5t9u

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(New page: '''Unreleased structure''' The entry 5t9u is ON HOLD Authors: Appleby, T.C., Steadman, V., Pettit, S., Schmitz, U., Mackman, R.L., Schultz, B. Description: Discovery of a Potent Cyclop...)
Current revision (14:19, 6 March 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 5t9u is ON HOLD
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==Discovery of a Potent Cyclophilin Inhibitor (Compound 3) based on Structural Simplification of Sanglifehrin A==
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<StructureSection load='5t9u' size='340' side='right'caption='[[5t9u]], [[Resolution|resolution]] 2.30&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5t9u]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5T9U OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5T9U 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]] 2.301&#8491;</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=7HG:3-[(3-HYDROXYPHENYL)METHYL]-10,12-DIMETHOXY-9,11-DIMETHYL-6-(PROPAN-2-YL)-19-OXA-1,4,7,25-TETRAAZABICYCLO[19.3.1]PENTACOSA-13,15-DIENE-2,5,8,20-TETRONE'>7HG</scene></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=5t9u FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5t9u OCA], [https://pdbe.org/5t9u PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5t9u RCSB], [https://www.ebi.ac.uk/pdbsum/5t9u PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5t9u ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/PPIA_HUMAN PPIA_HUMAN] PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides.
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Authors: Appleby, T.C., Steadman, V., Pettit, S., Schmitz, U., Mackman, R.L., Schultz, B.
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==See Also==
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*[[Cyclophilin 3D structures|Cyclophilin 3D structures]]
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Description: Discovery of a Potent Cyclophilin Inhibitor (Compound 2) based on Structural Simplification of Sanglifehrin A
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__TOC__
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[[Category: Unreleased Structures]]
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</StructureSection>
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[[Category: Pettit, S]]
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[[Category: Homo sapiens]]
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[[Category: Mackman, R.L]]
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[[Category: Large Structures]]
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[[Category: Schmitz, U]]
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[[Category: Appleby TC]]
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[[Category: Appleby, T.C]]
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[[Category: Mackman RL]]
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[[Category: Schultz, B]]
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[[Category: Pettit S]]
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[[Category: Steadman, V]]
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[[Category: Schmitz U]]
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[[Category: Schultz B]]
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[[Category: Steadman V]]

Current revision

Discovery of a Potent Cyclophilin Inhibitor (Compound 3) based on Structural Simplification of Sanglifehrin A

PDB ID 5t9u

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