{"id":916,"date":"2013-07-17T16:26:52","date_gmt":"2013-07-17T15:26:52","guid":{"rendered":"http:\/\/www.blopig.com\/blog\/?p=916"},"modified":"2013-07-17T16:28:50","modified_gmt":"2013-07-17T15:28:50","slug":"sabdab-thestructural-antibody-database","status":"publish","type":"post","link":"https:\/\/www.blopig.com\/blog\/2013\/07\/sabdab-thestructural-antibody-database\/","title":{"rendered":"[Database] SAbDab &#8211; the Structural Antibody Database"},"content":{"rendered":"<p><span style=\"line-height: 1.714285714;font-size: 1rem\">An increasing proportion of our research at OPIG is about the structure and function of <a title=\"Antibody Wikipedia\" href=\"http:\/\/en.wikipedia.org\/wiki\/Antibody\" target=\"_blank\">antibodies<\/a>.\u00a0<\/span>Compared to other types of proteins, there is a large number of antibody structures publicly available in the <a title=\"Protein Data Bank\" href=\"http:\/\/www.rcsb.org\/\" target=\"_blank\">PDB<\/a> (approximately 1.8% of structures contain an antibody chain).\u00a0For those of us working in the fields of antibody structure prediction, antibody-antigen docking and <a title=\"Nice review paper\" href=\"http:\/\/peds.oxfordjournals.org\/content\/early\/2012\/06\/02\/protein.gzs024\" target=\"_blank\">structure-based methods for therapeutic antibody design<\/a>, this is great news!<\/p>\n<p>However, we find that these data are not in a standard format with respect to antibody nomenclature. For instance, which chains are &#8220;<a title=\"The antibody heavy chain\" href=\"http:\/\/en.wikipedia.org\/wiki\/Heavy_chain\" target=\"_blank\">heavy<\/a>&#8221; chains and which are &#8220;<a title=\"The antibody light chain\" href=\"http:\/\/en.wikipedia.org\/wiki\/Immunoglobulin_light_chain\" target=\"_blank\">light<\/a>&#8220;? Which heavy and light chains pair? Is there an <a title=\"Antigens\" href=\"http:\/\/en.wikipedia.org\/wiki\/Antigen\" target=\"_blank\">antigen<\/a> present? If so, to which H-L pair does it bind to? Which <a title=\"Chothia numbering scheme\" href=\"http:\/\/www.bioinf.org.uk\/abs\/index.html#chothianum\" target=\"_blank\">numbering system<\/a> is used &#8230; etc.<\/p>\n<p>To address this problem, <a title=\"James\" href=\"http:\/\/www.stats.ox.ac.uk\/~dunbar\/\" target=\"_blank\">w<\/a><a title=\"Konrad\" href=\"http:\/\/www.stats.ox.ac.uk\/~krawczyk\/\" target=\"_blank\">e<\/a> have developed <a title=\"SAbDab\" href=\"http:\/\/opig.stats.ox.ac.uk\/webapps\/sabdab\" target=\"_blank\">SAbDab<\/a>: the Structural Antibody Database.\u00a0Its primary aim is for easy creation of antibody structure and antibody-antigen complex datasets for further analysis by researchers such as ourselves.\u00a0These sets can be selected using a number of criteria (e.g. experimental method, species, presence of constant domains&#8230;) and redundancy filters can be applied over the sequences of both the antibody and antigen. Thanks to <a title=\"Jin\" href=\"http:\/\/www.dtc.ox.ac.uk\/people\/12\/leem\/\" target=\"_blank\">Jin<\/a>, SAbDab now also includes associated curated affinity (Kd) values for around 190 antibody-antigen complexes. We hope this will serve as a benchmarking tool for antibody-antigen docking prediction algorithms.<\/p>\n<p><a href=\"https:\/\/i0.wp.com\/www.blopig.com\/blog\/wp-content\/uploads\/2013\/07\/sabdab.png?ssl=1\"><img data-recalc-dims=\"1\" decoding=\"async\" loading=\"lazy\" class=\"size-medium wp-image-958 aligncenter\" alt=\"sabdab\" src=\"https:\/\/i0.wp.com\/www.blopig.com\/blog\/wp-content\/uploads\/2013\/07\/sabdab.png?resize=290%2C300&#038;ssl=1\" width=\"290\" height=\"300\" srcset=\"https:\/\/i0.wp.com\/www.blopig.com\/blog\/wp-content\/uploads\/2013\/07\/sabdab.png?resize=290%2C300&amp;ssl=1 290w, https:\/\/i0.wp.com\/www.blopig.com\/blog\/wp-content\/uploads\/2013\/07\/sabdab.png?resize=624%2C645&amp;ssl=1 624w, https:\/\/i0.wp.com\/www.blopig.com\/blog\/wp-content\/uploads\/2013\/07\/sabdab.png?w=882&amp;ssl=1 882w\" sizes=\"auto, (max-width: 290px) 100vw, 290px\" \/><\/a><\/p>\n<p>Alternatively, the database can be used to inspect and compare properties of individual structures.\u00a0For instance, we have recently published a method to <a title=\"ABangle Paper\" href=\"http:\/\/peds.oxfordjournals.org\/content\/early\/2013\/05\/23\/protein.gzt020.short?rss=1\" target=\"_blank\">characterise the orientation between the two antibody variable domains<\/a>, VH and VL. Using the <a title=\"ABangle tool\" href=\"http:\/\/opig.stats.ox.ac.uk\/webapps\/abdb\/web_front\/ABangle.php\" target=\"_blank\">ABangle<\/a> tool, users can select structures with a particular VH-VL orientation, visualise and quantify conformational changes (e.g. between bound and unbound forms) and inspect the pose of structures with certain amino acids at specific positions. Similarly, the CDR (complimentary determining region) <a title=\"CDR Search\" href=\"http:\/\/opig.stats.ox.ac.uk\/webapps\/abdb\/web_front\/CDRTools.php\" target=\"_blank\">search<\/a> and <a title=\"Clustering\" href=\"http:\/\/opig.stats.ox.ac.uk\/webapps\/abdb\/web_front\/CDRClustering.php\" target=\"_blank\">clustering<\/a> tools, allow for the antibody hyper-variable loops to be selected by length, type and canonical class and their structures visualised or downloaded.