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| MMDB Description | |
|---|---|
| 55315 | Human Cyclin Dependent Kinase 2 Complexed With the Inhibitor Staurosporine |
| 86690 | Human Cyclin-dependent Kinase 2 |
| 86691 | Human Cyclin-dependent Kinase 2 Phosphorylated on THR 160 |
| 11979 | Crystal Structure of the Human Cdk2 Kinase Complex With Cell Cycle-regulatory Protein Ckshs1 |
| 12188 | Human Cyclin Dependent Kinase 2 Complexed With the Inhibitor Purvalanol B |
| 14472 | The Structure of Cyclin-dependent Kinase 2 (Cdk2) in Complex With 4-[3-hydroxyanilino]-6,7-dimethoxyquinazoline |
| 13361 | Human Cyclin-dependent Kinase 2 Complexed With the Inhibitor Hymenialdisine |
| 91067 | Human Cyclin Dependent Kinase 2 Complexed With the Inhibitor Nu2058 |
| 91068 | Human Cyclin Dependent Kinase 2 Complexed With the Inhibitor Nu6027 |
| 48841 | THR 160 Phosphorylated Cdk2-human Cyclin A3 Complex With the Inhibitor Indirubin-5-sulphonate Bound |
| 14968 | Crystal Structure of Murine Gamma Herpesvirus Cyclin Complexed to Human Cyclin Dependent Kinase 2 |
| 5224 | Cyclin A-cyclin-dependent Kinase 2 Complex |
| 16075 | Crystal Structure of Kinase Associated Phosphatase (Kap) in Complex With Phospho-cdk2 |
| 15423 | The Structure of Cyclin-dependent Kinase 2 (Cdk2) in Complex With an Oxindole Inhibitor |
| 15424 | The Structure of Cdk2cyclin a in Complex With an Oxindole Inhibitor |
| 17593 | Crystal Structure of Human Cyclin Dependent Kinase 2 (Cdk2) in Complex With the Inhibitor H717 |
| 18391 | Human Cyclin Dependent Kinase 2 Complexed With the Cdk4 Inhibitor |
| 18392 | Human Cyclin Dependent Kinase 2 Complexed With the Cdk4 Inhibitor |
| 18393 | Human Cyclin Dependent Kinase 2 Complexed With the Cdk4 Inhibitor |
| 19416 | Pcdk2cyclin a in Complex With Mgadp, Nitrate and Peptide Substrate |
| 72206 | Human Cyclin Dependent Kinase 2 Complexed With the Inhibitor 2-amino-6-(3'-methyl-2'-oxo)butoxypurine |
| 91106 | Cdk2 in Complex With a Disubstituted 4, 6-bis Anilino Pyrimidine Cdk4 Inhibitor |
| 23817 | Cdk2 in Complex With a Disubstituted 2, 4-bis Anilino Pyrimidine Cdk4 Inhibitor |
| 91107 | Cdk2 in Complex With a Disubstituted 4, 6-bis Anilino Pyrimidine Cdk4 Inhibitor |
| 91108 | Cdk2 in Complex With a Disubstituted 2, 4-bis Anilino Pyrimidine Cdk4 Inhibitor |
| 23241 | Human Cyclin Dependent Protein Kinase 2 in Complex With the Inhibitor 2-amino-6-[(r)-pyrrolidino-5'-yl]methoxypurine |
| 23242 | Human Cyclin Dependent Protein Kinase 2 in Complex With the Inhibitor 2-amino-6-[cyclohex-3-enyl]methoxypurine |
| 20562 | Structure of Human Thr160-phospho Cdk2cyclin a Complexed With the Inhibitor Nu2058 |
| 20563 | Structure of Human Thr160-phospho Cdk2cyclin a Complexed With the Inhibitor Nu6094 |
| 20564 | Structure of Human Thr160-phospho Cdk2cyclin a Complexed With the Inhibitor Nu6086 |
| 20565 | Structure of Human Thr160-phospho Cdk2cyclin a Complexed With the Inhibitor Nu6102 |
| 21606 | Cdk2cyclin a in Complex With a 9 Residue Recruitment Peptide From E2F |
| 21607 | Cdk2cyclin a in Complex With an 11-residue Recruitment Peptide From Retinoblastoma-associated Protein |
