Found 1111 chains in Genus chains table. Displaying 1 - 50. Applied filters: Proteins

Search results query ec: 2.7.10.1

Total Genus Sequence Length pdb Title
55 193 7d85A Crystal structure of anti-erbb3 fab isu104 in complex with human erbb3 extracellular domain 3
93 324 7aemA Studies towards a reversible egfr c797s triple mutant inhibitor series
91 316 6wa2A Crystal structure of egfr(t790m/v948r) in complex with ln3753
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
79 278 7b3wA Crystal structure of c-met bound by compound 4
81 283 6z4bA Crystal structure of egfr-t790m/v948r in complex with osimertinib and eai045
87 292 7b40A Crystal structure of c-met bound by compound 6
84 296 7ab0A Apo crystal structure of the mertk kinase domain
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
27 174 7czeI Crystal structure of epstein-barr virus (ebv) ghgl and in complex with the ligand binding domian (lbd) of epha2
77 283 7b3tA Crystal structure of c-met bound by compound 2
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
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
86 305 7jytA Halk in complex with 3-(3-methyl-1h-pyrazol-5-yl)pyridine