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PMID: 1125392 Published · ppublish English Journal Article

A model of myoglobin self-organization.

Biophysical chemistry ·Vol. 3 ·No. 1 ·1975-02-00 ·Pages 1-20

Ptitsyn OB, Rashin AA

Abstract

The self-organization of helical regions of myoglobin into a compact tertiary structure is considered on the basis of the hypothesis on the step-wise mechanism of self-organization of protein molecules. It is assumed that the self-organization begins with the formation of "centers of crystallization" and proceeds with the growth of on such center or by a sequential collapse of two or more grown centers. Different pathways of self-organization of myoglobin are considered; the most favourable structures corresponding to the greatest number of dehydrated bulky hydrophobic groups and to all the strongly hydrophilic groups exposed to water are selected at every stage of the given pathway and the others are neglected. One of the two most favourable structures obtained in such a way coincides in rough resolution with the native tertiary structure of protein.

MeSH Terms
Animals Binding Sites Models, Molecular Myoglobin Protein Binding Protein Conformation Whales
Chemicals
Myoglobin
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Ptitsyn O B
Rashin A A
Article Info
Journal
Biophysical chemistry
Abbr.
Biophys Chem
ISSN
0301-4622
Published
1975-02-00
Pages
1-20
Language
English
Region
Netherlands
NLM ID
0403171
Subset
IM
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