8kgw

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Current revision (05:33, 4 September 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 8kgw is ON HOLD
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==Molecular mechanism of prostaglandin transporter SLCO2A1==
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<StructureSection load='8kgw' size='340' side='right'caption='[[8kgw]], [[Resolution|resolution]] 3.40&Aring;' scene=''>
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Authors:
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== Structural highlights ==
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<table><tr><td colspan='2'>[[8kgw]] 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=8KGW OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8KGW 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]] 3.4&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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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=8kgw FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8kgw OCA], [https://pdbe.org/8kgw PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8kgw RCSB], [https://www.ebi.ac.uk/pdbsum/8kgw PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8kgw ProSAT]</span></td></tr>
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</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/SO2A1_HUMAN SO2A1_HUMAN] Defects in SLCO2A1 are the cause of hypertrophic osteoarthropathy, primary, autosomal recessive, type 2 (PHOAR2) [MIM:[https://omim.org/entry/614441 614441]. PHOAR2 is a disease characterized by digital clubbing, periostosis, acroosteolysis, painful joint enlargement, and variable features of pachydermia that include thickened facial skin and a thickened scalp. Other developmental anomalies include delayed closure of the cranial sutures and congenital heart disease.<ref>PMID:22331663</ref> <ref>PMID:22197487</ref> <ref>PMID:22553128</ref> <ref>PMID:22696055</ref>
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== Function ==
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[https://www.uniprot.org/uniprot/SO2A1_HUMAN SO2A1_HUMAN] May mediate the release of newly synthesized prostaglandins from cells, the transepithelial transport of prostaglandins, and the clearance of prostaglandins from the circulation. Transports PGD2, as well as PGE1, PGE2 and PGF2A.
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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: Chao YL]]
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[[Category: Li YH]]
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[[Category: Qu QH]]
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[[Category: Zhou ZX]]
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[[Category: Zhu ZN]]

Current revision

Molecular mechanism of prostaglandin transporter SLCO2A1

PDB ID 8kgw

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