PDB Information

PDB6CDJ
MethodX-RAY DIFFRACTION
Host OrganismEscherichia coli BL21(DE3)
Gene SourceHuman immunodeficiency virus 1
Primary Citation
Design and Synthesis of Highly Potent HIV-1 Protease Inhibitors Containing Tricyclic Fused Ring Systems as Novel P2 Ligands: Structure-Activity Studies, Biological and X-ray Structural Analysis.
Ghosh, A.K., R Nyalapatla, P., Kovela, S., Rao, K.V., Brindisi, M., Osswald, H.L., Amano, M., Aoki, M., Agniswamy, J., Wang, Y.F., Weber, I.T., Mitsuya, H.
J. Med. Chem.
HeaderHydrolase/Hydrolase Inhibitor
Released2018-02-08
Resolution1.130
CATH Insert Date06 Jul, 2018

PDB Images (5)

PDB Prints

PDB Chains (2)

Chain ID Date inserted into CATH CATH Status
A 06 Jul, 2018 Chopped
B 06 Jul, 2018 Chopped

CATH Domains (2)

Domain ID Date inserted into CATH Superfamily CATH Status
6cdjA00 19 Jul, 2018 2.40.70.10 Assigned
6cdjB00 19 Jul, 2018 2.40.70.10 Assigned

UniProtKB Entries (2)

Accession Gene ID Taxon Description
Q5RZ08 Q5RZ08_9HIV1 Human immunodeficiency virus 1 Protease
Q5RZ08 Q5RZ08_9HIV1 Human immunodeficiency virus 1 Protease