2X9V
High resolution structure of TbPTR1 with trimetrexate
2X9V の概要
| エントリーDOI | 10.2210/pdb2x9v/pdb |
| 関連するPDBエントリー | 2C7V 2VZ0 2WD7 2WD8 2X9N |
| 分子名称 | PTERIDINE REDUCTASE, NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, TRIMETREXATE, ... (5 entities in total) |
| 機能のキーワード | oxidoreductase, short chain dehydrogenase |
| 由来する生物種 | TRYPANOSOMA BRUCEI BRUCEI |
| タンパク質・核酸の鎖数 | 4 |
| 化学式量合計 | 127488.75 |
| 構造登録者 | Dawson, A.,Tulloch, L.B.,Barrack, K.L.,Hunter, W.N. (登録日: 2010-03-24, 公開日: 2010-06-23, 最終更新日: 2024-05-08) |
| 主引用文献 | Dawson, A.,Tulloch, L.B.,Barrack, K.L.,Hunter, W.N. High-Resolution Structures of Trypanosoma Brucei Pteridine Reductase Ligand Complexes Inform on the Placement of New Molecular Entities in the Active Site of a Potential Drug Target Acta Crystallogr.,Sect.D, 66:1334-, 2010 Cited by PubMed Abstract: Pteridine reductase (PTR1) is a potential target for drug development against parasitic Trypanosoma and Leishmania species. These protozoa cause serious diseases for which current therapies are inadequate. High-resolution structures have been determined, using data between 1.6 and 1.1 Å resolution, of T. brucei PTR1 in complex with pemetrexed, trimetrexate, cyromazine and a 2,4-diaminopyrimidine derivative. The structures provide insight into the interactions formed by new molecular entities in the enzyme active site with ligands that represent lead compounds for structure-based inhibitor development and to support early-stage drug discovery. PubMed: 21123874DOI: 10.1107/S0907444910040886 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.3 Å) |
構造検証レポート
検証レポート(詳細版)
をダウンロード






