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enzyme (lysozyme)

 
Enzymes
  Enzyme classes:
  EC 1: Oxidoreductases
  EC 2: Transferases
  EC 3: Hydrolases
    EC 3.1
    EC 3.2
    EC 3.3
    EC 3.4
      EC 3.4.1
      EC 3.4.2
      EC 3.4.3
      EC 3.4.4
      EC 3.4.11
      EC 3.4.12
      EC 3.4.13
      EC 3.4.14
      EC 3.4.15
      EC 3.4.16
      EC 3.4.17
      EC 3.4.18
      EC 3.4.19
      EC 3.4.21
      EC 3.4.22
        EC 3.4.22.1
        EC 3.4.22.2
        EC 3.4.22.3
        EC 3.4.22.4
        EC 3.4.22.5
        EC 3.4.22.6
        EC 3.4.22.7
        EC 3.4.22.8
        EC 3.4.22.9
        EC 3.4.22.10
        EC 3.4.22.11
        EC 3.4.22.12
        EC 3.4.22.13
        EC 3.4.22.14
        EC 3.4.22.15
        EC 3.4.22.16
        EC 3.4.22.17
        EC 3.4.22.18
        EC 3.4.22.19
        EC 3.4.22.20
        EC 3.4.22.21
        EC 3.4.22.22
        EC 3.4.22.23
        EC 3.4.22.24
        EC 3.4.22.25
        EC 3.4.22.26
        EC 3.4.22.27
        EC 3.4.22.28
        EC 3.4.22.29
        EC 3.4.22.30
        EC 3.4.22.31
        EC 3.4.22.32
        EC 3.4.22.33
        EC 3.4.22.34
        EC 3.4.22.35
        EC 3.4.22.36
        EC 3.4.22.37
        EC 3.4.22.38
        EC 3.4.22.39
        EC 3.4.22.40
        EC 3.4.22.41
        EC 3.4.22.42
        EC 3.4.22.43
        EC 3.4.22.44
        EC 3.4.22.45
        EC 3.4.22.46
        EC 3.4.22.47
        EC 3.4.22.48
        EC 3.4.22.49
        EC 3.4.22.50
        EC 3.4.22.51
        EC 3.4.22.52
        EC 3.4.22.53
        EC 3.4.22.54
        EC 3.4.22.55
        EC 3.4.22.56
        EC 3.4.22.57
        EC 3.4.22.58
        EC 3.4.22.59
        EC 3.4.22.60
        EC 3.4.22.61
        EC 3.4.22.62
        EC 3.4.22.63
        EC 3.4.22.64
        EC 3.4.22.65
        EC 3.4.22.66
        EC 3.4.22.67
        EC 3.4.22.68
      EC 3.4.23
      EC 3.4.24
      EC 3.4.25
      EC 3.4.99
    EC 3.5
    EC 3.6
    EC 3.7
    EC 3.8
    EC 3.9
    EC 3.10
    EC 3.11
    EC 3.12
    EC 3.13
  EC 4: Lyases
  EC 5: Isomerases
  EC 6: Ligases
  General information:
  Catalytic mechanism
  Enzyme kinetics
  Inhibitors
  Enzymes in industry

