4wf6

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'''Unreleased structure'''
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==Anthrax toxin lethal factor with bound small molecule inhibitor MK-31==
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<StructureSection load='4wf6' size='340' side='right' caption='[[4wf6]], [[Resolution|resolution]] 2.65&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[4wf6]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4WF6 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4WF6 FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=407:N~2~-[(4-FLUORO-3-METHYLPHENYL)SULFONYL]-N-HYDROXY-D-ALANINAMIDE'>407</scene>, <scene name='pdbligand=EDO:1,2-ETHANEDIOL'>EDO</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr>
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<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4pkq|4pkq]], [[4pkr|4pkr]], [[4pks|4pks]], [[4pkt|4pkt]], [[4pku|4pku]], [[4pkv|4pkv]], [[4pkw|4pkw]], [[1yqy|1yqy]]</td></tr>
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<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Hydrolase Hydrolase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.24.83 3.4.24.83] </span></td></tr>
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<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=4wf6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4wf6 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4wf6 RCSB], [http://www.ebi.ac.uk/pdbsum/4wf6 PDBsum]</span></td></tr>
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</table>
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== Function ==
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[[http://www.uniprot.org/uniprot/LEF_BACAN LEF_BACAN]] One of the three proteins composing the anthrax toxin, the agent which infects many mammalian species and that may cause death. LF is the lethal factor that, when associated with PA, causes death. LF is not toxic by itself. It is a protease that cleaves the N-terminal of most dual specificity mitogen-activated protein kinase kinases (MAPKKs or MAP2Ks) (except for MAP2K5). Cleavage invariably occurs within the N-terminal proline-rich region preceding the kinase domain, thus disrupting a sequence involved in directing specific protein-protein interactions necessary for the assembly of signaling complexes. There may be other cytosolic targets of LF involved in cytotoxicity. The proteasome may mediate a toxic process initiated by LF in the cell cytosol involving degradation of unidentified molecules that are essential for macrophage homeostasis. This is an early step in LeTx intoxication, but it is downstream of the cleavage by LF of MEK1 or other putative substrates.<ref>PMID:9563949</ref> <ref>PMID:9703991</ref> <ref>PMID:10475971</ref> <ref>PMID:11104681</ref> <ref>PMID:10338520</ref>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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A potent and selective anthrax LF inhibitor 40, (2R)-2-[(4-fluoro-3-methylphenyl)sulfonylamino]-N-hydroxy-2-(tetrahydro-2H-pyran- 4-yl)acetamide, was identified through SAR study of a high throughput screen lead. It has an IC50 of 54 nM in the enzyme assay and an IC50 of 210 nM in the macrophage cytotoxicity assay. Compound 40 is also effective in vivo in several animal model studies.
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The entry 4wf6 is ON HOLD until Paper Publication
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The discovery of a potent and selective lethal factor inhibitor for adjunct therapy of anthrax infection.,Xiong Y, Wiltsie J, Woods A, Guo J, Pivnichny JV, Tang W, Bansal A, Cummings RT, Cunningham BR, Friedlander AM, Douglas CM, Salowe SP, Zaller DM, Scolnick EM, Schmatz DM, Bartizal K, Hermes JD, MacCoss M, Chapman KT Bioorg Med Chem Lett. 2006 Feb 15;16(4):964-8. Epub 2005 Dec 9. PMID:16338135<ref>PMID:16338135</ref>
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Authors: Maize, K.M., De la Mora-Rey, T., Finzel, B.C.
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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</div>
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Description: Anthrax toxin lethal factor with bound small molecule inhibitor MK-31
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== References ==
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[[Category: Unreleased Structures]]
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<references/>
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[[Category: De La Mora-Rey, T]]
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__TOC__
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[[Category: Maize, K.M]]
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</StructureSection>
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[[Category: Finzel, B.C]]
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[[Category: Hydrolase]]
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[[Category: Finzel, B C]]
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[[Category: Maize, K M]]
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[[Category: Mora-Rey, T De la]]
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[[Category: Anthrax toxin]]
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[[Category: Hydrolase-hydrolase inhibitor complex]]
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[[Category: Lethal factor]]
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[[Category: Metalloprotease]]
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[[Category: Metalloproteinase]]

Revision as of 11:10, 9 September 2015

Anthrax toxin lethal factor with bound small molecule inhibitor MK-31

4wf6, resolution 2.65Å

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