105
|
348
|
3p5kA |
P38 inhibitor-bound |
85
|
287
|
3p1aA |
Structure of human membrane-associated tyrosine- and threonine-specific cdc2-inhibitory kinase myt1 (pkmyt1) |
105
|
337
|
3oxtA |
Human camp-dependent protein kinase in complex with an inhibitor |
95
|
348
|
3ohtA |
Crystal structure of salmo salar p38alpha |
110
|
337
|
3ovvA |
Human camp-dependent protein kinase in complex with an inhibitor |
88
|
290
|
3orpA |
Mycobacterium tuberculosis pknb kinase domain l33d mutant (crystal form 5) |
106
|
355
|
3oy1A |
Highly selective c-jun n-terminal kinase (jnk) 2 and 3 inhibitors with in vitro cns-like pharmacokinetic properties |
106
|
335
|
3oogA |
Human camp-dependent protein kinase in complex with a small fragment |
85
|
281
|
3oriA |
Mycobacterium tuberculosis pknb kinase domain l33d mutant (crystal form 1) |
116
|
378
|
3oz6A |
Crystal structure of mapk from cryptosporidium parvum, cgd2_1960 |
86
|
292
|
3orkA |
Mycobacterium tuberculosis pknb kinase domain l33d mutant (crystal form 2) |
110
|
336
|
3ow3A |
Discovery of dihydrothieno- and dihydrofuropyrimidines as potent pan akt inhibitors |
149
|
466
|
3nyvA |
Calcium-dependent protein kinase 1 from toxoplasma gondii (tgcdpk1) in complex with non-specific inhibitor whi-p180 |
99
|
348
|
3o8uA |
Conformational plasticity of p38 map kinase dfg motif mutants in response to inhibitor binding |
92
|
350
|
3odzX |
Crystal structure of p38alpha y323r active mutant |
102
|
348
|
3objA |
Conformational plasticity of p38 map kinase dfg mutants in response to inhibitor binding |
109
|
346
|
3o71A |
Crystal structure of erk2/dcc peptide complex |
113
|
349
|
3nwwA |
P38 alpha kinase complexed with a 2-aminothiazol-5-yl-pyrimidine based inhibitor |
82
|
277
|
3oezA |
Crystal structure of the l317i mutant of the chicken c-src tyrosine kinase domain complexed with imatinib |
87
|
334
|
3o7lB |
Crystal structure of phospholamban (1-19):pka c-subunit:amp-pnp:mg2+ complex |
68
|
263
|
3o51A |
Crystal structure of anthranilamide 10 bound to auroraa |
169
|
556
|
3nynA |
Crystal structure of g protein-coupled receptor kinase 6 in complex with sangivamycin |
81
|
263
|
3octA |
Crystal structure of bruton's tyrosine kinase mutant v555r in complex with dasatinib |
110
|
347
|
3o8pA |
Conformational plasticity of p38 map kinase dfg motif mutants in response to inhibitor binding |
94
|
293
|
3o23A |
Human unphosphorylated igf1-r kinase domain in complex with an hydantoin inhibitor |
76
|
277
|
3of0A |
Crystal structure of the l317i mutant of the chicken c-src tyrosine kinase domain |
101
|
348
|
3oc1A |
Conformational plasticity of p38 map kinase dfg motif mutants in response to inhibitor binding |
99
|
428
|
3o96A |
Crystal structure of human akt1 with an allosteric inhibitor |
88
|
338
|
3o7lD |
Crystal structure of phospholamban (1-19):pka c-subunit:amp-pnp:mg2+ complex |
111
|
358
|
3o2mA |
Crystal structure of jnk1-alpha1 isoform complex with a biaryl tetrazol (a-82118) |
110
|
348
|
3oefX |
Crystal structure of y323f inactive mutant of p38alpha map kinase |
96
|
349
|
3od6X |
Crystal structure of p38alpha y323t active mutant |
99
|
349
|
3ocgA |
P38 alpha kinase complexed with a 5-amino-pyrazole based inhibitor |
159
|
556
|
3nyoA |
Crystal structure of g protein-coupled receptor kinase 6 in complex with amp |
82
|
289
|
3o0gA |
Crystal structure of cdk5:p25 in complex with an atp analogue |
89
|
290
|
3nyxA |
Non-phosphorylated tyk2 jh1 domain with quinoline-thiadiazole-thiophene inhibitor |
102
|
348
|
3o8tA |
Conformational plasticity of p38 map kinase dfg-motif mutants in response to inhibitor binding |
102
|
357
|
3o17A |
Crystal structure of jnk1-alpha1 isoform |
96
|
335
|
3ocbA |
Akt1 kinase domain with pyrrolopyrimidine inhibitor |
94
|
348
|
3obgA |
Conformational plasticity of p38 map kinase dfg mutants in response to inhibitor binding |
89
|
264
|
3ocsA |
Crystal structure of bruton's tyrosine kinase in complex with inhibitor cgi1746 |
92
|
350
|
3odyX |
Crystal structure of p38alpha y323q active mutant |
70
|
263
|
3o50A |
Crystal structure of benzamide 9 bound to auroraa |
92
|
291
|
3nz0A |
Non-phosphorylated tyk2 kinase with cmp6 |
111
|
348
|
3nnvA |
Crystal structure of p38 alpha in complex with dp437 |
95
|
301
|
3nw6A |
Crystal structure of insulin-like growth factor 1 receptor (igf-1r-wt) complex with a carbon-linked proline isostere inhibitor (11a) |
84
|
288
|
3nunA |
Phosphoinositide-dependent kinase-1 (pdk1) with lead compound |
81
|
266
|
3nlbA |
Novel kinase profile highlights the temporal basis of context dependent checkpoint pathways to cell death |
52
|
227
|
3nvmB |
Structural basis for substrate placement by an archaeal box c/d ribonucleoprotein particle |
116
|
348
|
3nr9A |
Structure of human cdc2-like kinase 2 (clk2) |