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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 ssected the IVD gene locus-which encodes the isovaleryl-CoA dehydrogenase enzyme-implicated by select
22 eral expansion of the binding cavity seen in isovaleryl-CoA dehydrogenase is not observed in IBD.
23  with abstraction of a gamma-proton, whereas isovaleryl-CoA dehydrogenase is not significantly inhibi
24 the Glu254Gly/Ala375Glu double mutant) makes isovaleryl-CoA dehydrogenase sensitive to irreversible i
25 hose of medium chain acyl-CoA dehydrogenase, isovaleryl-CoA dehydrogenase, and bacterial short chain
26 ium is, however, similar to that observed in isovaleryl-CoA dehydrogenase.
27 ields a reduced flavin adduct with wild-type isovaleryl-CoA dehydrogenase.
28           The potato cDNAs Solanum tuberosum isovaleryl-CoA dehydrogenases 1 and 2 (St-IVD1 and St-IV
29 oA ligand for medium chain, short chain, and isovaleryl-CoA dehydrogenases suggests that the increase
30 rogenases) or on the G helix (long-chain and isovaleryl-CoA dehydrogenases).
31 ccumulation of Leu, 3-methylcrotonyl CoA and isovaleryl CoA indicates that mitochondrial and peroxiso
32 used as a carbon source by some bacteria and isovaleryl-CoA is an intermediate in leucine catabolism,
33 cmF yielded the following values: a K(m) for isovaleryl-CoA of 62 +/- 8 muM and V(max) of 0.021 +/- 0
34  Given the biotechnological potential of the isovaleryl-CoA/pivalyl-CoA mutase (PCM) reaction, we ini
35 382Leu mutants are 27.0, 2.8, and 6.9 microM isovaleryl-CoA, respectively, compared to 3.1 microM for
36 flavoenzyme that catalyzes the conversion of isovaleryl-CoA to 3-methylcrotonyl-CoA in the leucine ca
37 flavoenzyme that catalyzes the conversion of isovaleryl-CoA to 3-methylcrotonyl-CoA.
38 lavoenzyme which catalyzes the conversion of isovaleryl-CoA to 3-methylcrotonyl-CoA.
39                                              Isovaleryl-CoA was the preferred starter substrate of Fv