Anaphase
Anaphase-Promoting Complex-Cyclosome
An E3 ubiquitin ligase primarily involved in regulation of the metaphase-to-anaphase transition during MITOSIS through ubiquitination of specific CELL CYCLE PROTEINS. Enzyme activity is tightly regulated through subunits and cofactors, which modulate activation, inhibition, and substrate specificity. The anaphase-promoting complex, or APC-C, is also involved in tissue differentiation in the PLACENTA, CRYSTALLINE LENS, and SKELETAL MUSCLE, and in regulation of postmitotic NEURONAL PLASTICITY and excitability.
Ubiquitin-Protein Ligase Complexes
Complexes of enzymes that catalyze the covalent attachment of UBIQUITIN to other proteins by forming a peptide bond between the C-terminal GLYCINE of UBIQUITIN and the alpha-amino groups of LYSINE residues in the protein. The complexes play an important role in mediating the selective-degradation of short-lived and abnormal proteins. The complex of enzymes can be broken down into three components that involve activation of ubiquitin (UBIQUITIN-ACTIVATING ENZYMES), conjugation of ubiquitin to the ligase complex (UBIQUITIN-CONJUGATING ENZYMES), and ligation of ubiquitin to the substrate protein (UBIQUITIN-PROTEIN LIGASES).
Cdc20 Proteins
Highly conserved proteins that specifically bind to and activate the anaphase-promoting complex-cyclosome, promoting ubiquitination and proteolysis of cell-cycle-regulatory proteins. Cdc20 is essential for anaphase-promoting complex activity, initiation of anaphase, and cyclin proteolysis during mitosis.
Cdh1 Proteins
Mitosis
Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome
A highly evolutionarily conserved subunit of the anaphase-promoting complex (APC-C) containing multiple 34-amino-acid tetratricopeptide repeats. These domains, also found in Apc subunits 6, 7, and 8, have been shown to mediate protein-protein interactions, suggesting that Apc3 may assist in coordinating the juxtaposition of the catalytic and substrate recognition module subunits relative to co-activators and APC-C inhibitors.
Cell Cycle Proteins
Proteins that control the CELL DIVISION CYCLE. This family of proteins includes a wide variety of classes, including CYCLIN-DEPENDENT KINASES, mitogen-activated kinases, CYCLINS, and PHOSPHOPROTEIN PHOSPHATASES as well as their putative substrates such as chromatin-associated proteins, CYTOSKELETAL PROTEINS, and TRANSCRIPTION FACTORS.
Apc1 Subunit, Anaphase-Promoting Complex-Cyclosome
The largest subunit of the anaphase-promoting complex. It acts primarily as a scaffold for the proper organization and arrangement of subunits. The C-terminal region of Apc1 contains a series of tandem amino acid repeats that are also seen in the 26S proteasome regulatory particle, and may assist with forming and stabilizing protein-protein interactions.
Spindle Apparatus
Securin
Securin is involved in the control of the metaphase-anaphase transition during MITOSIS. It promotes the onset of anaphase by blocking SEPARASE function and preventing proteolysis of cohesin and separation of sister CHROMATIDS. Overexpression of securin is associated with NEOPLASTIC CELL TRANSFORMATION and tumor formation.
Cyclin B
F-Box Proteins
A family of proteins that share the F-BOX MOTIF and are involved in protein-protein interactions. They play an important role in process of protein ubiquition by associating with a variety of substrates and then associating into SCF UBIQUITIN LIGASE complexes. They are held in the ubiquitin-ligase complex via binding to SKP DOMAIN PROTEINS.
Genes, APC
Metaphase
Ligases
M Phase Cell Cycle Checkpoints
Cyclin A2
Apc5 Subunit, Anaphase-Promoting Complex-Cyclosome
Mad2 Proteins
Mad2 is a component of the spindle-assembly checkpoint apparatus. It binds to and inhibits the Cdc20 activator subunit of the anaphase-promoting complex, preventing the onset of anaphase until all chromosomes are properly aligned at the metaphase plate. Mad2 is required for proper microtubule capture at KINETOCHORES.
Cyclin B1
Ubiquitin-Protein Ligases
A diverse class of enzymes that interact with UBIQUITIN-CONJUGATING ENZYMES and ubiquitination-specific protein substrates. Each member of this enzyme group has its own distinct specificity for a substrate and ubiquitin-conjugating enzyme. Ubiquitin-protein ligases exist as both monomeric proteins multiprotein complexes.
Cell Cycle
The complex series of phenomena, occurring between the end of one CELL DIVISION and the end of the next, by which cellular material is duplicated and then divided between two daughter cells. The cell cycle includes INTERPHASE, which includes G0 PHASE; G1 PHASE; S PHASE; and G2 PHASE, and CELL DIVISION PHASE.
Prometaphase
CDC2 Protein Kinase
Phosphoprotein with protein kinase activity that functions in the G2/M phase transition of the CELL CYCLE. It is the catalytic subunit of the MATURATION-PROMOTING FACTOR and complexes with both CYCLIN A and CYCLIN B in mammalian cells. The maximal activity of cyclin-dependent kinase 1 is achieved when it is fully dephosphorylated.
HeLa Cells
Meiosis
Ubiquitination
Geminin
Schizosaccharomyces pombe Proteins
Apc2 Subunit, Anaphase-Promoting Complex-Cyclosome
Together with the Apc11 subunit, forms the catalytic core of the E3 ubiquitin ligase anaphase-promoting complex (APC-C). Its N-terminus has cullin domains which associate with the RING FINGER DOMAINS of Apc11. Apc2 also interacts with the E2 ubiquitin ligases involved in APC-C ubiquitination reactions.
Cyclin A
Saccharomyces cerevisiae Proteins
Protein-Serine-Threonine Kinases
Molecular Sequence Data
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.
Schizosaccharomyces
Apc8 Subunit, Anaphase-Promoting Complex-Cyclosome
A highly conserved subunit of the anaphase-promoting complex (APC-C) containing multiple 34-amino-acid tetratricopeptide repeats. These domains, also found in Apc3, Apc6, and Apc7, have been shown to mediate protein-protein interactions, suggesting that Apc8 may assist in coordinating the juxtaposition of the catalytic and substrate recognition module subunits relative to coactivators and APC-C inhibitors.
