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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 3.4.23
        EC 3.4.23.1
        EC 3.4.23.2
        EC 3.4.23.3
        EC 3.4.23.4
        EC 3.4.23.5
        EC 3.4.23.6
        EC 3.4.23.7
        EC 3.4.23.8
        EC 3.4.23.9
        EC 3.4.23.10
        EC 3.4.23.11
        EC 3.4.23.12
        EC 3.4.23.13
        EC 3.4.23.14
        EC 3.4.23.15
        EC 3.4.23.16
        EC 3.4.23.17
        EC 3.4.23.18
        EC 3.4.23.19
        EC 3.4.23.20
        EC 3.4.23.21
        EC 3.4.23.22
        EC 3.4.23.23
        EC 3.4.23.24
        EC 3.4.23.25
        EC 3.4.23.26
        EC 3.4.23.27
        EC 3.4.23.28
        EC 3.4.23.29
        EC 3.4.23.30
        EC 3.4.23.31
        EC 3.4.23.32
        EC 3.4.23.33
        EC 3.4.23.34
        EC 3.4.23.35
        EC 3.4.23.36
        EC 3.4.23.37
        EC 3.4.23.38
        EC 3.4.23.39
        EC 3.4.23.40
        EC 3.4.23.41
        EC 3.4.23.42
        EC 3.4.23.43
        EC 3.4.23.44
        EC 3.4.23.45
        EC 3.4.23.46
        EC 3.4.23.47
        EC 3.4.23.48
        EC 3.4.23.49
      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 3.4.23.5 - cathepsin D



3D structures of EC 3.4.23.5 - cathepsin D in Protein Data Bank

updated: 6 January 2022, 2:15

In total: 10 PDB structures of EC 3.4.23.5 - cathepsin D:
  1. 1lya: Crystal Structures of Native and Inhibited Forms of Human Cathepsin D: Implications for Lysosomal Targeting and Drug Design
  2. 1lyb: Crystal Structures of Native and Inhibited Forms of Human Cathepsin D: Implications for Lysosomal Targeting and Drug Design
  3. 1lyw: Cathepsin D at Ph 7.5
  4. 6qcb: Crystal Structure of Human Cathepsin D in Complex with Macrocyclic Inhibitor 9
  5. 4obz: Structure of Cathepsin D with Inhibitor 2-(3,4-dimethoxyphenyl)-n-[n- (4-methylbenzyl)carbamimidoyl]acetamide
  6. 4oc6: Structure of Cathepsin D with Inhibitor 2-bromo-n-[(2s,3s)-4-{[2-(2,4- Dichlorophenyl)ethyl][3-(1,3-dioxo-1,3-dihydro-2h-isoindol-2-yl) Propanoyl]amino}-3-hydroxy-1-(3-phenoxyphenyl)butan-2-yl]-4,5- Dimethoxybenzamide
  7. 4od9: Structure of Cathepsin D with Inhibitor N-(3,4-dimethoxybenzyl)- Nalpha-{n-[(3,4-dimethoxyphenyl)acetyl]carbamimidoyl}-d- Phenylalaninamide
  8. 6qbg: Crystal Structure of Human Cathepsin D in Complex with Macrocyclic Inhibitor 14
  9. 6qbh: Crystal Structure of Human Cathepsin D in Complex with Macrocyclic Inhibitor 33
  10. 5ux4: Crystal Structure of Rat Cathepsin D with (5s)-3-(5,6-dihydro-2h- Pyran-3-yl)-1-fluoro- 7-(2-fluoropyridin-3-yl)spiro[chromeno[2,3- C]pyridine-5,4'-[1,3]oxazol]-2'-amine
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