4DVB
The crystal structure of the Fab fragment of pro-uPA antibody mAb-112
4DVB の概要
エントリーDOI | 10.2210/pdb4dvb/pdb |
関連するPDBエントリー | 2BRR 2R4R 4DW2 |
分子名称 | Fab fragment of pro-uPA antibody mAb-112, SULFATE ION, TETRAETHYLENE GLYCOL, ... (5 entities in total) |
機能のキーワード | immune system, hydrolase |
由来する生物種 | Mus musculus 詳細 |
タンパク質・核酸の鎖数 | 4 |
化学式量合計 | 94074.44 |
構造登録者 | Jiang, L.,Botkjaer, K.A.,Andersen, L.M.,Yuan, C.,Andreasen, P.A.,Huang, M. (登録日: 2012-02-23, 公開日: 2013-01-16) |
主引用文献 | Jiang, L.,Botkjaer, K.A.,Andersen, L.M.,Yuan, C.,Andreasen, P.A.,Huang, M. Rezymogenation of active urokinase induced by an inhibitory antibody. Biochem.J., 449:161-166, 2013 Cited by PubMed Abstract: An important regulatory mechanism of serine proteases is the proteolytic conversion of the inactive pro-enzyme, or zymogen, into the active enzyme. This activation process is generally considered an irreversible process. In the present study, we demonstrate that an active enzyme can be converted back into its zymogen form. We determined the crystal structure of uPA (urokinase-type plasminogen activator) in complex with an inhibitory antibody, revealing that the antibody 'rezymogenizes' already activated uPA. The present study demonstrates a new regulatory mechanism of protease activity, which is also an extreme case of protein allostery. Mechanistically, the antibody binds a single surface-exposed loop, named the autolysis loop, thereby preventing the stabilization of uPA in its active conformation. We argue that this autolysis loop is a key structural element for rezymogenation of other proteases, and will be a new target site for pharmacological intervention with serine protease activity. PubMed: 23016918DOI: 10.1042/BJ20121132 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.93 Å) |
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