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enzyme (lysozyme)

 
Enzymes
  Enzyme classes:
  EC 1: Oxidoreductases
  EC 2: Transferases
    EC 2.1
    EC 2.2
    EC 2.3
    EC 2.4
    EC 2.5
    EC 2.6
    EC 2.7
      EC 2.7.1
      EC 2.7.2
      EC 2.7.3
      EC 2.7.4
      EC 2.7.5
      EC 2.7.6
      EC 2.7.7
      EC 2.7.8
      EC 2.7.9
      EC 2.7.10
        EC 2.7.10.1
        EC 2.7.10.2
      EC 2.7.11
      EC 2.7.12
      EC 2.7.13
      EC 2.7.14
    EC 2.8
    EC 2.9
  EC 3: Hydrolases
  EC 4: Lyases
  EC 5: Isomerases
  EC 6: Ligases
  General information:
  Catalytic mechanism
  Enzyme kinetics
  Inhibitors
  Enzymes in industry

EC 2.7.10.2 - ATP:[protein] - L- tyrosine O- phosphotransferase (non- specific) (non- specific protein- tyrosine kinase)



3D structures of EC 2.7.10.2 - non-specific protein-tyrosine kinase in Protein Data Bank

updated: 17 May 2012, 1:59

In total: 250 PDB structures of EC 2.7.10.2 - non-specific protein-tyrosine kinase:
  1. 3p08: Crystal Structure of The Human Btk Kinase Domain
  2. 3oct: Crystal Structure of Bruton's Tyrosine Kinase Mutant V555R in Complex with Dasatinib
  3. 3ocs: Crystal Structure of Bruton's Tyrosine Kinase in Complex with Inhibitor Cgi1746
  4. 3nz0: Non-phosphorylated Tyk2 Kinase with Cmp6
  5. 3nyx: Non-phosphorylated Tyk2 Jh1 Domain with Quinoline-thiadiazole- Thiophene Inhibitor
  6. 3nhn: Crystal Structure of The Src-family Kinase Hck Sh3-sh2-linker Regulatory Region
  7. 3mss: Abl Kinase in Complex with Imatinib and Fragment (frag2) in The Myristate Site
  8. 3ms9: Abl Kinase in Complex with Imatinib and a Fragment (frag1) in The Myristate Pocket
  9. 3mpm: Lck Complexed with a Pyrazolopyrimidine
  10. 3mj2: X-ray Crystal Structure of Itk Complexed with Inhibitor Bms-509744
  11. 3mj1: X-ray Crystal Structure of Itk Complexed with Inhibitor Ro5191614
  12. 3miy: X-ray Crystal Structure of Itk Complexed with Sunitinib
  13. 3lxp: Structural and Thermodynamic Characterization of The Tyk2 and Jak3 Kinase Domains in Complex with Cp-690550 and Cmp-6
  14. 3lxn: Structural and Thermodynamic Characterization of The Tyk2 and Jak3 Kinase Domains in Complex with Cp-690550 and Cmp-6
  15. 3lxl: Structural and Thermodynamic Characterization of The Tyk2 and Jak3 Kinase Domains in Complex with Cp-690550 and Cmp-6
  16. 3lxk: Structural and Thermodynamic Characterization of The Tyk2 and Jak3 Kinase Domains in Complex with Cp-690550 and Cmp-6
  17. 3lpb: Crystal Structure of Jak2 Complexed with a Potent 2,8-diaryl- Quinoxaline Inhibitor
  18. 3kxz: The Complex Crystal Structure of Lck with a Probe Molecule W259
  19. 3krr: Crystal Structure of Jak2 Complexed with a Potent Quinoxaline Atp Site Inhibitor
  20. 3kfa: Structural Analysis of Dfg-in and Dfg-out Dual Src-abl Inhibitors Sharing a Common Vinyl Purine Template
  21. 3kf4: Structural Analysis of Dfg-in and Dfg-out Dual Src-abl Inhibitors Sharing a Common Vinyl Purine Template
  22. 3kck: A Novel Chemotype of Kinase Inhibitors
  23. 3k5v: Structure of Abl Kinase in Complex with Imatinib and Gnf-2
  24. 3k54: Structures of Human Bruton's Tyrosine Kinase in Active and Inactive Conformations Suggests a Mechanism of Activation for Tec Family Kinases.
