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Molecular Modeling Of Endoglucanases August, 2007
INTRODUCTION
Cellulase ,[object Object]
Cellulases: Types of Action ,[object Object],[object Object],[object Object],[object Object],[object Object],CBM Cellulosome Scheme Cohensins Dockerins Catalytic domains
Application of Cellulases ,[object Object],[object Object],[object Object]
GH Classification ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
GH families ,[object Object],[object Object],[object Object],[object Object]
Pyrococcus horikoshii ,[object Object],[object Object],[object Object],[object Object]
EGPh ,[object Object],[object Object],[object Object],[object Object]
Protein Engineering ,[object Object],[object Object],[object Object],[object Object]
Homology Modeling ,[object Object],[object Object],[object Object],Amino acid sequence Protein 3D structure
Molecular Dynamics (MD) Simulation ,[object Object],[object Object],Protein Structure Protein Dynamics
METHODS
Overview ,[object Object],[object Object],[object Object],[object Object]
Programs and Tools ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Part 1 Homology Modeling
Homology Modeling ,[object Object],[object Object],[object Object],[object Object],[object Object]
1. Template Selection ,[object Object],[object Object],[object Object]
Template Selected ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Homology Modeling ,[object Object],[object Object],[object Object],[object Object],[object Object]
Structural-based Multiple Sequence Alignment
Locations of Conserved Residues ,[object Object],[object Object],cellotetraose E282 R62 N161 H238 Y240 H116 E162
Alignment of the endoglucanases sequences from  Acidothermus cellulolyticus  (1ece) [358 residues] and  Pyrococcus horikoshii  (EGPh) [458 residues] with ClustalW.  Extra loop?
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
EGPh Model  loop loop
Alignment from MODELLER (Align2d method)
Modeling for insertions in the loops ,[object Object],[object Object]
Secondary Structure Prediction by PSIDPRED
Homology Modeling ,[object Object],[object Object],[object Object],[object Object],[object Object]
Model Building ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Homology Modeling ,[object Object],[object Object],[object Object],[object Object],[object Object]
MODEL REFINEMENT ,[object Object],[object Object]
Evaluation of Models ,[object Object],[object Object],[object Object],[object Object],[object Object]
Z-score: -8.48 EGAc crystal structure (pdb code:1ece) EGPh model Z-score: -8.17
https://prosa.services.came.sbg.ac.at/prosa.php EGAc crystal structure (pdb code:1ece) EGPh model
Z-score (68.pdb)  -8.17
Z-score (after 2ns MD)  -9.1
Z-score(after 2ns&Bmin)  -9.32
DOPE profile before and after MD
Evaluation of Models ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
100% 314 Total 37+23+2 Gly+Pro+end residues 85.4% 2 68 Most favored regions 12.1% 35 Additional allowed regions 1.6% 5 Generously allowed regions 1.0% 3 Disallowed regions % # Residues in
 
[object Object]
Y 264 W 233 W 337 F 29 EGPh Y 245 W 213 W 319 F 29 EGAc
-2 -1 +1 +2
Nucleophile -E 282 E 162 – proton donor
Accepted Model ,[object Object]
 
Part 2 MD simulations of  EGPh & EGAc
Molecular Dynamics Protocol ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Preparation Obtain  pdb file Step 1 Check pKa &  add H atoms  accordingly Step 2 Solvate the  protein  in a water box Step 3 Add ions  (Na +  or Cl -  )
Molecular Dynamics Protocol ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
 
EGPh EGAc
 
 
 
