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1 rogenases) or on the G helix (long-chain and isovaleryl-CoA dehydrogenases).
2 ium is, however, similar to that observed in isovaleryl-CoA dehydrogenase.
3 ields a reduced flavin adduct with wild-type isovaleryl-CoA dehydrogenase.
5 bstrate for the ETC are not fully available, isovaleryl-CoA dehydrogenase and 2-hydroxyglutarate dehy
6 not due to weak binding: the complex between isovaleryl-CoA dehydrogenase and 2-pentynoyl-CoA shows a
7 hose of medium chain acyl-CoA dehydrogenase, isovaleryl-CoA dehydrogenase, and bacterial short chain
8 d branched chain amino acid catabolic enzyme isovaleryl-CoA dehydrogenase (encoded by gene At3g45300
9 ssected the IVD gene locus-which encodes the isovaleryl-CoA dehydrogenase enzyme-implicated by select
10 eral expansion of the binding cavity seen in isovaleryl-CoA dehydrogenase is not observed in IBD.
11 with abstraction of a gamma-proton, whereas isovaleryl-CoA dehydrogenase is not significantly inhibi
15 rror of metabolism caused by a deficiency of isovaleryl-CoA dehydrogenase (IVD), a nucleus-encoded, h
17 yl-CoA dehydrogenase (MCAD), Glu254 in human isovaleryl-CoA dehydrogenase (IVD), and Glu261 in human
19 the Glu254Gly/Ala375Glu double mutant) makes isovaleryl-CoA dehydrogenase sensitive to irreversible i
20 oA ligand for medium chain, short chain, and isovaleryl-CoA dehydrogenases suggests that the increase