REPULSIVE RESTRAINTS FOR HYDROGEN-BONDING IN LEAST-SQUARES REFINEMENT OF PROTEIN CRYSTALS - A NEUTRON-DIFFRACTION STUDY OF MYOGLOBIN CRYSTALS

被引：12

作者：

CHENG, XD

SCHOENBORN, BP

机构：

[1] BROOKHAVEN NATL LAB,DEPT BIOL,CTR STRUCT BIOL,UPTON,NY 11973

[2] SUNY STONY BROOK,DEPT PHYS,STONY BROOK,NY 11794

来源：

ACTA CRYSTALLOGRAPHICA SECTION A | 1991年 / 47卷

关键词：

D O I：

10.1107/S010876739001426X

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The purpose of this article is to describe stereochemical restraints on hydrogen bonding within proteins and their associated solvent which can be included in the refinement (PROLSQ) of X-ray or neutron structures of protein crystals. The parameters which define the geometry of hydrogen bonding, ie. the correlation between distances and angles, are based on the results of an analysis of hydrogen bonding in crystal structures of myoglobin derivatives analyzed by neutron diffraction.

引用

页码：314 / 317

页数：4

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