5kpn

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(New page: '''Unreleased structure''' The entry 5kpn is ON HOLD Authors: Cao, R., Wang, Y.L., Zhou, J., Yao, H.P., Huang, N., Xu, B.L. Description: Structure of human PARP1 catalytic domain bound...)
Current revision (10:50, 27 September 2023) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 5kpn is ON HOLD
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==Structure of human PARP1 catalytic domain bound to a quinazoline-2,4(1H,3H)-dione inhibitor==
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<StructureSection load='5kpn' size='340' side='right'caption='[[5kpn]], [[Resolution|resolution]] 2.30&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5kpn]] is a 2 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=5KPN OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5KPN 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]] 2.3&#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=6WX:1-[[4-FLUORANYL-3-(3-OXIDANYLIDENE-4-PROPYL-PIPERAZIN-1-YL)CARBONYL-PHENYL]METHYL]QUINAZOLINE-2,4-DIONE'>6WX</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=5kpn FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5kpn OCA], [https://pdbe.org/5kpn PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5kpn RCSB], [https://www.ebi.ac.uk/pdbsum/5kpn PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5kpn ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/PARP1_HUMAN PARP1_HUMAN] Involved in the base excision repair (BER) pathway, by catalyzing the poly(ADP-ribosyl)ation of a limited number of acceptor proteins involved in chromatin architecture and in DNA metabolism. This modification follows DNA damages and appears as an obligatory step in a detection/signaling pathway leading to the reparation of DNA strand breaks. Mediates the poly(ADP-ribosyl)ation of APLF and CHFR. Positively regulates the transcription of MTUS1 and negatively regulates the transcription of MTUS2/TIP150. With EEF1A1 and TXK, forms a complex that acts as a T-helper 1 (Th1) cell-specific transcription factor and binds the promoter of IFN-gamma to directly regulate its transcription, and is thus involved importantly in Th1 cytokine production.<ref>PMID:17177976</ref> <ref>PMID:18172500</ref> <ref>PMID:19344625</ref> <ref>PMID:19661379</ref>
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Authors: Cao, R., Wang, Y.L., Zhou, J., Yao, H.P., Huang, N., Xu, B.L.
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==See Also==
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*[[Poly(ADP-ribose) polymerase 3D structures|Poly(ADP-ribose) polymerase 3D structures]]
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Description: Structure of human PARP1 catalytic domain bound to a quinazoline-2,4(1H,3H)-dione inhibitor
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== References ==
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[[Category: Unreleased Structures]]
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<references/>
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[[Category: Huang, N]]
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__TOC__
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[[Category: Yao, H.P]]
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</StructureSection>
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[[Category: Wang, Y.L]]
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[[Category: Homo sapiens]]
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[[Category: Cao, R]]
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[[Category: Large Structures]]
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[[Category: Xu, B.L]]
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[[Category: Cao R]]
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[[Category: Zhou, J]]
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[[Category: Huang N]]
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[[Category: Wang YL]]
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[[Category: Xu BL]]
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[[Category: Yao HP]]
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[[Category: Zhou J]]

Current revision

Structure of human PARP1 catalytic domain bound to a quinazoline-2,4(1H,3H)-dione inhibitor

PDB ID 5kpn

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