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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 3.5
      EC 3.5.1
        EC 3.5.1.1
        EC 3.5.1.2
        EC 3.5.1.3
        EC 3.5.1.4
        EC 3.5.1.5
        EC 3.5.1.6
        EC 3.5.1.7
        EC 3.5.1.8
        EC 3.5.1.9
        EC 3.5.1.10
        EC 3.5.1.11
        EC 3.5.1.12
        EC 3.5.1.13
        EC 3.5.1.14
        EC 3.5.1.15
        EC 3.5.1.16
        EC 3.5.1.17
        EC 3.5.1.18
        EC 3.5.1.19
        EC 3.5.1.20
        EC 3.5.1.21
        EC 3.5.1.22
        EC 3.5.1.23
        EC 3.5.1.24
        EC 3.5.1.25
        EC 3.5.1.26
        EC 3.5.1.27
        EC 3.5.1.28
        EC 3.5.1.29
        EC 3.5.1.30
        EC 3.5.1.31
        EC 3.5.1.32
        EC 3.5.1.33
        EC 3.5.1.34
        EC 3.5.1.35
        EC 3.5.1.36
        EC 3.5.1.37
        EC 3.5.1.39
        EC 3.5.1.40
        EC 3.5.1.41
        EC 3.5.1.42
        EC 3.5.1.43
        EC 3.5.1.44
        EC 3.5.1.45
        EC 3.5.1.46
        EC 3.5.1.47
        EC 3.5.1.48
        EC 3.5.1.49
        EC 3.5.1.50
        EC 3.5.1.51
        EC 3.5.1.52
        EC 3.5.1.53
        EC 3.5.1.54
        EC 3.5.1.55
        EC 3.5.1.56
        EC 3.5.1.57
        EC 3.5.1.58
        EC 3.5.1.59
        EC 3.5.1.60
        EC 3.5.1.61
        EC 3.5.1.62
        EC 3.5.1.63
        EC 3.5.1.64
        EC 3.5.1.65
        EC 3.5.1.66
        EC 3.5.1.67
        EC 3.5.1.68
        EC 3.5.1.69
        EC 3.5.1.70
        EC 3.5.1.71
        EC 3.5.1.72
        EC 3.5.1.73
        EC 3.5.1.74
        EC 3.5.1.75
        EC 3.5.1.76
        EC 3.5.1.77
        EC 3.5.1.78
        EC 3.5.1.79
        EC 3.5.1.80
        EC 3.5.1.81
        EC 3.5.1.82
        EC 3.5.1.83
        EC 3.5.1.84
        EC 3.5.1.85
        EC 3.5.1.86
        EC 3.5.1.87
        EC 3.5.1.88
        EC 3.5.1.89
        EC 3.5.1.90
        EC 3.5.1.91
        EC 3.5.1.92
        EC 3.5.1.93
        EC 3.5.1.94
        EC 3.5.1.95
        EC 3.5.1.96
        EC 3.5.1.97
        EC 3.5.1.98
      EC 3.5.2
      EC 3.5.3
      EC 3.5.4
      EC 3.5.5
      EC 3.5.99
    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 3.5.1.98 - histone amidohydrolase (histone deacetylase)



3D structures of EC 3.5.1.98 - histone deacetylase in Protein Data Bank

updated: 6 January 2022, 2:15

In total: 152 PDB structures of EC 3.5.1.98 - histone deacetylase:
  1. 3mz7: Crystal Structure of D101L Co2+ Hdac8 Complexed with M344
  2. 3mz6: Crystal Structure of D101L Fe2+ Hdac8 Complexed with M344
  3. 3mz4: Crystal Structure of D101L Mn2+ Hdac8 Complexed with M344
  4. 3mz3: Crystal Structure of Co2+ Hdac8 Complexed with M344
  5. 3max: Crystal Structure of Human Hdac2 Complexed with an N-(2-aminophenyl) Benzamide
  6. 3gv4: Crystal Structure of Human Hdac6 Zinc Finger Domain and Ubiquitin C-terminal Peptide Rlrgg
  7. 3f0r: Crystal Structure Analysis of Human Hdac8 Complexed with Trichostatin a in a New Monoclinic Crystal Form
  8. 3f07: Crystal Structure Analysis of Human Hdac8 Complexed with Apha in a New Monoclinic Crystal Form
  9. 3f06: Crystal Structure Analysis of Human Hdac8 D101A Variant.
  10. 3ezt: Crystal Structure Analysis of Human Hdac8 D101E Variant
  11. 3ezp: Crystal Structure Analysis of Human Hdac8 D101N Variant
  12. 3ewf: Crystal Structure Analysis of Human Hdac8 H143A Variant Complexed with Substrate.
