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Ligands
Code Name Style Show Link
FB8 4-(2-methyl-3-propan-2-yl-imidazol-4-yl)-~{N}-(4-methylsulfonylphenyl)pyrimidin-2-amine
Non-standard Residues
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Glycosylation
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Code : 6GU7   PDBj   RCSB PDB   PDBe
Header : CELL CYCLE
Title : CDK1/Cks2 in complex with AZD5438
Release Data : 2018-12-05
Compound :
mol_id molecule chains synonym
1 Cyclin-dependent kinase 1 A,C,E,G CDK1,Cell division control protein 2 homolog,Cell division protein kinase 1,p34 protein kinase
ec: 2.7.11.22,2.7.11.23
mol_id molecule chains synonym
2 Cyclin-dependent kinases regulatory subunit 2 B,D,F,H CKS-2
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Spodoptera frugiperda  (taxid:7108)
gene: CDK1, CDC2, CDC28A, CDKN1, P34CDC2
expression_system_common: Fall armyworm
expression_system_cell_line: SF9
expression_system_plasmid: pVL1393
mol_id organism_scientific organism_common expression_system
2 Homo sapiens  (taxid:9606) Human Escherichia coli  (taxid:562)
gene: CKS2
Authors : Wood, D.J., Korolchuk, S., Tatum, N.J., Wang, L.Z., Endicott, J.A., Noble, M.E.M., Martin, M.P.
Keywords : CDK1, CKS2, INHIBITOR, CELL CYCLE
Exp. method : X-RAY DIFFRACTION ( 2.75 Å )
Citation :

Differences in the Conformational Energy Landscape of CDK1 and CDK2 Suggest a Mechanism for Achieving Selective CDK Inhibition.

Wood, D.J.,Korolchuk, S.,Tatum, N.J.  et al.
(2019)  Cell Chem Biol  26 : 121 - 130.e5

PubMed: 30472117
DOI: 10.1016/j.chembiol.2018.10.015

Chain : A, C, E, G
UniProt : P06493 (CDK1_HUMAN)
Reaction: EC: Evidence:
Physiological Direction:
ATP + L-seryl-[protein] = ADP + H(+) + O-phospho-L-seryl- [protein] 2.7.11.22 PubMed:23355470, PubMed:26829474, PubMed:30704899
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ATP + L-threonyl-[protein] = ADP + H(+) + O-phospho-L- threonyl-[protein] 2.7.11.22 PubMed:23355470, PubMed:26829474, PubMed:30704899
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[DNA-directed RNA polymerase] + ATP = ADP + H(+) + phospho- [DNA-directed RNA polymerase] 2.7.11.23 UniProtKB:P11440
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Chain : B, D, F, H
UniProt : P33552 (CKS2_HUMAN)
Reaction : -