5jjx
From Proteopedia
(Difference between revisions)
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<StructureSection load='5jjx' size='340' side='right'caption='[[5jjx]], [[Resolution|resolution]] 2.00Å' scene=''> | <StructureSection load='5jjx' size='340' side='right'caption='[[5jjx]], [[Resolution|resolution]] 2.00Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'>[[5jjx]] is a 1 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[5jjx]] 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=5JJX OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5JJX FirstGlance]. <br> |
- | </td></tr><tr id=' | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2Å</td></tr> |
- | <tr id=' | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=UNX:UNKNOWN+ATOM+OR+ION'>UNX</scene></td></tr> |
- | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=5jjx FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5jjx OCA], [https://pdbe.org/5jjx PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5jjx RCSB], [https://www.ebi.ac.uk/pdbsum/5jjx PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5jjx ProSAT]</span></td></tr> |
</table> | </table> | ||
== Disease == | == Disease == | ||
- | [ | + | [https://www.uniprot.org/uniprot/SART3_HUMAN SART3_HUMAN] Defects in SART3 are the cause of disseminated superficial actinic porokeratosis type 1 (DSAP1) [MIM:[https://omim.org/entry/175900 175900]. DSAP1 is an autosomal dominant disorder, characterized by multiple superficial keratotic lesions surrounded by a slightly raised keratotic border, developing during the third or fourth decade of life on sun-exposed areas of skin.<ref>PMID:15840095</ref> |
== Function == | == Function == | ||
- | [ | + | [https://www.uniprot.org/uniprot/SART3_HUMAN SART3_HUMAN] Regulates Tat transactivation activity through direct interaction. May be a cellular factor for HIV-1 gene expression and viral replication.<ref>PMID:11959860</ref> |
== References == | == References == | ||
<references/> | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
- | [[Category: | + | [[Category: Homo sapiens]] |
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
- | [[Category: Arrowsmith | + | [[Category: Arrowsmith CH]] |
- | [[Category: Bountra | + | [[Category: Bountra C]] |
- | [[Category: DONG | + | [[Category: DONG A]] |
- | [[Category: Edwards | + | [[Category: Edwards AM]] |
- | + | [[Category: TEMPEL W]] | |
- | [[Category: TEMPEL | + | [[Category: TONG Y]] |
- | [[Category: TONG | + | [[Category: ZHANG Q]] |
- | [[Category: ZHANG | + | |
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Current revision
Crystal structure of the HAT domain of sart3
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Categories: Homo sapiens | Large Structures | Arrowsmith CH | Bountra C | DONG A | Edwards AM | TEMPEL W | TONG Y | ZHANG Q