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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 2.7.11
      EC 2.7.12
        EC 2.7.12.1
        EC 2.7.12.2
      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 2.7.12.1 - ATP:protein phosphotransferase (Ser/Thr- and Tyr- phosphorylating) (dual- specificity kinase)



3D structures of EC 2.7.12.1 - dual-specificity kinase in Protein Data Bank

updated: 29 May 2015, 1:12

In total: 57 PDB structures of EC 2.7.12.1 - dual-specificity kinase:
  1. 3nr9: Structure of Human Cdc2-like Kinase 2 (clk2)
  2. 3kvw: Crystal Structure of Dual-specificity Tyrosine Phosphorylation Regulated Kinase 2 (dyrk2) in Complex with an Indirubin Ligand
  3. 3k2l: Crystal Structure of Dual-specificity Tyrosine Phosphorylation Regulated Kinase 2 (dyrk2)
  4. 3hmp: Crystal Structure of Human Mps1 Catalytic Domain in Complex with a Quinazolin Ligand Compound 4
  5. 3hmo: Crystal Structure of Human Mps1 Catalytic Domain in Complex with The Inhibitor Staurosporine
  6. 3hmn: Crystal Structure of Human Mps1 Catalytic Domain in Complex with Atp
  7. 3h9f: Crystal Structure of Human Dual Specificity Protein Kinase (ttk) in Complex with a Pyrimido-diazepin Ligand
  8. 3gfw: Crystal Structure of Human Dual Specificity Protein Kinase (ttk) in Complex with a Pyrolo-pyridin Ligand
  9. 3dbq: Crystal Structure of Ttk Kinase Domain
  10. 3cek: Crystal Structure of Human Dual Specificity Protein Kinase (ttk)
  11. 3anr: Human DYRK1A/HARMINE Complex
  12. 3anq: Human DYRK1A/INHIBITOR Complex
  13. 2zmd: Crystal Structure of Human Mps1 Catalytic Domain T686A Mutant in Complex with Sp600125 Inhibitor
  14. 2zmc: Crystal Structure of Human Mitotic Checkpoint Kinase Mps1 Catalytic Domain Apo Form
  15. 2wu7: Crystal Structure of The Human Clk3 in Complex with V25
  16. 2wu6: Crystal Structure of The Human Clk3 in Complex with Dki
  17. 2wo6: Human Dual-specificity Tyrosine-phosphorylation-regulated Kinase 1a in Complex with a Consensus Substrate Peptide
  18. 2vx3: Crystal Structure of The Human Dual Specificity Tyrosine- Phosphorylation-regulated Kinase 1a
  19. 2vag: Crystal Structure of Di-phosphorylated Human Clk1 in Complex with a Novel Substituted Indole Inhibitor
  20. 2x9e: Human Mps1 in Complex with Nms-p715
  21. 3raw: Crystal Structure of Human Cdc-like Kinase 3 Isoform in Complex with Leucettine L41
  22. 3vqu: Crystal Structure of Human Mps1 Catalytic Domain in Complex with 4- [(4-amino-5-cyano-6-ethoxypyridin-2- Yl)amino]benzamide
  23. 4aze: Human DYRK1A in Complex with Leucettine L41
  24. 4h7x: Crystal Structure of The Tetratricopeptide Repeat (tpr) Motif of Human Dual Specificity Protein Kinase Mps1
  25. 4h7y: Crystal Structure of The Tetratricopeptide Repeat (tpr) Motif of Human Dual Specificity Protein Kinase Mps1
  26. 4b94: Crystal Structure of Human Mps1 Tpr Domain
  27. 4bhz: Scaffold Focused Virtual Screening: Prospective Application to The Discovery of Ttk Inhibitor
  28. 4bi0: Scaffold Focused Virtual Screening: Prospective Application to The Discovery of Ttk Inhibitor
  29. 4bi1: Scaffold Focused Virtual Screening: Prospective Application to The Discovery of Ttk Inhibitor
