Biochemical characterization of a variant human medium-chain acyl-CoA dehydrogenase with a disease-associated mutation localized in the active site.
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Protein misfolding is the molecular mechanism underlying MCADD identified in newborn screeningEthylmalonic encephalopathy ETHE1 R163W/R163Q mutations alter protein stability and redox properties of the iron centre.Characterization of active site residues of nitroalkane oxidase.A novel mutation of the ACADM gene (c.145C>G) associated with the common c.985A>G mutation on the other ACADM allele causes mild MCAD deficiency: a case reportPotential of mean force calculation for the proton and hydride transfer reactions catalyzed by medium-chain acyl-CoA dehydrogenase: effect of mutations on enzyme catalysis.Structural basis for substrate specificity of methylsuccinyl-CoA dehydrogenase: an unusual member of the acyl-CoA dehydrogenase family.
P2860
Biochemical characterization of a variant human medium-chain acyl-CoA dehydrogenase with a disease-associated mutation localized in the active site.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh-hant
name
Biochemical characterization o ...... localized in the active site.
@en
Biochemical characterization o ...... localized in the active site.
@nl
type
label
Biochemical characterization o ...... localized in the active site.
@en
Biochemical characterization o ...... localized in the active site.
@nl
prefLabel
Biochemical characterization o ...... localized in the active site.
@en
Biochemical characterization o ...... localized in the active site.
@nl
P2093
P2860
P1433
P1476
Biochemical characterization o ...... localized in the active site.
@en
P2093
P2860
P304
P356
10.1042/0264-6021:3370225
P407
P478
337 ( Pt 2)
P577
1999-01-01T00:00:00Z