Rerefined model
PDB 6G97|dpdb_7j0fi61m
Rerefined model
Fragment-based discovery of a highly potent, orally bioavailable inhibitor which modulates the phosphorylation and catalytic activity of ERK1/2
- Program
- PHENIX 2.0_5824
- Model type
- Multiconformer
- Purpose
- Refinement
- Atoms
- 3,256
- Residues
- 344
- Protein chains
- 1
- Alternate-location fraction
- 0.58%
- Ligands
- CME, EQZ, SO4
Evaluations
R-work
0.186
R-free
0.231
Clashscore
6.6
Macromolecules
The same in every model of this entry.
Data
L0 Raw
L1 Processed
L2 Models
L3 Evaluations