  25. 3k2m: Crystal Structure of Monobody Ha4/abl1 Sh2 Domain Complex
  26. 3jy9: Janus Kinase 2 Inhibitors
  27. 3iok: 2-aminopyrazolo[1,5-a]pyrimidines as Potent and Selective Inhibitors of Jak2
  28. 3io7: 2-aminopyrazolo[1,5-a]pyrimidines as Potent and Selective Inhibitors of Jak2
  29. 3ik3: Ap24534, a Pan-bcr-abl Inhibitor for Chronic Myeloid Leukemia, Potently Inhibits The T315I Mutant and Overcomes Mutation-based Resistance
  30. 3hmi: The Crystal Structure of Human Abl2 in Complex with 5-amino- 3-{[4-(aminosulfonyl)phenyl]amino}-n-(2,6-difluorophenyl)- 1h-1,2,4-triazole-1-carbothioamide
  31. 3hck: Nmr Ensemble of The Uncomplexed Human Hck Sh2 Domain, 20 Structures
  32. 3h3c: Crystal Structure of Pyk2 in Complex with Sulfoximine- Substituted Trifluoromethylpyrimidine Analog
  33. 3h0i: Human Fyn Sh3 Domain R96I Mutant, Crystal Form II
  34. 3h0h: Human Fyn Sh3 Domain R96I Mutant, Crystal Form I
  35. 3h0f: Crystal Structure of The Human Fyn Sh3 R96W Mutant
  36. 3gvu: The Crystal Structure of Human Abl2 in Complex with Gleevec
  37. 3gm3: Crystal Structure of The Focal Adhesion Targeting (fat) Domain of Pyk2
  38. 3gm2: Crystal Structure of The Focal Adhesion Targeting (fat) Domain of Pyk2
  39. 3gm1: Crystal Structure of The Focal Adhesion Targeting (fat) Domain of Pyk2 in Complex with Paxillin Ld4 Motif-derived Peptides
  40. 3geq: Structural Basis for The Chemical Rescue of Src Kinase Activity
  41. 3gen: The 1.6 a Crystal Structure of Human Bruton's Tyrosine Kinase Bound to a Pyrrolopyrimidine-containing Compound
  42. 3g6h: Src THR338ILE Inhibited in The Dfg-asp-out Conformation
  43. 3g6g: Equally Potent Inhibition of C-src and Abl by Compounds That Recognize Inactive Kinase Conformations
  44. 3g5d: Kinase Domain of Csrc in Complex with Dasatinib
  45. 3fzt: Crystal Structure of Pyk2 Complexed with Pf-4618433
  46. 3fzs: Crystal Structure of Pyk2 Complexed with Birb796
  47. 3fzr: Crystal Structure of Pyk2 Complexed with Pf-431396
  48. 3fzp: Crystal Structure of Pyk2 Complexed with Atpgs
  49. 3fzo: Crystal Structure of Pyk2-apo, Proline-rich Tyrosine Kinase
  50. 3fup: Crystal Structures of Jak1 and Jak2 Inhibitor Complexes
  51. 3fqs: Crystal Structure of Spleen Tyrosine Kinase Complexed with R406
  52. 3fqh: Crystal Structure of Spleen Tyrosine Kinase Complexed with a 2-substituted 7-azaindole
  53. 3fqe: Crystal Structure of Spleen Tyrosine Kinase Complexed with Ym193306
  54. 3fj5: Crystal Structure of The C-src-sh3 Domain
  55. 3f6x: C-src Kinase Domain in Complex with Small Molecule Inhibitor
  56. 3f3w: Drug Resistant Csrc Kinase Domain in Complex with Inhibitor Rl45 (type Ii)
  57. 3f3v: Kinase Domain of Csrc in Complex with Inhibitor Rl45 (type Ii)
  58. 3f3u: Kinase Domain of Csrc in Complex with Inhibitor Rl37 (type Iii)
  59. 3f3t: Kinase Domain of Csrc in Complex with Inhibitor Rl38 (type Iii)
  60. 3eyh: Crystal Structures of Jak1 and Jak2 Inhibitor Complexes
  61. 3eyg: Crystal Structures of Jak1 and Jak2 Inhibitor Complexes
  62. 3et7: Crystal Structure of Pyk2 Complexed with Pf-2318841
  63. 3eqr: Crystal Structure of Ack1 with Compound T74
