Thr 160 phosphorylated CDK2 - Human cyclin A3 complex with the inhibitor indirubin-5-sulphonate bound

Summary for 1E9H

Related1AQ1 1B38 1B39 1CKP 1DM2 1E1V 1E1X 1HCK 1HCL 1JSU 1FIN 1JST 1QMZ
DescriptorCELL DIVISION PROTEIN KINASE 2, CYCLIN A3, 2',3-DIOXO-1,1',2',3-TETRAHYDRO-2,3'-BIINDOLE-5'-SULFONIC ACID, ... (4 entities in total)
Functional Keywordscell cycle, complex (protein kinase-cyclin), kinases, inhibitor, cyclin, complex, phosphorylation
Biological sourceHOMO SAPIENS (HUMAN)
Cellular locationNucleus P20248
Total number of polymer chains4
Total molecular weight128360.47
Davies, T.G.,Tunnah, P.,Noble, M.E.M.,Endicott, J.A. (deposition date: 2000-10-16, release date: 2001-10-11, Last modification date: 2011-07-13)
Primary citation
Davies, T.G.,Tunnah, P.,Meijer, L.,Marko, D.,Eisenbrand, G.,Endicott, J.A.,Noble, M.E.
Inhibitor Binding to Active and Inactive Cdk2: The Crystal Structure of Cdk2-Cyclin A/Indirubin-5-Sulphonate
Structure, 9:389-, 2001
PubMed: 11377199 (PDB entries with the same primary citation)
DOI: 10.1016/S0969-2126(01)00598-6
MImport into Mendeley
Experimental method

Structure validation

ClashscoreRamachandran outliersSidechain outliers282.4%7.7%MetricValuePercentile RanksWorseBetterPercentile relative to all X-ray structuresPercentile relative to X-ray structures of similar resolution
Download full validation report