ライフサイエンスコーパス: isovaleryl-CoA

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1 ith 2-methylbutyryl-CoA and no activity with isovaleryl-CoA.

2 nt enzymes could also isomerize pivalyl- and isovaleryl-CoA, albeit at >10 times lower rates than the

3 ificant accumulation of several amino acids, isovaleryl CoA and phytanoyl CoA during dark-induced car

4 A also catalyzes the interconversion between isovaleryl-CoA and pivalyl-CoA, albeit with low efficien

5 , IcmF also catalyzes the interconversion of isovaleryl-CoA and pivalyl-CoA.

6 iated with IcmF, i.e. the interconversion of isovaleryl-CoA and pivalyl-CoA.

7 aproate is converted via the BKDH complex to isovaleryl-CoA and subsequently converted into isovalera

8 ith the substrates valeryl-coenzyme A (CoA), isovaleryl-CoA, and isobutyryl-CoA.

9 rred modest protection during utilization of isovaleryl-CoA as substrate.

10 as an IV-HSL synthase, which was active with isovaleryl-CoA but not detectably so with isovaleryl-ACP

11 d branched chain amino acid catabolic enzyme isovaleryl-CoA dehydrogenase (encoded by gene At3g45300

12 Isovaleryl-CoA dehydrogenase (IVD) belongs to an importa

13 Isovaleryl-CoA dehydrogenase (IVD) is a homotetrameric m

14 Isovaleryl-CoA dehydrogenase (IVD) is an intramitochondr

15 rror of metabolism caused by a deficiency of isovaleryl-CoA dehydrogenase (IVD), a nucleus-encoded, h

16 ancestral glutaryl-CoA dehydrogenase (GCD), isovaleryl-CoA dehydrogenase (IVD), and ACAD10/11.

17 yl-CoA dehydrogenase (MCAD), Glu254 in human isovaleryl-CoA dehydrogenase (IVD), and Glu261 in human

18 recessive disorder caused by a deficiency of isovaleryl-CoA dehydrogenase (IVD).

19 bstrate for the ETC are not fully available, isovaleryl-CoA dehydrogenase and 2-hydroxyglutarate dehy

20 not due to weak binding: the complex between isovaleryl-CoA dehydrogenase and 2-pentynoyl-CoA shows a

21 eral expansion of the binding cavity seen in isovaleryl-CoA dehydrogenase is not observed in IBD.

22 with abstraction of a gamma-proton, whereas isovaleryl-CoA dehydrogenase is not significantly inhibi

23 the Glu254Gly/Ala375Glu double mutant) makes isovaleryl-CoA dehydrogenase sensitive to irreversible i

24 hose of medium chain acyl-CoA dehydrogenase, isovaleryl-CoA dehydrogenase, and bacterial short chain

25 ium is, however, similar to that observed in isovaleryl-CoA dehydrogenase.

26 ields a reduced flavin adduct with wild-type isovaleryl-CoA dehydrogenase.

27 The potato cDNAs Solanum tuberosum isovaleryl-CoA dehydrogenases 1 and 2 (St-IVD1 and St-IV

28 oA ligand for medium chain, short chain, and isovaleryl-CoA dehydrogenases suggests that the increase

29 rogenases) or on the G helix (long-chain and isovaleryl-CoA dehydrogenases).

30 ccumulation of Leu, 3-methylcrotonyl CoA and isovaleryl CoA indicates that mitochondrial and peroxiso

31 used as a carbon source by some bacteria and isovaleryl-CoA is an intermediate in leucine catabolism,

32 cmF yielded the following values: a K(m) for isovaleryl-CoA of 62 +/- 8 muM and V(max) of 0.021 +/- 0

33 Given the biotechnological potential of the isovaleryl-CoA/pivalyl-CoA mutase (PCM) reaction, we ini

34 382Leu mutants are 27.0, 2.8, and 6.9 microM isovaleryl-CoA, respectively, compared to 3.1 microM for

35 flavoenzyme that catalyzes the conversion of isovaleryl-CoA to 3-methylcrotonyl-CoA in the leucine ca

36 flavoenzyme that catalyzes the conversion of isovaleryl-CoA to 3-methylcrotonyl-CoA.

37 lavoenzyme which catalyzes the conversion of isovaleryl-CoA to 3-methylcrotonyl-CoA.

38 Isovaleryl-CoA was the preferred starter substrate of Fv

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