Found 1048 chains in Genus chains table. Displaying 1 - 50. Applied filters: Proteins

Search results query ec: 2.7.10.2

Total Genus Sequence Length pdb Title
6 58 1a0nB Nmr study of the sh3 domain from fyn proto-oncogene tyrosine kinase complexed with the synthetic peptide p2l corresponding to residues 91-104 of the p85 subunit of pi3-kinase, family of 25 structures
10 60 1jegA Solution structure of the sh3 domain from c-terminal src kinase complexed with a peptide from the tyrosine phosphatase pep
11 114 1bljA Nmr ensemble of blk sh2 domain, 20 structures
1 44 1cf4B Cdc42/ack gtpase-binding domain complex
5 67 1awwA Sh3 domain from bruton's tyrosine kinase, nmr, 42 structures
53 139 1ktmA Solution structure of fat domain of focal adhesion kinase
4 57 1awoA The solution nmr structure of abl sh3 and its relationship to sh2 in the sh(32) construct, 20 structures
14 107 1hctB Nmr structure of the human src sh2 domain complex
10 51 1f62A Wstf-phd
14 114 1blkA Nmr ensemble of blk sh2 domain using chemical shift refinement, 20 structures
7 63 1h92A Sh3 domain of human lck tyrosine kinase
11 106 1aouF Nmr structure of the fyn sh2 domain complexed with a phosphotyrosyl peptide, 22 structures
8 57 1kikA Sh3 domain of lymphocyte specific kinase (lck)
11 67 1gl5A Nmr structure of the sh3 domain from the tec protein tyrosine kinase
13 109 1ab2A Three-dimensional solution structure of the src homology 2 domain of c-abl
11 112 1csyA Syk tyrosine kinase c-terminal sh2 domain complexed with a phosphopeptidefrom the gamma chain of the high affinity immunoglobin g receptor, nmr
74 289 6d3kA Crystal structure of unphosphorylated human pkr kinase domain in complex with adp
66 284 6d3lA Crystal structure of unphosphorylated human pkr
0 8 6ehjD Human n-myristoyltransferase (nmt1) with myristoyl-coa and peptide bound
12 58 2o88A Crystal structure of the n114a mutant of abl-sh3 domain complexed with a designed high-affinity peptide ligand: implications for sh3-ligand interactions
0 9 1fbvB Structure of a cbl-ubch7 complex: ring domain function in ubiquitin-protein ligases
0 9 3zniB Structure of phosphotyr363-cbl-b - ubch5b-ub - zap-70 peptide complex
0 9 3buwA Crystal structure of c-cbl-tkb domain complexed with its binding motif in syk
12 63 6ipzZ Fyn sh3 domain r96w mutant, crystallized with 18-crown-6
89 271 6hm7A Crystal structure of spleen tyrosine kinase (syk) in complex with a 2-(phenoxymethyl)pyridine inhibitor
11 67 6ipyA His-tagged fyn sh3 domain r96i mutant
86 269 6hm6A Crystal structure of spleen tyrosine kinase (syk) in complex with a 2-(pyridinyloxymethyl)pyridine inhibitor
89 306 6hmxA Rip2 kinase catalytic domain complex with n(4,5dimethyl1hpyrazol3yl)7methoxy6(2methylpropane2sulfonyl)quinolin4amine
90 288 6hd4A Abl1 in complex with compound 7 and imatinib (sti-571)
86 287 6dudA Jak3 with cyanamide cp12
18 86 6ggsA Structure of rip2 card filament
87 287 6db4A Jak3 with cyanamide cp34
90 301 6elrA Human jak1 kinase domain in complex with compound 7
91 271 6di1A Crystal structure of btk in complex with covalent fragment ligand
84 287 6db3A Jak3 with cyanamide cp23
92 271 6di0A Crystal structure of btk in complex with fragment ligand
84 285 6da4A Jak3 with cyanamide cp10
88 266 6bkwA Btk complex with compound 12
87 263 6bkhA Btk complex with compound 11
87 264 6blnA Btk complex with compound 13
86 264 6bikA Btk complex with compound 7
82 264 6bkeA Btk complex with compound 10
88 269 6npeA C-abl kinase domain with the activator(cmpd6), 2-cyano-n-(4-(3,4-dichlorophenyl)thiazol-2-yl)acetamide
88 269 6npvA C-abl kinase domain with the activator(cmpd51), n-(1-(3,4-dichlorophenyl)-4-(2-hydroxyethyl)-4,5-dihydro-1h-pyrazol-3-yl)isonicotinamide
86 269 6npuA C-abl kinase domain with the activator(cmpd29), n-(1-(3,4-dichlorophenyl)-4,5-dihydro-1h-pyrazol-3-yl)acetamide
26 87 5yrnA Structure of rip2 card domain
89 271 6n9pA Discovery of affinity-based probes for btk occupancy assay
79 268 6nfiA Btk in complex with inhibitor n-(3-{[(2,6-dimethylphenyl)methyl]amino}-7-methoxyindeno[1,2-c]pyrazol-6-yl)methanesulfonamide
90 271 6nfhA Btk in complex with inhibitor 8-(2,3-dihydro-1h-inden-5-yl)-2-({4-[(2s)-3-(dimethylamino)-2-hydroxypropoxy]phenyl}amino)-5,8-dihydropteridine-6,7-dione
84 275 6i8zA Crystal structure of ptk2 in complex with bi-4464.