通过X射线晶体学确定双产物类似物L-苄基琥珀酸与嗜热菌蛋白酶的结合。 - Suppr | 超能文献

Binding of the biproduct analog L-benzylsuccinic acid to thermolysin determined by X-ray crystallography.

作者信息

Bolognesi M C, Matthews B W

出版信息

J Biol Chem. 1979 Feb 10;254(3):634-9.

Abstract

摘要

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Binding of the biproduct analog L-benzylsuccinic acid to thermolysin determined by X-ray crystallography.通过X射线晶体学确定双产物类似物L-苄基琥珀酸与嗜热菌蛋白酶的结合。

J Biol Chem. 1979 Feb 10;254(3):634-9.

2

Redetermination and refinement of the complex of benzylsuccinic acid with thermolysin and its relation to the complex with carboxypeptidase A.

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3

Structural basis for the action of thermolysin.嗜热菌蛋白酶作用的结构基础。

Matrix Suppl. 1992;1:107-11.

4

Crystal structure of the complex between carboxypeptidase A and the biproduct analog inhibitor L-benzylsuccinate at 2.0 A resolution.羧肽酶A与双产物类似物抑制剂L-苄基琥珀酸复合物在2.0埃分辨率下的晶体结构。

J Mol Biol. 1992 Jan 20;223(2):573-8. doi: 10.1016/0022-2836(92)90671-6.

5

The structure of thermolysin: an electron density map at 2-3 A resolution.嗜热菌蛋白酶的结构：分辨率为2 - 3埃的电子密度图。

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6

The conformation of thermolysin.嗜热菌蛋白酶的构象。

J Biol Chem. 1974 Dec 25;249(24):8030-44.

7

Binding of hydroxamic acid inhibitors to crystalline thermolysin suggests a pentacoordinate zinc intermediate in catalysis.异羟肟酸抑制剂与结晶嗜热菌蛋白酶的结合表明在催化过程中存在五配位锌中间体。

Biochemistry. 1981 Nov 24;20(24):6912-20. doi: 10.1021/bi00527a026.

8

Structure of thermolysin refined at 1.6 A resolution.在1.6埃分辨率下精修的嗜热菌蛋白酶结构。

J Mol Biol. 1982 Oct 5;160(4):623-39. doi: 10.1016/0022-2836(82)90319-9.

9

Structures of two thermolysin-inhibitor complexes that differ by a single hydrogen bond.

Science. 1987 Jan 30;235(4788):571-4. doi: 10.1126/science.3810156.

10

The primary structure of the 16 S rRNA binding protein S 8 from Escherichia coli ribosomes.来自大肠杆菌核糖体的16 S rRNA结合蛋白S 8的一级结构。

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引用本文的文献

1

Structure of an actively exchanging complex between carboxypeptidase A and a substrate analogue.羧肽酶A与底物类似物之间的活性交换复合物的结构。

Proc Natl Acad Sci U S A. 1980 Jun;77(6):3288-91. doi: 10.1073/pnas.77.6.3288.

2

3-Phosphonopropionic acids inhibit carboxypeptidase A as multisubstrate analogues or transition-state analogues.3-膦基丙酸作为多底物类似物或过渡态类似物可抑制羧肽酶A。

Biochem J. 1985 Nov 15;232(1):15-9. doi: 10.1042/bj2320015.