An essential amino acid. It is often added to animal feed.
Addition of methyl groups. In histo-chemistry methylation is used to esterify carboxyl groups and remove sulfate groups by treating tissue sections with hot methanol in the presence of hydrochloric acid. (From Stedman, 25th ed)
Small chromosomal proteins (approx 12-20 kD) possessing an open, unfolded structure and attached to the DNA in cell nuclei by ionic linkages. Classification into the various types (designated histone I, histone II, etc.) is based on the relative amounts of arginine and lysine in each.
Formation of an acetyl derivative. (Stedman, 25th ed)
The order of amino acids as they occur in a polypeptide chain. This is referred to as the primary structure of proteins. It is of fundamental importance in determining PROTEIN CONFORMATION.
Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories.
Organic compounds that generally contain an amino (-NH2) and a carboxyl (-COOH) group. Twenty alpha-amino acids are the subunits which are polymerized to form proteins.
A metabolite in the principal biochemical pathway of lysine. It antagonizes neuroexcitatory activity modulated by the glutamate receptor, N-METHYL-D-ASPARTATE; (NMDA).
Amine oxidoreductases that use either NAD+ (EC 1.5.1.7) or NADP+ (EC 1.5.1.8) as an acceptor to form L-LYSINE or NAD+ (EC 1.5.1.9) or NADP+ (EC 1.5.1.10) as an acceptor to form L-GLUTAMATE. Deficiency of this enzyme causes HYPERLYSINEMIAS.
An essential amino acid that is physiologically active in the L-form.
The parts of a macromolecule that directly participate in its specific combination with another molecule.
Enzymes that catalyse the removal of methyl groups from LYSINE or ARGININE residues found on HISTONES. Many histone demethylases generally function through an oxidoreductive mechanism.
The process in which substances, either endogenous or exogenous, bind to proteins, peptides, enzymes, protein precursors, or allied compounds. Specific protein-binding measures are often used as assays in diagnostic assessments.
Any of various enzymatically catalyzed post-translational modifications of PEPTIDES or PROTEINS in the cell of origin. These modifications include carboxylation; HYDROXYLATION; ACETYLATION; PHOSPHORYLATION; METHYLATION; GLYCOSYLATION; ubiquitination; oxidation; proteolysis; and crosslinking and result in changes in molecular weight and electrophoretic motility.
Enzymes that catalyze the methylation of amino acids after their incorporation into a polypeptide chain. S-Adenosyl-L-methionine acts as the methylating agent. EC 2.1.1.
Any detectable and heritable change in the genetic material that causes a change in the GENOTYPE and which is transmitted to daughter cells and to succeeding generations.
Compounds used extensively as acetylation, oxidation and dehydrating agents and in the modification of proteins and enzymes.
Genetically engineered MUTAGENESIS at a specific site in the DNA molecule that introduces a base substitution, or an insertion or deletion.
Any of various animals that constitute the family Suidae and comprise stout-bodied, short-legged omnivorous mammals with thick skin, usually covered with coarse bristles, a rather long mobile snout, and small tail. Included are the genera Babyrousa, Phacochoerus (wart hogs), and Sus, the latter containing the domestic pig (see SUS SCROFA).
The amounts of various substances in food needed by an organism to sustain healthy life.
The rate dynamics in chemical or physical systems.
Models used experimentally or theoretically to study molecular shape, electronic properties, or interactions; includes analogous molecules, computer-generated graphics, and mechanical structures.
The act of ligating UBIQUITINS to PROTEINS to form ubiquitin-protein ligase complexes to label proteins for transport to the PROTEASOME ENDOPEPTIDASE COMPLEX where proteolysis occurs.
The level of protein structure in which combinations of secondary protein structures (alpha helices, beta sheets, loop regions, and motifs) pack together to form folded shapes called domains. Disulfide bridges between cysteines in two different parts of the polypeptide chain along with other interactions between the chains play a role in the formation and stabilization of tertiary structure. Small proteins usually consist of only one domain but larger proteins may contain a number of domains connected by segments of polypeptide chain which lack regular secondary structure.
Enzymes that catalyze acyl group transfer from ACETYL-CoA to HISTONES forming CoA and acetyl-histones.
A family of histone demethylases that share a conserved Jumonji C domain. The enzymes function via an iron-dependent dioxygenase mechanism that couples the conversion of 2-oxoglutarate to succinate to the hydroxylation of N-methyl groups.
The material of CHROMOSOMES. It is a complex of DNA; HISTONES; and nonhistone proteins (CHROMOSOMAL PROTEINS, NON-HISTONE) found within the nucleus of a cell.
Foodstuff used especially for domestic and laboratory animals, or livestock.
This is the active form of VITAMIN B 6 serving as a coenzyme for synthesis of amino acids, neurotransmitters (serotonin, norepinephrine), sphingolipids, aminolevulinic acid. During transamination of amino acids, pyridoxal phosphate is transiently converted into pyridoxamine phosphate (PYRIDOXAMINE).
Proteins obtained from foods. They are the main source of the ESSENTIAL AMINO ACIDS.
A family of histone acetyltransferases that is structurally-related to CREB-BINDING PROTEIN and to E1A-ASSOCIATED P300 PROTEIN. They function as transcriptional coactivators by bridging between DNA-binding TRANSCRIPTION FACTORS and the basal transcription machinery. They also modify transcription factors and CHROMATIN through ACETYLATION.
'Homoarginine' is a non-proteinogenic amino acid, meaning it is not used in the formation of proteins, and is primarily found in small quantities in certain foods and synthesized in the human body from the amino acid lysine.
A highly conserved 76-amino acid peptide universally found in eukaryotic cells that functions as a marker for intracellular PROTEIN TRANSPORT and degradation. Ubiquitin becomes activated through a series of complicated steps and forms an isopeptide bond to lysine residues of specific proteins within the cell. These "ubiquitinated" proteins can be recognized and degraded by proteosomes or be transported to specific compartments within the cell.
The characteristic 3-dimensional shape of a protein, including the secondary, supersecondary (motifs), tertiary (domains) and quaternary structure of the peptide chain. PROTEIN STRUCTURE, QUATERNARY describes the conformation assumed by multimeric proteins (aggregates of more than one polypeptide chain).
A characteristic feature of enzyme activity in relation to the kind of substrate on which the enzyme or catalytic molecule reacts.
A species of gram-negative, facultatively anaerobic, rod-shaped bacteria (GRAM-NEGATIVE FACULTATIVELY ANAEROBIC RODS) commonly found in the lower part of the intestine of warm-blooded animals. It is usually nonpathogenic, but some strains are known to produce DIARRHEA and pyogenic infections. Pathogenic strains (virotypes) are classified by their specific pathogenic mechanisms such as toxins (ENTEROTOXIGENIC ESCHERICHIA COLI), etc.
A foul-smelling diamine formed by bacterial decarboxylation of lysine.
The naturally occurring or experimentally induced replacement of one or more AMINO ACIDS in a protein with another. If a functionally equivalent amino acid is substituted, the protein may retain wild-type activity. Substitution may also diminish, enhance, or eliminate protein function. Experimentally induced substitution is often used to study enzyme activities and binding site properties.
Amino acids that are not synthesized by the human body in amounts sufficient to carry out physiological functions. They are obtained from dietary foodstuffs.
The sequence of PURINES and PYRIMIDINES in nucleic acids and polynucleotides. It is also called nucleotide sequence.
Members of the class of compounds composed of AMINO ACIDS joined together by peptide bonds between adjacent amino acids into linear, branched or cyclical structures. OLIGOPEPTIDES are composed of approximately 2-12 amino acids. Polypeptides are composed of approximately 13 or more amino acids. PROTEINS are linear polypeptides that are normally synthesized on RIBOSOMES.
A subclass of enzymes of the transferase class that catalyze the transfer of a methyl group from one compound to another. (Dorland, 28th ed) EC 2.1.1.
The relationship between the chemical structure of a compound and its biological or pharmacological activity. Compounds are often classed together because they have structural characteristics in common including shape, size, stereochemical arrangement, and distribution of functional groups.
Enzymes that catalyze the addition of a carboxyl group to a compound (carboxylases) or the removal of a carboxyl group from a compound (decarboxylases). EC 4.1.1.
An oligomer formed from the repetitive linking of the C-terminal glycine of one UBIQUITIN molecule via an isopeptide bond to a lysine residue on a second ubiquitin molecule. It is structurally distinct from UBIQUITIN C, which is a single protein containing a tandemly arrayed ubiquitin peptide sequence.
An enzyme that catalyzes the formation of beta-aspartyl phosphate from aspartic acid and ATP. Threonine serves as an allosteric regulator of this enzyme to control the biosynthetic pathway from aspartic acid to threonine. EC 2.7.2.4.
A genetic process by which the adult organism is realized via mechanisms that lead to the restriction in the possible fates of cells, eventually leading to their differentiated state. Mechanisms involved cause heritable changes to cells without changes to DNA sequence such as DNA METHYLATION; HISTONE modification; DNA REPLICATION TIMING; NUCLEOSOME positioning; and heterochromatization which result in selective gene expression or repression.
An amino acid produced in the urea cycle by the splitting off of urea from arginine.
The degree of similarity between sequences of amino acids. This information is useful for the analyzing genetic relatedness of proteins and species.
Derivatives of adipic acid. Included under this heading are a broad variety of acid forms, salts, esters, and amides that contain a 1,6-carboxy terminated aliphatic structure.
A 1.5-kDa small ubiquitin-related modifier protein that can covalently bind via an isopeptide link to a number of cellular proteins. It may play a role in intracellular protein transport and a number of other cellular processes.

