Literature DB >> 7849592

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

J W Seale1, R Srinivasan, G D Rose.   

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).

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Year:  1994        PMID: 7849592      PMCID: PMC2142610          DOI: 10.1002/pro.5560031014

Source DB:  PubMed          Journal:  Protein Sci        ISSN: 0961-8368            Impact factor:   6.725


  33 in total

1.  Effect of central-residue replacements on the helical stability of a monomeric peptide.

Authors:  G Merutka; W Lipton; W Shalongo; S H Park; E Stellwagen
Journal:  Biochemistry       Date:  1990-08-14       Impact factor: 3.162

2.  Hydrophobicity of amino acid subgroups in proteins.

Authors:  G J Lesser; G D Rose
Journal:  Proteins       Date:  1990

3.  A thermodynamic scale for the helix-forming tendencies of the commonly occurring amino acids.

Authors:  K T O'Neil; W F DeGrado
Journal:  Science       Date:  1990-11-02       Impact factor: 47.728

4.  Side chain contributions to the stability of alpha-helical structure in peptides.

Authors:  P C Lyu; M I Liff; L A Marky; N R Kallenbach
Journal:  Science       Date:  1990-11-02       Impact factor: 47.728

5.  Side-chain entropy opposes alpha-helix formation but rationalizes experimentally determined helix-forming propensities.

Authors:  T P Creamer; G D Rose
Journal:  Proc Natl Acad Sci U S A       Date:  1992-07-01       Impact factor: 11.205

6.  A segment-based approach to protein secondary structure prediction.

Authors:  S R Presnell; B I Cohen; F E Cohen
Journal:  Biochemistry       Date:  1992-02-04       Impact factor: 3.162

7.  Amino acid preferences for specific locations at the ends of alpha helices.

Authors:  J S Richardson; D C Richardson
Journal:  Science       Date:  1988-06-17       Impact factor: 47.728

8.  Capping and alpha-helix stability.

Authors:  L Serrano; A R Fersht
Journal:  Nature       Date:  1989-11-16       Impact factor: 49.962

9.  Conformational equilibria of valine studied by dynamics simulation.

Authors:  R H Yun; J Hermans
Journal:  Protein Eng       Date:  1991-10

10.  Side chain-backbone hydrogen bonding contributes to helix stability in peptides derived from an alpha-helical region of carboxypeptidase A.

Authors:  M D Bruch; M M Dhingra; L M Gierasch
Journal:  Proteins       Date:  1991
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  23 in total

1.  The role of helix stabilizing residues in GCN4 basic region folding and DNA binding.

Authors:  Jessica J Hollenbeck; Diana L McClain; Martha G Oakley
Journal:  Protein Sci       Date:  2002-11       Impact factor: 6.725

2.  Noncharged amino acid residues at the solvent-exposed positions in the middle and at the C terminus of the alpha-helix have the same helical propensity.

Authors:  Dmitri N Ermolenko; John M Richardson; George I Makhatadze
Journal:  Protein Sci       Date:  2003-06       Impact factor: 6.725

3.  Importance of alpha-helix N-capping motif in stabilization of betabetaalpha fold.

Authors:  Katarzyna Koscielska-Kasprzak; Tomasz Cierpicki; Jacek Otlewski
Journal:  Protein Sci       Date:  2003-06       Impact factor: 6.725

4.  Molecular dynamics as a tool to detect protein foldability. A mutant of domain B1 of protein G with non-native secondary structure propensities.

Authors:  D Cregut; L Serrano
Journal:  Protein Sci       Date:  1999-02       Impact factor: 6.725

5.  Visualization of conformational distribution of short to medium size segments in globular proteins and identification of local structural motifs.

Authors:  Kazuyoshi Ikeda; Kentaro Tomii; Tsuyoshi Yokomizo; Daisuke Mitomo; Keiichiro Maruyama; Shinya Suzuki; Junichi Higo
Journal:  Protein Sci       Date:  2005-03-31       Impact factor: 6.725

6.  Prion disease susceptibility is affected by beta-structure folding propensity and local side-chain interactions in PrP.

Authors:  M Qasim Khan; Braden Sweeting; Vikram Khipple Mulligan; Pharhad Eli Arslan; Neil R Cashman; Emil F Pai; Avijit Chakrabartty
Journal:  Proc Natl Acad Sci U S A       Date:  2010-11-01       Impact factor: 11.205

Review 7.  Helix capping.

Authors:  R Aurora; G D Rose
Journal:  Protein Sci       Date:  1998-01       Impact factor: 6.725

8.  Empirical parameterization of a model for predicting peptide helix/coil equilibrium populations.

Authors:  N H Andersen; H Tong
Journal:  Protein Sci       Date:  1997-09       Impact factor: 6.725

9.  Side-chain conformation at the selectivity filter shapes the permeation free-energy landscape of an ion channel.

Authors:  Tyler J Harpole; Claudio Grosman
Journal:  Proc Natl Acad Sci U S A       Date:  2014-07-21       Impact factor: 11.205

10.  A conformational equilibrium in a protein fragment caused by two consecutive capping boxes: 1H-, 13C-NMR, and mutational analysis.

Authors:  R Guerois; F Cordier-Ochsenbein; F Baleux; T Huynh-Dinh; J M Neumann; A Sanson
Journal:  Protein Sci       Date:  1998-07       Impact factor: 6.725

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