Found 114 chains in Genus chains table. Displaying 1 - 50. Applied filters: Proteins

Search results query: protein binding/inhibitor

Total Genus Sequence Length pdb Title
1 8 6keyB Structural basis for the regulation of inducible nitric oxide synthase (inos) by the spry domain-containing socs box protein 2 (spsb2)
53 200 6keyA Structural basis for the regulation of inducible nitric oxide synthase (inos) by the spry domain-containing socs box protein 2 (spsb2)
1 13 6pw8B Hydrocarbon-stapled paxillin peptide bound to the focal adhesion targeting (fat) domain of the focal adhesion kinase (fak)
57 126 6pw8A Hydrocarbon-stapled paxillin peptide bound to the focal adhesion targeting (fat) domain of the focal adhesion kinase (fak)
67 285 6v6zA Crystal structure of n-(4-((4-methoxy-n-(2,2,2-trifluoroethyl)phenyl)sulfonamido)isoquinolin-1-yl)-n-((4-methoxyphenyl)sulfonyl)glycine bound to human keap1 kelch domain
51 193 6jwnA Crystal structure of the spry domain of spsb2 in complex with cr9, a cyclic peptide inhibitor of spsb-inos interaction
56 203 6jwmA Crystal structure of the spry domain of spsb2 in complex with cr7, a potent cyclic peptide inhibitor of spsb2-inos interaction
0 7 6jwmB Crystal structure of the spry domain of spsb2 in complex with cr7, a potent cyclic peptide inhibitor of spsb2-inos interaction
0 9 6jwnB Crystal structure of the spry domain of spsb2 in complex with cr9, a cyclic peptide inhibitor of spsb-inos interaction
105 305 6pgdA Wdr5delta32 bound to peptidomimetic
97 305 6pgaA Wdr5delta32 bound to methyl (4-(4-(hydroxymethyl)-1h-imidazol-2-yl)butyl)carbamate
104 305 6pgcA Wdr5delta32 bound to methyl benzyl(4-(4-(hydroxymethyl)-1h-imidazol-2-yl)butyl)carbamate
103 304 6pg9A Wdr5delta23 bound to n-(4-(5-(hydroxymethyl)-1h-imidazol-2-yl)butyl)benzamide
104 305 6pgfA Wdr5delta32 bound to n-(4-(4-(hydroxymethyl)-1h-imidazol-2-yl)butyl)acrylamide
104 305 6pg4A Wdr5delta32 bound to (2-methyl-1h-imidazol-4-yl)methanol
102 305 6pg5A Wdr5delta32 bound to benzyl (4-(5-(hydroxymethyl)-1h-imidazol-2-yl)butyl)carbamate
99 305 6pg7A Wdr5delta32 bound to (2-(3-methoxy-3-phenylpropyl)-1h-imidazol-4-yl)methanol
102 304 6pg3A Wdr5delta23 bound to (2-butyl-1h-imidazol-4-yl)methanol
103 305 6pgbA Wdr5delta32 bound to n-(4-(5-(hydroxymethyl)-1h-imidazol-2-yl)butyl)-2-phenylacetamide
104 304 6pg8A Wdr5delta23 bound to (2-(3-phenylpropyl)-1h-imidazol-4-yl)methanol
100 305 6pgeA Wdr5delta32 bound to ethyl 3-(4-(hydroxymethyl)-1h-imidazol-2-yl)propanoate
102 304 6pg6A Wdr5delta23 bound to n-(4-(5-(hydroxymethyl)-1h-imidazol-2-yl)butyl)acetamide
38 127 6mh7A Crystal structure of the first bromodomain of human brd4 in complex with skt-68, a 1,4,5-trisubstituted imidazole analogue
0 7 5z8hB Apc with an inhibitor
55 233 6albA Crebbp bromodomain in complex with cpd 30 (1-(3-(3-(1-methyl-1h-pyrazol-4-yl)isoquinolin-8-yl)-1-(tetrahydro-2h-pyran-4-yl)-1,4,6,7-tetrahydro-5h-pyrazolo[4,3-c]pyridin-5-yl)ethan-1-one)
44 124 6c3lA Crystal structure of bcl6 btb domain with compound 15f
146 339 5z8hA Apc with an inhibitor
42 110 6duvA Crystal structure of the second bromodomain of human brd4 in complex with ms417 inhibitor
43 123 6cq1A Bcl6 btb domain in complex with 15a
143 343 5iz8A Protein-protein interaction
151 339 5iz6A Protein-protein interaction
155 341 5izaA Protein-protein interaction
54 139 5i29A Taf1(2) bound to a pyrrolopyridone compound
40 114 5i83A Crystal structure of the bromodomain of human crebbp bound to the benzodiazepinone g02773986
41 115 5i86A Crystal structure of the bromodomain of human crebbp bound to the benzodiazepinone g02778174
56 135 5i1qA Second bromodomain of taf1 bound to a pyrrolopyridone compound
169 520 6b41A Menin bound to m-525
39 114 6alcA Crebbp bromodomain in complex with cpd 4 (1-(1-(cyclopropylmethyl)-3-(1h-indol-4-yl)-1,4,6,7-tetrahydro-5h-pyrazolo[4,3-c]pyridin-5-yl)ethan-1-one)
0 8 5xn3B Crystal structure of spsb2 in complex with a rational designed rgd containing cyclic peptide inhibitor of spsb2-inos interaction
51 199 5xn3A Crystal structure of spsb2 in complex with a rational designed rgd containing cyclic peptide inhibitor of spsb2-inos interaction
44 203 5y2qA X-ray structure of acetylcholine binding protein (achbp) complexed with a small molecule
151 339 5b6gA Protein-protein interaction
43 124 4e96A Crystal structure of the first bromodomain of human brd4 in complex with the inhibitor pfi-1
100 235 4dhqA Small-molecule inhibitors of 14-3-3 protein-protein interactions from virtual screening
101 235 4dhpA Small-molecule inhibitors of 14-3-3 protein-protein interactions from virtual screening
102 235 4dhuA Small-molecule inhibitors of 14-3-3 protein-protein interactions from virtual screening
102 235 4dhrA Small-molecule inhibitors of 14-3-3 protein-protein interactions from virtual screening
100 235 4dhsA Small-molecule inhibitors of 14-3-3 protein-protein interactions from virtual screening
99 235 4dhnA Small-molecule inhibitors of 14-3-3 protein-protein interactions from virtual screening
100 235 4dhoA Small-molecule inhibitors of 14-3-3 protein-protein interactions from virtual screening