  64. 3eqp: Crystal Structure of Ack1 with Compound T95
  65. 3en7: Targeted Polypharmacology: Crystal Structure of The C-src Kinase Domain in Complex with S1, a Multitargeted Kinase Inhibitor
  66. 3en6: Targeted Polypharmacology: Crystal Structure of The C-src Kinase Domain in Complex with Pp102, a Multitargeted Kinase Inhibitor
  67. 3en5: Targeted Polypharmacology: Crystal Structure of The C-src Kinase Domain in Complex with Pp494, a Multitargeted Kinase Inhibitor
  68. 3en4: Targeted Polypharmacology: Crystal Structure of The C-src Kinase Domain in Complex with Pp121, a Multitargeted Kinase Inhibitor
  69. 3emg: Discovery and Sar of Novel 4-thiazolyl-2- Phenylaminopyrimidines as Potent Inhibitors of Spleen Tyrosine Kinase (syk)
  70. 3el8: Crystal Structure of C-src in Complex with Pyrazolopyrimidine 5
  71. 3el7: Crystal Structure of C-src in Complex with Pyrazolopyrimidine 3
  72. 3egu: Crystal Structure of The N114A Mutant of Abl-sh3 Domain
  73. 3eg3: Crystal Structure of The N114A Mutant of Abl-sh3 Domain
  74. 3eg2: Crystal Structure of The N114Q Mutant of Abl-sh3 Domain
  75. 3eg1: Crystal Structure of The N114Q Mutant of Abl-sh3 Domain Complexed with a Designed High-affinity Peptide Ligand: Implications for Sh3-ligand Interactions
  76. 3eg0: Crystal Structure of The N114T Mutant of Abl-sh3 Domain
  77. 3eaz: Crystal Structure of Sh2 Domain of Human Csk (carboxyl- Terminal Src Kinase), C122S Mutant.
  78. 3eac: Crystal Structure of Sh2 Domain of Human Csk (carboxyl- Terminal Src Kinase), Oxidized Form.
  79. 3e64: Fragment Based Discovery of Jak-2 Inhibitors
  80. 3e63: Fragment Based Discovery of Jak-2 Inhibitors
  81. 3e62: Fragment Based Discovery of Jak-2 Inhibitors
  82. 3dqx: Chicken C-src Kinase Domain in Complex with Atpgs
  83. 3dqw: C-src Kinase Domain THR338ILE Mutant in Complex with Atpgs
  84. 3dk7: Crystal Structure of Mutant Abl Kinase Domain in Complex with Small Molecule Fragment
  85. 3dk6: Crystal Structure of Mutant Abl Kinase Domain in Complex with Small Molecule Fragment
  86. 3dk3: Crystal Structure of Mutant Abl Kinase Domain in Complex with Small Molecule Fragment
  87. 3d7u: Structural Basis for The Recognition of C-src by Its Inactivator Csk
  88. 3d7t: Structural Basis for The Recognition of C-src by Its Inactivator Csk
  89. 3cs9: Human Abl Kinase in Complex with Nilotinib
  90. 3cr0: Wee1 Kinase Complex with Inhibitor Pd259_809
  91. 3cqt: N53I V55L Mutant of Fyn Sh3 Domain
  92. 3cqe: Wee1 Kinase Complex with Inhibitor Pd074291
  93. 3cio: The Kinase Domain of Escherichia Coli Tyrosine Kinase Etk
  94. 3cd3: Crystal Structure of Phosphorylated Human Feline Sarcoma Viral Oncogene Homologue (v-fes) in Complex with Staurosporine and a Consensus Peptide
  95. 3cc6: Crystal Structure of Kinase Domain of Protein Tyrosine Kinase 2 Beta (PTK2B)
  96. 3cbl: Crystal Structure of Human Feline Sarcoma Viral Oncogene Homologue (v-fes) in Complex with Staurosporine and a Consensus Peptide
  97. 3bz3: Crystal Structure Analysis of Focal Adhesion Kinase with a Methanesulfonamide Diaminopyrimidine Inhibitor