  30. 4bi2: Scaffold Focused Virtual Screening: Prospective Application to The Discovery of Ttk Inhibitor
  31. 3w1f: Crystal Structure of Human Mps1 Catalytic Domain in Complex with 5-(5- Ethoxy-6-(1-methyl-1h-pyrazol-4-yl)-1h-indazol-3-yl)-2- Methylbenzenesulfonamide
  32. 4c4e: Structure-based Design of Orally Bioavailable Pyrrolopyridine Inhibitors of The Mitotic Kinase Mps1
  33. 4c4f: Structure-based Design of Orally Bioavailable Pyrrolopyridine Inhibitors of The Mitotic Kinase Mps1
  34. 4c4g: Structure-based Design of Orally Bioavailable Pyrrolopyridine Inhibitors of The Mitotic Kinase Mps1
  35. 4c4h: Structure-based Design of Orally Bioavailable Pyrrolopyridine Inhibitors of The Mitotic Kinase Mps1
  36. 4c4i: Structure-based Design of Orally Bioavailable Pyrrolopyridine Inhibitors of The Mitotic Kinase Mps1
  37. 4c4j: Structure-based Design of Orally Bioavailable Pyrrolopyridine Inhibitors of The Mitotic Kinase Mps1
  38. 4js8: Crystal Structure of Ttk Kinase Domain with an Inhibitor: 401348
  39. 4jt3: Crystal Structure of Ttk Kinase Domain with an Inhibitor: 400740
  40. 4mq1: The Crystal Structure of DYRK1A with a Bound Pyrido[2,3-d]pyrimidine Inhibitor
  41. 4mq2: The Crystal Structure of DYRK1A with a Bound Pyrido[2,3-d]pyrimidine Inhibitor
  42. 4pdp: Crystal Structure of Rad53 Kinase Domain and Scd2
  43. 4pds: Crystal Structure of Rad53 Kinase Domain and Scd2 in Complex with Amppnp
  44. 4o6l: Crystal Structure of Ttk Kinase Domain with an Inhibitor: 401498 (n- [(1r)-1-(2-chlorophenyl)propyl]-3-{4-[(1-methylpiperidin-4-yl) Oxy]phenyl}-1h-indazole-5-carboxamide)
  45. 3wzj: Crystal Structure of Human Mps1 Catalytic Domain in Complex with 4-(6- (cyclohexylamino)-8-(((tetrahydro-2h-pyran-4-yl)methyl)amino) Imidazo[1,2-b]pyridazin-3-yl)-n-cyclopropylbenzamide
  46. 3wzk: Crystal Structure of Human Mps1 Catalytic Domain in Complex with N- Cyclopropyl-4-(8-((thiophen-2-ylmethyl)amino)imidazo[1,2-a]pyrazin-3- Yl)benzamide
  47. 4ylj: Crystal Structure of DYRK1A in Complex with 10-iodo-substituted 11h- Indolo[3,2-c]quinoline-6-carboxylic Acid Inhibitor 5j
  48. 4ylk: Crystal Structure of DYRK1A in Complex with 10-chloro-substituted 11h- Indolo[3,2-c]quinolone-6-carboxylic Acid Inhibitor 5s
  49. 4yll: Crystal Structure of DYRK1AA in Complex with 10-bromo-substituted 11h- Indolo[3,2-c]quinolone-6-carboxylic Acid Inhibitor 5t
  50. 4yu2: Crystal Structure of DYRK1A with Harmine-derivatized Annh-75 Inhibitor
  51. 4nct: Human DYRK1A in Complex with Pkc412
  52. 3wyx: Crystal Structure of Human Mps1 Catalytic Domain in Complex with 6- ((3-(cyanomethoxy)-4-(1-methyl-1h-pyrazol-4-yl)phenyl)amino)-2- (cyclohexylamino)nicotinonitrile
  53. 3wyy: Crystal Structure of Human Mps1 Catalytic Domain in Complex with (e)- 3-(4-((6-(((3s,5s,7s)-adamantan-1-yl)amino)-4-amino-5-cyanopyridin-2- Yl)amino)-2-(cyanomethoxy)phenyl)-n-(2-methoxyethyl)acrylamide
  54. 4cv8: Mps1 Kinase with 3-aminopyridin-2-one Inhibitors
  55. 4cv9: Mps1 Kinase with 3-aminopyridin-2-one Inhibitors
  56. 4cva: Mps1 Kinase with 3-aminopyridin-2-one Inhibitors
  57. 4d2s: Human Ttk in Complex with a DYRK1B Inhibitor
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