HUMAN P38 MAP KINASE INHIBITOR COMPLEX
The structure was published by Tong, L., Pav, S., White, D.M., et al., Cywin, C.L., Brown, M.L., and Pargellis, C.A., in 1997 in a paper entitled "A highly specific inhibitor of human p38 MAP kinase binds in the ATP pocket." (abstract).
This crystal structure was determined using X-ray diffraction at a resolution of 2.0 Å and deposited in 1997.
The experimental data on which the structure is based was not deposited.
The PDB entry contains the structure of P38 MAP KINASE. This molecule has the UniProt identifier Q16539 (MK14_HUMAN). The sample contained 366 residues which is 100% of the natural sequence. Out of 366 residues 43 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: