|
105
|
336
|
3dndA |
Camp-dependent protein kinase pka catalytic subunit with pki-5-24 |
|
104
|
341
|
3bwjA |
Complex of pka with the bisubstrate protein kinase inhibitor lead compound arc-1034 |
|
109
|
348
|
3ambA |
Protein kinase a sixfold mutant model of aurora b with inhibitor vx-680 |
|
108
|
350
|
3amaA |
Protein kinase a sixfold mutant model of aurora b with inhibitor jnj-7706621 |
|
107
|
339
|
3agmA |
Complex of pka with the bisubstrate protein kinase inhibitor arc-670 |
|
112
|
340
|
3aglA |
Complex of pka with the bisubstrate protein kinase inhibitor arc-1039 |
|
106
|
337
|
3ag9A |
Complex of pka with the bisubstrate protein kinase inhibitor arc-1012 |
|
105
|
337
|
2vo3A |
Structure of pka-pkb chimera complexed with c-(4-(4-chlorophenyl)-1-(7h-pyrrolo(2,3-d)pyrimidin-4-yl)piperidin-4-yl)methylamine |
|
105
|
337
|
2vnyA |
Structure of pka-pkb chimera complexed with (1-(9h-purin-6-yl) piperidin-4-yl)amine |
|
107
|
337
|
2vo7A |
Structure of pka complexed with 4-(4-chlorobenzyl)-1-(7h-pyrrolo(2,3- d)pyrimidin-4-yl)piperidin-4-ylamine |
|
108
|
343
|
2vo0A |
Structure of pka-pkb chimera complexed with c-(4-(4-chlorophenyl)-1-(7h-pyrrolo(2,3-d)pyrimidin-4-yl)piperidin-4-yl)methylamine |
|
110
|
338
|
2vo6A |
Structure of pka-pkb chimera complexed with 4-(4-chlorobenzyl)-1-(7h- pyrrolo(2,3-d)pyrimidin-4-yl)piperidin-4-ylamine |
|
106
|
337
|
2vnwA |
Structure of pka-pkb chimera complexed with (1-(9h-purin-6-yl) piperidin-4-yl)methanamine |
|
107
|
337
|
2uw0A |
Structure of pka-pkb chimera complexed with 6-(4-(4-(4-chloro-phenyl) -piperidin-4-yl)-phenyl)-9h-purine |
|
108
|
336
|
2uzvA |
Pka structures of indazole-pyridine series of akt inhibitors |
|
108
|
337
|
2uvxA |
Structure of pka-pkb chimera complexed with 7-azaindole |
|
111
|
336
|
2uztA |
Pka structures of akt, indazole-pyridine inhibitors |
|
109
|
337
|
2uw7A |
Structure of pka-pkb chimera complexed with 4-(4-chloro-phenyl)-4-(4- (1h-pyrazol-4-yl)-phenyl)-piperidine |
|
106
|
336
|
2uzuE |
Pka structures of indazole-pyridine series of akt inhibitors |
|
108
|
337
|
2uvzA |
Structure of pka-pkb chimera complexed with c-phenyl-c-(4-(9h-purin-6- yl)-phenyl)-methylamine |
|
104
|
337
|
2uw4A |
Structure of pka-pkb chimera complexed with 2-(4-(5-methyl-1h-pyrazol- 4-yl)-phenyl)-ethylamine |
|
100
|
336
|
2uzwE |
Pka structures of indazole-pyridine series of akt inhibitors |
|
104
|
337
|
2uw6A |
Structure of pka-pkb chimera complexed with (s)-2-(4-chloro-phenyl)- 2-(4-1h-pyrazol-4-yl)-phenyl)-ethylamine |
|
106
|
337
|
2uw3A |
Structure of pka-pkb chimera complexed with 5-methyl-4-phenyl-1h- pyrazole |
|
107
|
337
|
2uw8A |
Structure of pka-pkb chimera complexed with 2-(4-chloro-phenyl)-2- phenyl-ethylamine |
|
107
|
336
|
2uw5A |
Structure of pka-pkb chimera complexed with (r)-2-(4-chloro-phenyl)- 2-(4-1h-pyrazol-4-yl)-phenyl)-ethylamine |
|
108
|
336
|
2uvyA |
Structure of pka-pkb chimera complexed with methyl-(4-(9h-purin-6-yl)- benzyl)-amine |
|
87
|
338
|
2qvsE |
Crystal structure of type iia holoenzyme of camp-dependent protein kinase |
|
96
|
340
|
2qurA |
Crystal structure of f327a/k285p mutant of camp-dependent protein kinase |
|
99
|
338
|
2qcsA |
A complex structure between the catalytic and regulatory subunit of protein kinase a that represents the inhibited state |
|
107
|
336
|
2oh0E |
Crystal structure of protein kinase a in complex with pyridine-pyrazolopyridine based inhibitors |
|
113
|
336
|
2ojfE |
Crystal structure of protein kinase a in complex with pyridine-pyrazolopyridine based inhibitors |
|
105
|
336
|
2jdtA |
Structure of pka-pkb chimera complexed with isoquinoline-5-sulfonic acid (2-(2-(4-chlorobenzyloxy) ethylamino)ethyl)amide |
|
107
|
336
|
2jdvA |
Structure of pka-pkb chimera complexed with a-443654 |
|
109
|
337
|
2jdsA |
Structure of camp-dependent protein kinase complexed with a-443654 |
|
17
|
47
|
2izyA |
Molecular basis of akap specificity for pka regulatory subunits |
|
14
|
39
|
2izxA |
Molecular basis of akap specificity for pka regulatory subunits |
|
13
|
39
|
2hwnA |
Crystal structure of rii alpha dimerization/docking domain of pka bound to the d-akap2 peptide |
|
105
|
337
|
2gu8A |
Discovery of 2-pyrimidyl-5-amidothiophenes as novel and potent inhibitors for akt: synthesis and sar studies |
|
108
|
340
|
2gniA |
Pka fivefold mutant model of rho-kinase with inhibitor fasudil (ha1077) |
|
105
|
340
|
2gnhA |
Pka five fold mutant model of rho-kinase with h1152p |
|
107
|
341
|
2gnfA |
Protein kinase a fivefold mutant model of rho-kinase with y-27632 |
|
110
|
337
|
2gnjA |
Pka three fold mutant model of rho-kinase with y-27632 |
|
106
|
340
|
2gnlA |
Pka threefold mutant model of rho-kinase with inhibitor h-1152p |
|
108
|
340
|
2gngA |
Protein kinase a fivefold mutant model of rho-kinase |
|
109
|
337
|
2gfcA |
Camp-dependent protein kinase pka catalytic subunit with pki-5-24 |
|
108
|
336
|
2f7eE |
Pka complexed with (s)-2-(1h-indol-3-yl)-1-(5-isoquinolin-6-yl-pyridin-3-yloxymethyl-etylamine |
|
107
|
336
|
2erzE |
Crystal structure of c-amp dependent kinase (pka) bound to hydroxyfasudil |
|
108
|
336
|
2f7xE |
Protein kinase a bound to (s)-2-(1h-indol-3-yl)-1-[5-((e)-2-pyridin-4-yl-vinyl)-pyridin-3-yloxymethyl]-ethylamine |
|
100
|
336
|
2f7zE |
Protein kinase a bound to (r)-1-(1h-indol-3-ylmethyl)-2-(2-pyridin-4-yl-[1,7]naphtyridin-5-yloxy)-ehylamine |