 
Thermostability ,[object Object],[object Object],[object Object],[object Object],[object Object]
Comparison of Amino Acids Composition in EGAc and EGPh Charged residues: 55 vs. 80 3.99 15 5.87 21 Ala  (A) 5.85 22 6.42 23 Val  (V) 6.65 25 5.31 19 Ile  (I) 7.18 27 8.38 30 Leu  (L) 1.86 7 1.40 5 Met  (M) 6.12 23 5.87 21 Pro  (P) Hydrophobic 4.79 18 3.35 12 Phe  (F) 9.84 37 9.22 33 Gly  (G) Residues Mol% # Mol% # EGPh (total 376aa) EGAc (total 358aa)
# 80 7.18 27 7.26 26 Asp  (D) Charged 5.05 19 1.96 7 Glu  (E) 2.66 10 3.63 13 Arg  (R) 6.38 24 2.51 9 Lys  (K) 6.12 23 6.70 24 Asn  (N) 1.86 7 5.59 20 Gln  (Q) 1.06 4 1.12 4 Cys  (C) 4.79 18 7.26 26 Ser  (S) 5.32 20 5.31 19 Tyr  (Y) Polar 5.05 19 5.03 18 Trp  (W) 5.32 20 6.15 22 Thr  (T) 2.93 11 1.68 6 His  (H) Residues Mol% # Mol% # EGPh (total 376aa) EGAc (total 358aa) # 55
 
Salt Bridges
CONCLUSION ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
References
Extras
RMSD (Root mean square deviation) ,[object Object]
Root Mean Square Deviation ,[object Object],[object Object]
12 Families with endoglucanse activity Asp (experimental)   Not known   Glu   Asp (experimental)   Not known Glu (experimental)   Glu (experimental)   Glu (experimental)   Glu (experimental)   Glu (experimental)   Asp (experimental)  Glu (experimental)   Catalytic Proton Donor  Fold 7-fold  β -propeller  --- Fold ( α / α  ) 6   --- Not available Fold ( β  / α  ) 8   Fold -jelly roll  Fold ( α / α  ) 6   Fold ( α / α  ) 6   Fold -jelly roll  --- Fold ( β  / α  ) 8   Fold Asp (experimental)   I endoglucanase; etc 74 Not known   -- endoglucanase 61 Not known   I endoglucanase; cellobiohydrolase.  48  Clan M Asp (experimental)   I endoglucanase.   45 Not known I endoglucanase; xyloglucanase  44 Glu (experimental)   R mannanase; -1,3-xylanase 26 Clan A Glu (experimental)   R endoglucanase; xyloglucan hydrolase ; -1,3-1,4-glucanase 12 Clan C Asp (experimental)   I endoglucanase; cellobiohydrolase; -glucosidase 9 Asp (inferred)   I Chitosanase; Cellulase; Licheninase; Endo-1,4--xylanase  8 Clan M Glu (experimental)   R endoglucanase; reducing end-acting cellobiohydrolase 7 Clan B Asp (experimental)  I Endoglucanase;cellobiohydrolase 6 Glu (experimental)   R Cellulase (EC 3.2.1.4); Glucan 1,3--glucosidase (EC 3.2.1.58); Endo-1,4--xylanase (EC 3.2.1.8); Cellulose 1,4--cellobiosidase (EC 3.2.1.91), etc  5 Clan A Catalytic Nucleophile/Base  Mechanism Known Activity CAZY Family
Ligand: cellutetraose Catalytic Site
Classification ,[object Object],[object Object],[object Object],[object Object]

