View source for 9hld


==TRPML1 in complex with compound 13==
<StructureSection load='9hld' size='340' side='right'caption='[[9hld]], [[Resolution|resolution]] 2.20&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[9hld]] is a 4 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=9HLD OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9HLD FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.2&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=8K6:OCTADECANE'>8K6</scene>, <scene name='pdbligand=A1IV6:1-[(8~{R},9~{S},13~{S},14~{S},17~{S})-13-methyl-17-oxidanyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-yl]ethanone'>A1IV6</scene>, <scene name='pdbligand=D10:DECANE'>D10</scene>, <scene name='pdbligand=D12:DODECANE'>D12</scene>, <scene name='pdbligand=EUJ:(2R)-3-{[(S)-hydroxy{[(1S,2R,3R,4S,5S,6R)-2,4,6-trihydroxy-3,5-bis(phosphonooxy)cyclohexyl]oxy}phosphoryl]oxy}propane-1,2-diyl+dioctanoate'>EUJ</scene>, <scene name='pdbligand=HEX:HEXANE'>HEX</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>, <scene name='pdbligand=OCT:N-OCTANE'>OCT</scene></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=9hld FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9hld OCA], [https://pdbe.org/9hld PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9hld RCSB], [https://www.ebi.ac.uk/pdbsum/9hld PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9hld ProSAT]</span></td></tr>
</table>
== Disease ==
[https://www.uniprot.org/uniprot/MCLN1_HUMAN MCLN1_HUMAN] Mucolipidosis type 4. The disease is caused by mutations affecting the gene represented in this entry.
== Function ==
[https://www.uniprot.org/uniprot/MCLN1_HUMAN MCLN1_HUMAN] Cation channel probably playing a role in the endocytic pathway and in the control of membrane trafficking of proteins and lipids. Could play a major role in Ca(2+) transport regulating lysosomal exocytosis.<ref>PMID:12459486</ref> <ref>PMID:14749347</ref> 
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Clark M]]
[[Category: Cowan SR]]
[[Category: Di Daniel E]]
[[Category: Earl CP]]
[[Category: Fisher S]]
[[Category: Holvey RS]]
[[Category: Jackson SM]]
[[Category: Johnson CN]]
[[Category: Lloyd-Evans E]]
[[Category: Mahajan P]]
[[Category: Morgillo CM]]
[[Category: Mortenson PN]]
[[Category: O'Reilly M]]
[[Category: Reeks J]]
[[Category: Richardson CJ]]
[[Category: Schopf P]]
[[Category: Tams DM]]
[[Category: Waller-Evans H]]
[[Category: Ward SE]]
[[Category: Whibley S]]
[[Category: Williams PA]]