Search results query: Phosphorylase Kinase; domain 1

Found 4147 chains in Genus chains table. Displaying 901 - 950. Applied filters: Proteins

Total Genus	Sequence Length	pdb	Title
75	276	3skcA	Human b-raf kinase in complex with an amide linked pyrazolopyridine inhibitor
84	298	3sqqA	Cdk2 in complex with inhibitor rc-3-96
99	307	3socA	Crystal structure of activin receptor type-iia (acvr2a) kinase domain in complex with a quinazolin
103	298	3sg8A	Crystal structure of aminoglycoside-2''-phosphotransferase type iva tobramycin complex
91	304	3slsA	Crystal structure of human mek-1 kinase in complex with ucb1353770 and amppnp
124	438	3soaA	Full-length human camkii
107	350	3sd0A	Identification of a glycogen synthase kinase-3b inhibitor that attenuates hyperactivity in clock mutant mice
88	316	3sheA	Novel atp-competitive mk2 inhibitors with potent biochemical and cell-based activity throughout the series
77	287	3sc1A	Novel isoquinolone pdk1 inhibitors discovered through fragment-based lead discovery
95	296	3sgcA	Crystal structure of apo aminoglycoside-2''-phosphotransferase type iva
96	418	3sdjA	Structure of rnase-inactive point mutant of oligomeric kinase/rnase ire1
100	297	3sg9A	Crystal structure of aminoglycoside-2''-phosphotransferase type iva kanamycin a complex
104	350	3sayA	Crystal structure of human glycogen synthase kinase 3 beta (gsk3b) in complex with inhibitor 142
94	310	3s95A	Crystal structure of the human limk1 kinase domain in complex with staurosporine
75	298	3s2pA	Crystal structure of cdk2 with a 2-aminopyrimidine compound
80	298	3rzbA	Cdk2 in complex with inhibitor rc-2-23
96	355	3rtpA	Design and synthesis of brain penetrant selective jnk inhibitors with improved pharmacokinetic properties for the prevention of neurodegeneration
85	349	3s4qA	P38 alpha kinase complexed with a pyrazolo-triazine based inhibitor
84	288	3rwqA	Discovery of a novel, potent and selective inhibitor of 3-phosphoinositide dependent kinase (pdk1)
104	349	3s3iA	P38 kinase crystal structure in complex with small molecule inhibitor
88	292	3rvgA	Crystals structure of jak2 with a 1-amino-5h-pyrido[4,3-b]indol-4-carboxamide inhibitor
82	287	3rwpA	Discovery of a novel, potent and selective inhibitor of 3-phosphoinositide dependent kinase (pdk1)
104	334	3rpsA	Structure of human ck2alpha in complex with the atp-competitive inhibitor 3-(4,5,6,7-tetrabromo-1h-benzotriazol-1-yl)propan-1-ol
85	298	3royA	Cdk2 in complex with inhibitor kvr-1-154
83	298	3rm6A	Cdk2 in complex with inhibitor kvr-2-80
86	298	3rprA	Cdk2 in complex with inhibitor rc-2-49
110	348	3rocA	Crystal structure of human p38 alpha complexed with a pyrimidinone compound
82	298	3rpvA	Cdk2 in complex with inhibitor rc-2-88
79	298	3rniA	Cdk2 in complex with inhibitor rc-3-86
83	298	3rpoA	Cdk2 in complex with inhibitor kvr-1-156
79	298	3rmfA	Cdk2 in complex with inhibitor rc-2-33
77	290	3rnyA	Crystal structure of human rsk1 c-terminal kinase domain
79	298	3rpyA	Cdk2 in complex with inhibitor rc-2-40
117	406	3rp9A	Crystal structure of the apo mapk from toxoplasma gondii, 25.m01780 or tgme49_007820
83	298	3rm7A	Cdk2 in complex with inhibitor kvr-1-91
114	351	3rawA	Crystal structure of human cdc-like kinase 3 isoform in complex with leucettine l41
79	298	3r8uA	Cdk2 in complex with inhibitor rc-1-132
83	282	3rcjA	Rapid preparation of triazolyl substituted nh-heterocyclic kinase inhibitors via one-pot sonogashira coupling tms-deprotection cuaac sequence
88	298	3r9nA	Cdk2 in complex with inhibitor rc-2-21
77	298	3r8lA	Cdk2 in complex with inhibitor l3-4
79	298	3rjcA	Cdk2 in complex with inhibitor l4-12
94	355	3rgfA	Crystal structure of human cdk8/cycc
82	298	3rahA	Cdk2 in complex with inhibitor rc-2-22
79	298	3ralA	Cdk2 in complex with inhibitor rc-2-34
79	298	3r7uA	Cdk2 in complex with inhibitor kvr-1-75
79	298	3r8mA	Cdk2 in complex with inhibitor l3-3
78	298	3rkbA	Cdk2 in complex with inhibitor rc-2-73
83	298	3r83A	Cdk2 in complex with inhibitor kvr-2-92
78	298	3r9hA	Cdk2 in complex with inhibitor rc-2-142
79	298	3r7iA	Cdk2 in complex with inhibitor kvr-1-74