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MMDB Description
48841THR 160 Phosphorylated Cdk2-human Cyclin A3 Complex With the Inhibitor Indirubin-5-sulphonate Bound
5224Cyclin A-cyclin-dependent Kinase 2 Complex
15424The Structure of Cdk2cyclin a in Complex With an Oxindole Inhibitor
19416Pcdk2cyclin a in Complex With Mgadp, Nitrate and Peptide Substrate
20562Structure of Human Thr160-phospho Cdk2cyclin a Complexed With the Inhibitor Nu2058
20563Structure of Human Thr160-phospho Cdk2cyclin a Complexed With the Inhibitor Nu6094
20564Structure of Human Thr160-phospho Cdk2cyclin a Complexed With the Inhibitor Nu6086
20565Structure of Human Thr160-phospho Cdk2cyclin a Complexed With the Inhibitor Nu6102
21606Cdk2cyclin a in Complex With a 9 Residue Recruitment Peptide From E2F
21607Cdk2cyclin a in Complex With an 11-residue Recruitment Peptide From Retinoblastoma-associated Protein
21608Cdk2cyclin a in Complex With an 11-residue Recruitment Peptide From P53
21609Cdk2cyclin a in Complex With an 11-residue Recruitment Peptide From P27
21610Cdk2cyclin a in Complex With an 11-residue Recruitment Peptide From P107
5324Phosphorylated Cyclin-dependent Kinase-2 Bound to Cyclin a
49840P27(kip1)cyclin Acdk2 Complex
23920Structure of Human Thr160-phospho Cdk2cyclin a Complexed With a 2-arylamino-4-cyclohexylmethyl-5-nitroso-6- Aminopyrimidine Inhibitor
28467Structure of Human Thr160-phospho Cdk2cyclin a Complexed With a 6-cyclohexylmethyloxy-2-anilino-purine Inhibitor
28468Structure of Human Thr160-phospho Cdk2cyclin a Complexed With a 6-cyclohexylmethyloxy-2-anilino-purine Inhibitor
28469Structure of Human Thr160-phospho Cdk2cyclin a Complexed With a 6-cyclohexylmethyloxy-2-anilino-purine Inhibitor
74114Cyclin a Binding Groove Inhibitor H-arg-arg-leu-ile-phe-nh2
74115Cyclin a Binding Groove Inhibitor Ac-arg-arg-leu-asn- (M-cl-phe)-nh2
73405Cyclin a Binding Groove Inhibitor H-cit-cit-leu-ile-(p-f-phe)-nh2
74116Cyclin a Binding Groove Inhibitor H-arg-arg-leu-asn-(p-f-phe)-nh2
23597The Strucure of Phospho-cdk2cyclin a in Complex With the Inhibitor 4,5,6,7-tetrabromobenzotriazole (Tbs)
23656The Crystal Structure of Ucn-01 in Complex With Phospho- Cdk2cyclin a
11811Phosphorylated Cdk2-cyclyin A-substrate Peptide Complex
74367Cyclin a Binding Groove Inhibitor Ace-arg-lys-leu- Phe-gly
57599Bovine Cyclin A3
28447Structure of Cdk2cyclin a With Pnu-292137
38056Structure of Cdk2-cyclin a With Pha-404611
36731Structure of Cdk2-cyclin a With Pha-630529
36260Structure of Cdk2-cyclin a With Pha-533514
38076Differential Binding of Inhibitors to Active and Inactive Cdk2 Provides Insights for Drug Design
38077Differential Binding of Inhibitors to Active and Inactive Cdk2 Provides Insights for Drug Design
52746Differential Binding of Inhibitors to Active and Inactive Cdk2 Provides Insights for Drug Design
38081Differential Binding of Inhibitors to Active and Inactive Cdk2 Provides Insights for Drug Design
36766Crystal Structure of the Human Cdk2 Complexed With the Triazolopyrimidine Inhibitor
39101The Crystal Structure of Cdk2 Cyclin a in Complex With a Substrate Peptide Derived From CDC Modified With a Gamma- Linked ATP Analogue
