ID F2PQI4_TRIEC Unreviewed; 323 AA. AC F2PQI4; DT 31-MAY-2011, integrated into UniProtKB/TrEMBL. DT 31-MAY-2011, sequence version 1. DT 11-DEC-2019, entry version 29. DE SubName: Full=Chorismate mutase/prephenate dehydratase {ECO:0000313,EMBL:EGE04152.1}; GN ORFNames=TEQG_03185 {ECO:0000313,EMBL:EGE04152.1}; OS Trichophyton equinum (strain ATCC MYA-4606 / CBS 127.97) (Horse ringworm OS fungus). OC Eukaryota; Fungi; Dikarya; Ascomycota; Pezizomycotina; Eurotiomycetes; OC Eurotiomycetidae; Onygenales; Arthrodermataceae; Trichophyton. OX NCBI_TaxID=559882 {ECO:0000313,Proteomes:UP000009169}; RN [1] {ECO:0000313,Proteomes:UP000009169} RP NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. RC STRAIN=ATCC MYA-4606 / CBS 127.97 {ECO:0000313,Proteomes:UP000009169}; RX PubMed=22951933; DOI=10.1128/mBio.00259-12; RA Martinez D.A., Oliver B.G., Graeser Y., Goldberg J.M., Li W., RA Martinez-Rossi N.M., Monod M., Shelest E., Barton R.C., Birch E., RA Brakhage A.A., Chen Z., Gurr S.J., Heiman D., Heitman J., Kosti ...

Several derivatives of phenylalanine and tyrosine were prepared and tested for inhibition of chorismate mutase-prephenate dehydrogenase (EC 1.3.1.12) from Escherichia coli K12 (strain JP 232). The best inhibitors were N-toluene-p-sulphonyl-L-phenylalanine, N-benzenesulphonyl-L-phenylalanine and N-benzloxycarbonyl-L-phenylalanine. Consequently two compounds, N-toluene-sulphonyl-L-p-aminophenylalanine and N-p-aminobenzenesulphonyl-L-phenylalanine, were synthesized for coupling to CNBr-activated Sepharose-4B. The N-toluene-p-sulphonyl-L-p-aminophenylalanine-Sepharose-4B conjugate was shown to bind the enzyme very strongly at pH 7.5. The enzyme was not eluted by various eluents, including 1 M-NaCl, but could be quantitatively recovered by washing with buffer of pH9. Elution was more effective in the presence of 10 mM-1-adamantaneacetic acid, a competitive inhibitor of the enzyme. This affinity-chromatography procedure results in a high degree of purification of the enzyme and can be used to prepare ...

Regulation and Cell signalingRegulation and Cell signaling - no subcategoryCell envelope-associated LytR-CpsA-Psr transcriptional attenuators Prephenate dehydratase (EC 4.2.1.51) ...

Description: The chemical reactions and pathways resulting in the formation of phenylalanine and tyrosine from other compounds, including chorismate, via the intermediate prephenate.. ...

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The bacterial pheL gene encodes the leader peptide for the phenylalanine biosynthetic operon. Translation of pheL mRNA controls transcription attenuation and, consequently, expression of the downstream pheA gene. Fifty-three unique pheL genes have been identified in sequenced genomes of the gamma subdivision. There are two groups of pheL genes, both of which are short and contain a run(s) of phenylalanine codons at an inteRNAl position. One group is somewhat diverse and features different termination and 5-flanking codons. The other group, mostly restricted to Enterobacteria and including Escherichia coli pheL, has a conserved nucleotide sequence that ends with UUC_CCC_UGA. When these three codons in E. coli pheL mRNA are in the ribosomal E-, P- and A-sites, there is an unusually high level, 15%, of +1 ribosomal frameshifting due to features of the nascent peptide sequence that include the penultimate phenylalanine. This level increases to 60% with a natural, heterologous, nas... ...

1COM: The monofunctional chorismate mutase from Bacillus subtilis. Structure determination of chorismate mutase and its complexes with a transition state analog and prephenate, and implications for the mechanism of the enzymatic reaction.

