Search results query ec: 2.7.11.1

Found 3590 chains in Genus chains table. Displaying 2151 - 2200. Applied filters: Proteins

Total Genus	Sequence Length	pdb	Title
94	295	5deyA	Crystal structure of pak1 in complex with an inhibitor compound g-5555
97	293	5dfpA	Crystal structure of pak1 in complex with an inhibitor compound frax1036
107	389	5cyzA	Structure of s. cerevisiae hrr25:mam1 complex, form 1
84	297	5di1A	Map4k4 in complex with an inhibitor
2	16	5de2C	Structural mechanism of nek7 activation by nek9-induced dimerisation
100	295	5dewA	Crystal structure of pak1 in complex with an inhibitor compound 5
81	298	5d9kA	Rsk2 n-terminal kinase in complex with bi-d1870
97	332	4yomB	Structure of sad kinase
102	297	4yo6A	Irak4-inhibitor co-structure
101	328	5cquA	Monoclinic complex structure of protein kinase ck2 catalytic subunit with a benzotriazole-based inhibitor generated by click-chemistry
73	318	4z8lA	Crystal structure of dcaf1/siv-mnd vpx/mnd samhd1 ntd ternary complex
113	328	5cx9A	Crystal structure of ck2alpha with (methyl 4-((3-(3-chloro-4-(phenyl)benzylamino)propyl)amino)-4-oxobutanoate bound
100	335	4ynzA	Structure of the n-terminal domain of sad
112	327	5cu6A	Crystal structure of ck2alpha
78	273	5csxA	Crystal structure of b-raf in complex with bi 882370
112	327	5cu4A	Crystal structure of ck2alpha with compound 10 bound
78	273	5ct7A	Braf in complex with raf265
107	331	5cqwA	Tetragonal complex structure of protein kinase ck2 catalytic subunit with a benzotriazole-based inhibitor generated by click-chemistry
82	318	5ajaA	Crystal structure of mandrill samhd1 (amino acid residues 1-114) bound to vpx isolated from mandrill and human dcaf1 (amino acid residues 1058-1396)
80	282	4yffA	Tnni3k complexed with inhibitor 2
92	294	4ypdA	Crystal structure of dapk1 catalytic domain in complex with the hinge binding fragment 4-methylpyridazine
116	325	5cu3A	Crystal structure of ck2alpha with compound 10 bound
1	36	5csjC	S100b-rsk1 crystal structure b
84	274	4yznA	Humanized roco4 bound to compound 19
75	273	5cswA	B-raf in complex with dabrafenib
84	296	4zp5A	Map4k4 in complex with inhibitor
118	400	4yveA	Rock 1 bound to methoxyphenyl thiazole inhibitor
113	326	5cvgA	Crystal structure of ck2alpha with a novel closed conformation of the ad loop
111	327	5cvfA	Crystal structure of ck2alpha with compound 5 bound
110	324	5cshA	Crystal structure of ck2alpha with compound 4 bound
113	328	5cu2A	Crystal structure of ck2alpha with 2-hydroxy-5-methylbenzoic acid and (methyl 4-((3-(3-chloro-4-(phenyl)benzylamino)propyl)amino)-4-oxobutanoat bound
112	327	5cs6A	Crystal structure of ck2alpha with compound 3 bound
80	289	5ajqA	Human lok (stk10) in complex with bosutinib
107	402	4yzdA	Crystal structure of human phosphorylated ire1alpha in complex with adp-mg
101	358	5airA	Structural analysis of mouse gsk3beta fused with lrp6 peptide.
78	286	4yfiA	Tnni3k complexed with inhibitor 1
112	327	5cvhA	Crystal structure of ck2alpha
23	118	4yomA	Structure of sad kinase
111	326	5ct0A	Crystal structure of ck2alpha with 3-(3-chloro-4-(phenyl)benzylamino)propan-1-ol bound
110	327	5csvA	Crystal structure of ck2alpha with compound 6 bound
2	19	5csnC	S100b-rsk1 crystal structure c
77	271	4yhtA	Braf complexed with an inhibitor
84	297	5cwzA	Crystal structure of the kinase domain of human traf2 and nck-interacting protein kinase
60	276	4yzmA	Humanized roco4 bound to lrrk2-in1
111	324	5ctpA	Crystal structure of ck2alpha with n-(3-(3-chloro-4-(phenyl)benzylamino)propyl)acetamide bound
105	402	4yzcA	Crystal structure of pire1alpha in complex with staurosporine
269	949	4xx5A	Structure of pi3k gamma in complex with an inhibitor
102	403	4yz9A	Crystal structure of human phosphorylated ire1alpha in complex with a type iii kinase inhibitor (gsk2850163a)
278	943	4wwpA	Crystal structure of human pi3k-gamma in complex with pyridinylquinoline inhibitor n-{(1s)-1-[8-chloro-2-(2-methylpyridin-3-yl)quinolin-3-yl]ethyl}-9h-purin-6-amine
78	277	5ci7A	Structure of ulk1 bound to a selective inhibitor