  13. 3ew8: Crystal Structure Analysis of Human Hdac8 D101L Variant
  14. 2vqw: Structure of Inhibitor-free Hdac4 Catalytic Domain (with Gain-of-function Mutation HIS332TYR)
  15. 7jvw: Crystal Structure of Human Histone Deacetylase 8 (hdac8) G320R Mutation Complexed with M344
  16. 7jvv: Crystal Structure of Human Histone Deacetylase 8 (hdac8) E66D/Y306F Double Mutation Complexed with a Tetrapeptide Substrate
  17. 7jvu: Crystal Structure of Human Histone Deacetylase 8 (hdac8) I45T Mutation Complexed with Saha
  18. 7aoa: Structure of The Extended Mta1/hdac1/mbd2/rbbp4 Nurd Deacetylase Complex
  19. 7ao9: Structure of The Core Mta1/hdac1/mbd2 Nurd Deacetylase Complex
  20. 7ao8: Structure of The Mta1/hdac1/mbd2 Nurd Deacetylase Complex
  21. 6z2k: The Structure of The Tetrameric Hdac1/mideas/dnttip1 Midac Deacetylase Complex
  22. 6z2j: The Structure of The Dimeric Hdac1/mideas/dnttip1 Midac Deacetylase Complex
  23. 5zop: Crystal Structure of Histone Deacetylase 4 (hdac4) in Complex with a Smrt Corepressor Sp2 Fragment
  24. 5zoo: Crystal Structure of Histone Deacetylase 4 (hdac4) in Complex with a Smrt Corepressor Sp1 Fragment
  25. 6xec: Structure of Human Hdac2 in Complex with Ketone Inhibitor (compound O)
  26. 6xeb: Structure of Human Hdac2 in Complex with Ketone Inhibitor (compound E)
  27. 6xdm: Structure of Human Hdac2 in Complex with an Aryl Ketone Inhibitor
  28. 3phd: Crystal Structure of Human Hdac6 in Complex with Ubiquitin
  29. 6wbz: Structure of Human Hdac2 in Complex with an Ethyl Ketone Inhibitor Containing a Spiro-bicyclic Group
  30. 6wbw: Structure of Human Hdac2 in Complex with an Ethyl Ketone Inhibitor
  31. 6odc: Crystal Structure of Hdac8 in Complex with Compound 30
  32. 6odb: Crystal Structure of Hdac8 in Complex with Compound 3
  33. 6oda: Crystal Structure of Hdac8 in Complex with Compound 2
  34. 3sff: Crystal Structure of Human Hdac8 Inhibitor Complex, an Amino Acid Derived Inhibitor
  35. 3sfh: Crystal Structure of Human Hdac8 Inhibitor Complex, an Amino Acid Derived Inhibitor
  36. 3rqd: Ideal Thiolate-zinc Coordination Geometry in Depsipeptide Binding to Histone Deacetylase 8
  37. 4a69: Structure of Hdac3 Bound to Corepressor and Inositol Tetraphosphate
  38. 3uzd: Crystal Structure of 14-3-3 Gamma
  39. 3v31: Crystal Structure of The Peptide Bound Complex of The Ankyrin Repeat Domains of Human Ankra2
  40. 3uxg: Crystal Structure of Rfxank
  41. 6hu3: Crystal Structure of Schistosoma Mansoni Hdac8 Complexed with a Triazole Hydroxamate Inhibitor
  42. 6hu2: Crystal Structure of Schistosoma Mansoni Hdac8 Complexed with a Benzohydroxamate Inhibitor 11
  43. 6hu1: Crystal Structure of Schistosoma Mansoni Hdac8 Complexed with a Benzohydroxamate Inhibitor 10
  44. 6hu0: Crystal Structure of Schistosoma Mansoni Hdac8 Complexed with a Benzohydroxamate Inhibitor 9
  45. 6htz: Crystal Structure of Schistosoma Mansoni Hdac8 Complexed with a Benzohydroxamate Inhibitor 8
  46. 6htt: Crystal Structure of Schistosoma Mansoni Hdac8 Complexed with a Benzohydroxamate Inhibitor 7
  47. 6hti: Crystal Structure of Schistosoma Mansoni Hdac8 Complexed with a Benzohydroxamate Inhibitor 6
  48. 6hth: Crystal Structure of Schistosoma Mansoni Hdac8 Complexed with a Benzohydroxamate Inhibitor 5
  49. 6htg: Crystal Structure of Schistosoma Mansoni Hdac8 Complexed with a Benzohydroxamate Inhibitor 4
