Found 1100 chains in Genus chains table. Displaying 1 - 50. Applied filters: Proteins

Search results query ec: 2.7.10.2

Total Genus Sequence Length pdb Title
96 298 6vnkA Jak2 jh1 in complex with pn4-073
95 298 6vnbA Jak2 jh1 in complex with bl2-084
93 297 6vncA Jak2 jh1 in complex with bl2-096
93 298 6vnfA Jak2 jh1 in complex with ma9-086
96 298 6vnhA Jak2 jh1 in complex with pn2-123
97 299 6vnjA Jak2 jh1 in complex with pn4-014
96 298 6vn8A Jak2 jh1 in complex with baricitinib
98 289 6vs3A Jak2 jh1 in complex with bl2-057
98 298 6vsnA Jak2 jh1 in complex with bl2-110
94 291 6vniA Jak2 jh1 in complex with pn3-115
93 298 6vnmA Jak2 jh1 in complex with sy5-103
94 292 6vngA Jak2 jh1 in complex with pn2-118
90 298 6vnlA Jak2 jh1 in complex with sg3-179
92 292 6vneA Jak2 jh1 in complex with fedratinib
57 273 6l8lA C-src in complex with ibrutinib
94 290 7apfA Crystal structure of jak3 in complex with fm601 (compound 10a)
90 290 6x8gA Crystal structure of tyk2 with compound 22
93 290 6x8fA Crystal structure of tyk2 with compound 11
91 291 7apgA Crystal structure of jak3 in complex with fm587 (compound 9a)
31 167 6tvnA Crystal structure of 5-bromoindoline-2,3-dione covalently bound to the ph domain of bruton's tyrosine kinase
97 305 6vglA Jak2 jh1 in complex with ruxolitinib
84 267 6vxqA Bruton's tyrosine kinase in complex with compound 5
91 288 6x8eA Crystal structure of jak2 with compound 11
91 267 6w06A Bruton's tyrosine kinase in complex with compound 6
87 266 6w07A Bruton's tyrosine kinase in complex with compound 1
80 261 6w7oA Ternary complex structure - btk ciap compound 17
34 168 6tt2A The ph domain of bruton's tyrosine kinase mutant r28c
86 269 6xjkA Jak2 jh2 in complex with jak067
33 167 6tuhA The ph domain of bruton's tyrosine kinase mutant r28c
73 265 6w8iA Ternary complex structure - btk ciap compound 15
32 168 6tseA Crystal structure of 1-methylindoline-2,3-dione covalently bound to the ph domain of bruton's tyrosine kinase mutant r28c
71 287 6xrgA Abl 1b isoform inactive2 state
75 287 6xr6A Abl 1b isoform active state
80 287 6xr7A Abl isoform 1b inactive1 state
86 266 6i99A Bone marrow tyrosine kinase in chromosome x in complex with a newly designed covalent inhibitor js24
24 104 6htfA Crystal structure of human btk sh2 domain bound to rf10 repebody
97 289 7c3nA Crystal structure of jak3 in complex with delgocitinib
14 61 6xx5A Crystal structure of the c-src sh3 domain h122r-q128k mutant in complex with ni(ii) at ph 7.5 co-crystallized with methyl beta-cyclodextrin
85 264 6xe4A Btk fluorocyclopropyl amide inhibitor, compound 25
83 268 6x3nA Co-structure of btk kinase domain with l-005085737 inhibitor
93 266 6x3pA Co-structure of btk kinase domain with l-005298385 inhibitor
88 265 6x3oA Co-structure of btk kinase domain with l-005191930 inhibitor
79 275 6wiwA C-src bound to atp-competitive inhibitor i14
80 290 6tpfA Fragment-based discovery of pyrazolopyridones as jak1 inhibitors with excellent subtype selectivity
92 289 6tpdA Fragment-based discovery of pyrazolopyridones as jak1 inhibitors with excellent subtype selectivity
73 290 6tpeA Fragment-based discovery of pyrazolopyridones as jak1 inhibitors with excellent subtype selectivity
86 290 6rshA Structure based optimization of jak1-atp binding pocket inhibitors in the aminopyrazole class
88 290 6rscA Structure based optimization of jak1-atp binding pocket inhibitors in the aminopyrazole class
87 290 6rsdA Structure based optimization of jak1-atp binding pocket inhibitors in the aminopyrazole class
87 290 6rsbA Structure based optimization of jak1-atp binding pocket inhibitors in the aminopyrazole class