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Mm Of Endoglucanases

  • 1. Molecular Modeling Of Endoglucanases August, 2007
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  • 16. Part 1 Homology Modeling
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  • 23. Alignment of the endoglucanases sequences from Acidothermus cellulolyticus (1ece) [358 residues] and Pyrococcus horikoshii (EGPh) [458 residues] with ClustalW. Extra loop?
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  • 25. EGPh Model loop loop
  • 26. Alignment from MODELLER (Align2d method)
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  • 34. Z-score: -8.48 EGAc crystal structure (pdb code:1ece) EGPh model Z-score: -8.17
  • 35. https://prosa.services.came.sbg.ac.at/prosa.php EGAc crystal structure (pdb code:1ece) EGPh model
  • 37. Z-score (after 2ns MD) -9.1
  • 39. DOPE profile before and after MD
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  • 41. 100% 314 Total 37+23+2 Gly+Pro+end residues 85.4% 2 68 Most favored regions 12.1% 35 Additional allowed regions 1.6% 5 Generously allowed regions 1.0% 3 Disallowed regions % # Residues in
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  • 44. Y 264 W 233 W 337 F 29 EGPh Y 245 W 213 W 319 F 29 EGAc
  • 45. -2 -1 +1 +2
  • 46. Nucleophile -E 282 E 162 – proton donor
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  • 49. Part 2 MD simulations of EGPh & EGAc
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  • 51. Preparation Obtain pdb file Step 1 Check pKa & add H atoms accordingly Step 2 Solvate the protein in a water box Step 3 Add ions (Na + or Cl - )
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  • 60. Comparison of Amino Acids Composition in EGAc and EGPh Charged residues: 55 vs. 80 3.99 15 5.87 21 Ala (A) 5.85 22 6.42 23 Val (V) 6.65 25 5.31 19 Ile (I) 7.18 27 8.38 30 Leu (L) 1.86 7 1.40 5 Met (M) 6.12 23 5.87 21 Pro (P) Hydrophobic 4.79 18 3.35 12 Phe (F) 9.84 37 9.22 33 Gly (G) Residues Mol% # Mol% # EGPh (total 376aa) EGAc (total 358aa)
  • 61. # 80 7.18 27 7.26 26 Asp (D) Charged 5.05 19 1.96 7 Glu (E) 2.66 10 3.63 13 Arg (R) 6.38 24 2.51 9 Lys (K) 6.12 23 6.70 24 Asn (N) 1.86 7 5.59 20 Gln (Q) 1.06 4 1.12 4 Cys (C) 4.79 18 7.26 26 Ser (S) 5.32 20 5.31 19 Tyr (Y) Polar 5.05 19 5.03 18 Trp (W) 5.32 20 6.15 22 Thr (T) 2.93 11 1.68 6 His (H) Residues Mol% # Mol% # EGPh (total 376aa) EGAc (total 358aa) # 55
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  • 69. 12 Families with endoglucanse activity Asp (experimental)  Not known  Glu  Asp (experimental)  Not known Glu (experimental)  Glu (experimental)  Glu (experimental)  Glu (experimental)  Glu (experimental)  Asp (experimental)  Glu (experimental)  Catalytic Proton Donor Fold 7-fold β -propeller --- Fold ( α / α ) 6 --- Not available Fold ( β / α ) 8 Fold -jelly roll Fold ( α / α ) 6 Fold ( α / α ) 6 Fold -jelly roll --- Fold ( β / α ) 8 Fold Asp (experimental)  I endoglucanase; etc 74 Not known  -- endoglucanase 61 Not known  I endoglucanase; cellobiohydrolase. 48 Clan M Asp (experimental)  I endoglucanase.  45 Not known I endoglucanase; xyloglucanase 44 Glu (experimental)  R mannanase; -1,3-xylanase 26 Clan A Glu (experimental)  R endoglucanase; xyloglucan hydrolase ; -1,3-1,4-glucanase 12 Clan C Asp (experimental)  I endoglucanase; cellobiohydrolase; -glucosidase 9 Asp (inferred)  I Chitosanase; Cellulase; Licheninase; Endo-1,4--xylanase 8 Clan M Glu (experimental)  R endoglucanase; reducing end-acting cellobiohydrolase 7 Clan B Asp (experimental)  I Endoglucanase;cellobiohydrolase 6 Glu (experimental)  R Cellulase (EC 3.2.1.4); Glucan 1,3--glucosidase (EC 3.2.1.58); Endo-1,4--xylanase (EC 3.2.1.8); Cellulose 1,4--cellobiosidase (EC 3.2.1.91), etc 5 Clan A Catalytic Nucleophile/Base Mechanism Known Activity CAZY Family
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