  98. 3byu: Co-crystal Structure of Lck and Aminopyrimidine Reverse Amide 23
  99. 3bys: Co-crystal Structure of Lck and Aminopyrimidine Amide 10b
  100. 3byo: X-ray Co-crystal Structure of 2-amino-6-phenylpyrimido[5', 4':5,6]pyrimido[1,2-a]benzimidazol-5(6h)-one 25 Bound to Lck
  101. 3bym: X-ray Co-crystal Structure Aminobenzimidazole Triazine 1 Bound to Lck
  102. 3bkb: Crystal Structure of Human Feline Sarcoma Viral Oncogene Homologue (v-fes)
  103. 3biz: Wee1 Kinase Complex with Inhibitor Pd331618
  104. 3bi6: Wee1 Kinase Complex with Inhibitor Pd352396
  105. 3b71: Cd4 Endocytosis Motif Bound to The Focal Adhesion Targeting (fat) Domain of The Focal Adhesion Kinase
  106. 3b2w: Crystal Structure of Pyrimidine Amide 11 Bound to Lck
  107. 3ack: Crystal Structure of Pyrrolo Pyrazine Derivative Bound to The Kinase Domain of Human Lck, (auto-phosphorylated on Tyr394)
  108. 3acj: Crystal Structure of Imidazo Pyrimidine Derivative Bound to The Kinase Domain of Human Lck, (auto-phosphorylated on Tyr394)
  109. 3ac8: Crystal Structure of Pyrazolo Pyrimidine Derivative Bound to The Kinase Domain of Human Lck, (auto-phosphorylated on Tyr394)
  110. 3ac5: Crystal Structure of Triazolo Pyrimidine Derivative Bound to The Kinase Domain of Human Lck, (auto-phosphorylated on Tyr394)
  111. 3ac4: Crystal Structure of Triazolo Pyrimidine Derivative Bound to The Kinase Domain of Human Lck, (auto-phosphorylated on Tyr394)
  112. 3ac3: Crystal Structure of Pyrazolo Pyrimidine Derivative Bound to The Kinase Domain of Human Lck, (auto-phosphorylated on Tyr394)
  113. 3ac2: Crystal Structure of Pyrazolo Pyrimidine Derivative Bound to The Kinase Domain of Human Lck, (auto-phosphorylated on Tyr394)
  114. 3ac1: Crystal Structure of Pyrazin Derivative Bound to The Kinase Domain of Human Lck, (auto-phosphorylated on Tyr394)
  115. 3a4o: Lyn Kinase Domain
  116. 2zyb: Crystal Structure of Phenylimidazo Pyrazin 2 Bound to The Kinase Domain of Human Lck, (auto-phosphorylated on Tyr394)
  117. 2zva: Lyn Tyrosine Kinase Domain-dasatinib Complex
  118. 2zv9: Lyn Tyrosine Kinase Domain-pp2 Complex
  119. 2zv8: Lyn Tyrosine Kinase Domain-amp-pnp Complex
  120. 2zv7: Lyn Tyrosine Kinase Domain, Apo Form
  121. 2zm4: Crystal Structure of Imidazo Quinoxaline 1 Bound to The Kinase Domain of Human Lck, Activated Form (auto- Phosphorylated on Tyr394)
  122. 2zm1: Crystal Structure of Imidazo Pyrazin 1 Bound to The Kinase Domain of Human Lck, (auto-phosphorylated on Tyr394)
  123. 2z60: Crystal Structure of The T315I Mutant of Abl Kinase Bound with Ppy-a
  124. 2z2w: Humand Wee1 Kinase Complexed with Inhibitor Pf0335770
  125. 2z0p: Crystal Structure of Ph Domain of Bruton's Tyrosine Kinase
  126. 2yuq: Solution Structure of The Sh3 Domain of Human Tyrosine- Protein Kinase Itk/tsk
  127. 2ys2: Solution Structure of The Btk Motif of Human Cytoplasmic Tyrosine-protein Kinase Bmx
  128. 2xyn: Human Abl2 in Complex with Aurora Kinase Inhibitor Vx-680
  129. 2w1i: Structure Determination of Aurora Kinase in Complex with Inhibitor
  130. 2v7a: Crystal Structure of The T315I Abl Mutant in Complex with The Inhibitor Pha-739358
