1ECV
CRYSTAL STRUCTURE OF PROTEIN TYROSINE PHOSPHATASE 1B COMPLEXED WITH 5-IODO-2-(OXALYL-AMINO)-BENZOIC ACID
1ECV の概要
| エントリーDOI | 10.2210/pdb1ecv/pdb |
| 関連するPDBエントリー | 1C83 1C84 1C85 1C86 1C87 1C88 |
| 分子名称 | PROTEIN-TYROSINE PHOSPHATASE 1B, ACETATE ION, 5-IODO-2-(OXALYL-AMINO)-BENZOIC ACID, ... (4 entities in total) |
| 機能のキーワード | hydrolase, phosphorylation, ligand, inhibitor |
| 由来する生物種 | Homo sapiens (human) |
| 細胞内の位置 | Endoplasmic reticulum membrane ; Peripheral membrane protein ; Cytoplasmic side : P18031 |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 35232.75 |
| 構造登録者 | Andersen, H.S.,Iversen, L.F.,Branner, S.,Rasmussen, H.B.,Moller, N.P.H. (登録日: 2000-01-26, 公開日: 2000-03-15, 最終更新日: 2024-02-07) |
| 主引用文献 | Andersen, H.S.,Iversen, L.F.,Jeppesen, C.B.,Branner, S.,Norris, K.,Rasmussen, H.B.,Moller, K.B.,Moller, N.P. 2-(oxalylamino)-benzoic acid is a general, competitive inhibitor of protein-tyrosine phosphatases. J.Biol.Chem., 275:7101-7108, 2000 Cited by PubMed Abstract: Protein-tyrosine phosphatases (PTPs) are critically involved in regulation of signal transduction processes. Members of this class of enzymes are considered attractive therapeutic targets in several disease states, e.g. diabetes, cancer, and inflammation. However, most reported PTP inhibitors have been phosphorus-containing compounds, tight binding inhibitors, and/or inhibitors that covalently modify the enzymes. We therefore embarked on identifying a general, reversible, competitive PTP inhibitor that could be used as a common scaffold for lead optimization for specific PTPs. We here report the identification of 2-(oxalylamino)-benzoic acid (OBA) as a classical competitive inhibitor of several PTPs. X-ray crystallography of PTP1B complexed with OBA and related non-phosphate low molecular weight derivatives reveals that the binding mode of these molecules to a large extent mimics that of the natural substrate including hydrogen bonding to the PTP signature motif. In addition, binding of OBA to the active site of PTP1B creates a unique arrangement involving Asp(181), Lys(120), and Tyr(46). PTP inhibitors are essential tools in elucidating the biological function of specific PTPs and they may eventually be developed into selective drug candidates. The unique enzyme kinetic features and the low molecular weight of OBA makes it an ideal starting point for further optimization. PubMed: 10702277DOI: 10.1074/jbc.275.10.7101 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.95 Å) |
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