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3l3l
From Proteopedia
(Difference between revisions)
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| + | [[Image:3l3l.jpg|left|200px]] | ||
| - | The | + | <!-- |
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| + | {{STRUCTURE_3l3l| PDB=3l3l | SCENE= }} | ||
| - | + | ===PARP complexed with A906894=== | |
| - | Description: PARP complexed with A906894 | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | + | <!-- |
| + | The line below this paragraph, {{ABSTRACT_PUBMED_20045315}}, adds the Publication Abstract to the page | ||
| + | (as it appears on PubMed at http://www.pubmed.gov), where 20045315 is the PubMed ID number. | ||
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| + | {{ABSTRACT_PUBMED_20045315}} | ||
| + | |||
| + | ==About this Structure== | ||
| + | 3L3L is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3L3L OCA]. | ||
| + | |||
| + | ==Reference== | ||
| + | <ref group="xtra">PMID:20045315</ref><references group="xtra"/> | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Park, C H.]] | ||
| + | [[Category: Adp-ribosylation]] | ||
| + | [[Category: Dna damage]] | ||
| + | [[Category: Dna repair]] | ||
| + | [[Category: Dna-binding]] | ||
| + | [[Category: Glycosyltransferase]] | ||
| + | [[Category: Metal-binding]] | ||
| + | [[Category: Nad]] | ||
| + | [[Category: Nucleus]] | ||
| + | [[Category: Phosphoprotein]] | ||
| + | [[Category: Protein-inhibitor complex]] | ||
| + | [[Category: Transcription]] | ||
| + | [[Category: Transcription regulation]] | ||
| + | [[Category: Transferase]] | ||
| + | |||
| + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Dec 22 09:52:38 2010'' | ||
Revision as of 06:40, 22 December 2010
PARP complexed with A906894
Template:ABSTRACT PUBMED 20045315
About this Structure
3L3L is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Gandhi VB, Luo Y, Liu X, Shi Y, Klinghofer V, Johnson EF, Park C, Giranda VL, Penning TD, Zhu GD. Discovery and SAR of substituted 3-oxoisoindoline-4-carboxamides as potent inhibitors of poly(ADP-ribose) polymerase (PARP) for the treatment of cancer. Bioorg Med Chem Lett. 2010 Feb 1;20(3):1023-6. Epub 2009 Dec 14. PMID:20045315 doi:10.1016/j.bmcl.2009.12.042
Page seeded by OCA on Wed Dec 22 09:52:38 2010