  131. 2rna: Itk Sh3 Average Minimized
  132. 2rn8: Nmr Structure Note: Murine Itk Sh3 Domain
  133. 2ra7: Crystal Structure of Focal Adhesion Kinase Fat Domain Complexed with a Specific Small Molecule Inhibitor
  134. 2qq7: Crystal Structure of Drug Resistant Src Kinase Domain with Irreversible Inhibitor
  135. 2qoh: Crystal Structure of Abl Kinase Bound with Ppy-a
  136. 2qlq: Crystal Structure of Src Kinase Domain with Covalent Inhibitor Rl3
  137. 2qi8: Crystal Structure of Drug Resistant Src Kinase Domain
  138. 2pl0: Lck Bound to Imatinib
  139. 2ozo: Autoinhibited Intact Human Zap-70
  140. 2oq1: Tandem Sh2 Domains of Zap-70 with 19-mer Zeta1 Peptide
  141. 2dm0: Solution Structure of The Sh2 Domain of Human Tyrosine- Protein Kinase Txk
  142. 2oiq: Crystal Structure of Chicken C-src Kinase Domain in Complex with The Cancer Drug Imatinib.
  143. 2oi3: Nmr Structure Analysis of The Hematopoetic Cell Kinase Sh3 Domain Complexed with an Artificial High Affinity Ligand (pd1)
  144. 2og8: Crystal Structure of Aminoquinazoline 36 Bound to Lck
  145. 2ofv: Crystal Structure of Aminoquinazoline 1 Bound to Lck
  146. 2ofu: X-ray Crystal Structure of 2-aminopyrimidine Carbamate 43 Bound to Lck
  147. 2of4: Crystal Structure of Furanopyrimidine 1 Bound to Lck
  148. 2of2: Crystal Structure of Furanopyrimidine 8 Bound to Lck
  149. 2dq7: Crystal Structure of Fyn Kinase Domain Complexed with Staurosporine
  150. 2o88: Crystal Structure of The N114A Mutant of Abl-sh3 Domain Complexed with a Designed High-affinity Peptide Ligand: Implications for Sh3-ligand Interactions
  151. 2e2b: Crystal Structure of The C-abl Kinase Domain in Complex with Inno-406
  152. 2e6i: Solution Structure of The Btk Motif of Tyrosine-protein Kinase Itk from Human
  153. 2ecd: Solution Structure of The Human Abl2 Sh2 Domain
  154. 2ekx: Solution Structure of The Human Bmx Sh2 Domain
  155. 2gqg: X-ray Crystal Structure of Dasatinib (bms-354825) Bound to Activated Abl Kinase Domain
  156. 2h8h: Src Kinase in Complex with a Quinazoline Inhibitor
  157. 2hda: Yes Sh3 Domain
  158. 2hiw: Crystal Structure of Inactive Conformation Abl Kinase Catalytic Domain Complexed with Type II Inhibitor
  159. 2hk5: Hck Kinase in Complex with Lck Targetted Inhibitor Pg- 1009247
  160. 2hwo: Crystal Structure of Src Kinase Domain in Complex with Covalent Inhibitor
  161. 2hwp: Crystal Structure of Src Kinase Domain in Complex with Covalent Inhibitor Pd168393
  162. 2hyy: Human Abl Kinase Domain in Complex with Imatinib (sti571, Glivec)
  163. 2hz0: Abl Kinase Domain in Complex with Nvp-aeg082
  164. 2hz4: Abl Kinase Domain Unligated and in Complex with Tetrahydrostaurosporine
  165. 2hzi: Abl Kinase Domain in Complex with Pd180970
  166. 2hzn: Abl Kinase Domain in Complex with Nvp-afg210
  167. 2ijm: Crystal Structure of Focal Adhesion Kinase Domain with 2 Molecules in The Asymmetric Unit Complexed with Adp and Atp
  168. 2in6: Wee1 Kinase Complex with Inhibitor Pd311839
  169. 2io6: Wee1 Kinase Complexed with Inhibitor Pd330961
  170. 2j0j: Crystal Structure of a Fragment of Focal Adhesion Kinase Containing The Ferm and Kinase Domains.