  50. 6ht8: Crystal Structure of Schistosoma Mansoni Hdac8 Complexed with a Benzohydroxamate Inhibitor 3
  51. 6hsz: Crystal Structure of Schistosoma Mansoni Hdac8 Complexed with a Benzohydroxamate Inhibitor 2
  52. 6hsk: Crystal Structure of a Human Hdac8 L6 Loop Mutant Complexed with Quisinostat
  53. 6hsh: Crystal Structure of Schistosoma Mansoni Hdac8 Complexed with Quisinostat
  54. 6hsg: Crystal Structure of Schistosoma Mansoni Hdac8 H292M Mutant Complexed with Ncc-149
  55. 6hsf: Crystal Structure of Schistosoma Mansoni Hdac8 Mutant H292M Complexed with Pci-34051
  56. 6hrq: Crystal Structure of Schistosoma Mansoni Hdac8 Complexed with Ncc-149
  57. 6hqy: Crystal Structure of Schistosoma Mansoni Hdac8 Complexed with Pci- 34051
  58. 3znr: Hdac7 Bound with Inhibitor Tmp269
  59. 3zns: Hdac7 Bound with Tfmo Inhibitor Tmp942
  60. 6gxw: Crystal Structure of Schistosoma Mansoni Hdac8 Complexed with an Hydroxamate 4
  61. 6gxu: Crystal Structure of Schistosoma Mansoni Hdac8 Complexed with an Hydroxamate 3
  62. 6gxa: Crystal Structure of Schistosoma Mansoni Hdac8 Complexed with an Hydroxamate 2
  63. 6gx3: Crystal Structure of Schistosoma Mansoni Hdac8 Complexed with an Hydroxamate 1
  64. 6g3o: Crystal Structure of Human Hdac2 in Complex with (r)-6-[3,4-dioxo-2- (4-trifluoromethoxy-phenylamino)-cyclobut-1-enylamino]-heptanoic Acid Hydroxyamide
  65. 6fyz: Development and Characterization of a Cns-penetrant Benzhydryl Hydroxamic Acid Class Iia Histone Deacetylase Inhibitor
  66. 6fu1: Crystal Structure of Schistosoma Mansoni Hdac8 Complexed with a N- Alkyl Hydroxamate
  67. 4bkx: The Structure of Hdac1 in Complex with The Dimeric Elm2-sant Domain of Mta1 from The Nurd Complex
  68. 6cef: Crystal Structure of Fragment 3-(1,3-benzothiazol-2-yl)propanoic Acid Bound in The Ubiquitin Binding Pocket of The Hdac6 Zinc-finger Domain
  69. 6cee: Crystal Structure of Fragment 3-(1-methyl-2-oxo-1,2-dihydroquinoxalin- 3-yl)propionic Acid Bound in The Ubiquitin Binding Pocket of The Hdac6 Zinc-finger Domain
  70. 6ced: Crystal Structure of Fragment 3-(3-methyl-4-oxo-3,4-dihydroquinazolin- 2-yl)propanoic Acid Bound in The Ubiquitin Binding Pocket of The Hdac6 Zinc-finger Domain
  71. 6cec: Crystal Structure of Fragment 3-(3-methoxy-2-quinoxalinyl)propanoic Acid Bound in The Ubiquitin Binding Pocket of The Hdac6 Zinc-finger Domain
  72. 6cea: Crystal Structure of Fragment 3-(quinolin-2-yl)propanoic Acid Bound in The Ubiquitin Binding Pocket of The Hdac6 Zinc-finger Domain
  73. 6ce8: Crystal Structure of Fragment 2-(benzo[d]thiazol-2-yl)acetic Acid Bound in The Ubiquitin Binding Pocket of The Hdac6 Zinc-finger Domain
  74. 6ce6: Structure of Hdac6 Zinc-finger Ubiquitin Binding Domain Soaked with 3, 3'-(benzo[1,2-d:5,4-d']bis(thiazole)-2,6-diyl)dipropionic Acid
  75. 4cbt: Design, Synthesis, and Biological Evaluation of Potent and Selective Class Iia Hdac Inhibitors as a Potential Therapy for Huntingtons Disease
  76. 4cby: Design, Synthesis, and Biological Evaluation of Potent and Selective Class Iia Hdac Inhibitors as a Potential Therapy for Huntingtons Disease
  77. 4lxz: Structure of Human Hdac2 in Complex with Saha (vorinostat)
  78. 4ly1: Structure of Human Hdac2 in Complex with Inhibitor 4-(acetylamino)-n- [2-amino-5-(thiophen-2-yl)phenyl]benzamide
  79. 4qa0: Crystal Structure of C153F Hdac8 in Complex with Saha
  80. 4qa1: Crystal Structure of A188T Hdac8 in Complex with M344
