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1 of our target proteins, the small subunit of glutamate synthase.
2 ty is inhibited by glutamate, the product of glutamate synthase.
3 he large (GltB) and small (GltD) subunits of glutamate synthase.
4 ism are induced by iron deprivation, whereas glutamate synthase, a key enzyme in nitrogen assimilatio
6 cient cells also had decreased aconitase and glutamate synthase activities, suggesting a general defe
7 and genes encoding various ABC transporters, glutamate synthase and CO oxidation were particularly up
9 reductase, the nitrate transporter NRT1, and glutamate synthase) appeared in the 40 most strongly nit
11 ylic acid cycle and the glutamine synthetase/glutamate synthase cycles are linked directly with the o
15 aconitase B, 6-phosphogluconate dehydratase, glutamate synthase, fumarase A, and FNR) and membrane-bo
16 ation (gltR24) that allows Bacillus subtilis glutamate synthase (gltAB) gene expression in the absenc
17 rmease and the iron-sulfur-containing enzyme glutamate synthase (GltAB), which serves as a central li
18 peptides identified as ferredoxin-dependent glutamate synthase (GltB2), large subunit of putative he
19 rginine repressed the specific activities of glutamate synthase (GltBD) and anabolic NADP-dependent G
21 d Klebsiella aerogenes that are deficient in glutamate synthase (glutamate-oxoglutarate amidotransfer
23 ists of three enzymes: glutamine synthetase, glutamate synthase (GOGAT), and glutamate dehydrogenase
25 combined action of glutamine synthetase and glutamate synthase (GS/GOGAT cycle) or the action of bio
26 ied four novel filament systems comprised of glutamate synthase, guanosine diphosphate-mannose pyroph
27 etase, glucosamine 6-phosphate synthase, and glutamate synthase, implying a common function in the fo
28 impairs the pathway for Glu biosynthesis via glutamate synthase, leading to decreased intracellular l
29 nd 90, Rubisco large subunit, and ferredoxin-glutamate synthase), likely reflecting functional regula
30 mino acid biosynthesis [PAA], NADH-dependent glutamate synthase [NGS], lovastatin nonaketide synthase
31 scription start site of the Escherichia coli glutamate synthase operon (gltBDF) and activates transcr
32 and in vitro activity studies confirmed that glutamate synthase rapidly inactivates upon NO treatment
33 ctive in these pathways, biotin synthase and glutamate synthase, require an iron-sulfur cluster for a
34 The Bacillus subtilis gltAB operon, encoding glutamate synthase, requires a specific positive regulat
35 acillus subtilis, the gltAB operon, encoding glutamate synthase, requires a specific positive regulat
36 lation by the plastidic glutamine synthetase/glutamate synthase system requires 2-oxoglutarate (2-OG)
37 functional nitrogen assimilation pathway via glutamate synthase, the simulations predict an unexpecte
38 requires alpha-ketoglutarate, a substrate of glutamate synthase, to fully activate gltA transcription
39 tory protein (Lrp) controls the synthesis of glutamate synthase, which controls the Ntr response, pre
40 eal that two genes, glutamine synthetase and glutamate synthase, which potentially work together in t
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