ID A0A076MGV6_AMYME Unreviewed; 538 AA. AC A0A076MGV6; DT 29-OCT-2014, integrated into UniProtKB/TrEMBL. DT 29-OCT-2014, sequence version 1. DT 25-OCT-2017, entry version 27. DE RecName: Full=Chromosomal replication initiator protein DnaA {ECO:0000256,HAMAP-Rule:MF_00377, ECO:0000256,RuleBase:RU000577}; GN Name=dnaA {ECO:0000256,HAMAP-Rule:MF_00377, GN ECO:0000313,EMBL:AIJ20093.1}; GN ORFNames=AMETH_0001 {ECO:0000313,EMBL:AIJ20093.1}; OS Amycolatopsis methanolica 239. OC Bacteria; Actinobacteria; Pseudonocardiales; Pseudonocardiaceae; OC Amycolatopsis. OX NCBI_TaxID=1068978 {ECO:0000313,EMBL:AIJ20093.1, ECO:0000313,Proteomes:UP000062973}; RN [1] {ECO:0000313,EMBL:AIJ20093.1, ECO:0000313,Proteomes:UP000062973} RP NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. RC STRAIN=239 {ECO:0000313,EMBL:AIJ20093.1, RC ECO:0000313,Proteomes:UP000062973}; RA Tang B.; RT Whole Genome Sequence of the Amycolatopsis methanolica 239.; RL Submitted (JUL-2014) to the EMBL/GenBank/DDBJ databases. CC -!- FUNCTION: ...

Cite as: IUPAC. Compendium of Chemical Terminology, 2nd ed. (the Gold Book). Compiled by A. D. McNaught and A. Wilkinson. Blackwell Scientific Publications, Oxford (1997). XML on-line corrected version: http://goldbook.iupac.org (2006-) created by M. Nic, J. Jirat, B. Kosata; updates compiled by A. Jenkins. ISBN 0-9678550-9-8. https://doi.org/10.1351/goldbook. ...

EaseChem provides information about Z-(4-tert-butyloxycarbonyl)-L-phenylalanine, Z-(4-tert-butyloxycarbonyl)-L-phenylalanine, CAS No.: 270567-85-6.,Z-(4-tert-butyloxycarbonyl)-L-phenylalanine

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An additional stabilizing factor in this enzyme-substrate complex is hydrogen bonding between the lone pair of the oxygen in the vinyl ether system and hydrogen bond donor residues. Not only does this stabilize the complex, but disruption of resonance within the vinyl ether destabilizes the ground state and reduces the energy barrier for this transformation. An alternative view is that electrostatic stabilization of the polarized transition state is of great importance in this reaction. In the chorismate mutase active site, the transition-state analog is stabilized by 12 electrostatic and hydrogen-bonding interactions.[8] This is shown in mutants of the native enzyme in which Arg90 is replaced with citrulline to demonstrate the importance of hydrogen bonding to stabilize the transition state.[9] Other work using chorismate mutase from Bacillus subtilis showed evidence that when a cation was aptly placed in the active site, the electrostatic interactions between it and the negatively charged ...

Sigma-Aldrich offers abstracts and full-text articles by [Feng Xie, Shengwang Dai, Jinzhao Shen, Biao Ren, Pei Huang, Qiushui Wang, Xueting Liu, Buchang Zhang, Huanqin Dai, Lixin Zhang].

BioAssay record AID 52148 submitted by ChEMBL: The compound was tested for inhibition of Bacillus subtilis chorismate mutase (BcCM).

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Definition of phenylpyruvate oligophrenia. Provided by Stedmans medical dictionary and Drugs.com. Includes medical terms and definitions.

prephenic acid: nonaromatic biosynthetic intermediate, probable immediate precursor of aromatic systems such as phenylalanine, tyrosine, tannins, flavanoids; isolated from cultures of mutant E coli; structure

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Information of L-Phenylalanine. L-Phenylalanine essential amino acid is classified as neutral and nonpolar because of the inert and hydrophobic.

