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| | ==MPZL1 mutant - V145G, Q146K, P147T and G148S== | | ==MPZL1 mutant - V145G, Q146K, P147T and G148S== |
| - | <StructureSection load='6igt' size='340' side='right' caption='[[6igt]], [[Resolution|resolution]] 2.40Å' scene=''> | + | <StructureSection load='6igt' size='340' side='right'caption='[[6igt]], [[Resolution|resolution]] 2.40Å' scene=''> |
| | == Structural highlights == | | == Structural highlights == |
| - | <table><tr><td colspan='2'>[[6igt]] is a 4 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6IGT OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6IGT FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[6igt]] is a 4 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=6IGT OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6IGT FirstGlance]. <br> |
| - | </td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">MPZL1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.404Å</td></tr> |
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6igt FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6igt OCA], [http://pdbe.org/6igt PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6igt RCSB], [http://www.ebi.ac.uk/pdbsum/6igt PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6igt 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=6igt FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6igt OCA], [https://pdbe.org/6igt PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6igt RCSB], [https://www.ebi.ac.uk/pdbsum/6igt PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6igt ProSAT]</span></td></tr> |
| | </table> | | </table> |
| | == Function == | | == Function == |
| - | [[http://www.uniprot.org/uniprot/MPZL1_HUMAN MPZL1_HUMAN]] Cell surface receptor, which is involved in signal transduction processes. Recruits PTPN11/SHP-2 to the cell membrane and is a putative substrate of PTPN11/SHP-2. Is a major receptor for concanavalin-A (ConA) and is involved in cellular signaling induced by ConA, which probably includes Src family tyrosine-protein kinases. Isoform 3 seems to have a dominant negative role; it blocks tyrosine phosphorylation of MPZL1 induced by ConA. Isoform 1, but not isoform 2 and isoform 3, may be involved in regulation of integrin-mediated cell motility.<ref>PMID:11751924</ref> <ref>PMID:12410637</ref> | + | [https://www.uniprot.org/uniprot/MPZL1_HUMAN MPZL1_HUMAN] Cell surface receptor, which is involved in signal transduction processes. Recruits PTPN11/SHP-2 to the cell membrane and is a putative substrate of PTPN11/SHP-2. Is a major receptor for concanavalin-A (ConA) and is involved in cellular signaling induced by ConA, which probably includes Src family tyrosine-protein kinases. Isoform 3 seems to have a dominant negative role; it blocks tyrosine phosphorylation of MPZL1 induced by ConA. Isoform 1, but not isoform 2 and isoform 3, may be involved in regulation of integrin-mediated cell motility.<ref>PMID:11751924</ref> <ref>PMID:12410637</ref> |
| | <div style="background-color:#fffaf0;"> | | <div style="background-color:#fffaf0;"> |
| | == Publication Abstract from PubMed == | | == Publication Abstract from PubMed == |
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| | __TOC__ | | __TOC__ |
| | </StructureSection> | | </StructureSection> |
| - | [[Category: Human]] | + | [[Category: Homo sapiens]] |
| - | [[Category: Yu, T]] | + | [[Category: Large Structures]] |
| - | [[Category: Glycoprotein]] | + | [[Category: Yu T]] |
| - | [[Category: Immunoglobulin]]
| + | |
| - | [[Category: Membrane protein]]
| + | |
| - | [[Category: Receptor]]
| + | |
| - | [[Category: Transmembrane]]
| + | |
| Structural highlights
Function
MPZL1_HUMAN Cell surface receptor, which is involved in signal transduction processes. Recruits PTPN11/SHP-2 to the cell membrane and is a putative substrate of PTPN11/SHP-2. Is a major receptor for concanavalin-A (ConA) and is involved in cellular signaling induced by ConA, which probably includes Src family tyrosine-protein kinases. Isoform 3 seems to have a dominant negative role; it blocks tyrosine phosphorylation of MPZL1 induced by ConA. Isoform 1, but not isoform 2 and isoform 3, may be involved in regulation of integrin-mediated cell motility.[1] [2]
Publication Abstract from PubMed
Myelin protein zero-like protein 1 (MPZL1) is a member of the immunoglobulin superfamily, and is also a receptor of concanavalin A (ConA). MPZL1 is upregulated in hepatocellular carcinoma (HCC) and accelerates migration of HCC cells. However, function of MPZL1 as a receptor of ConA and its role in HCC development are largely unknown. To elucidate the functional basis, we have determined the crystal structure of the extracellular domain of MPZL1 at 2.7A resolution. Overall, it folds like a typical immunoglobulin variable-like domain that is much like MPZ. Unexpectedly, we found Asn50 is a unique glycosylation site and the glycosylation mediates its interaction with ConA. Furthermore, we also found that MPZL1 exists as a homodimer in the crystal, in which hydrogen bonds between Ser86 and Val145 play an important role. Our results demonstrate that glycosylation of Asn50 is essential for its function as a receptor of ConA. We propose that dimerization of MPZL1 participates in control of its signal transmission in cell adhesion.
Structural and biochemical studies of the extracellular domain of Myelin protein zero-like protein 1.,Yu T, Liang L, Zhao X, Yin Y Biochem Biophys Res Commun. 2018 Dec 2;506(4):883-890. doi:, 10.1016/j.bbrc.2018.10.161. Epub 2018 Nov 2. PMID:30392906[3]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
References
- ↑ Zhao R, Guerrah A, Tang H, Zhao ZJ. Cell surface glycoprotein PZR is a major mediator of concanavalin A-induced cell signaling. J Biol Chem. 2002 Mar 8;277(10):7882-8. Epub 2001 Dec 20. PMID:11751924 doi:http://dx.doi.org/10.1074/jbc.M111914200
- ↑ Zannettino AC, Roubelakis M, Welldon KJ, Jackson DE, Simmons PJ, Bendall LJ, Henniker A, Harrison KL, Niutta S, Bradstock KF, Watt SM. Novel mesenchymal and haematopoietic cell isoforms of the SHP-2 docking receptor, PZR: identification, molecular cloning and effects on cell migration. Biochem J. 2003 Mar 1;370(Pt 2):537-49. doi: 10.1042/BJ20020935. PMID:12410637 doi:http://dx.doi.org/10.1042/BJ20020935
- ↑ Yu T, Liang L, Zhao X, Yin Y. Structural and biochemical studies of the extracellular domain of Myelin protein zero-like protein 1. Biochem Biophys Res Commun. 2018 Dec 2;506(4):883-890. doi:, 10.1016/j.bbrc.2018.10.161. Epub 2018 Nov 2. PMID:30392906 doi:http://dx.doi.org/10.1016/j.bbrc.2018.10.161
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