qFit model
PDB 6GE0|dpdb_22p0fs6k
qFit 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
- Model Building
- Atoms
- 5,402
- Residues
- 343
- Protein chains
- 1
- Alternate-location fraction
- 78.43%
- Ligands
- CME, DMS, EVQ, SO4
Evaluations
R-work
0.178
R-free
0.234
Clashscore
—
Macromolecules
The same in every model of this entry.
Data
L0 Raw
L1 Processed
L2 Models
L3 Evaluations