4ln7
From Proteopedia
(Difference between revisions)
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- | + | {{STRUCTURE_4ln7| PDB=4ln7 | SCENE= }} | |
+ | ===5,6-bis(4-fluorophenyl)-3-hydroxy-2,5-dihydropyridin-2-one bound to influenza 2009 pH1N1 endonuclease=== | ||
+ | {{ABSTRACT_PUBMED_23978130}} | ||
- | + | ==Function== | |
+ | [[http://www.uniprot.org/uniprot/F0TRT1_9INFA F0TRT1_9INFA]] Implicated in endonuclease cleavage of capped RNA primers. Displays an elongation factor activity in viral RNA synthesis. Dispensable for viral transcription, but not replication (By similarity).[SAAS:SAAS001009_004_020464] | ||
- | + | ==About this Structure== | |
+ | [[4ln7]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Influenza_a_virus_(a/lima/wrair1695p/2009(h1n1)) Influenza a virus (a/lima/wrair1695p/2009(h1n1))]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4LN7 OCA]. | ||
- | + | ==Reference== | |
+ | <ref group="xtra">PMID:023978130</ref><references group="xtra"/><references/> | ||
+ | [[Category: Arnold, E.]] | ||
+ | [[Category: Bauman, J D.]] | ||
+ | [[Category: Das, K.]] | ||
+ | [[Category: Patel, D.]] | ||
+ | [[Category: Cap-snatching]] | ||
+ | [[Category: Rna binding protein-inhibitor]] | ||
+ | [[Category: Rna binding protein-inhibitor complex]] |
Revision as of 04:15, 20 September 2013
Contents |
5,6-bis(4-fluorophenyl)-3-hydroxy-2,5-dihydropyridin-2-one bound to influenza 2009 pH1N1 endonuclease
Template:ABSTRACT PUBMED 23978130
Function
[F0TRT1_9INFA] Implicated in endonuclease cleavage of capped RNA primers. Displays an elongation factor activity in viral RNA synthesis. Dispensable for viral transcription, but not replication (By similarity).[SAAS:SAAS001009_004_020464]
About this Structure
4ln7 is a 1 chain structure with sequence from Influenza a virus (a/lima/wrair1695p/2009(h1n1)). Full crystallographic information is available from OCA.
Reference
- Bauman JD, Patel D, Baker SF, Vijayan RS, Xiang A, Parhi AK, Martinez-Sobrido L, Lavoie EJ, Das K, Arnold E. Crystallographic Fragment Screening and Structure-Based Optimization Yields a New Class of Influenza Endonuclease Inhibitors. ACS Chem Biol. 2013 Sep 13. PMID:23978130 doi:10.1021/cb400400j