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1 espectively), which both likely evolved from asparagine synthetase.
2 e inhibitor of the ammonia-dependent E. coli asparagine synthetase A (AS-A) can be regarded as such a
4 . possess asparagine-tRNA synthetase paralog asparagine synthetase A (LdASNA) that is ammonia-depende
7 acid is also a partial substrate for E. coli asparagine synthetase, acting as a nucleophile to form t
9 ndent asparagine formation in this bacterial asparagine synthetase and (ii) ammonia in bulk solution
10 (p-eIF2) leading to increased mRNA levels of asparagine synthetase and CCAAT/enhancer-binding protein
13 ion of the amino acid stress response genes, asparagine synthetase and CHOP/GADD153, increased as a r
14 We report the transactivation of two genes, asparagine synthetase and human telomerase reverse trans
15 ns genome of genes encoding tRNA-independent asparagine synthetase and the lack of this enzyme in D.
17 ative pentose pathway, malate dehydrogenase, asparagine synthetase, and histidine decarboxylase; and
19 o and in vitro characterizations of FdmV, an asparagine synthetase (AS) B-like protein, as an amide s
23 nd trans-factors affecting the expression of asparagine synthetase (AS) genes whose transcription is
24 ene for the amino acid biosynthetic activity asparagine synthetase (AS) is induced by both amino acid
26 f this family of ATP/Mg2+-dependent enzymes, asparagine synthetase (AS-B), catalyzes intermolecular,
27 AS1 and SAS2) encoding different isoforms of asparagine synthetase (AS; EC 6.3.5.4) were isolated.
29 clones, LJAS1 and LJAS2, encoding different asparagine synthetases (AS) have been identified and seq
31 genes such as glutamine synthetase (GLN) and asparagine synthetase (ASN) are modulated by carbon and
32 get genes involved in nitrogen assimilation: asparagine synthetase (ASN1 and ASN2) and glutamine synt
34 of ATF4 significantly reduced the levels of asparagine synthetase (ASNS) and overexpression of ASNS
38 P suppressed the induction of the endogenous asparagine synthetase (ASNS) gene and inhibited transcri
39 ted analysis of these data revealed that the asparagine synthetase (ASNS) gene showed a gain in copy
42 ntigen 1 (FOSL1), transglutaminase 2 (TGM2), asparagine synthetase (ASNS), PLAB, PAOh1 and ELF3, whil
46 While ECs can take up asparagine, silencing asparagine synthetase (ASNS, which converts glutamine-de
47 ave examined the methylation profiles of the asparagine synthetase (ASY) promoter in a number of huma
48 mall-molecule inhibitors of Escherichia coli asparagine synthetase B (AS-B) as a model system for the
51 e aspartate binding site of Escherichia coli asparagine synthetase B (AS-B) using a number of stereoc
57 ragine synthetase A (AsnA), and the other is asparagine synthetase B (AsnB) that uses glutamine or am
58 osine (5'-FSBA) inactivates Escherichia coli asparagine synthetase B activity following pseudo-first-
60 in the synthetase active site of the enzyme asparagine synthetase B from Escherichia coli (AS-B).
62 nal architecture of the N-terminal domain of asparagine synthetase B is similar to that observed for
63 s of the homologous primary metabolic enzyme asparagine synthetase B, and a chemical mechanism is pro
64 constitute a clinically useful inhibitor of asparagine synthetase B, these results suggested that re
68 other glutamine amidotransferases including asparagine synthetase, cytidine 5'-triphosphate (CTP) sy
70 rans and Thermus thermophilus do not possess asparagine synthetase (encoded by asnA or asnB), the enz
73 subfamily of amidotransferases that includes asparagine synthetase, glucosamine 6-phosphate synthase,
74 horibosylpyrophosphate amidotransferase, and asparagine synthetase have revealed the relative locatio
78 synthesis was suppressed, and expression of asparagine synthetase was statistically correlated with
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