| 21608 | Cdk2cyclin a in Complex With an 11-residue Recruitment Peptide From P53 |
| 21609 | Cdk2cyclin a in Complex With an 11-residue Recruitment Peptide From P27 |
| 21610 | Cdk2cyclin a in Complex With an 11-residue Recruitment Peptide From P107 |
| 56308 | Human Cyclin-dependent Kinase 2 |
| 56309 | Human Cyclin-dependent Kinase 2 |
| 5324 | Phosphorylated Cyclin-dependent Kinase-2 Bound to Cyclin a |
| 49840 | P27(kip1)cyclin Acdk2 Complex |
| 17097 | The Structure of Cyclin-dependent Kinase 2 (Cdk2) in Complex With 4-[(6-amino-4-pyrimidinyl) Amino]benzenesulfonamide |
| 18308 | Crystal Structure of Human Cdk2 (Unphosphorylated) in Complex With Pkf049-365 |
| 19534 | Cdk2 Complexed With N-methyl-4-{[(2-oxo-1,2-dihydro-3h- Indol-3-ylidene)methyl]amino}benzenesulfonamide |
| 19535 | Cyclin-dependent Kinase 2 (Cdk2) Complexed With N-methyl-{4- [2-(7-oxo-6,7-dihydro-8h-[1,3]thiazolo[5,4-e]indol-8- Ylidene)hydrazino]phenyl}methanesulfonamide |
| 19536 | Cyclin-dependent Kinase 2 (Cdk2) Complexed With 3-{[(2,2- Dioxido-1,3-dihydro-2-benzothien-5-yl)amino]methylene}-5- (1,3-oxazol-5-yl)-1,3-dihydro-2h-indol-2-one |
| 19537 | Cyclin-dependent Kinase 2 (Cdk2) Complexed With 4-{[(2-oxo- 1,2-dihydro-3h-indol-3-ylidene)methyl]amino}-n-(1,3- Thiazol-2-yl)benzenesulfonamide |
| 19538 | Cyclin-dependent Kinase 2 (Cdk2) Complexed With 3-{[4- ({[amino(imino)methyl]aminosulfonyl)anilino]methylene}-2- Oxo-2,3-dihydro-1h-indole |
| 23920 | Structure of Human Thr160-phospho Cdk2cyclin a Complexed With a 2-arylamino-4-cyclohexylmethyl-5-nitroso-6- Aminopyrimidine Inhibitor |
| 28467 | Structure of Human Thr160-phospho Cdk2cyclin a Complexed With a 6-cyclohexylmethyloxy-2-anilino-purine Inhibitor |
| 50636 | Imidazopyridines: a Potent and Selective Class of Cyclin- Dependent Kinase Inhibitors Identified Through Structure- Based Hybridisation |
| 50637 | Imidazopyridines: a Potent and Selective Class of Cyclin- Dependent Kinase Inhibitors Identified Through Structure- Based Hybridisation |
| 50639 | Imidazopyridines: a Potent and Selective Class of Cyclin- Dependent Kinase Inhibitors Identified Through Structure- Based Hybridisation |
| 28468 | Structure of Human Thr160-phospho Cdk2cyclin a Complexed With a 6-cyclohexylmethyloxy-2-anilino-purine Inhibitor |
| 28469 | Structure of Human Thr160-phospho Cdk2cyclin a Complexed With a 6-cyclohexylmethyloxy-2-anilino-purine Inhibitor |
| 74114 | Cyclin a Binding Groove Inhibitor H-arg-arg-leu-ile-phe-nh2 |
| 74115 | Cyclin a Binding Groove Inhibitor Ac-arg-arg-leu-asn- (M-cl-phe)-nh2 |
| 73405 | Cyclin a Binding Groove Inhibitor H-cit-cit-leu-ile-(p-f-phe)-nh2 |
| 74116 | Cyclin a Binding Groove Inhibitor H-arg-arg-leu-asn-(p-f-phe)-nh2 |
| 24473 | The Structure of Cyclin Dependent Kinase 2 (Ckd2) With a Trisubstituted Naphthostyril Inhibitor |
| 23597 | The Strucure of Phospho-cdk2cyclin a in Complex With the Inhibitor 4,5,6,7-tetrabromobenzotriazole (Tbs) |
| 25687 | Crystal Structure of Human Cyclin-dependent Kinase 2 Complexed With a Nucleoside Inhibitor |
| 23656 | The Crystal Structure of Ucn-01 in Complex With Phospho- Cdk2cyclin a |
