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PMID: 2837824 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Helix signals in proteins.

Science (New York, N.Y.) ·Vol. 240 ·No. 4859 ·1988-06-17 ·Pages 1632-41

Presta LG, Rose GD

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.

MeSH Terms
Amino Acid Sequence Animals Carboxypeptidases Carboxypeptidases A Cytochrome c Group Flavodoxin Humans Hydrogen Bonding Models, Chemical Molecular Sequence Data Muramidase Myoglobin Pancreatic Polypeptide Parvalbumins Plastocyanin Protein Conformation Ribonucleases Scorpion Venoms Tetrahydrofolate Dehydrogenase Triose-Phosphate Isomerase Trypsin Inhibitors X-Ray Diffraction
Chemicals
Cytochrome c Group Flavodoxin Myoglobin Parvalbumins Scorpion Venoms Trypsin Inhibitors pancreatic polypeptide, avian Pancreatic Polypeptide Plastocyanin Tetrahydrofolate Dehydrogenase Ribonucleases Muramidase Carboxypeptidases Carboxypeptidases A Triose-Phosphate Isomerase
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Presta L G
Department of Biological Chemistry, Hershey Medical Center, Pennsylvania State University, Hershey 17033.
Rose G D
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1988-06-17
Pages
1632-41
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NIA NIH HHS · AG 06084 · United States
NIGMS NIH HHS · GM 29458 · United States
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