Separase
Amino Acid Sequence
Nocodazole
Mutation
Nuclear Proteins
Telophase
Aurora Kinases
A family of highly conserved serine-threonine kinases that are involved in the regulation of MITOSIS. They are involved in many aspects of cell division, including centrosome duplication, SPINDLE APPARATUS formation, chromosome alignment, attachment to the spindle, checkpoint activation, and CYTOKINESIS.
Chromatids
Either of the two longitudinally adjacent threads formed when a eukaryotic chromosome replicates prior to mitosis. The chromatids are held together at the centromere. Sister chromatids are derived from the same chromosome. (Singleton & Sainsbury, Dictionary of Microbiology and Molecular Biology, 2d ed)
Proto-Oncogene Proteins c-mos
Xenopus Proteins
G1 Phase
Genes, cdc
Protein Binding
Oocytes
Protein Subunits
Microtubules
Ubiquitin
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.
Ubiquitin-Conjugating Enzymes
Xenopus
Apc6 Subunit, Anaphase-Promoting Complex-Cyclosome
A highly conserved subunit of the anaphase-promoting complex (APC-C) containing multiple 34 amino acid tetratricopeptide repeats. These domains, also found in Apc3, Apc7, and Apc8, have been shown to mediate protein-protein interactions, suggesting that Apc6 may assist in coordinating the juxtaposition of the catalytic and substrate recognition module subunits relative to coactivators and APC-C inhibitors.
SKP Cullin F-Box Protein Ligases
Saccharomyces cerevisiae
Ubiquitins
Kinetochores
Proteasome Endopeptidase Complex
A large multisubunit complex that plays an important role in the degradation of most of the cytosolic and nuclear proteins in eukaryotic cells. It contains a 700-kDa catalytic sub-complex and two 700-kDa regulatory sub-complexes. The complex digests ubiquitinated proteins and protein activated via ornithine decarboxylase antizyme.
Phosphorylation
RNA Interference
A gene silencing phenomenon whereby specific dsRNAs (RNA, DOUBLE-STRANDED) trigger the degradation of homologous mRNA (RNA, MESSENGER). The specific dsRNAs are processed into SMALL INTERFERING RNA (siRNA) which serves as a guide for cleavage of the homologous mRNA in the RNA-INDUCED SILENCING COMPLEX. DNA METHYLATION may also be triggered during this process.
Chromosomes
Recombinant Fusion Proteins
S Phase
Amino Acid Motifs
Calcium-Binding Proteins
Drosophila Proteins
Models, Biological
G2 Phase
Protein Kinases
Substrate Specificity
Centromere
Apc11 Subunit, Anaphase-Promoting Complex-Cyclosome
Carrier Proteins
Repressor Proteins
Adenomatous Polyposis Coli Protein
Cadherins
Calcium-dependent cell adhesion proteins. They are important in the formation of ADHERENS JUNCTIONS between cells. Cadherins are classified by their distinct immunological and tissue specificities, either by letters (E- for epithelial, N- for neural, and P- for placental cadherins) or by numbers (cadherin-12 or N-cadherin 2 for brain-cadherin). Cadherins promote cell adhesion via a homophilic mechanism as in the construction of tissues and of the whole animal body.
Protein Processing, Post-Translational
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.
Cyclins
Drosophila
RNA, Small Interfering
Small double-stranded, non-protein coding RNAs (21-31 nucleotides) involved in GENE SILENCING functions, especially RNA INTERFERENCE (RNAi). Endogenously, siRNAs are generated from dsRNAs (RNA, DOUBLE-STRANDED) by the same ribonuclease, Dicer, that generates miRNAs (MICRORNAS). The perfect match of the siRNAs' antisense strand to their target RNAs mediates RNAi by siRNA-guided RNA cleavage. siRNAs fall into different classes including trans-acting siRNA (tasiRNA), repeat-associated RNA (rasiRNA), small-scan RNA (scnRNA), and Piwi protein-interacting RNA (piRNA) and have different specific gene silencing functions.
Protein Stability
Chromosomal Proteins, Non-Histone
Macromolecular Substances
Apc7 Subunit, Anaphase-Promoting Complex-Cyclosome
A highly conserved subunit of the anaphase-promoting complex (APC-C) containing multiple 34 amino acid tetratricopeptide repeats. These domains, also found in Apc3, Apc6, and Apc8, have been shown to mediate protein-protein interactions, suggesting that Apc7 may assist in coordinating the juxtaposition of the catalytic and substrate recognition module subunits relative to coactivators and APC-C inhibitors.
Cyclin-Dependent Kinases
Base Sequence
Microtubule-Associated Proteins
Sequence Homology, Amino Acid
Kinesin
A microtubule-associated mechanical adenosine triphosphatase, that uses the energy of ATP hydrolysis to move organelles along microtubules toward the plus end of the microtubule. The protein is found in squid axoplasm, optic lobes, and in bovine brain. Bovine kinesin is a heterotetramer composed of two heavy (120 kDa) and two light (62 kDa) chains. EC 3.6.1.-.
Prophase
Bivalvia
Endoreduplication
Endopeptidases
Tubulin
A microtubule subunit protein found in large quantities in mammalian brain. It has also been isolated from SPERM FLAGELLUM; CILIA; and other sources. Structurally, the protein is a dimer with a molecular weight of approximately 120,000 and a sedimentation coefficient of 5.8S. It binds to COLCHICINE; VINCRISTINE; and VINBLASTINE.
Interphase
Aurora Kinase B
Protein Structure, Tertiary
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.
Spermatocytes
Cell Nucleus
Within a eukaryotic cell, a membrane-limited body which contains chromosomes and one or more nucleoli (CELL NUCLEOLUS). The nuclear membrane consists of a double unit-type membrane which is perforated by a number of pores; the outermost membrane is continuous with the ENDOPLASMIC RETICULUM. A cell may contain more than one nucleus. (From Singleton & Sainsbury, Dictionary of Microbiology and Molecular Biology, 2d ed)
Cell Division
Apc10 Subunit, Anaphase-Promoting Complex-Cyclosome
Centrosome
The cell center, consisting of a pair of CENTRIOLES surrounded by a cloud of amorphous material called the pericentriolar region. During interphase, the centrosome nucleates microtubule outgrowth. The centrosome duplicates and, during mitosis, separates to form the two poles of the mitotic spindle (MITOTIC SPINDLE APPARATUS).