| 25698 | APO Structure of Human Cyclin-dependent Kinase 2 |
| 25700 | Human Cyclin Dependent Kinase 2 Complexed With the Inhibitor 4-(2,5-dichloro-thiophen-3-yl)-pyrimidin-2- Ylamine |
| 25701 | Human Cyclin Dependent Kinase 2 Complexed With the Inhibitor 4-(2,4-dimethyl-thiazol-5-yl)-pyrimidin-2-ylamine |
| 25702 | Human Cyclin Dependent Kinase 2 Complexed With the Inhibitor N-[4-(2,4-dimethyl-thiazol-5-yl)pyrimidin-2-yl]- N'-hydroxyiminoformamide |
| 25703 | Human Cyclin Dependent Kinase 2 Complexed With the Inhibitor [4-(2,4-dimethyl-thiazol-5-yl)-pyrimidin-2-yl]- (4-trifluoromethyl-phenyl)-amine |
| 27269 | Human Cyclin Dependent Kinase 2 Complexed With the Inhibitor 3-[4-(2,4-dimethyl-thiazol-5-yl)-pyrimidin-2- Ylamino]-phenol |
| 27270 | Human Cyclin Dependent Kinase 2 Complexed With the Inhibitor 4-[4-(4-methyl-2-methylamino-thiazol-5-yl)- Pyrimidin-2-ylamino]-phenol |
| 27271 | Human Cyclin Dependent Kinase 2 Complexed With the Inhibitor [4-(2-amino-4-methyl-thiazol-5-yl)-pyrimidin-2- Yl]-(3-nitro-phenyl)-amine |
| 27272 | Human Cyclin Dependent Kinase 2 Complexed With the Inhibitor N-[4-(2,4-dimethyl-thiazol-5-yl)-pyrimidin-2-yl]- N',n'-dimethyl-benzene-1,4-diamine |
| 28501 | Crystal Structure of Cdk2 With Inhibitor |
| 11811 | Phosphorylated Cdk2-cyclyin A-substrate Peptide Complex |
| 26171 | Cdk2 Complex With a 4-alkynyl Oxindole Inhibitor |
| 74367 | Cyclin a Binding Groove Inhibitor Ace-arg-lys-leu- Phe-gly |
| 51705 | Cdk2 in Complex With an Imidazo[1,2-b]pyridazine |
| 51756 | Cdk2 in Complex With a Disubstituted 4, 6-bis Anilino Pyrimidine Cdk4 Inhibitor |
| 28447 | Structure of Cdk2cyclin a With Pnu-292137 |
| 28448 | Structure of Cdk2 Complexed With Pnu-181227 |
| 31343 | Crystals Structure of Human Cdk2 in Complex With the Inhibitor Olomoucine |
| 51877 | Co-crystal Structure of 6-cyclohexylmethoxy-8-isopropyl-9h- Purin-2-ylamine and Monomeric Cdk2 |
| 31900 | The Structural Basis of Cdk2 Activation by Cyclin E |
| 31391 | Screening for Fragment Binding by X-ray Crystallography |
| 32043 | Crystal Structure of Human Cdk2 Complexed With a Pyrazolo[1, 5-a]pyrimidine Inhibitor |
| 32044 | Crystal Structure of Human Cdk2 Complexed With a Pyrazolo[1, 5-a]pyrimidine Inhibitor |
| 36955 | Crystal Structure of Cdk2 With an Aminoimidazo Pyridine Inhibitor |
| 37020 | Human Cdk2 in Complex With Olomoucine II, a Novel 2,6,9- Trisubstituted Purine Cyclin-dependent Kinase Inhibitor |
| 41297 | Human Cyclin-dependent Kinase 2 in Complex With Roscovitine |
| 35692 | Human Cyclin Dependent Kinase 2 (Cdk2) Complexed With Dph- 042562 |
| 35693 | Human Cyclin Dependent Kinase 2 (Cdk2) Complexed With Din- 234325 |
| 35694 | Human Cyclin Dependent Kinase 2 (Ckd2)complexed With Din- 232305 |
| 35695 | Human Cyclin Dependent Kinase 2 (Cdk2) Complexed With Indenopyraxole Din-101312 |
| 32662 | Human Cyclin Dependent Protein Kinase 2 in Complex With the Inhibitor 5-bromo-indirubine |
| 32663 | Human Cyclin Dependent Protein Kinase 2 in Complex With the Inhibitor 4-hydroxypiperindinesulfonyl-indirubine |
| 38056 | Structure of Cdk2-cyclin a With Pha-404611 |