Lysine deficiency alters diet selection without depressing food intake in rats. (1/9069)

Under states of protein deficiency, the dietary limiting amino acid, rather than protein content, can act as the dietary stimulus to control diet selection. If fact, threonine-deficient rats will alter their diet selection patterns solely on the basis of very small changes (0.009 g/100 g) in the dietary threonine concentration. In these studies, we assessed whether lysine-deficient rats will also alter their diet selection patterns on the basis of small changes in dietary Lys concentration. In all experiments, growing rats were adapted to diets in which the protein fraction (purified amino acids or wheat gluten) was limiting in Lys. They were then given a choice between the adaptation diet (AD) diet and a slightly more deficient diet. Rats that were adapted to a Lys-deficient diet (0.25 g Lys/100 g) selected their AD over diets containing as little as 0.01% less Lys (P < 0.01) within 5 d. To determine how deficient rats must be before they alter their selection patterns, rats were adapted to diets containing various levels of Lys, i.e., 2 levels below the requirement for growth and 2 levels above the requirement for growth, but below the requirement for maximal nitrogen retention. Only rats adapted to diets containing Lys below their requirement for growth selected their AD over a diet containing 0.05% less Lys (P < 0.005). Finally, to determine whether rats will alter their selection to whole protein-based diets, rats were adapted to 25% wheat gluten diets supplemented with 0.03-0.21% Lys. Rats selected the AD over a diet containing as little as 0.09% less supplemental Lys by d 4 of the trial (P < 0.05). We conclude that rats are sensitive to changes as small as 0.01% in dietary Lys concentration, but that sensitivity requires prior adaptation to Lys-deficient diets.  (+info)

Expanded lysine acetylation specificity of Gcn5 in native complexes. (2/9069)

The coactivator/adaptor protein Gcn5 is a conserved histone acetyltransferase, which functions as the catalytic subunit in multiple yeast transcriptional regulatory complexes. The ability of Gcn5 to acetylate nucleosomal histones is significantly reduced relative to its activity on free histones, where it predominantly modifies histone H3 at lysine 14. However, the association of Gcn5 in multisubunit complexes potentiates its nucleosomal histone acetyltransferase activity. Here, we show that the association of Gcn5 with other proteins in two native yeast complexes, Ada and SAGA (Spt-Ada-Gcn5-acetyltransferase), directly confers upon Gcn5 the ability to acetylate an expanded set of lysines on H3. Furthermore Ada and SAGA have overlapping, yet distinct, patterns of acetylation, suggesting that the association of specific subunits determines site specificity.  (+info)

Control of ketogenesis from amino acids. IV. Tissue specificity in oxidation of leucine, tyrosine, and lysine. (3/9069)

In vitro and in vivo studies were made on the tissue specificity of oxidation of the ketogenic amino acids, leucine, tyrosine, and lysine. In in vitro studies the abilities of slices of various tissues of rats to form 14CO2 from 14C-amino acids were examined. With liver, but not kidney slices, addition of alpha-ketoglutarate was required for the maximum activities with these amino acids. Among the various tissues tested, kidney had the highest activity for lysine oxidation, followed by liver; other tissues showed very low activity. Kidney also had the highest activity for leucine oxidation, followed by diaphragm; liver and adipose tissue had lower activities. Liver had the highest activity for tyrosine oxidation, but kidney also showed considerable activity; other tissues had negligible activity. In in vivo studies the blood flow through the liver or kidney was stopped by ligation of the blood vessels. Then labeled amino acids were injected and recovery of radioactivity in respiratory 14CO2 was measured. In contrast to results with slices, no difference was found in the respiratory 14CO2 when the renal blood vessels were or were not ligated. On the contrary ligation of the hepatic vessels suppressed the oxidations of lysine and tyrosine completely and that of leucine partially. Thus in vivo, lysine and tyrosine seem to be metabolized mainly in the liver, whereas leucine is metabolized mostly in extrahepatic tissues and partly in liver. Use of tissue slices seems to be of only limited value in elucidating the metabolisms of these amino acids.  (+info)

Actions of a pair of identified cerebral-buccal interneurons (CBI-8/9) in Aplysia that contain the peptide myomodulin. (4/9069)

A combination of biocytin back-fills of the cerebral-buccal connectives and immunocytochemistry of the cerebral ganglion demonstrated that of the 13 bilateral pairs of cerebral-buccal interneurons in the cerebral ganglion, a subpopulation of 3 are immunopositive for the peptide myomodulin. The present paper describes the properties of two of these cells, which we have termed CBI-8 and CBI-9. CBI-8 and CBI-9 were found to be dye coupled and electrically coupled. The cells have virtually identical properties, and consequently we consider them to be "twin" pairs and refer to them as CBI-8/9. CBI-8/9 were identified by electrophysiological criteria and then labeled with dye. Labeled cells were found to be immunopositive for myomodulin, and, using high pressure liquid chromatography, the cells were shown to contain authentic myomodulin. CBI-8/9 were found to receive synaptic input after mechanical stimulation of the tentacles. They also received excitatory input from C-PR, a neuron involved in neck lengthening, and received a slow inhibitory input from CC5, a cell involved in neck shortening, suggesting that CBI-8/9 may be active during forward movements of the head or buccal mass. Firing of CBI-8 or CBI-9 resulted in the activation of a relatively small number of buccal neurons as evidenced by extracellular recordings from buccal nerves. Firing also produced local movements of the buccal mass, in particular a strong contraction of the I7 muscle, which mediates radula opening. CBI-8/9 were found to produce a slow depolarization and rhythmic activity of B48, the motor neuron for the I7 muscle. The data provide continuing evidence that the small population of cerebral buccal interneurons is composed of neurons that are highly diverse in their functional roles. CBI-8/9 may function as a type of premotor neuron, or perhaps as a peptidergic modulatory neuron, the functions of which are dependent on the coactivity of other neurons.  (+info)

pKa calculations for class A beta-lactamases: influence of substrate binding. (5/9069)

Beta-Lactamases are responsible for bacterial resistance to beta-lactams and are thus of major clinical importance. However, the identity of the general base involved in their mechanism of action is still unclear. Two candidate residues, Glu166 and Lys73, have been proposed to fulfill this role. Previous studies support the proposal that Glu166 acts during the deacylation, but there is no consensus on the possible role of this residue in the acylation step. Recent experimental data and theoretical considerations indicate that Lys73 is protonated in the free beta-lactamases, showing that this residue is unlikely to act as a proton abstractor. On the other hand, it has been proposed that the pKa of Lys73 would be dramatically reduced upon substrate binding and would thus be able to act as a base. To check this hypothesis, we performed continuum electrostatic calculations for five wild-type and three beta-lactamase mutants to estimate the pKa of Lys73 in the presence of substrates, both in the Henri-Michaelis complex and in the tetrahedral intermediate. In all cases, the pKa of Lys73 was computed to be above 10, showing that it is unlikely to act as a proton abstractor, even when a beta-lactam substrate is bound in the enzyme active site. The pKa of Lys234 is also raised in the tetrahedral intermediate, thus confirming a probable role of this residue in the stabilization of the tetrahedral intermediate. The influence of the beta-lactam carboxylate on the pKa values of the active-site lysines is also discussed.  (+info)

Characterisation of the conformational and quaternary structure-dependent heparin-binding region of bovine seminal plasma protein PDC-109. (6/9069)

PDC-109, the major heparin-binding protein of bull seminal plasma, binds to sperm choline lipids at ejaculation and modulates capacitation mediated by heparin. Affinity chromatography on heparin-Sepharose showed that polydisperse, but not monomeric, PDC-109 displayed heparin-binding capability. We sought to characterise the surface topology of the quaternary structure-dependent heparin-binding region of PDC-109 by comparing the arginine- and lysine-selective chemical modification patterns of the free and the heparin-bound protein. A combination of reversed-phase peptide mapping of endoproteinase Lys-C-digested PDC-109 derivatives and mass spectrometry was employed to identify modified and heparin-protected residues. PDC-109 contains two tandemly arranged fibronectin type II domains (a, Cys24-Cys61; b, Cys69-Cys109). The results show that six basic residues (Lys34, Arg57, Lys59, Arg64, Lys68, and Arg104) were shielded from reaction with acetic anhydride and 1,2-cyclohexanedione in heparin-bound PDC-109 oligomers. In the 1H-NMR solution structures of single fibronectin type II domains, residues topologically equivalent to PDC-109 Arg57 (Arg104) and Lys59 lay around beta-strand D on the same face of the domain. In full-length PDC-109, Arg64 and Lys68 are both located in the intervening polypeptide between domains a and b. Our data suggest possible quaternary structure arrangements of PDC-109 molecules to form a heparin-binding oligomer.  (+info)

Role of a conserved lysine residue in the peripheral cannabinoid receptor (CB2): evidence for subtype specificity. (7/9069)

The human cannabinoid receptors, central cannabinoid receptor (CB1) and peripheral cannabinoid receptor (CB2), share only 44% amino acid identity overall, yet most ligands do not discriminate between receptor subtypes. Site-directed mutagenesis was employed as a means of mapping the ligand recognition site for the human CB2 cannabinoid receptor. A lysine residue in the third transmembrane domain of the CB2 receptor (K109), which is conserved between the CB1 and CB2 receptors, was mutated to alanine or arginine to determine the role of this charged amino acid in receptor function. The analogous mutation in the CB1 receptor (K192A) was found to be crucial for recognition of several cannabinoid compounds excluding (R)-(+)-[2, 3-dihydro-5-methyl-3-[(4-morpholinyl)methyl]pyrrolo[1,2,3-de]-1, 4-benzoxazin-6-yl](1-naphthalenyl)methanone (WIN 55,212-2). In contrast, in human embryonic kidney (HEK)-293 cells expressing the mutant or wild-type CB2 receptors, we found no significant differences in either the binding profile of several cannabinoid ligands nor in inhibition of cAMP accumulation. We identified a high-affinity site for (-)-3-[2-hydroxyl-4-(1, 1-dimethylheptyl)phenyl]-4-[3-hydroxyl propyl] cyclohexan-1-ol (CP-55,940) in the region of helices 3, 6, and 7, with S3.31(112), T3.35(116), and N7.49(295) in the K109A mutant using molecular modeling. The serine residue, unique to the CB2 receptor, was then mutated to glycine in the K109A mutant. This double mutant, K109AS112G, retains the ability to bind aminoalkylindoles but loses affinity for classical cannabinoids, as predicted by the molecular model. Distinct cellular localization of the mutant receptors observed with immunofluorescence also suggests differences in receptor function. In summary, we identified amino acid residues in the CB2 receptor that could lead to subtype specificity.  (+info)

Passive electrotonic properties of rat hippocampal CA3 interneurones. (8/9069)

1. The linear membrane responses of CA3 interneurones were determined with the use of whole-cell patch recording methods. The mean input resistance (RN) for all cells in this study was 526 +/- 16 MOmega and the slowest membrane time constant (tau0) was 73 +/- 3 ms. 2. The three-dimensional morphology of 63 biocytin-labelled neurones was used to construct compartmental models. Specific membrane resistivity (Rm) and specific membrane capacitance (Cm) were estimated by fitting the linear membrane response. Acceptable fits were obtained for 24 CA3 interneurones. The mean Rm was 61.9 +/- 34.2 Omega cm2 and the mean Cm was 0.9 +/- 0.3 microF cm-2. Intracellular resistance (Ri) could not be resolved in this study. 3. Examination of voltage attenuation revealed a significantly low synaptic efficiency from most dendritic synaptic input locations to the soma. 4. Simulations of excitatory postsynaptic potentials (EPSPs) were analysed at both the site of synaptic input and at the soma. There was little variability in the depolarization at the soma from synaptic inputs placed at different locations along the dendritic tree. The EPSP amplitude at the site of synaptic input was progressively larger with distance from the soma, consistent with a progressive increase in input impedance. 5. The 'iso-efficiency' of spatially different synaptic inputs arose from two opposing factors: an increase in EPSP amplitude at the synapse with distance from the soma was opposed by a nearly equivalent increase in voltage attenuation. These simulations suggest that, in these particular neurones, the amplitude of EPSPs measured at the soma will not be significantly affected by the location of synaptic inputs.  (+info)

Lysine is an essential amino acid, which means that it cannot be synthesized by the human body and must be obtained through the diet. Its chemical formula is (2S)-2,6-diaminohexanoic acid. Lysine is necessary for the growth and maintenance of tissues in the body, and it plays a crucial role in the production of enzymes, hormones, and antibodies. It is also essential for the absorption of calcium and the formation of collagen, which is an important component of bones and connective tissue. Foods that are good sources of lysine include meat, poultry, fish, eggs, and dairy products.