Sequence Alignment
The arrangement of two or more amino acid or base sequences from an organism or organisms in such a way as to align areas of the sequences sharing common properties. The degree of relatedness or homology between the sequences is predicted computationally or statistically based on weights assigned to the elements aligned between the sequences. This in turn can serve as a potential indicator of the genetic relatedness between the organisms.
Microscopy, Fluorescence
Adenomatous Polyposis Coli
Binding Sites
Embryo, Nonmammalian
Saccharomycetales
Cloning, Molecular
Macropodidae
Two-Hybrid System Techniques
Screening techniques first developed in yeast to identify genes encoding interacting proteins. Variations are used to evaluate interplay between proteins and other molecules. Two-hybrid techniques refer to analysis for protein-protein interactions, one-hybrid for DNA-protein interactions, three-hybrid interactions for RNA-protein interactions or ligand-based interactions. Reverse n-hybrid techniques refer to analysis for mutations or other small molecules that dissociate known interactions.
Chromosomes, Fungal
Caenorhabditis elegans
Signal Transduction
The intracellular transfer of information (biological activation/inhibition) through a signal pathway. In each signal transduction system, an activation/inhibition signal from a biologically active molecule (hormone, neurotransmitter) is mediated via the coupling of a receptor/enzyme to a second messenger system or to an ion channel. Signal transduction plays an important role in activating cellular functions, cell differentiation, and cell proliferation. Examples of signal transduction systems are the GAMMA-AMINOBUTYRIC ACID-postsynaptic receptor-calcium ion channel system, the receptor-mediated T-cell activation pathway, and the receptor-mediated activation of phospholipases. Those coupled to membrane depolarization or intracellular release of calcium include the receptor-mediated activation of cytotoxic functions in granulocytes and the synaptic potentiation of protein kinase activation. Some signal transduction pathways may be part of larger signal transduction pathways; for example, protein kinase activation is part of the platelet activation signal pathway.
Enzyme Activation
Cell Cycle Checkpoints
Regulatory signaling systems that control the progression through the CELL CYCLE. They ensure that the cell has completed, in the correct order and without mistakes, all the processes required to replicate the GENOME and CYTOPLASM, and divide them equally between two daughter cells. If cells sense they have not completed these processes or that the environment does not have the nutrients and growth hormones in place to proceed, then the cells are restrained (or "arrested") until the processes are completed and growth conditions are suitable.
Dyneins
Chromosomes, Human
Nondisjunction, Genetic
Escherichia coli
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.
Proteolysis
Multiprotein Complexes
Protein Conformation
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).
Gene Expression Regulation, Fungal
Fluorescent Antibody Technique
Test for tissue antigen using either a direct method, by conjugation of antibody with fluorescent dye (FLUORESCENT ANTIBODY TECHNIQUE, DIRECT) or an indirect method, by formation of antigen-antibody complex which is then labeled with fluorescein-conjugated anti-immunoglobulin antibody (FLUORESCENT ANTIBODY TECHNIQUE, INDIRECT). The tissue is then examined by fluorescence microscopy.
Phosphoprotein Phosphatases
DNA-Binding Proteins
Green Fluorescent Proteins
Cell Nucleolus
Within most types of eukaryotic CELL NUCLEUS, a distinct region, not delimited by a membrane, in which some species of rRNA (RNA, RIBOSOMAL) are synthesized and assembled into ribonucleoprotein subunits of ribosomes. In the nucleolus rRNA is transcribed from a nucleolar organizer, i.e., a group of tandemly repeated chromosomal genes which encode rRNA and which are transcribed by RNA polymerase I. (Singleton & Sainsbury, Dictionary of Microbiology & Molecular Biology, 2d ed)
Cells, Cultured
Electrophoresis, Polyacrylamide Gel
Proton-Translocating ATPases
Protein Phosphatase 2
A phosphoprotein phosphatase subtype that is comprised of a catalytic subunit and two different regulatory subunits. At least two genes encode isoforms of the protein phosphatase catalytic subunit, while several isoforms of regulatory subunits exist due to the presence of multiple genes and the alternative splicing of their mRNAs. Protein phosphatase 2 acts on a broad variety of cellular proteins and may play a role as a regulator of intracellular signaling processes.
Models, Molecular
DNA, Catenated
Phenotype
Potoroidae
RNA, Messenger
RNA sequences that serve as templates for protein synthesis. Bacterial mRNAs are generally primary transcripts in that they do not require post-transcriptional processing. Eukaryotic mRNA is synthesized in the nucleus and must be exported to the cytoplasm for translation. Most eukaryotic mRNAs have a sequence of polyadenylic acid at the 3' end, referred to as the poly(A) tail. The function of this tail is not known for certain, but it may play a role in the export of mature mRNA from the nucleus as well as in helping stabilize some mRNA molecules by retarding their degradation in the cytoplasm.
Protein Tyrosine Phosphatases
Chromosomal Instability
Protein C
Cytoskeletal Proteins
Dipodomys
Mutagenesis, Site-Directed
Aneuploidy
The chromosomal constitution of cells which deviate from the normal by the addition or subtraction of CHROMOSOMES, chromosome pairs, or chromosome fragments. In a normally diploid cell (DIPLOIDY) the loss of a chromosome pair is termed nullisomy (symbol: 2N-2), the loss of a single chromosome is MONOSOMY (symbol: 2N-1), the addition of a chromosome pair is tetrasomy (symbol: 2N+2), the addition of a single chromosome is TRISOMY (symbol: 2N+1).
Proteins
Linear POLYPEPTIDES that are synthesized on RIBOSOMES and may be further modified, crosslinked, cleaved, or assembled into complex proteins with several subunits. The specific sequence of AMINO ACIDS determines the shape the polypeptide will take, during PROTEIN FOLDING, and the function of the protein.
Protein Transport
Sister Chromatid Exchange
An exchange of segments between the sister chromatids of a chromosome, either between the sister chromatids of a meiotic tetrad or between the sister chromatids of a duplicated somatic chromosome. Its frequency is increased by ultraviolet and ionizing radiation and other mutagenic agents and is particularly high in BLOOM SYNDROME.
Blotting, Western
Microscopy, Video
Diptera
An order of the class Insecta. Wings, when present, number two and distinguish Diptera from other so-called flies, while the halteres, or reduced hindwings, separate Diptera from other insects with one pair of wings. The order includes the families Calliphoridae, Oestridae, Phoridae, SARCOPHAGIDAE, Scatophagidae, Sciaridae, SIMULIIDAE, Tabanidae, Therevidae, Trypetidae, CERATOPOGONIDAE; CHIRONOMIDAE; CULICIDAE; DROSOPHILIDAE; GLOSSINIDAE; MUSCIDAE; TEPHRITIDAE; and PSYCHODIDAE. The larval form of Diptera species are called maggots (see LARVA).
