IDENTIFICATION OF RESIDUES LINKED TO THE SLOW-]FAST TRANSITION OF THROMBIN

被引:46
作者
GUINTO, ER [1 ]
VINDIGNI, A [1 ]
AYALA, YM [1 ]
DANG, QD [1 ]
DICERA, E [1 ]
机构
[1] WASHINGTON UNIV,SCH MED,DEPT BIOCHEM & MOLEC BIOPHYS,ST LOUIS,MO 63110
关键词
ALLOSTERY; FIBRINOGEN; HIRUDIN; MOLECULAR RECOGNITION; SITE-DIRECTED MUTAGENESIS;
D O I
10.1073/pnas.92.24.11185
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Residues energetically linked to the allosteric transition of thrombin from its anticoagulant slow form to the procoagulant fast form have been identified by site-directed mutagenesis, The energetics of recognition by the two forms of the enzyme were probed by using a synthetic chromogenic substrate, fibrinogen, and hirudin, The thrombin residues E39, W60d, E192, D221, and D222 are linked to the slow --> fast transition and are part of an ''allosteric core'' through which events originating at the Na+ binding loop propagate to other regions of the enzyme, The thrombin residues Y76, W96, W148, and R173 lie at the periphery of the allosteric core, affect recognition of fibrinogen and hirudin to the same extent in both forms, and are not linked to the slow. --> fast transition.
引用
收藏
页码:11185 / 11189
页数:5
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