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1.98埃分辨率下嗜热栖热菌蛋白酶-埃格林-C复合物的分子动力学精修以及两种钙含量不同的晶体形式的比较。

Molecular dynamics refinement of a thermitase-eglin-c complex at 1.98 A resolution and comparison of two crystal forms that differ in calcium content.

作者信息

Gros P, Betzel C, Dauter Z, Wilson K S, Hol W G

机构信息

Laboratory of Chemical Physics, University of Groningen, The Netherlands.

出版信息

J Mol Biol. 1989 Nov 20;210(2):347-67. doi: 10.1016/0022-2836(89)90336-7.

Abstract

The crystal structure of the complex of thermitase with eglin-c in crystal form II, obtained in the presence of 5 mM-CaCl2, has been determined at 1.98 A resolution. The structure was solved by a molecular replacement method, then molecular dynamics crystallographic refinement was started using the thermitase-eglin-c structure as determined for crystal form I. A ten degrees rigid body misplacement of the core of eglin-c was corrected by the molecular dynamics crystallographic refinement without any need for manual rebuilding on a graphics system. A final crystallographic R-factor of 16.5% was obtained for crystal form II. The comparison of the complexes of thermitase with eglin-c in the two crystal forms shows that the eglin-c cores are differently oriented with respect to the protease. The inhibiting loop of eglin binds in a similar way to thermitase as to subtilisin Carlsberg. A tryptophanyl residue at the S4 site explains the preference of thermitase for aromatic residues of the substrate at the P4 site. The difference in the P1 binding pocket, asparagine in thermitase instead of glycine in subtilisin Carlsberg, does not change the binding of eglin-c. The preference for an arginyl residue at the P1 site of thermitase can be explained by the hydrogen bonding with Asn170 in thermitase. Three ion-binding sites of thermitase have been identified. The strong and weak calcium-binding sites resemble the equivalent sites of subtilisin Carlsberg and subtilisin BPN', though there are important amino acid differences at the calcium-binding sites. The medium-strength calcium-binding site of thermitase is observed in the subtilisin family for the first time. The calcium is bound to residues from the loop 57 to 66. A difference in chelation is observed at this site between the two crystal forms of thermitase, which differ in calcium concentration. Additional electron density is observed near Asp60 in crystal form II, which has more calcium bound than form I. This density is possibly due to a water molecule ligating the calcium ion or the result of Asp60 assuming two significantly different conformations.

摘要

在5 mM氯化钙存在的情况下获得的热解酶与II型晶体形式的依格林 - c复合物的晶体结构已在1.98 Å分辨率下测定。该结构通过分子置换法解析,然后使用针对I型晶体测定的热解酶 - 依格林 - c结构开始进行分子动力学晶体学精修。依格林 - c核心的十度刚体错位通过分子动力学晶体学精修得到校正,无需在图形系统上进行任何手动重建。II型晶体的最终晶体学R因子为16.5%。两种晶体形式的热解酶与依格林 - c复合物的比较表明,依格林 - c核心相对于蛋白酶的取向不同。依格林的抑制环以与枯草杆菌蛋白酶卡尔伯格类似的方式与热解酶结合。S4位点的一个色氨酸残基解释了热解酶对P4位点底物芳香族残基的偏好。P1结合口袋的差异,热解酶中的天冬酰胺而非枯草杆菌蛋白酶卡尔伯格中的甘氨酸,并未改变依格林 - c的结合。热解酶对P1位点精氨酸残基的偏好可以通过与热解酶中Asn170的氢键作用来解释。已鉴定出热解酶的三个离子结合位点。强和弱钙结合位点类似于枯草杆菌蛋白酶卡尔伯格和枯草杆菌蛋白酶BPN'的等效位点,尽管在钙结合位点存在重要的氨基酸差异。热解酶的中等强度钙结合位点首次在枯草杆菌蛋白酶家族中观察到。钙与57至66环的残基结合。在热解酶的两种晶体形式之间,该位点观察到螯合差异,它们在钙浓度上有所不同。在II型晶体中,靠近Asp60处观察到额外的电子密度,其结合的钙比I型晶体更多。这种密度可能是由于一个水分子连接钙离子,或者是Asp60呈现两种明显不同构象的结果。

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