| 36731 | Structure of Cdk2-cyclin a With Pha-630529 |
| 36215 | Structure of Cdk2 Complexed With Pnu-198873 |
| 36216 | Structure of Cdk2 Complexed With Pnu-230032 |
| 36260 | Structure of Cdk2-cyclin a With Pha-533514 |
| 38076 | Differential Binding of Inhibitors to Active and Inactive Cdk2 Provides Insights for Drug Design |
| 38077 | Differential Binding of Inhibitors to Active and Inactive Cdk2 Provides Insights for Drug Design |
| 86903 | Differential Binding of Inhibitors to Active and Inactive Cdk2 Provides Insights for Drug Design |
| 38081 | Differential Binding of Inhibitors to Active and Inactive Cdk2 Provides Insights for Drug Design |
| 38082 | Differential Binding of Inhibitors to Active and Inactive Cdk2 Provides Insights for Drug Design |
| 86905 | Crystal Structure of the Human Cdk2 Complexed With the Triazolopyrimidine Inhibitor |
| 36760 | Crystal Structure of the Human Cdk2 Complexed With the Triazolopyrimidine Inhibitor |
| 36761 | Crystal Structure of the Human Cdk2 Complexed With the Triazolopyrimidine Inhibitor |
| 36762 | Crystal Structure of the Human Cdk2 Complexed With the Triazolopyrimidine Inhibitor |
| 36763 | Crystal Structure of the Human Cdk2 Complexed With the Triazolopyrimidine Inhibitor |
| 86907 | Crystal Structure of the Human Cdk2 Complexed With the Triazolopyrimidine Inhibitor |
| 86908 | Crystal Structure of the Human Cdk2 Complexed With the Triazolopyrimidine Inhibitor |
| 36766 | Crystal Structure of the Human Cdk2 Complexed With the Triazolopyrimidine Inhibitor |
| 39101 | The Crystal Structure of Cdk2 Cyclin a in Complex With a Substrate Peptide Derived From CDC Modified With a Gamma- Linked ATP Analogue |
| 39102 | Crystal Structure of Phospho-cdk2 Cyclin a in Complex With a Peptide Containing Both the Substrate and Recruitment Sites of Cdc6 |
| 38626 | Mechanism of CDK Inhibition by Active Site Phosphorylation: Cdk2 Y15p T160p in Complex With Cyclin a Structure |
| 42581 | 4-arylazo-3,5-diamino-1h-pyrazole CDK Inhibitors: SAR Study, Crystal Structure in Complex With Cdk2, Selectivity, and Cellular Effects |
| 46879 | Human Cyclin Dependent Kinase 2 Complexed With the Cdk4 Inhibitor |
| 43718 | Structure of Cdk2 With a 3-hydroxychromones |
| 36838 | Human Cdk2 in Complex With Isopentenyladenine |
| 42189 | Cyclin Dependent Kinase 2 (Cdk2) With Diaminopyrimidine Inhibitor |
| 39347 | Structure of THR 160 Phosphorylated Cdk2cyclin a in Complex With the Inhibitor Nu6271 |
| 42325 | Cdk2cyclin a Complexed With a Thiophene Carboxamide Inhibitor |
| 41817 | Structure of Human Thr160-phospho Cdk2-cyclin a Complexed With a Bisanilinopyrimidine Inhibitor |
| 41818 | Structure of Human Thr160-phospho Cdk2-cyclin a F82h-l83v- H84d Mutant With an O6-cyclohexylmethylguanine Inhibitor |
| 41819 | Structure of Human Thr160-phospho Cdk2-cyclin a Complexed With a Bisanilinopyrimidine Inhibitor |
| 60474 | Crystal Structure of Cdk2 in Complex With Macrocyclic Aminopyrimidine |
| 46324 | Crystal Structure of Phospho-cdk2 in Complex With Cyclin B |
| 61984 | Crystal Structure of Cyclin-dependent Kinase 2 With Inhibitor |
