Search results query ec: 2.7.11.24

Found 710 chains in Genus chains table. Displaying 451 - 500. Applied filters: Proteins

Total Genus	Sequence Length	pdb	Title
111	350	4fv8A	Crystal structure of the erk2 complexed with e63
98	349	4fv5A	Crystal structure of the erk2 complexed with ek9
108	347	4fv2A	Crystal structure of the erk2 complexed with ek5
103	349	4fv4A	Crystal structure of the erk2 complexed with ek7
105	348	4fuyA	Crystal structure of the erk2 complexed with ek2
105	346	4fv1A	Crystal structure of the erk2 complexed with ek4
103	350	4fv9A	Crystal structure of the erk2 complexed with e71
121	346	3qyzA	Crystal structure of erk2 in complex with an inhibitor
111	350	4fmqA	Crystal structure of human erk2 complexed with a mapk docking peptide
114	355	3r63A	Structure of erk2 (spe) mutant (s246e)
114	346	3qywA	Crystal structure of erk2 in complex with an inhibitor
107	351	3qudA	Human p38 map kinase in complex with 2-amino-phenylamino-benzophenone
106	349	3queA	Human p38 map kinase in complex with skepinone-l
109	356	3pzeA	Jnk1 in complex with inhibitor
112	357	3py3A	Crystal structure of phosphorylated p38alpha map kinase
98	356	3ptgA	Design and synthesis of a novel, orally efficacious tri-substituted thiophene based jnk inhibitor
108	350	3pg3A	Human p38 map kinase in complex with rl182
107	348	3p79A	P38 inhibitor-bound
103	348	3p78A	P38 inhibitor-bound
106	348	3p7bA	P38 inhibitor-bound
100	348	3p7cA	P38 inhibitor-bound
100	348	3p7aA	P38 inhibitor-bound
95	355	3oxiA	Design and synthesis of disubstituted thiophene and thiazole based inhibitors of jnk for the treatment of neurodegenerative diseases
105	350	3p4kA	The third conformation of p38a map kinase observed in phosphorylated p38a and in solution
105	348	3p5kA	P38 inhibitor-bound
106	355	3oy1A	Highly selective c-jun n-terminal kinase (jnk) 2 and 3 inhibitors with in vitro cns-like pharmacokinetic properties
92	350	3odzX	Crystal structure of p38alpha y323r active mutant
109	346	3o71A	Crystal structure of erk2/dcc peptide complex
101	348	3oc1A	Conformational plasticity of p38 map kinase dfg motif mutants in response to inhibitor binding
110	347	3o8pA	Conformational plasticity of p38 map kinase dfg motif mutants in response to inhibitor binding
113	349	3nwwA	P38 alpha kinase complexed with a 2-aminothiazol-5-yl-pyrimidine based inhibitor
102	348	3objA	Conformational plasticity of p38 map kinase dfg mutants in response to inhibitor binding
99	348	3o8uA	Conformational plasticity of p38 map kinase dfg motif mutants in response to inhibitor binding
99	349	3ocgA	P38 alpha kinase complexed with a 5-amino-pyrazole based inhibitor
92	350	3odyX	Crystal structure of p38alpha y323q active mutant
94	348	3obgA	Conformational plasticity of p38 map kinase dfg mutants in response to inhibitor binding
111	358	3o2mA	Crystal structure of jnk1-alpha1 isoform complex with a biaryl tetrazol (a-82118)
110	348	3oefX	Crystal structure of y323f inactive mutant of p38alpha map kinase
96	349	3od6X	Crystal structure of p38alpha y323t active mutant
102	348	3o8tA	Conformational plasticity of p38 map kinase dfg-motif mutants in response to inhibitor binding
102	357	3o17A	Crystal structure of jnk1-alpha1 isoform
106	348	3nnxA	Crystal structure of phosphorylated p38 alpha in complex with dp802
111	348	3nnvA	Crystal structure of p38 alpha in complex with dp437
103	348	3newA	P38-alpha complexed with compound 10
118	357	3npcA	Crystal structure of jnk2 complexed with birb796
112	348	3nnuA	Crystal structure of p38 alpha in complex with dp1376
113	349	3nnwA	Crystal structure of p38 alpha in complex with dp802
107	349	3mw1A	P38 kinase crystal structure in complex with small molecule inhibitor
114	349	3mptA	Crystal structure of p38 kinase in complex with a pyrrole-2-carboxamide inhibitor
103	349	3mvmA	P38 alpha map kinase complexed with pyrrolotriazine inhibitor 7v