4WRY
Crystal structure of Mycobacterium tuberculosis uracil-DNA glycosylase in complex with 5-fluorouracil(B), Form I
4WRY の概要
| エントリーDOI | 10.2210/pdb4wry/pdb |
| 関連するPDBエントリー | 4WRU 4WRV 4WRW 4WRX 4WRZ 4WS0 4WS1 4WS2 4WS3 4WS4 4WS5 4WS6 4WS7 4WS8 |
| 分子名称 | Uracil-DNA glycosylase, CITRIC ACID, 5-FLUOROURACIL, ... (5 entities in total) |
| 機能のキーワード | dna-repair, excision repair, conformational selection, ligand binding, hydrolase |
| 由来する生物種 | Mycobacterium tuberculosis |
| 細胞内の位置 | Cytoplasm : P9WFQ9 |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 26171.20 |
| 構造登録者 | Arif, S.M.,Geethanandan, K.,Mishra, P.,Surolia, A.,Varshney, U.,Vijayan, M. (登録日: 2014-10-25, 公開日: 2015-07-15, 最終更新日: 2023-09-27) |
| 主引用文献 | Arif, S.M.,Geethanandan, K.,Mishra, P.,Surolia, A.,Varshney, U.,Vijayan, M. Structural plasticity in Mycobacterium tuberculosis uracil-DNA glycosylase (MtUng) and its functional implications. Acta Crystallogr.,Sect.D, 71:1514-1527, 2015 Cited by PubMed Abstract: 17 independent crystal structures of family I uracil-DNA glycosylase from Mycobacterium tuberculosis (MtUng) and its complexes with uracil and its derivatives, distributed among five distinct crystal forms, have been determined. Thermodynamic parameters of binding in the complexes have been measured using isothermal titration calorimetry. The two-domain protein exhibits open and closed conformations, suggesting that the closure of the domain on DNA binding involves conformational selection. Segmental mobility in the enzyme molecule is confined to a 32-residue stretch which plays a major role in DNA binding. Uracil and its derivatives can bind to the protein in two possible orientations. Only one of them is possible when there is a bulky substituent at the 5' position. The crystal structures of the complexes provide a reasonable rationale for the observed thermodynamic parameters. In addition to providing fresh insights into the structure, plasticity and interactions of the protein molecule, the results of the present investigation provide a platform for structure-based inhibitor design. PubMed: 26143923DOI: 10.1107/S1399004715009311 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.43 Å) |
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