1vcj
From Proteopedia
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[[Image:1vcj.gif|left|200px]] | [[Image:1vcj.gif|left|200px]] | ||
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| - | | | + | {{STRUCTURE_1vcj| PDB=1vcj | SCENE= }} |
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'''Influenza B virus neuraminidase complexed with 1-(4-Carboxy-2-(3-pentylamino)phenyl)-5-aminomethyl-5-hydroxymethyl-pyrrolidin-2-one''' | '''Influenza B virus neuraminidase complexed with 1-(4-Carboxy-2-(3-pentylamino)phenyl)-5-aminomethyl-5-hydroxymethyl-pyrrolidin-2-one''' | ||
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==About this Structure== | ==About this Structure== | ||
| - | 1VCJ is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Influenza_b_virus Influenza b virus]. This structure supersedes the now removed PDB entry | + | 1VCJ is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Influenza_b_virus Influenza b virus]. This structure supersedes the now removed PDB entry [http://oca.weizmann.ac.il/oca-bin/send-pdb?obs=1&id=1uja 1uja]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1VCJ OCA]. |
==Reference== | ==Reference== | ||
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[[Category: Lommer, B S.]] | [[Category: Lommer, B S.]] | ||
[[Category: Luo, M.]] | [[Category: Luo, M.]] | ||
| - | [[Category: | + | [[Category: Benzoic acid inhibitor]] |
| - | [[Category: | + | [[Category: Neuraminidase]] |
| - | [[Category: | + | [[Category: Protein-inhibitor complex]] |
| - | [[Category: | + | [[Category: Small molecule inhibitor]] |
| - | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 12:22:21 2008'' | |
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | |
Revision as of 09:22, 3 May 2008
Influenza B virus neuraminidase complexed with 1-(4-Carboxy-2-(3-pentylamino)phenyl)-5-aminomethyl-5-hydroxymethyl-pyrrolidin-2-one
Overview
Owing to the highly conserved nature of its active site, Influenza B virus neuraminidase (NA) has emerged as a major target for the design of novel anti-influenza drugs. A benzene-ring scaffold has been used in place of the pyranose ring of sialic acid to develop simpler NA inhibitors that contain a minimal number of chiral centers. A new compound belonging to this series, BANA 207, showed significant improvement in inhibitory activity against Influenza B virus NA compared with its parent compound. Here, the structural analysis of a complex of BANA 207 with influenza virus B/Lee/40 NA is reported. The results indicate that BANA 207 forms an unexpected interaction with the crucial active-site residue Glu275 that stabilizes the side chain of this residue in a conformation previously unobserved in NA-inhibitor complexes. This change in the side-chain orientation of Glu275 alters the topology of the triglycerol pocket, which accommodates an additional lipophilic substitution at the benzene ring and may provide an explanation for the increased activity of BANA 207 against Influenza B virus NA.
About this Structure
1VCJ is a Single protein structure of sequence from Influenza b virus. This structure supersedes the now removed PDB entry 1uja. Full crystallographic information is available from OCA.
Reference
A benzoic acid inhibitor induces a novel conformational change in the active site of Influenza B virus neuraminidase., Lommer BS, Ali SM, Bajpai SN, Brouillette WJ, Air GM, Luo M, Acta Crystallogr D Biol Crystallogr. 2004 Jun;60(Pt 6):1017-23. Epub 2004, May 21. PMID:15159560 Page seeded by OCA on Sat May 3 12:22:21 2008