  171. 2j0k: Crystal Structure of a Fragment of Focal Adhesion Kinase Containing The Ferm and Kinase Domains.
  172. 2j0l: Crystal Structure of a The Active Conformation of The Kinase Domain of Focal Adhesion Kinase with a Phosphorylated Activation Loop.
  173. 2j0m: Crystal Structure a Two-chain Complex between The Ferm and Kinase Domains of Focal Adhesion Kinase.
  174. 2jkk: Focal Adhesion Kinase Catalytic Domain in Complex with Bis- Anilino Pyrimidine Inhibitor
  175. 2jkm: Focal Adhesion Kinase Catalytic Domain in Complex with Bis- Anilino Pyrimidine Inhibitor
  176. 2jko: Focal Adhesion Kinase Catalytic Domain in Complex with Bis- Anilino Pyrimidine Inhibitor
  177. 2jkq: Focal Adhesion Kinase Catalytic Domain in Complex with Bis- Anilino Pyrimidine Inhibitor
  178. 2jyq: Nmr Structure of The Apo V-src Sh2 Domain
  179. 2k79: Solution Structure of The Binary Complex between The Sh3 and Sh2 Domain of Interleukin-2 Tyrosine Kinase
  180. 2k7a: Ensemble Structures of The Binary Complex between The Sh3 and Sh2 Domain of Interleukin-2 Tyrosine Kinase.
  181. 2kk1: Solution Structure of C-terminal Domain of Tyrosine-protein Kinase Abl2 from Homo Sapiens, Northeast Structural Genomics Consortium (nesg) Target HR5537A
  182. 2kk6: Solution Structure of Sh2 Domain of Proto-oncogene Tyrosine- Protein Kinase fer from Homo Sapiens, Northeast Structural Genomics Consortium (nesg) Target HR3461D
  183. 3kmm: Structure of Human Lck Kinase with a Small Molecule Inhibitor
  184. 2xa4: Inhibitors of Jak2 Kinase Domain
  185. 3ad4: Crystal Structure of Methoxy Benzofuran Derivative Bound to The Kinase Domain of Human Lck, (auto-phosphorylated on Tyr394)
  186. 3ad5: Crystal Structure of Triazolone Derivative Bound to The Kinase Domain of Human Lck, (auto-phosphorylated on Tyr394)
  187. 3ad6: Crystal Structure of Pyrazolo Pyrimidine Derivative Bound to The Kinase Domain of Human Lck, (auto-phosphorylated on Tyr394)
  188. 3lok: Drug Resistant Csrc Kinase Domain in Complex with Covalent Inhibitor Pd168393
  189. 3oxz: Crystal Structure of Abl Kinase Domain Bound with a Dfg-out Inhibitor Ap24534
  190. 3oy3: Crystal Structure of Abl T315I Mutant Kinase Domain Bound with a Dfg- out Inhibitor Ap24589
  191. 3pix: Crystal Structure of Btk Kinase Domain Complexed with 2-isopropyl-7- (4-methyl-piperazin-1-yl)-4-(5-methyl-2h-pyrazol-3-ylamino)-2h- Phthalazin-1-one
  192. 3piy: Crystal Structure of Btk Kinase Domain Complexed with R406
  193. 3piz: Crystal Structure of Btk Kinase Domain Complexed with (5-amino-1-o- Tolyl-1h-pyrazol-4-yl)-[3-(1-methanesulfonyl-piperidin-4-yl)-phenyl]- Methanone
  194. 3pj1: Crystal Structure of Btk Kinase Domain Complexed with 3-(2,6-dichloro- Phenyl)-7-[4-(2-diethylamino-ethoxy)-phenylamino]-1-methyl-3,4- Dihydro-1h-pyrimido[4,5-d]pyrimidin-2-one
  195. 3pj2: Crystal Structure of Btk Kinase Domain Complexed with 2-[4-(2- Diethylamino-ethoxy)-phenylamino]-6-(4-fluoro-phenoxy)-8-methyl-8h- Pyrido[2,3-d]pyrimidin-7-one
  196. 3pj3: Crystal Structure of Btk Kinase Domain Complexed with 2-methyl-5-[(e)- (3-phenyl-acryloyl)amino]-n-(2-phenyl-3h-imidazo[4,5-b]pyridin-6-yl)- Benzamide
