Found 475 chains in Knotted chains table. Displaying 1 - 150. Applied filters: Probabilistic

Search results query: topological notation: K +31

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#pdbid|chain|deposition date|is S/K-not|(slip)knot types;
      
  6eda|A|2018-12-02|K|+3.1;
  6eea|A|2018-12-02|K|+3.1;
  3iqk|A|2018-10-21|K|+3.1;
  5fl5|A|2018-10-21|K|+3.1;
  1cak|A|2018-10-21|K|+3.1;
  4qk1|A|2018-10-20|K|+3.1;
  5flo|A|2018-10-20|K|+3.1;
  5th4|A|2018-10-20|K|+3.1;
  5cjf|A|2018-10-20|K|+3.1;
  1z97|A|2018-10-20|K|+3.1;
  5sz5|A|2018-10-20|K|+3.1;
  1fsq|A|2018-10-20|K|+3.1;
  3ryj|B|2018-10-20|K|+3.1;
  1ze8|A|2018-10-20|K|+3.1;
  4ygn|A|2018-10-20|K|+3.1;
  5lmd|A|2018-10-20|K|+3.1;
  5jgs|B|2018-10-20|K|+3.1;
  4mlt|A|2018-10-20|K|+3.1;
  5eij|A|2018-10-20|K|+3.1;
  4r59|A|2018-10-20|K|+3.1;
  4mdg|A|2018-10-20|K|+3.1;
  3mnu|A|2018-10-20|K|+3.1;
  2nno|A|2018-10-20|K|+3.1;
  1cao|A|2018-10-20|K|+3.1;
  3v2j|A|2018-10-20|K|+3.1;
  3kon|A|2018-10-20|K|+3.1;
  4m2r|A|2018-10-20|K|+3.1;
  2nwo|A|2018-10-20|K|+3.1;
  5msa|A|2018-10-20|K|+3.1;
  5flp|A|2018-10-20|K|+3.1;
  5flr|A|2018-10-20|K|+3.1;
  4xz5|A|2018-10-20|K|+3.1;
  3ml5|A|2018-10-20|K|+3.1;
  4qsb|A|2018-10-20|K|+3.1;
  5ty1|A|2018-10-20|K|+3.1;
  1cnj|A|2018-10-20|K|+3.1;
  3mhc|A|2018-10-20|K|+3.1;
  5fls|A|2018-10-20|K|+3.1;
  5umc|A|2018-10-20|K|+3.1;
  5tt3|A|2018-10-20|K|+3.1;
  5g01|A|2018-10-20|K|+3.1;
  4ywp|A|2018-10-20|K|+3.1;
  4mdl|A|2018-10-20|K|+3.1;
  4fpt|A|2018-10-20|K|+3.1;
  3s72|B|2018-10-20|K|+3.1;
  3daz|A|2018-10-20|K|+3.1;
  2vvb|X|2018-10-20|K|+3.1;
  4z1e|A|2018-10-20|K|+3.1;
  3kkx|A|2018-10-20|K|+3.1;
  4kp5|A|2018-10-20|K|+3.1;
  4l5v|A|2018-10-20|K|+3.1;
  3u3a|X|2018-10-20|K|+3.1;
  3hkn|A|2018-10-20|K|+3.1;
  5tfx|A|2018-10-20|K|+3.1;
  2fnn|A|2018-10-20|K|+3.1;
  5jdf|A|2018-10-20|K|+3.1;
  1ugd|A|2018-10-20|K|+3.1;
  3p3j|A|2018-10-20|K|+3.1;
  5jes|B|2018-10-20|K|+3.1;
  3gz0|A|2018-10-20|K|+3.1;
  4kp8|A|2018-10-19|K|+3.1;
  4z1k|A|2018-10-19|K|+3.1;
  2pou|A|2018-10-19|K|+3.1;
  6b00|A|2018-10-19|K|+3.1;
  5u0e|A|2018-10-19|K|+3.1;
  5g0b|A|2018-10-19|K|+3.1;
  5ll9|A|2018-10-19|K|+3.1;
  4m2u|A|2018-10-19|K|+3.1;
  4r5a|A|2018-10-19|K|+3.1;
  2fnk|A|2018-10-19|K|+3.1;
  5fnm|A|2018-10-19|K|+3.1;
  4iwz|A|2018-10-19|K|+3.1;
  4ht2|A|2018-10-19|K|+3.1;
  3s74|B|2018-10-19|K|+3.1;
  3v7x|A|2018-10-19|K|+3.1;
  3dv7|A|2018-10-19|K|+3.1;
  4qjm|A|2018-10-19|K|+3.1;
  6bbs|A|2018-10-19|K|+3.1;
  4mdm|A|2018-10-19|K|+3.1;
  3n0n|A|2018-10-19|K|+3.1;
  4q8z|A|2018-10-19|K|+3.1;
  4fl7|A|2018-10-19|K|+3.1;
  5fdc|A|2018-10-19|K|+3.1;
  5vgy|A|2018-10-19|K|+3.1;
  2wd3|A|2018-10-19|K|+3.1;
  4e5q|A|2018-10-19|K|+3.1;
  4wl4|A|2018-10-19|K|+3.1;
  5u0f|A|2018-10-19|K|+3.1;
  4kuy|A|2018-10-19|K|+3.1;
  3v2m|A|2018-10-19|K|+3.1;
  1g0f|A|2018-10-19|K|+3.1;
  5tya|A|2018-10-19|K|+3.1;
  4pyx|A|2018-10-19|K|+3.1;
  6fe1|A|2018-10-19|K|+3.1;
  3ryx|B|2018-10-19|K|+3.1;
  1raz|A|2018-10-19|K|+3.1;
  4e4a|A|2018-10-19|K|+3.1;
  2fnm|A|2018-10-19|K|+3.1;