Methylation, in the context of genetics and epigenetics, refers to the addition of a methyl group (CH3) to a molecule, usually to the nitrogenous base of DNA or to the side chain of amino acids in proteins. In DNA methylation, this process typically occurs at the 5-carbon position of cytosine residues that precede guanine residues (CpG sites) and is catalyzed by enzymes called DNA methyltransferases (DNMTs).

DNA methylation plays a crucial role in regulating gene expression, genomic imprinting, X-chromosome inactivation, and suppression of repetitive elements. Hypermethylation or hypomethylation of specific genes can lead to altered gene expression patterns, which have been associated with various human diseases, including cancer.

In summary, methylation is a fundamental epigenetic modification that influences genomic stability, gene regulation, and cellular function by introducing methyl groups to DNA or proteins.

Histones are highly alkaline proteins found in the chromatin of eukaryotic cells. They are rich in basic amino acid residues, such as arginine and lysine, which give them their positive charge. Histones play a crucial role in packaging DNA into a more compact structure within the nucleus by forming a complex with it called a nucleosome. Each nucleosome contains about 146 base pairs of DNA wrapped around an octamer of eight histone proteins (two each of H2A, H2B, H3, and H4). The N-terminal tails of these histones are subject to various post-translational modifications, such as methylation, acetylation, and phosphorylation, which can influence chromatin structure and gene expression. Histone variants also exist, which can contribute to the regulation of specific genes and other nuclear processes.

Acetylation is a chemical process that involves the addition of an acetyl group (-COCH3) to a molecule. In the context of medical biochemistry, acetylation often refers to the post-translational modification of proteins, where an acetyl group is added to the amino group of a lysine residue in a protein by an enzyme called acetyltransferase. This modification can alter the function or stability of the protein and plays a crucial role in regulating various cellular processes such as gene expression, DNA repair, and cell signaling. Acetylation can also occur on other types of molecules, including lipids and carbohydrates, and has important implications for drug metabolism and toxicity.

An amino acid sequence is the specific order of amino acids in a protein or peptide molecule, formed by the linking of the amino group (-NH2) of one amino acid to the carboxyl group (-COOH) of another amino acid through a peptide bond. The sequence is determined by the genetic code and is unique to each type of protein or peptide. It plays a crucial role in determining the three-dimensional structure and function of proteins.

Molecular sequence data refers to the specific arrangement of molecules, most commonly nucleotides in DNA or RNA, or amino acids in proteins, that make up a biological macromolecule. This data is generated through laboratory techniques such as sequencing, and provides information about the exact order of the constituent molecules. This data is crucial in various fields of biology, including genetics, evolution, and molecular biology, allowing for comparisons between different organisms, identification of genetic variations, and studies of gene function and regulation.

Amino acids are organic compounds that serve as the building blocks of proteins. They consist of a central carbon atom, also known as the alpha carbon, which is bonded to an amino group (-NH2), a carboxyl group (-COOH), a hydrogen atom (H), and a variable side chain (R group). The R group can be composed of various combinations of atoms such as hydrogen, oxygen, sulfur, nitrogen, and carbon, which determine the unique properties of each amino acid.

There are 20 standard amino acids that are encoded by the genetic code and incorporated into proteins during translation. These include:

1. Alanine (Ala)
2. Arginine (Arg)
3. Asparagine (Asn)
4. Aspartic acid (Asp)
5. Cysteine (Cys)
6. Glutamine (Gln)
7. Glutamic acid (Glu)
8. Glycine (Gly)
9. Histidine (His)
10. Isoleucine (Ile)
11. Leucine (Leu)
12. Lysine (Lys)
13. Methionine (Met)
14. Phenylalanine (Phe)
15. Proline (Pro)
16. Serine (Ser)
17. Threonine (Thr)
18. Tryptophan (Trp)
19. Tyrosine (Tyr)
20. Valine (Val)

Additionally, there are several non-standard or modified amino acids that can be incorporated into proteins through post-translational modifications, such as hydroxylation, methylation, and phosphorylation. These modifications expand the functional diversity of proteins and play crucial roles in various cellular processes.

Amino acids are essential for numerous biological functions, including protein synthesis, enzyme catalysis, neurotransmitter production, energy metabolism, and immune response regulation. Some amino acids can be synthesized by the human body (non-essential), while others must be obtained through dietary sources (essential).

2-Aminoadipic acid (2-AAA) is a type of amino acid that is formed as a byproduct of the metabolism of lysine, which is an essential amino acid. It is not commonly considered a building block of proteins, but it does play a role in various biochemical pathways in the body.

Abnormally high levels of 2-AAA have been found in certain medical conditions, such as genetic disorders of lysine metabolism and in some neurodegenerative diseases like multiple sclerosis and Alzheimer's disease. However, it is not currently clear whether elevated levels of 2-AAA are a cause or a consequence of these conditions.

Research is ongoing to better understand the role of 2-AAA in human health and disease.

Saccharopine dehydrogenases are enzymes involved in the metabolism of the amino acid lysine. These enzymes catalyze the conversion of saccharopine, an intermediate compound in the lysine degradation pathway, into α-aminoadipic semialdehyde and glutamate. Saccharopine dehydrogenases play a crucial role in maintaining the balance of amino acids in the body and are found in various organisms, including bacteria, plants, and animals. In humans, mutations in the gene encoding one form of saccharopine dehydrogenase (Lysine Ketoglutarate Reductase/Saccharopine Dehydrogenase) have been associated with a rare genetic disorder called saccharopinuria, which is characterized by elevated levels of saccharopine in the urine and neurological symptoms.

Arginine is an α-amino acid that is classified as a semi-essential or conditionally essential amino acid, depending on the developmental stage and health status of the individual. The adult human body can normally synthesize sufficient amounts of arginine to meet its needs, but there are certain circumstances, such as periods of rapid growth or injury, where the dietary intake of arginine may become necessary.

The chemical formula for arginine is C6H14N4O2. It has a molecular weight of 174.20 g/mol and a pKa value of 12.48. Arginine is a basic amino acid, which means that it contains a side chain with a positive charge at physiological pH levels. The side chain of arginine is composed of a guanidino group, which is a functional group consisting of a nitrogen atom bonded to three methyl groups.

In the body, arginine plays several important roles. It is a precursor for the synthesis of nitric oxide, a molecule that helps regulate blood flow and immune function. Arginine is also involved in the detoxification of ammonia, a waste product produced by the breakdown of proteins. Additionally, arginine can be converted into other amino acids, such as ornithine and citrulline, which are involved in various metabolic processes.

Foods that are good sources of arginine include meat, poultry, fish, dairy products, nuts, seeds, and legumes. Arginine supplements are available and may be used for a variety of purposes, such as improving exercise performance, enhancing wound healing, and boosting immune function. However, it is important to consult with a healthcare provider before taking arginine supplements, as they can interact with certain medications and have potential side effects.

In the context of medical and biological sciences, a "binding site" refers to a specific location on a protein, molecule, or cell where another molecule can attach or bind. This binding interaction can lead to various functional changes in the original protein or molecule. The other molecule that binds to the binding site is often referred to as a ligand, which can be a small molecule, ion, or even another protein.

The binding between a ligand and its target binding site can be specific and selective, meaning that only certain ligands can bind to particular binding sites with high affinity. This specificity plays a crucial role in various biological processes, such as signal transduction, enzyme catalysis, or drug action.

In the case of drug development, understanding the location and properties of binding sites on target proteins is essential for designing drugs that can selectively bind to these sites and modulate protein function. This knowledge can help create more effective and safer therapeutic options for various diseases.

Histone demethylases are enzymes that remove methyl groups from histone proteins, which are the structural components around which DNA is wound in chromosomes. These enzymes play a crucial role in regulating gene expression by modifying the chromatin structure and influencing the accessibility of DNA to transcription factors and other regulatory proteins.

Histones can be methylated at various residues, including lysine and arginine residues, and different histone demethylases specifically target these modified residues. Histone demethylases are classified into two main categories based on their mechanisms of action:

1. Lysine-specific demethylases (LSDs): These enzymes belong to the flavin adenine dinucleotide (FAD)-dependent amine oxidase family and specifically remove methyl groups from lysine residues. They target mono- and di-methylated lysines but cannot act on tri-methylated lysines.
2. Jumonji C (JmjC) domain-containing histone demethylases: These enzymes utilize Fe(II) and α-ketoglutarate as cofactors to hydroxylate methyl groups on lysine residues, leading to their removal. JmjC domain-containing histone demethylases can target all three states of lysine methylation (mono-, di-, and tri-methylated).

Dysregulation of histone demethylases has been implicated in various human diseases, including cancer, neurological disorders, and cardiovascular diseases. Therefore, understanding the functions and regulation of these enzymes is essential for developing novel therapeutic strategies to target these conditions.

Protein binding, in the context of medical and biological sciences, refers to the interaction between a protein and another molecule (known as the ligand) that results in a stable complex. This process is often reversible and can be influenced by various factors such as pH, temperature, and concentration of the involved molecules.

In clinical chemistry, protein binding is particularly important when it comes to drugs, as many of them bind to proteins (especially albumin) in the bloodstream. The degree of protein binding can affect a drug's distribution, metabolism, and excretion, which in turn influence its therapeutic effectiveness and potential side effects.

Protein-bound drugs may be less available for interaction with their target tissues, as only the unbound or "free" fraction of the drug is active. Therefore, understanding protein binding can help optimize dosing regimens and minimize adverse reactions.

Post-translational protein processing refers to the modifications and changes that proteins undergo after their synthesis on ribosomes, which are complex molecular machines responsible for protein synthesis. These modifications occur through various biochemical processes and play a crucial role in determining the final structure, function, and stability of the protein.

The process begins with the translation of messenger RNA (mRNA) into a linear polypeptide chain, which is then subjected to several post-translational modifications. These modifications can include:

1. Proteolytic cleavage: The removal of specific segments or domains from the polypeptide chain by proteases, resulting in the formation of mature, functional protein subunits.
2. Chemical modifications: Addition or modification of chemical groups to the side chains of amino acids, such as phosphorylation (addition of a phosphate group), glycosylation (addition of sugar moieties), methylation (addition of a methyl group), acetylation (addition of an acetyl group), and ubiquitination (addition of a ubiquitin protein).
3. Disulfide bond formation: The oxidation of specific cysteine residues within the polypeptide chain, leading to the formation of disulfide bonds between them. This process helps stabilize the three-dimensional structure of proteins, particularly in extracellular environments.
4. Folding and assembly: The acquisition of a specific three-dimensional conformation by the polypeptide chain, which is essential for its function. Chaperone proteins assist in this process to ensure proper folding and prevent aggregation.
5. Protein targeting: The directed transport of proteins to their appropriate cellular locations, such as the nucleus, mitochondria, endoplasmic reticulum, or plasma membrane. This is often facilitated by specific signal sequences within the protein that are recognized and bound by transport machinery.

Collectively, these post-translational modifications contribute to the functional diversity of proteins in living organisms, allowing them to perform a wide range of cellular processes, including signaling, catalysis, regulation, and structural support.

