IMIDAZOPYRIDINES: A POTENT AND SELECTIVE CLASS OF CYCLIN-DEPENDENT KINASE INHIBITORS IDENTIFIED THROUGH STRUCTURE-BASED HYBRIDISATION
The structure was published by Anderson, M., Beattie, J.F., Breault, G.A., et al., Stanway, J., Thomas, A.P., and Jewsbury, P.J., in 2003 in a paper entitled "Imidazo[1,2-A]Pyridines: A Potent and Selective Class of Cyclin-Dependent Kinase Inhibitors Identified Through Structure-Based Hybridisation" (abstract).
This crystal structure was determined using X-ray diffraction at a resolution of 1.6 Å and deposited in 2003.
The experimental data on which the structure is based was also deposited.
The PDB entry contains the structure of CELL DIVISION PROTEIN KINASE 2.
It also contains one or more heterogenic compounds (e.g., ligands, co-factors, ions, modified amino acids, etc.); see here for a complete list.
The molecule is most likely monomeric.
The following tables show cross-reference information to other databases (to obtain a list of all PDB entries sharing the same property or classification, click on the magnifying glass icon):
This entry contains 1 unique UniProt protein: