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8B54

CDK2/cyclin A2 in complex with pyrazolo[4,3-d]pyrimidine inhibitor LGR6768

Summary for 8B54
Entry DOI10.2210/pdb8b54/pdb
DescriptorCyclin-dependent kinase 2, Cyclin-A2, ~{N}-[(2-phenylphenyl)methyl]-5-piperidin-4-ylsulfanyl-3-propan-2-yl-2~{H}-pyrazolo[4,3-d]pyrimidin-7-amine, ... (6 entities in total)
Functional Keywordscyclin-dependent kinase 2, cyclin a2, cancer, cell cycle
Biological sourceHomo sapiens (human)
More
Total number of polymer chains4
Total formula weight128945.44
Authors
Djukic, S.,Skerlova, J.,Rezacova, P. (deposition date: 2022-09-21, release date: 2023-03-29, Last modification date: 2024-02-07)
Primary citationKovalova, M.,Havlicek, L.,Djukic, S.,Skerlova, J.,Perina, M.,Pospisil, T.,Reznickova, E.,Rezacova, P.,Jorda, R.,Krystof, V.
Characterization of new highly selective pyrazolo[4,3-d]pyrimidine inhibitor of CDK7.
Biomed Pharmacother, 161:114492-114492, 2023
Cited by
PubMed: 36931035
DOI: 10.1016/j.biopha.2023.114492
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.6 Å)
Structure validation

222926

數據於2024-07-24公開中

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