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1hfn

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[[Image:1hfn.gif|left|200px]]
 
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{{Structure
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==NMR solution structures of vMIP-II 1-71 from Kaposi's sarcoma-associated herpesvirus.==
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|PDB= 1hfn |SIZE=350|CAPTION= <scene name='initialview01'>1hfn</scene>
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<StructureSection load='1hfn' size='340' side='right'caption='[[1hfn]]' scene=''>
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|SITE=
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== Structural highlights ==
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|LIGAND=
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<table><tr><td colspan='2'>[[1hfn]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Human_gammaherpesvirus_8 Human gammaherpesvirus 8]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1HFN OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1HFN FirstGlance]. <br>
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|ACTIVITY=
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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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|GENE=
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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=1hfn FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1hfn OCA], [https://pdbe.org/1hfn PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1hfn RCSB], [https://www.ebi.ac.uk/pdbsum/1hfn PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1hfn ProSAT]</span></td></tr>
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}}
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</table>
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== Function ==
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'''NMR SOLUTION STRUCTURES OF VMIP-II 1-71 FROM KAPOSI'S SARCOMA-ASSOCIATED HERPESVIRUS.'''
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[https://www.uniprot.org/uniprot/VMI2_HHV8P VMI2_HHV8P] Blocks infection by several different human immunodeficiency virus type 1 (HIV-1) strains. This occurs because vMIP-II binds to a wide range of chemokine receptors. May form part of the response to host defenses contributing to virus-induced neoplasia and may have relevance to KSHV and HIV-I interactions.
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== Evolutionary Conservation ==
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[[Image:Consurf_key_small.gif|200px|right]]
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==Overview==
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Check<jmol>
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Kaposi's sarcoma-associated herpesvirus encodes a chemokine called vMIP-II that has been shown to be a broad range human chemokine receptor antagonist. Two N-terminal peptides, vMIP-II(1-10) and vMIP-II(1-11)dimer (dimerised through Cys11) were synthesised. Both peptides are shown to bind the CXC chemokine receptor 4 (CXCR4). vMIP-II(1-10) was 1400-fold less potent than the native protein whilst the vMIP-II(1-11)dimer was only 180-fold less potent. In addition, both peptides are CXCR4 antagonists. Through analysis of non-standard, long mixing time two-dimensional nuclear Overhauser enhancement spectroscopy experiments, 13C relaxation data and amide chemical shift temperature gradients for the N-terminus of vMIP-II, we show that this region populates a turn-like structure over residues 5-8, both in the presence and absence of the full protein scaffold. This major conformation is likely to be in fast exchange with other conformational states but it has not previously been detected in monomeric chemokine structures. This and other studies [Elisseeva et al. (2000) J. Biol. Chem. 275, 26799-26805] suggest that there may be a link between the structuring of the short N-terminal chemokine peptides and their ability to bind their receptor.
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<jmolCheckbox>
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<scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/hf/1hfn_consurf.spt"</scriptWhenChecked>
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==About this Structure==
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<scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
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1HFN is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Human_herpesvirus_4 Human herpesvirus 4]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1HFN OCA].
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<text>to colour the structure by Evolutionary Conservation</text>
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</jmolCheckbox>
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==Reference==
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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=1hfn ConSurf].
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Structure/function of human herpesvirus-8 MIP-II (1-71) and the antagonist N-terminal segment (1-10)., Crump MP, Elisseeva E, Gong J, Clark-Lewis I, Sykes BD, FEBS Lett. 2001 Feb 2;489(2-3):171-5. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/11165244 11165244]
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<div style="clear:both"></div>
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[[Category: Human herpesvirus 4]]
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__TOC__
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[[Category: Single protein]]
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</StructureSection>
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[[Category: Clark-Lewis, I.]]
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[[Category: Human gammaherpesvirus 8]]
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[[Category: Crump, M P.]]
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[[Category: Large Structures]]
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[[Category: Elisseeva, E.]]
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[[Category: Clark-Lewis I]]
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[[Category: Gong, J H.]]
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[[Category: Crump MP]]
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[[Category: Sykes, B D.]]
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[[Category: Elisseeva E]]
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[[Category: anatagonist]]
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[[Category: Gong J-H]]
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[[Category: chemokine]]
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[[Category: Sykes BD]]
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[[Category: cxcr4]]
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[[Category: vmip-ii]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 11:36:32 2008''
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Current revision

NMR solution structures of vMIP-II 1-71 from Kaposi's sarcoma-associated herpesvirus.

PDB ID 1hfn

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