WebMay 1, 2024 · 3-phosphoshikimate 1-carboxyvinyltransferase activity. Specific Function. Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5 … WebChorismate synthase catalyzes the conversion of 5-enolpyruvylshikimate 3-phosphate to chorismate in the shikimate pathway, which represents an attractive target for discovering antimicrobial agents and herbicides.
Crystal structure of 5-enolpyruvylshikimate-3-phosphate ... - PubMed
The enzyme belongs to the family of transferases, to be specific those transferring aryl or alkyl groups other than methyl groups. The systematic name of this enzyme class is phosphoenolpyruvate:3-phosphoshikimate 5-O-(1-carboxyvinyl)-transferase. Other names in common use include: 5-enolpyruvylshikimate-3 … See more 5-enolpyruvylshikimate-3-phosphate (EPSP) synthase is an enzyme produced by plants and microorganisms. EPSPS catalyzes the chemical reaction: phosphoenolpyruvate (PEP) + 3-phospho shikimate (S3P) ⇌ … See more EPSP synthase participates in the biosynthesis of the aromatic amino acids phenylalanine, tyrosine, and tryptophan via the shikimate pathway in bacteria, fungi, and plants. EPSP synthase is produced only by plants and micro-organisms; the gene coding for it is … See more • Morell H, Clark MJ, Knowles PF, Sprinson DB (Jan 1967). "The enzymic synthesis of chorismic and prephenic acids from 3-enolpyruvylshikimic acid 5-phosphate". The Journal of Biological Chemistry. 242 (1): 82–90. doi:10.1016/S0021-9258(18)96321-0 See more EPSP synthase is a monomeric enzyme with a molecular mass of about 46,000. It is composed of two domains, which are joined by protein … See more EPSP synthase is the biological target for the herbicide glyphosate. Glyphosate is a competitive inhibitor of EPSP synthase, acting as a transition state analog that binds more tightly to … See more WebApr 12, 2024 · enzyme that performs the metabolism of 3-phosphoshikimate int o 5-enolpyruvylshikimate-3- phosphate, which is a fundamental step for the s ynthesis of aromatic amino acids, such as . how to remove rat trap glue from skin
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WebMay 1, 2024 · 2.5.1.19 3-phosphoshikimate 1-carboxyvinyltransferase BSNT_08655 (aroE) BRITE hierarchy: SSDB: Ortholog Paralog Gene cluster GFIT: Motif: Pfam: EPSP_synthase: Motif: Other DBs: NCBI-ProteinID: BAI85758: UniProt: D4FY27: Position: complement(2156611..2157918) Genome browser: AA seq: 435 aa AA seq DB search WebJun 13, 2005 · Generic Name Glyphosate DrugBank Accession Number DB04539 Background Not Available Type Small Molecule Groups Experimental Structure 3D Download Similar Structures Weight Average: 170.081 Monoisotopic: 170.021833915 Chemical Formula C 3 H 9 NO 5 P Synonyms Not Available Pharmacology Indication Not Available Web5-O- (1-carboxyvinyl)-3-phosphoshikimate 5-ENOLPYRUVYLSHIKIMATE-3-PHOSPHATE DTXSID70331414 BDBM50281341 1-cyclohexene-1-carboxylic acid, 5- [ (1-carboxyethenyl)oxy]-4-hydroxy-3- (phosphonooxy)-, (3R,4S,5R)- O5- (1-carboxyvinyl)-3-phosphate shikimate C01269 Q3604489 how to remove rawl plugs from plasterboard