Towards Symmetry-Based Explanation of (Approximate) Shapes of Alpha-Helices and Beta-Sheets (and Beta-Barrels) in Protein Structure 英文参考文献.docVIP
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Towards Symmetry-Based Explanation of (Approximate) Shapes of Alpha-Helices and Beta-Sheets (and Beta-Barrels) in Protein Structure 英文参考文献
Symmetry2012,4,15-25;doi:10.3390/sym4010015
OPENACCESS
symmetry
ISSN2073-8994
/journal/symmetry
Article
TowardsSymmetry-BasedExplanationof(Approximate)Shapes
ofAlpha-HelicesandBeta-Sheets(andBeta-Barrels)in
ProteinStructure
JaimeNavaandVladikKreinovich*
DepartmentofComputerScience,UniversityofTexasatElPaso,500WestUniversityAvenue,ElPaso,
TX79968,USA;E-Mail:jenava@
*Authortowhomcorrespondenceshouldbeaddressed;E-Mail:vladik@;
Tel.:+1-915-747-6951;Fax:+1-915-747-5030.
Received:22December2011;inrevisedform:6January2012/Accepted:12January2012/
Published:19January2012
Abstract: Protein structure is invariably connected to protein function. There are two
important secondary structure elements: alpha-helices and beta-sheets (which sometimes
comeinashapeofbeta-barrels). Theactualshapesofthesestructurescanbecomplicated,
butinthe?rstapproximation,theyareusuallyapproximatedby,correspondingly,cylindrical
spirals and planes (and cylinders, for beta-barrels). In this paper, following the ideas
pioneered by a renowned mathematician M. Gromov, we use natural symmetries to
show that, under reasonable assumptions, these geometric shapes are indeed the best
approximatingfamiliesforsecondarystructures.
Keywords:symmetries;secondaryproteinstructures;alpha-helices;beta-sheets;beta-barrels
1.Introduction
Alpha-helicesandbeta-sheets:briefreminder.Proteinsarebiologicalpolymersthatperformmostof
life’sfunction.Asinglechainpolymer(protein)isfoldedinsuchawaythatitformslocalsubstructures
called secondary structure elements. In order to study the structure and function of proteins it is
extremelyimportanttohaveagoodgeometricaldescriptionoftheproteinsstructure. Therearetwo
importantsecondarystructureelements: alpha-helicesandbeta-sheets. Apartoftheproteinstructure
wheredifferentfragmentsofthepolypeptidealignnexttoeachotherinextendedconformationforming
Symmetry2012,4
16
aline-likefeaturede?nesasecondarystructurecalledanalpha-helix. Apartoftheproteinstructure
wheredifferentfragme
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