4avx
From Proteopedia
(Difference between revisions)
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<StructureSection load='4avx' size='340' side='right'caption='[[4avx]], [[Resolution|resolution]] 1.68Å' scene=''> | <StructureSection load='4avx' size='340' side='right'caption='[[4avx]], [[Resolution|resolution]] 1.68Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
- | <table><tr><td colspan='2'>[[4avx]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/ | + | <table><tr><td colspan='2'>[[4avx]] 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=4AVX OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4AVX FirstGlance]. <br> |
- | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=ITP:PHOSPHORIC+ACID+MONO-(2,3,4,6-TETRAHYDROXY-5-PHOSPHONOOXY-CYCLOHEXYL)+ESTER'>ITP</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.68Å</td></tr> |
- | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=ITP:PHOSPHORIC+ACID+MONO-(2,3,4,6-TETRAHYDROXY-5-PHOSPHONOOXY-CYCLOHEXYL)+ESTER'>ITP</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</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=4avx FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4avx OCA], [https://pdbe.org/4avx PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4avx RCSB], [https://www.ebi.ac.uk/pdbsum/4avx PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4avx ProSAT]</span></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=4avx FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4avx OCA], [https://pdbe.org/4avx PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4avx RCSB], [https://www.ebi.ac.uk/pdbsum/4avx PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4avx ProSAT]</span></td></tr> | ||
</table> | </table> | ||
== Function == | == Function == | ||
- | + | [https://www.uniprot.org/uniprot/HGS_HUMAN HGS_HUMAN] Involved in intracellular signal transduction mediated by cytokines and growth factors. When associated with STAM, it suppresses DNA signaling upon stimulation by IL-2 and GM-CSF. Could be a direct effector of PI3-kinase in vesicular pathway via early endosomes and may regulate trafficking to early and late endosomes by recruiting clathrin. May concentrate ubiquitinated receptors within clathrin-coated regions. Involved in down-regulation of receptor tyrosine kinase via multivesicular body (MVBs) when complexed with STAM (ESCRT-0 complex). The ESCRT-0 complex binds ubiquitin and acts as sorting machinery that recognizes ubiquitinated receptors and transfers them to further sequential lysosomal sorting/trafficking processes. May contribute to the efficient recruitment of SMADs to the activin receptor complex. Involved in receptor recycling via its association with the CART complex, a multiprotein complex required for efficient transferrin receptor recycling but not for EGFR degradation. | |
__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: Bullock | + | [[Category: Bullock A]] |
- | [[Category: Canning | + | [[Category: Canning P]] |
- | [[Category: Conway | + | [[Category: Conway S]] |
- | + | [[Category: Edwards AM]] | |
- | [[Category: Edwards | + | [[Category: Krojer T]] |
- | [[Category: Krojer | + | [[Category: Shrestha L]] |
- | [[Category: Shrestha | + | [[Category: Slowey A]] |
- | [[Category: Slowey | + | [[Category: Vollmar M]] |
- | [[Category: Vollmar | + | [[Category: Weigelt J]] |
- | [[Category: Weigelt | + | [[Category: Williams E]] |
- | [[Category: Williams | + | [[Category: Von Delft F]] |
- | [[Category: | + | |
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- | + | ||
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Current revision
Hepatocyte Growth Factor-Regulated Tyrosine Kinase Substrate (Hgs-Hrs) bound to an IP2 compound at 1.68 A Resolution
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Categories: Homo sapiens | Large Structures | Arrowsmith CH | Bountra C | Bullock A | Canning P | Conway S | Edwards AM | Krojer T | Shrestha L | Slowey A | Vollmar M | Weigelt J | Williams E | Von Delft F