Found 146 chains in Genus chains table. Displaying 1 - 50. Applied filters: Proteins

Search results query: signaling protein/inhibitor

Total Genus Sequence Length pdb Title
66 286 7m5zA Crystal structure of the mertk kinase domain in complex with inhibitor mips15692
0 16 6vxgA Structure of the c-terminal domain of rage and its inhibitor
0 15 6wgnE Crystal structure of k-ras(g12d) gppnhp bound to cyclic peptide ligand kd2
64 169 6wgnA Crystal structure of k-ras(g12d) gppnhp bound to cyclic peptide ligand kd2
98 297 6juxA Crystal structure of human alk2 kinase domain with r206h mutation in complex with rk-71807
60 169 6p0iB Crystal structure of gdp-bound human rala in a covalent complex with aryl sulfonyl fluoride compounds.
61 168 6p0kB Crystal structure of gdp-bound human rala in a covalent complex with aryl sulfonyl fluoride compounds.
61 168 6p0mB Crystal structure of gdp-bound human rala in a covalent complex with aryl sulfonyl fluoride compounds.
59 168 6p0nB Crystal structure of gdp-bound human rala in a covalent complex with aryl sulfonyl fluoride compounds.
61 168 6p0lB Crystal structure of gdp-bound human rala in a covalent complex with aryl sulfonyl fluoride compounds.
44 125 6jj5A Brd4 in complex with 259
43 125 6jj6A Brd4 in complex with 500
41 125 6jjbA Brd4 in complex with zzm1
44 125 6jj3A Brd4 in complex with 138a
63 169 6pgpA Crystal structure of human kras g12c covalently bound to a quinazolinone inhibitor
55 167 6pgoA Crystal structure of human kras g12c covalently bound to a phthalazine inhibitor
137 396 6nfaA Vav1 inhibited by an allosteric inhibitor: vav1 inhibitors block gef activity
53 169 6v5lA The haddock structure model of gdp kras in complex with its allosteric inhibitor e22
102 296 6uyaA Crystal structure of compound 19 bound to irak4
87 1063 6nzdI Cryo-em structure of the lysosomal folliculin complex (flcn-fnip2-raga-ragc-ragulator)
34 121 6nzdC Cryo-em structure of the lysosomal folliculin complex (flcn-fnip2-raga-ragc-ragulator)
19 109 6nzdA Cryo-em structure of the lysosomal folliculin complex (flcn-fnip2-raga-ragc-ragulator)
107 557 6nzdH Cryo-em structure of the lysosomal folliculin complex (flcn-fnip2-raga-ragc-ragulator)
24 91 6nzdE Cryo-em structure of the lysosomal folliculin complex (flcn-fnip2-raga-ragc-ragulator)
60 286 6nzdF Cryo-em structure of the lysosomal folliculin complex (flcn-fnip2-raga-ragc-ragulator)
18 90 6nzdD Cryo-em structure of the lysosomal folliculin complex (flcn-fnip2-raga-ragc-ragulator)
33 126 6nzdB Cryo-em structure of the lysosomal folliculin complex (flcn-fnip2-raga-ragc-ragulator)
83 306 6nzdG Cryo-em structure of the lysosomal folliculin complex (flcn-fnip2-raga-ragc-ragulator)
81 279 6pdjA Tyrosine-protein kinase lck bound to compound 11
13 81 6ak2A Crystal structure of the syntenin pdz1 domain in complex with the peptide inhibitor ksl-128018
57 166 6p8yA Crystal structure of human kras g12c covalently bound to an acryloylazetidine acetamide inhibitor.
58 169 6p8wA Crystal structure of human kras g12c covalently bound to an acryloylazetidine acetamide inhibitor.
61 169 6p8zA Crystal structure of human kras g12c covalently bound to an acryloylazetidine acetamide inhibitor
58 166 6p8xA Crystal structure of human kras g12c covalently bound to an acryloylazetidine acetamide inhibitor.
42 127 6afrA Crystal structure of the first bromodomain of human brd4 in complex with 5-((4-fluoro-1h-imidazol-1-yl)methyl)quinolin-8-ol
76 287 6ocqA Crystal structure of rip1 kinase in complex with a pyrrolidine
44 127 3u5jA Crystal structure of the first bromodomain of human brd4 in complex with alprazolam
0 6 5h10D Traf1-tank complex
93 270 6e4fA Crystal structure of arq 531 in complex with the kinase domain of btk
169 517 6dm8A Understanding the species selectivity of myeloid cell leukemia-1 (mcl-1) inhibitors
60 150 6b4lA Crystal structure of mcl-1 in complex with a bim competitive inhibitor
58 155 6b4uA Crystal structure of mcl-1 in complex with a bim competitive inhibitor
61 170 6arkA Crystal structure of compound 10 covalently bound to k-ras g12c
40 108 5uvxA Brd4 bromodomain 2 with a-1359643
41 109 5uvsA Brd4_bd2_a-1406537
40 109 5uvzA Brd4 bromodomain 2 with a-1354689
25 83 5vk1A Crystal structure of human mdm4 in complex with a 12-mer lysine-cysteine side chain dithiocarbamate stapled peptide inhibitor pmi
43 131 5cy9A Crystal structure of the first bromodomain of human brd4 in complex with benzo[cd]indol-2(1h)-one ligand
41 129 5d0cA Crystal structure of the first bromodomain of human brd4 in complex with benzo[cd]indol-2(1h)-one ligand
41 132 5coiA Crystal structure of the first bromodomain of human brd4 in complex with benzo[cd]indol-2(1h)-one ligand