68
|
289
|
7dxlA |
Fragment-based lead discovery of indazole-based compounds as axl kinase inhibitors |
83
|
296
|
7eecA |
Crystal structure of epha7 mutant g656r |
85
|
296
|
7eedA |
Crystal structure of epha7 mutant d751h |
84
|
297
|
7eefA |
Crystal structure of epha7 mutant g656e |
90
|
308
|
6xl4A |
Egfr(t790m/v948r) in complex with azd9291 and ddc4002 |
72
|
525
|
7mobC |
Cryo-em structure of 2:2 c-met/nk1 complex |
94
|
713
|
7mo9E |
Cryo-em map of the c-met ii/hgf i/hgf ii (k4 and sph) sub-complex |
96
|
713
|
7moaE |
Cryo-em structure of the c-met ii/hgf i complex bound with hgf ii in a rigid conformation |
114
|
715
|
7mo7B |
Cryo-em structure of 2:2 c-met/hgf holo-complex |
86
|
322
|
7aeiA |
Studies towards a reversible egfr c797s triple mutant inhibitor series |
75
|
289
|
7oamA |
Kinase domain of mertk in complex with compound 8 |
92
|
316
|
6wxnA |
Egfr(t790m/v948r) in complex with ln3844 |
55
|
193
|
7d85A |
Crystal structure of anti-erbb3 fab isu104 in complex with human erbb3 extracellular domain 3 |
91
|
316
|
6wa2A |
Crystal structure of egfr(t790m/v948r) in complex with ln3753 |
93
|
324
|
7aemA |
Studies towards a reversible egfr c797s triple mutant inhibitor series |
92
|
312
|
6wakA |
A crystal structure of egfr(t790m/v948r) in complex with ln3754 |
102
|
309
|
7bttA |
A x-ray cocrystal structure of xmu-mp-5 bound to the alk kinase domain |
80
|
278
|
7kpmA |
Crystal structure of hephb1 bound with adp |
86
|
295
|
7aw1A |
Mertk kinase domain in complex with a type 2 inhibitor |
87
|
295
|
7avzA |
Mertk kinase domain in complex with a bisaminopyrimidine inhibitor |
82
|
286
|
7avxA |
Mertk kinase domain in complex with nps-1034 |
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 |