3dk1
From Proteopedia
Wild Type HIV-1 Protease with potent Antiviral inhibitor GRL-0105A
Template:ABSTRACT PUBMED 18843400
About this Structure
3DK1 is a 2 chains structure of sequences from Human immunodeficiency virus 1. Full crystallographic information is available from OCA.
Reference
- Ghosh AK, Gemma S, Takayama J, Baldridge A, Leshchenko-Yashchuk S, Miller HB, Wang YF, Kovalevsky AY, Koh Y, Weber IT, Mitsuya H. Potent HIV-1 protease inhibitors incorporating meso-bicyclic urethanes as P2-ligands: structure-based design, synthesis, biological evaluation and protein-ligand X-ray studies. Org Biomol Chem. 2008 Oct 21;6(20):3703-13. Epub 2008 Aug 11. PMID:18843400 doi:10.1039/b809178a
Page seeded by OCA on Wed May 13 09:57:29 2009
Categories: HIV-1 retropepsin | Human immunodeficiency virus 1 | Wang, Y F. | Weber, I T. | Aid | Aspartyl protease | Capsid maturation | Capsid protein | Cytoplasm | Dna integration | Dna recombination | Dna-directed dna polymerase | Endonuclease | Hiv-1 | Hydrolase | Lipoprotein | Magnesium | Metal-binding | Multifunctional enzyme | Myristate | Nuclease | Nucleotidyltransferase | Nucleus | Phosphoprotein | Protease | Protease inhibitor | Ribosomal frameshifting | Rna-binding | Rna-directed dna polymerase | Transferase | Viral nucleoprotein | Virion | Wild type protease | Zinc | Zinc-finger