  81. 4qa2: Crystal Structure of I243N Hdac8 in Complex with Saha
  82. 4qa3: Crystal Structure of T311M Hdac8 in Complex with Trichostatin a (tsa)
  83. 4qa4: Crystal Structure of H334R Hdac8 in Complex with M344
  84. 4qa5: Crystal Structure of A188T/Y306F Hdac8 in Complex with a Tetrapeptide Substrate
  85. 4qa6: Crystal Structure of I243N/Y306F Hdac8 in Complex with a Tetrapeptide Substrate
  86. 4qa7: Crystal Structure of H334R/Y306F Hdac8 in Complex with a Tetrapeptide Substrate
  87. 5wpb: Crystal Structure of Fragment 3-(3-(pyridin-2-ylmethoxy)quinoxalin-2- Yl)propanoic Acid Bound in The Ubiquitin Binding Pocket of The Hdac6 Zinc-finger Domain
  88. 5wbn: Crystal Structure of Fragment 3-(3-benzyl-2-oxo-2h-[1,2,4]triazino[2, 3-c]quinazolin-6-yl)propanoic Acid Bound in The Ubiquitin Binding Pocket of The Hdac6 Zinc-finger Domain
  89. 6pzo: Crystal Structure of Danio Rerio Histone Deacetylase 6 Catalytic Domain 2 Complexed with Yx-153
  90. 6pzr: Crystal Structure of Danio Rerio Histone Deacetylase 6 Catalytic Domain 2 Complexed with Resminostat
  91. 6pzs: Crystal Structure of Danio Rerio Histone Deacetylase 6 Catalytic Domain 2 Complexed with Jr005
  92. 6j6t: Crystal Structure of Hda15 Hd Domain
  93. 5vi6: Crystal Structure of Histone Deacetylase 8 in Complex with Trapoxin a
  94. 5thv: Crystal Structure of G305A Hdac8 in Complex with M344
  95. 5thu: Crystal Structure of G304A Hdac8 in Complex with M344
  96. 5tht: Crystal Structure of G303A Hdac8 in Complex with M344
  97. 5ths: Crystal Structure of G302A Hdac8 in Complex with M344
  98. 5kh9: Crystal Structure of a Low Occupancy Fragment Candidate (5-[(4- Isopropylphenyl)amino]-6-methyl-1,2,4-triazin-3(2h)-one) Bound in The Ubiquitin Binding Pocket of The Hdac6 Zinc-finger Domain
  99. 5kh7: Crystal Structure of Fragment (3-[6-oxo-3-(3-pyridinyl)-1(6h)- Pyridazinyl]propanoic Acid) Bound in The Ubiquitin Binding Pocket of The Hdac6 Zinc-finger Domain
  100. 5kh3: Crystal Structure of Fragment (3-(5-chloro-1,3-benzothiazol-2-yl) Propanoic Acid) Bound in The Ubiquitin Binding Pocket of The Hdac6 Zinc-finger Domain
  101. 5j8j: A Histone Deacetylase from Saccharomyces Cerevisiae
  102. 5ix0: Hdac2 with Ligand Brd7232
  103. 5iwg: Hdac2 with Ligand Brd4884
  104. 5ikk: Structure of The Histone Deacetylase Clr3
  105. 5icn: Hdac1:mta1 in Complex with Inositol-6-phosphate and a Novel Peptide Inhibitor Based on Histone H4
  106. 5fcw: Hdac8 Complexed with a Hydroxamic Acid
  107. 5efn: Crystal Structure of Danio Rerio Histone Deacetylase 6 Catalytic Domain 2 (H574A) in Complex with Histone H4 Lys6 Tripeptide Substrate
  108. 5efk: Crystal Structure of Danio Rerio Histone Deacetylase 6 Catalytic Domain 2 (Y745F Mutant) in Complex with Alpha Tubulin K40 Tripeptide Substrate
  109. 5efj: Crystal Structure of Danio Rerio Histone Deacetylase 6 Catalytic Domain 2 in Complex with Hc Toxin
  110. 5efh: Crystal Structure of Danio Rerio Histone Deacetylase 6 Catalytic Domain 2 in Complex with Trifluoroketone Transition State Analogue
  111. 5efg: Crystal Structure of Danio Rerio Histone Deacetylase 6 Catalytic Domain 2 in Complex with Acetate
  112. 5efb: Crystal Structure of Danio Rerio Histone Deacetylase 6 Catalytic Domain 2 in Complex with Oxamflatin
  113. 5ef8: Crystal Structure of Danio Rerio Histone Deacetylase 6 Catalytic Domain 2 in Complex with Panobinostat
