 |
1FYN |
PHOSPHOTRANSFERASE |
B |
A |
SH3-like barrel |
|
 |
1H27 |
CDK2/CYCLIN A IN COMPLEX WITH AN 11-RESIDUE RECRUITMENT PEPTIDE FROM P27 |
E |
B |
Cyclin-like |
|
 |
1Q8T |
The Catalytic Subunit of cAMP-dependent Protein Kinase (PKA) in Complex with Rho-kinase Inhibitor Y-27632 |
B |
A |
Protein kinase-like (PK-like) |
|
 |
1Q8U |
The Catalytic Subunit of cAMP-dependent Protein Kinase in Complex with Rho-kinase Inhibitor H-1152P |
B |
A |
Protein kinase-like (PK-like) |
|
 |
1Q8W |
The Catalytic Subunit of cAMP-dependent Protein Kinase in Complex with Rho-kinase Inhibitor Fasudil (HA-1077) |
B |
A |
Protein kinase-like (PK-like) |
|
 |
1WBP |
SRPK1 BOUND TO 9MER DOCKING MOTIF PEPTIDE |
B |
C |
|
|
 |
1YDR |
STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE, ALPHA-CATALYTIC SUBUNIT IN COMPLEX WITH H7 PROTEIN KINASE INHIBITOR 1-(5-ISOQUINOLINESULFONYL)-2-METHYLPIPERAZINE |
I |
E |
Protein kinase-like (PK-like) |
|
 |
1YDS |
STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE, ALPHA-CATALYTIC SUBUNIT IN COMPLEX WITH H8 PROTEIN KINASE INHIBITOR [N-(2-METHYLAMINO)ETHYL]-5-ISOQUINOLINESULFONAMIDE |
I |
E |
Protein kinase-like (PK-like) |
|
 |
1YDT |
STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE, ALPHA-CATALYTIC SUBUNIT IN COMPLEX WITH H89 PROTEIN KINASE INHIBITOR N-[2-(4-BROMOCINNAMYLAMINO)ETHYL]-5-ISOQUINOLINE |
I |
E |
Protein kinase-like (PK-like) |
|
 |
2BZK |
CRYSTAL STRUCTURE OF THE HUMAN PIM1 IN COMPLEX WITH AMPPNP AND PIMTIDE |
A |
B |
|
|
 |
2C1A |
STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE COMPLEXED WITH ISOQUINOLINE-5-SULFONIC ACID (2-(2-(4-CHLOROBENZYLOXY) ETHYLAMINO)ETHYL)AMIDE |
I |
A |
Protein kinase-like (PK-like) |
|
 |
2C1B |
STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE COMPLEXED WITH (4R,2S)-5\'-(4-(4-CHLOROBENZYLOXY)PYRROLIDIN-2-YLMETHANESULFONYL)ISOQUINOLINE |
I |
A |
Protein kinase-like (PK-like) |
|
 |
2C3I |
CRYSTAL STRUCTURE OF HUMAN PIM1 IN COMPLEX WITH IMIDAZOPYRIDAZIN I |
A |
B |
|
|
 |
2CCH |
THE CRYSTAL STRUCTURE OF CDK2 CYCLIN A IN COMPLEX WITH A SUBSTRATE PEPTIDE DERIVED FROM CDC MODIFIED WITH A GAMMA-LINKED ATP ANALOGUE |
E |
B |
Cyclin-like |
|
 |
2CK3 |
AZIDE INHIBITED BOVINE F1-ATPASE |
I |
HG |
Epsilon subunit of F1F0-ATP synthase N-terminal domain |
|
 |
2JAM |
CRYSTAL STRUCTURE OF HUMAN CALMODULIN-DEPENDENT PROTEIN KINASE I G |
D |
A |
|
|
 |
2JDI |
GROUND STATE STRUCTURE OF F1-ATPASE FROM BOVINE HEART MITOCHONDRIA (BOVINE F1-ATPASE CRYSTALLISED IN THE ABSENCE OF AZIDE) |
I |
HG |
Epsilon subunit of F1F0-ATP synthase N-terminal domain |
|
 |
2JDO |
STRUCTURE OF PKB-BETA (AKT2) COMPLEXED WITH ISOQUINOLINE-5-SULFONIC ACID (2-(2-(4-CHLOROBENZYLOXY) ETHYLAMINO)ETHYL) AMIDE |
C |
A |
Protein kinase-like (PK-like) |
|
 |
2JDR |
STRUCTURE OF PKB-BETA (AKT2) COMPLEXED WITH THE INHIBITOR A-443654 |
C |
A |
Protein kinase-like (PK-like) |
|
 |
2JDS |
STRUCTURE OF CAMP-DEPENDENT PROTEIN KINASE COMPLEXED WITH A-443654 |
I |
A |
Protein kinase-like (PK-like) |
|
 |
2JDT |
STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH ISOQUINOLINE-5-SULFONIC ACID (2-(2-(4-CHLOROBENZYLOXY) ETHYLAMINO)ETHYL) AMIDE |
I |
A |
|
|
 |
2JDV |
STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH A-443654 |
I |
A |
|
|
 |
2JLD |
EXTREMELY TIGHT BINDING OF RUTHENIUM COMPLEX TO GLYCOGEN SYNTHASE KINASE 3 |
E |
A |
|
|
