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封端盒的序列决定因素,α螺旋N端的一种稳定基序。

Sequence determinants of the capping box, a stabilizing motif at the N-termini of alpha-helices.

作者信息

Seale J W, Srinivasan R, Rose G D

机构信息

Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, Missouri 63110.

出版信息

Protein Sci. 1994 Oct;3(10):1741-5. doi: 10.1002/pro.5560031014.

Abstract

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).

摘要

封端盒是α-螺旋N端反复出现的氢键基序,封端螺旋最初4个主链酰胺氢供体中的2个(哈珀等人,罗斯·G·D,1993年,《生物化学》32:7605 - 7609)。具体而言,第一个螺旋残基的侧链与第四个螺旋残基的主链形成氢键,反之,第四个残基的侧链与第一个残基的主链形成氢键。我们现在扩大了这个基序的早期定义,以包括在封端盒序列两侧的残基之间伴随的疏水相互作用。扩展后的盒式基序——其中2个氢键和1个疏水相互作用位于连续6个残基内——类似于在螺旋C端发现的基于甘氨酸的封端基序(奥罗拉·R,斯里尼瓦桑·R,罗斯·G·D,1994年,《科学》264:1126 - 1130)。

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