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3e7b
From Proteopedia
(Difference between revisions)
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===Crystal Structure of Protein Phosphatase-1 Bound to the natural toxin inhibitor Tautomycin=== | ===Crystal Structure of Protein Phosphatase-1 Bound to the natural toxin inhibitor Tautomycin=== | ||
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| + | The line below this paragraph, {{ABSTRACT_PUBMED_18992256}}, adds the Publication Abstract to the page | ||
| + | (as it appears on PubMed at http://www.pubmed.gov), where 18992256 is the PubMed ID number. | ||
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| + | {{ABSTRACT_PUBMED_18992256}} | ||
==About this Structure== | ==About this Structure== | ||
| - | 3E7B is a | + | 3E7B is a 2 chains structure of sequences 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=3E7B OCA]. |
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| + | ==Reference== | ||
| + | Crystal structures of protein phosphatase-1 bound to nodularin-R and tautomycin: a novel scaffold for structure-based drug design of serine/threonine phosphatase inhibitors., Kelker MS, Page R, Peti W, J Mol Biol. 2009 Jan 9;385(1):11-21. Epub 2008 Nov 1. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/18992256 18992256] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Phosphoprotein phosphatase]] | [[Category: Phosphoprotein phosphatase]] | ||
| - | [[Category: Single protein]] | ||
[[Category: Kelker, M S.]] | [[Category: Kelker, M S.]] | ||
[[Category: Page, R.]] | [[Category: Page, R.]] | ||
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[[Category: Tautomycin]] | [[Category: Tautomycin]] | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jan 14 12:41:53 2009'' |
Revision as of 10:41, 14 January 2009
Crystal Structure of Protein Phosphatase-1 Bound to the natural toxin inhibitor Tautomycin
Template:ABSTRACT PUBMED 18992256
About this Structure
3E7B is a 2 chains structure of sequences from Homo sapiens. Full crystallographic information is available from OCA.
Reference
Crystal structures of protein phosphatase-1 bound to nodularin-R and tautomycin: a novel scaffold for structure-based drug design of serine/threonine phosphatase inhibitors., Kelker MS, Page R, Peti W, J Mol Biol. 2009 Jan 9;385(1):11-21. Epub 2008 Nov 1. PMID:18992256
Page seeded by OCA on Wed Jan 14 12:41:53 2009
