Rerefined model
PDB 6DAK|dpdb_eykq9zp7
Rerefined model
Discovery of Potent 2-Aryl-6,7-Dihydro-5HPyrrolo[ 1,2-a]imidazoles as WDR5 WIN-site Inhibitors Using Fragment-Based Methods and Structure-Based Design
- Program
- PHENIX 2.0_5824
- Model type
- Multiconformer
- Purpose
- Refinement
- Atoms
- 2,825
- Residues
- 304
- Protein chains
- 1
- Alternate-location fraction
- 3.29%
- Ligands
- DMS, G1Y
Evaluations
R-work
0.181
R-free
0.220
Clashscore
3.9
Macromolecules
The same in every model of this entry.
Data
L0 Raw
L1 Processed
L2 Models
L3 Evaluations