1rtl: Difference between revisions
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[[Image:1rtl.png|left|200px]] | [[Image:1rtl.png|left|200px]] | ||
{{STRUCTURE_1rtl| PDB=1rtl | SCENE= }} | {{STRUCTURE_1rtl| PDB=1rtl | SCENE= }} | ||
===CRYSTAL STRUCTURE OF HCV NS3 PROTEASE DOMAIN: NS4A PEPTIDE COMPLEX WITH COVALENTLY BOUND PYRROLIDINE-5,5-TRANSLACTAM INHIBITOR=== | ===CRYSTAL STRUCTURE OF HCV NS3 PROTEASE DOMAIN: NS4A PEPTIDE COMPLEX WITH COVALENTLY BOUND PYRROLIDINE-5,5-TRANSLACTAM INHIBITOR=== | ||
{{ABSTRACT_PUBMED_14627400}} | {{ABSTRACT_PUBMED_14627400}} | ||
==About this Structure== | ==About this Structure== | ||
[[1rtl]] is a 4 chain structure of [[Helicase]] with sequence from [http://en.wikipedia.org/wiki/Hepatitis_c_virus Hepatitis c virus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1RTL OCA]. | |||
==See Also== | |||
*[[Helicase|Helicase]] | |||
==Reference== | ==Reference== | ||
<ref group="xtra">PMID: | <ref group="xtra">PMID:014627400</ref><references group="xtra"/> | ||
[[Category: Hepatitis c virus]] | [[Category: Hepatitis c virus]] | ||
[[Category: Skarzynski, T.]] | [[Category: Skarzynski, T.]] | ||
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[[Category: Translactam]] | [[Category: Translactam]] | ||
[[Category: Viral protein]] | [[Category: Viral protein]] | ||
[[Category: Viral protein complex]] | |||
Revision as of 11:11, 26 July 2012
CRYSTAL STRUCTURE OF HCV NS3 PROTEASE DOMAIN: NS4A PEPTIDE COMPLEX WITH COVALENTLY BOUND PYRROLIDINE-5,5-TRANSLACTAM INHIBITORCRYSTAL STRUCTURE OF HCV NS3 PROTEASE DOMAIN: NS4A PEPTIDE COMPLEX WITH COVALENTLY BOUND PYRROLIDINE-5,5-TRANSLACTAM INHIBITOR
Template:ABSTRACT PUBMED 14627400
About this StructureAbout this Structure
1rtl is a 4 chain structure of Helicase with sequence from Hepatitis c virus. Full crystallographic information is available from OCA.
See AlsoSee Also
ReferenceReference
- ↑ Slater MJ, Amphlett EM, Andrews DM, Bamborough P, Carey SJ, Johnson MR, Jones PS, Mills G, Parry NR, Somers DO, Stewart AJ, Skarzynski T. Pyrrolidine-5,5-trans-lactams. 4. Incorporation of a P3/P4 urea leads to potent intracellular inhibitors of hepatitis C virus NS3/4A protease. Org Lett. 2003 Nov 27;5(24):4627-30. PMID:14627400 doi:10.1021/ol035826v