5w3r

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(New page: '''Unreleased structure''' The entry 5w3r is ON HOLD until Paper Publication Authors: McKercher, M.A., Wuttke, D.S. Description: SH2B1 SH2 Domain Category: Unreleased Structures [[...)
Current revision (14:06, 4 October 2023) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 5w3r is ON HOLD until Paper Publication
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==SH2B1 SH2 Domain==
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<StructureSection load='5w3r' size='340' side='right'caption='[[5w3r]], [[Resolution|resolution]] 1.39&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5w3r]] 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=5W3R OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5W3R FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.386&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=IPH:PHENOL'>IPH</scene>, <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</scene></td></tr>
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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=5w3r FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5w3r OCA], [https://pdbe.org/5w3r PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5w3r RCSB], [https://www.ebi.ac.uk/pdbsum/5w3r PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5w3r ProSAT]</span></td></tr>
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</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/SH2B1_HUMAN SH2B1_HUMAN] Severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency;Proximal 16p11.2 microdeletion syndrome;Distal 16p11.2 microdeletion syndrome.
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== Function ==
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[https://www.uniprot.org/uniprot/SH2B1_HUMAN SH2B1_HUMAN] Adapter protein for several members of the tyrosine kinase receptor family. Involved in multiple signaling pathways mediated by Janus kinase (JAK) and receptor tyrosine kinases, including the receptors of insulin (INS), insulin-like growth factor I (IGF1), nerve growth factor (NGF), brain-derived neurotrophic factor (BDNF), glial cell line-derived neurotrophic factor (GDNF), platelet-derived growth factor (PDGF) and fibroblast growth factors (FGFs). In growth hormone (GH) signaling, autophosphorylated ('Tyr-813') JAK2 recruits SH2B1, which in turn is phosphorylated by JAK2 on tyrosine residues. These phosphotyrosines form potential binding sites for other signaling proteins. GH also promotes serine/threonine phosphorylation of SH2B1 and these phosphorylated residues may serve to recruit other proteins to the GHR-JAK2-SH2B1 complexes, such as RAC1. In leptin (LEP) signaling, binds to and potentiates the activation of JAK2 by globally enhancing downstream pathways. In response to leptin, binds simultaneously to both, JAK2 and IRS1 or IRS2, thus mediating formation of a complex of JAK2, SH2B1 and IRS1 or IRS2. Mediates tyrosine phosphorylation of IRS1 and IRS2, resulting in activation of the PI 3-kinase pathway. Acts as positive regulator of NGF-mediated activation of the Akt/Forkhead pathway; prolongs NGF-induced phosphorylation of AKT1 on 'Ser-473' and AKT1 enzymatic activity. Enhances the kinase activity of the cytokine receptor-associated tyrosine kinase JAK2 and of other receptor tyrosine kinases, such as FGFR3 and NTRK1. For JAK2, the mechanism seems to involve dimerization of both, SH2B1 and JAK2. Enhances RET phosphorylation and kinase activity. Isoforms seem to be differentially involved in IGF-I and PDGF-induced mitogenesis (By similarity).<ref>PMID:11827956</ref> <ref>PMID:14565960</ref> <ref>PMID:15767667</ref> <ref>PMID:16569669</ref> <ref>PMID:17471236</ref> <ref>PMID:9694882</ref> <ref>PMID:9742218</ref>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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SH2B1 is a multidomain protein that serves as a key adapter to regulate numerous cellular events, such as insulin, leptin, and growth hormone signaling pathways. Many of these protein-protein interactions are mediated by the SH2 domain of SH2B1, which recognizes ligands containing a phosphorylated tyrosine (pY), including peptides derived from janus kinase 2, insulin receptor, and insulin receptor substrate-1 and -2. Specificity for the SH2 domain of SH2B1 is conferred in these ligands either a hydrophobic or an acidic side chain at the +3 position C-terminal to the pY. This specificity for chemically disparate species suggests that SH2B1 relies on distinct thermodynamic or structural mechanisms to bind to peptides. Using binding and structural strategies, we have identified unique thermodynamic signatures for each peptide binding mode, and several SH2B1 residues, including K575 and R578, that play distinct roles in peptide binding. The high-resolution structure of the SH2 domain of SH2B1 further reveals conformationally plastic protein loops that may contribute to the ability of the protein to recognize dissimilar ligands. Together, numerous hydrophobic and electrostatic interactions, in addition to backbone conformational flexibility, permit the recognition of diverse peptides by SH2B1. An understanding of this expanded peptide recognition will allow for the identification of novel physiologically relevant SH2B1/peptide interactions, which can contribute to the design of obesity and diabetes pharmaceuticals to target the ligand-binding interface of SH2B1 with high specificity. This article is protected by copyright. All rights reserved.
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Authors: McKercher, M.A., Wuttke, D.S.
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Diversity in Peptide Recognition by the SH2 Domain of SH2B1.,McKercher MA, Guan X, Tan Z, Wuttke DS Proteins. 2017 Nov 11. doi: 10.1002/prot.25420. PMID:29127727<ref>PMID:29127727</ref>
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Description: SH2B1 SH2 Domain
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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[[Category: Wuttke, D.S]]
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<div class="pdbe-citations 5w3r" style="background-color:#fffaf0;"></div>
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[[Category: Mckercher, M.A]]
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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: McKercher MA]]
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[[Category: Wuttke DS]]

Current revision

SH2B1 SH2 Domain

PDB ID 5w3r

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