Domain relationships in thiamine diphosphate-dependent enzymes
Data(s) |
01/01/2006
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Resumo |
Three-dimensional structures have been determined for 13 different enzymes that use thiamine diphosphate (ThDP) as a cofactor. These enzymes fall into five families, where members within a family have similar structures. In different families, there are similarities between some domains that clearly point to a common ancestor for all of these enzymes. Where the enzyme structures differ, evolutionary relationships between families can be discerned. Here, I present an analysis of these families and propose an evolutionary pathway to explain the diversity of structures that are now known. |
Identificador | |
Idioma(s) |
eng |
Publicador |
Amer Chemical Soc |
Palavras-Chave | #Chemistry, Multidisciplinary #Pyruvate-ferredoxin Oxidoreductase #Acetohydroxyacid Synthase #Multienzyme Complex #Angstrom Resolution #Crystal-structures #Active-site #Decarboxylase #Dehydrogenase #Binding #Transketolase #C1 #270108 Enzymes #270208 Molecular Evolution #780105 Biological sciences |
Tipo |
Journal Article |