Found 462 chains in Genus chains table. Displaying 51 - 100. Applied filters: Proteins

Search results query: SH3_1

Total Genus Sequence Length pdb Title
9 59 1gfdA Solution structure and ligand-binding site of the c-terminal sh3 domain of grb2
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
7 63 1h92A Sh3 domain of human lck tyrosine kinase
6 60 1h3hA Structural basis for specific recognition of an rxxk-containing slp-76 peptide by the gads c-terminal sh3 domain
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
12 63 6ipzZ Fyn sh3 domain r96w mutant, crystallized with 18-crown-6
11 67 6ipyA His-tagged fyn sh3 domain r96i mutant
13 74 6c4sA Human csrc sh3 domain in complex with choline kinase fragment 60-69
58 202 6ghmC Structure of pp1 alpha phosphatase bound to aspp2
15 63 6nmwA Crystal structure of the human lyn sh3 domain
16 77 6edfA Fragment of a tyrosine-protein kinase
134 449 5mo4A Abl1 kinase (t334i_d382n) in complex with asciminib and nilotinib
10 58 5l23A Crystal structure of the complex between the n-terminal sh3 domain of crkii and a proline-rich ligand
107 339 5jmqA Crystal structures of a methyl transferase
10 68 5ixfA Solution structure of the stam2 sh3 with amsh derived peptide complex
12 56 5ihkA Crystal structure of the alpha spectrin sh3 domain mutant n47a
10 58 5ih2A Structure, thermodynamics, and the role of conformational dynamics in the interactions between the n-terminal sh3 domain of crkii and proline-rich motifs in cabl
6 56 5i11A Crystal structure of the intertwined form of the src tyrosine kinase sh3 domain t114s-q128r mutant
128 447 5h0gA Crystal structure of hck complexed with a pyrrolo-pyrimidine inhibitor (s)-2-(((1r,4s)-4-(4-amino-5-(4-phenoxyphenyl)-7h-pyrrolo[2,3-d]pyrimidin-7-yl)cyclohexyl)amino)-n,4-dimethylpentanamide
125 447 5h0eA Crystal structure of hck complexed with a pyrrolo-pyrimidine inhibitor (s)-2-(((1r,4s)-4-(4-amino-5-(4-phenoxyphenyl)-7h-pyrrolo[2,3-d]pyrimidin-7-yl)cyclohexyl)amino)-4-methylpentanamide
124 449 6f3fA Autoinhibited src kinase bound to adp
22 115 6b25A Crystal structure of human stac1 tandem sh3 domains (288-402)
58 255 6amvA Abl 1b regulatory module 'inhibiting state'
9 58 6atvA The molecular mechanisms by which ns1 of the 1918 spanish influenza a virus hijack host protein-protein interactions
48 255 6amwA Abl1b regulatory module 'activating' conformation
74 293 5yprA Crystal structure of psd-95 sh3-gk domain in complex with a synthesized inhibitor
12 64 5xggA Crystal structure c-terminal sh3 domain of myosin ib from entamoeba histolytica
11 55 4f17A Crystal structure of the alpha spectrin sh3 domain at ph 9
12 57 4f16A Crystal structure of the alpha spectrin sh3 domain at ph 5
15 65 4esrA Molecular and structural characterization of the sh3 domain of ahi-1 in regulation of cellular resistance of bcr-abl+ chronic myeloid leukemia cells to tyrosine kinase inhibitors
13 58 4eikA Crystal structure of the human fyn sh3 domain in complex with the synthetic peptide vsl12
12 57 4d8dA Crystal structure of hiv-1 nef fyn-sh3 r96w variant
32 163 4d8kA Crystal structure of a sh3-sh2 domains of a lymphocyte-specific protein tyrosine kinase (lck) from homo sapiens at 2.36 a resolution
10 67 4cc4B Complex of inlc of listeria monocytogenes and human tuba c-terminal sh3 domain
11 61 4cc3A Complex of human tuba c-terminal sh3 domain and mena proline-rich peptide - h3
12 58 4cc7A Crystal structure of the sixth or c-terminal sh3 domain of human tuba in complex with proline-rich peptides of n-wasp. space group p41
12 63 4cc2A Complex of human tuba c-terminal sh3 domain with human n-wasp proline- rich peptide - p212121
127 290 4bneA Pacsin2 interacts with membranes and actin-filaments
59 202 4a63B Crystal structure of the p73-aspp2 complex at 2.6a resolution
117 447 3vs6A Crystal structure of hck complexed with a pyrazolo-pyrimidine inhibitor tert-butyl {4-[4-amino-1-(propan-2-yl)-1h-pyrazolo[3,4-d]pyrimidin-3-yl]-2-methoxyphenyl}carbamate
116 447 3vs2A Crystal structure of hck complexed with a pyrrolo-pyrimidine inhibitor 7-[cis-4-(4-methylpiperazin-1-yl)cyclohexyl]-5-(4-phenoxyphenyl)-7h-pyrrolo[2,3-d]pyrimidin-4-amine
112 447 3vs1A Crystal structure of hck complexed with a pyrrolo-pyrimidine inhibitor 1-[4-(4-amino-7-cyclopentyl-7h-pyrrolo[2,3-d]pyrimidin-5-yl)phenyl]-3-phenylurea
117 447 3vrzA Crystal structure of hck complexed with a pyrrolo-pyrimidine inhibitor 1-[4-(4-amino-7-cyclopentyl-7h-pyrrolo[2,3-d]pyrimidin-5-yl)phenyl]-3-benzylurea
116 447 3vs5A Crystal structure of hck complexed with a pyrrolo-pyrimidine inhibitor 7-(1-methylpiperidin-4-yl)-5-(4-phenoxyphenyl)-7h-pyrrolo[2,3-d]pyrimidin-4-amine
122 447 3vryA Crystal structure of hck complexed with a pyrrolo-pyrimidine inhibitor 4-amino-5-(4-phenoxyphenyl)-7h-pyrrolo[2,3-d]pyrimidin-7-yl-cyclopentane
110 447 3vs4A Crystal structure of hck complexed with a pyrrolo-pyrimidine inhibitor 5-(4-phenoxyphenyl)-7-(tetrahydro-2h-pyran-4-yl)-7h-pyrrolo[2,3-d]pyrimidin-4-amine
123 447 3vs3A Crystal structure of hck complexed with a pyrrolo-pyrimidine inhibitor 7-[trans-4-(4-methylpiperazin-1-yl)cyclohexyl]-5-(4-phenoxyphenyl)-7h-pyrrolo[2,3-d]pyrimidin-4-amine
106 447 3vs7A Crystal structure of hck complexed with a pyrazolo-pyrimidine inhibitor 1-cyclopentyl-3-(1h-pyrrolo[2,3-b]pyridin-5-yl)-1h-pyrazolo[3,4-d]pyrimidin-4-amine
109 447 3vs0A Crystal structure of hck complexed with a pyrrolo-pyrimidine inhibitor n-[4-(4-amino-7-cyclopentyl-7h-pyrrolo[2,3-d]pyrimidin-5-yl)phenyl]benzamide