5ccr

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'''Unreleased structure'''
 
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The entry 5ccr is ON HOLD until Paper Publication
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==Human Cyclophilin D Complexed with Inhibitor==
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<StructureSection load='5ccr' size='340' side='right' caption='[[5ccr]], [[Resolution|resolution]] 1.90&Aring;' scene=''>
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Authors:
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5ccr]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5CCR OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5CCR FirstGlance]. <br>
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Description:
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=4ZT:ETHYL+N-[(4-AMINOBENZYL)CARBAMOYL]-L-METHIONINATE'>4ZT</scene>, <scene name='pdbligand=FMT:FORMIC+ACID'>FMT</scene>, <scene name='pdbligand=K:POTASSIUM+ION'>K</scene>, <scene name='pdbligand=PEG:DI(HYDROXYETHYL)ETHER'>PEG</scene>, <scene name='pdbligand=PG4:TETRAETHYLENE+GLYCOL'>PG4</scene>, <scene name='pdbligand=PGE:TRIETHYLENE+GLYCOL'>PGE</scene></td></tr>
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[[Category: Unreleased Structures]]
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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/Peptidylprolyl_isomerase Peptidylprolyl isomerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=5.2.1.8 5.2.1.8] </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=5ccr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5ccr OCA], [http://pdbe.org/5ccr PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5ccr RCSB], [http://www.ebi.ac.uk/pdbsum/5ccr PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5ccr ProSAT]</span></td></tr>
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</table>
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== Function ==
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[[http://www.uniprot.org/uniprot/PPIF_HUMAN PPIF_HUMAN]] PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides. Involved in regulation of the mitochondrial permeability transition pore (mPTP). It is proposed that its association with the mPTP is masking a binding site for inhibiting inorganic phosphate (Pi) and promotes the open probablity of the mPTP leading to apoptosis or necrosis; the requirement of the PPIase activity for this function is debated. In cooperation with mitochondrial TP53 is involved in activating oxidative stress-induced necrosis. Involved in modulation of mitochondrial membrane F(1)F(0) ATP synthase activity and regulation of mitochondrial matrix adenine nucleotide levels. Has anti-apoptotic activity independently of mPTP and in cooperation with BCL2 inhibits cytochrome c-dependent apoptosis.<ref>PMID:19228691</ref> <ref>PMID:22726440</ref>
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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: Peptidylprolyl isomerase]]
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[[Category: Awais, M]]
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[[Category: Berry, N]]
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[[Category: Gibson, R P]]
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[[Category: Javed, A]]
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[[Category: Kershaw, N]]
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[[Category: Latawiec, D]]
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[[Category: Lian, L Y]]
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[[Category: Neill, P O]]
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[[Category: Pandalaneni, S]]
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[[Category: Shore, E]]
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[[Category: Sutton, R]]
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[[Category: Wen, L]]
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[[Category: Complex]]
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[[Category: Cyclophilin]]
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[[Category: Inhibitor]]
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[[Category: Isomerase]]

Revision as of 15:26, 26 July 2016

Human Cyclophilin D Complexed with Inhibitor

5ccr, resolution 1.90Å

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