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enzyme (lysozyme)

 
Enzymes
  Enzyme classes:
  EC 1: Oxidoreductases
    EC 1.1
    EC 1.2
    EC 1.3
      EC 1.3.1
      EC 1.3.2
      EC 1.3.3
      EC 1.3.5
      EC 1.3.7
      EC 1.3.99
        EC 1.3.99.1
        EC 1.3.99.2
        EC 1.3.99.3
        EC 1.3.99.4
        EC 1.3.99.5
        EC 1.3.99.6
        EC 1.3.99.7
        EC 1.3.99.8
        EC 1.3.99.9
        EC 1.3.99.10
        EC 1.3.99.11
        EC 1.3.99.12
        EC 1.3.99.13
        EC 1.3.99.14
        EC 1.3.99.15
        EC 1.3.99.16
        EC 1.3.99.17
        EC 1.3.99.18
        EC 1.3.99.19
        EC 1.3.99.20
        EC 1.3.99.21
        EC 1.3.99.22
        EC 1.3.99.23
        EC 1.3.99.24
        EC 1.3.99.25
    EC 1.4
    EC 1.5
    EC 1.6
    EC 1.7
    EC 1.8
    EC 1.9
    EC 1.10
    EC 1.11
    EC 1.12
    EC 1.13
    EC 1.14
    EC 1.15
    EC 1.16
    EC 1.17
    EC 1.18
    EC 1.19
    EC 1.20
    EC 1.21
    EC 1.97
    EC 1.98
    EC 1.99
  EC 2: Transferases
  EC 3: Hydrolases
  EC 4: Lyases
  EC 5: Isomerases
  EC 6: Ligases
  General information:
  Catalytic mechanism
  Enzyme kinetics
  Inhibitors
  Enzymes in industry

EC 1.3.99.11 - ( S ) - dihydroorotate:acceptor oxidoreductase



3D structures of EC 1.3.99.11 in Protein Data Bank

updated: 29 October 2020, 11:13

In total: 9 PDB structures of EC 1.3.99.11:
  1. 1tv5: Plasmodium Falciparum Dihydroorotate Dehydrogenase with a Bound Inhibitor
  2. 1uum: Rat Dihydroorotate Dehydrogenase (dhod)in Complex with Atovaquone
  3. 1uuo: Rat Dihydroorotate Dehydrogenase (dhod)in Complex with Brequinar
  4. 3c61: Crystal Structure of Dihydroorotate Dehydrogenase from Leishmania Donovani
  5. 2b4g: Dihydroorotate Dehydrogenase
  6. 2bsl: Crystal Structure of L. Lactis Dihydroorotate Dehydrogense a in Complex with 3,4-dihydroxybenzoate
  7. 2prm: The Structures of Apo- and Inhibitor Bound Human Dihydroorotate Dehydrogenase Reveal Conformational Flexibility within The Inhibitor Binding Site
  8. 2prl: The Structures of Apo- and Inhibitor Bound Human Dihydroorotate Dehydrogenase Reveal Conformational Flexibility within The Inhibitor Binding Site
  9. 2prh: The Structures of Apo- and Inhibitor Bound Human Dihydroorotate Dehydrogenase Reveal Conformational Flexibility within The Inhibitor Binding Site
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