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3ZO2

The Synthesis and Evaluation of Diazaspirocyclic Protein Kinase Inhibitors

Summary for 3ZO2
Entry DOI10.2210/pdb3zo2/pdb
Related3ZO1 3ZO3 3ZO4
DescriptorCAMP-DEPENDENT PROTEIN KINASE CATALYTIC SUBUNIT ALPHA, CAMP-DEPENDENT PROTEIN KINASE INHIBITOR ALPHA, 6-(2,9-Diazaspiro[5.5]undecan-9-yl)-9H-purine, ... (6 entities in total)
Functional Keywordstransferase-inhibitor complex, transferase/inhibitor
Biological sourceBOS TAURUS (BOVINE)
More
Total number of polymer chains2
Total formula weight43798.69
Authors
Allen, C.E.,Chow, C.L.,Caldwell, J.J.,Westwood, I.M.,van Montfort, R.L.,Collins, I. (deposition date: 2013-02-20, release date: 2013-03-06, Last modification date: 2023-12-20)
Primary citationAllen, C.E.,Chow, C.L.,Caldwell, J.J.,Westwood, I.M.,van Montfort, R.L.,Collins, I.
Synthesis and evaluation of heteroaryl substituted diazaspirocycles as scaffolds to probe the ATP-binding site of protein kinases.
Bioorg. Med. Chem., 21:5707-5724, 2013
Cited by
PubMed: 23920481
DOI: 10.1016/j.bmc.2013.07.021
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.98 Å)
Structure validation

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