  3r16|A|2018-10-19|K|+3.1;
  5wlr|A|2018-10-19|K|+3.1;
  6d1l|A|2018-10-19|K|+3.1;
  3vbd|A|2018-10-19|K|+3.1;
  5jeh|B|2018-10-19|K|+3.1;
  4q90|A|2018-10-19|K|+3.1;
  2nns|A|2018-10-19|K|+3.1;
  3myq|A|2018-10-19|K|+3.1;
  3m1q|A|2018-10-19|K|+3.1;
  5tuo|A|2018-10-19|K|+3.1;
  2eu2|A|2018-10-19|K|+3.1;
  4e3f|A|2018-10-19|K|+3.1;
  3p55|A|2018-10-18|K|+3.1;
  2nwz|A|2018-10-18|K|+3.1;
  3uyn|A|2018-10-18|K|+3.1;
  5t71|A|2018-10-18|K|+3.1;
  2hfx|A|2018-10-18|K|+3.1;
  3ml2|A|2018-10-18|K|+3.1;
  4k1q|A|2018-10-18|K|+3.1;
  5ty8|A|2018-10-18|K|+3.1;
  5g0c|A|2018-10-18|K|+3.1;
  1fsr|A|2018-10-18|K|+3.1;
  6g98|A|2018-10-18|K|+3.1;
  5dvx|A|2018-10-18|K|+3.1;
  5amd|A|2018-10-18|K|+3.1;
  4qef|A|2018-10-18|K|+3.1;
  4hew|A|2018-10-18|K|+3.1;
  3oku|A|2018-10-18|K|+3.1;
  1z93|A|2018-10-18|K|+3.1;
  5brw|A|2018-10-18|K|+3.1;
  5wex|A|2018-10-18|K|+3.1;
  4q06|A|2018-10-18|K|+3.1;
  3p5a|A|2018-10-18|K|+3.1;
  5je7|B|2018-10-18|K|+3.1;
  5ekm|A|2018-10-18|K|+3.1;
  4z1j|A|2018-10-18|K|+3.1;
  2wej|A|2018-10-18|K|+3.1;
  3oys|A|2018-10-18|K|+3.1;
  4itp|A|2018-10-18|K|+3.1;
  3k34|A|2018-10-18|K|+3.1;
  3dvb|A|2018-10-18|K|+3.1;
  2pow|A|2018-10-18|K|+3.1;
  4e3g|A|2018-10-18|K|+3.1;
  2x7t|A|2018-10-18|K|+3.1;
  2ili|A|2018-10-18|K|+3.1;
  4fik|A|2018-10-18|K|+3.1;
  4knn|A|2018-10-17|K|+3.1;
  3sax|A|2018-10-17|K|+3.1;
  4qsa|A|2018-10-17|K|+3.1;
  3s8x|A|2018-10-17|K|+3.1;
  6got|A|2018-10-13|K|+3.1;
  3s73|B|2018-10-04|K|+3.1;
  2cbc|A|2018-10-03|K|+3.1;
  4lu3|A|2018-10-03|K|+3.1;
  1thk|A|2018-10-03|K|+3.1;
  5yuj|A|2018-10-03|K|+3.1;
  2osf|A|2018-10-03|K|+3.1;
  4kap|A|2018-10-03|K|+3.1;
  1g0e|A|2018-10-03|K|+3.1;
  2ez7|A|2018-10-03|K|+3.1;
  1if9|A|2018-10-03|K|+3.1;
  1if7|A|2018-10-03|K|+3.1;
  3rz0|B|2018-10-02|K|+3.1;
  3t85|A|2018-10-02|K|+3.1;
  3czv|A|2018-10-01|K|+3.1;
  3okv|A|2018-10-01|K|+3.1;
  3sbi|A|2018-10-01|K|+3.1;
  3bl0|A|2018-10-01|K|+3.1;
  2fos|A|2018-09-29|K|+3.1;
  1fqm|A|2018-09-29|K|+3.1;
  1xev|A|2018-09-28|K|+3.1;
  2nxt|A|2018-09-28|K|+3.1;
  5gmn|A|2018-09-26|K|+3.1;
  2ax2|A|2018-09-26|K|+3.1;
  5l70|A|2018-09-26|K|+3.1;
  4cnd|B|2018-09-16|K|+3.1;
  5vm8|A|2018-09-13|K|+3.1;
  5dsq|A|2018-09-12|K|+3.1;
  5dso|A|2018-09-12|K|+3.1;
  1hva|A|2018-09-12|K|+3.1;
  1fsn|A|2018-09-12|K|+3.1;
  2w2j|A|2018-09-12|K|+3.1;
  3bet|A|2018-09-12|K|+3.1;
  2cbe|A|2018-09-12|K|+3.1;
  3caj|A|2018-09-12|K|+3.1;
  3ibu|A|2018-09-12|K|+3.1;
  3ibn|A|2018-09-12|K|+3.1;
  3ibl|A|2018-09-12|K|+3.1;
  3rz5|A|2018-09-12|K|+3.1;
  3rz7|A|2018-09-12|K|+3.1;
  3s76|A|2018-09-12|K|+3.1;
  5a19|A|2018-09-12|K|+3.1;
  1cng|A|2018-09-12|K|+3.1;
  3mhl|A|2018-09-12|K|+3.1;
  3m5e|A|2018-09-12|K|+3.1;
  3m40|A|2018-09-12|K|+3.1;
  3m3x|A|2018-09-12|K|+3.1;
  3m67|A|2018-09-12|K|+3.1;
  3m98|A|2018-09-12|K|+3.1;
  3m2n|A|2018-09-12|K|+3.1;
  3mhm|A|2018-09-12|K|+3.1;
  1zsa|A|2018-09-12|K|+3.1;
  3m96|A|2018-09-12|K|+3.1;
  3po6|A|2018-09-12|K|+3.1;
  1cnh|A|2018-09-12|K|+3.1;
  4twm|A|2018-09-12|K|+3.1;
  4twl|A|2018-09-12|K|+3.1;
  5a1g|A|2018-09-12|K|+3.1;
