Literature DB >> 5253650

The influence of short-range interactions on protein onformation. II. A model for predicting the alpha-helical regions of proteins.

D Kotelchuck, H A Scheraga.   

Abstract

On the basis of earlier energy computations, the various single peptide units in proteins were designated as helix-making or helix-breaking.(1) With the use of these designations, empirical rules for distinguishing between alpha-helical and non-alpha-helical regions of proteins have been formulated. These rules include conditions for initiation and termination of a helical segment which, when combined with changes in the designation of three peptide units, correctly identify the helical or nonhelical character of over three fourths of the individual peptide units in four proteins of known amino acid sequence and structure: myoglobin, lysozyme, tosyl-alpha-chymotrypsin, and ribonuclease-A. The model is discussed, some of its predictions are checked, and further predictions about the structure of various proteins are made.

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Year:  1969        PMID: 5253650      PMCID: PMC285948          DOI: 10.1073/pnas.62.1.14

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  19 in total

1.  Three-dimensional structure of tosyl-alpha-chymotrypsin.

Authors:  B W Matthews; P B Sigler; R Henderson; D M Blow
Journal:  Nature       Date:  1967-05-13       Impact factor: 49.962

2.  Use of helical wheels to represent the structures of proteins and to identify segments with helical potential.

Authors:  M Schiffer; A B Edmundson
Journal:  Biophys J       Date:  1967-03       Impact factor: 4.033

3.  Tertiary structure of ribonuclease.

Authors:  G Kartha; J Bello; D Harker
Journal:  Nature       Date:  1967-03-04       Impact factor: 49.962

4.  Three-dimensional Fourier synthesis of horse oxyhaemoglobin at 2.8 A resolution: the atomic model.

Authors:  M F Perutz; H Muirhead; J M Cox; L C Goaman
Journal:  Nature       Date:  1968-07-13       Impact factor: 49.962

5.  Minimization of polypeptide energy. I. Preliminary structures of bovine pancreatic ribonuclease S-peptide.

Authors:  K D Gibson; H A Scheraga
Journal:  Proc Natl Acad Sci U S A       Date:  1967-08       Impact factor: 11.205

6.  The influence of amino-acid sequence on protein structure.

Authors:  A V Guzzo
Journal:  Biophys J       Date:  1965-11       Impact factor: 4.033

7.  Structure of hen egg-white lysozyme. A three-dimensional Fourier synthesis at 2 Angstrom resolution.

Authors:  C C Blake; D F Koenig; G A Mair; A C North; D C Phillips; V R Sarma
Journal:  Nature       Date:  1965-05-22       Impact factor: 49.962

8.  Recognition of alpha-helical segments in proteins of known primary structure.

Authors:  P F Periti; G Quagliarotti; A M Liquori
Journal:  J Mol Biol       Date:  1967-03-14       Impact factor: 5.469

9.  Correlation between the distribution of amino acids and alpha helices.

Authors:  J W Prothero
Journal:  Biophys J       Date:  1966-05       Impact factor: 4.033

10.  A study of the correlation between the amino acid composition and the helical content of proteins.

Authors:  B H Havsteen
Journal:  J Theor Biol       Date:  1966-01       Impact factor: 2.691

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  11 in total

Review 1.  Structural determinants of protein folding.

Authors:  Tse Siang Kang; R Manjunatha Kini
Journal:  Cell Mol Life Sci       Date:  2009-04-15       Impact factor: 9.261

2.  The mechanism of folding of globular proteins. Suitability of a penicillinase from Staphylococcus Aureus as a model for refolding studies.

Authors:  B Robson; R H Pain
Journal:  Biochem J       Date:  1976-05-01       Impact factor: 3.857

3.  Analysis of the code relating sequence to conformation in globular proteins. An informational analysis of the role of the residue in determining the conformation of its neighbours in the primary sequence.

Authors:  B Robson; R H Pain
Journal:  Biochem J       Date:  1974-09       Impact factor: 3.857

4.  Construction of a three-dimensional model of the polypeptide backbone of the variable region of kappa immunoglobulin light chains.

Authors:  E A Kabat; T T Wu
Journal:  Proc Natl Acad Sci U S A       Date:  1972-04       Impact factor: 11.205

5.  Prediction of alpha-helices in glucagon.

Authors:  M Schiffer; A B Edmundson
Journal:  Biophys J       Date:  1970-03       Impact factor: 4.033

6.  Fibrinogen structure and evolution.

Authors:  T Söderqvist; B Blombäck
Journal:  Naturwissenschaften       Date:  1971-01

7.  Regeneration of RNase A from the reduced protein: models of regeneration pathways.

Authors:  Y Konishi; T Ooi; H A Scheraga
Journal:  Proc Natl Acad Sci U S A       Date:  1982-09       Impact factor: 11.205

8.  Local structure involving histidine-12 in reduced S-sulfonated ribonuclease A detected by proton NMR spectroscopy under folding conditions.

Authors:  J K Swadesh; G T Montelione; T W Thannhauser; H A Scheraga
Journal:  Proc Natl Acad Sci U S A       Date:  1984-07       Impact factor: 11.205

9.  An attempt to locate the non-helical and permissively helical sequences of proteins: application to the variable regions of immunoglobulin light and heavy chains.

Authors:  T T Wu; E A Kabat
Journal:  Proc Natl Acad Sci U S A       Date:  1971-07       Impact factor: 11.205

10.  Covalent structure of bovine neurophysin-II: localization of the disulfide bonds.

Authors:  D H Schlesinger; B Frangione; R Walter
Journal:  Proc Natl Acad Sci U S A       Date:  1972-11       Impact factor: 11.205

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