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1 e mutant phenotype, which encodes a putative serine hydroxymethyltransferase.
2 (5-CHO-THF) is formed by a side reaction of serine hydroxymethyltransferase.
3 rotein, two tRNA synthetases, and a putative serine hydroxymethyltransferase.
4 f several folate-dependent enzymes including serine hydroxymethyltransferase.
9 ation and repair and consists of the enzymes serine hydroxymethyltransferase 1 and 2alpha (SHMT1 and
12 which in turn promotes the succinylation of serine hydroxymethyltransferase 2 (SHMT2) within the mit
15 d serine metabolism enzymes Psat1 and Shmt2 (serine hydroxymethyltransferase 2), as well as translati
17 ng serine to glycine conversion catalyzed by serine hydroxymethyltransferase-2 as well as ornithine a
18 min B6 media can be explained by the loss of serine hydroxymethyltransferase-2-dependent production o
19 validated by the pharmacologic inhibition of serine hydroxymethyltransferase, a key enzyme that feeds
20 ded a 30 kDa chloroplast membrane protein, a serine hydroxymethyltransferase, a nuclease, and two pro
21 and PLP-stimulated (35%; P=0.004) lymphocyte serine hydroxymethyltransferase activities in vitro.
22 show that this assay can be used to measure serine hydroxymethyltransferase activity at 10(-8) to 10
23 ggest that 5-formyltetrahydrofolate inhibits serine hydroxymethyltransferase activity in vivo and tha
24 s assay, the 5,10-CH(2)-H(4)PteGlu formed by serine hydroxymethyltransferase activity is reduced to 5
26 ric quaternary structure of liganded E. coli serine hydroxymethyltransferase also differs in symmetry
28 red to the other two enzymes in the cytosol, serine hydroxymethyltransferase and C1-tetrahydrofolate
29 o thymidylate synthesis, and suggesting that serine hydroxymethyltransferase and FTHFS compete for a
30 s that are inhibited in the PPIP5K KO cells: serine hydroxymethyltransferase and phosphoribosyl pyrop
31 h define the folate cofactor binding site in serine hydroxymethyltransferase and the differences in o
33 of genes encoding a glycine cleavage system, serine hydroxymethyltransferase, and serine dehydratase.
35 ing the in vitro folding of Escherichia coli serine hydroxymethyltransferase at 4 degrees C, both mon
37 orted to be the viable in vivo substrate for serine hydroxymethyltransferase-catalyzed formation of 5
39 ism is associated with decreased cytoplasmic serine hydroxymethyltransferase (cSHMT) expression in MC
42 slated region (UTR) of the human cytoplasmic serine hydroxymethyltransferase (cSHMT) message is alter
44 the preferential partitioning of cytoplasmic serine hydroxymethyltransferase (cSHMT)-derived methylen
49 it was an indirect consequence of damage to serine hydroxymethyltransferase (GlyA; E.C. 2.1.2.1).
50 In soybeans, eighteen members constitute the serine hydroxymethyltransferase (GmSHMT) gene family, of
51 the Rhg4 gene encodes a predicted cytosolic serine hydroxymethyltransferase (GmSHMT08); however, the
52 in vitro folding pathway of Escherichia coli serine hydroxymethyltransferase has both monomer and dim
53 nal lethality of the yggS and glyA (encoding serine hydroxymethyltransferase) has been described, but
55 ture at 2.4 A resolution of Escherichia coli serine hydroxymethyltransferase in ternary complex with
60 ehydrogenase reaction to an excess of either serine hydroxymethyltransferase or C1-tetrahydrofolate s
61 n 16 days were viable and lacked cytoplasmic serine hydroxymethyltransferase protein, confirming that
62 coding a protein with sequence similarity to serine hydroxymethyltransferases, resulting in the propo
64 Unexpectedly, mutation of both cytosolic serine hydroxymethyltransferase (SHM2) and one-carbon te
65 PLC)-based fluorometric method for measuring serine hydroxymethyltransferase (SHMT) activity toward f
67 is formed via a second catalytic activity of serine hydroxymethyltransferase (SHMT) and strongly inhi
74 etrahydrofolate dehydrogenase 1 (MTHFD1) and serine hydroxymethyltransferase (SHMT) generate 5,10-met
79 on the folding mechanism of Escherichia coli serine hydroxymethyltransferase (SHMT) showed that the f
80 olyglutamate forms to rabbit liver cytosolic serine hydroxymethyltransferase (SHMT) were determined b
81 methylenetetrahydrofolate reductase (MTHFR), serine hydroxymethyltransferase (SHMT), and cystathionin
83 opyran-based inhibitors targeting the enzyme serine hydroxymethyltransferase (SHMT), designed to impr
85 synthesis, a pathway composed of the enzymes serine hydroxymethyltransferase (SHMT), thymidylate synt
86 ormylTHF, a slow, tight-binding inhibitor of serine hydroxymethyltransferase (SHMT), was enriched in
89 olo[3,2-d]pyrimidine antifolate that targets serine hydroxymethyltransferase (SHMT)2 in the mitochond
92 structures of the human and rabbit cytosolic serine hydroxymethyltransferases (SHMT) confirmed their
93 disrupted at the genes encoding one or both serine hydroxymethyltransferases (SHMT) or at the genes
94 reductase-thymidylate synthase, dhfr-ts, and serine hydroxymethyltransferase, shmt) gave the most abu
95 n methionine synthase (MS A2756G), cytosolic serine hydroxymethyltransferase (SHMT1 C1420T), and a do
96 folate reductase (MTHFR 677C>T and 1298A>C); serine hydroxymethyltransferase (SHMT1 C1420T); reduced
97 onucleotide transformylase (ATIC) 347GG, and serine hydroxymethyltransferase (SHMT1) 1420CC were meas
100 human glioblastoma multiforme, mitochondrial serine hydroxymethyltransferase (SHMT2) and glycine deca
101 ine, through the activities of mitochondrial serine hydroxymethyltransferase (SHMT2), thymidylate syn
103 parison with the unliganded rabbit cytosolic serine hydroxymethyltransferase structure identifies cha
104 in vivo of specific proteins indicated that serine hydroxymethyltransferase was affected in icp55.