4FB8

Crystal Structure of apo Acyl-CoA Carboxylase

4FB8 の概要

• エントリーDOI: 10.2210/pdb4fb8/pdb
• 関連するPDBエントリー: 4G2R
• 分子名称: Probable propionyl-CoA carboxylase beta chain 6 (2 entities in total)
• 機能のキーワード: structural genomics, tb structural genomics consortium, tbsgc, crotonase fold, acyl-coa carboxylase, ligase, psi-2, protein structure initiative
• 由来する生物種: Mycobacterium tuberculosis
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 100397.87

構造登録者

Reddy, M.C.M.,Bruning, J.B.,Sherekar, M.,Valluru, S.,Ehrenfeld, H.,Sacchettini, J.C.,TB Structural Genomics Consortium (TBSGC) (登録日: 2012-05-22, 公開日: 2014-02-19, 最終更新日: 2023-09-13)

主引用文献

Reddy, M.C.,Breda, A.,Bruning, J.B.,Sherekar, M.,Valluru, S.,Thurman, C.,Ehrenfeld, H.,Sacchettini, J.C.
Structure, Activity, and Inhibition of the Carboxyltransferase beta-Subunit of Acetyl Coenzyme A Carboxylase (AccD6) from Mycobacterium tuberculosis.
Antimicrob.Agents Chemother., 58:6122-6132, 2014

PubMed Abstract: In Mycobacterium tuberculosis, the carboxylation of acetyl coenzyme A (acetyl-CoA) to produce malonyl-CoA, a building block in long-chain fatty acid biosynthesis, is catalyzed by two enzymes working sequentially: a biotin carboxylase (AccA) and a carboxyltransferase (AccD). While the exact roles of the three different biotin carboxylases (AccA1 to -3) and the six carboxyltransferases (AccD1 to -6) in M. tuberculosis are still not clear, AccD6 in complex with AccA3 can synthesize malonyl-CoA from acetyl-CoA. A series of 10 herbicides that target plant acetyl-CoA carboxylases (ACC) were tested for inhibition of AccD6 and for whole-cell activity against M. tuberculosis. From the tested herbicides, haloxyfop, an arylophenoxypropionate, showed in vitro inhibition of M. tuberculosis AccD6, with a 50% inhibitory concentration (IC50) of 21.4 ± 1 μM. Here, we report the crystal structures of M. tuberculosis AccD6 in the apo form (3.0 Å) and in complex with haloxyfop-R (2.3 Å). The structure of M. tuberculosis AccD6 in complex with haloxyfop-R shows two molecules of the inhibitor bound on each AccD6 subunit. These results indicate the potential for developing novel therapeutics for tuberculosis based on herbicides with low human toxicity.

PubMed: 25092705
DOI: 10.1128/AAC.02574-13

実験手法

X-RAY DIFFRACTION (3 Å)