| 61985 | Crystal Structure of Cyclin-dependent Kinase 2 With Inhibitor |
| 61986 | Crystal Structure of Cyclin-dependent Kinase 2 With Inhibitor |
| 61987 | Crystal Structure of Cyclin-dependent Kinase 2 With Inhibitor |
| 61988 | Crystal Structure of Cyclin-dependent Kinase 2 With Inhibitor |
| 61989 | Crystal Structure of Cyclin-dependent Kinase 2 With Inhibitor |
| 61990 | Crystal Structure of Cyclin-dependent Kinase 2 With Inhibitor |
| 61991 | Crystal Structure of Cyclin-dependent Kinase 2 With Inhibitor |
| 61992 | Crystal Structure of Cyclin-dependent Kinase 2 With Inhibitor |
| 61993 | Crystal Structure of Cyclin-dependent Kinase 2 With Inhibitor |
| 61994 | Crystal Structure of Cyclin-dependent Kinase 2 With Inhibitor |
| 61995 | Crystal Structure of Cyclin-dependent Kinase 2 With Inhibitor |
| 61996 | Crystal Structure of Cyclin-dependent Kinase 2 With Inhibitor |
| 66553 | Crystal Structure of a 3-aminoindazole Compound With Cdk2 |
| 45391 | Replace: a Strategy for Iterative Design of Cyclin Binding Groove Inhibitors |
| 47311 | Crystal Structure of Human Cdk2 Complexed With a Thiazolidinone Inhibitor |
| 47312 | Crystal Structure of Human Cdk2 Complexed With a Thiazolidinone Inhibitor |
| 47313 | Crystal Structure of Human Cdk2 Complexed With a Thiazolidinone Inhibitor |
| 47315 | Crystal Structure of Human Cdk2 Complexed With a Thiazolidinone Inhibitor |
| 47316 | Crystal Structure of Human Cdk2 Complexed With a Thiazolidinone Inhibitor |
| 47317 | Crystal Structure of Human Cdk2 Complexed With a Thiazolidinone Inhibitor |
| 47319 | Crystal Structure of Human Cdk2 Complexed With a Thiazolidinone Inhibitor |
| 62126 | Replace: a Strategy for Iterative Design of Cyclin Binding Groove Inhibitors |
| 65828 | Identification of N-(4-piperidinyl)-4-(2,6- Dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (At7519), a Novel Cyclin Dependent Kinase Inhibitor Using Fragment- Based X-ray Crystallography and Structure Based Drug Design |
| 65829 | Identification of N-(4-piperidinyl)-4-(2,6- Dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (At7519), a Novel Cyclin Dependent Kinase Inhibitor Using Fragment- Based X-ray Crystallography and Structure Based Drug Design |
| 65830 | Identification of N-(4-piperidinyl)-4-(2,6- Dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (At7519), a Novel Cyclin Dependent Kinase Inhibitor Using Fragment- Based X-ray Crystallography and Structure Based Drug Design |
| 65831 | Identification of N-(4-piperidinyl)-4-(2,6- Dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (At7519), a Novel Cyclin Dependent Kinase Inhibitor Using Fragment- Based X-ray Crystallography and Structure Based Drug Design |
| 65832 | Identification of N-(4-piperidinyl)-4-(2,6- Dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (At7519), a Novel Cyclin Dependent Kinase Inhibitor Using Fragment- Based X-ray Crystallography and Structure Based Drug Design |
| 65833 | Identification of N-(4-piperidinyl)-4-(2,6- Dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (At7519), a Novel Cyclin Dependent Kinase Inhibitor Using Fragment- Based X-ray Crystallography and Structure Based Drug Design |
