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1CI1

CRYSTAL STRUCTURE OF TRIOSEPHOSPHATE ISOMERASE FROM TRYPANOSOMA CRUZI IN HEXANE

1CI1 の概要
エントリーDOI10.2210/pdb1ci1/pdb
分子名称PROTEIN (TRIOSEPHOSPHATE ISOMERASE), HEXANE (3 entities in total)
機能のキーワードtriosephosphate isomerase, trypanosoma cruzi, organic solvent, hexane, oligomeric protein
由来する生物種Trypanosoma cruzi
タンパク質・核酸の鎖数2
化学式量合計54979.40
構造登録者
Gao, X.-G.,Maldondo, E.,Perez-Montfort, R.,De Gomez-Puyou, M.T.,Gomez-Puyou, A.,Rodriguez-Romero, A. (登録日: 1999-04-06, 公開日: 1999-09-01, 最終更新日: 2023-08-09)
主引用文献Gao, X.G.,Maldonado, E.,Perez-Montfort, R.,Garza-Ramos, G.,de Gomez-Puyou, M.T.,Gomez-Puyou, A.,Rodriguez-Romero, A.
Crystal structure of triosephosphate isomerase from Trypanosoma cruzi in hexane.
Proc.Natl.Acad.Sci.USA, 96:10062-10067, 1999
Cited by
PubMed Abstract: To gain insight into the mechanisms of enzyme catalysis in organic solvents, the x-ray structure of some monomeric enzymes in organic solvents was determined. However, it remained to be explored whether the structure of oligomeric proteins is also amenable to such analysis. The field acquired new perspectives when it was proposed that the x-ray structure of enzymes in nonaqueous media could reveal binding sites for organic solvents that in principle could represent the starting point for drug design. Here, a crystal of the dimeric enzyme triosephosphate isomerase from the pathogenic parasite Trypanosoma cruzi was soaked and diffracted in hexane and its structure solved at 2-A resolution. Its overall structure and the dimer interface were not altered by hexane. However, there were differences in the orientation of the side chains of several amino acids, including that of the catalytic Glu-168 in one of the monomers. No hexane molecules were detected in the active site or in the dimer interface. However, three hexane molecules were identified on the surface of the protein at sites, which in the native crystal did not have water molecules. The number of water molecules in the hexane structure was higher than in the native crystal. Two hexanes localized at <4 A from residues that form the dimer interface; they were in close proximity to a site that has been considered a potential target for drug design.
PubMed: 10468562
DOI: 10.1073/pnas.96.18.10062
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2 Å)
構造検証レポート
Validation report summary of 1ci1
検証レポート(詳細版)ダウンロードをダウンロード

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件を2024-10-30に公開中

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