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dc.contributor.authorChamberlain, AK-
dc.contributor.authorLee, Y-
dc.contributor.authorKim, S-
dc.contributor.authorBowie, JU-
dc.date.accessioned2016-04-01T08:49:16Z-
dc.date.available2016-04-01T08:49:16Z-
dc.date.created2009-09-30-
dc.date.issued2004-05-28-
dc.identifier.issn0022-2836-
dc.identifier.other2004-OAK-0000016786-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/28840-
dc.description.abstractBy analyzing transmembrane (TM) helices in known structures, we find that some polar amino acids are more frequent at the N terminus than at the C terminus. We propose the asymmetry occurs because most polar amino acids are better able to snorkel their polar atoms away from the membrane core at the N terminus than at the C terminus. Two findings lead us to this proposition: (1) side-chain conformations are influenced strongly by the N or C-terminal position of the amino acid in the bilayer, and (2) the favored snorkeling direction of an amino acid correlates well with its N to C-terminal composition bias. Our results suggest that TM helix predictions should incorporate an N to C-terminal composition bias, that rotamer preferences of TM side-chains are position-dependent, and that the ability to snorkel influences the evolutionary selection of amino acids for the helix N and C termini. (C) 2004 Elsevier Ltd. All rights reserved.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherACADEMIC PRESS LTD ELSEVIER SCIENCE L-
dc.relation.isPartOfJOURNAL OF MOLECULAR BIOLOGY-
dc.subjectmembrane-
dc.subjectprotein-
dc.subjectside-chain-
dc.subjectpolarity-
dc.subjectrotamer-
dc.subjectMEMBRANE-PROTEIN TOPOLOGY-
dc.subjectSTATISTICAL-ANALYSIS-
dc.subjectCHARGED RESIDUES-
dc.subjectBACTERIORHODOPSIN LATTICE-
dc.subjectSECONDARY STRUCTURE-
dc.subjectAMPHIPATHIC HELIX-
dc.subjectCRYSTAL-STRUCTURE-
dc.subjectSTRUCTURAL BASIS-
dc.subjectSIDE-CHAINS-
dc.subjectASSOCIATION-
dc.titleSNORKELING PREFERENCES FOSTER AN AMINO ACID COMPOSITION BIAS IN TRANSMEMBRANE HELICES-
dc.typeArticle-
dc.contributor.college생명과학과-
dc.identifier.doi10.1016/J.JMB.2004.0-
dc.author.googleChamberlain, AK-
dc.author.googleLee, Y-
dc.author.googleKim, S-
dc.author.googleBowie, JU-
dc.relation.volume339-
dc.relation.issue2-
dc.relation.startpage471-
dc.relation.lastpage479-
dc.contributor.id10136479-
dc.relation.journalJOURNAL OF MOLECULAR BIOLOGY-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationJOURNAL OF MOLECULAR BIOLOGY, v.339, no.2, pp.471 - 479-
dc.identifier.wosid000221561800019-
dc.date.tcdate2019-02-01-
dc.citation.endPage479-
dc.citation.number2-
dc.citation.startPage471-
dc.citation.titleJOURNAL OF MOLECULAR BIOLOGY-
dc.citation.volume339-
dc.contributor.affiliatedAuthorKim, S-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc57-
dc.type.docTypeArticle-
dc.subject.keywordPlusMEMBRANE-PROTEIN TOPOLOGY-
dc.subject.keywordPlusSTATISTICAL-ANALYSIS-
dc.subject.keywordPlusCHARGED RESIDUES-
dc.subject.keywordPlusBACTERIORHODOPSIN LATTICE-
dc.subject.keywordPlusSECONDARY STRUCTURE-
dc.subject.keywordPlusAMPHIPATHIC HELIX-
dc.subject.keywordPlusCRYSTAL-STRUCTURE-
dc.subject.keywordPlusSTRUCTURAL BASIS-
dc.subject.keywordPlusSIDE-CHAINS-
dc.subject.keywordPlusASSOCIATION-
dc.subject.keywordAuthormembrane-
dc.subject.keywordAuthorprotein-
dc.subject.keywordAuthorside-chain-
dc.subject.keywordAuthorpolarity-
dc.subject.keywordAuthorrotamer-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-

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