3djk
From Proteopedia
Wild Type HIV-1 Protease with potent Antiviral inhibitor GRL-0255A
Template:ABSTRACT PUBMED 18783203
About this Structure
3DJK is a 2 chains structure of sequences from Human immunodeficiency virus 1. Full crystallographic information is available from OCA.
Reference
- Ghosh AK, Gemma S, Baldridge A, Wang YF, Kovalevsky AY, Koh Y, Weber IT, Mitsuya H. Flexible Cyclic Ethers/Polyethers as Novel P2-Ligands for HIV-1 Protease Inhibitors: Design, Synthesis, Biological Evaluation, and Protein-Ligand X-ray Studies. J Med Chem. 2008 Sep 11. PMID:18783203 doi:10.1021/jm8004543
Page seeded by OCA on Wed Feb 18 09:43:42 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
