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1 ne and sulfate or with 9-deazaadenine and Mg-phosphoribosylpyrophosphate.
2 he Km value of the Y96F and Y96V mutants for phosphoribosylpyrophosphate.
3 their substrates hypoxanthine, guanine, and phosphoribosylpyrophosphate.
6 overexpression of (His)(6)-tagged glutamine phosphoribosylpyrophosphate amidotransferase (PurF) unex
7 he first enzyme of de novo purine synthesis, phosphoribosylpyrophosphate amidotransferase (PurF), in
10 B is similar to that observed for glutamine phosphoribosylpyrophosphate amidotransferase while the m
12 e, carbamoyl phosphate synthetase, glutamine phosphoribosylpyrophosphate amidotransferase, and aspara
13 portion of the pathway and is generated from phosphoribosylpyrophosphate and glutamine by the PurF en
15 n the catalytic loop, subunit interface, and phosphoribosylpyrophosphate binding site indicates criti
16 orylation causes stabilization of the enzyme-phosphoribosylpyrophosphate complex, permitting efficien
17 ld of CobT is unrelated to the type I and II phosphoribosylpyrophosphate dependent transferases and d
18 alysis of [(14)C]uracil-UMP and [(32)P]PP(i)-phosphoribosylpyrophosphate exchange reactions could be
19 idine nucleotide pool balance and by sparing phosphoribosylpyrophosphate for consumption by the nutri
22 rly steps of de novo synthesis by modulating phosphoribosylpyrophosphate production by the non-oxidat
23 ne and is generated in bacteria by glutamine phosphoribosylpyrophosphate (PRPP) amidotransferase (EC
26 ransition of ligand-free, inactive glutamine phosphoribosylpyrophosphate (PRPP) amidotransferase to t
28 a ternary complex with the primary substrate phosphoribosylpyrophosphate (PRPP) and an analogue of th
30 he magnesium-dependent conversion of alpha-D-phosphoribosylpyrophosphate (PRPP) and orotate to orotid
31 rotidine 5'-monophosphate (OMP) from alpha-D-phosphoribosylpyrophosphate (PRPP) and orotate, an essen
35 99 muM for the natural substrates uracil and phosphoribosylpyrophosphate, respectively, as well as ap
37 an N-terminal glutaminase domain to a distal phosphoribosylpyrophosphate site in a C-terminal domain
38 the enzymatic and genetic basis of X-linked phosphoribosylpyrophosphate synthetase (PRS) catalytic s
40 r A, haptoglobin, tyrosine aminotransferase, phosphoribosylpyrophosphate synthetase subunit II, and 6
42 the condensation of p-aminobenzoic acid with phosphoribosylpyrophosphate to form beta-RFAP, CO2, and
43 on six enzymes to catalyze the conversion of phosphoribosylpyrophosphate to inosine 5'-monophosphate.
44 ans that catalyze the 10 chemical steps from phosphoribosylpyrophosphate to inosine monophosphate wer
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