  5dsr|A|2018-09-06|K|+3.1;
  1j85|A|2018-08-14|K|+3.1;
  6emu|A|2018-07-22|K|+3.1;
  5y2r|A|2018-02-14|K|+3.1;
  5y2s|A|2018-02-14|K|+3.1;
  5nxg|A|2018-01-17|K|+3.1;
  5nxi|A|2018-01-17|K|+3.1;
  5nxo|A|2018-01-17|K|+3.1;
  5nxp|A|2018-01-17|K|+3.1;
  5nxv|A|2018-01-17|K|+3.1;
  5nxw|A|2018-01-17|K|+3.1;
  5ny1|A|2018-01-17|K|+3.1;
  5ny3|A|2018-01-17|K|+3.1;
  5ny6|A|2018-01-17|K|+3.1;
  5nya|A|2018-01-17|K|+3.1;
  5msb|A|2018-01-17|K|+3.1;
  5yud|A|2018-01-03|K|+3.1;
  5m78|A|2017-12-20|K|+3.1;
  5wyr|A|2017-12-20|K|+3.1;
  5wyq|A|2017-12-20|K|+3.1;
  5o95|A|2017-11-08|K|+3.1;
  5o96|A|2017-11-08|K|+3.1;
  5oql|e|2017-10-11|K|+3.1;
  5tv3|A|2017-09-20|K|+3.1;
  5t75|A|2017-09-14|K|+3.1;
  5tt8|A|2017-09-13|K|+3.1;
  5l0z|A|2017-08-28|K|+3.1;
  5kzk|A|2017-08-28|K|+3.1;
  5ku6|A|2017-08-28|K|+3.1;
  5lle|A|2017-08-28|K|+3.1;
  5llg|A|2017-08-28|K|+3.1;
  5llo|A|2017-08-28|K|+3.1;
  5lln|A|2017-08-28|K|+3.1;
  5llp|A|2017-08-28|K|+3.1;
  5gra|A|2017-06-21|K|+3.1;
  5twj|A|2017-05-06|K|+3.1;
  5jnc|A|2017-05-04|K|+3.1;
  5thj|A|2017-05-03|K|+3.1;
  5jn8|A|2017-05-03|K|+3.1;
  5jna|A|2017-05-03|K|+3.1;
  5jn3|A|2017-05-03|K|+3.1;
  5twk|A|2017-05-03|K|+3.1;
  5wyk|E1|2017-04-07|K|+3.1;
  5ipz|A|2017-03-29|K|+3.1;
  5l6k|A|2017-03-02|K|+3.1;
  5sz7|A|2017-02-06|K|+3.1;
  5sz0|A|2017-02-05|K|+3.1;
  5sz1|A|2017-02-05|K|+3.1;
  5sz2|A|2017-02-05|K|+3.1;
  5sz3|A|2017-02-05|K|+3.1;
  5sz4|A|2017-02-05|K|+3.1;
  5h5f|A|2017-01-23|K|+3.1;
  5h5e|A|2017-01-23|K|+3.1;
  5jir|A|2016-11-27|K|+3.1;
  5gm8|A|2016-10-28|K|+3.1;
  5gmc|A|2016-10-28|K|+3.1;
  5gmb|A|2016-10-28|K|+3.1;
  5t8s|A|2016-10-03|K|+3.1;
  5t8t|A|2016-10-03|K|+3.1;
  5drs|A|2016-09-29|K|+3.1;
  5dog|A|2016-09-28|K|+3.1;
  5doh|A|2016-09-28|K|+3.1;
  5cjl|A|2016-09-28|K|+3.1;
  5e5r|A|2016-08-31|K|+3.1;
  5jpq|e|2016-07-29|K|+3.1;
  5co4|A|2016-07-20|K|+3.1;
  5g03|A|2016-05-26|K|+3.1;
  5hwy|A|2016-05-22|K|+3.1;
  5apg|A|2016-04-27|K|+3.1;
  5ap8|A|2016-04-27|K|+3.1;
  4yqt|A|2016-03-16|K|+3.1;
  4yqs|A|2016-03-16|K|+3.1;
  4yqr|A|2016-03-16|K|+3.1;
  4ypx|A|2016-03-16|K|+3.1;
  5a1i|A|2016-03-10|K|+3.1;
  4x3l|A|2016-01-22|K|+3.1;
  5fai|A|2016-01-21|K|+3.1;
  5c77|A|2016-01-14|K|+3.1;
  5c74|A|2016-01-14|K|+3.1;
  5a7y|A|2016-01-13|K|+3.1;
  5a7z|A|2016-01-13|K|+3.1;
  5a7t|A|2016-01-13|K|+3.1;
  4yvk|A|2015-12-25|K|+3.1;
  4yvj|A|2015-12-25|K|+3.1;
  4yvi|A|2015-12-25|K|+3.1;
  4yvh|A|2015-12-25|K|+3.1;
  4yvg|A|2015-12-25|K|+3.1;
  4xbo|A|2015-12-23|K|+3.1;
  4x3m|A|2015-11-11|K|+3.1;
  4yqd|A|2015-11-11|K|+3.1;
  4ws9|A|2015-02-10|K|+3.1;
  4rg1|A|2015-02-07|K|+3.1;
  2fg7|C|2014-10-08|K|+3.1;
  3s97|A|2014-10-08|K|+3.1;
  3kld|B|2014-10-08|K|+3.1;
  4etq|C|2014-10-08|K|+3.1;
  3v5s|A|2014-09-25|K|+3.1;
  4cng|A|2014-09-25|K|+3.1;
  4cnf|A|2014-09-25|K|+3.1;
  4cne|A|2014-09-25|K|+3.1;
  4cnd|A|2014-09-25|K|+3.1;
  4j3c|A|2014-09-11|K|+3.1;
  3cwo|X|2014-08-23|K|+3.1;
  4jal|A|2014-08-19|K|+3.1;
  4mcc|A|2014-08-19|K|+3.1;
  4mcb|A|2014-08-19|K|+3.1;
  4l2z|A|2014-08-19|K|+3.1;
  4k0b|A|2014-08-19|K|+3.1;
  3axz|A|2014-08-19|K|+3.1;
  4ig6|A|2014-08-19|K|+3.1;
  4hpv|A|2014-08-19|K|+3.1;
  4h3y|A|2014-08-19|K|+3.1;
  3kzm|A|2014-08-19|K|+3.1;
  4jwg|A|2014-08-19|K|+3.1;
  3so4|A|2014-08-18|K|+3.1;
  4pzk|B|2014-08-13|K|+3.1;
  4pzk|A|2014-08-13|K|+3.1;
  4ndn|A|2014-08-13|K|+3.1;
  4ndn|B|2014-08-13|K|+3.1;
  4ndn|C|2014-08-13|K|+3.1;
  4l4q|A|2014-08-13|K|+3.1;
  4ndn|D|2014-08-13|K|+3.1;
  4ktv|D|2014-08-13|K|+3.1;
  4ktv|C|2014-08-13|K|+3.1;
  4ktv|B|2014-08-13|K|+3.1;
  4ktv|A|2014-08-13|K|+3.1;
  4ktt|D|2014-08-13|K|+3.1;
  4ktt|C|2014-08-13|K|+3.1;
  4ktt|B|2014-08-13|K|+3.1;
  4ktt|A|2014-08-13|K|+3.1;
  1uak|A|2014-07-31|K|+3.1;
  3ai9|X|2014-07-31|K|+3.1;
  3aia|A|2014-07-31|K|+3.1;
  3b1b|A|2014-07-31|K|+3.1;
  3bbd|A|2014-07-31|K|+3.1;
  3v5u|A|2014-07-31|K|+3.1;
  3bbe|A|2014-07-31|K|+3.1;
  3bbh|A|2014-07-31|K|+3.1;
  3znc|A|2014-07-31|K|+3.1;
  1to0|A|2014-07-31|K|+3.1;
  1uaj|A|2014-07-31|K|+3.1;
  1ual|A|2014-07-31|K|+3.1;
  1uam|A|2014-07-31|K|+3.1;
  4e8b|A|2014-07-31|K|+3.1;
  4fak|A|2014-07-31|K|+3.1;
  4fmw|A|2014-07-31|K|+3.1;
  4gge|A|2014-07-31|K|+3.1;
  1v2x|A|2014-07-31|K|+3.1;
  1by7|A|2014-07-31|K|+3.1;
  1v6z|A|2014-07-31|K|+3.1;
  4h3z|A|2014-07-31|K|+3.1;
  1vh0|A|2014-07-31|K|+3.1;
  4h6v|A|2014-07-31|K|+3.1;
  1vhk|A|2014-07-31|K|+3.1;
  3dcm|X|2014-07-31|K|+3.1;
  1vhy|A|2014-07-31|K|+3.1;
  4jak|A|2014-07-31|K|+3.1;
  1x7o|A|2014-07-31|K|+3.1;
  1x7p|A|2014-07-31|K|+3.1;
  4jwf|A|2014-07-31|K|+3.1;
  4jwh|A|2014-07-31|K|+3.1;
  4jwj|A|2014-07-31|K|+3.1;
  4k1c|A|2014-07-31|K|+3.1;
  3e5y|A|2014-07-31|K|+3.1;
  4kdz|A|2014-07-31|K|+3.1;
  1xra|A|2014-07-31|K|+3.1;
  4kgn|A|2014-07-31|K|+3.1;
  1xrb|A|2014-07-31|K|+3.1;
  1xrc|A|2014-07-31|K|+3.1;
  3ed7|A|2014-07-31|K|+3.1;
  4kjr|A|2014-07-31|K|+3.1;
  1y7w|A|2014-07-31|K|+3.1;
  4kpp|A|2014-07-31|K|+3.1;
  4l69|A|2014-07-31|K|+3.1;
  4l7i|A|2014-07-31|K|+3.1;
  4le5|A|2014-07-31|K|+3.1;
  1yh1|A|2014-07-31|K|+3.1;
  3f7b|A|2014-07-31|K|+3.1;
  3fw3|A|2014-07-31|K|+3.1;
  4mcd|A|2014-07-31|K|+3.1;
  1zjr|A|2014-07-31|K|+3.1;
  1znc|A|2014-07-31|K|+3.1;
  4o6d|A|2014-07-31|K|+3.1;
  3gyq|A|2014-07-31|K|+3.1;
  4o6d|B|2014-07-31|K|+3.1;
  4odj|A|2014-07-31|K|+3.1;
  1eku|A|2014-07-31|K|+3.1;
  3ic6|A|2014-07-31|K|+3.1;
  3ief|A|2014-07-31|K|+3.1;
  1f48|A|2014-07-31|K|+3.1;
  2cx8|A|2014-07-31|K|+3.1;
  3ilk|A|2014-07-31|K|+3.1;
  3iml|A|2014-07-31|K|+3.1;
  2egv|A|2014-07-31|K|+3.1;
  2egw|A|2014-07-31|K|+3.1;
  3jxf|A|2014-07-31|K|+3.1;
  3jxg|A|2014-07-31|K|+3.1;
  1fug|A|2014-07-31|K|+3.1;
  3jxh|C|2014-07-31|K|+3.1;
  3jyw|E|2014-07-31|K|+3.1;
  2fg6|C|2014-07-31|K|+3.1;
  2fg7|X|2014-07-31|K|+3.1;
  3knu|A|2014-07-31|K|+3.1;
  3kty|A|2014-07-31|K|+3.1;
  2g7m|C|2014-07-31|K|+3.1;
  3kw2|A|2014-07-31|K|+3.1;
  1gz0|A|2014-07-31|K|+3.1;
  3ky7|A|2014-07-31|K|+3.1;
  3kzc|A|2014-07-31|K|+3.1;
  3kzk|A|2014-07-31|K|+3.1;
  3kzn|A|2014-07-31|K|+3.1;
  3kzo|A|2014-07-31|K|+3.1;
  3l02|A|2014-07-31|K|+3.1;
  2ha8|A|2014-07-31|K|+3.1;
  3l04|A|2014-07-31|K|+3.1;
  3l05|A|2014-07-31|K|+3.1;
