Found 318 chains in Genus chains table. Displaying 1 - 50. Applied filters: Proteins

Search results query: transferase/inhibitor

Total Genus Sequence Length pdb Title
54 186 7lunA Human parp14 (artd8), catalytic fragment in complex with rbn011980
134 381 7kdbA Crystal structure of human methionine adenosyltransferase 2a (mat2a) in complex with sam and allosteric inhibitor compound 35
134 382 7kccA Crystal structure of human methionine adenosyltransferase 2a (mat2a) in complex with sam and allosteric inhibitor ag-270
137 380 7kceA Crystal structure of human methionine adenosyltransferase 2a (mat2a) in complex with sam and allosteric inhibitor compound 2
51 187 7l9yA Human parp14 (artd8), catalytic fragment in complex with rbn012042
134 382 7kcfA Crystal structure of human methionine adenosyltransferase 2a (mat2a) in complex with sam and allosteric inhibitor agi-24512
133 381 7kdaA Crystal structure of human methionine adenosyltransferase 2a (mat2a) in complex with sam and allosteric inhibitor compound 34
123 404 6xddA Crystal structure of ire1 in complex with g-3053
108 425 7kwuB Crystal structure of hiv-1 rt in complex with 16c (k07-15)
159 556 7kwuA Crystal structure of hiv-1 rt in complex with 16c (k07-15)
55 211 7cajA Crystal structure of setdb1 tudor domain in complexed with compound 2.
263 949 7kkeA Phosphoinositide 3-kinase gamma bound to a thiazole inhibitor
50 189 6we2A Human parp14 (artd8), catalytic fragment in complex with rbn012759
162 625 7m05A Cryoem structure of prmt5 bound to covalent pbm-site inhibitor brd-6988
48 306 7m05B Cryoem structure of prmt5 bound to covalent pbm-site inhibitor brd-6988
100 356 7kskA Thiophenyl-pyrazolourea derivatives as potent, brian penetrant, orally bioavailable, and isoform-selective jnk3 inhibitors
130 380 7l1aA Human methionine adenosyltransferase 2a bound to methylthioadenosine and inhibitor, di-imido triphosphate (pnpnp)
105 356 7ksiA Thiophenyl-pyrazolourea derivatives as potent, brian penetrant, orally bioavailable, and isoform-selective jnk3 inhibitors
79 273 6l17A Crystal structure of ser/thr kinase pim1 in complex with 10-debc derivatives
41 158 7kdoA Crystal structure of escherichia coli hppk in complex with bisubstrate inhibitor hp-73
41 158 7kdrA Crystal structure of escherichia coli hppk in complex with bisubstrate inhibitor hp-75
86 269 6xjkA Jak2 jh2 in complex with jak067
105 336 6wl6A Cocomplex structure of deoxyhypusine synthase with inhibitor 6-[(2r)-1-amino-4-methylpentan-2-yl]-3-(pyridin-3-yl)-4h,5h,6h,7h-thieno[2,3-c]pyridin-7-one
109 336 6wkzA Cocomplex structure of deoxyhypusine synthase with inhibitor 6-[(1r)-2-amino-1-phenylethyl]-3-(pyridin-3-yl)-4h,5h,6h,7h-thieno[2,3-c]pyridin-7-one
80 273 6l11A Crystal structure of ser/thr kinase pim1 in complex with 10-debc derivatives
83 273 6l12A Crystal structure of ser/thr kinase pim1 in complex with 10-debc derivatives
77 273 6l13A Crystal structure of ser/thr kinase pim1 in complex with 10-debc derivatives
79 273 6l15A Crystal structure of ser/thr kinase pim1 in complex with 10-debc derivatives
79 273 6l16A Crystal structure of ser/thr kinase pim1 in complex with 10-debc derivatives
80 273 6l14A Crystal structure of ser/thr kinase pim1 in complex with 10-debc derivatives
79 275 6wiwA C-src bound to atp-competitive inhibitor i14
42 150 6wfgA Crystal structure of human naa50 in complex with an inhibitor (compound 3) identified using dna encoded library technology
42 151 6wfnA Crystal structure of human naa50 in complex with accoa and an inhibitor (compound 4a) identified using dna encoded library technology
38 165 6wf5A Crystal structure of human naa50 in complex with a truncated cofactor derived inhibitor (compound 2)
42 150 6wf3A Crystal structure of human naa50 in complex with a cofactor derived inhibitor (compound 1)
40 153 6wfoA Crystal structure of human naa50 in complex with accoa and an inhibitor (compound 4b) identified using dna encoded library technology
83 348 6vkqA Crystal structure of human parp-1 cat domain bound to inhibitor eb-47
92 348 6vkoA Crystal structure of human parp-1 cat domain bound to inhibitor uktt15
106 350 6vkkA Crystal structure of human parp-1 cat domain bound to inhibitor rucaparib
83 288 6w8lA Crystal structure of jak1 kinase with compound 10
94 290 6vnsA Crystal structure of tyk2 kinase with compound 13
96 290 6vnvA Crystal structure of tyk2 kinase with compound 14
96 290 6vnxA Crystal structure of tyk2 kinase with compound 19
95 290 6vnyA Crystal structure of tyk2 kinase with compound 10
126 336 6p4vA 1.65 angstrom ternary complex of deoxyhypusine synthase with cofactor nad and spermidine mimic inhibitor gc7
105 321 6v8kA Crystal structure of the p300 acetyltransferase domain with peptide-competitive inhibitor 2
112 344 6v90A Crystal structure of the p300 acetyltransferase domain with accoa competitive inhibitor 12
108 342 6v8nA Crystal structure of the p300 acetyltransferase domain with accoa competitive inhibitor 17
121 351 6pgrA Cocomplex structure of deoxyhypusine synthase with inhibitor 6-bromo-n-(1h-indol-4-yl)-1-benzothiophene-2-carboxamide
94 347 6v8bA Crystal structure of the p300 acetyltransferase domain with accoa competitive inhibitor 1