Protein methyltransferases (PMTs) are a family of enzymes that transfer methyl groups from a donor, such as S-adenosylmethionine (SAM), to specific residues on protein substrates. This post-translational modification plays a crucial role in various cellular processes, including epigenetic regulation, signal transduction, and protein stability.

PMTs can methylate different amino acid residues, such as lysine, arginine, and histidine, on proteins. The methylation of these residues can lead to changes in the charge, hydrophobicity, or interaction properties of the target protein, thereby modulating its function.

For example, lysine methyltransferases (KMTs) are a subclass of PMTs that specifically methylate lysine residues on histone proteins, which are the core components of nucleosomes in chromatin. Histone methylation can either activate or repress gene transcription, depending on the specific residue and degree of methylation.

Protein arginine methyltransferases (PRMTs) are another subclass of PMTs that methylate arginine residues on various protein substrates, including histones, transcription factors, and RNA-binding proteins. Arginine methylation can also affect protein function by altering its interaction with other molecules or modulating its stability.

Overall, protein methyltransferases are essential regulators of cellular processes and have been implicated in various diseases, including cancer, neurodegenerative disorders, and cardiovascular diseases. Therefore, understanding the mechanisms and functions of PMTs is crucial for developing novel therapeutic strategies to target these diseases.

A mutation is a permanent change in the DNA sequence of an organism's genome. Mutations can occur spontaneously or be caused by environmental factors such as exposure to radiation, chemicals, or viruses. They may have various effects on the organism, ranging from benign to harmful, depending on where they occur and whether they alter the function of essential proteins. In some cases, mutations can increase an individual's susceptibility to certain diseases or disorders, while in others, they may confer a survival advantage. Mutations are the driving force behind evolution, as they introduce new genetic variability into populations, which can then be acted upon by natural selection.

Acetic anhydride is a chemical compound with the formula (CH3CO)2O. It is a colorless liquid that is used as a reagent in organic synthesis, particularly in the production of cellulose acetate and other acetate esters. Acetic anhydride is also an important intermediate in the synthesis of certain pharmaceuticals and dyes.

In medical terminology, acetic anhydride is not typically used as a diagnostic or therapeutic agent. However, it can be used in laboratory settings to synthesize compounds that may have medical applications. For example, acetic anhydride has been used to produce certain antiviral drugs and antibiotics.

It is important to note that acetic anhydride can be harmful or fatal if swallowed, inhaled, or absorbed through the skin. It can cause burns and eye damage, and may be harmful to the respiratory system if inhaled. Therefore, it should be handled with care and used only in well-ventilated areas with appropriate personal protective equipment.

Site-directed mutagenesis is a molecular biology technique used to introduce specific and targeted changes to a specific DNA sequence. This process involves creating a new variant of a gene or a specific region of interest within a DNA molecule by introducing a planned, deliberate change, or mutation, at a predetermined site within the DNA sequence.

The methodology typically involves the use of molecular tools such as PCR (polymerase chain reaction), restriction enzymes, and/or ligases to introduce the desired mutation(s) into a plasmid or other vector containing the target DNA sequence. The resulting modified DNA molecule can then be used to transform host cells, allowing for the production of large quantities of the mutated gene or protein for further study.

Site-directed mutagenesis is a valuable tool in basic research, drug discovery, and biotechnology applications where specific changes to a DNA sequence are required to understand gene function, investigate protein structure/function relationships, or engineer novel biological properties into existing genes or proteins.

"Swine" is a common term used to refer to even-toed ungulates of the family Suidae, including domestic pigs and wild boars. However, in a medical context, "swine" often appears in the phrase "swine flu," which is a strain of influenza virus that typically infects pigs but can also cause illness in humans. The 2009 H1N1 pandemic was caused by a new strain of swine-origin influenza A virus, which was commonly referred to as "swine flu." It's important to note that this virus is not transmitted through eating cooked pork products; it spreads from person to person, mainly through respiratory droplets produced when an infected person coughs or sneezes.

Nutritional requirements refer to the necessary amount of nutrients, including macronutrients (carbohydrates, proteins, and fats) and micronutrients (vitamins and minerals), that an individual requires to maintain good health, support normal growth and development, and promote optimal bodily functions. These requirements vary based on factors such as age, sex, body size, pregnancy status, and physical activity level. Meeting one's nutritional requirements typically involves consuming a balanced and varied diet, with additional consideration given to any specific dietary restrictions or medical conditions that may influence nutrient needs.

In the context of medicine and pharmacology, "kinetics" refers to the study of how a drug moves throughout the body, including its absorption, distribution, metabolism, and excretion (often abbreviated as ADME). This field is called "pharmacokinetics."

1. Absorption: This is the process of a drug moving from its site of administration into the bloodstream. Factors such as the route of administration (e.g., oral, intravenous, etc.), formulation, and individual physiological differences can affect absorption.

2. Distribution: Once a drug is in the bloodstream, it gets distributed throughout the body to various tissues and organs. This process is influenced by factors like blood flow, protein binding, and lipid solubility of the drug.

3. Metabolism: Drugs are often chemically modified in the body, typically in the liver, through processes known as metabolism. These changes can lead to the formation of active or inactive metabolites, which may then be further distributed, excreted, or undergo additional metabolic transformations.

4. Excretion: This is the process by which drugs and their metabolites are eliminated from the body, primarily through the kidneys (urine) and the liver (bile).

Understanding the kinetics of a drug is crucial for determining its optimal dosing regimen, potential interactions with other medications or foods, and any necessary adjustments for special populations like pediatric or geriatric patients, or those with impaired renal or hepatic function.

Molecular models are three-dimensional representations of molecular structures that are used in the field of molecular biology and chemistry to visualize and understand the spatial arrangement of atoms and bonds within a molecule. These models can be physical or computer-generated and allow researchers to study the shape, size, and behavior of molecules, which is crucial for understanding their function and interactions with other molecules.

Physical molecular models are often made up of balls (representing atoms) connected by rods or sticks (representing bonds). These models can be constructed manually using materials such as plastic or wooden balls and rods, or they can be created using 3D printing technology.

Computer-generated molecular models, on the other hand, are created using specialized software that allows researchers to visualize and manipulate molecular structures in three dimensions. These models can be used to simulate molecular interactions, predict molecular behavior, and design new drugs or chemicals with specific properties. Overall, molecular models play a critical role in advancing our understanding of molecular structures and their functions.

Ubiquitination is a post-translational modification process in which a ubiquitin protein is covalently attached to a target protein. This process plays a crucial role in regulating various cellular functions, including protein degradation, DNA repair, and signal transduction. The addition of ubiquitin can lead to different outcomes depending on the number and location of ubiquitin molecules attached to the target protein. Monoubiquitination (the attachment of a single ubiquitin molecule) or multiubiquitination (the attachment of multiple ubiquitin molecules) can mark proteins for degradation by the 26S proteasome, while specific types of ubiquitination (e.g., K63-linked polyubiquitination) can serve as a signal for nonproteolytic functions such as endocytosis, autophagy, or DNA repair. Ubiquitination is a highly regulated process that involves the coordinated action of three enzymes: E1 ubiquitin-activating enzyme, E2 ubiquitin-conjugating enzyme, and E3 ubiquitin ligase. Dysregulation of ubiquitination has been implicated in various diseases, including cancer, neurodegenerative disorders, and inflammatory conditions.

Tertiary protein structure refers to the three-dimensional arrangement of all the elements (polypeptide chains) of a single protein molecule. It is the highest level of structural organization and results from interactions between various side chains (R groups) of the amino acids that make up the protein. These interactions, which include hydrogen bonds, ionic bonds, van der Waals forces, and disulfide bridges, give the protein its unique shape and stability, which in turn determines its function. The tertiary structure of a protein can be stabilized by various factors such as temperature, pH, and the presence of certain ions. Any changes in these factors can lead to denaturation, where the protein loses its tertiary structure and thus its function.

Histone Acetyltransferases (HATs) are a group of enzymes that play a crucial role in the regulation of gene expression. They function by adding acetyl groups to specific lysine residues on the N-terminal tails of histone proteins, which make up the structural core of nucleosomes - the fundamental units of chromatin.

The process of histone acetylation neutralizes the positive charge of lysine residues, reducing their attraction to the negatively charged DNA backbone. This leads to a more open and relaxed chromatin structure, facilitating the access of transcription factors and other regulatory proteins to the DNA, thereby promoting gene transcription.

HATs are classified into two main categories: type A HATs, which are primarily found in the nucleus and associated with transcriptional activation, and type B HATs, which are located in the cytoplasm and participate in chromatin assembly during DNA replication and repair. Dysregulation of HAT activity has been implicated in various human diseases, including cancer, neurodevelopmental disorders, and cardiovascular diseases.

Jumonji domain-containing histone demethylases (JHDMs) are a family of enzymes that are responsible for removing methyl groups from specific residues on histone proteins. These enzymes play crucial roles in the regulation of gene expression by modifying the chromatin structure and influencing the accessibility of transcription factors to DNA.

JHDMs contain a conserved Jumonji C (JmjC) domain, which is responsible for their demethylase activity. They are classified into two main groups based on the type of methyl group they remove: lysine-specific demethylases (KDMs) and arginine-specific demethylases (RDMs).

KDMs can be further divided into several subfamilies, including KDM2/7, KDM3, KDM4, KDM5, and KDM6, based on their substrate specificity and the number of methyl groups they remove. For example, KDM4 enzymes specifically demethylate di- and tri-methylated lysine 9 and lysine 36 residues on histone H3, while KDM5 enzymes target mono-, di-, and tri-methylated lysine 4 residues on histone H3.

RDMs, on the other hand, are responsible for demethylating arginine residues on histones, including symmetrically or asymmetrically dimethylated arginine 2, 8, 17, and 26 residues on histone H3 and H4.

Dysregulation of JHDMs has been implicated in various human diseases, including cancer, neurological disorders, and cardiovascular diseases. Therefore, understanding the functions and regulation of JHDMs is essential for developing novel therapeutic strategies to treat these diseases.

Chromatin is the complex of DNA, RNA, and proteins that make up the chromosomes in the nucleus of a cell. It is responsible for packaging the long DNA molecules into a more compact form that fits within the nucleus. Chromatin is made up of repeating units called nucleosomes, which consist of a histone protein octamer wrapped tightly by DNA. The structure of chromatin can be altered through chemical modifications to the histone proteins and DNA, which can influence gene expression and other cellular processes.

Animal feed refers to any substance or mixture of substances, whether processed, unprocessed, or partially processed, which is intended to be used as food for animals, including fish, without further processing. It includes ingredients such as grains, hay, straw, oilseed meals, and by-products from the milling, processing, and manufacturing industries. Animal feed can be in the form of pellets, crumbles, mash, or other forms, and is used to provide nutrients such as energy, protein, fiber, vitamins, and minerals to support the growth, reproduction, and maintenance of animals. It's important to note that animal feed must be safe, nutritious, and properly labeled to ensure the health and well-being of the animals that consume it.

