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1 from the reported crystal structure of human glutathione synthetase.
2 eductase, gamma-glutamyl transpeptidase, and glutathione synthetase.
3 uble mutants missing atx1 and gshB (encoding glutathione synthetase) accumulate the same number of at
4 glycosyltransferase activity that increases glutathione synthetase activity to protect the bacterium
6 expressed in a S. pombe mutant deficient in glutathione synthetase activity, the plant cDNA was able
7 ily of ATP-utilizing enzymes, which includes glutathione synthetase and D-alanine:D-alanine ligase.
9 any changes in sequence or protein levels of glutathione synthetase and gamma-glutamylcysteine synthe
10 CphA1 has domains that are homologous to glutathione synthetases and muramyl ligases, but no othe
12 hesis, gamma-glutamylcysteine synthetase and glutathione synthetase, as well as glutathione reductase
13 synthetase is an enzyme that belongs to the glutathione synthetase ATP-binding domain-like superfami
14 o observed in D-alanine:D-alanine ligase and glutathione synthetase, both of which belong to the "ATP
15 in this superfamily are d-Ala d-Ala ligase, glutathione synthetase, carbamyl phosphate synthetase, N
16 ibition against glutamylcysteine synthetase, glutathione synthetase, catalase, and superoxide dismuta
17 7 other genes (CRISPR, lanthionine synthase, glutathione synthetase, catalase, Na+/H+ antiporter, etc
19 ne:D-alanine ligase, biotin carboxylase, and glutathione synthetase, despite low sequence similarity.
22 n of catalase, glutathione peroxidase 4, and glutathione synthetase genes, increased levels of mangan
23 and four highly conserved residues of human glutathione synthetase (Glu-144, Asn-146, Lys-305, and L
24 S) scavenging machinery, including catalase, glutathione synthetase, glutathione reductase, NADPH-cyt
26 -glutamylcysteine synthetase (gamma-GCS) and glutathione synthetase (GS), distinct enzymes that toget
27 ma-glutamylcysteine synthetase (gammaGCS) or glutathione synthetase (GS), the two enzymes synthesizin
28 enzymes homoglutathione synthetase (hGS) and glutathione synthetase (GS), we determined the structure
31 evated 4-fold in these mice, while those for glutathione synthetase (GSH syn) are elevated 2-fold.
33 ants of glutamate-cysteine ligase (gshA) and glutathione synthetase (gshB) in Synechocystis sp. PCC 6
34 we unexpectedly observed that the bacterial glutathione synthetase (GshB) is glycosylated by NleB on
35 nuria (pyroglutamic aciduria) resulting from glutathione synthetase (GSS) deficiency is an inherited
38 n of GSH to 21.4 +/- 3.3% of controls by the glutathione synthetase inhibitor buthionine sulfoximine
39 lutathione was removed from the cells by the glutathione synthetase inhibitor L-buthionine-(S,R)-sulf
41 ee-dimensional coordinates for several human glutathione synthetase mutant enzymes were obtained usin
43 inal cyclic imide formation on proteins like glutathione synthetase that are susceptible to aggregati
44 B mutants lacking gamma-glutamylcysteine and glutathione synthetases to NO and S-nitrosoglutathione i
45 tI fragment containing the genomic clone for glutathione synthetase was also isolated and sequenced.