 |
2Q0N |
Structure of human p21 activating kinase 4 (PAK4) in complex with a consensus peptide |
B |
A |
|
|
 |
2QME |
Crystal structure of human RAC3 in complex with CRIB domain of human p21-activated kinase 1 (PAK1) |
I |
A |
|
|
 |
2UVY |
STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH METHYL-(4-(9H-PURIN-6-YL)-BENZYL)-AMINE |
I |
A |
|
|
 |
2UVZ |
STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH C-PHENYL-C-(4-(9H-PURIN-6-YL)-PHENYL)-METHYLAMINE |
I |
A |
|
|
 |
2UW0 |
STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 6-(4-(4-(4-CHLORO-PHENYL)-PIPERIDIN-4-YL)-PHENYL)-9H-PURINE |
I |
A |
|
|
 |
2UW3 |
STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 5-METHYL-4-PHENYL-1H-PYRAZOLE |
I |
A |
|
|
 |
2UW4 |
STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 2-(4-(5-METHYL-1H-PYRAZOL-4-YL)-PHENYL)-ETHYLAMINE |
I |
A |
|
|
 |
2UW5 |
STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH (R)-2-(4-CHLORO-PHENYL)-2-(4-1H-PYRAZOL-4-YL)-PHENYL)-ETHYLAMINE |
I |
A |
|
|
 |
2UW6 |
STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH (S)-2-(4-CHLORO-PHENYL)-2-(4-1H-PYRAZOL-4-YL)-PHENYL)-ETHYLAMINE |
I |
A |
|
|
 |
2UW7 |
STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 4-(4-CHLORO-PHENYL)-4-(4-(1H-PYRAZOL-4-YL)-PHENYL)-PIPERIDINE |
I |
A |
|
|
 |
2UW8 |
STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 2-(4-CHLORO-PHENYL)-2-PHENYL-ETHYLAMINE |
I |
A |
|
|
 |
2UW9 |
STRUCTURE OF PKB-BETA (AKT2) COMPLEXED WITH 4-(4-CHLORO-PHENYL)-4-(4-(1H-PYRAZOL-4-YL)-PHENYL)-PIPERIDINE |
C |
A |
Protein kinase-like (PK-like) |
|
 |
2UZV |
PKA STRUCTURES OF INDAZOLE-PYRIDINE SERIES OF AKT INHIBITORS |
2 |
A |
|
|
 |
2UZW |
PKA STRUCTURES OF INDAZOLE-PYRIDINE SERIES OF AKT INHIBITORS |
I |
E |
|
|
 |
2V3S |
STRUCTURAL INSIGHTS INTO THE RECOGNITION OF SUBSTRATES AND ACTIVATORS BY THE OSR1 KINASE |
D |
A |
|
|
 |
2V51 |
STRUCTURE OF MAL-RPEL1 COMPLEXED TO ACTIN |
E |
A |
|
|
 |
2V52 |
STRUCTURE OF MAL-RPEL2 COMPLEXED TO G-ACTIN |
M |
A |
|
|
 |
2VNW |
STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH (1-(9H-PURIN-6-YL)PIPERIDIN-4-YL)METHANAMINE |
I |
A |
|
|
 |
2VNY |
STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH (1-(9H-PURIN-6-YL)PIPERIDIN-4-YL)AMINE |
I |
A |
|
|
 |
2VO0 |
STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH C-(4-(4-CHLOROPHENYL)-1-(7H-PYRROLO(2,3-D)PYRIMIDIN-4-YL)PIPERIDIN-4-YL)METHYLAMINE |
I |
A |
|
|
 |
2VO3 |
STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH C-(4-(4-CHLOROPHENYL)-1-(7H-PYRROLO(2,3-D)PYRIMIDIN-4-YL)PIPERIDIN-4-YL)METHYLAMINE |
I |
A |
|
|
 |
2VO6 |
STRUCTURE OF PKA-PKB CHIMERA COMPLEXED WITH 4-(4-CHLOROBENZYL)-1-(7H-PYRROLO(2,3-D)PYRIMIDIN-4-YL)PIPERIDIN-4-YLAMINE |
I |
A |
|
|
 |
2VO7 |
STRUCTURE OF PKA COMPLEXED WITH 4-(4-CHLOROBENZYL)-1-(7H-PYRROLO(2,3-D)PYRIMIDIN-4-YL)PIPERIDIN-4-YLAMINE |
I |
A |
Protein kinase-like (PK-like) |
|
 |
2WAX |
STRUCTURE OF THE HUMAN DDX6 C-TERMINAL DOMAIN IN COMPLEX WITH AN EDC3-FDF PEPTIDE |
B |
A |
|
|
 |
2WAY |
STRUCTURE OF THE HUMAN DDX6 C-TERMINAL DOMAIN IN COMPLEX WITH AN EDC3-FDF PEPTIDE |
B |
A |
|
|
 |
3BU3 |
Crystal structure of the insulin receptor kinase in complex with IRS2 KRLB peptide |
B |
A |
Protein kinase-like (PK-like) |
|
 |
3BU5 |
Crystal structure of the insulin receptor kinase in complex with IRS2 KRLB peptide and ATP |
B |
C |
|
|