Deposited model
PDB 1MHW|dpdb_lc6xjkmk
Deposited model
Design of non-covalent inhibitors of human cathepsin L. From the 96-residue proregion to optimized tripeptides
- Program
- CNS 1.0
- Model type
- Deposited
- Purpose
- Reference
- Authors
- Chowdhury, S., Sivaraman, J., Wang, J., Devanathan, G., Lachance, P., Qi, H., Menard, R., Lefebvre, J., Konishi, Y., Cygler, M., Sulea, T., Purisima, E.O.
- Atoms
- 4,007
- Residues
- 446
- Protein chains
- 8
- Unmodeled fraction
- 1.76%
Evaluations
R-work
0.185
R-free
0.230
Clashscore
8.5
Macromolecules
The same in every model of this entry.
| Entity 3 | |||||
|---|---|---|---|---|---|
| Molecule | Chains | Length | Organism | UniProt | Details |
| 4-biphenylacetyl-Cys-(D)Arg-Tyr-N-(2-phenylethyl) amide | 5 | — | — | — | |
Data
L0 Raw
L1 Processed
L2 Models
L3 Evaluations