{"id":68,"date":"2013-07-09T14:19:55","date_gmt":"2013-07-09T05:19:55","guid":{"rendered":"http:\/\/120.29.164.89\/?page_id=68"},"modified":"2015-11-05T17:42:55","modified_gmt":"2015-11-05T08:42:55","slug":"modified_peptides","status":"publish","type":"page","link":"https:\/\/www.peptide.co.jp\/en\/custom\/peptide_synthesis\/modified_peptides","title":{"rendered":"Modified Peptides"},"content":{"rendered":"<table>\n<tbody>\n<tr class=\"odd\">\n<th>-NH<sub>2<\/sub><\/th>\n<td>\n<ul>\n<li>Biotinylation, Myristoylation, Palmitoylation, Acetylation, Malonylation, Maleimide, Aoa\u2026<\/li>\n<li>Methylation[Lys(Me), Lys(Me)<sub>2<\/sub>, Lys(Me)<sub>3<\/sub>, Arg(Me), Arg(Me)<sub>2<\/sub> ] \u2026<\/li>\n<\/ul>\n<\/td>\n<\/tr>\n<tr>\n<th>-COOH<\/th>\n<td>\n<ul>\n<li>Amidation (Amide, Methyl amide, Ethyl amide, <em>-p<\/em>NA, -MCA\u2026)<\/li>\n<li>Esterification (Methly ester, Ethyl ester, Thioester\u2026)<\/li>\n<li>Aldehyde, FMK, CMK, Alcohol\u2026<\/li>\n<\/ul>\n<\/td>\n<\/tr>\n<tr class=\"odd\">\n<th>-SH<\/th>\n<td>\n<ul>\n<li>Farnesylation, Geranylation, Methylation, Palmitoylation \u2026<\/li>\n<li>Sulfinic acid [Cys(O<sub>2<\/sub>H)], Sulfonic acid [Cys(O<sub>3<\/sub>H)]\u2026<\/li>\n<\/ul>\n<\/td>\n<\/tr>\n<tr>\n<th>-OH<\/th>\n<td>\n<ul>\n<li>Phosphorylation (Ser, Thr, Tyr), Sulfation [Tyr(SO<sub>3<\/sub>H)]\u2026<\/li>\n<li>Octanoylation, Palmitoylation, Palmitoleoylation, Acetylation\u2026<\/li>\n<\/ul>\n<\/td>\n<\/tr>\n<tr class=\"odd\">\n<th>Fluorescence labeling<\/th>\n<td>\n<ul>\n<li>FITC, FAM, Rhodamine, BODIPY, DY-series, NBD, MCA \u2026<\/li>\n<\/ul>\n<\/td>\n<\/tr>\n<tr>\n<th>Pegylation<\/th>\n<td>\n<ul>\n<li>MW from150\uff5e40000<\/li>\n<\/ul>\n<\/td>\n<\/tr>\n<tr class=\"odd\">\n<th>Photoaffinity labeling<\/th>\n<td>\n<ul>\n<li>N<sub>3<\/sub>-, Benzophenone, Diazirine\u2026<\/li>\n<\/ul>\n<\/td>\n<\/tr>\n<tr>\n<th>Cell penetrating peptides<\/th>\n<td>\n<ul>\n<li>Tat, Oligoarginine, Penetratin\u2026<\/li>\n<\/ul>\n<\/td>\n<\/tr>\n<tr class=\"odd\">\n<th>Click Peptides<\/th>\n<td>\n<ul>\n<li>N<sub>3<\/sub>-, alkyne\u2026<\/li>\n<\/ul>\n<\/td>\n<\/tr>\n<th>Others<\/th>\n<td>\n<ul>\n<li>Peptides containing unnatural amino acids, D-amino acids, spacers<\/li>\n<li>Nonhydrolyzable phosphonopeptide (Ser, Thr, Tyr, His, Asp) mimics<\/li>\n<li>Protease resistant peptides (Statine, -CH<sub>2<\/sub>-NH-\u2026)<\/li>\n<\/ul>\n<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<div class=\"floatbox_wrapper\">\n<div class=\"floatbox span1-2\">\n<h4>Histidine phosphorylation mimetic<\/h4>\n<p class=\"aligncenter\"><img class=\"alignnone\" alt=\"Histidine phosphorylation mimetic\" src=\"https:\/\/www.peptide.co.jp\/en\/wp-content\/uploads\/2013\/08\/202-1_e.gif\" \/><\/p>\n<p class=\"ref\">J. M. Kee, et al., J.Am.Chem.Soc., <b>132<\/b>, 14327. (2010)<\/p>\n<\/div>\n<div class=\"floatbox span1-2\">\n<h4>Sulfinic acid<\/h4>\n<p class=\"aligncenter\"><img loading=\"lazy\" class=\"alignnone\" alt=\"Sulfinic acid\" src=\"https:\/\/www.peptide.co.jp\/en\/wp-content\/uploads\/2013\/08\/202-2.gif\" width=\"113\" height=\"119\" \/><\/p>\n<\/div>\n<p><!-- \/.floatbox_wrapper --><\/p>\n<\/div>\n<ul class=\"liststyle_inline clear\">\n<li><a href=\"labeled-peptides\">Stable isotope<br \/>\nlabeled peptides<\/a><\/li>\n<li><a href=\"glycopeptides\">Glycopeptides<\/a><\/li>\n<li><a href=\"inhibitors\">Fluorescence-quenching<br \/>\nsubstrates<\/a><\/li>\n<li><a href=\"disulfide_bond\">Disulfide bond<br \/>\nformation<\/a><\/li>\n<li><a href=\"cyclic_branched-peptides\">Cyclic peptides<\/a><\/li>\n<\/ul>\n","protected":false},"excerpt":{"rendered":"<p>-NH2 Biotinylation, Myristoylation, Palmitoylation, Acetylation, Malonylation, Maleimide, Aoa\u2026 Methylation[Lys [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":999,"parent":65,"menu_order":3402,"comment_status":"open","ping_status":"closed","template":"page-custom.php","meta":[],"acf":[],"_links":{"self":[{"href":"https:\/\/www.peptide.co.jp\/en\/wp-json\/wp\/v2\/pages\/68"}],"collection":[{"href":"https:\/\/www.peptide.co.jp\/en\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.peptide.co.jp\/en\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.peptide.co.jp\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.peptide.co.jp\/en\/wp-json\/wp\/v2\/comments?post=68"}],"version-history":[{"count":3,"href":"https:\/\/www.peptide.co.jp\/en\/wp-json\/wp\/v2\/pages\/68\/revisions"}],"predecessor-version":[{"id":3438,"href":"https:\/\/www.peptide.co.jp\/en\/wp-json\/wp\/v2\/pages\/68\/revisions\/3438"}],"up":[{"embeddable":true,"href":"https:\/\/www.peptide.co.jp\/en\/wp-json\/wp\/v2\/pages\/65"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.peptide.co.jp\/en\/wp-json\/wp\/v2\/media\/999"}],"wp:attachment":[{"href":"https:\/\/www.peptide.co.jp\/en\/wp-json\/wp\/v2\/media?parent=68"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}