Mutation of Tyr375 to Lys375 allows medium-chain acyl-CoA dehydrogenase to acquire acyl-CoA oxidase activity

Biochimica et Biophysica Acta - Proteins and Proteomics

Volumn 1774, Issue 12, 2007, Pages 1628-1634

  Zeng, Jia ^a,b   Liu, Yuandong ^b   Wu, Long ^a   Li, Ding ^a  

^a CITY UNIVERSITY OF HONG KONG   (Hong Kong)

^b CENTRAL SOUTH UNIVERSITY   (China)

Author keywords

Oxidation; Acyl CoA dehydrogenase; Acyl CoA oxidase; Fatty acid; Solvent accessible area

Indexed keywords

ACYL COENZYME A OXIDASE; ENZYME VARIANT; LYSINE; MEDIUM CHAIN ACYL COENZYME A DEHYDROGENASE; TYROSINE;

ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME ANALYSIS; ENZYME BINDING; ENZYME MECHANISM; ENZYME SUBSTRATE; GENE MUTATION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MAMMAL; NONHUMAN; PRIORITY JOURNAL; RAT; WILD TYPE;

ACYL-COA DEHYDROGENASE; ACYL-COA OXIDASE; AMINO ACID SUBSTITUTION; ANIMALS; BASE SEQUENCE; CATALYTIC DOMAIN; COENZYMES; FLAVIN-ADENINE DINUCLEOTIDE; LIVER; LYSINE; MODELS, BIOLOGICAL; MODELS, MOLECULAR; MUTAGENESIS, SITE-DIRECTED; MUTANT PROTEINS; MUTATION; RATS; SUBSTRATE SPECIFICITY; TYROSINE;

MAMMALIA; RATTUS;

EID: 36849042575     PISSN: 15709639     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbapap.2007.08.018     Document Type: Article

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