4C2K
Crystal structure of human mitochondrial 3-ketoacyl-CoA thiolase
4C2K の概要
| エントリーDOI | 10.2210/pdb4c2k/pdb |
| 関連するPDBエントリー | 4C2J |
| 分子名称 | 3-KETOACYL-COA THIOLASE, MITOCHONDRIAL, 1,2-ETHANEDIOL, 2,3-DIHYDROXY-1,4-DITHIOBUTANE, ... (5 entities in total) |
| 機能のキーワード | transferase, fatty acid metabolism, mitochondrial beta-oxidation, thiolytic cleavage |
| 由来する生物種 | HOMO SAPIENS (HUMAN) |
| 細胞内の位置 | Mitochondrion : P42765 |
| タンパク質・核酸の鎖数 | 4 |
| 化学式量合計 | 178820.30 |
| 構造登録者 | |
| 主引用文献 | Kiema, T.-R.,Harijan, R.K.,Strozyk, M.,Fukao, T.,Alexson, S.E.H.,Wierenga, R.K. The Crystal Structure of Human Mitochondrial 3-Ketoacyl-Coa Thiolase (T1): Insight Into the Reaction Mechanism of its Thiolase and Thioesterase Activities Acta Crystallogr.,Sect.D, 70:3212-, 2014 Cited by PubMed Abstract: Crystal structures of human mitochondrial 3-ketoacyl-CoA thiolase (hT1) in the apo form and in complex with CoA have been determined at 2.0 Å resolution. The structures confirm the tetrameric quaternary structure of this degradative thiolase. The active site is surprisingly similar to the active site of the Zoogloea ramigera biosynthetic tetrameric thiolase (PDB entries 1dm3 and 1m1o) and different from the active site of the peroxisomal dimeric degradative thiolase (PDB entries 1afw and 2iik). A cavity analysis suggests a mode of binding for the fatty-acyl tail in a tunnel lined by the Nβ2-Nα2 loop of the adjacent subunit and the Lα1 helix of the loop domain. Soaking of the apo hT1 crystals with octanoyl-CoA resulted in a crystal structure in complex with CoA owing to the intrinsic acyl-CoA thioesterase activity of hT1. Solution studies confirm that hT1 has low acyl-CoA thioesterase activity for fatty acyl-CoA substrates. The fastest rate is observed for the hydrolysis of butyryl-CoA. It is also shown that T1 has significant biosynthetic thiolase activity, which is predicted to be of physiological importance. PubMed: 25478839DOI: 10.1107/S1399004714023827 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (2 Å) |
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