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Estimating the total number of protein folds

dc.contributor.authorGovindarajan, Sridharen_US
dc.contributor.authorRecabarren, Rubenen_US
dc.contributor.authorGoldstein, Richard A.en_US
dc.date.accessioned2006-04-19T14:01:35Z
dc.date.available2006-04-19T14:01:35Z
dc.date.issued1999-06-01en_US
dc.identifier.citationGovindarajan, Sridhar; Recabarren, Ruben; Goldstein, Richard A. (1999)."Estimating the total number of protein folds." Proteins: Structure, Function, and Genetics 35(4): 408-414. <http://hdl.handle.net/2027.42/34969>en_US
dc.identifier.issn0887-3585en_US
dc.identifier.issn1097-0134en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/34969
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=10382668&dopt=citationen_US
dc.description.abstractMany seemingly unrelated protein families share common folds. Theoretical models based on structure designability have suggested that a few folds should be very common while many others have low probability. In agreement with the predictions of these models, we show that the distribution of observed protein families over different folds can be modeled with a highly-stretched exponential. Our results suggest that there are approximately 4,000 possible folds, some so unlikely that only approximately 2,000 folds existing among naturally-occurring proteins. Due to the large number of extremely rare folds, constructing a comprehensive database of all existent folds would be difficult. Constructing a database of the most-likely folds representing the vast majority of protein families would be considerably easier. Proteins 1999;35:408–414. © 1999 Wiley-Liss, Inc.en_US
dc.format.extent120557 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherJohn Wiley & Sons, Inc.en_US
dc.subject.otherChemistryen_US
dc.subject.otherBiochemistry and Biotechnologyen_US
dc.titleEstimating the total number of protein foldsen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, Michigan ; Biophysics Research Division, University of Michigan, Ann Arbor, Michigan ; Department of Chemistry, University of Michigan, Ann Arbor, MI 48109-1055.en_US
dc.identifier.pmid10382668en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/34969/1/4_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/(SICI)1097-0134(19990601)35:4<408::AID-PROT4>3.0.CO;2-Aen_US
dc.identifier.sourceProteins: Structure, Function, and Geneticsen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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