PYRROLIDINE RING PUCKERING IN CIS AND TRANS-PROLINE RESIDUES IN PROTEINS AND POLYPEPTIDES - DIFFERENT PUCKERS ARE FAVORED IN CERTAIN SITUATIONS

被引:141
作者
MILNERWHITE, EJ
BELL, LH
MACCALLUM, PH
机构
[1] Department of Biochemistry, University of Glasgow, Glasgow
关键词
PROLINE; ALPHA-HELIX; BETA-SHEET; BETA-TURN; PROTEINS;
D O I
10.1016/0022-2836(92)90859-I
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In a set of proteins studied at high resolution by X-ray crystallography over a half of all cis and trans-proline residues could be unambiguously assigned to one of the two forms of pyrrolidine ring puckering, called UP and DOWN. Of these, 89% of the cis-proline residues exhibit the DOWN pucker, while the trans-proline residues, on average, are about evenly distributed between the two forms. Of trans-proline residues found in α-helices, 79% have the UP ring pucker. trans-proline residues occurring in other situations are more equally distributed between the two forms of pucker, although further generalizations may be possible. Proline residues in a set of crystal structures of short polypeptides were also examined. As in the protein sample, a tendency for the cis-proline residues to have the DOWN pucker was observed, but the effect was less pronounced. © 1992.
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页码:725 / 734
页数:10
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