9n1y: Difference between revisions

From Proteopedia
Jump to navigationJump to search
← Older edit
OCA (talk | contribs)
Bots, Bureaucrats, journal, Administrators
3,332,843 edits
No edit summary
OCA (talk | contribs)
Bots, Bureaucrats, journal, Administrators
3,332,843 edits
No edit summary
 
Line 1: Line 1:
'''Unreleased structure'''


The entry 9n1y is ON HOLD  until Paper Publication
==BSEP E297G Apo Structure in GDN==
 
<StructureSection load='9n1y' size='340' side='right'caption='[[9n1y]], [[Resolution|resolution]] 3.23&Aring;' scene=''>
Authors: Reddy, B.G., Gruget, C., Moore, J.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[9n1y]] 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=9N1Y OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9N1Y FirstGlance]. <br>
Description: BSEP E297G Apo Structure in GDN
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.23&#8491;</td></tr>
[[Category: Unreleased Structures]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9n1y FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9n1y OCA], [https://pdbe.org/9n1y PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9n1y RCSB], [https://www.ebi.ac.uk/pdbsum/9n1y PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9n1y ProSAT]</span></td></tr>
[[Category: Reddy, B.G]]
</table>
[[Category: Gruget, C]]
== Disease ==
[[Category: Moore, J]]
[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.
== Function ==
[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>
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Gruget C]]
[[Category: Moore J]]
[[Category: Reddy BG]]
Retrieved from "https://proteopedia.org/9n1y"