Literature DB >> 2837824

Helix signals in proteins.

L G Presta1, G D Rose.   

Abstract

The alpha helix, first proposed by Pauling and co-workers, is a hallmark of protein structure, and much effort has been directed toward understanding which sequences can form helices. The helix hypothesis, introduced here, provides a tentative answer to this question. The hypothesis states that a necessary condition for helix formation is the presence of residues flanking the helix termini whose side chains can form hydrogen bonds with the initial four-helix greater than N-H groups and final four-helix greater than C-O groups; these eight groups would otherwise lack intrahelical partners. This simple hypothesis implies the existence of a stereochemical code in which certain sequences have the hydrogen-bonding capacity to function as helix boundaries and thereby enable the helix to form autonomously. The three-dimensional structure of a protein is a consequence of the genetic code, but the rules relating sequence to structure are still unknown. The ensuing analysis supports the idea that a stereochemical code for the alpha helix resides in its boundary residues.

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Year:  1988        PMID: 2837824     DOI: 10.1126/science.2837824

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  150 in total

1.  N- and C-terminal residues combine in the fusion-pH influenza hemagglutinin HA(2) subunit to form an N cap that terminates the triple-stranded coiled coil.

Authors:  J Chen; J J Skehel; D C Wiley
Journal:  Proc Natl Acad Sci U S A       Date:  1999-08-03       Impact factor: 11.205

2.  Determination of alpha-helix N1 energies after addition of N1, N2, and N3 preferences to helix/coil theory.

Authors:  J K Sun; S Penel; A J Doig
Journal:  Protein Sci       Date:  2000-04       Impact factor: 6.725

3.  Patterned library analysis: a method for the quantitative assessment of hypotheses concerning the determinants of protein structure.

Authors:  S J Lahr; A Broadwater; C W Carter; M L Collier; L Hensley; J C Waldner; G J Pielak; M H Edgell
Journal:  Proc Natl Acad Sci U S A       Date:  1999-12-21       Impact factor: 11.205

4.  A survey of left-handed polyproline II helices.

Authors:  B J Stapley; T P Creamer
Journal:  Protein Sci       Date:  1999-03       Impact factor: 6.725

5.  The Flory isolated-pair hypothesis is not valid for polypeptide chains: implications for protein folding.

Authors:  R V Pappu; R Srinivasan; G D Rose
Journal:  Proc Natl Acad Sci U S A       Date:  2000-11-07       Impact factor: 11.205

6.  Conformational behavior of ionic self-complementary peptides.

Authors:  M Altman; P Lee; A Rich; S Zhang
Journal:  Protein Sci       Date:  2000-06       Impact factor: 6.725

7.  A test of proposed rules for helix capping: implications for protein design.

Authors:  Martin Sagermann; Lars-Göran Mårtensson; Walter A Baase; Brian W Matthews
Journal:  Protein Sci       Date:  2002-03       Impact factor: 6.725

8.  Effects of charged amino acids at b and c heptad positions on specificity and stability of four-chain coiled coils.

Authors:  C Vu; J Robblee; K M Werner; R Fairman
Journal:  Protein Sci       Date:  2001-03       Impact factor: 6.725

9.  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

10.  TRILOGY: Discovery of sequence-structure patterns across diverse proteins.

Authors:  Philip Bradley; Peter S Kim; Bonnie Berger
Journal:  Proc Natl Acad Sci U S A       Date:  2002-06-25       Impact factor: 11.205

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