EC 3.4.22.38 - cathepsin K



3D structures of EC 3.4.22.38 - cathepsin K in Protein Data Bank

updated: 6 January 2022, 2:15

In total: 67 PDB structures of EC 3.4.22.38 - cathepsin K:
  1. 1atk: Crystal Structure of The Cysteine Protease Human Cathepsin K in Complex with The Covalent Inhibitor E-64
  2. 1au0: Crystal Structure of The Cysteine Protease Human Cathepsin K in Complex with a Covalent Symmetric Diacylaminomethyl Ketone Inhibitor
  3. 1au2: Crystal Structure of The Cysteine Protease Human Cathepsin K in Complex with a Covalent Propanone Inhibitor
  4. 1au3: Crystal Structure of The Cysteine Protease Human Cathepsin K in Complex with a Covalent Pyrrolidinone Inhibitor
  5. 1au4: Crystal Structure of The Cysteine Protease Human Cathepsin K in Complex with a Covalent Pyrrolidinone Inhibitor
  6. 1ayu: Crystal Structure of Cysteine Protease Human Cathepsin K in Complex with a Covalent Symmetric Biscarbohydrazide Inhibitor
  7. 1ayv: Crystal Structure of Cysteine Protease Human Cathepsin K in Complex with a Covalent Thiazolhydrazide Inhibitor
  8. 1ayw: Crystal Structure of Cysteine Protease Human Cathepsin K in Complex with a Covalent Benzyloxybenzoylcarbohydrazide Inhibitor
  9. 1bgo: Crystal Structure of Cysteine Protease Human Cathepsin K in Complex with a Covalent Peptidomimetic Inhibitor
  10. 1by8: The Crystal Structure of Human Procathepsin K
  11. 7pck: Crystal Structure of Wild Type Human Procathepsin K
  12. 3o1g: Cathepsin K Covalently Bound to a 2-cyano Pyrimidine Inhibitor with a Benzyl P3 Group.
  13. 1mem: Crystal Structure of Cathepsin K Complexed with a Potent Vinyl Sulfone Inhibitor
  14. 1nl6: Crystal Structure of The Cysteine Protease Human Cathepsin K in Complex with a Covalent Azepanone Inhibitor
  15. 1nlj: Crystal Structure of The Cysteine Protease Human Cathepsin K in Complex with a Covalent Azepanone Inhibitor
  16. 6ql8: Cathepsin-k in Complex with Miv-711
  17. 3kx1: Cathepsin K in Complex with a Selective 2-cyano-pyrimidine Inhibitor
  18. 3kwz: Cathepsin K in Complex with a Non-selective 2-cyano- Pyrimidine Inhibitor
  19. 3kwb: Structure of Catk Covalently Bound to a Dioxo-triazine Inhibitor
  20. 3kw9: X-ray Structure of Cathepsin K Covalently Bound to a Triazine Ligand
  21. 1q6k: Cathepsin K Complexed with T-butyl(1s)-1-cyclohexyl-2- Oxoethylcarbamate
  22. 3h7d: The Crystal Structure of The Cathepsin K Variant M5 in Complex with Chondroitin-4-sulfate
  23. 1snk: Cathepsin K Complexed with Carbamate Derivatized Norleucine Aldehyde
  24. 6qlm: Cathepsin-k in Complex with Miv-701
  25. 1tu6: Cathepsin K Complexed with a Ketoamide Inhibitor
  26. 1u9v: Crystal Structure of The Cysteine Protease Human Cathepsin K in Complex with The Covalent Inhibitor Nvp-abe854
  27. 1u9w: Crystal Structure of The Cysteine Protease Human Cathepsin K in Complex with The Covalent Inhibitor Nvp-abi491
  28. 1u9x: Crystal Structure of The Cysteine Protease Human Cathepsin K in Complex with The Covalent Inhibitor Nvp-abj688
  29. 3c9e: Crystal Structure of The Cathepsin K : Chondroitin Sulfate Complex.
  30. 1vsn: Crystal Structure of a Potent Small Molecule Inhibitor Bound to Cathepsin K
  31. 6qlw: Cathepsin-k in Complex with Miv-710
  32. 6qlx: Cathepsin-k in Complex with Fluoro-oxa-azabicyclo[3.3.0]octanyl Containing Inhibitor
  33. 1yk7: Cathepsin K Complexed with a Cyanopyrrolidine Inhibitor
  34. 1yk8: Cathepsin K Complexed with a Cyanamide-based Inhibitor
  35. 1yt7: Cathepsin K Complexed with a Constrained Ketoamide Inhibitor
  36. 2ato: Crystal Structure of Human Cathepsin K in Complex with Myocrisin
  37. 2aux: Cathepsin K Complexed with a Semicarbazone Inhibitor
  38. 2auz: Cathepsin K Complexed with a Semicarbazone Inhibitor
  39. 2bdl: Cathepsin K Complexed with a Pyrrolidine Ketoamide-based Inhibitor
  40. 2r6n: Crystal Structure of a Pyrrolopyrimidine Inhibitor in Complex with Human Cathepsin K
  41. 6bki: Crystal Structure of T101A Variant Mouse Cathepsin K at 2.94 Angstrom Resolution.
  42. 6ash: Crystal Structure of Human Cathepsin K with a Non-active Site Inhibitor at 1.42 Angstrom Resolution
  43. 2f7d: A Mutant Rabbit Cathepsin K with a Nitrile Inhibitor
  44. 2ftd: Crystal Structure of Cathepsin K Complexed with 7-methyl- Substituted Azepan-3-one Compound
  45. 5z5o: Structure of Pycnonodysostosis Disease Related I249T Mutant of Human Cathepsin K
  46. 6pxf: Structure of Human Cathepsin K with an Ectosteric Inhibitor at 1.85 Angstrom Resolution
  47. 3ovz: Cathepsin K in Complex with a Covalent Inhibitor with a Ketoamide Warhead
  48. 3o0u: Cathepsin K Covalently Bound to a Cyano-pyrimidine Inhibitor with Improved Selectivity over Herg
  49. 6qbs: The Alkyne Moiety as a Latent Electrophile in Irreversible Covalent Small Molecule Inhibitors of Cathepsin K
  50. 4dmx: Cathepsin K Inhibitor
  51. 4dmy: Cathepsin K Inhibitor
  52. 6qm0: Cathepsin-k in Complex with Amino-oxaazabicyclo[3.3.0]octanyl Containing Inhibitor
  53. 6hgy: Crystal Structure of Cathepsin K with N-desmethyl Thalassospiramide C
  54. 4n79: Structure of Cathepsin K-dermatan Sulfate Complex
  55. 4n8w: Cathepsin K - Chondroitin Sulfate Complex
  56. 5tun: Crystal Structure of Uninhibited Human Cathepsin K at 1.62 Angstrom Resolution
  57. 5tdi: Crystal Structure of Cathepsin K with a Covalently-linked Inhibitor at 1.4 Angstrom Resolution.
  58. 5t6u: Crystal Structure of Mouse Cathepsin K at 2.9 Angstroms Resolution.
  59. 5jh3: Human Cathepsin K Mutant C25S
  60. 5ja7: Human Cathepsin K Mutant C25S in Complex with The Allosteric Effector Nsc94914
  61. 5j94: Human Cathepsin K Mutant C25S in Complex with The Allosteric Effector Nsc13345
  62. 4yva: Cathepsin K Co-crystallized with Actinomycetes Extract
  63. 4yv8: Crystal Structure of Cathepsin K Bound to The Covalent Inhibitor Lichostatinal
  64. 4x6h: Development of N-(functionalized Benzoyl)-homocycloleucyl- Glycinonitriles as Potent Cathepsin K Inhibitors.
  65. 4x6i: Development of N-(functionalized Benzoyl)-homocycloleucyl- Glycinonitriles as Potent Cathepsin K Inhibitors.
  66. 4x6j: Development of N-(functionalized Benzoyl)-homocycloleucyl- Glycinonitriles as Potent Cathepsin K Inhibitors.
  67. 7nxm: Structure of Human Cathepsin K in Complex with The Selective Activity- Based Probe Gu3416
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