1EWX
Crystal structure of native tryparedoxin I from Crithidia fasciculata
1EWX の概要
| エントリーDOI | 10.2210/pdb1ewx/pdb |
| 関連するPDBエントリー | 1ezk |
| 分子名称 | TRYPAREDOXIN I (2 entities in total) |
| 機能のキーワード | electron transport |
| 由来する生物種 | Crithidia fasciculata |
| タンパク質・核酸の鎖数 | 1 |
| 化学式量合計 | 16393.47 |
| 構造登録者 | Hofmann, B.,Guerrero, S.A.,Kalisz, H.M.,Menge, U.,Nogoceke, E.,Montemartini, M.,Singh, M.,Flohe, L.,Hecht, H.J. (登録日: 2000-04-28, 公開日: 2000-05-10, 最終更新日: 2024-11-20) |
| 主引用文献 | Hofmann, B.,Budde, H.,Bruns, K.,Guerrero, S.A.,Kalisz, H.M.,Menge, U.,Montemartini, M.,Nogoceke, E.,Steinert, P.,Wissing, J.B.,Flohe, L.,Hecht, H.J. Structures of tryparedoxins revealing interaction with trypanothione. Biol.Chem., 382:459-471, 2001 Cited by PubMed Abstract: Tryparedoxins (TXNs) catalyse the reduction of peroxiredoxin-type peroxidases by the bis-glutathionyl derivative of spermidine, trypanothione, and are relevant to hydroperoxide detoxification and virulence of trypanosomes. The 3D-structures of the following tryparedoxins are presented: authentic tryparedoxin1 of Crithidia fasciculata, CfTXN1; the his-tagged recombinant protein, CfTXN1H6; reduced and oxidised CfTXN2, and an alternative substrate derivative of the mutein CfTXN2H6-Cys44Ser. Cys41 (Cys40 in TXN1) of the active site motif 40-WCPPCR-45 proved to be the only solvent-exposed redox active residue in CfTXN2. In reduced TXNs, its nucleophilicity is increased by a network of hydrogen bonds. In oxidised TXNs it can be attacked by the thiol of the 1N-glutathionyl residue of trypanothione, as evidenced by the structure of 1N-glutathionylspermidine-derivatised CfTXN2H6-Cys44Ser. Modelling suggests Arg45 (44), Glu73 (72), the Ile110 (109) cis-Pro111 (110)-bond and Arg129 (128) to be involved in the binding of trypanothione to CfTXN2 (CfTXN1). The model of TXN-substrate interaction is consistent with functional characteristics of known and newly designed muteins (CfTXN2H6-Arg129Asp and Glu73Arg) and the 1N-glutathionyl-spermidine binding in the CfTXN2H6-Cys44Ser structure. PubMed: 11347894DOI: 10.1515/BC.2001.056 主引用文献が同じPDBエントリー |
| 実験手法 | X-RAY DIFFRACTION (1.7 Å) |
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