9hl3

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Current revision (08:29, 4 June 2025) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 9hl3 is ON HOLD until Paper Publication
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==TRPML1 in complex with compound 1a==
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<StructureSection load='9hl3' size='340' side='right'caption='[[9hl3]], [[Resolution|resolution]] 2.10&Aring;' scene=''>
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Authors:
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== Structural highlights ==
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<table><tr><td colspan='2'>[[9hl3]] 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=9HL3 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9HL3 FirstGlance]. <br>
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Description:
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 2.1&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=A1IVZ:2-[2-oxidanylidene-2-[(4~{R})-2,2,4-trimethyl-3,4-dihydroquinolin-1-yl]ethyl]isoindole-1,3-dione'>A1IVZ</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=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>, <scene name='pdbligand=OCT:N-OCTANE'>OCT</scene></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9hl3 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9hl3 OCA], [https://pdbe.org/9hl3 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9hl3 RCSB], [https://www.ebi.ac.uk/pdbsum/9hl3 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9hl3 ProSAT]</span></td></tr>
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</table>
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== Disease ==
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[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.
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== Function ==
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[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>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Clark M]]
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[[Category: Cowan SR]]
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[[Category: Di Daniel E]]
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[[Category: Earl CP]]
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[[Category: Fisher S]]
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[[Category: Holvey RS]]
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[[Category: Jackson SM]]
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[[Category: Johnson CN]]
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[[Category: Lloyd-Evans E]]
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[[Category: Mahajan P]]
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[[Category: Morgillo CM]]
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[[Category: Mortenson PN]]
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[[Category: O'Reilly M]]
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[[Category: Reeks J]]
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[[Category: Richardson CJ]]
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[[Category: Schopf P]]
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[[Category: Tams DM]]
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[[Category: Waller-Evans H]]
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[[Category: Ward SE]]
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[[Category: Whibley S]]
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[[Category: Williams PA]]

Current revision

TRPML1 in complex with compound 1a

PDB ID 9hl3

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