2VAV
Crystal structure of deacetylcephalosporin C acetyltransferase (DAC-Soak)
2VAV の概要
エントリーDOI | 10.2210/pdb2vav/pdb |
関連するPDBエントリー | 2VAT 2VAX |
分子名称 | ACETYL-COA--DEACETYLCEPHALOSPORIN C ACETYLTRANSFERASE, 4-(3-ACETOXYMETHYL-2-CARBOXY-8-OXO-5-THIA-1-AZA-BICYCLO[4.2.0]OCT-2-EN-7-YLCARBAMOYL)-1-CARBOXY-BUTYL-AMMONIUM, ACETATE ION, ... (4 entities in total) |
機能のキーワード | acetyl transferase, a/b- hydrolase fold, transferase, acyltransferase, acetyl coenzyme a, antibiotic biosynthesis, cephalosporin biosynthesis |
由来する生物種 | ACREMONIUM CHRYSOGENUM |
タンパク質・核酸の鎖数 | 12 |
化学式量合計 | 596998.74 |
構造登録者 | |
主引用文献 | Lejon, S.,Ellis, J.,Valegard, K. The last step in cephalosporin C formation revealed: crystal structures of deacetylcephalosporin C acetyltransferase from Acremonium chrysogenum in complexes with reaction intermediates. J. Mol. Biol., 377:935-944, 2008 Cited by PubMed Abstract: Deacetylcephalosporin C acetyltransferase (DAC-AT) catalyses the last step in the biosynthesis of cephalosporin C, a broad-spectrum beta-lactam antibiotic of large clinical importance. The acetyl transfer step has been suggested to be limiting for cephalosporin C biosynthesis, but has so far escaped detailed structural analysis. We present here the crystal structures of DAC-AT in complexes with reaction intermediates, providing crystallographic snapshots of the reaction mechanism. The enzyme is found to belong to the alpha/beta hydrolase class of acetyltransferases, and the structures support previous observations of a double displacement mechanism for the acetyl transfer reaction in other members of this class of enzymes. The structures of DAC-AT reported here provide evidence of a stable acyl-enzyme complex, thus underpinning a mechanism involving acetylation of a catalytic serine residue by acetyl coenzyme A, followed by transfer of the acetyl group to deacetylcephalosporin C through a suggested tetrahedral transition state. PubMed: 18279889DOI: 10.1016/j.jmb.2008.01.047 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.5 Å) |
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