{"context":{"query":">>uniprot>>pdb","source_dataset":"uniprot","target_dataset":"pdb"},"stats":{"queried":1,"total":22,"mapped":1},"pagination":{"has_next":false},"schema":"id|title|method|resolution|source_organism|chain_count|header","mappings":[{"input":"Q00534","source":"Q00534|Cyclin-dependent kinase 6","targets":["1BI7|MECHANISM OF G1 CYCLIN DEPENDENT KINASE INHIBITION FROM THE STRUCTURE OF THE CDK6-P16INK4A TUMOR SUPPRESSOR COMPLEX|X-RAY DIFFRACTION|3.4|Homo sapiens|0|COMPLEX (KINASE/ANTI-ONCOGENE)","1BI8|MECHANISM OF G1 CYCLIN DEPENDENT KINASE INHIBITION FROM THE STRUCTURES CDK6-P19INK4D INHIBITOR COMPLEX|X-RAY DIFFRACTION|2.8|Homo sapiens|0|COMPLEX (KINASE/INHIBITOR)","1BLX|P19INK4D/CDK6 COMPLEX|X-RAY DIFFRACTION|1.9|Homo sapiens; Mus musculus|0|COMPLEX (INHIBITOR PROTEIN/KINASE)","1G3N|STRUCTURE OF A P18(INK4C)-CDK6-K-CYCLIN TERNARY COMPLEX|X-RAY DIFFRACTION|2.9|Homo sapiens; Human herpesvirus 8|0|cell cycle, signaling protein","1JOW|Crystal structure of a complex of human CDK6 and a viral cyclin|X-RAY DIFFRACTION|3.1|Homo sapiens; Saimiriine herpesvirus 2|0|CELL CYCLE/TRANSFERASE","1XO2|Crystal structure of a human cyclin-dependent kinase 6 complex with a flavonol inhibitor, fisetin|X-RAY DIFFRACTION|2.9|Homo sapiens; Saimiriine herpesvirus 2|0|CELL CYCLE/TRANSFERASE","2EUF|X-ray structure of human CDK6-Vcyclin in complex with the inhibitor PD0332991|X-RAY DIFFRACTION|3|Herpesvirus saimiri (strain 11); Homo sapiens|0|CELL CYCLE/TRANSFERASE","2F2C|X-ray structure of human CDK6-Vcyclinwith the inhibitor aminopurvalanol|X-RAY DIFFRACTION|2.8|Herpesvirus saimiri (strain 11); Homo sapiens|0|CELL CYCLE/TRANSFERASE","3NUP|CDK6 (monomeric) in complex with inhibitor|X-RAY DIFFRACTION|2.6|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","3NUX|CDK6 (monomeric) in complex with inhibitor|X-RAY DIFFRACTION|2.7|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","4AUA|Liganded X-ray crystal structure of cyclin dependent kinase 6 (CDK6)|X-RAY DIFFRACTION|2.31|HOMO SAPIENS|0|TRANSFERASE","4EZ5|CDK6 (monomeric) in complex with inhibitor|X-RAY DIFFRACTION|2.7|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","4TTH|Crystal structure of a CDK6/Vcyclin complex with inhibitor bound|X-RAY DIFFRACTION|2.9|Homo sapiens; Saimiriine herpesvirus 2|0|TRANSFERASE/CELL CYCLE/INHIBITOR","5L2I|The X-ray co-crystal structure of human CDK6 and Palbociclib.|X-RAY DIFFRACTION|2.75|Homo sapiens|0|Transferase/Transferase Inhibitor","5L2S|The X-ray co-crystal structure of human CDK6 and Abemaciclib.|X-RAY DIFFRACTION|2.27|Homo sapiens|0|Transferase/Transferase Inhibitor","5L2T|The X-ray co-crystal structure of human CDK6 and Ribociclib.|X-RAY DIFFRACTION|2.37|Homo sapiens|0|Transferase/Transferase Inhibitor","6OQL|CDK6 in complex with Cpd13 (R)-5-fluoro-4-(4-methyl-5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a]azepin-3-yl)-N-(5-(4-methylpiperazin-1-yl)pyridin-2-yl)pyrimidin-2-amine|X-RAY DIFFRACTION|2.707|Homo sapiens|0|TRANSFERASE/TRANSFERASE inhibitor","6OQO|CDK6 in complex with Cpd24 N-(5-(6-ethyl-2,6-diazaspiro[3.3]heptan-2-yl)pyridin-2-yl)-5-fluoro-4-(4-methyl-5,6,7,8-tetrahydro-4H-pyrazolo[1,5-a]azepin-3-yl)pyrimidin-2-amine|X-RAY DIFFRACTION|1.977|Homo sapiens|0|TRANSFERASE/TRANSFERASE inhibitor","8I0M|Structure of CDK6 in complex with inhibitor|X-RAY DIFFRACTION|2.7772|Homo sapiens|0|CELL CYCLE/INHIBITOR","9D8U|Crystal structure of CDK6 in complex with atirmociclib|X-RAY DIFFRACTION|2|Homo sapiens|0|TRANSFERASE","9PE7|CDK6 to CDK4 active site surrogate in complex with compound 6|X-RAY DIFFRACTION|2.05|Homo sapiens|0|TRANSFERASE/INHIBITOR","9PE8|CDK6 to CDK4 active site surrogate in complex with PF-07220060|X-RAY DIFFRACTION|1.8|Homo sapiens|0|TRANSFERASE/INHIBITOR"]}]}