This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.
Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.
7xlm
From Proteopedia
(Difference between revisions)
m (Protected "7xlm" [edit=sysop:move=sysop]) |
|||
| Line 1: | Line 1: | ||
| - | '''Unreleased structure''' | ||
| - | The entry | + | ==Human diastrophic dysplasia sulfate transporter SLC26A2== |
| - | + | <StructureSection load='7xlm' size='340' side='right'caption='[[7xlm]], [[Resolution|resolution]] 3.73Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[7xlm]] is a 2 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=7XLM OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7XLM FirstGlance]. <br> | |
| - | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr> | |
| - | [[Category: | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7xlm FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7xlm OCA], [https://pdbe.org/7xlm PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7xlm RCSB], [https://www.ebi.ac.uk/pdbsum/7xlm PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7xlm ProSAT]</span></td></tr> |
| + | </table> | ||
| + | == Disease == | ||
| + | [https://www.uniprot.org/uniprot/S26A2_HUMAN S26A2_HUMAN] Multiple epiphyseal dysplasia type 4;Atelosteogenesis type II;Achondrogenesis type 1B;Diastrophic dysplasia. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry. | ||
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/S26A2_HUMAN S26A2_HUMAN] Sulfate transporter. May play a role in endochondral bone formation.<ref>PMID:7923357</ref> | ||
| + | == References == | ||
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Chi XM]] | ||
| + | [[Category: Zhou Q]] | ||
Current revision
Human diastrophic dysplasia sulfate transporter SLC26A2
| |||||||||||
