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5eeq
From Proteopedia
(Difference between revisions)
(New page: '''Unreleased structure''' The entry 5eeq is ON HOLD Authors: Ambaye, N.D., Watson, G.M., Wilce, M.C.J., Wilce, G.M. Description: Grb7 SH2 with the G7-B1 bicyclic peptide inhibitor [[C...) |
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| - | '''Unreleased structure''' | ||
| - | + | ==Grb7 SH2 with the G7-B1 bicyclic peptide inhibitor== | |
| + | <StructureSection load='5eeq' size='340' side='right'caption='[[5eeq]], [[Resolution|resolution]] 1.60Å' scene=''> | ||
| + | == Structural highlights == | ||
| + | <table><tr><td colspan='2'>[[5eeq]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [https://en.wikipedia.org/wiki/Synthetic_construct Synthetic construct]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5EEQ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5EEQ FirstGlance]. <br> | ||
| + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.6Å</td></tr> | ||
| + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=48V:{[(2R)-2,3-DIAMINO-3-OXOPROPYL]SULFANYL}ACETIC+ACID'>48V</scene>, <scene name='pdbligand=73C:(2~{S})-2-AZANYL-3-BUTOXY-PROPANOIC+ACID'>73C</scene>, <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</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=5eeq FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5eeq OCA], [https://pdbe.org/5eeq PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5eeq RCSB], [https://www.ebi.ac.uk/pdbsum/5eeq PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5eeq ProSAT]</span></td></tr> | ||
| + | </table> | ||
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/GRB7_HUMAN GRB7_HUMAN] Adapter protein that interacts with the cytoplasmic domain of numerous receptor kinases and modulates down-stream signaling. Promotes activation of down-stream protein kinases, including STAT3, AKT1, MAPK1 and/or MAPK3. Promotes activation of HRAS. Plays a role in signal transduction in response to EGF. Plays a role in the regulation of cell proliferation and cell migration. Plays a role in the assembly and stability of RNA stress granules. Binds to the 5'UTR of target mRNA molecules and represses translation of target mRNA species, when not phosphorylated. Phosphorylation impairs RNA binding and promotes stress granule disassembly during recovery after cellular stress (By similarity).<ref>PMID:10893408</ref> <ref>PMID:12021278</ref> <ref>PMID:12223469</ref> <ref>PMID:20622016</ref> | ||
| - | + | ==See Also== | |
| - | + | *[[Growth factor receptor-bound proteins 3D structures|Growth factor receptor-bound proteins 3D structures]] | |
| - | + | == References == | |
| - | [[Category: | + | <references/> |
| - | [[Category: | + | __TOC__ |
| - | [[Category: | + | </StructureSection> |
| - | [[Category: Ambaye | + | [[Category: Homo sapiens]] |
| - | [[Category: Watson | + | [[Category: Large Structures]] |
| + | [[Category: Synthetic construct]] | ||
| + | [[Category: Ambaye ND]] | ||
| + | [[Category: Watson GM]] | ||
| + | [[Category: Wilce GM]] | ||
| + | [[Category: Wilce MCJ]] | ||
Current revision
Grb7 SH2 with the G7-B1 bicyclic peptide inhibitor
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