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1 citric acid cycle directly producing energy; succinyl-CoA synthetase.
2 rate synthase, isocitrate dehydrogenase, and succinyl-CoA synthetase.
3 e alpha- and beta-subunits, respectively, of succinyl-CoA synthetase.
4 lly replace 2-oxoglutarate dehydrogenase and succinyl-CoA synthetase.
5 stic alpha- and beta-subunits found in other succinyl-CoA synthetases.
6 hosphorylation of troponin I (190+/-23%) and succinyl CoA synthetase (160+/-16%), whereas the phospho
8 ed that AP33 had significant identity to the succinyl-CoA synthetase alpha-subunit of several differe
9 an tissues, which suggests that ATP-specific succinyl-CoA synthetase also plays an important role in
10 nslated regions of the endogenous gene alpha-succinyl CoA synthetase B (alpha-SCSB) to drive transcri
13 gues and by the sisterhood of the eukaryotic succinyl-CoA synthetase clade with alpha-proteobacteria.
15 , highlighting the probable role of an ALAS2-succinyl-CoA synthetase complex in the regulation of ery
17 ates nucleoside diphosphate kinase (Ndk) and succinyl-CoA synthetase, enzymes critical in nucleoside
18 rified and characterized both an ADP-forming succinyl-CoA synthetase from pigeon breast muscle and th
19 While both hydrogenosomal and mitochondrial succinyl-CoA synthetase homologues have been identified,
22 Highly ATP- and GTP-specific isoforms of succinyl-CoA synthetase in pigeon incorporate the same a
25 nthetase homologues have been identified, no succinyl-CoA synthetase proteins were identifiable in ta
29 es the enzymatic step typically performed by succinyl-CoA synthetase (SCS), has arisen in diverse bac
30 e GTPase linking hydrolysis of mtGTP made by succinyl-CoA synthetase (SCS-GTP) to an anaplerotic path
31 Because ALAS2 binds to the beta subunit of succinyl-CoA synthetase (SUCLA2), the mutant proteins we
32 at a DeltasucCD mutant (succinyl coenzyme A [succinyl-CoA] synthetase), which prevents the conversion
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