9ege: Difference between revisions

From Proteopedia
Jump to navigationJump to search
OCA (talk | contribs)
Bots, Bureaucrats, journal, Administrators
3,332,843 edits
New page: '''Unreleased structure''' The entry 9ege is ON HOLD Authors: Reddy, B.G., Gruget, C., Moore, J. Description: BSEP Apo Structure in GDN Category: Unreleased Structures [[Category: ...
 
OCA (talk | contribs)
Bots, Bureaucrats, journal, Administrators
3,332,843 edits
No edit summary
 
(2 intermediate revisions by the same user not shown)
Line 1: Line 1:
'''Unreleased structure'''


The entry 9ege is ON HOLD
==BSEP Apo Structure in GDN==
 
<StructureSection load='9ege' size='340' side='right'caption='[[9ege]], [[Resolution|resolution]] 2.80&Aring;' scene=''>
Authors: Reddy, B.G., Gruget, C., Moore, J.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[9ege]] 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=9EGE OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9EGE FirstGlance]. <br>
Description: BSEP 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]] 2.8&#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=9ege FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9ege OCA], [https://pdbe.org/9ege PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9ege RCSB], [https://www.ebi.ac.uk/pdbsum/9ege PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9ege ProSAT]</span></td></tr>
[[Category: Moore, J]]
</table>
[[Category: Gruget, C]]
== Disease ==
[[Category: Reddy, B.G]]
[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/9ege"