Adenosine Triphosphatases
Mutagenesis
Luminescent Proteins
DNA Primers
Drosophila melanogaster
DNA
A deoxyribonucleotide polymer that is the primary genetic material of all cells. Eukaryotic and prokaryotic organisms normally contain DNA in a double-stranded state, yet several important biological processes transiently involve single-stranded regions. DNA, which consists of a polysugar-phosphate backbone possessing projections of purines (adenine and guanine) and pyrimidines (thymine and cytosine), forms a double helix that is held together by hydrogen bonds between these purines and pyrimidines (adenine to thymine and guanine to cytosine).
Microinjections
Cytoplasm
Gene Deletion
Transfection
Peptide Fragments
Proto-Oncogene Proteins
Vaccines, Subunit
Nuclear Matrix-Associated Proteins
beta Catenin
A multi-functional catenin that participates in CELL ADHESION and nuclear signaling. Beta catenin binds CADHERINS and helps link their cytoplasmic tails to the ACTIN in the CYTOSKELETON via ALPHA CATENIN. It also serves as a transcriptional co-activator and downstream component of WNT PROTEIN-mediated SIGNAL TRANSDUCTION PATHWAYS.
DNA, Complementary
Chromatin
Vacuolar Proton-Translocating ATPases
Salamandridae
Xenopus laevis
Antigen-Presenting Cells
A heterogeneous group of immunocompetent cells that mediate the cellular immune response by processing and presenting antigens to the T-cells. Traditional antigen-presenting cells include MACROPHAGES; DENDRITIC CELLS; LANGERHANS CELLS; and B-LYMPHOCYTES. FOLLICULAR DENDRITIC CELLS are not traditional antigen-presenting cells, but because they hold antigen on their cell surface in the form of IMMUNE COMPLEXES for B-cell recognition they are considered so by some authors.
Transcription, Genetic
Precipitin Tests
The schizosaccharomyces pombe dim1(+) gene interacts with the anaphase-promoting complex or cyclosome (APC/C) component lid1(+) and is required for APC/C function. (1/54)
The Schizosaccharomyces pombe dim1(+) gene is required for entry into mitosis and for chromosome segregation during mitosis. To further understand dim1p function, we undertook a synthetic lethal screen with the temperature-sensitive dim1-35 mutant and isolated lid (for lethal in dim1-35) mutants. Here, we describe the temperature-sensitive lid1-6 mutant. At the restrictive temperature of 36 degrees C, lid1-6 mutant cells arrest with a "cut" phenotype similar to that of cut4 and cut9 mutants. An epitope-tagged version of lid1p is a component of a multiprotein approximately 20S complex; the presence of lid1p in this complex depends upon functional cut9(+). lid1p-myc coimmunoprecipitates with several other proteins, including cut9p and nuc2p, and the presence of cut9p in a 20S complex depends upon the activity of lid1(+). Further, lid1(+) function is required for the multiubiquitination of cut2p, an anaphase-promoting complex or cyclosome (APC/C) target. Thus, lid1p is a component of the S. pombe APC/C. In dim1 mutants, the abundances of lid1p and the APC/C complex decline significantly, and the ubiquitination of an APC/C target is abolished. These data suggest that at least one role of dim1p is to maintain or establish the steady-state level of the APC/C. (+info)Isolation and identification of the third subunit of mammalian DNA polymerase delta by PCNA-affinity chromatography of mouse FM3A cell extracts. (2/54)
Using proliferating cell nuclear antigen affinity chroma-tography and glycerol gradient centrifugation of partially purified fractions from mouse FM3A cells we have been able to isolate novel complexes of DNA polymerase delta and DNA ligase 1 containing clearly defined subunit compositions. In addition to the well known catalytic subunit of 125 kDa and accessory subunit of 48 kDa, the DNA polymerase delta complex contained three supplementary components, one of which reacted with antibodies directed against the p40 and p37 subunits of RF-C. Of the two remaining components, one termed p66 turned out to be coded by a gene whose putative C-terminal domain displayed significant homology with that of the Cdc27 subunit of Schizosaccharomyces pombe polymerase delta. On the basis of these and other observations, we propose p66 to be the missing third subunit of mammalian DNA polymerase delta. The DNA ligase 1 complex was made up of three novel components in addition to the 125 kDa catalytic subunit, two of which, p48 and p66, were common to DNA polymerase delta. We discuss the implications of our findings within the current framework of our understanding of DNA replication. (+info)Cloning genes encoding MHC class II-restricted antigens: mutated CDC27 as a tumor antigen. (3/54)
In an effort to identify tumor-specific antigens recognized by CD4(+) T cells, an approach was developed that allows the screening of an invariant chain-complementary DNA fusion library in a genetically engineered cell line expressing the essential components of the major histocompatibility complex (MHC) class II processing and presentation pathway. This led to the identification of a mutated form of human CDC27, which gave rise to an HLA-DR4-restricted melanoma antigen. A mutated form of triosephosphate isomerase, isolated by a biochemical method, was also identified as an HLA-DR1-restricted antigen. Thus, this approach may be generally applicable to the identification of antigens recognized by CD4(+) T cells, which could aid the development of strategies for the treatment of patients with cancer, autoimmune diseases, or infectious diseases. (+info)Expression of the CDH1-associated form of the anaphase-promoting complex in postmitotic neurons. (4/54)
The anaphase-promoting complex/cyclosome (APC) is a tightly cell cycle-regulated ubiquitin-protein ligase that targets cyclin B and other destruction box-containing proteins for proteolysis at the end of mitosis and in G1. Recent work has shown that activation of the APC in mitosis depends on CDC20, whereas APC is maintained active in G1 via association with the CDC20-related protein CDH1. Here we show that the mitotic activator CDC20 is the only component of the APC ubiquitination pathway whose expression is restricted to proliferating cells, whereas the APC and CDH1 are also expressed in several mammalian tissues that predominantly contain differentiated cells, such as adult brain. Immunocytochemical analyses of cultured rat hippocampal neurons and of mouse and human brain sections indicate that the APC and CDH1 are ubiquitously expressed in the nuclei of postmitotic terminally differentiated neurons. The APC purified from brain contains all core subunits known from proliferating cells and is tightly associated with CDH1. Purified brain APC(CDH1) has a high cyclin B ubiquitination activity that depends less on the destruction box than on the activity of mitotic APC(CDC20). On the basis of these results, we propose that the functions of APC(CDH1) are not restricted to controlling cell-cycle progression but may include the ubiquitination of yet unidentified substrates in differentiated cells. (+info)Cdc20 protein contains a destruction-box but, unlike Clb2, its proteolysisis not acutely dependent on the activity of anaphase-promoting complex. (5/54)
