Search results query: Transferase(Phosphotransferase); domain 1

Found 4011 chains in Genus chains table. Displaying 1901 - 1950. Applied filters: Proteins

Total Genus	Sequence Length	pdb	Title
115	356	4h3bA	Crystal structure of jnk3 in complex with sab peptide
92	286	4hgtA	Crystal structure of ck1d with compound 13
100	349	4h3pA	Crystal structure of human erk2 complexed with a mapk docking peptide
90	263	4hcvA	Crystal structure of itk in complex with compound 53
105	356	4h39A	Crystal structure of jnk3 in complex with jip1 peptide
92	291	4hniA	Crystal structure of ck1e in complex with pf4800567
92	290	4hgeA	Jak2 kinase (jh1 domain) in complex with compound 8
72	275	4h58A	Braf in complex with compound 3
91	265	4hctA	Crystal structure of itk in complex with compound 52
104	352	4h3qA	Crystal structure of human erk2 complexed with a mapk docking peptide
103	341	4gygA	Crystal structure of the rio2 kinase from chaetomium thermophilum
82	273	4gw8A	Human proto-oncogene serine threonine kinase (pim1) in complex with a consensus peptide and leucettine l41
81	272	4h1jA	Crystal structure of pyk2 with the pyrazole 13a
92	273	4gu6A	Focal adhesion kinase catalytic domain in complex with n-{3-[(5-cyano-2-phenyl-1h-pyrrolo[2,3-b]pyridin-4-ylamino)- methyl]-pyridin-2-yl}-n-methyl-methanesulfonamide
83	299	4gueA	Structure of n-terminal kinase domain of rsk2 with flavonoid glycoside quercitrin
118	327	4grbA	Casein kinase 2 (ck2) bound to inhibitor
89	296	4gt5A	Crystal structure of the inactive trka kinase domain
106	341	4gyiA	Crystal structure of the rio2 kinase-adp/mg2+-phosphoaspartate complex from chaetomium thermophilum
83	272	4gu9A	Focal adhesion kinase catalytic domain in complex with (2-fluoro-phenyl)-(1h-pyrazolo[3,4-d]pyrimidin-4-yl)-amine
106	348	4gt3A	Atp-bound form of the erk2 kinase
93	307	4gs6A	Irreversible inhibition of tak1 kinase by 5z-7-oxozeaenol
83	271	4h1mA	Crystal structure of pyk2 with the indole 10c
100	329	4gubA	Casein kinase ii bound to inhibitor
85	288	4gt4A	Structure of unliganded, inactive ror2 kinase domain
111	348	4gsbA	Monoclinic crystal form of the apo-erk2
94	290	4gvjA	Tyk2 (jh1) in complex with adenosine di-phosphate
105	335	4gv1A	Pkb alpha in complex with azd5363
112	346	4gvaA	Adp-bound form of the erk2 kinase
77	274	4g9rA	B-raf v600e kinase domain bound to a type ii dihydroquinazoline inhibitor
107	333	4g3fA	Crystal structure of murine nf-kappab inducing kinase (nik) bound to a 2-(aminothiazoly)phenol (cmp2)
87	295	4gk2A	Human epha3 kinase domain in complex with ligand 66
97	291	4gfmA	Jak2 kinase (jh1 domain) with 2,6-dichloro-n-(2-oxo-2,5-dihydropyridin-4-yl)benzamide
99	362	4g6lA	Crystal structure of human cdk8/cycc in the dmg-in conformation
101	341	4g3dA	Crystal structure of human nf-kappab inducing kinase (nik)
90	295	4gk3A	Human epha3 kinase domain in complex with ligand 87
88	288	4gj3A	Tyk2 (jh1) in complex with 2,6-dichloro-4-cyano-n-[2-({[(1r,2r)-2-fluorocyclopropyl]carbonyl}amino)pyridin-4-yl]benzamide
64	276	4g9cA	Human b-raf kinase domain bound to a type ii pyrazolopyridine inhibitor
104	333	4g3gA	Crystal structure of murine nf-kappab inducing kinase (nik) v408l bound to a 2-(aminothiazolyl)phenol (cmp3)
77	278	4gh2A	Crystal structure of the chk1
89	304	4gcjA	Cdk2 in complex with inhibitor rc-3-89
106	347	4g6oA	Crystal structure of the erk2
111	342	4g3cA	Crystal structure of apo murine nf-kappab inducing kinase (nik)
109	348	4g6nA	Crystal structure of the erk2
76	321	4g5pA	Crystal structure of egfr kinase t790m in complex with bibw2992
87	289	4giiA	Tyk2 (jh1) in complex with 2,6-dichloro-4-cyano-n-{2-[(cyclopropylcarbonyl)amino]pyridin-4-yl}benzamide
91	277	4gfgA	Crystal structure of spleen tyrosine kinase complexed with r9021
84	321	4g5jA	Crystal structure of egfr kinase in complex with bibw2992
92	300	4gmyA	Jak2 kinase (jh1 domain) in complex with 2,6-dichloro-n-{2-[(cyclopropylcarbonyl)amino]pyridin-4-yl}benzamide
109	347	4geoA	P38a map kinase def-pocket penta mutant (m194a, l195a, h228a, i229a, y258a)
84	281	4gg5A	Crystal structure of cmet in complex with novel inhibitor