|
40
|
284
|
7lbfD |
Cryoem structure of the hcmv trimer ghglgo in complex with human platelet-derived growth factor receptor alpha and neutralizing fabs 13h11 and msl-109 |
|
83
|
295
|
7aw0A |
Mertk kinase domain in complex with purine inhibitor |
|
76
|
278
|
7kplA |
Crystal structure of hephb1 in apo form |
|
82
|
295
|
7aw3A |
Mertk kinase domain with type 1 inhibitor from a dna-encoded library |
|
87
|
306
|
7bcmA |
The ddr1 kinase domain bound to sr302 |
|
97
|
313
|
7be6A |
Structure of ddr1 receptor tyrosine kinase in complex with inhibitor sr159 |
|
85
|
295
|
7aw2A |
Mertk kinase domain with type 1.5 inhibitor from a dna-encoded library |
|
80
|
287
|
7aw4A |
Mertk kinase domain with type 3 inhibitor from a dna-encoded library |
|
12
|
72
|
6lbxB |
Crystal structure of her2 domain iv and rb-h2 |
|
51
|
596
|
7amlA |
Ret/gdnf/gfra1 extracellular complex cryo-em structure |
|
78
|
285
|
7a2aA |
Crystal structure of egfr-t790m/v948r in complex with spebrutinib and eai001 |
|
86
|
295
|
7ab2A |
Crystal structure of mertk kinase domain in complex with unc2025 |
|
85
|
290
|
7aazA |
Crystal structure of mertk in complex with a type 1.5 aminopyridine inhibitor |
|
88
|
290
|
7b42A |
Crystal structure of c-met bound by compound 8 |
|
87
|
290
|
7b3qA |
Crystal structure of c-met bound by compound 1 |
|
83
|
290
|
7b43A |
Crystal structure of c-met bound by compound 9 |
|
78
|
306
|
7aymA |
Structure of ddr2 kinase domain in complex with ibz3 |
|
85
|
288
|
7b3vA |
Crystal structure of c-met bound by compound 3 |
|
35
|
160
|
7azbA |
Structure of ddr2 ds domain in complex with vhh |
|
81
|
283
|
6z4bA |
Crystal structure of egfr-t790m/v948r in complex with osimertinib and eai045 |
|
79
|
278
|
7b3wA |
Crystal structure of c-met bound by compound 4 |
|
84
|
296
|
7ab0A |
Apo crystal structure of the mertk kinase domain |
|
87
|
292
|
7b40A |
Crystal structure of c-met bound by compound 6 |
|
29
|
174
|
7b7nE |
Human herpesvirus-8 gh/gl in complex with epha2 |
|
87
|
292
|
7b41A |
Crystal structure of c-met bound by compound 7 |
|
97
|
300
|
7ju6A |
Structure of ret protein tyrosine kinase in complex with selpercatinib |
|
91
|
292
|
7b44A |
Crystal structure of c-met bound by compound s1 |
|
77
|
283
|
7b3tA |
Crystal structure of c-met bound by compound 2 |
|
27
|
174
|
7czeI |
Crystal structure of epstein-barr virus (ebv) ghgl and in complex with the ligand binding domian (lbd) of epha2 |
|
98
|
314
|
7ju5A |
Structure of ret protein tyrosine kinase in complex with pralsetinib |
|
88
|
291
|
7aayA |
Crystal structure of mertk kinase domain in complex with merestinib |
|
86
|
296
|
7aaxA |
Crystal structure of mertk kinase domain in complex with ldc1267 |
|
84
|
290
|
7b3zA |
Crystal structure of c-met bound by compound 5 |
|
21
|
183
|
7czfA |
Crystal structure of kaposi sarcoma associated herpesvirus (kshv ) ghgl in complex with the ligand binding domian (lbd) of epha2 |
|
86
|
295
|
7ab1A |
Crystal structure of mertk kinase domain in complex with gilteritinib |
|
72
|
284
|
7cqeA |
Crystal structure of the catalytic domain of the proto-oncogene tyrosine-protein kinase mer in complex with azd-7762 |
|
90
|
300
|
6v6qA |
Crystal structure of monophosphorylated fgf receptor 2 isoform iiib with ptr657 |
|
83
|
284
|
6z4dA |
Crystal structure of egfr-t790m/v948r in complex with mavelertinib and eai001 |
|
82
|
305
|
7jysA |
Halk in complex with 3-(3-chlorophenyl)-5-methyl-1h-pyrazole |
|
86
|
305
|
7jytA |
Halk in complex with 3-(3-methyl-1h-pyrazol-5-yl)pyridine |
|
87
|
305
|
7jyrA |
Halk in complex with 1-[(1r,2r)-1-(2,4-difluorophenyl)-2-[2-(5-methyl-1h-pyrazol-3-yl)-4-(trifluoromethyl)phenoxy]cyclopropyl]methanamine |
|
84
|
304
|
7jy4A |
Halk in complex with ((1s,2s)-1-(2,4-difluorophenyl)-2-(2-(3-methyl-1h-pyrazol-5-yl)-4-(trifluoromethyl)phenoxy)cyclopropyl)methanamine |
|
92
|
323
|
6ludA |
Crystal structure of egfr(l858r/t790m/c797s) in complex with osimertinib |
|
92
|
323
|
6lubA |
Crystal structure of egfr(l858r/t790m/c797s) in complex with ch7233163 |
|
96
|
334
|
6y23A |
Ddr1 kinase autoinhibited by its juxtamembrane region |
|
134
|
573
|
6kbiA |
Crystal structure of erbb3 n418q mutant |
|
89
|
300
|
6jpeA |
Crystal structure of fgfr4 kinase domain with irreversible inhibitor 1 |
|
103
|
305
|
6xvjA |
Crystal structure of the kdr (vegfr2) kinase domain in complex with a type-ii inhibitor |
|
97
|
306
|
6xv9A |
Crystal structure of the kinase domain of human c-kit in complex with a type-ii inhibitor |
|
98
|
303
|
6xvbA |
Crystal structure of the kinase domain of human c-kit with a cyclic imidate inhibitor covalently bound to cys788 |
