PDB Information

PDB5IMX
MethodX-RAY DIFFRACTION
Host OrganismEscherichia coli
Gene SourceHomo sapiens
Primary Citation
Design and synthesis of novel 3-sulfonylpyrazol-4-amino pyrimidines as potent anaplastic lymphoma kinase (ALK) inhibitors.
Zhang, P., Dong, J., Zhong, B., Zhang, D., Yuan, H., Jin, C., Xu, X., Li, H., Zhou, Y., Liang, Z., Ji, M., Xu, T., Song, G., Zhang, L., Chen, G., Meng, X., Sun, D., Shih, J., Zhang, R., Hou, G., Wang, C., Jin, Y., Yang, Q.
Bioorg.Med.Chem.Lett.
HeaderTransferase/Transferase Inhibitor
Released2016-03-07
Resolution2.120
CATH Insert Date15 May, 2016

PDB Images (4)

PDB Prints

PDB Chains (1)

Chain ID Date inserted into CATH CATH Status
A 16 May, 2016 Chopped

CATH Domains (2)

Domain ID Date inserted into CATH Superfamily CATH Status
5imxA01 18 Jul, 2016 3.30.200.20 Assigned
5imxA02 18 Jul, 2016 1.10.510.10 Assigned

UniProtKB Entries (1)

Accession Gene ID Taxon Description
Q9UM73 ALK_HUMAN Homo sapiens ALK tyrosine kinase receptor
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