  3l06|A|2014-07-31|K|+3.1;
  2hfy|A|2014-07-31|K|+3.1;
  3l8u|A|2014-07-31|K|+3.1;
  2i6d|A|2014-07-31|K|+3.1;
  3m4j|A|2014-07-31|K|+3.1;
  3m4n|A|2014-07-31|K|+3.1;
  3m5c|A|2014-07-31|K|+3.1;
  3m5d|A|2014-07-31|K|+3.1;
  1ipa|A|2014-07-31|K|+3.1;
  1js1|X|2014-07-31|K|+3.1;
  1k3r|A|2014-07-31|K|+3.1;
  2o3a|A|2014-07-31|K|+3.1;
  2obv|A|2014-07-31|K|+3.1;
  2p02|A|2014-07-31|K|+3.1;
  3n4j|A|2014-07-31|K|+3.1;
  3n4k|A|2014-07-31|K|+3.1;
  2qmm|A|2014-07-31|K|+3.1;
  3nk6|A|2014-07-31|K|+3.1;
  3nk7|A|2014-07-31|K|+3.1;
  2qwv|A|2014-07-31|K|+3.1;
  3o7b|A|2014-07-31|K|+3.1;
  3oii|A|2014-07-31|K|+3.1;
  2v3j|A|2014-07-31|K|+3.1;
  3oij|A|2014-07-31|K|+3.1;
  2v3k|A|2014-07-31|K|+3.1;
  3oin|A|2014-07-31|K|+3.1;
  1mxa|A|2014-07-31|K|+3.1;
  3onp|A|2014-07-31|K|+3.1;
  1mxb|A|2014-07-31|K|+3.1;
  1mxc|A|2014-07-31|K|+3.1;
  1mxi|A|2014-07-31|K|+3.1;
  1ns5|A|2014-07-31|K|+3.1;
  1nxz|A|2014-07-31|K|+3.1;
  1o6d|A|2014-07-31|K|+3.1;
  3q98|A|2014-07-31|K|+3.1;
  1o90|A|2014-07-31|K|+3.1;
  1o92|A|2014-07-31|K|+3.1;
  1o93|A|2014-07-31|K|+3.1;
  1o9t|A|2014-07-31|K|+3.1;
  3quv|A|2014-07-31|K|+3.1;
  3rv2|A|2014-07-31|K|+3.1;
  3s82|A|2014-07-31|K|+3.1;
  3sig|A|2014-07-31|K|+3.1;
  1p7l|A|2014-07-31|K|+3.1;
  3sij|A|2014-07-31|K|+3.1;
  1p9p|A|2014-07-31|K|+3.1;
  3tde|A|2014-07-31|K|+3.1;
  1qm4|A|2014-07-31|K|+3.1;
  1rg9|A|2014-07-31|K|+3.1;
  2yfk|A|2014-07-31|K|+3.1;
  2yy8|A|2014-07-31|K|+3.1;
  2z0y|A|2014-07-31|K|+3.1;
  2znc|A|2014-07-31|K|+3.1;

      
Knot types Knot loop types pdb Title
K +31 K 3x +31 6edaA Bioreductive 4-hydroxy-3-nitro-5-ureido-benzenesulfonamides selectively target the tumor-associated carbonic anhydrase isoforms ix and xii and show hypoxia-enhanced cytotoxicity against human cancer cell lines.
K +31 K 3x +31 6eeaA Bioreductive 4-hydroxy-3-nitro-5-ureido-benzenesulfonamides selectively target the tumor-associated carbonic anhydrase isoforms ix and xii and show hypoxia-enhanced cytotoxicity against human cancer cell lines.
K +31 K 3x +31 3iqkA Human carbonic anhydrase ii h64a complexed with thioxolone hydrolysis products
K +31 K 3x +31 5fl5A Three dimensional structure of human carbonic anhydrase ix in complex with 5-(1-(4-methoxyphenyl)-1h-1,2,3-triazol-4-yl)thiophene-2- sulfonamide
K +31 K 3x +31 1cakA Structural analysis of the zinc hydroxide-thr 199-glu 106 hydrogen bonding network in human carbonic anhydrase ii
K +31 K 3x +31 4qk1A Structural and catalytic effects of proline substitution and surface loop deletion in the extended active site of human carbonic anhydrase ii - k170p
K +31 K 3x +31 5floA Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
K +31 K 3x +31 5th4A Crystal structure of 1-hydroxypyridine-2(1h)-thione bound to human carbonic anhydrase 2 l198g
K +31 K 3x +31 5cjfA The crystal structure of the human carbonic anhydrase xiv in complex with a 1,1'-biphenyl-4-sulfonamide inhibitor.
K +31 K 3x +31 1z97A Human carbonic anhydrase iii: structural and kinetic study of catalysis and proton transfer.
