SEQUENCE DETERMINANTS OF THE CAPPING BOX, A STABILIZING MOTIF AT THE N-TERMINI OF ALPHA-HELICES

被引:118
作者
SEALE, JW [1 ]
SRINIVASAN, R [1 ]
ROSE, GD [1 ]
机构
[1] WASHINGTON UNIV,SCH MED,DEPT BIOCHEM & MOLEC BIOPHYS,ST LOUIS,MO 63110
关键词
ALPHA-HELICES; CAPPING BOX; HYDROPHOBIC INTERACTIONS;
D O I
10.1002/pro.5560031014
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
The capping box, a recurrent hydrogen bonded motif at the N-termini of alpha-helices, caps 2 of the initial 4 backbone amide hydrogen donors of the helix (Harper ET, Rose GD, 1993, Biochemistry 32:7605-7609). In detail, the side chain of the first helical residue forms a hydrogen bond with the backbone of the fourth helical residue and, reciprocally, the side chain of the fourth residue forms a hydrogen bond with the backbone of the first residue. We now enlarge the earlier definition of this motif to include an accompanying hydrophobic interaction between residues that bracket the capping box sequence on either side. The expanded box motif-in which 2 hydrogen bonds and a hydrophobic interaction are localized within 6 consecutive residues - resembles a glycine-based capping motif found at helix C-termini (Aurora R, Srinivasan R, Rose GD, 1994, Science 264:1126-1130).
引用
收藏
页码:1741 / 1745
页数:5
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