Rerefined model

PDB 5U9D|dpdb_p1fiehnv

Rerefined model

Discovery of a potent BTK inhibitor with a novel binding mode using parallel selections with a DNA-encoded chemical library

Program
PHENIX 2.0_5824
Model type
Multiconformer
Purpose
Refinement
Atoms
2,831
Residues
271
Protein chains
1
Alternate-location fraction
9.59%
Ligands
83P, EDO, PEG

Evaluations

R-work
0.168
R-free
0.193
Clashscore
7.8

Macromolecules

The same in every model of this entry.

Entity 1
MoleculeChainsLengthOrganismUniProtDetails
Tyrosine-protein kinase BTK271
  • ConstructKINASE DOMAIN, UNP residues 423-693

Data

L0 Raw
L1 Processed
L2 Models
L3 Evaluations