K +31 K 3x +31 5sz5A Carbonic anhydrase ix-mimic in complex with 4-(2-methylphenyl)-benzenesulfonamide
K +31 K 3x +31 1fsqA X-ray crystal structure of cobalt-bound f93s/f95l/w97m carbonic anhydrase (caii) variant
K +31 K 3x +31 3ryjB Carbonic anhydrase complexed with 4-sulfamoyl-n-(2,2,2-trifluoroethyl)benzamide
K +31 K 7x +31 1ze8A Carbonic anhydrase ii in complex with a membrane-impermeant sulfonamide inhibitor
K +31 K 3x +31 4ygnA Nai--interactions between hofmeister anions and the binding pocket of a protein
K +31 K 3x +31 5lmdA The crystal structure of hca ii in complex with a benzoxaborole inhibitor
K +31 K 3x +31
4
5jgsB Human carbonic anhydrase ii (f131y/l198a) complexed with benzo[d]thiazole-2-sulfonamide
K +31 K 3x +31 4mltA Structure of a monodentate 3-hydroxy-4h-pyran-4-thione ligand bound to hcaii
K +31 K 3x +31 5eijA Carbonic anhydrase ii in complex with sulfonamide inhibitor
K +31 K 3x +31 4r59A A carbonic anhydrase ix mimic in complex with a carbohydrate-based sulfamate
K +31 K 3x +31 4mdgA Closo carborane carbonic anhydrase inhibitor
K +31 K 3x +31 3mnuA Carbonic anhydrase inhibitors: crystallographic and solution binding studies for the interaction of a boron containing aromatic sulfamide with mammalian isoforms i-xv
K +31 K 3x +31
4
2nnoA Structure of inhibitor binding to carbonic anhydrase ii
K +31 K 3x +31 1caoA Crystallographic studies of the binding of protonated and unprotonated inhibitors to carbonic anhydrase using hydrogen sulphide and nitrate anions
K +31 K 3x +31 3v2jA Effect of sucrose and glycerol as cryoprotectans, on the inhibition of human carbonic anhydrase ii
K +31 K 3x +31 3konA Crystal structure of cobalt (ii) human carbonic anhydrase ii at ph 11.0
K +31 K 3x +31 4m2rA Human carbonic anhydrase ii in complex with brinzolamide
K +31 K 3x +31 2nwoA Structural and kinetic effect of hydrophobic mutations in the active site of human carbonic anhydrase ii
K +31 K 3x +31 5msaA Crystal structure of human carbonic anhydrase isozyme xii with 2,3,5,6-tetrafluoro-4-(propylthio)benzenesulfonamide
K +31 K 3x +31 5flpA Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
K +31 K 3x +31 5flrA Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
K +31 K 3x +31 4xz5A Structure of the thermostable alpha-carbonic anydrase from thiomicrospira crunogena xcl-2 gammaproteobacterium
K +31 K 4x +31 3ml5A Crystal structure of the c183s/c217s mutant of human ca vii in complex with acetazolamide
K +31 K 3x +31 4qsbA Crystal structure of human carbonic anhydrase isozyme ii with 3-{[(4-methyl-6-oxo-1,6-dihydropyrimidin-2-yl)thio]acetyl}benzenesulfonamide
K +31 K 3x +31 5ty1A Identification of a new zinc binding chemotype by fragment screening
K +31 K 5x +31 1cnjA X-ray crystallographic studies of engineered hydrogen bond networks in a protein-zinc binding site
K +31 K 3x +31 3mhcA Crystal structure of human cabonic anhydrase ii in adduct with an adamantyl analogue of acetazolamide in a novel hydrophobic binding pocket
K +31 K 3x +31 5flsA Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
K +31 K 3x +31 5umcA Synthesis of novel seleno ureido containing compounds as slc-0111 analogs. investigations on carbonic anhydrases activity, glutathione peroxidase and x-ray crystallography
K +31 K 3x +31
4
5tt3A Crystal structure of the complex of helicobacter pylori alpha-carbonic anhydrase with ethoxzolamide
K +31 K 3x +31 5g01A An unusual natural product primary sulfonamide: synthesis, carbonic anhydrase inhibition and protein x-ray structure of psammaplin c
K +31 K 3x +31 4ywpA Sucrose binding site in genetically engineered carbonic anhydrase ix
K +31 K 11x +31 4mdlA Meta carborane carbonic anhydrase inhibitor
K +31 K 11x +31 4fptA Carbonic anhydrase ii in complex with ethyl (2z,4r)-2-(sulfamoylimino)-1,3-thiazolidine-4-carboxylate
K +31 K 3x +31
4
3s72B The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
K +31 K 3x +31 3dazA Use of carbonic anhydrase ii, ix active-site mimic, for the purpose of screening inhibitors for possible anti-cancer properties
K +31 K 3x +31 2vvbX Human carbonic anhydrase ii in complex with bicarbonate
K +31 K 3x +31 4z1eA Carbonic anhydrase inhibitors: design and synthesis of new heteroaryl-n-carbonylbenzenesulfonamides targeting druggable human carbonic anhydrase isoforms (hca vii, hca ix, and hca xiv)
K +31 K 3x +31 3kkxA Neutron structure of human carbonic anhydrase ii
K +31 K 3x +31 4kp5A Crystal structure of catalytic domain of human carbonic anhydrase isozyme xii with 2-chloro-4-[(pyrimidin-2-ylsulfanyl)acetyl]benzenesulfonamide
K +31 K 3x +31 4l5vA The structural implications of the secondary co2 binding pocket in human carbonic anhydrase ii
K +31 K 3x +31 3u3aX Structure of human carbonic anhydrase ii v143i
K +31 K 3x +31 3hknA Human carbonic anhydrase ii in complex with (2,3,4,6-tetra-o-acetyl-beta-d-galactopyranosyl) -(1-4)-1,2,3,6-tetra-o-acetyl-1-thio-beta-d-glucopyranosylsulfonamide
K +31 K 3x +31 5tfxA New method for synthesis of benzoxazole amide inhibitors of carbonic anhydrase
K +31 K 3x +31 2fnnA Activation of human carbonic anhydrase ii by exogenous proton donors
K +31 K 29x +31
30
5jdfA Structural mechanisms of extracellular ion exchange and induced binding-site occlusion in the sodium-calcium exchanger ncx_mj soaked with 2.5 mm na+ and 1mm ca2+
K +31 K 3x +31 1ugdA Human carbonic anhydrase ii[hcaii] (e.c.4.2.1.1) mutant with ala 65 replaced by ser (a65s)
K +31 K 3x +31 3p3jA Human carbonic anhydrase ii in complex with p-(5-ruthenocenyl-1h-1,2,3-triazol-1-yl)benzenesulfonamide
K +31 K 3x +31 5jesB Human carbonic anhydrase ii (v121t) complexed with benzo[d]thiazole-2-sulfonamide
K +31 K 3x +31 3gz0A Apo-human carbonic anhydrase ii revisited: implications of the loss of a metal in protein structure, stability and solvent network
K +31 K 3x +31 4kp8A Crystal structure of catalytic domain of human carbonic anhydrase isozyme xii with 3-[(pyrimidin-2-ylsulfanyl)acetyl]benzenesulfonamide
K +31 K 3x +31 4z1kA Carbonic anhydrase inhibitors: design and synthesis of new heteroaryl-n-carbonylbenzenesulfonamides targeting druggable human carbonic anhydrase isoforms (hca vii, hca ix, and hca xiv)
K +31 K 3x +31 2pouA The crystal structure of the human carbonic anhydrase ii in complex with 4,5-dichloro-benzene-1,3-disulfonamide
K +31 K 3x +31 6b00A Thermostabilized mutant of human carbonic anhydrase ii - a65t l100h k154n l224s l240p a248t
K +31 K 3x +31 5u0eA Identification of a new zinc binding chemotype by fragment screening
K +31 K 3x +31 5g0bA An unusual natural product primary sulfonamide: synthesis, carbonic anhydrase inhibition and protein x-ray structure of psammaplin c
K +31 K 3x +31 5ll9A Crystal structure of human carbonic anhydrase isozyme xii with 4-(1h-benzimidazol-1-ylacetyl)-2-chlorobenzenesulfonamide
K +31 K 3x +31 4m2uA Carbonic anhydrase ii in complex with dorzolamide
K +31 K 3x +31
4
4r5aA A carbonic anhydrase ix mimic in complex with a carbohydrate-based sulfamate
K +31 K 3x +31 2fnkA Activation of human carbonic anhydrase ii by exogenous proton donors
K +31 K 3x +31 5fnmA Native state mass spectrometry, surface plasmon resonance and x-ray crystallography correlate strongly as a fragment screening combination
K +31 K 3x +31 4iwzA Structure of hcaii in complex with an acetazolamide derivative
K +31 K 3x +31 4ht2A Crystal structure of human carbonic anhydrase isozyme xii with the inhibitor.