Pyridoxal phosphate (PLP) is the active form of vitamin B6 and functions as a cofactor in various enzymatic reactions in the human body. It plays a crucial role in the metabolism of amino acids, carbohydrates, lipids, and neurotransmitters. Pyridoxal phosphate is involved in more than 140 different enzyme-catalyzed reactions, making it one of the most versatile cofactors in human biochemistry.

As a cofactor, pyridoxal phosphate helps enzymes carry out their functions by facilitating chemical transformations in substrates (the molecules on which enzymes act). In particular, PLP is essential for transamination, decarboxylation, racemization, and elimination reactions involving amino acids. These processes are vital for the synthesis and degradation of amino acids, neurotransmitters, hemoglobin, and other crucial molecules in the body.

Pyridoxal phosphate is formed from the conversion of pyridoxal (a form of vitamin B6) by the enzyme pyridoxal kinase, using ATP as a phosphate donor. The human body obtains vitamin B6 through dietary sources such as whole grains, legumes, vegetables, nuts, and animal products like poultry, fish, and pork. It is essential to maintain adequate levels of pyridoxal phosphate for optimal enzymatic function and overall health.

Dietary proteins are sources of protein that come from the foods we eat. Protein is an essential nutrient for the human body, required for various bodily functions such as growth, repair, and immune function. Dietary proteins are broken down into amino acids during digestion, which are then absorbed and used to synthesize new proteins in the body.

Dietary proteins can be classified as complete or incomplete based on their essential amino acid content. Complete proteins contain all nine essential amino acids that cannot be produced by the human body and must be obtained through the diet. Examples of complete protein sources include meat, poultry, fish, eggs, dairy products, soy, and quinoa.

Incomplete proteins lack one or more essential amino acids and are typically found in plant-based foods such as grains, legumes, nuts, and seeds. However, by combining different incomplete protein sources, it is possible to obtain all the essential amino acids needed for a complete protein diet. This concept is known as complementary proteins.

It's important to note that while dietary proteins are essential for good health, excessive protein intake can have negative effects on the body, such as increased stress on the kidneys and bones. Therefore, it's recommended to consume protein in moderation as part of a balanced and varied diet.

P300 and CREB binding protein (CBP) are both transcriptional coactivators that play crucial roles in regulating gene expression. They function by binding to various transcription factors and modifying the chromatin structure to allow for the recruitment of the transcriptional machinery. The P300-CBP complex is essential for many cellular processes, including development, differentiation, and oncogenesis.

P300-CBP transcription factors refer to a family of proteins that include both p300 and CBP, as well as their various isoforms and splice variants. These proteins share structural and functional similarities and are often referred to together due to their overlapping roles in transcriptional regulation.

The P300-CBP complex plays a key role in the P300-CBP-mediated signal integration, which allows for the coordinated regulation of gene expression in response to various signals and stimuli. Dysregulation of P300-CBP transcription factors has been implicated in several diseases, including cancer, neurodevelopmental disorders, and inflammatory diseases.

In summary, P300-CBP transcription factors are a family of proteins that play crucial roles in regulating gene expression through their ability to bind to various transcription factors and modify the chromatin structure. Dysregulation of these proteins has been implicated in several diseases, making them important targets for therapeutic intervention.

Homoarginine is not a medical condition, but it's a naturally occurring amino acid in the human body. It is considered a non-proteinogenic amino acid because it is not used in the synthesis of proteins. Homoarginine is formed from the essential amino acid lysine and has been studied for its potential role in cardiovascular health, kidney function, and other physiological processes. However, more research is needed to fully understand its functions and clinical significance.

Ubiquitin is a small protein that is present in all eukaryotic cells and plays a crucial role in the regulation of various cellular processes, such as protein degradation, DNA repair, and stress response. It is involved in marking proteins for destruction by attaching to them, a process known as ubiquitination. This modification can target proteins for degradation by the proteasome, a large protein complex that breaks down unneeded or damaged proteins in the cell. Ubiquitin also has other functions, such as regulating the localization and activity of certain proteins. The ability of ubiquitin to modify many different proteins and play a role in multiple cellular processes makes it an essential player in maintaining cellular homeostasis.

Protein conformation refers to the specific three-dimensional shape that a protein molecule assumes due to the spatial arrangement of its constituent amino acid residues and their associated chemical groups. This complex structure is determined by several factors, including covalent bonds (disulfide bridges), hydrogen bonds, van der Waals forces, and ionic bonds, which help stabilize the protein's unique conformation.

Protein conformations can be broadly classified into two categories: primary, secondary, tertiary, and quaternary structures. The primary structure represents the linear sequence of amino acids in a polypeptide chain. The secondary structure arises from local interactions between adjacent amino acid residues, leading to the formation of recurring motifs such as α-helices and β-sheets. Tertiary structure refers to the overall three-dimensional folding pattern of a single polypeptide chain, while quaternary structure describes the spatial arrangement of multiple folded polypeptide chains (subunits) that interact to form a functional protein complex.

Understanding protein conformation is crucial for elucidating protein function, as the specific three-dimensional shape of a protein directly influences its ability to interact with other molecules, such as ligands, nucleic acids, or other proteins. Any alterations in protein conformation due to genetic mutations, environmental factors, or chemical modifications can lead to loss of function, misfolding, aggregation, and disease states like neurodegenerative disorders and cancer.

Substrate specificity in the context of medical biochemistry and enzymology refers to the ability of an enzyme to selectively bind and catalyze a chemical reaction with a particular substrate (or a group of similar substrates) while discriminating against other molecules that are not substrates. This specificity arises from the three-dimensional structure of the enzyme, which has evolved to match the shape, charge distribution, and functional groups of its physiological substrate(s).

Substrate specificity is a fundamental property of enzymes that enables them to carry out highly selective chemical transformations in the complex cellular environment. The active site of an enzyme, where the catalysis takes place, has a unique conformation that complements the shape and charge distribution of its substrate(s). This ensures efficient recognition, binding, and conversion of the substrate into the desired product while minimizing unwanted side reactions with other molecules.

Substrate specificity can be categorized as:

1. Absolute specificity: An enzyme that can only act on a single substrate or a very narrow group of structurally related substrates, showing no activity towards any other molecule.
2. Group specificity: An enzyme that prefers to act on a particular functional group or class of compounds but can still accommodate minor structural variations within the substrate.
3. Broad or promiscuous specificity: An enzyme that can act on a wide range of structurally diverse substrates, albeit with varying catalytic efficiencies.

Understanding substrate specificity is crucial for elucidating enzymatic mechanisms, designing drugs that target specific enzymes or pathways, and developing biotechnological applications that rely on the controlled manipulation of enzyme activities.

'Escherichia coli' (E. coli) is a type of gram-negative, facultatively anaerobic, rod-shaped bacterium that commonly inhabits the intestinal tract of humans and warm-blooded animals. It is a member of the family Enterobacteriaceae and one of the most well-studied prokaryotic model organisms in molecular biology.

While most E. coli strains are harmless and even beneficial to their hosts, some serotypes can cause various forms of gastrointestinal and extraintestinal illnesses in humans and animals. These pathogenic strains possess virulence factors that enable them to colonize and damage host tissues, leading to diseases such as diarrhea, urinary tract infections, pneumonia, and sepsis.

E. coli is a versatile organism with remarkable genetic diversity, which allows it to adapt to various environmental niches. It can be found in water, soil, food, and various man-made environments, making it an essential indicator of fecal contamination and a common cause of foodborne illnesses. The study of E. coli has contributed significantly to our understanding of fundamental biological processes, including DNA replication, gene regulation, and protein synthesis.

Cadaverine is a foul-smelling organic compound that is produced by the breakdown of certain amino acids in dead bodies. It is formed through the decarboxylation of lysine, an essential amino acid, and is characterized by its strong, unpleasant odor. Cadaverine is often used as a forensic indicator of decomposition and is also being studied for its potential role in various physiological processes, such as inflammation and cancer.

An amino acid substitution is a type of mutation in which one amino acid in a protein is replaced by another. This occurs when there is a change in the DNA sequence that codes for a particular amino acid in a protein. The genetic code is redundant, meaning that most amino acids are encoded by more than one codon (a sequence of three nucleotides). As a result, a single base pair change in the DNA sequence may not necessarily lead to an amino acid substitution. However, if a change does occur, it can have a variety of effects on the protein's structure and function, depending on the nature of the substituted amino acids. Some substitutions may be harmless, while others may alter the protein's activity or stability, leading to disease.

Essential amino acids are a group of 9 out of the 20 standard amino acids that cannot be synthesized by the human body and must be obtained through diet. They include: histidine, isoleucine, leucine, lysine, methionine, phenylalanine, threonine, tryptophan, and valine. These amino acids are essential for various biological processes such as protein synthesis, growth, and repair of body tissues. A deficiency in any of these essential amino acids can lead to impaired physical development and compromised immune function. Foods that provide all nine essential amino acids are considered complete proteins and include animal-derived products like meat, poultry, fish, eggs, and dairy, as well as soy and quinoa.

A base sequence in the context of molecular biology refers to the specific order of nucleotides in a DNA or RNA molecule. In DNA, these nucleotides are adenine (A), guanine (G), cytosine (C), and thymine (T). In RNA, uracil (U) takes the place of thymine. The base sequence contains genetic information that is transcribed into RNA and ultimately translated into proteins. It is the exact order of these bases that determines the genetic code and thus the function of the DNA or RNA molecule.

Peptides are short chains of amino acid residues linked by covalent bonds, known as peptide bonds. They are formed when two or more amino acids are joined together through a condensation reaction, which results in the elimination of a water molecule and the formation of an amide bond between the carboxyl group of one amino acid and the amino group of another.

Peptides can vary in length from two to about fifty amino acids, and they are often classified based on their size. For example, dipeptides contain two amino acids, tripeptides contain three, and so on. Oligopeptides typically contain up to ten amino acids, while polypeptides can contain dozens or even hundreds of amino acids.

Peptides play many important roles in the body, including serving as hormones, neurotransmitters, enzymes, and antibiotics. They are also used in medical research and therapeutic applications, such as drug delivery and tissue engineering.

Methyltransferases are a class of enzymes that catalyze the transfer of a methyl group (-CH3) from a donor molecule to an acceptor molecule, which is often a protein, DNA, or RNA. This transfer of a methyl group can modify the chemical and physical properties of the acceptor molecule, playing a crucial role in various cellular processes such as gene expression, signal transduction, and DNA repair.

In biochemistry, methyltransferases are classified based on the type of donor molecule they use for the transfer of the methyl group. The most common methyl donor is S-adenosylmethionine (SAM), a universal methyl group donor found in many organisms. Methyltransferases that utilize SAM as a cofactor are called SAM-dependent methyltransferases.

Abnormal regulation or function of methyltransferases has been implicated in several diseases, including cancer and neurological disorders. Therefore, understanding the structure, function, and regulation of these enzymes is essential for developing targeted therapies to treat these conditions.

A Structure-Activity Relationship (SAR) in the context of medicinal chemistry and pharmacology refers to the relationship between the chemical structure of a drug or molecule and its biological activity or effect on a target protein, cell, or organism. SAR studies aim to identify patterns and correlations between structural features of a compound and its ability to interact with a specific biological target, leading to a desired therapeutic response or undesired side effects.

