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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
2
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pubmed:dateCreated |
2002-3-20
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pubmed:databankReference |
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pubmed:abstractText |
Acetohydroxyacid synthase (AHAS; EC 4.1.3.18) catalyzes the first step in branched-chain amino acid biosynthesis. The enzyme requires thiamin diphosphate and FAD for activity, but the latter is unexpected, because the reaction involves no oxidation or reduction. Due to its presence in plants, AHAS is a target for sulfonylurea and imidazolinone herbicides. Here, the crystal structure to 2.6 A resolution of the catalytic subunit of yeast AHAS is reported. The active site is located at the dimer interface and is near the proposed herbicide-binding site. The conformation of FAD and its position in the active site are defined. The structure of AHAS provides a starting point for the rational design of new herbicides.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0022-2836
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pubmed:author |
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pubmed:copyrightInfo |
Copyright 2002 Elsevier Science Ltd.
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pubmed:issnType |
Print
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pubmed:day |
22
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pubmed:volume |
317
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
249-62
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11902841-Acetolactate Synthase,
pubmed-meshheading:11902841-Amino Acid Sequence,
pubmed-meshheading:11902841-Binding Sites,
pubmed-meshheading:11902841-Catalytic Domain,
pubmed-meshheading:11902841-Crystallography, X-Ray,
pubmed-meshheading:11902841-Dimerization,
pubmed-meshheading:11902841-Enzyme Inhibitors,
pubmed-meshheading:11902841-Flavin-Adenine Dinucleotide,
pubmed-meshheading:11902841-Herbicides,
pubmed-meshheading:11902841-Imidazoles,
pubmed-meshheading:11902841-Magnesium,
pubmed-meshheading:11902841-Models, Molecular,
pubmed-meshheading:11902841-Molecular Sequence Data,
pubmed-meshheading:11902841-Mutation,
pubmed-meshheading:11902841-Niacin,
pubmed-meshheading:11902841-Protein Conformation,
pubmed-meshheading:11902841-Sequence Homology, Amino Acid,
pubmed-meshheading:11902841-Thiamine Pyrophosphate,
pubmed-meshheading:11902841-Yeasts
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pubmed:year |
2002
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pubmed:articleTitle |
Crystal structure of yeast acetohydroxyacid synthase: a target for herbicidal inhibitors.
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pubmed:affiliation |
Centre for Protein Structure Function and Engineering, Department of Biochemistry and Molecular Biology, School of Molecular and Microbial Sciences, The University of Queensland, Brisbane, QLD 4072, Australia.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
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