2uzy

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[[Image:2uzy.jpg|left|200px]]<br /><applet load="2uzy" size="350" color="white" frame="true" align="right" spinBox="true"
 
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caption="2uzy, resolution 4.0&Aring;" />
 
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'''STRUCTURE OF THE HUMAN RECEPTOR TYROSINE KINASE MET IN COMPLEX WITH THE LISTERIA MONOCYTOGENES INVASION PROTEIN INLB: LOW RESOLUTION, CRYSTAL FORM II'''<br />
 
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==Overview==
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==Structure of the human receptor tyrosine kinase Met in complex with the Listeria monocytogenes invasion protein inlb: low resolution, Crystal form II==
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The tyrosine kinase Met, the product of the c-met proto-oncogene and the, receptor for hepatocyte growth factor/scatter factor (HGF/SF), mediates, signals critical for cell survival and migration. The human pathogen, Listeria monocytogenes exploits Met signaling for invasion of host cells, via its surface protein InlB. We present the crystal structure of the, complex between a large fragment of the human Met ectodomain and the, Met-binding domain of InlB. The concave face of the InlB leucine-rich, repeat region interacts tightly with the first immunoglobulin-like domain, of the Met stalk, a domain which does not bind HGF/SF. A second contact, between InlB and the Met Sema domain locks the otherwise flexible receptor, in a rigid, signaling competent conformation. Full Met activation requires, the additional C-terminal domains of InlB which induce heparin-mediated, receptor clustering and potent signaling. Thus, although it elicits a, similar cellular response, InlB is not a structural mimic of HGF/SF.
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<StructureSection load='2uzy' size='340' side='right'caption='[[2uzy]], [[Resolution|resolution]] 4.00&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[2uzy]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [https://en.wikipedia.org/wiki/Listeria_monocytogenes_EGD-e Listeria monocytogenes EGD-e]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2UZY OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2UZY 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]] 4&#8491;</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=2uzy FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2uzy OCA], [https://pdbe.org/2uzy PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2uzy RCSB], [https://www.ebi.ac.uk/pdbsum/2uzy PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2uzy ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/INLB_LISMO INLB_LISMO] Mediates the entry of Listeria monocytogenes into cells.
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== Evolutionary Conservation ==
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[[Image:Consurf_key_small.gif|200px|right]]
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Check<jmol>
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<jmolCheckbox>
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<scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/uz/2uzy_consurf.spt"</scriptWhenChecked>
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<scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview03.spt</scriptWhenUnchecked>
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<text>to colour the structure by Evolutionary Conservation</text>
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</jmolCheckbox>
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</jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=2uzy ConSurf].
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<div style="clear:both"></div>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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The tyrosine kinase Met, the product of the c-met proto-oncogene and the receptor for hepatocyte growth factor/scatter factor (HGF/SF), mediates signals critical for cell survival and migration. The human pathogen Listeria monocytogenes exploits Met signaling for invasion of host cells via its surface protein InlB. We present the crystal structure of the complex between a large fragment of the human Met ectodomain and the Met-binding domain of InlB. The concave face of the InlB leucine-rich repeat region interacts tightly with the first immunoglobulin-like domain of the Met stalk, a domain which does not bind HGF/SF. A second contact between InlB and the Met Sema domain locks the otherwise flexible receptor in a rigid, signaling competent conformation. Full Met activation requires the additional C-terminal domains of InlB which induce heparin-mediated receptor clustering and potent signaling. Thus, although it elicits a similar cellular response, InlB is not a structural mimic of HGF/SF.
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==About this Structure==
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Structure of the human receptor tyrosine kinase met in complex with the Listeria invasion protein InlB.,Niemann HH, Jager V, Butler PJ, van den Heuvel J, Schmidt S, Ferraris D, Gherardi E, Heinz DW Cell. 2007 Jul 27;130(2):235-46. PMID:17662939<ref>PMID:17662939</ref>
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2UZY is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [http://en.wikipedia.org/wiki/Listeria_monocytogenes Listeria monocytogenes]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2UZY OCA].
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==Reference==
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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Structure of the Human Receptor Tyrosine Kinase Met in Complex with the Listeria Invasion Protein InlB., Niemann HH, Jager V, Butler PJ, van den Heuvel J, Schmidt S, Ferraris D, Gherardi E, Heinz DW, Cell. 2007 Jul 27;130(2):235-246. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=17662939 17662939]
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</div>
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[[Category: Homo sapiens]]
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<div class="pdbe-citations 2uzy" style="background-color:#fffaf0;"></div>
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[[Category: Listeria monocytogenes]]
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[[Category: Protein complex]]
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[[Category: Butler, P.J.G.]]
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[[Category: Ferraris, D.]]
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[[Category: Gherardi, E.]]
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[[Category: Heinz, D.W.]]
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[[Category: Heuvel, J.Van.Den.]]
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[[Category: Jager, V.]]
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[[Category: Niemann, H.H.]]
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[[Category: Schmidt, S.]]
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[[Category: alternative splicing]]
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[[Category: atp-binding]]
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[[Category: chromosomal rearrangement]]
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[[Category: disease mutation]]
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[[Category: glycoprotein]]
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[[Category: hepatocyte growth factor receptor]]
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[[Category: hgfr]]
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[[Category: internalin]]
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[[Category: kinase]]
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[[Category: leucine rich repeat]]
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[[Category: leucine-rich repeat]]
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[[Category: lrr]]
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[[Category: membrane]]
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[[Category: nucleotide-binding]]
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[[Category: phosphorylation]]
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[[Category: polymorphism]]
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[[Category: proto-oncogene]]
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[[Category: receptor]]
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[[Category: receptor ectodomain]]
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[[Category: signaling protein/receptor complex]]
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[[Category: transferase]]
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[[Category: transmembrane]]
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[[Category: tyrosine-protein kinase]]
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[[Category: virulence factor]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jan 23 14:18:49 2008''
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==See Also==
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*[[Hepatocyte growth factor receptor 3D structures|Hepatocyte growth factor receptor 3D structures]]
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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: Listeria monocytogenes EGD-e]]
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[[Category: Butler PJG]]
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[[Category: Ferraris D]]
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[[Category: Gherardi E]]
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[[Category: Heinz DW]]
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[[Category: Jager V]]
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[[Category: Niemann HH]]
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[[Category: Schmidt S]]
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[[Category: Van den Heuvel J]]

Current revision

Structure of the human receptor tyrosine kinase Met in complex with the Listeria monocytogenes invasion protein inlb: low resolution, Crystal form II

PDB ID 2uzy

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