K +31 K 3x +31 3s74B The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase
K +31 K 3x +31 3v7xA Complex of human carbonic anhydrase ii with n-[2-(3,4-dimethoxyphenyl)ethyl]-4-sulfamoylbenzamide
K +31 K 3x +31 3dv7A Role of hydrophilic residues in proton transfer during catalysis by human carbonic anhydrase ii (n62a)
K +31 K 3x +31 4qjmA Crystal structure of human carbonic anhydrase isozyme ii with inhibitor
K +31 K 3x +31 6bbsA Joint x-ray/neutron structure of human carbonic anhydrase ii in complex with brinzolamide
K +31 K 3x +31 4mdmA Nido-carborane carbonic anhydrase inhibitor
K +31 K 3x +31 3n0nA Crystal structure of human carbonic anhydrase ii in complex with a benzenesulfonamide inhibitor
K +31 K 7x +31 4q8zA Crystal structure of 1-hydroxy-4-methylpyridin-2(1h)-one bound to human carbonic anhydrase ii
K +31 K 3x +31 4fl7A The crystal structure of human carbonic anhydrase ii in complex with n-(hydroxy)-benzamide
K +31 K 7x +31 5fdcA Crystal structure of human carbonic anhydrase ii in complex with the anticonvulsant sulfamide jnj-26990990 and its s,s-dioxide analog.
K +31 K 4x +31 5vgyA Identification of a new zinc binding chemotype by fragment screening
K +31 K 3x +31 2wd3A Highly potent first examples of dual aromatase-steroid sulfatase inhibitors based on a biphenyl template
K +31 K 3x +31 4e5qA Human carbonic anhydrase ii in complex with cyanate
K +31 K 3x +31 4wl4A Crystal structure of human carbonic anhydrase ii in complex with the 6-hydroxy-chromene-2-thione inhibitor
K +31 K 3x +31 5u0fA Identification of a new zinc binding chemotype by fragment screening
K +31 K 3x +31 4kuyA Crystal structure of human carbonic anhydrase ii in complex with the 5-(3-(o-tolylsulfonyl)ureido)pyridine-2-sulfonamide inhibitor
K +31 K 3x +31 3v2mA Effect of sucrose and glycerol as cryoprotectans, on the inhibition of human carbonic anhydrase ii
K +31 K 11x +31 1g0fA Site-specific mutant (his64 replaced with ala) of human carbonic anhydrase ii
K +31 K 3x +31 5tyaA Identification of a new zinc binding chemotype by fragment screening
K +31 K 3x +31 4pyxA Crystal structure of human carbonic anhydrase isozyme ii with inhibitor
K +31 K 3x +31 6fe1A Three dimensional structure of human carbonic anhydrase ix in complex with benzenesulfonamide.
K +31 K 3x +31 3ryxB Fluoroalkyl and alkyl chains have similar hydrophobicities in binding to the hydrophobic wall of carbonic anhydrase
K +31 K 3x +31 1razA The structure of human carbonic anhydrase ii in complex with bromide and azide
K +31 K 3x +31 4e4aA Nucleophile recognition as an alternative inhibition mode for benzoic acid based carbonic anhydrase inhibitors
K +31 K 3x +31 2fnmA Activation of human carbonic anhdyrase ii by exogenous proton donors
K +31 K 3x +31 3r16A Human caii bound to n-(4-sulfamoylphenyl)-2-(thiophen-2-yl) acetamide
K +31 K 3x +31 5wlrA Carbonic anhydrase ix-mimic in complex with aryloxy-2-hydroxypropylammine sulfonamide
K +31 K 3x +31 6d1lA Design, synthesis, and x-ray of selenides bearing benzenesulfonamide moiety with neuropathic pain modulating effects
K +31 K 3x +31 3vbdA Complex of human carbonic anhydrase ii with 4-(6-methoxy-3,4-dihydroisoquinolin-1-yl)benzenesulfonamide
K +31 K 3x +31 5jehB Human carbonic anhydrase ii (l198a) complexed with benzo[d]thiazole-2-sulfonamide
K +31 K 3x +31 4q90A Crystal structure of 4-methylpyridine-2(1h)-thione bound to human carbonic anhydrase ii
K +31 K 3x +31
4
2nnsA Structure of inhibitor binding to carbonic anhydrase ii
K +31 K 3x +31 3myqA Crystal structure of human carbonic anhydrase isozyme ii with 2-chloro-5-[(1h-imidazo[4,5-c]quinolin-2-ylsulfanyl)acetyl]benzenesulfonamide
K +31 K 3x +31 3m1qA Carbonic anhydrase ii mutant w5c-h64c with opened disulfide bond
K +31 K 3x +31
4
5tuoA Crystal structure of the complex of helicobacter pylori alpha-carbonic anhydrase with 5-amino-1,3,4-thiadiazole-2-sulfonamide inhibitor.