By analyzing the SAR, researchers can optimize the chemical structure of lead compounds to enhance their potency, selectivity, safety, and pharmacokinetic properties, ultimately guiding the design and development of novel drugs with improved efficacy and reduced toxicity.

Carboxy-lyases are a class of enzymes that catalyze the removal of a carboxyl group from a substrate, often releasing carbon dioxide in the process. These enzymes play important roles in various metabolic pathways, such as the biosynthesis and degradation of amino acids, sugars, and other organic compounds.

Carboxy-lyases are classified under EC number 4.2 in the Enzyme Commission (EC) system. They can be further divided into several subclasses based on their specific mechanisms and substrates. For example, some carboxy-lyases require a cofactor such as biotin or thiamine pyrophosphate to facilitate the decarboxylation reaction, while others do not.

Examples of carboxy-lyases include:

1. Pyruvate decarboxylase: This enzyme catalyzes the conversion of pyruvate to acetaldehyde and carbon dioxide during fermentation in yeast and other organisms.
2. Ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBisCO): This enzyme is essential for photosynthesis in plants and some bacteria, as it catalyzes the fixation of carbon dioxide into an organic molecule during the Calvin cycle.
3. Phosphoenolpyruvate carboxylase: Found in plants, algae, and some bacteria, this enzyme plays a role in anaplerotic reactions that replenish intermediates in the citric acid cycle. It catalyzes the conversion of phosphoenolpyruvate to oxaloacetate and inorganic phosphate.
4. Aspartate transcarbamylase: This enzyme is involved in the biosynthesis of pyrimidines, a class of nucleotides. It catalyzes the transfer of a carboxyl group from carbamoyl aspartate to carbamoyl phosphate, forming cytidine triphosphate (CTP) and fumarate.
5. Urocanase: Found in animals, this enzyme is involved in histidine catabolism. It catalyzes the conversion of urocanate to formiminoglutamate and ammonia.

Polyubiquitin refers to the formation of chains of ubiquitin molecules that are attached to a protein substrate. Ubiquitination is a post-translational modification where ubiquitin, a small regulatory protein, is covalently attached to lysine residues on target proteins. When multiple ubiquitin molecules are linked together through their C-terminal glycine residue to one of the seven lysine residues (K6, K11, K27, K29, K33, K48, or K63) on another ubiquitin molecule, it results in the formation of polyubiquitin chains.

Different types of polyubiquitination chains have distinct functions within the cell. For instance, K48-linked polyubiquitin chains typically target proteins for proteasomal degradation, while K63-linked polyubiquitin chains are involved in various signaling pathways, including DNA damage response, endocytosis, and inflammation.

Polyubiquitination is a dynamic process that can be reversed by the action of deubiquitinating enzymes (DUBs), which cleave ubiquitin chains from substrate proteins or disassemble polyubiquitin chains into individual ubiquitin molecules. Dysregulation of polyubiquitination and deubiquitination processes has been implicated in various diseases, including cancer, neurodegenerative disorders, and inflammatory conditions.

Aspartate kinase is a type of enzyme that plays a crucial role in the biosynthesis of several amino acids, including aspartate, methionine, and threonine. This enzyme catalyzes the phosphorylation of aspartic acid to form phosphoaspartate, which is the first step in the synthesis of these essential amino acids.

Aspartate kinase exists in different forms or isozymes in various organisms, and it can be regulated by feedback inhibition. This means that the enzyme's activity can be suppressed when the concentration of one or more of the amino acids it helps to synthesize becomes too high, preventing further production and maintaining a balanced level of these essential nutrients in the body.

In humans, aspartate kinase is involved in several metabolic pathways and is an essential enzyme for normal growth and development. Defects or mutations in the genes encoding aspartate kinase can lead to various genetic disorders and metabolic imbalances.

Epigenetics is the study of heritable changes in gene function that occur without a change in the underlying DNA sequence. These changes can be caused by various mechanisms such as DNA methylation, histone modification, and non-coding RNA molecules. Epigenetic changes can be influenced by various factors including age, environment, lifestyle, and disease state.

Genetic epigenesis specifically refers to the study of how genetic factors influence these epigenetic modifications. Genetic variations between individuals can lead to differences in epigenetic patterns, which in turn can contribute to phenotypic variation and susceptibility to diseases. For example, certain genetic variants may predispose an individual to develop cancer, and environmental factors such as smoking or exposure to chemicals can interact with these genetic variants to trigger epigenetic changes that promote tumor growth.

Overall, the field of genetic epigenesis aims to understand how genetic and environmental factors interact to regulate gene expression and contribute to disease susceptibility.

Ornithine is not a medical condition but a naturally occurring alpha-amino acid, which is involved in the urea cycle, a process that eliminates ammonia from the body. Here's a brief medical/biochemical definition of Ornithine:

Ornithine (NH₂-CH₂-CH₂-CH(NH₃)-COOH) is an α-amino acid without a carbon atom attached to the amino group, classified as a non-proteinogenic amino acid because it is not encoded by the standard genetic code and not commonly found in proteins. It plays a crucial role in the urea cycle, where it helps convert harmful ammonia into urea, which can then be excreted by the body through urine. Ornithine is produced from the breakdown of arginine, another amino acid, via the enzyme arginase. In some medical and nutritional contexts, ornithine supplementation may be recommended to support liver function, wound healing, or muscle growth, but its effectiveness for these uses remains a subject of ongoing research and debate.

Sequence homology, amino acid, refers to the similarity in the order of amino acids in a protein or a portion of a protein between two or more species. This similarity can be used to infer evolutionary relationships and functional similarities between proteins. The higher the degree of sequence homology, the more likely it is that the proteins are related and have similar functions. Sequence homology can be determined through various methods such as pairwise alignment or multiple sequence alignment, which compare the sequences and calculate a score based on the number and type of matching amino acids.

Adipates are a group of chemical compounds that are esters of adipic acid. Adipic acid is a dicarboxylic acid with the formula (CH₂)₄(COOH)₂. Adipates are commonly used as plasticizers in the manufacture of polyvinyl chloride (PVC) products, such as pipes, cables, and flooring. They can also be found in cosmetics, personal care products, and some food additives.

Adipates are generally considered to be safe for use in consumer products, but like all chemicals, they should be used with caution and in accordance with recommended guidelines. Some adipates have been shown to have potential health effects, such as endocrine disruption and reproductive toxicity, at high levels of exposure. Therefore, it is important to follow proper handling and disposal procedures to minimize exposure.

SUMO-1 (Small Ubiquitin-like Modifier 1) protein is a member of the SUMO family of post-translational modifiers, which are involved in the regulation of various cellular processes such as nuclear-cytoplasmic transport, transcriptional regulation, and DNA repair. The SUMO-1 protein is covalently attached to specific lysine residues on target proteins through a process called sumoylation, which can alter the activity, localization, or stability of the modified protein. Sumoylation plays a crucial role in maintaining cellular homeostasis and has been implicated in several human diseases, including cancer and neurodegenerative disorders.

