{"id":16,"date":"2012-10-12T12:35:52","date_gmt":"2012-10-12T10:35:52","guid":{"rendered":"https:\/\/protsci-us2b.univ-nantes.fr\/FP2B\/?page_id=16"},"modified":"2023-03-28T16:53:44","modified_gmt":"2023-03-28T14:53:44","slug":"help","status":"publish","type":"page","link":"https:\/\/protsci-us2b.univ-nantes.fr\/forsa\/?page_id=16","title":{"rendered":"HELP"},"content":{"rendered":"<table class=\"table1\" style=\"width: 100%;\">\n<tbody>\n<tr>\n<td class=\"column1\" style=\"text-align: center;\"><a href=\".\/?page_id=170\"><span style=\"text-decoration: underline;\">FoRSA help<\/span><\/a><\/td>\n<td class=\"column1\" style=\"text-align: center;\"><a href=\".\/?page_id=172\"><span style=\"text-decoration: underline;\">Fold_comPB help<\/span><\/a><\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>PBs are a set of 16 pentapeptide structural motifs (<a href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/11025540\" target=\"_blank\" rel=\"noopener\">de Brevern et al, Proteins 41:271-287, 2000<\/a>). They are abstraction of the unique local backbone structures present in proteins and upon which the backbone model of the proteins can be built. Each of the 16 protein blocks is defined by a vector of 8 dihedral angles associated with five consecutive residues and represented by an alphabet character from <em>a<\/em> to <em>p<\/em> (see picture below).<\/p>\n<p><a href=\"https:\/\/i0.wp.com\/protsci-us2b.univ-nantes.fr\/forsa\/wp-content\/uploads\/2012\/04\/PBs.png?ssl=1\"><img data-recalc-dims=\"1\" loading=\"lazy\" decoding=\"async\" src=\"https:\/\/i0.wp.com\/protsci-us2b.univ-nantes.fr\/forsa\/wp-content\/uploads\/2012\/04\/PBs.png?resize=300%2C225&#038;ssl=1\" alt=\"\" title=\"PBs\" class=\"aligncenter size-medium wp-image-331\" width=\"300\" height=\"225\"><\/a><\/p>\n<p>This ability to abstract protein 3D structures into 1D sequences of PBs (<a href=\"..\/pbe\/?page_id=10\">PBE-T<\/a>) lead to the development of new approaches for protein structure analysis (<a href=\"http:\/\/www.ingentaconnect.com\/content\/ben\/cbio\/2007\/00000002\/00000003\/art00002\" target=\"_blank\" rel=\"noopener\">Offmann et al, Current Bioinformatics,  2:165-202, 2007<\/a> ;  <a href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/21731588\" target=\"_blank\" rel=\"noopener\">Joseph A.P. et al, Biophys. Rev., 2:137-145, 2010<\/a>).<br \/>\n<img data-recalc-dims=\"1\" loading=\"lazy\" decoding=\"async\" alt=\"\" src=\"https:\/\/i0.wp.com\/protsci-us2b.univ-nantes.fr\/forsa\/wp-content\/uploads\/pbe-t.jpg?resize=973%2C381&#038;ssl=1\" class=\"aligncenter\" width=\"973\" height=\"381\"><br \/>\nIn the same line, web services were proposed by us earlier: <a href=\"..\/pbe\/\" target=\"_blank\" rel=\"noopener\">PBE <\/a>(<a href=\"http:\/\/nar.oxfordjournals.org\/cgi\/content\/full\/34\/suppl_2\/W119\" target=\"_blank\" rel=\"noopener\">Tyagi et al, Nucl. Acids. Res., 34:W119-123, 2006<\/a>) available at <a href=\"..\/pbe\/\">PBE<\/a> and more recently, <a href=\"http:\/\/www.dsimb.inserm.fr\/dsimb_tools\/ipba\/\" target=\"_blank\" rel=\"noopener\">iPBa <\/a>(\u201ciPBA: a tool for protein structure comparison using sequence alignment strategies\u201d, Gelly J-C et al, Nucl. Acids. Res., in press, 2011) available at <a href=\"http:\/\/www.dsimb.inserm.fr\/dsimb_tools\/ipba\/\" target=\"_blank\" rel=\"noopener\">http:\/\/www.dsimb.inserm.fr\/dsimb_tools\/ipba\/<\/a>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>FoRSA help Fold_comPB help PBs are a set of 16 pentapeptide structural motifs (de Brevern et al, Proteins 41:271-287, 2000). They are abstraction of the unique local backbone structures present in proteins and upon which the backbone model of the proteins can be built. Each of the 16 protein blocks is defined by a vector [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"parent":0,"menu_order":4,"comment_status":"closed","ping_status":"closed","template":"full-width-page.php","meta":{"footnotes":""},"class_list":["post-16","page","type-page","status-publish","hentry"],"blocksy_meta":[],"jetpack_sharing_enabled":true,"_links":{"self":[{"href":"https:\/\/protsci-us2b.univ-nantes.fr\/forsa\/index.php?rest_route=\/wp\/v2\/pages\/16","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/protsci-us2b.univ-nantes.fr\/forsa\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/protsci-us2b.univ-nantes.fr\/forsa\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/protsci-us2b.univ-nantes.fr\/forsa\/index.php?rest_route=\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/protsci-us2b.univ-nantes.fr\/forsa\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=16"}],"version-history":[{"count":11,"href":"https:\/\/protsci-us2b.univ-nantes.fr\/forsa\/index.php?rest_route=\/wp\/v2\/pages\/16\/revisions"}],"predecessor-version":[{"id":269,"href":"https:\/\/protsci-us2b.univ-nantes.fr\/forsa\/index.php?rest_route=\/wp\/v2\/pages\/16\/revisions\/269"}],"wp:attachment":[{"href":"https:\/\/protsci-us2b.univ-nantes.fr\/forsa\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=16"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}