6lr0: Difference between revisions

<table><tr><td colspan='2'>[[6lr0]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6LR0 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6LR0 FirstGlance]. <br>

</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6lr0 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6lr0 OCA], [https://pdbe.org/6lr0 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6lr0 RCSB], [https://www.ebi.ac.uk/pdbsum/6lr0 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6lr0 ProSAT]</span></td></tr>

[https://www.uniprot.org/uniprot/ABCBB_HUMAN ABCBB_HUMAN] Progressive familial intrahepatic cholestasis type 2;Intrahepatic cholestasis of pregnancy;Benign recurrent intrahepatic cholestasis type 2. The disease is caused by mutations affecting the gene represented in this entry.  The disease is caused by mutations affecting the gene represented in this entry.

[https://www.uniprot.org/uniprot/ABCBB_HUMAN ABCBB_HUMAN] Catalyzes the secretion of conjugated bile salts across the canalicular membrane of hepatocytes in an ATP-dependent manner (PubMed:16332456). Transports taurine-conjugated bile salts more rapidly than glycine-conjugated bile salts (PubMed:16332456).<ref>PMID:16332456</ref>  

[[Category: Homo sapiens]]

[[Category: Chen L]]

[[Category: Chen Y]]

[[Category: Hou WT]]

[[Category: Jiang YL]]

[[Category: Sun LF]]

[[Category: Wang L]]

[[Category: Xu D]]

[[Category: Zhou CZ]]