  114. 5ef7: Crystal Structure of Danio Rerio Histone Deacetylase 6 Catalytic Domain 2 in Complex with Hpob
  115. 5een: Crystal Structure of Danio Rerio Histone Deacetylase 6 Catalytic Domain 2 in Complex with Belinostat
  116. 5eem: Crystal Structure of Danio Rerio Histone Deacetylase 6 Catalytic Domain 2
  117. 5eek: Crystal Structure of Danio Rerio Histone Deacetylase 6 Catalytic Domain 2 in Complex with Trichostatin a
  118. 5eei: Crystal Structure of Danio Rerio Histone Deacetylase 6 Catalytic Domain 2 in Complex with Saha
  119. 5edu: Crystal Structure of Human Histone Deacetylase 6 Catalytic Domain 2 in Complex with Trichostatin a
  120. 5dc8: Crystal Structure of H142A-Y306F Hdac8 in Complex with a Tetrapeptide Substrate
  121. 5dc7: Crystal Structure of D176A-Y306F Hdac8 in Complex with a Tetrapeptide Substrate
  122. 5dc6: Crystal Structure of D176N-Y306F Hdac8 in Complex with a Tetrapeptide Substrate
  123. 5dc5: Crystal Structure of D176N Hdac8 in Complex with M344
  124. 5d1d: Crystal Structure of P91L-Y306F Hdac8 in Complex with a Tetrapeptide Substrate
  125. 5d1c: Crystal Structure of D233G-Y306F Hdac8 in Complex with a Tetrapeptide Substrate
  126. 5d1b: Crystal Structure of G117E Hdac8 in Complex with Tsa
  127. 5bwz: Crystal Structure of S39E Hdac8 in Complex with Droxinostat
  128. 5b8d: Crystal Structure of a Low Occupancy Fragment Candidate (n-(4-methyl- 1,3-thiazol-2-yl)propanamide) Bound Adjacent to The Ubiquitin Binding Pocket of The Hdac6 Zinc-finger Domain
  129. 5a2s: Potent, Selective and Cns-penetrant Tetrasubstituted Cyclopropane Class Iia Histone Deacetylase (hdac) Inhibitors
  130. 4rn0: Crystal Structure of S39D Hdac8 in Complex with a Largazole Analogue.
  131. 4rn1: Crystal Structure of S39D Hdac8 in Complex with a Largazole Analogue.
  132. 4rn2: Crystal Structure of S39D Hdac8 in Complex with a Largazole Analogue.
  133. 7kbg: Structure of Human Hdac2 in Complex with a 2-substituted Benzamide Inhibitor (compound 20)
  134. 7kbh: Structure of Human Hdac2 in Complex with a 2-substituted Benzamide Inhibitor (compound 16)
  135. 6z6f: Hdac-pc
  136. 6z6h: Hdac-dc
  137. 6z6o: Hdac-tc
  138. 6z6p: Hdac-pc-nuc
  139. 6whn: Histone Deacetylases Complex with Peptide Macrocycles
  140. 6who: Histone Deacetylases Complex with Peptide Macrocycles
  141. 6whq: Histone Deacetylases Complex with Peptide Macrocycles
  142. 6whz: Histone Deacetylases Complex with Peptide Macrocycles
  143. 6wi3: Histone Deacetylases Complex with Peptide Macrocycles
  144. 7ltg: Structure of Human Hdac2 in Complex with Apicidin
  145. 7ltk: Structure of Human Hdac2 in Complex with an Inhibitor That Lacks a Zinc Binding Group (compound 12)
  146. 7ltl: Structure of Human Hdac2 in Complex with an Inhibitor Lacking a Zinc Binding Group (compound 19)
  147. 7mos: Structure of Hdac2 in Complex with a Macrocyclic Inhibitor (compound 4)
  148. 7mot: Structure of Hdac2 in Complex with an Inhibitor (compound 9)
  149. 7mox: Structure of Hdac2 in Complex with an Inhibitor (compound 14)
  150. 7moy: Structure of Hdac2 in Complex with an Inhibitor (compound 19)
  151. 7moz: Structure of Hdac2 in Complex with a Macrocyclic Inhibitor (compound 25)
  152. 7js8: Structure of Human Hdac2 in Complex with an Ethyl Ketone Inhibitor Containing a Spiro-bicyclic Group (compound 22)
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