1QA7
CRYSTAL COMPLEX OF THE 3C PROTEINASE FROM HEPATITIS A VIRUS WITH ITS INHIBITOR AND IMPLICATIONS FOR THE POLYPROTEIN PROCESSING IN HAV
1QA7 の概要
エントリーDOI | 10.2210/pdb1qa7/pdb |
分子名称 | HAV 3C PROTEINASE, N-(iodoacetyl)-L-valyl-L-phenylalaninamide, DIMETHYL SULFOXIDE, ... (5 entities in total) |
機能のキーワード | chymotrypsin-like cysteine proteinase viral protease p'-site inhibitor, hydrolase, hydrolase-hydrolase inhibitor complex, hydrolase/hydrolase inhibitor |
由来する生物種 | Hepatitis A virus |
タンパク質・核酸の鎖数 | 4 |
化学式量合計 | 97209.18 |
構造登録者 | Bergmann, E.M.,Cherney, M.M.,Mckendrick, J.,Vederas, J.C.,James, M.N.G. (登録日: 1999-04-15, 公開日: 1999-04-20, 最終更新日: 2023-08-16) |
主引用文献 | Bergmann, E.M.,Cherney, M.M.,Mckendrick, J.,Frormann, S.,Luo, C.,Malcolm, B.A.,Vederas, J.C.,James, M.N. Crystal structure of an inhibitor complex of the 3C proteinase from hepatitis A virus (HAV) and implications for the polyprotein processing in HAV. Virology, 265:153-163, 1999 Cited by PubMed: 10603326DOI: 10.1006/viro.1999.9968 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.9 Å) |
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