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anthranilate phosphoribosyltransferase <enzyme> An enzyme that catalyses the formation of n-5'-phosphoribosylanthranilic acid from anthranilate and phosphoribosylpyrophosphate, the first step in tryptophan synthesis in e. Coli. It exists in a complex with anthranilate synthase in bacteria.
Chemical name: N-(5-Phospho-D-ribosyl)-anthranilate:pyrophosphate phospho-alpha-D-ribosyltransferase
Registry number: EC 2.4.2.18
(12 Dec 1998)
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anthranilate monooxygenase <enzyme> Catalyses the hydroxylation of anthranilate to hydroxyanthranilate in the presence of tetrahydropteridine and molecular oxygen; anthranilate hydroxylase is a synonym for this and EC 1.14.12.1 and EC 1.14.13.35 (formerly EC 1.14.12.2)
Registry number: EC 1.14.16.3
Synonym: anthranilate 3-hydroxylase, anthranilate 3-monooxygenase
(26 Jun 1999)
anthranilate synthase <enzyme> An enzyme that catalyses the formation of anthranilate (o-aminobenzoate) and pyruvic acid from chorismate and glutamine. Anthranilate is the biosynthetic precurser of tryptophan and numerous secondary metabolites, including inducible plant defense compounds.
Chemical name: Chorismate pyruvate-lyase (amino-accepting)
Registry number: EC 4.1.3.27
(12 Dec 1998)
benzoyl-CoA-anthranilate N-benzoyltransferase <enzyme> Specific for anthranilate; almost no activity towards 4-hydroxyanthranilate; involved in phytoalexin biosyntesis
Registry number: EC 2.3.1.-
Synonym: b-CoA-anb transferase, benzoyl-coenzyme a-anthranilate n-benzoyltransferase
(26 Jun 1999)
adenine phosphoribosyltransferase <enzyme> An enzyme catalyzing the formation of AMP from adenine and phosphoribosylpyrophosphate. It can act as a salvage enzyme for recycling of adenine into nucleic acids.
Chemical name: AMP:pyrophosphate phospho-D-ribosyltransferase
Registry number: EC 2.4.2.7
(12 Dec 1998)
aminoglycoside phosphoribosyltransferase <enzyme> Coded by neo-gene; involved in kanamycin resistance; no other information given on reaction 8/93
Registry number: EC 2.4.2.-
Synonym: aminoglycosidephosphoribosyltransferase
(26 Jun 1999)
ATP phosphoribosyltransferase <enzyme> An enzyme that catalyses the first step of the pathway for histidine biosynthesis in salmonella typhimurium. ATP reacts reversibly with 5-phosphoribosyl-1-pyrophosphate to yield n-1-(5'-phosphoribosyl)-ATP and pyrophosphate.
Chemical name: 1-(5-Phospho-D-ribosyl)-ATP:pyrophosphate phospho-alpha-D- ribosyltransferase
Registry number: EC 2.4.2.17
(12 Dec 1998)
phosphoribosyltransferase One of a group of enzymes (EC sub-subclass 2.4.2, pentosyltransferases) that transfers d-ribose 5-phosphate from 5-phospho-alpha-d-ribosyl pyrophosphate to a purine, pyrimidine, or pyridine acceptor, forming a 5'-nucleotide and inorganic pyrophosphate, or d-ribose from d-ribosyl phosphate to a base, forming a nucleoside, or similar pentose transfers; important in nucleotide biosynthesis. Specific phosphoribosyltransferases are preceded by the name of the acceptor base, e.g., uracil phosphoribosyltransferase (i.e., uracil + PRPP &dblarr; UMP + pyrophosphate).
(05 Mar 2000)
purine phosphoribosyltransferase <enzyme> Specific purine phosphoribosyltransferases are EC 2.4.2.7 and 2.4.2.8.
Registry number: EC 2.4.2.-
(26 Jun 1999)
pyrimidine phosphoribosyltransferase <enzyme> Pyrimidine monophosphate and pyrophosphate gives pyrimidine and phosphoribosyl pyrophosphate; acts with uracil, orotic acid or fluorouracil
Registry number: EC 2.4.2.-
(26 Jun 1999)
hypoxanthine guanine phosphoribosyltransferase <enzyme> An enzyme that catalyses the conversion of 5-phosphoribosyl-1-pyrophosphate and hypoxanthine, guanine, or 6-mercaptopurine to the corresponding 5'-mononucleotides and pyrophosphate. The enzyme is important in purine biosynthesis as well as central nervous system functions. Complete lack of enzyme activity is associated with the lesch-nyhan syndrome, while partial deficiency results in overproduction of uric acid.
Chemical name: IMP:pyrophosphate phospho-D-ribosyltransferase
Registry number: EC 2.4.2.8
(12 Dec 1998)
hypoxanthine guanine phosphoribosyltransferase deficiency A sex-linked inherited metabolic disorder; complete deficiency results in Lesch-Nyhan syndrome; incomplete deficiency is associated with acute gouty arthritis and renal stones.
(05 Mar 2000)
hypoxanthine-guanine-xanthine phosphoribosyltransferase <enzyme> From tritrichomonas foetus; in contrast to EC 2.4.2.8, this enzyme also uses xanthine as substrate; mw 24 kD
Registry number: EC 2.4.2.-
Synonym: hgxprtase
(26 Jun 1999)
hypoxanthine phosphoribosyltransferase <enzyme> An enzyme that catalyses the conversion of 5-phosphoribosyl-1-pyrophosphate and hypoxanthine, guanine, or 6-mercaptopurine to the corresponding 5'-mononucleotides and pyrophosphate. The enzyme is important in purine biosynthesis as well as central nervous system functions. Complete lack of enzyme activity is associated with the lesch-nyhan syndrome, while partial deficiency results in overproduction of uric acid.
Chemical name: IMP:pyrophosphate phospho-D-ribosyltransferase
Registry number: EC 2.4.2.8
(12 Dec 1998)
nicotinamide phosphoribosyltransferase <enzyme> Utilises nicotinamide, mg(2+), prpp and ATP
Registry number: EC 2.4.2.12
Synonym: nmn pyrophosphorylase
(26 Jun 1999)
nicotinatenucleotide-dimethylbenzimidazole phosphoribosyltransferase <enzyme> Involved in the synthesis of adenosyl-cobalamin (coenzyme b12); amino acid sequence given in second source
Registry number: EC 2.4.2.21
Synonym: nicotinate ribonucleotide benzimidazole phosphoribosyltransferase, trans-n-glycosidase, nicotinate-nucleotide-dimethylbenzimidazole phosphoribosyltransferase, cobu gene product, cobt protein, scobt protein, cobt gene product
(26 Jun 1999)
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