Found 206 chains in Genus chains table. Displaying 1 - 50. Applied filters: Proteins

Search results query ec: 2.7.1.153

Total Genus Sequence Length pdb Title
295 926 6zacA Pi3k delta in complex with [(dimethylamino)methyldihydrobenzoxazin2methoxypyridinyl]methanesulfonamide
289 926 6zaaA Pi3k delta in complex with methoxy(methylsulfamoyl)pyridinyln(methylpiperidinyl)dihydrobenzoxazinecarboxamide
301 1012 6g6wA Human pi3kdelta in complex with ligand lasw1976
296 926 6q6yA Pi3k delta in complex with n(2chloro5phenylpyridin3yl)benzenesulfonamide
296 926 6q73A Pi3k delta in complex with n[2chloro5(3,6dihydro2hpyran4yl)pyridin3yl]methanesulfonamide
261 918 6gy0A Mpi3kd in complex with az3
243 942 6fh5A Pi3kg in complex with compound 7
276 1084 6nctA Structure of p110alpha/nish2 - vector data collection
253 919 6mulA Murine pi3k delta kinsae domain - cpd 1
252 919 6mumA Murine pi3k delta kinsae domain - cpd 3
325 1058 5itdA Crystal structure of pi3k alpha with pi3k delta inhibitor
309 1052 5xgiA Crystal structure of pi3k complex with an inhibitor
295 1048 5xghA Crystal structure of pi3k complex with an inhibitor
292 1048 5xgjA Crystal structure of pi3k complex with an inhibitor
287 1013 5vlrA Crystal structure of pi3k delta in complex with a trifluoro-ethyl-pyrazol-pyrolotriazine inhibitor
298 1079 5swoA Crystal structure of pi3kalpha in complex with fragments 4 and 19
281 919 5ncyA Mpi3kd in complex with inh1
275 919 5ngbA X-ray diffraction crystal structure of the murine pi3k p110delta in complex with a pan inhibitor
281 916 5nczA Mpi3kd in complex with inh1
275 919 5t2lA Mpi3kd in complex with 7l
264 1011 5m6uA Human pi3kdelta in complex with lasw1579
267 925 5l72A Pi3 kinase delta in complex with n-[6-(5-methanesulfonamido-6-methoxypyridin-3-yl)-1,3-dihydro-2-benzofuran-4-yl]-2-(morpholin-4-yl)acetamide
251 944 5jhaA Structure of phosphoinositide 3-kinase gamma (pi3k) bound to the potent inhibitor pikin2
229 948 5jhbA Structure of phosphoinositide 3-kinase gamma (pi3k) bound to the potent inhibitor pikin3
269 917 5i4uA The crystal structure of pi3kdelta with compound 34
232 918 5i6uA The crystal structure of pi3kdelta with compound 32
340 1061 5fi4A Discovery of imidazo[1,2-a]-pyridine inhibitors of pan-pi3 kinases that are efficacious in a mouse xenograft model
294 1015 5dxuA P110delta/p85alpha with gdc-0326
321 1061 5dxhA P110alpha/p85alpha with compound 5
265 942 5edsA Crystal structure of human pi3k-gamma in complex with benzimidazole inhibitor 5
258 948 4urkA Pi3kg in complex with azd6482
243 942 6gq7A Pi3kg in complex with inh
281 919 6ftnA Mpi3kd in complex with az2
293 926 6ez6A Pi3 kinase delta in complex with methyl 5-(4-(5-((4-isopropylpiperazin-1-yl)methyl)oxazol-2-yl)-1h-indazol-6-yl)-2-methoxynicotinate
262 914 6dgtA Selective pi3k beta inhibitor bound to pi3k delta
263 947 6c1sA Phosphoinositide 3-kinase gamma bound to an pyrrolopyridinone inhibitor
274 949 6audA Pi3k-gamma k802t in complex with cpd 8 10-((1-(tert-butyl)piperidin-4-yl)sulfinyl)-2-(1-isopropyl-1h-1,2,4-triazol-5-yl)-5,6-dihydrobenzo[f]imidazo[1,2-d][1,4]oxazepine
395 1347 4yknA Pi3k alpha lipid kinase with active site inhibitor
278 925 5ae9A Crystal structure of mouse pi3 kinase delta in complex with gsk2292767
277 925 5ae8A Crystal structure of mouse pi3 kinase delta in complex with gsk2269557
334 1060 4zopA Co-crystal structure of lipid kinase pi3k alpha with a selective phosphatidylinositol-3 kinase alpha inhibitor
242 946 4hleA Compound 21 (1-alkyl-substituted 1,2,4-triazoles)
279 951 4ezlA Potent and selective inhibitors of pi3k-delta: obtaining isoform selectivity from the affinity pocket and tryptophan shelf
264 947 4hvbA Catalytic unit of pi3kg in complex with pi3k/mtor dual inhibitor pf-04979064
267 949 4fa6A Design and synthesis of a novel pyrrolidinyl pyrido pyrimidinone derivative as a potent inhibitor of pi3ka and mtor
265 945 4f1sA Crystal structure of human pi3k-gamma in complex with a pyridyl-triazine-sulfonamide inhibitor
275 949 4ezkA Potent and selective inhibitors of pi3k-delta: obtaining isoform selectivity from the affinity pocket and tryptophan shelf
253 950 4fadA Design and synthesis of a novel pyrrolidinyl pyrido pyrimidinone derivative as a potent inhibitor of pi3ka and mtor
273 951 4ezjA Potent and selective inhibitors of pi3k-delta: obtaining isoform selectivity from the affinity pocket and tryptophan shelf
256 945 4dk5A Crystal structure of human pi3k-gamma in complex with a pyridyl-triazine inhibitor