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5a28

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'''Unreleased structure'''
 
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The entry 5a28 is ON HOLD until Paper Publication
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==Leishmania major N-myristoyltransferase in complex with a chlorophenyl inhibitor (compound 13).==
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<StructureSection load='5a28' size='340' side='right' caption='[[5a28]], [[Resolution|resolution]] 1.48&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5a28]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5A28 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5A28 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=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=MYA:TETRADECANOYL-COA'>MYA</scene>, <scene name='pdbligand=TUQ:4-(4-CHLORO-2-{5-[(TRIMETHYL-1H-PYRAZOL-4-YL)METHYL]-1,3,4-OXADIAZOL-2-YL}PHENOXY)PIPERIDINE'>TUQ</scene></td></tr>
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<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[5a27|5a27]]</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/Glycylpeptide_N-tetradecanoyltransferase Glycylpeptide N-tetradecanoyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.3.1.97 2.3.1.97] </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=5a28 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5a28 OCA], [http://pdbe.org/5a28 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5a28 RCSB], [http://www.ebi.ac.uk/pdbsum/5a28 PDBsum]</span></td></tr>
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</table>
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== Function ==
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[[http://www.uniprot.org/uniprot/Q4Q5S8_LEIMA Q4Q5S8_LEIMA]] Adds a myristoyl group to the N-terminal glycine residue of certain cellular proteins (By similarity).
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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N-Myristoyltransferase (NMT) is a potential drug target in Leishmania parasites. Scaffold-hopping from published inhibitors yielded the serendipitous discovery of a chemotype selective for Leishmania donovani NMT; development led to high affinity inhibitors with excellent ligand efficiency. The binding mode was characterised by crystallography and provides a structural rationale for selectivity.
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Authors: Rackham, M.D., Yu, Z., Brannigan, J.A., Heal, W.P., Paape, D., Barker, K.V., Wilkinson, A.J., Smith, D.F., Tate, E.W., Leatherbarrow, R.J.
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Discovery of high affinity inhibitors of -myristoyltransferase.,Rackham MD, Yu Z, Brannigan JA, Heal WP, Paape D, Barker KV, Wilkinson AJ, Smith DF, Leatherbarrow RJ, Tate EW Medchemcomm. 2015 Oct 8;6(10):1761-1766. Epub 2015 Aug 19. PMID:26962429<ref>PMID:26962429</ref>
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Description: Leishmania major N-myristoyltransferase in complex with a chlorophenyl inhibitor (compound 13).
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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<div class="pdbe-citations 5a28" style="background-color:#fffaf0;"></div>
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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: Glycylpeptide N-tetradecanoyltransferase]]
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[[Category: Barker, K V]]
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[[Category: Brannigan, J A]]
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[[Category: Heal, W P]]
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[[Category: Leatherbarrow, R J]]
[[Category: Paape, D]]
[[Category: Paape, D]]
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[[Category: Rackham, M D]]
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[[Category: Smith, D F]]
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[[Category: Tate, E W]]
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[[Category: Wilkinson, A J]]
[[Category: Yu, Z]]
[[Category: Yu, Z]]
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[[Category: Tate, E.W]]
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[[Category: Drug design]]
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[[Category: Wilkinson, A.J]]
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[[Category: Inhibitor]]
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[[Category: Barker, K.V]]
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[[Category: Myristoylation]]
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[[Category: Leatherbarrow, R.J]]
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[[Category: Transferase]]
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[[Category: Brannigan, J.A]]
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[[Category: Rackham, M.D]]
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[[Category: Smith, D.F]]
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[[Category: Heal, W.P]]
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Revision as of 12:58, 11 May 2016

Leishmania major N-myristoyltransferase in complex with a chlorophenyl inhibitor (compound 13).

5a28, resolution 1.48Å

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