|
106
|
294
|
9igqA |
Crystal structure of ppk2 class iii from erysipelotrichaceae bacterium in complex with appch2p and polyphosphate |
|
110
|
349
|
9im8A |
Mutated adp-ribosyltransferase 2 (parp2) catalytic domain bound to a pyrimidine 2,4-diketone derivative inhibitor |
|
107
|
361
|
9hv3A |
Crystal structure of human gsk3b in complex with arn25657 |
|
96
|
361
|
9hukA |
Crystal structure of human gsk3b in complex with arn24161 |
|
106
|
361
|
9hulA |
Crystal structure of human gsk3b in complex with arn25423 |
|
115
|
331
|
9hl7B |
Protein kinase ck2 and small molecule ligands |
|
11
|
65
|
9hiyH |
Cryo-em structure of cak (cdk7 d97n mutant) in complex with atpgs |
|
111
|
331
|
9hphA |
Protein kinase ck2 bound to kdx1381 |
|
108
|
331
|
9hkpA |
Protein kinase ck2 with small molecule ligands |
|
106
|
331
|
9hl0A |
Protein kinase ck2 and small molecule ligands |
|
108
|
330
|
9hksA |
Protein kinase ck2 and small molecule ligands |
|
72
|
303
|
9hixJ |
Cryo-em structure of cak (cdk7 d97n mutant) in complex with thz1 |
|
12
|
65
|
9hj0H |
Cryo-em structure of cak (cdk7 d97n mutant) in complex with samuraciclib |
|
106
|
282
|
9hj0I |
Cryo-em structure of cak (cdk7 d97n mutant) in complex with samuraciclib |
|
103
|
283
|
9hixI |
Cryo-em structure of cak (cdk7 d97n mutant) in complex with thz1 |
|
10
|
65
|
9hixH |
Cryo-em structure of cak (cdk7 d97n mutant) in complex with thz1 |
|
105
|
281
|
9hiyI |
Cryo-em structure of cak (cdk7 d97n mutant) in complex with atpgs |
|
64
|
299
|
9hj0J |
Cryo-em structure of cak (cdk7 d97n mutant) in complex with samuraciclib |
|
78
|
301
|
9hiyJ |
Cryo-em structure of cak (cdk7 d97n mutant) in complex with atpgs |
|
121
|
395
|
9hfpA |
Rock2 in complex with cpd7 |
|
92
|
346
|
9hgmA |
Structure of human dnmt2 with bound allosteric inhibitor |
|
110
|
328
|
9h9dA |
Protein kinase ck2 catalytic subunit alpha (csnk2a1 gene product) in complex the the indenoindole-type inhibitor mc11 |
|
122
|
327
|
9h96A |
Structure of protein kinase ck2 catalytic subunit (isoform ck2alpha'; csnk2a2 gene product) in complex with the indenoindole-type inhibitor mc11 |
|
137
|
481
|
9h6jA |
Human b4galnt1 apo structure |
|
117
|
333
|
9h97A |
Structure of protein kinase ck2 catalytic subunit ck2alpha (csnk2a1 gene product) in complex with the indenoindole-type inhibitor mc11 at high-salt conditions |
|
137
|
483
|
9h6lA |
Human b4galnt1 in complex with udp |
|
138
|
483
|
9h6kA |
Human b4galnt1 in complex with udp-galnac |
|
73
|
234
|
9gp9A |
Crystal structure of polyphosphate kinase 2-ii (ppk2-ii) from lysinibacillus fusiformis bound to adp (form i) |
|
76
|
268
|
9gucA |
Adhiron-mediated identification of a novel and selective allosteric pocket in aurora kinase a |
|
75
|
287
|
9gtyA |
Ripk1 in complex with az"320 |
|
74
|
287
|
9gtgA |
Ripk1 in complex with az"902 |
|
16
|
82
|
9gucB |
Adhiron-mediated identification of a novel and selective allosteric pocket in aurora kinase a |
|
120
|
327
|
9gxyA |
Crystal structure of protein kinase ck2 catalytic subunit (csnk2a2 gene product) in complex with the dual ck2/hdac inhibitor ior-160 |
|
232
|
845
|
9godA |
Crystal structure of dpp9 in complex with n-phosphono-(s)-3-aminopiperidine-2-one-based inhibitor |
|
253
|
844
|
9gonA |
Crystal structure of dpp9 in complex with sulphostin |
|
98
|
321
|
9gsrA |
Crystal structure of m. hassiacum gpgs co-crystallized with udp-glucose (ph 7.2) |
|
251
|
845
|
9gocA |
Crystal structure of dpp9 ser730ala in complex with sulphostin. |
|
204
|
728
|
9gohA |
Crystal structure of dpp4 in complex with sulphostin. |
|
157
|
453
|
9gh9A |
A novel aminotransferase from streptomyces sp. |
|
100
|
304
|
9gfsA |
Psim in complex with sah |
|
96
|
251
|
9giaA |
Crystal structure of polyphosphate kinase 2-ii (ppk2-ii) from bacillus cereus apo-form |
|
97
|
275
|
9gopB |
Crystal structure of cdk2-cyclin e1 bound by compound 30 |
|
79
|
298
|
9gopA |
Crystal structure of cdk2-cyclin e1 bound by compound 30 |
|
94
|
274
|
9gp3B |
Crystal structure of cdk2-cyclin e1 bound by compound 11 (azd8421) |
|
124
|
403
|
9gowA |
Crystal structure of phosphorylated human ire1a in complex with ia107 |
|
78
|
298
|
9gp3A |
Crystal structure of cdk2-cyclin e1 bound by compound 11 (azd8421) |
|
170
|
455
|
9gnfA |
A novel aminotransferase from streptomyces sp. gabaculine complex |
|
83
|
298
|
9gnoA |
Crystal structure of cdk2 bound by compound 4 |
|
40
|
118
|
9getA |
Crystal structure of crebbp bromodomain in complex with (r,e)-6-(5-(7-methoxy-3,4-dihydroquinolin-1(2h)-yl)pent-1-en-1-yl)-4-methyl-8-(morpholine-4-carbonyl)-1,3,4,5-tetrahydro-2h-benzo[b][1,4]diazepin-2-one |
|
158
|
482
|
9g5yA |
The structure of aspergillus fumigatus udp-glcnac pyrophosphorylase in complex with a fragment |
