ライフサイエンスコーパス: oxoglutarate dehydrogenase

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1 ing domain of a large multienzyme complex, 2-oxoglutarate dehydrogenase.

2 mplete in many other anaerobes (absence of 2-oxoglutarate dehydrogenase activity), isotopic labeling

3 ccinyltransferase (Dlst), a subunit of the 2-oxoglutarate dehydrogenase (alpha-KGDH) complex.

4 cid as a cofactor (pyruvate dehydrogenase, 2-oxoglutarate dehydrogenase and glycine decarboxylase).

5 to succinate and thus functionally replace 2-oxoglutarate dehydrogenase and succinyl-CoA synthetase.

6 boxylic acid (TCA) cycle because they lack 2-oxoglutarate dehydrogenase and thus cannot convert 2-oxo

7 Pyruvate and 2-oxoglutarate dehydrogenases are substituted by 'ancient'

8 id dehydrogenase complex (BCOADC), and the 2-oxoglutarate dehydrogenase complex (OGDC).

9 The 2-oxoglutarate dehydrogenase complex (OGHDC) (also known a

10 ependent E1o component (EC 1.2.4.2) of the 2-oxoglutarate dehydrogenase complex catalyses a rate-limi

11 hydrogenase complex E (BCOADC-E2), and the 2-oxoglutarate dehydrogenase complex E (OGDC-E2).

12 2) in 6 of 19 patients (31.6%), and to the 2-oxoglutarate dehydrogenase complex E2 (OGDC-E2) in 1 of

13 (BCOADC-E2) in 4 of 49 (8%), to PDC-E2 and 2-oxoglutarate dehydrogenase complex E2 (OGDC-E2) in 9 of

14 of the gene encoding the E1 subunit of the 2-oxoglutarate dehydrogenase complex in the antisense orie

15 A traditional 2-oxoglutarate dehydrogenase complex is missing in the cya

16 e enzymes, pyruvate dehydrogenase complex, 2-oxoglutarate dehydrogenase complex, NAD-malic enzyme, an

17 -oxo-acid dehydrogenase, and E2 subunit of 2-oxoglutarate dehydrogenase complex.

18 2-oxoglutarate decarboxylase (E1o) of the 2-oxoglutarate dehydrogenase complex.

19 ents of pyruvate dehydrogenase complex and 2-oxoglutarate dehydrogenase complex.

20 We report that the intact pyruvate and 2-oxoglutarate dehydrogenase complexes specifically copuri

21 yl CoA ligase, aconitase, and pyruvate and 2-oxoglutarate dehydrogenase complexes.

22 (a) Functionally competent 2-oxoglutarate dehydrogenase (E1o-h) and dihydrolipoyl suc

23 h engineered variants of the E2 subunit of 2-oxoglutarate dehydrogenase indicate that binding sites f

24 n this organism, even though a traditional 2-oxoglutarate dehydrogenase is lacking.

25 to enzymes of the tricarboxylic acid cycle (oxoglutarate dehydrogenase, isocitrate dehydrogenase) an

26 re reported unique properties of the human 2-oxoglutarate dehydrogenase multienzyme complex (OGDHc),

27 nit binding domain from Escherichia coli's 2-oxoglutarate dehydrogenase multienzyme complex (termed B

28 succinyltransferase (E2o) component of the 2-oxoglutarate dehydrogenase multienzyme complex is compos

29 ccinyltransferase polypeptide chain of the 2-oxoglutarate dehydrogenase multienzyme complex of Escher

30 interactions with other components of the 2-oxoglutarate dehydrogenase multienzyme complex.

31 (E2p, E2o) components of the pyruvate and 2-oxoglutarate dehydrogenase multienzyme complexes are spe

32 ogenase E1 component subunit beta (PDHB) and oxoglutarate dehydrogenase (OGDH) required dual phosphor

33 ived from alpha-ketoglutarate dehydrogenase (oxoglutarate dehydrogenase (OGDH)), a ubiquitous intrace

34 However, the 2-oxoglutarate dehydrogenase (OGDH), branched-chain 2-oxoa

35 ire the expression of the TCA cycle enzyme 2-oxoglutarate dehydrogenase (OGDH).

36 s and thus upregulates ATP citrate lyase and oxoglutarate dehydrogenase, two key enzymes that determi

37 ine diphosphate-dependent Escherichia coli 2-oxoglutarate dehydrogenase, which is a key component of

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