K +31 K 1x +31 2eu2A Human carbonic anhydrase ii in complex with novel inhibitors
K +31 K 3x +31 4e3fA Nucleophile recognition as an alternative inhibition mode for benzoic acid based carbonic anhydrase inhibitors
K +31 K 3x +31 3p55A Human carbonic anhydrase ii in complex with p-(4-ferrocenyl-1h-1,2,3-triazol-1-yl)benzenesulfonamide
K +31 K 3x +31 2nwzA Structural and kinetic effects of hydrophobic mutations on the active site of human carbonic anhydrase ii
K +31 K 3x +31 3uynA Hca 3
K +31 K 3x +31 5t71A Human carboanhydrase f131c_c206s double mutant in complex with sa-2
K +31 K 1x +31 2hfxA Structural and kinetic analysis of proton shuttle residues in the active site of human carbonic anhydrase iii
K +31 K 3x +31 3ml2A Human carbonic anhydsase ii in complex with an aryl sulfonamide inhibitor
K +31 K 3x +31 4k1qA Structure of hcaix mimic (hcaii with 5 mutations in active site)
K +31 K 3x +31 5ty8A Identification of a new zinc binding chemotype by fragment screening
K +31 K 3x +31 5g0cA An unusual natural product primary sulfonamide: synthesis, carbonic anhydrase inhibition and protein x-ray structure of psammaplin c
K +31 K 3x +31 1fsrA X-ray crystal structure of copper-bound f93s/f95l/w97m carbonic anhydrase (caii) variant
K +31 K 3x +31 6g98A Three dimensional structure of human carbonic anhydrase ix in complex with sulfonamide
K +31 K 3x +31 5dvxA Crystal structure of the catalytic-domain of human carbonic anhydrase ix at 1.6 angstrom resolution
K +31 K 3x +31 5amdA Three dimensional structure of human carbonic anhydrase ii in complex with 2-((2-phenylethyl)sulfamoyl)-4-sulfamoylbenzoic acid
K +31 K 3x +31 4qefA Human carbonic anhydrase ii v207i - cyanate inhibitor complex
K +31 K 3x +31 4hewA Activity enhancers of h64a variant of human carbonic anhydrase ii possess multiple binding sites within and around the enzyme structure
K +31 K 3x +31 3okuA Human carbonic anhydrase ii in complex with 2-ethylestrone-3-o-sulfamate
K +31 K 3x +31 1z93A Human carbonic anhydrase iii:structural and kinetic study of catalysis and proton transfer.
K +31 K 3x +31 5brwA Catalytic improvement of an artificial metalloenzyme by computational design
K +31 K 3x +31 5wexA Discovery of new selenoureido analogs of 4-(4-fluorophenylureido) benzenesulfonamides as carbonic anhydrase inhibitors
K +31 K 3x +31 4q06A Crystal structure of chimeric carbonic anhydrase ix with inhibitor
K +31 K 3x +31 3p5aA Human carbonic anhydrase complexed with sodium morpholinocarbodithioate
K +31 K 3x +31 5je7B Human carbonic anhydrase ii (f131y) complexed with benzo[d]thiazole-2-sulfonamide
K +31 K 3x +31 5ekmA Human carbonic anhydrase ii complexed with a two-faced guest
K +31 K 3x +31 4z1jA Carbonic anhydrase inhibitors: design and synthesis of new heteroaryl-n-carbonylbenzenesulfonamides targeting druggable human carbonic anhydrase isoforms (hca vii, hca ix, and hca xiv)
K +31 K 3x +31 2wejA Thermodynamic optimisation of carbonic anhydrase fragment inhibitors
K +31 K 3x +31 3oysA Human carbonic anhydrase ii complexed with 2-{[4-amino-3-(3-hydroxyprop-1-yn-1-yl)-1h-pyrazolo[3,4-d]pyrimidin-1-yl]methyl}-5-methyl-3-(2-methylphenyl)quinazolin-4(3h)-one
K +31 K 3x +31 4itpA Structure of human carbonic anhydrase ii bound to a benzene sulfonamide
K +31 K 11x +31 3k34A Human carbonic anhydrase ii with a sulfonamide inhibitor
K +31 K 3x +31 3dvbA X-ray crystal structure of mutant n62v human carbonic anhydrase ii
K +31 K 3x +31 2powA The crystal structure of the human carbonic anhydrase ii in complex with 4-amino-6-trifluoromethyl-benzene-1,3-disulfonamide
K +31 K 3x +31 4e3gA Nucleophile recognition as an alternative inhibition mode for benzoic acid based carbonic anhydrase inhibitors
K +31 K 2x +31 2x7tA Structures of human carbonic anhydrase ii inhibitor complexes reveal a second binding site for steroidal and non-steroidal inhibitors.
K +31 K 3x +31 2iliA Refine atomic structure of human carbonic anhydrase ii
K +31 K 3x +31 4fikA Human carbonic anhydrase ii h64a complexed with thioxolone hydrolysis products
K +31 K 3x +31 4knnA Crystal structure of human carbonic anhydrase isozyme xiii with 2-chloro-4-[(pyrimidin-2-ylsulfanyl)acetyl]benzenesulfonamide
K +31 K 3x +31 3saxA Crystal structure of human carbonic anhydrase isozyme ii with 2-chloro-5-{[(5-ethyl-2-pyrimidinyl)sulfanyl]acetyl}benzenesulfonamide
K +31 K 3x +31 4qsaA Crystal structure of human carbonic anhydrase isozyme ii with 2-chloro-4-{[(4-methyl-6-oxo-1,6-dihydropyrimidin-2-yl)thio]acetyl}benzenesulfonamide
K +31 K 3x +31 3s8xA Crystal structure of human carbonic anhydrase isozyme ii with 4-{[(4-methyl-6-oxo-1,6-dihydro-2-pyrimidinyl)sulfanyl]acetyl}benzenesulfonamide
K +31 K 3x +31 6gotA Crystal structure of human carbonic anhydrase ii in complex with the inhibitor 4-(phenethylthio)benzenesulfonamide
K +31 K 3x +31 3s73B The origin of the hydrophobic effect in the molecular recognition of arylsulfonamides by carbonic anhydrase

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