  197. 3pjc: Crystal Structure of Jak3 Complexed with a Potent Atp Site Inhibitor Showing High Selectivity within The Janus Kinase Family
  198. 3q32: Structure of Janus Kinase 2 with a Pyrrolotriazine Inhibitor
  199. 3rbb: Hiv-1 Nef Protein in Complex with Engineered Hck Sh3 Domain
  200. 2lct: Solution Structure of The Vav1 Sh2 Domain Complexed with a Syk-derived Doubly Phosphorylated Peptide
  201. 3qgw: Crystal Structure of Itk Kinase Bound to an Inhibitor
  202. 3qgy: Crystal Structure of Itk Inhibitor Complex
  203. 3qri: The Crystal Structure of Human Abl1 Kinase Domain in Complex with Dcc- 2036
  204. 3qrj: The Crystal Structure of Human Abl1 Kinase Domain T315I Mutant in Complex with Dcc-2036
  205. 3qrk: The Crystal Structure of Human Abl1 Kinase Domain in Complex with Dp- 987
  206. 3rea: Hiv-1 Nef Protein in Complex with Engineered Hck-sh3 Domain
  207. 3reb: Hiv-1 Nef Protein in Complex with Engineered Hck-sh3 Domain
  208. 3oez: Crystal Structure of The L317I Mutant of The Chicken C-src Tyrosine Kinase Domain Complexed with Imatinib
  209. 3of0: Crystal Structure of The L317I Mutant of The Chicken C-src Tyrosine Kinase Domain
  210. 3svv: Crystal Structure of T338C C-src Covalently Bound to Vinylsulfonamide- Pyrazolopyrimidine 9
  211. 2l2p: Folding Intermediate of The Fyn Sh3 A39V/N53P/V55L from Nmr Relaxation Dispersion Experiments
  212. 3srv: Crystal Structure of Spleen Tyrosine Kinase (syk) in Complex with a Diaminopyrimidine Carboxamide Inhibitor
  213. 3sxr: Crystal Structure of Bmx Non-receptor Tyrosine Kinase Complex with Dasatinib
  214. 3sxs: Crystal Structure of Bmx Non-receptor Tyrosine Kinase Complexed with Pp2
  215. 3t9t: Crystal Structure of Btk Mutant (F435T,K596R) Complexed with Imidazo[1,5-a]quinoxaline
  216. 3t04: Crystal Structure of Monobody 7c12/abl1 Sh2 Domain Complex
  217. 3pxk: Focal Adhesion Kinase Catalytic Domain in Complex with Pyrrolo[2,3- D]thiazole
  218. 3tjc: Co-crystal Structure of Jak2 with Thienopyridine 8
  219. 3tjd: Co-crystal Structure of Jak2 with Thienopyridine 19
  220. 3uf4: Crystal Structure of a Sh3 and Sh2 Domains of Fyn Protein (proto- Concogene Tyrosine-protein Kinase Fyn) from Mus Musculus at 1.98 a Resolution
  221. 3us4: Crystal Structure of a Sh2 Domain of a Megakaryocyte-associated Tyrosine Kinase (matk) from Homo Sapiens at 1.50 a Resolution
  222. 3uyo: Crystal Structure of Monobody Sh13/abl1 Sh2 Domain Complex
  223. 2y1n: Structure of C-cbl-zap-70 Peptide Complex
  224. 4a4b: Structure of Modified PHOSPHOTYR371-C-CBL-UBCH5B-ZAP-70 Complex
  225. 4a4c: Structure of PHOSPHOTYR371-C-CBL-UBCH5B-ZAP-70 Complex
  226. 4d8k: Crystal Structure of a Sh3-sh2 Domains of a Lymphocyte-specific Protein Tyrosine Kinase (lck) from Homo Sapiens at 2.36 a Resolution
  227. 3qlf: Crystal Structure of The L317I Mutant of The C-src Tyrosine Kinase Domain Complexed with Pyrazolopyrimidine 5
  228. 3qlg: Crystal Structure of The L317I Mutant of The C-src Tyrosine Kinase Domain Complexed with Dasatinib
  229. 3s9k: Crystal Structure of The Itk Sh2 Domain.
