THE 1.7 A CRYSTAL STRUCTURE OF HUMAN CELL CYCLE CHECKPOINT KINASE CHK1
The structure was published by Chen, P., Luo, C., Deng, Y., et al., Lundgren, K., Kan, C.C., and O'Connor, P.M., in 2000 in a paper entitled "The 1.7 A crystal structure of human cell cycle checkpoint kinase Chk1: implications for Chk1 regulation." (abstract).
This crystal structure was determined using X-ray diffraction at a resolution of 1.7 Å and deposited in 2001.
The experimental data on which the structure is based was not deposited.
The PDB entry contains the structure of CHK1 CHECKPOINT KINASE. This molecule has the UniProt identifier O14757 (CHK1_HUMAN). The sample contained 289 residues which is < 90% of the natural sequence. Out of 289 residues 269 were observed and are deposited in the PDB.
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: