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dc.contributor.authorLo, Wei-Chengen_US
dc.contributor.authorWang, Li-Fenen_US
dc.contributor.authorLiu, Yen-Yien_US
dc.contributor.authorDai, Tianen_US
dc.contributor.authorHwang, Jenn-Kangen_US
dc.contributor.authorLyu, Ping-Chiangen_US
dc.date.accessioned2014-12-08T15:23:54Z-
dc.date.available2014-12-08T15:23:54Z-
dc.date.issued2012-07-01en_US
dc.identifier.issn0305-1048en_US
dc.identifier.urihttp://hdl.handle.net/11536/16640-
dc.description.abstract"Circular permutation (CP) is a protein structural rearrangement phenomenon, through which nature allows structural homologs to have different locations of termini and thus varied activities, stabilities and functional properties. It can be applied in many fields of protein research and bioengineering. The limitation of applying CP lies in its technical complexity, high cost and uncertainty of the viability of the resulting protein variants. Not every position in a protein can be used to create a viable circular permutant, but there is still a lack of practical computational tools for evaluating the positional feasibility of CP before costly experiments are carried out. We have previously designed a comprehensive method for predicting viable CP cleavage sites in proteins. In this work, we implement that method into an efficient and user-friendly web server named CPred (CP site predictor), which is supposed to be helpful to promote fundamental researches and biotechnological applications of CP. The CPred is accessible at http://sarst.life.nthu.edu.tw/CPred."en_US
dc.language.isoen_USen_US
dc.titleCPred: a web server for predicting viable circular permutations in proteinsen_US
dc.typeArticleen_US
dc.identifier.journalNUCLEIC ACIDS RESEARCHen_US
dc.citation.volume40en_US
dc.citation.issueW1en_US
dc.citation.epageW232en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000306670900038-
dc.citation.woscount4-
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