2l7w

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[[Image:2l7w.jpg|left|200px]]
 
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==Solution structure of the human Raf-1 kinase inhibitor protein==
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The line below this paragraph, containing "STRUCTURE_2l7w", creates the "Structure Box" on the page.
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<StructureSection load='2l7w' size='340' side='right'caption='[[2l7w]]' scene=''>
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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== Structural highlights ==
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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<table><tr><td colspan='2'>[[2l7w]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2L7W OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2L7W FirstGlance]. <br>
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or leave the SCENE parameter empty for the default display.
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</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=2l7w FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2l7w OCA], [https://pdbe.org/2l7w PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2l7w RCSB], [https://www.ebi.ac.uk/pdbsum/2l7w PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2l7w ProSAT]</span></td></tr>
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{{STRUCTURE_2l7w| PDB=2l7w | SCENE= }}
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</table>
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== Function ==
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===Solution structure of the human Raf-1 kinase inhibitor protein===
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[https://www.uniprot.org/uniprot/PEBP1_HUMAN PEBP1_HUMAN] Binds ATP, opioids and phosphatidylethanolamine. Has lower affinity for phosphatidylinositol and phosphatidylcholine. Serine protease inhibitor which inhibits thrombin, neuropsin and chymotrypsin but not trypsin, tissue type plasminogen activator and elastase (By similarity). Inhibits the kinase activity of RAF1 by inhibiting its activation and by dissociating the RAF1/MEK complex and acting as a competitive inhibitor of MEK phosphorylation.<ref>PMID:18294816</ref> HCNP may be involved in the function of the presynaptic cholinergic neurons of the central nervous system. HCNP increases the production of choline acetyltransferase but not acetylcholinesterase. Seems to be mediated by a specific receptor (By similarity).<ref>PMID:18294816</ref>
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== References ==
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<references/>
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==About this Structure==
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__TOC__
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[[2l7w]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2L7W OCA].
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</StructureSection>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Yi, C Y.]]
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[[Category: Large Structures]]
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[[Category: Raf-1 kinase inhibitor protein]]
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[[Category: Yi CY]]
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[[Category: Signaling protein inhibitor]]
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Current revision

Solution structure of the human Raf-1 kinase inhibitor protein

PDB ID 2l7w

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OCA

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