Both chromosome segregation and the final exit from mitosis require a ubiquitin-protein ligase called anaphase-promoting complex (APC) or cyclosome. This multiprotein complex ubiquitinates various substrates, such as the anaphase inhibitor Pds1 and mitotic cyclins, and thus targets them for proteolysis by the 26S proteasome. The ubiquitination by APC is dependent on the presence of a destruction-box sequence in the N-terminus of target proteins. Recent reports have strongly suggested that Cdc20, a WD40 repeat-containing protein required for nuclear division in the budding yeast Saccharomyces cerevisiae, is essential for the APC-mediated proteolysis. To understand the function of CDC20, we have studied its regulation in some detail. The expression of the CDC20 gene is cell-cycle regulated such that it is transcribed only during late S phase and mitosis. Although the protein is unstable to some extent through out the cell cycle, its degradation is particularly enhanced in G1. Cdc20 contains a destruction box sequence which, when mutated or deleted, stabilizes it considerably in G1. Surprisingly, we find that while the inactivation of APC subunits Cdc16, Cdc23 or Cdc27 results in stabilization of the mitotic cyclin Clb2 in G1, the proteolytic destruction of Cdc20 remains largely unaffected. This suggests the existence of proteolytic mechanisms in G1 that can degrade destruction-box containing proteins, such as Cdc20, in an APC-independent manner. (+info)Essential interaction between the fission yeast DNA polymerase delta subunit Cdc27 and Pcn1 (PCNA) mediated through a C-terminal p21(Cip1)-like PCNA binding motif. (6/54)
Direct interaction between DNA polymerase delta and its processivity factor proliferating cell nuclear antigen (PCNA) is essential for effective replication of the eukaryotic genome, yet the precise manner by which this occurs is unclear. We show that the 54 kDa subunit of DNA polymerase delta from Schizosaccharomyces pombe interacts directly with Pcn1 (PCNA) both in vivo and in vitro. Binding is effected via a short sequence at the C-terminus of Cdc27 with significant similarity to the canonical PCNA binding motif first identified in the mammalian p21(Cip1) protein. This motif is both necessary and sufficient for binding of Pcn1 by Cdc27 in vitro and is essential for Cdc27 function in vivo. We also show that the Pcn1 binding motif in Cdc27 is distinct from its binding site for Cdc1, the 55 kDa B-subunit of polymerase delta, and present evidence that Cdc27 can bind to Pcn1 and Cdc1 simultaneously. Finally, we show that Cdc27 performs at least two distinct essential functions, one of which is independent of Pcn1 binding. (+info)Phosphorylation by Cdc28 activates the Cdc20-dependent activity of the anaphase-promoting complex. (7/54)
Budding yeast initiates anaphase by activating the Cdc20-dependent anaphase-promoting complex (APC). The mitotic activity of Cdc28 (Cdk1) is required to activate this form of the APC, and mutants that are impaired in mitotic Cdc28 function have difficulty leaving mitosis. This defect can be explained by a defect in APC phosphorylation, which depends on mitotic Cdc28 activity in vivo and can be catalyzed by purified Cdc28 in vitro. Mutating putative Cdc28 phosphorylation sites in three components of the APC, Cdc16, Cdc23, and Cdc27, makes the APC resistant to phosphorylation both in vivo and in vitro. The nonphosphorylatable APC has normal activity in G1, but its mitotic, Cdc20-dependent activity is compromised. These results show that Cdc28 activates the APC in budding yeast to trigger anaphase. Previous reports have shown that the budding yeast Cdc5 homologue, Plk, can also phosphorylate and activate the APC in vitro. We show that, like cdc28 mutants, cdc5 mutants affect APC phosphorylation in vivo. However, although Cdc5 can phosphorylate Cdc16 and Cdc27 in vitro, this in vitro phosphorylation does not occur on in vivo sites of phosphorylation. (+info)The human homologue of fission Yeast cdc27, p66, is a component of active human DNA polymerase delta. (8/54)
An essential eukaryotic DNA polymerase, DNA polymerase delta (pol delta), synthesizes DNA processively in the presence of proliferating cell nuclear antigen (PCNA). Recently, a 66 kDa polypeptide (p66) that displays significant homology within its PCNA binding domain to that of fission yeast cdc27 was identified as a component of mouse and calf thymus pol delta. Our studies show that p66 interacts tightly with other subunits of pol delta during size fractionation of human cell extracts, and co-immunoprecipitates with these subunits along with PCNA-dependent polymerase activity. Active human pol delta could be reconstituted by co-expressing p125, p50, and p66 recombinant baculoviruses, but not by co-expressing p125 and p50 alone. Interaction studies demonstrated that p66 stabilizes the association between p125 and p50. Pull-down assays with PCNA-linked beads demonstrated that p66 increases the overall affinity of pol delta for PCNA. These results indicate that p66 is a functionally important subunit of human pol delta that stabilizes the pol delta complex and increases the affinity of pol delta for PCNA. (+info)
Mendeley Data - Helicase subunit Cdc45 targets the checkpoint kinase Rad53 to both replication initiation and elongation...
Anaphase-promoting complex, subunit CDC26 (IPR018860) | InterPro | EMBL-EBI
C Functions
Addgene: pmKalama1-Nuc
Identification of the C. elegansanaphase promoting complex subunit Cdc26 by phenotypic profiling and functional rescue in yeast
CDC23 - Anaphase-promoting complex subunit CDC23 - Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Bakers yeast) -...
