3FF6
Human ACC2 CT domain with CP-640186
3FF6 の概要
| エントリーDOI | 10.2210/pdb3ff6/pdb |
| 関連するPDBエントリー | 1od2 1w2x |
| 分子名称 | Acetyl-CoA carboxylase 2, (3R)-1'-(9-ANTHRYLCARBONYL)-3-(MORPHOLIN-4-YLCARBONYL)-1,4'-BIPIPERIDINE (3 entities in total) |
| 機能のキーワード | acetyl coa carboxylase, acc2, acc, metabolic disorder, fatty acid metabolism, atp-binding, biotin, fatty acid biosynthesis, ligase, lipid synthesis, manganese, membrane, metal-binding, multifunctional enzyme, nucleotide-binding, phosphoprotein |
| 由来する生物種 | Homo sapiens (human) |
| 細胞内の位置 | Mitochondrion : O00763 |
| タンパク質・核酸の鎖数 | 4 |
| 化学式量合計 | 346508.25 |
| 構造登録者 | |
| 主引用文献 | Madauss, K.P.,Burkhart, W.A.,Consler, T.G.,Cowan, D.J.,Gottschalk, W.K.,Miller, A.B.,Short, S.A.,Tran, T.B.,Williams, S.P. The human ACC2 CT-domain C-terminus is required for full functionality and has a novel twist. Acta Crystallogr.,Sect.D, 65:449-461, 2009 Cited by PubMed Abstract: Inhibition of acetyl-CoA carboxylase (ACC) may prevent lipid-induced insulin resistance and type 2 diabetes, making the enzyme an attractive pharmaceutical target. Although the enzyme is highly conserved amongst animals, only the yeast enzyme structure is available for rational drug design. The use of biophysical assays has permitted the identification of a specific C-terminal truncation of the 826-residue human ACC2 carboxyl transferase (CT) domain that is both functionally competent to bind inhibitors and crystallizes in their presence. This C-terminal truncation led to the determination of the human ACC2 CT domain-CP-640186 complex crystal structure, which revealed distinctions from the yeast-enzyme complex. The human ACC2 CT-domain C-terminus is comprised of three intertwined alpha-helices that extend outwards from the enzyme on the opposite side to the ligand-binding site. Differences in the observed inhibitor conformation between the yeast and human structures are caused by differing residues in the binding pocket. PubMed: 19390150DOI: 10.1107/S0907444909008014 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (3.19 Å) |
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