<\/p>\n<p><a href=\"https:\/\/i0.wp.com\/www.blopig.com\/blog\/wp-content\/uploads\/2013\/07\/structure_viewer.png?ssl=1\"><img data-recalc-dims=\"1\" decoding=\"async\" loading=\"lazy\" class=\"size-medium wp-image-959 aligncenter\" alt=\"structure_viewer\" src=\"https:\/\/i0.wp.com\/www.blopig.com\/blog\/wp-content\/uploads\/2013\/07\/structure_viewer.png?resize=228%2C300&#038;ssl=1\" width=\"228\" height=\"300\" srcset=\"https:\/\/i0.wp.com\/www.blopig.com\/blog\/wp-content\/uploads\/2013\/07\/structure_viewer.png?resize=228%2C300&amp;ssl=1 228w, https:\/\/i0.wp.com\/www.blopig.com\/blog\/wp-content\/uploads\/2013\/07\/structure_viewer.png?resize=624%2C820&amp;ssl=1 624w, https:\/\/i0.wp.com\/www.blopig.com\/blog\/wp-content\/uploads\/2013\/07\/structure_viewer.png?w=669&amp;ssl=1 669w\" sizes=\"auto, (max-width: 228px) 100vw, 228px\" \/><\/a><\/p>\n<p>&nbsp;<\/p>\n<p>SAbDab also contains features such as the <a title=\"Template Search\" href=\"http:\/\/opig.stats.ox.ac.uk\/webapps\/abdb\/web_front\/SeqAlignment.php\" target=\"_blank\">template search<\/a>. This allows a user to submit the sequence of either an antibody heavy or light chain (or both) and to find structures in the database that may offer good templates to use in a homology modelling protocol.\u00a0Specific regions of the antibody can be isolated so that structures with a high sequence identity over, for example, the CDR H3 loop can be found.\u00a0SAbDab&#8217;s weekly automatic updates ensures that it contains the latest available data.\u00a0Using each method of selection, the structure, a standardised and re-numbered version of the structure, and a summary file containing information about the antibody, can be downloaded both individually or <em>en-masse<\/em> as a dataset. SAbDab will continue to develop with new <a title=\"Antibody tools\" href=\"http:\/\/opig.stats.ox.ac.uk\/webapps\/abdb\/web_front\/Tools.php\" target=\"_blank\">tools<\/a> and features and is freely available at: <a title=\"SAbDab\" href=\"http:\/\/opig.stats.ox.ac.uk\/webapps\/sabdab\" target=\"_blank\">opig.stats.ox.ac.uk\/webapps\/sabdab<\/a>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>An increasing proportion of our research at OPIG is about the structure and function of antibodies.\u00a0Compared to other types of proteins, there is a large number of antibody structures publicly available in the PDB (approximately 1.8% of structures contain an antibody chain).\u00a0For those of us working in the fields of antibody structure prediction, antibody-antigen docking [&hellip;]<\/p>\n","protected":false},"author":10,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"nf_dc_page":"","wikipediapreview_detectlinks":true,"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"ngg_post_thumbnail":0,"_jetpack_memberships_contains_paid_content":false,"footnotes":""},"categories":[29,10,30,48],"tags":[],"ppma_author":[489],"class_list":["post-916","post","type-post","status-publish","format-standard","hentry","category-code","category-groupmeetings","category-links","category-publication"],"jetpack_featured_media_url":"","jetpack_sharing_enabled":true,"authors":[{"term_id":489,"user_id":10,"is_guest":0,"slug":"james","display_name":"James Dunbar","avatar_url":"https:\/\/secure.gravatar.com\/avatar\/7dbfd5f8cfa0385032a6b9d425335f52669ae5d89e784a5e65c14ecfe7dbea14?s=96&d=mm&r=g","0":null,"1":"","2":"","3":"","4":"","5":"","6":"","7":"","8":""}],"_links":{"self":[{"href":"https:\/\/www.blopig.com\/blog\/wp-json\/wp\/v2\/posts\/916","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.blopig.com\/blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.blopig.com\/blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.blopig.com\/blog\/wp-json\/wp\/v2\/users\/10"}],"replies":[{"embeddable":true,"href":"https:\/\/www.blopig.com\/blog\/wp-json\/wp\/v2\/comments?post=916"}],"version-history":[{"count":7,"href":"https:\/\/www.blopig.com\/blog\/wp-json\/wp\/v2\/posts\/916\/revisions"}],"predecessor-version":[{"id":965,"href":"https:\/\/www.blopig.com\/blog\/wp-json\/wp\/v2\/posts\/916\/revisions\/965"}],"wp:attachment":[{"href":"https:\/\/www.blopig.com\/blog\/wp-json\/wp\/v2\/media?parent=916"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.blopig.com\/blog\/wp-json\/wp\/v2\/categories?post=916"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.blopig.com\/blog\/wp-json\/wp\/v2\/tags?post=916"},{"taxonomy":"author","embeddable":true,"href":"https:\/\/www.blopig.com\/blog\/wp-json\/wp\/v2\/ppma_author?post=916"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}