  230. 4agw: Discovery of a Small Molecule Type II Inhibitor of Wild- Type and Gatekeeper Mutants of Bcr-abl, Pdgfralpha, Kit, and Src Kinases
  231. 3u4w: Src in Complex with Dna-templated Macrocyclic Inhibitor MC4B
  232. 3u51: Src in Complex with Dna-templated Macrocyclic Inhibitor Mc1
  233. 3uqf: C-src Kinase Domain in Complex with Bki Rm-1-89
  234. 3uqg: C-src Kinase Domain in Complex with Bumpless Bki Analog Uw1243
  235. 3rvg: Crystals Structure of Jak2 with a 1-amino-5h-pyrido[4,3-b]indol-4- Carboxamide Inhibitor
  236. 4dyl: F-bar Domain of Human Fes Tyrosine Kinase
  237. 3ue4: Structural and Spectroscopic Analysis of The Kinase Inhibitor Bosutinib Binding to The Abl Tyrosine Kinase Domain
  238. 4e93: Crystal Structure of Human Feline Sarcoma Viral Oncogene Homologue (v- Fes)in Complex with Tae684
  239. 4aqc: Triazolopyridine-based Inhibitor of Janus Kinase 2
  240. 4dfl: Crystal Structure of Spleen Tyrosine Kinase Complexed with a Sulfonamidopyrazine Piperidine Inhibitor
  241. 4dfn: Crystal Structure of Spleen Tyrosine Kinase Complexed with an Adamantylpyrazine Inhibitor
  242. 4eku: Crystal Structure of Ferm Domain of Proline-rich Tyrosine Kinase 2
  243. 3v5j: Crystal Structure of Interleukin-2 Inducible T-cell Kinase Itk Catalytic Domain with Thienopyrazolylindole Inhibitor 090
  244. 3v5l: Crystal Structure of Interleukin-2 Inducible T-cell Kinase Itk Catalytic Domain with Thienopyrazolylindole Inhibitor 542
  245. 3v8t: Crystal Structure of Interleukin-2 Inducible T-cell Kinase Itk Catalytic Domain with Thienopyrazolylindole Inhibitor 477
  246. 3v8w: Crystal Structure of Interleukin-2 Inducible T-cell Kinase Itk Catalytic Domain with Thienopyrazolylindole Inhibitor 469
  247. 3vf8: Crystal Structure of Spleen Tyrosine Kinase Syk Catalytic Domain with Pyrazolylbenzimidazole Inhibitor 416
  248. 3vf9: Crystal Structure of Spleen Tyrosine Kinase Syk Catalytic Domain with Thienopyrazolylindole Inhibitor 027
  249. 2lp5: Native Structure of The Fyn Sh3 A39V/N53P/V55L
  250. 3ugc: Structural Basis of Jak2 Inhibition by The Type II Inhibtor Nvp-bbt594
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