CDC26 - Anaphase-promoting complex subunit CDC26 - Homo sapiens (Human) - CDC26 gene & protein
Frunze de Nuc Negru | Ekilibrium.ro
Intel nuc displayport not working
英特尔® Trusted Execution Engine NUC5CPYH、NUC5PPYH、NUC5PGYH 的驱动程序(英特尔® TXE)驱动程序
Fun Shapes with Pedal Equation
Dental Specialist, Cosmetic Dentistry, Tooth Whitening, Ahmedabad, Dental Cosmetic Surgeon
ffi pack for SWI...
downloads for intel nuc kits in tanzania
Analysis Library C Function Reference - LabVIEW NXG 3.0 Manual - National Instruments
Intel NUC Kit NUC8i7HVK (Hades Canyon) Review | PCMag
Linking Excel to C - 2 | Newton Excel Bach, not (just) an Excel Blog
Linking Excel to C - 2 | Newton Excel Bach, not (just) an Excel Blog
NUC7i7BNH freezing on workload / not with Hyper... |Intel Communities
Actualización del BIOS para el kit para computadoras portátiles Intel® NUC M15: LAPBCx10 [BCTGL357]
Examining Inducible Expression of the Poxvirus Anaphase-promoting Complex Regulator (PACR)
Cdk1 phosphorylation sites on Cdc27 are required for correct chromosomal localisation and APC/C function in syncytial...
Intel NUC NUC6i7KYK Skull Canyon Internal USB 3.0 Header Cable
NUC122LC1AN - Nuvoton
Intel® NUC Rugged Chassis Element CMCR1ABB
Dynamic ubiquitin signaling in cell cycle regulation | JCB
RCSB PDB - 5L9U: Model of human Anaphase-promoting complex/Cyclosome (APC/C-CDH1) with a cross linked Ubiquitin variant...
Anaphase-promoting complex subunit 1 (IPR024990) | InterPro | EMBL-EBI
Chicken (Scheme implementation) - Wikipedia
Chapter 3 Macromolecules - d Important sugars e Polysaccharides IV NUCLEIC ACIDS a Monomer b Linkage c Functions store genetic...
Intel® NUC Chassis Elements
Animal Cell Diagram - Nevron Diagram for .NET is a fully managed,
The anaphase-promoting complex/cyclosome › Research Explorer
University of Birmingham research gateway
RADIOSHOW
ANTIGEN PRESENTATION AND ASSEMBLY BY MOUSE I-A(K) CLASS-II MOLECULES IN HUMAN APC CONTAINING DELETED OR MUTATED HLA DM GENES -...
5:49 am
Intel Launching Skull Canyon Platform In Q1 2016 - Flagship SKU Will Be Most Powerful NUC To Date, Features Iris Pro 580...
Solved: Re: Network Unlocking Code (NUC) - Page 2 - Community home
Didattica
Anti ANAPC7 Antibody (PrecisionAb Monoclonal Antibody) | Bio-Rad
Sequence Similarity
- 1GQP: APC10/DOC1 SUBUNIT OF S. cerevisiae Sequence Similarity Report Page
Networking and Storage Performance - The Intel Skull Canyon NUC6i7KYK mini-PC Review
Identification of Subunits of the Anaphase-Promoting Complex of Saccharomyces cerevisiae | Science
josie lyrics meaning
Noise Club TakeOver on the App WOOV
Solved: Re: Network Unlocking Code (NUC) - Community home
Download PDF From ideas to expression by Aspen Institute Forum (1997) Ebook
Anaphase-promoting complex
April 2015). "Structure of an APC3-APC16 complex: insights into assembly of the anaphase-promoting complex/cyclosome". Journal ... a Drosophila gene encoding the Cdc27 subunit of the anaphase promoting complex, enhance centrosomal defects in polo and are ... Evidence shows that APC3 and APC7 serve to recruit Cdh1 to the anaphase-promoting complex. This further supports that Cdh1 is ... Anaphase-promoting complex (also called the cyclosome or APC/C) is an E3 ubiquitin ligase that marks target cell cycle proteins ...
ANAPC5
The anaphase-promoting complex (APC) consists of at least 8 protein subunits, including APC5, CDC27 (APC3; MIM 116946), CDC16 ( ... 2004). "The Apc5 Subunit of the Anaphase-Promoting Complex/Cyclosome Interacts with Poly(A) Binding Protein and Represses ... "The Apc5 Subunit of the Anaphase-Promoting Complex/Cyclosome Interacts with Poly(A) Binding Protein and Represses Internal ... 2004). "TPR subunits of the anaphase-promoting complex mediate binding to the activator protein CDH1". Curr. Biol. 13 (17): ...
CDC27
"The Apc5 subunit of the anaphase-promoting complex/cyclosome interacts with poly(A) binding protein and represses internal ... "The dephosphorylated form of the anaphase-promoting complex protein Cdc27/Apc3 concentrates on kinetochores and chromosome arms ... "TPR subunits of the anaphase-promoting complex mediate binding to the activator protein CDH1". Current Biology. 13 (17): 1459- ... This protein is a component of anaphase-promoting complex (APC), which is composed of eight protein subunits and highly ...
Genes search | AnalogYeast
Anaphase-promoting complex subunit cut9 (20S cyclosome/APC complex protein cut9) (Cell untimely torn protein 9) ... Cell division cycle protein 27 homolog (Anaphase-promoting complex subunit 3) (APC3) (CDC27 homolog) (CDC27Hs) (H-NUC) ... UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit (EC 2.4.1.255) (O-GlcNAc transferase subunit ... Anaphase-promoting complex subunit 7 (APC7) (Cyclosome subunit 7). Homo sapiens 4ui9_y Q9UJX3 ENSG00000196510 ANAPC7 99.80 9.90 ...
Publications | NECAT
Structure of an APC3-APC16 complex: insights into assembly of the anaphase-promoting complex/cyclosome. J Mol Biol. 427, 1748- ... Insights into the ribosome function from the structures of non-arrested ribosome-nascent chain complexes. Nat Chem. 10.1038/ ...
DeCS
Apc3 Subunit, Anaphase Promoting Complex Apc3 Subunit, Anaphase Promoting Complex Cyclosome Apc3 Subunit, Anaphase-Promoting ... Apc3 Subunit, Anaphase Promoting Complex. Apc3 Subunit, Anaphase Promoting Complex Cyclosome. Apc3 Subunit, Anaphase-Promoting ... Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome [D08.811.464.938.750.092.875] Apc3 Subunit, Anaphase-Promoting Complex- ... Apc1 Subunit, Anaphase-Promoting Complex-Cyclosome [D08.811.464.938.750.092.500] Apc1 Subunit, Anaphase-Promoting Complex- ...