| 65834 | Identification of N-(4-piperidinyl)-4-(2,6- Dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (At7519), a Novel Cyclin Dependent Kinase Inhibitor Using Fragment- Based X-ray Crystallography and Structure Based Drug Design |
| 65835 | Identification of N-(4-piperidinyl)-4-(2,6- Dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (At7519), a Novel Cyclin Dependent Kinase Inhibitor Using Fragment- Based X-ray Crystallography and Structure Based Drug Design |
| 65836 | Identification of N-(4-piperidinyl)-4-(2,6- Dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (At7519), a Novel Cyclin Dependent Kinase Inhibitor Using Fragment- Based X-ray Crystallography and Structure Based Drug Design |
| 65837 | Identification of N-(4-piperidinyl)-4-(2,6- Dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (At7519), a Novel Cyclin Dependent Kinase Inhibitor Using Fragment- Based X-ray Crystallography and Structure Based Drug Design |
| 65838 | Identification of N-(4-piperidinyl)-4-(2,6- Dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (At7519), a Novel Cyclin Dependent Kinase Inhibitor Using Fragment- Based X-ray Crystallography and Structure Based Drug Design |
| 65839 | Identification of N-(4-piperidinyl)-4-(2,6- Dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (At7519), a Novel Cyclin Dependent Kinase Inhibitor Using Fragment- Based X-ray Crystallography and Structure Based Drug Design |
| 65840 | Identification of N-(4-piperidinyl)-4-(2,6- Dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (At7519), a Novel Cyclin Dependent Kinase Inhibitor Using Fragment- Based X-ray Crystallography and Structure Based Drug Design |
| 65841 | Identification of N-(4-piperidinyl)-4-(2,6- Dichlorobenzoylamino)-1h-pyrazole-3-carboxamide (At7519), a Novel Cyclin Dependent Kinase Inhibitor Using Fragment- Based X-ray Crystallography and Structure Based Drug Design |
| 65845 | Cdk2 in Complex With an Imidazole Piperazine |
| 67301 | Structure of Cdk2 in Complex With an Imidazolyl Pyrimidine, Compound 5B |
| 66860 | Structure of Cdk2 in Complex With an Imidazolyl Pyrimidine, Compound 5C |
| 67710 | Cdk2 in Complex With the Imidazole Pyrimidine Amide, Compound (S)-8b |
| 69247 | Fragment-based Discovery of the Pyrazol-4-yl Urea (At9283), a Multi-targeted Kinase Inhibitor With Potent Aurora Kinase Activity |
| 82117 | Truncation and Optimisation of Peptide Inhibitors of Cdk2, Cyclin a Through Structure Guided Design |
| 73105 | Truncation and Optimisation of Peptide Inhibitors of Cdk2, Cyclin a Through Structure Guided Design |
| 73109 | Truncation and Optimisation of Peptide Inhibitors of Cdk2, Cyclin a Through Structure Guided Design |
| 75550 | Structure of Cdk2-cyclin a With Pha-848125 |
| 75551 | Structure of Cdk2-cyclin a Complexed With 8-anilino-1- Methyl-4,5-dihydro-1h-pyrazolo[4,3-h] Quinazoline-3- Carboxylic Acid |
| 84494 | Structural and Thermodynamic Consequences of Cyclization of Peptide Ligands for the Recruitment Site of Cyclin a |
