Crystal structures of xanthomonas campestris OleA reveal features that promote head-to-head condensation of two long-chain fatty acids

Biochemistry

Volumn 51, Issue 20, 2012, Pages 4138-4146

  Goblirsch, Brandon R ^a   Frias, Janice A ^a   Wackett, Lawrence P ^a   Wilmot, Carrie M ^a  

^a UNIVERSITY OF MINNESOTA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVE SITE; ALKYL CHAIN LENGTHS; ALKYL GROUPS; ASSIGNMENT OF; CATALYTIC BASE; CATALYTIC CYSTEINES; CERULENIN; CRYSTAL FORMS; FATTY ACID BIOSYNTHESIS; GENE CLUSTERS; GLUTAMIC ACID RESIDUES; LONG CHAIN OLEFINS; LONG-CHAIN FATTY ACIDS; PING-PONG MECHANISM; SUBSTRATE BINDING; SYNTHASES; XANTHOMONAS CAMPESTRIS; XENON BINDING;

AMINO ACIDS; BIOCHEMISTRY; BIOSYNTHESIS; CONDENSATION; DIMERS; ENZYMES; GENES; OLEFINS; REACTION INTERMEDIATES;

SUBSTRATES;

3 HYDROXY 3 METHYLGLUTARYL COENZYME A; ACETYL COENZYME A; ACETYL COENZYME A ACETYLTRANSFERASE; ACYL COENZYME A; BETA ACETYL COENZYME A; CERULENIN; CYSTEINE; GLUTAMIC ACID; LONG CHAIN FATTY ACID; OLEA ENZYME; THIOESTER; UNCLASSIFIED DRUG; XENON;

ALKYLATION; ARTICLE; BINDING SITE; CATALYSIS; CLAISEN CONDENSATION; CRYSTAL STRUCTURE; ENZYME ACTIVE SITE; ENZYME KINETICS; ENZYME METABOLISM; FATTY ACID SYNTHESIS; POLYMERIZATION; PRIORITY JOURNAL; XANTHOMONAS CAMPESTRIS;

BACTERIAL PROTEINS; CATALYTIC DOMAIN; CERULENIN; COENZYME A; CYSTEINE; FATTY ACIDS; GLUTAMIC ACID; MODELS, MOLECULAR; SUBSTRATE SPECIFICITY; XANTHOMONAS CAMPESTRIS;

XANTHOMONAS CAMPESTRIS;

EID: 84861414604     PISSN: 00062960     EISSN: 15204995     Source Type: Journal    
DOI: 10.1021/bi300386m     Document Type: Article

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