As such, 1 g of L-lysine is contained in 1.25 g of L-lysine HCl. The most common role for lysine is proteinogenesis. Lysine ... lysine). L-lysine HCl is used as a dietary supplement, providing 80.03% L-lysine. ... Lysine has also been shown to play a role in anaemia, as lysine is suspected to have an effect on the uptake of iron and, ... A food is considered to have sufficient lysine if it has at least 51 mg of lysine per gram of protein (so that the protein is ...
β-Lysine (3,6-diaminohexanoic acid) is an amino acid produced by platelets during coagulation and is directly antibacterial by ... curehunter.com > beta-lysine Retrieved on April 18, 2010 IMMUNOLOGY - CHAPTER ONE > INNATE (NON-SPECIFIC) IMMUNITY Gene Mayer, ...
In enzymology, a lysine carbamoyltransferase (EC 2.1.3.8) is an enzyme that catalyzes the chemical reaction carbamoyl phosphate ... This enzyme is also called lysine transcarbamylase. Hommes FA, Eller AG, Scott DF, Carter AL (1983). "Separation of ornithine ... The systematic name of this enzyme class is carbamoyl-phosphate:L-lysine carbamoyltransferase. ... L-lysine ⇌ {\displaystyle \rightleftharpoons } phosphate + L-homocitrulline Thus, the two substrates of this enzyme are ...
In enzymology, a lysine dehydrogenase (EC 1.4.1.15) is an enzyme that catalyzes the chemical reaction L-lysine + NAD+ ⇌ {\ ... "L-Lysine dehydrogenase deficiency in a patient with congenital lysine intolerance". Nature. 211 (5051): 854-5. doi:10.1038/ ... The systematic name of this enzyme class is L-lysine:NAD+ oxidoreductase (deaminating, cyclizing). Burgi W, Richterich R, ... the two substrates of this enzyme are L-lysine and NAD+, whereas its 4 products are 1,2-didehydropiperidine-2-carboxylate, NH3 ...
... , also known as aspirin DL-lysine or lysine aspirin, is a more soluble form of acetylsalicylic acid ( ... Lysine acetylsalicylate is used as a challenge test to diagnose NSAID-exacerbated respiratory disease. Drops of lysine ... It is composed of the ammonium form of the amino acid lysine paired with the conjugate base of aspirin. Lysine acetylsalicylate ... After administration, lysine acetylsalicylate is hydrolyzed, separating into lysine and acetylsalicylate compounds. Two forms ...
The enzyme functions to break off arginine or lysine from the C-terminal of a polypeptide chain. Lysine is hydrolyzed more ... Lysine carboxypeptidase is in sub-subclass 17: metallocarboxypeptidases. This subclass first defines lysine carboxypeptidase as ... For plasminogen receptors, cleaving lysine prevents plasminogen's activation into plasmin. Lysine carboxypeptidase regulates ... pocket of the active site is responsible for the preference of lysine over arginine as the P1' residue. Unlike arginine, lysine ...
The generalized transport reaction for LysE is: Lysine (in) + [nH+ (out) or nOH− (in)] Lysine (out) + [nH+ (in) or nOH− (out ... Lysine Exporters are a superfamily of transmembrane proteins which export amino acids, lipids and heavy metal ions. They ... Vrljic M, Sahm H, Eggeling L (December 1996). "A new type of transporter with a new type of cellular function: L-lysine export ... LysE appears to catalyze unidirectional efflux of L-lysine (and other basic amino acids such as L-arginine), and it provides ...
Page for Lysine riboswitch at Rfam PDB entry for the lysine riboswitch tertiary structure v t e (Cis-regulatory RNA elements, ... The lysine riboswitch has also been identified independently and called the L box. The lysine riboswitch controls metabolic ... The structure of the lysine riboswitch has recently been determined. The lysine amino acid is bound in the pocket formed by the ... Grundy, FJ; Lehman SC; Henkin TM (2003). "The L box regulon: Lysine sensing by leader RNAs of bacterial lysine biosynthesis ...
The enzyme Lysine decarboxylase (EC 4.1.1.18) converts lysine to cadaverine. Gale EF, Epps HM (1944). "Studies on bacterial ... lysine+decarboxylase at the U.S. National Library of Medicine Medical Subject Headings (MeSH) Portal: Biology v t e (EC 4.1.1, ... Soda K, Moriguchi M (January 1969). "Crystalline lysine decarboxylase". Biochem. Biophys. Res. Commun. 34 (1): 34-9. doi: ... amino-acid decarboxylases: 1. l(+)-lysine decarboxylase". Biochem. J. 38 (3): 232-42. doi:10.1042/bj0380232. PMC 1258073. PMID ...
In enzymology, a lysine racemase (EC 5.1.1.5) is an enzyme that catalyzes the chemical reaction L-lysine ⇌ D-lysine Hence, this ... The systematic name of this enzyme class is lysine racemase. This enzyme participates in lysine degradation. Huang HT (1960). " ... enzyme has one substrate, L-lysine, and one product, D-lysine. This enzyme belongs to the family of isomerases, specifically ...
... (EC 1.4.1.18, L-lysine epsilon-dehydrogenase, L-lysine 6-dehydrogenase, LysDH) is an enzyme with ... Lysine+6-dehydrogenase at the U.S. National Library of Medicine Medical Subject Headings (MeSH) Portal: Biology v t e (EC 1.4.1 ... Misono H, Hashimoto H, Uehigashi H, Nagata S, Nagasaki S (June 1989). "Properties of L-lysine epsilon-dehydrogenase from ... Heydari M, Ohshima T, Nunoura-Kominato N, Sakuraba H (February 2004). "Highly stable L-lysine 6-dehydrogenase from the ...
This enzyme participates in lysine degradation. PAIK WK, KIM S (1964). "ENZYMIC SYNTHESIS OF EPSILON-N-ACETYL-L-LYSINE". Arch. ... Other names in common use include lysine acetyltransferase, and acetyl-phosphate:L-lysine 6-N-acetyltransferase. ... N6-acetyl-L-lysine Thus, the two substrates of this enzyme are acetyl phosphate and L-lysine, whereas its two products are ... In enzymology, a lysine N-acetyltransferase (EC 2.3.1.32) is an enzyme that catalyzes the chemical reaction acetyl phosphate + ...
In enzymology, a L-lysine oxidase (EC 1.4.3.14) is an enzyme that catalyzes the chemical reaction L-lysine + O2 + H2O ⇌ {\ ... Other names in common use include L-lysine alpha-oxidase, and L-lysyl-alpha-oxidase. This enzyme participates in lysine ... Kusakabe H, Kodama K, Kuninaka A, Yoshino H, Misono H, Soda K (1980). "A new antitumor enzyme, L-lysine alpha-oxidase from ... Lukasheva, EV; Berezov, TT (October 2002). "L-Lysine alpha-oxidase: physicochemical and biological properties". Biochemistry ( ...
Other names in common use include ornithine(lysine) aminotransferase, lysine/ornithine:2-oxoglutarate aminotransferase, and L- ... In enzymology, an ornithine(lysine) transaminase (EC 2.6.1.68) is an enzyme that catalyzes the chemical reaction L-ornithine + ... ornithine(L-lysine):2-oxoglutarate-aminotransferase. Lowe PN, Rowe AF (1986). "Aminotransferase activities in Trichomonas ...
L-lysine Thus, the two substrates of this enzyme are L-lysine 1,6-lactam and H2O, whereas its product is L-lysine. This enzyme ... In enzymology, a L-lysine-lactamase (EC 3.5.2.11) is an enzyme that catalyzes the chemical reaction L-lysine 1,6-lactam + H2O ... The systematic name of this enzyme class is L-lysine-1,6-lactam lactamhydrolase. Other names in common use include L-alpha- ...
L-lysine-transfer RNA ligase, lysine-tRNA synthetase, and lysine translase. Allen EH, Glassman E, Schweet RS (April 1960). " ... In enzymology, a lysine-tRNA ligase (EC 6.1.1.6) is an enzyme that catalyzes the chemical reaction ATP + L-lysine + tRNALys ... The systematic name of this enzyme class is L-lysine:tRNALys ligase (AMP-forming). Other names in common use include lysyl-tRNA ... Lagerkvist U, Rymo L, Lindqvist O, Andersson E (June 1972). "Some properties of crystals of lysine transfer ribonucleic acid ...
... (EC 4.3.1.28, rapL (gene), fkbL (gene), tubZ (gene), visC (gene)) is an enzyme with systematic name L- ... L-lysine+cyclodeaminase at the U.S. National Library of Medicine Medical Subject Headings (MeSH) Portal: Biology (EC 4.3.1). ... Gatto GJ, Boyne MT, Kelleher NL, Walsh CT (March 2006). "Biosynthesis of pipecolic acid by RapL, a lysine cyclodeaminase ... Tsotsou GE, Barbirato F (May 2007). "Biochemical characterisation of recombinant Streptomyces pristinaespiralis L-lysine ...
In enzymology, an acyl-lysine deacylase (EC 3.5.1.17) is an enzyme that catalyzes the chemical reaction N6-acyl-L-lysine + H2O ... The systematic name of this enzyme class is N6-acyl-L-lysine amidohydrolase. Other names in common use include epsilon-lysine ... the two substrates of this enzyme are N6-acyl-L-lysine and H2O, whereas its two products are carboxylate and L-lysine. This ... This enzyme participates in lysine degradation. PAIK WK, BLOCH-FRANKENTHAL L, BIRNBAUM SM, WINITZ M, GREENSTEIN JP (1957). " ...
L-lysine The 3 substrates of this enzyme are ATP, (indol-3-yl)acetate, and L-lysine, whereas its 3 products are ADP, phosphate ... L-lysine ligase (ADP-forming). This enzyme is also called indoleacetate:L-lysine ligase (ADP-forming). Glass NL, Kosuge T (1986 ... In enzymology, an indoleacetate-lysine synthetase (EC 6.3.2.20) is an enzyme that catalyzes the chemical reaction ATP + (indol- ... 3. The isolation and characterization of indole-3-acetyl-epsilon-L-lysine". Biochemistry. 7 (2): 601-5. doi:10.1021/bi00842a013 ...
A liter of lysine iron agar contains 13.5g of the gelling agent agar, as well as the nutrients lysine (10 g), pancreatic digest ... Lysine iron agar or LIA is a differential media used to distinguish bacteria that are able to decarboxylate lysine and/or ... Bacteria able to decarboxylate lysine will leave the media purple colored. Bacteria producing hydrogen sulfide will appear ...
... lysine monooxygenase, and L-lysine-2-monooxygenase. This enzyme participates in lysine degradation. It employs one cofactor, ... In enzymology, a lysine 2-monooxygenase (EC 1.13.12.2) is an enzyme that catalyzes the chemical reaction L-lysine + O2 ⇌ {\ ... V. Manifestation of amino acid oxidase activity by L-lysine monooxygenase". J. Biol. Chem. 247 (11): 3439-44. PMID 4624115. ... Takeda H, Hayaishi O (1966). "Crystalline L-lysine oxygenase". J. Biol. Chem. 241 (11): 2733-6. PMID 5911646. Takeda H, ...
a EINECS number 200-294-2 (Lysine) ^a CID 866 from PubChem (DL-Lysine) ^a CID 5962 from PubChem (L-Lysine) (Articles with short ...
Enzyme Binding: Lysine 2,3-aminomutase binds to pyridoxal phosphate (PLP). Amino Acid Binding: The amino acid (Lysine or Beta- ... is a radical SAM enzyme that facilitates the conversion of the amino acid lysine to beta-lysine. It accomplishes this ... Lysine+2,3-aminomutase at the U.S. National Library of Medicine Medical Subject Headings (MeSH) Portal: Biology (EC 5.4.3). ... Lepore BW, Ruzicka FJ, Frey PA, Ringe D (September 2005). "The x-ray crystal structure of lysine-2,3-aminomutase from ...
The lysine price-fixing conspiracy was an organized effort during the mid-1990s to raise the price of the animal feed additive ... Buyers of lysine in the United States and Canada sued and recovered $80 to $100 million in damages from the five cartel members ... The lysine cartel was the first successful prosecution of an international cartel by the U.S. Department of Justice (DOJ) in ... The cartel had been able to raise lysine prices 70% within their first nine months of cooperation. The investigation yielded $ ...
In enzymology, a N6-methyl-lysine oxidase (EC 1.5.3.4) is an enzyme that catalyzes the chemical reaction N6-methyl-L-lysine + ... H2O2 The 3 substrates of this enzyme are N6-methyl-L-lysine, H2O, and O2, whereas its 3 products are L-lysine, formaldehyde, ... The systematic name of this enzyme class is N6-methyl-L-lysine:oxygen oxidoreductase (demethylating). Other names in common use ... and 6-N-methyl-L-lysine:oxygen oxidoreductase (demethylating). Kim S, Benoiton L, Paik WK (1964). "alpha-Alkyllysinase. ...
... calmodulin-L-lysine 6-N-methyltransferase. This enzyme participates in lysine degradation. Sitaramayya A, Wright LS, Siegel FL ... calmodulin L-lysine ⇌ {\displaystyle \rightleftharpoons } S-adenosyl-L-homocysteine + calmodulin N6-methyl-L-lysine Thus, the ... The systematic name of this enzyme class is S-adenosyl-L-methionine:calmodulin-L-lysine N6-methyltransferase. Other names in ... In enzymology, a calmodulin-lysine N-methyltransferase (EC 2.1.1.60) is an enzyme that catalyzes the chemical reaction S- ...