39102Crystal Structure of Phospho-cdk2 Cyclin a in Complex With a Peptide Containing Both the Substrate and Recruitment Sites of Cdc6
38626Mechanism of CDK Inhibition by Active Site Phosphorylation: Cdk2 Y15p T160p in Complex With Cyclin a Structure
39347Structure of THR 160 Phosphorylated Cdk2cyclin a in Complex With the Inhibitor Nu6271
42325Cdk2cyclin a Complexed With a Thiophene Carboxamide Inhibitor
41817Structure of Human Thr160-phospho Cdk2-cyclin a Complexed With a Bisanilinopyrimidine Inhibitor
41818Structure of Human Thr160-phospho Cdk2-cyclin a F82h-l83v- H84d Mutant With an O6-cyclohexylmethylguanine Inhibitor
41819Structure of Human Thr160-phospho Cdk2-cyclin a Complexed With a Bisanilinopyrimidine Inhibitor
45391Replace: a Strategy for Iterative Design of Cyclin Binding Groove Inhibitors
47311Crystal Structure of Human Cdk2 Complexed With a Thiazolidinone Inhibitor
47312Crystal Structure of Human Cdk2 Complexed With a Thiazolidinone Inhibitor
47313Crystal Structure of Human Cdk2 Complexed With a Thiazolidinone Inhibitor
47315Crystal Structure of Human Cdk2 Complexed With a Thiazolidinone Inhibitor
62126Replace: a Strategy for Iterative Design of Cyclin Binding Groove Inhibitors
82117Truncation and Optimisation of Peptide Inhibitors of Cdk2, Cyclin a Through Structure Guided Design
73105Truncation and Optimisation of Peptide Inhibitors of Cdk2, Cyclin a Through Structure Guided Design
73109Truncation and Optimisation of Peptide Inhibitors of Cdk2, Cyclin a Through Structure Guided Design
75550Structure of Cdk2-cyclin a With Pha-848125
75551Structure of Cdk2-cyclin a Complexed With 8-anilino-1- Methyl-4,5-dihydro-1h-pyrazolo[4,3-h] Quinazoline-3- Carboxylic Acid
84494Structural and Thermodynamic Consequences of Cyclization of Peptide Ligands for the Recruitment Site of Cyclin a
84495Structural and Thermodynamic Consequences of Cyclization of Peptide Ligands for the Recruitment Site of Cyclin a
80223Optimisation of 6,6-dimethyl Pyrrolo 3,4-c Pyrazoles: Identification of Pha-793887, a Potent CDK Inhibitor Suitable for Intravenous Dosing
80229Structure of Cdk2-cyclin a With a Pyrazolo(4,3-h) Quinazoline-3-carboxamide Inhibitor
80073Truncation and Optimisation of Peptide Inhibitors of Cdk2, Cyclin a Through Structure Guided Design
62420Structure of Phosphorylated Thr160 Cdk2cyclin a in Complex With the Inhibitor Meriolin 3
62421Structure of Phosphorylated Thr160 Cdk2cyclin a in Complex With the Inhibitor Meriolin 5
62422Structure of Phosphorylated Thr160 Cdk2cyclin a in Complex With the Inhibitor Variolin B
65636Structure of Phosphorylated Thr160 Cdk2cyclin a in Complex With the Inhibitor CR8
65637Structure of Phosphorylated Thr160 Cdk2cyclin a in Complex With the Inhibitor Roscovitine
67039Structure of THR 160 Phosphorylated Cdk2cyclin a in Complex With the Inhibitor N-&-n1
67507Cdk2cyclina Complexed With a Pyrazolopyridazine Inhibitor
67508Cdk2cyclina Complexed With a Pyrazolopyridazine Inhibitor
67795Cdk2cyclina Complexed With a Imidazo Triazin-2-amine
69436Cdk-2-cyclin Complex With Indazole Inhibitor 9 Bound at ITS Active Site