Genes search | AnalogYeast
Anaphase-promoting complex subunit cut9 (20S cyclosome/APC complex protein cut9) (Cell untimely torn protein 9) ... Cell division cycle protein 27 homolog (Anaphase-promoting complex subunit 3) (APC3) (CDC27 homolog) (CDC27Hs) (H-NUC) ... UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit (EC 2.4.1.255) (O-GlcNAc transferase subunit ... Anaphase-promoting complex subunit 7 (APC7) (Cyclosome subunit 7). Homo sapiens 4ui9_y Q9UJX3 ENSG00000196510 ANAPC7 99.80 9.90 ...
DeCS 2014 - New terms
Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc3 ... Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc3 ... Apc1 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc1 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc1 ... Apc2 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc2 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc2 ...
DeCS 2014 - New terms
Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc3 ... Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc3 ... Apc1 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc1 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc1 ... Apc2 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc2 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc2 ...
DeCS 2014 - New terms
Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc3 ... Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc3 ... Apc1 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc1 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc1 ... Apc2 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc2 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc2 ...
DeCS 2014 - New terms
Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc3 ... Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc3 ... Apc1 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc1 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc1 ... Apc2 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc2 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc2 ...
DeCS 2014 - New terms
Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc3 ... Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc3 ... Apc1 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc1 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc1 ... Apc2 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc2 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc2 ...
DeCS 2014 - New terms
Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc3 ... Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc3 ... Apc1 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc1 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc1 ... Apc2 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc2 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc2 ...
DeCS 2014 - New terms
Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc3 ... Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc3 ... Apc1 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc1 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc1 ... Apc2 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc2 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc2 ...
DeCS 2014 - Novos termos
Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidad Apc3 ... Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidad Apc3 ... Apc1 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidad Apc1 del Ciclosoma-Complejo Promotor de la Anafase. ... Apc10 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidad Apc10 del Ciclosoma-Complejo Promotor de la Anafase. ...
ANAPC16 (anaphase promoting complex subunit 16)
Structure of an APC3-APC16 complex: insights into assembly of the anaphase-promoting complex/cyclosome.. 17. ... Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components. ... Inactivation of APC/C via direct inhibition of the APC/C complex. REACTOME. R-HSA-141430. ... Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase. REACTOME. R-HSA-176407. ...
MeSH Browser
Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome [D12.776.167.024.875] * Apc4 Subunit, Anaphase-Promoting Complex-Cyclosome [ ... Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome [D08.811.464.938.750.092.875] * Apc4 Subunit, Anaphase-Promoting Complex- ... Apc5 Subunit, Anaphase-Promoting Complex-Cyclosome [D12.776.167.024.968] * Apc6 Subunit, Anaphase-Promoting Complex-Cyclosome [ ... Apc7 Subunit, Anaphase-Promoting Complex-Cyclosome [D12.776.167.024.992] * Apc8 Subunit, Anaphase-Promoting Complex-Cyclosome [ ...
Association between polymorphisms in cdc27 and breast cancer in a Chinese population - PubMed
... as a core component of anaphase-promoting complex (APC), is a cell cycle regulator, which participates in control of mitotic ... Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome / genetics* Actions. * Search in PubMed * Search in MeSH ... Cdc27, as a core component of anaphase-promoting complex (APC), is a cell cycle regulator, which participates in control of ... Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome Actions. * Search in PubMed * Search in MeSH ...
MeSH Browser
Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome [D12.776.167.024.875] * Apc4 Subunit, Anaphase-Promoting Complex-Cyclosome [ ... Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome [D08.811.464.938.750.092.875] * Apc4 Subunit, Anaphase-Promoting Complex- ... Apc5 Subunit, Anaphase-Promoting Complex-Cyclosome [D12.776.167.024.968] * Apc6 Subunit, Anaphase-Promoting Complex-Cyclosome [ ... Apc7 Subunit, Anaphase-Promoting Complex-Cyclosome [D12.776.167.024.992] * Apc8 Subunit, Anaphase-Promoting Complex-Cyclosome [ ...
NDF-RT Code NDF-RT Name
Anaphase-Promoting Complex-Cyclosome N0000189465 Apc2 Subunit, Anaphase-Promoting Complex-Cyclosome N0000189462 Apc3 Subunit, ... Anaphase-Promoting Complex-Cyclosome N0000189466 Apc4 Subunit, Anaphase-Promoting Complex-Cyclosome N0000189467 Apc5 Subunit, ... Anaphase-Promoting Complex-Cyclosome N0000189464 Apc6 Subunit, Anaphase-Promoting Complex-Cyclosome N0000189457 Apc7 Subunit, ... Anaphase-Promoting Complex-Cyclosome N0000189463 Apc10 Subunit, Anaphase-Promoting Complex-Cyclosome N0000189459 Apc11 Subunit ...
NEW (2014) MESH HEADINGS WITH SCOPE NOTES (UNIT RECORD FORMAT; 7/29/2013
HN - 2014 MH - Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome UI - D064191 MN - D8.811.464.938.750.92.875 MN - D12.776. ... HN - 2014 MH - Apc10 Subunit, Anaphase-Promoting Complex-Cyclosome UI - D064197 MN - D8.811.464.938.750.92.625 MN - D12.776. ... HN - 2014 MH - Apc11 Subunit, Anaphase-Promoting Complex-Cyclosome UI - D064198 MN - D8.811.464.938.750.92.687 MN - D12.776. ... HN - 2014 MH - Apc2 Subunit, Anaphase-Promoting Complex-Cyclosome UI - D064190 MN - D8.811.464.938.750.92.750 MN - D12.776. ...
Biomarkers Search
2. Structure of an APC3-APC16 complex: insights into assembly of the anaphase-promoting complex/cyclosome.. Yamaguchi M; Yu S; ... 4. TPR subunits of the anaphase-promoting complex mediate binding to the activator protein CDH1.. Vodermaier HC; Gieffers C; ... Functional characterization of Anaphase Promoting Complex/Cyclosome (APC/C) E3 ubiquitin ligases in tumorigenesis.. Zhang J; ... 9. The HECT type ubiquitin ligase NEDL2 is degraded by anaphase-promoting complex/cyclosome (APC/C)-Cdh1, and its tight ...
Pharos : Target Details - CDC27
This protein is a component of the anaphase-promoting complex (APC), which is composed of eight protein subunits and is highly ... The APC/C complex acts by mediating ubiquitination and subsequent degradation of target proteins: it mainly mediates the ... This complex catalyzes the formation of cyclin B-ubiquitin conjugate, which is responsible for the ubiquitin-mediated ... The protein encoded by this gene and three other members of the APC complex contain tetratricopeptide (TPR) repeats, which are ...