In enzymology, a L-lysine 6-oxidase (EC 1.4.3.20) is an enzyme that catalyzes the chemical reaction L-lysine + O2 + H2O ⇌ {\ ... Gomez D, Lucas-Elio P, Sanchez-Amat A, Solano F (2006). "A novel type of lysine oxidase: L-lysine-epsilon-oxidase". Biochim. ... The systematic name of this enzyme class is L-lysine:oxygen 6-oxidoreductase (deaminating). Other names in common use include L ... lysine-epsilon-oxidase, Lod, LodA, and marinocine. Lucas-Elio P, Gomez D, Solano F, Sanchez-Amat A (2006). "The antimicrobial ...
In enzymology, a lysine-pyruvate 6-transaminase (EC 2.6.1.71) is an enzyme that catalyzes the chemical reaction L-lysine + ... The systematic name of this enzyme class is L-lysine:pyruvate aminotransferase. Other names in common use include lysine- ... Schmidt H, Bode R, Birnbaum D (1988). "A novel enzyme, L-lysine : pyruvate aminotransferase, catalyses the first step of lysine ... pyruvate ⇌ L-2-aminoadipate 6-semialdehyde + L-alanine Thus, the two substrates of this enzyme are L-lysine and pyruvate, ...
... lysine epsilon-aminotransferase, lysine epsilon-transaminase, lysine:2-ketoglutarate 6-aminotransferase, L-lysine-alpha- ... L-lysine 6-transaminase belongs to the aminotransferase class-III family. Crystal structures of L-lysine 6-transaminase reveal ... In enzymology, a L-lysine 6-transaminase (EC 2.6.1.36) is an enzyme that catalyzes the chemical reaction L-lysine + 2- ... The systematic name of this enzyme class is L-lysine:2-oxoglutarate 6-aminotransferase. Other names in common use include ...
In enzymology, a lysine-tRNAPyl ligase (EC 6.1.1.25) is an enzyme that catalyzes the chemical reaction ATP + L-lysine + tRNAPyl ... The systematic name of this enzyme class is L-lysine:tRNAPyl ligase (AMP-forming). Srinivasan G, James CM, Krzycki JA (2002). " ... L-lysine, and tRNA(Pyl), whereas its 3 products are AMP, diphosphate, and L-lysyl-tRNA(Pyl). This enzyme belongs to the family ...
As such, 1 g of L-lysine is contained in 1.25 g of L-lysine HCl. The most common role for lysine is proteinogenesis. Lysine ... lysine). L-lysine HCl is used as a dietary supplement, providing 80.03% L-lysine. ... Lysine has also been shown to play a role in anaemia, as lysine is suspected to have an effect on the uptake of iron and, ... A food is considered to have sufficient lysine if it has at least 51 mg of lysine per gram of protein (so that the protein is ...
... lysine (CHEBI:25094). D-lysine (CHEBI:16855) is a lysine (CHEBI:25094). L-lysine (CHEBI:18019) is a lysine (CHEBI:25094). ... lysine (CHEBI:25094). N6-(2,4-dinitrophenyl)lysine (CHEBI:53078) has functional parent lysine (CHEBI:25094). lysine derivative ... lysine (CHEBI:25094) is a α-amino acid (CHEBI:33704) lysine (CHEBI:25094) is a diamino acid (CHEBI:35987) lysine (CHEBI:25094) ... lysine (CHEBI:25094) has part 4-aminobutyl group (CHEBI:50339) lysine (CHEBI:25094) has role Daphnia magna metabolite (CHEBI: ...
Histone lysine acylation is a major class of histone post-translational modifications involved in essential biological ...
Lysine is an essential amino acid that is used to produce proteins in the body. The body cannot make lysine on its own; ... All posts tagged with L-lysine. * A simple amino acid treatment protocol helps covid-19 patients recover faster. ... L-lysine is responsible for […] in: alternative medicine,Amino Acids,antiviral,coronavirus treatment,covid-19,goodhealth, ... Natural News) One of the essential amino acids, L-lysine, can block SARS-CoV-2 and prevent severe illness in covid-19 patients ...
FDAs Bacteriological Analytical Manual (BAM) presents the agencys preferred laboratory procedures for microbiological analyses of foods and cosmetics.
... Mol Syst Biol. 2012 Feb 28:8:571. doi: ... The measured M. pneumoniae phosphoproteome and lysine acetylome revealed that both PTMs are very common, that (as in Eukaryotes ... but also a modulation of proteome abundance and lysine acetylation patterns, mostly in the absence of transcriptional changes. ... results imply previously unreported hidden layers of post-transcriptional regulation intertwining phosphorylation with lysine ...
LYSINE. C6 H15 N2 O2. KDXKERNSBIXSRK-YFKPBYRVSA-O. Interactions *Focus chain C [auth A] ... Defining a Molecular Determinant of Lysine-Mediated Allosteric Inhibition of DHDPS.. Wubben, J.M., Paxman, J.J., Dogovski, C., ... SHEWANELLA BENTHICA DHDPS WITH LYSINE AND PYRUVATE. *PDB DOI: https://doi.org/10.2210/pdb4PFM/pdb ... SHEWANELLA BENTHICA DHDPS WITH LYSINE AND PYRUVATE ...
What is L-Lysine with Vitamin B-6?. L-Lysine with Vitamin B-6 combines 1,000 mg of the amino acid L-lysine with 25 mg of ... Vitacost® L-Lysine is a targeted wellness solution - just for you.. * Supplies 1,000 mg of L-lysine and 25 mg of vitamin B-6 ... Vitacost L-Lysine Description. Natural amino acid L-lysine with added vitamin B6 offers support during times of mental anxiety ... L-lysine may support a healthy cardiovascular system* * L-lysine supports calcium absorption, making it more available for ...
multifunctional procollagen lysine hydroxylase and glycosyltransferase LH3. Names. lysine hydroxylase 3. lysyl hydroxlase 3. ... PLOD3 procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 [Homo sapiens] PLOD3 procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 ... procollagen-lysine,2-oxoglutarate 5-dioxygenase 3provided by HGNC. Primary source. HGNC:HGNC:9083 See related. Ensembl: ... PLOD3 procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 [ Homo sapiens (human) ] Gene ID: 8985, updated on 23-Nov-2023 ...
... was 31982337 Kilograms. Discover more data with ... How does Netherlands rank in Production of Lysine, Glutamic Acid and Their Salts?. #. 13 Countries. Kilograms. Last. YoY. 5‑ ... At 31,982,336.68 Kilograms in 2019, the country was number 3 comparing other countries in Production of Lysine, Glutamic Acid ... Netherlands - Production of Lysine, Glutamic Acid and Their Salts Kilograms - 1995 to 2019 ...
Natures Bounty® L-Lysine supplements offer a convenient way to add more of this essential amino acid to your diet. Benefits of ... L-Lysine is an essential amino acid that your body cant produce on its own-you must get it from nutritional sources. ... L-Lysine may include supporting immune function and maintaining the health ... L-Lysine L-Lysine is an essential amino acid that your body cant produce on its own-you must get it from nutritional sources. ...
The crystal structures of pea Rubisco large subunit methyltransferase (LSMT) in ternary complexes with either lysine or ε-N- ... to specific lysine residues of protein substrates, such as the N-terminal tails of histones H3 and H4 and the large subunit of ... Figure 6: Space filling comparison of the lysine-binding sites of LSMT and SET7/9.. ... Mechanism of histone lysine methyl transfer revealed by the structure of SET7/9-AdoMet. EMBO J. 22, 292-303 (2003). ...
Quantum Lipclear® Lysine Plus® Cold Sore Treatment -- 0.25 oz * Shop all Quantum ... Lysine - Well-researched amino acid that suppresses the activity of arginine, which is a common trigger ... lysine, melaleuca alternifolia oil, melaleuca cajuputi oil, olea europaea (olive) fruit oil, propolis extract, vitamin A ( ...
View mouse Kat14 Chr2:144210952-144249595 with: phenotypes, sequences, polymorphisms, proteins, references, function, expression
L-lysine can also help manage a variety of health conditions. The nutrient can be used to control cholesterol levels, prevent ... I googled lysine-gallstones and found conflicting info- but tried 5 g of lysine and the pain was releived and I slept without ... L-lysine, a simple, low cost cure. They now are tried & true users of L-lysine, and have almost become heroes with their ... L-Lysine Cures #poststop:before { content: ""; display: block; height: 120px; margin: -120px 0 0; } Sort by Default New Loved ...
Lysine for Covid? Yes, IF YOU WANT IT REAL BAD. Lysine is used for biosynthesis of proteins. It is like giving a virus or the ... Lysine for Covid? Yes, IF YOU WANT IT REAL BAD. Lysine is used for biosynthesis of proteins. It is like giving a virus or the ... So I looked it up again lysine cellular mitosis were the words I typed, And from what I can see, all lysine is going to do is ... So I looked it up again lysine cellular mitosis were the words I typed, And from what I can see, all lysine is going to do is ...
View mouse Kdm2a Chr19:4366172-4448749 with: phenotypes, sequences, polymorphisms, proteins, references, function, expression
Füßl, Magdalena (2022): The role of lysine acetylation in photosynthesis. Dissertation, LMU München: Faculty of Biology ...
In this study, we have aimed to improve the functionality and stemness of MSCs during culture using poly-L-lysine (PLL). ... Poly-L-lysine (PLL) of extracellular matrix proteins is a small natural homopolymer of the essential amino acid L-lysine that ... Poly-L-lysine Prevents Senescence and Augments Growth in Culturing Mesenchymal Stem Cells Ex Vivo. June Seok Heo. ,1Hyun Ok Kim ... K.-S. Park, J. Ahn, J. Y. Kim, H. Park, H. O. Kim, and S.-H. Lee, "Poly-L-lysine increases the ex vivo expansion and erythroid ...
Addition of a sulfonyl group to lysine, an amino acid that is a constituent of most proteins, is of growing interest to the ... ELECTROSULF is exploiting the technology in a flow microreactor for oxidative sulfonylation of lysine, creating a new eco- ... Several transformations as alkylation, arylation, oxidation, acylation and condensation have been described for lysine. However ... being lysine with its free amine one of the most preferred handles used by chemists to introduce a new moieties, e.g. cytotoxic ...
The directed movement of a L-lysine into, out of or within a cell, or between cells, by means of some agent such as a ...
Healing lip balm made with hydrating coconut and soothing lysine, an amino acid that alleviates burning, itching, and ...
Shop Corning Polystyrene Poly-D-Lysine Coated Microplates at Thomas Scientific, your trusted partner in Science. ... Polystyrene Poly-D-Lysine Coated Microplates. * PRODUCT AVAILABILITY: Did you know you can view a products availability right ... 96 Well Flat Clear Bottom Black Poly-D-Lysine Coated Microplate, with Lid, Aseptically Manufactured. ... 96 Well Flat Clear Bottom White Poly-D-Lysine Coated Microplate, with Lid, Aseptically Manufactured. ...
Lysine methylation marks manifest their biological effect via... ... Lysine methylation marks manifest their biological effect via ... Protein methylation at lysine residues modulates chromatin structure, affects gene expression and mammalian development. ... Protein methylation at lysine residues modulates chromatin structure, affects gene expression and mammalian development. ... KMET-READ plans to investigate the biological role of these reading domains in essential histone lysine methyltransferases - ...
Home / Beauty / L-Lysine 1000 mg Tablets / L-Lysine 1000 mg Tablets ...
Enhance cell attachment to the culture surface with the extracellular matrix coating on Nunc Poly-D-Lysine or Collagen I Coated ... Poly-D-Lysine. Poly-D-Lysine (PDL) is a chemically synthesized extracellular matrix that is used to promote cell adhesion by ... Enhance cell attachment to the culture surface with the extracellular matrix coating on Thermo Scientific™ Nunc™ Poly-D-Lysine ...
Histone lysine demethylases in breast cancer.. Critical Reviews in Oncology/Hematology, 86(2) pp. 97-103. ... Histone lysine demethylases (KDMs) have been recently discovered in mammals and have been nicknamed "erasers" for their ability ...
Shop Pure Lysine™ Equine Supplement at Murdochs Ranch & Home Supply ... Contains pure Lysine, which is recommended for equine diets low in alfalfa, clover and soy. ...
... and L-Lysine has a chemical structure so similar to L-arginine that at least some viruses mistakenly incorporate L-Lysine ... Several viruses have been proven to be stopped indirectly by the dietary essential amino acid, L-Lysine. This is because at ... Lysine Reported to Halt Coronaviruses: An Interview with Bill Sardi. March 18, 2021 ...

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