2EFT

Methanethiol-CYS 112 inhibition complex of E. coli ketoacyl synthase III (FABH) and Coenzyme A (high concentration (1.7mM) soak)

2EFT の概要

• エントリーDOI: 10.2210/pdb2eft/pdb
• 関連するPDBエントリー: 1EBL 1HND 2GYO
• 分子名称: 3-oxoacyl-[acyl-carrier-protein] synthase 3, SULFATE ION, COENZYME A, ... (5 entities in total)
• 機能のキーワード: fatty acid biosynthesis, alkyl-coa-disulfide, mechanism-based inhibitor, e. coli, half sites occupancy, transferase
• 由来する生物種: Escherichia coli
• 細胞内の位置: Cytoplasm: P0A6R0
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 68149.93

構造登録者

Alhamadsheh, M.M.,Musayev, F.,Komissarov, A.A.,Sachdeva, S.,Wright, H.T.,Scarsdale, N.,Florova, G.,Reynolds, K.A. (登録日: 2007-02-24, 公開日: 2007-06-12, 最終更新日: 2023-10-25)

主引用文献

Alhamadsheh, M.M.,Musayev, F.,Komissarov, A.A.,Sachdeva, S.,Wright, H.T.,Scarsdale, N.,Florova, G.,Reynolds, K.A.
Alkyl-CoA Disulfides as Inhibitors and Mechanistic Probes for FabH Enzymes
Chem.Biol., 14:513-524, 2007

PubMed Abstract: The first step of the reaction catalyzed by the homodimeric FabH from a dissociated fatty acid synthase is acyl transfer from acyl-CoA to an active site cysteine. We report that C1 to C10 alkyl-CoA disulfides irreversibly inhibit Escherichia coli FabH (ecFabH) and Mycobacterium tuberculosis FabH with relative efficiencies that reflect these enzymes' differential acyl-group specificity. Crystallographic and kinetic studies with MeSSCoA show rapid inhibition of one monomer of ecFabH through formation of a methyl disulfide conjugate with this cysteine. Reaction of the second subunit with either MeSSCoA or acetyl-CoA is much slower. In the presence of malonyl-ACP, the acylation rate of the second subunit is restored to that of the native ecFabH. These observations suggest a catalytic model in which a structurally disordered apo-ecFabH dimer orders on binding either the first substrate, acetyl-CoA, or the inhibitor MeSSCoA, and is restored to a disordered state on binding of malonyl-ACP.

PubMed: 17524982
DOI: 10.1016/j.chembiol.2007.03.013

実験手法

X-RAY DIFFRACTION (2 Å)