PDB 6cdj
PDB Information
PDB | 6CDJ |
Method | X-RAY DIFFRACTION |
Host Organism | Escherichia coli BL21(DE3) |
Gene Source | Human 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.
J. Med. Chem.
|
Header | Hydrolase/Hydrolase Inhibitor |
Released | 2018-02-08 |
Resolution | 1.130 |
CATH Insert Date | 06 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 |