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putative dTDP-glucose 4,6-dehydratase [dNDP-glucose 4,6-dehydratase] ATGAACATCCTGGTCACCGGCGCGGCCGGTTTCATCGGCTCGCACTTCGTCCGCAGCCTG CTGGCCGACACCTACTCCGGCTGGGAGGGAGCCCGGGTCACTGCCCTGGACAAACTGACC TACGCGGGCAACCGGAACAACCTGCCGCCCTCAAACCCGCGCCTGGAGTTCGTGCGGGGC GACGTGTGCGACCGCGCCCTGCTCCGCGAGCTGCTGCCCGGGCACCACGCCGTGGTCCAT TTCGCGGCGGAATCCCACGTGGACCGCTCCCTCGAAGGCGCGGGCGAGTTCTTCCGCACG AACGTCCTCGGTACGCAGACACTCCTCGACGCCGTACTGGACAGCGGAGTCGAGCGGGTC GTTCACGTCTCCACCGACGAGGTGTACGGCTCGATCGAGCAAGGCTCCTGGACCGAGGAC TGGCCGCTGCAGCCCAATTCTCCGTACGCCGCCTCGAAGGCATGCTCGGACCTGGTCGCG CGAGCCTACTGCGCACCCACGGAGGTGGACCTCTCCATCACCCGCTGCTCCAACAACTAC GGCCCGCACCAGCACCCTGAGAAGGTCATTCCCAGGTTCGTCACGAACCTCCTCGAAGGA CGCCAGGTCCCGCTGTACGGCGACGGCCGCAATGTGCGCGAGTGGCTCCACGTGGAGGAC CACTGCCGCGGTATCCACCTGGTGCTCAACAAGGGGCAGGCCGGCGAGATCTACAACATC GGCGGGGGCAACGAGTACACCAACCTCGCCCTCACCGAGAAACTGCTCGAACTGACGGGT GCCGGCCCGGAGATGATCCGCCGCGTCCCCGACCGCAAGGCGCACGACCTGCGGTACTCG ATCGACGAGTCCAAGATCCGCGAGAAGCTCGGCTACGCCCCGCGGATCAGCTTCGAACAG ...

MetabolismEnergy metabolismAmino acids and aminesL-serine dehydratase, iron-sulfur-dependent, beta subunit (TIGR00719; EC 4.3.1.17; HMM-score: 170.8) ...

Department of Chemistry, UBC Faculty of Science. Vancouver Campus. 2036 Main Mall. Vancouver, BC Canada V6T 1Z1. Tel: 604.822.3266. Fax: 604.822.2847. ...

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N-dimethyl-4-nitrosoaniline oxidoreductase alcohol - N: a group III alcohol oxidoreductase from Rhodococcus sp, Amycolatopsis methanolica and Mycobacterium gastri; amino acid sequence given in first source; GenBank U21071

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L-Phenylalanine, an essential amino acid, is a predecessor of the amino acid tyrosine and a whole series of neurotransmitters and hormones. Phenylalanine is fir

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You are viewing an interactive 3D depiction of the molecule 4-[difluoro(phosphono)methyl]-l-phenylalanine (C10H12F2NO5P) from the PQR.

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Arogenate dehydratases (ADTs) perform the final step of phenylalanine (Phe) biosynthesis in plants. As one of twenty protein-coding amino acids, Phe is essential in all living organisms, and in plants it is also a precursor ...

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This aminocoumarin antibiotic consists of three major substituents. The 3-dimethylallyl-4-hydroxybenzoic acid moiety, known as ring A, is derived from prephenate and dimethylallyl pyrophosphate. The aminocoumarin moiety, known as ring B, is derived from L-tyrosine. The final component of novobiocin is the sugar derivative L-noviose, known as ring C, which is derived from glucose-1-phosphate. The biosynthetic gene cluster for novobiocin was identified by Heide and coworkers in 1999 (published 2000) from Streptomyces spheroides NCIB 11891.[18] They identified 23 putative open reading frames (ORFs) and more than 11 other ORFs that may play a role in novobiocin biosynthesis. The biosynthesis of ring A (see Fig. 1) begins with prephenate which is a derived from the shikimic acid biosynthetic pathway. The enzyme NovF catalyzes the decarboxylation of prephenate while simultaneously reducing nicotinamide adenine dinucleotide phosphate (NADP+) to produce NADPH. Following this NovQ catalyzes the ...

Accepted name: aspartate phenylpyruvate transaminase. Reaction: L-aspartate + phenylpyruvate = oxaloacetate + L-phenylalanine. For diagram click here (mechanism).. Other name(s): aspartate-phenylpyruvate aminotransferase. Systematic name: L-aspartate:phenylpyruvate aminotransferase. Comments: The enzyme from Pseudomonas putida also acts on 4-hydroxy-phenylpyruvate and, more slowly, on L-glutamate and L-histidine.. Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 99533-45-6. References: 1. Holger, Z. and Kula, M.-R. Isolation and characterization of a highly inducible L-aspartate-phenylpyruvate transaminase from Pseudomonas putida. J. Biotechnol. 3 (1985) 19-31.. ...

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The chemical reactions and pathways involving L-phenylalanine, the L-enantiomer of 2-amino-3-phenylpropanoic acid, i.e. (2S)-2-amino-3-phenylpropanoic acid. [CHEBI:17295, GOC:go_curators, GOC:jsg, GOC:mah]. ...

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L-Tyrosine is a non-essential amino acid that can be synthesized by the body. It can be used to regulate mood and stimulate the nervous system. Its a...

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