| 84495 | Structural and Thermodynamic Consequences of Cyclization of Peptide Ligands for the Recruitment Site of Cyclin a |
| 80223 | Optimisation of 6,6-dimethyl Pyrrolo 3,4-c Pyrazoles: Identification of Pha-793887, a Potent CDK Inhibitor Suitable for Intravenous Dosing |
| 80229 | Structure of Cdk2-cyclin a With a Pyrazolo(4,3-h) Quinazoline-3-carboxamide Inhibitor |
| 80073 | Truncation and Optimisation of Peptide Inhibitors of Cdk2, Cyclin a Through Structure Guided Design |
| 86033 | Discovery and Characterisation of 2-anilino-4-(thiazol-5-yl) Pyrimidine Transcriptional CDK Inhibitors as Anticancer Agents |
| 86035 | Discovery and Characterisation of 2-anilino-4-(thiazol-5-yl) Pyrimidine Transcriptional CDK Inhibitors as Anticancer Agents |
| 62420 | Structure of Phosphorylated Thr160 Cdk2cyclin a in Complex With the Inhibitor Meriolin 3 |
| 62421 | Structure of Phosphorylated Thr160 Cdk2cyclin a in Complex With the Inhibitor Meriolin 5 |
| 62422 | Structure of Phosphorylated Thr160 Cdk2cyclin a in Complex With the Inhibitor Variolin B |
| 65636 | Structure of Phosphorylated Thr160 Cdk2cyclin a in Complex With the Inhibitor CR8 |
| 65637 | Structure of Phosphorylated Thr160 Cdk2cyclin a in Complex With the Inhibitor Roscovitine |
| 67039 | Structure of THR 160 Phosphorylated Cdk2cyclin a in Complex With the Inhibitor N-&-n1 |
| 67507 | Cdk2cyclina Complexed With a Pyrazolopyridazine Inhibitor |
| 67508 | Cdk2cyclina Complexed With a Pyrazolopyridazine Inhibitor |
| 67795 | Cdk2cyclina Complexed With a Imidazo Triazin-2-amine |
| 69433 | Cdk-2 With Indazole Inhibitor 17 Bound at ITS Active Site |
| 69434 | Cdk-2 With Indazole Inhibitor 9 Bound at ITS Active Site |
| 69436 | Cdk-2-cyclin Complex With Indazole Inhibitor 9 Bound at ITS Active Site |
| 70716 | Crystal Structure of a Benzthiophene Inhibitor Bound to Human Cyclin-dependent Kinase-2 (Cdk-2) |
| 76611 | Novel Cdk-5 Inhibitors - Crystal Structure of Inhibitor EFP With Cdk-2 |
| 76612 | Novel Cdk-5 Inhibitors - Crystal Structure of Inhibitor EFQ With Cdk-2 |
| 86234 | The Structure of Cyclin Dependent Kinase 2 (Ckd2) With a Pyrazolobenzodiazepine Inhibitor |
| 80523 | Crystal Structure of Cdk2 With Sar57, an Aminoindazole Type Inhibitor |
| 80524 | Crystal Structure of Cdk2 With Sar60, an Aminoindazole Type Inhibitor |
| 80525 | Crystal Structure of Cdk2 With Sar37, an Aminoindazole Type Inhibitor |
| 85224 | Cdk2cyclina in Complex With DRB |
| 87178 | Crystal Structure of Cdk2 in Complex With Inhibitor Bs-194 |
| 89696 | Structure of Cdk2 in Complex With a Pyrazolo[4,3-d]pyrimidine Bioisostere of Roscovitine |
| 88696 | Cdk2 in Complex With Two Molecules of 8-anilino-1-naphthalene Sulfonate |
| 88698 | Cdk2 in Complex With 3 Molecules of 8-anilino-1-naphthalene Sulfonate |
| 88699 | APO Cdk2 Crystallized From Jeffamine |
| 88700 | Cdk2 in Complex With Inhibitor Jws648 |
| 88701 | Cdk2 Ternary Complex With Jws648 and ANS |
| 88702 | Cdk2 in Complex With Inhibitor Su9516 |
| 88703 | Cdk2 Ternary Complex With Su9516 and ANS |
| 90830 | Structure of a Pcdk2cyclina Transition-state Mimic |
| 90831 | Structure of a Pcdk2cyclina Transition-state Mimic |