DeCS 2014 - New terms
Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc3 ... Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc3 ... Apc1 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc1 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc1 ... Apc2 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidade Apc2 do Ciclossomo-Complexo Promotor de Anáfase. Subunidad Apc2 ...
DeCS 2014 - Novos termos
Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidad Apc3 ... Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidad Apc3 ... Apc1 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidad Apc1 del Ciclosoma-Complejo Promotor de la Anafase. ... Apc10 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidad Apc10 del Ciclosoma-Complejo Promotor de la Anafase. ...
DeCS 2014 - Novos termos
Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidad Apc3 ... Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidad Apc3 ... Apc1 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidad Apc1 del Ciclosoma-Complejo Promotor de la Anafase. ... Apc10 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidad Apc10 del Ciclosoma-Complejo Promotor de la Anafase. ...
DeCS 2014 - Novos termos
Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidad Apc3 ... Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidad Apc3 ... Apc1 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidad Apc1 del Ciclosoma-Complejo Promotor de la Anafase. ... Apc10 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidad Apc10 del Ciclosoma-Complejo Promotor de la Anafase. ...
DeCS 2014 - Novos termos
Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidad Apc3 ... Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidad Apc3 ... Apc1 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidad Apc1 del Ciclosoma-Complejo Promotor de la Anafase. ... Apc10 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidad Apc10 del Ciclosoma-Complejo Promotor de la Anafase. ...
DeCS 2014 - Novos termos
Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidad Apc3 ... Subunidade Apc3 do Ciclossomo-Complexo Promotor de Anáfase. Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidad Apc3 ... Apc1 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidad Apc1 del Ciclosoma-Complejo Promotor de la Anafase. ... Apc10 Subunit, Anaphase-Promoting Complex-Cyclosome. Subunidad Apc10 del Ciclosoma-Complejo Promotor de la Anafase. ...
MeSH Browser
Apc2 Subunit, Anaphase-Promoting Complex-Cyclosome [D12.776.167.024.750] * Apc3 Subunit, Anaphase-Promoting Complex-Cyclosome [ ... Apc2 Subunit, Anaphase-Promoting Complex-Cyclosome [D08.811.464.938.750.092.750] * Apc3 Subunit, Anaphase-Promoting Complex- ... Apc4 Subunit, Anaphase-Promoting Complex-Cyclosome [D12.776.167.024.937] * Apc5 Subunit, Anaphase-Promoting Complex-Cyclosome [ ... Apc6 Subunit, Anaphase-Promoting Complex-Cyclosome [D12.776.167.024.984] * Apc7 Subunit, Anaphase-Promoting Complex-Cyclosome [ ...
Component of anaphase-promoti2
- Cdc27, as a core component of anaphase-promoting complex (APC), is a cell cycle regulator, which participates in control of mitotic checkpoint and surveys the mitotic spindle to maintain chromosomal integrity. (nih.gov)
- 16. Cdh1, a substrate-recruiting component of anaphase-promoting complex/cyclosome (APC/C) ubiquitin E3 ligase, specifically interacts with phosphatase and tensin homolog (PTEN) and promotes its removal from chromatin. (nih.gov)
Metaphase-to-anaphase transition3
- HN - 2014 FX - Ammonia MH - Anaphase-Promoting Complex-Cyclosome UI - D064173 MN - D8.811.464.938.750.92 MN - D12.776.167.24 MS - An E3 ubiquitin ligase primarily involved in regulation of the metaphase-to-anaphase transition during MITOSIS through ubiquitination of specific CELL CYCLE PROTEINS. (nih.gov)
- 9. The HECT type ubiquitin ligase NEDL2 is degraded by anaphase-promoting complex/cyclosome (APC/C)-Cdh1, and its tight regulation maintains the metaphase to anaphase transition. (nih.gov)
- An E3 ubiquitin ligase primarily involved in regulation of the metaphase-to-anaphase transition during MITOSIS through ubiquitination of specific CELL CYCLE PROTEINS . (nih.gov)
Substrate2
- These domains, also found in Apc subunits 6, 7, and 8, have been shown to mediate protein-protein interactions, suggesting that Apc3 may assist in coordinating the juxtaposition of the catalytic and substrate recognition module subunits relative to co-activators and APC-C inhibitors. (nih.gov)
- Enzyme activity is tightly regulated through subunits and cofactors, which modulate activation, inhibition, and substrate specificity. (nih.gov)
Mediate1
- 4. TPR subunits of the anaphase-promoting complex mediate binding to the activator protein CDH1. (nih.gov)
Postmitotic2
- 5. Expression of the CDH1-associated form of the anaphase-promoting complex in postmitotic neurons. (nih.gov)
- The anaphase-promoting complex, or APC-C, is also involved in tissue differentiation in the PLACENTA, CRYSTALLINE LENS, and SKELETAL MUSCLE , and in regulation of postmitotic NEURONAL PLASTICITY and excitability. (nih.gov)
Ligase1
- Component of the anaphase promoting complex/cyclosome (APC/C), a cell cycle-regulated E3 ubiquitin ligase that controls progression through mitosis and the G1 phase of the cell cycle. (nih.gov)
Protein1
- This protein is a component of the anaphase-promoting complex (APC), which is composed of eight protein subunits and is highly conserved in eukaryotic cells. (nih.gov)
Ubiquitination1
- The APC/C complex acts by mediating ubiquitination and subsequent degradation of target proteins: it mainly mediates the formation of 'Lys-11'-linked polyubiquitin chains and, to a lower extent, the formation of 'Lys-48'- and 'Lys-63'-linked polyubiquitin chains. (nih.gov)
Regulation1
- 18. Mitotic regulation of the human anaphase-promoting complex by phosphorylation. (nih.gov)
Highly1
- A highly evolutionarily conserved subunit of the anaphase-promoting complex (APC-C) containing multiple 34-amino-acid tetratricopeptide repeats. (nih.gov)
Structure2
- Structure of an APC3-APC16 complex: insights into assembly of the anaphase-promoting complex/cyclosome. (atlasgeneticsoncology.org)
- 12. Recombinant expression, reconstitution and structure of human anaphase-promoting complex (APC/C). (nih.gov)
Activation1
- 8. Sequestration of CDH1 by MAD2L2 prevents premature APC/C activation prior to anaphase onset. (nih.gov)