91
|
295
|
7xdyA |
Crystal structure of a receptor like kinase from arabidopsis |
95
|
295
|
7xdwA |
Crystal structure of a receptor like kinase from arabidopsis |
0
|
24
|
8ib0A |
The amyloid structure of mouse ripk1 rhim-containing domain by solid-state nmr |
333
|
1043
|
8aj8A |
Structure of p110 gamma bound to the p84 regulatory subunit |
291
|
940
|
8bfuA |
Crystal structure of the apo p110alpha catalytic subunit from homo sapiens |
48
|
298
|
8bxrA |
Titin fniii-domain i109-i111 (i/a4-a/a6) from the mir region |
32
|
198
|
8bvoA |
Titin i110-i111 fniii tandem from the mir region (i/a5-i/a6) |
71
|
270
|
8edhA |
Identification of a class of wnk isoform-specific inhibitors through high-throughput screening |
82
|
311
|
8f8eA |
Crystal structure of the wdr domain of human dcaf1 in complex with oicr-8268 compound |
13
|
99
|
8bw6A |
Titin fniii-domain i110 (i/a6) from the mir region |
81
|
264
|
8e80A |
Structure of lrrk2-chk1 10-pt. mutant complex with heteroaryl-1h-indazole lrrk2 inhibitor 14 |
83
|
274
|
8c7xA |
Crystal structure of braf in complex with a hybrid compound 6 |
76
|
268
|
8e81A |
Structure of lrrk2-chk1 10-pt. mutant complex with heteroaryl-1h-indazole lrrk2 inhibitor 25 |
83
|
275
|
8c7yA |
Crystal structure of braf v600e in complex with a hybrid compound 6 |
114
|
370
|
7zksA |
Srpk1 in complex with inhibitor |
128
|
552
|
7z6eA |
Structure of the c1-ph-cnh regulatory module of mrck1 |
111
|
618
|
7zkxA |
Srpk2 in complex with inhibitor |
104
|
327
|
7a4qA |
The crystal structure of ro4613269 bound to ck2alpha |
82
|
271
|
8afrA |
Pim1 in complex with 4-((6-hydroxybenzofuran-3-yl)methyl)benzoic acid and pimtide |
83
|
273
|
7z6uA |
Pim1 in complex with (e)-4-((6-amino-2-oxoindolin-3-ylidene)methyl)benzoic acid and pimtide |
84
|
233
|
7szaA |
Crystal structure analysis of human prpk complex with a compound |
96
|
466
|
7pt78 |
Structure of mcm2-7 dh complexed with cdc7-dbf4 in the presence of adp:bef3, state i |
84
|
232
|
7szbA |
Crystal structure analysis of human prpk complex with a compound |
78
|
281
|
8bzjA |
Human mst3 (stk24) kinase in complex with inhibitor mrlw5 |
102
|
325
|
7xyhA |
Crystal structure of ck2a2 complexed with ag1112 |
118
|
334
|
7x4hA |
Crystal structure of ck2a1 complexed with ag1112 |
87
|
264
|
7ztlA |
Crystal structure of a covalently linked aurora-a n-myc complex |
88
|
282
|
8bziA |
Human mst3 (stk24) kinase in complex with inhibitor mr39 |
97
|
292
|
7qrbA |
Crystal structure of ck1 delta in complex with pk-09-129 |
92
|
292
|
7qraA |
Crystal structure of ck1 delta in complex with vn725 |
96
|
292
|
7qr9A |
Crystal structure of ck1 delta in complex with pk-09-82 |
43
|
174
|
7ur2A |
Crystal structure of the sec14 domain of the rhogef kalirin |
57
|
318
|
8c01r |
Enp1tap_a population of yeast small ribosomal subunit precursors |
49
|
253
|
8c00r |
Enp1tap-s21_a population of yeast small ribosomal subunit precursors depleted of rps21/es21 |
39
|
194
|
7thzA |
Structure of leucine rich repeat kinase 2's roc domain interacting with the microtubule facing the plus end |
46
|
194
|
7thyA |
Structure of leucine rich repeat kinase 2's roc domain interacting with the microtubule facing the minus end |
31
|
204
|
7zr6K |
Cryoem structure of hsp90-cdc37-braf(v600e)-pp5(open) complex |
113
|
330
|
7quxA |
Crystal structure of p7c8 bound to ck2alpha |
80
|
273
|
7qfmA |
Pim1 in complex with (e)-4-((2-oxoindolin-3-ylidene)methyl)benzoic acid and pimtide |
52
|
278
|
8ej4K |
Cryo-em structure of the active nlrp3 inflammasome disk |
93
|
466
|
7pt68 |
Structure of mcm2-7 dh complexed with cdc7-dbf4 in the presence of atpgs, state iii |
31
|
204
|
7zr0K |
Cryoem structure of hsp90-cdc37-braf(v600e) complex. |
35
|
204
|
7zr5K |
Cryoem structure of hsp90-cdc37-braf(v600e)-pp5(closed) complex |
231
|
944
|
8guaA |
Cryo-em structure of cancer-specific pi3kalpha mutant e542k in complex with byl-719 |
307
|
1051
|
7tz7A |
Pi3k alpha in complex with an inhibitor |
319
|
945
|
8exuA |
Crystal structure of pi3k-alpha in complex with compound 30 |
71
|
232
|
7szdA |
Crystal structure analysis of human prpk complex with a compound |
306
|
945
|
8exoA |
Crystal structure of pi3k-alpha in complex with compound 19 |
305
|
945
|
8exlA |
Crystal structure of pi3k-alpha in complex with taselisib |
310
|
945
|
8exvA |
Crystal structure of pi3k-alpha in complex with compound 32 |