8Z2I

Substrate analog a011 bound form of PET-degrading cutinase mutant Cut190**SS_S176A


Experimental Data Snapshot

  • Method: X-RAY DIFFRACTION
  • Resolution: 1.38 Å
  • R-Value Free: 0.168 
  • R-Value Work: 0.144 
  • R-Value Observed: 0.155 

Starting Model: experimental
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Literature

Structural dynamics of the Ca 2+ -regulated cutinase towards structure-based improvement of PET degradation activity.

Numoto, N.Kondo, F.Bekker, G.J.Liao, Z.Yamashita, M.Iida, A.Ito, N.Kamiya, N.Oda, M.

(2024) Int J Biol Macromol 281: 136597-136597

  • DOI: https://doi.org/10.1016/j.ijbiomac.2024.136597
  • Primary Citation of Related Structures:  
    8Z2G, 8Z2H, 8Z2I, 8Z2J, 8Z2K

  • PubMed Abstract: 

    We previously revealed the structural basis of Ca 2+ dependent regulation of a polyethylene terephthalate (PET)-degrading enzyme, Cut190, and proposed a unique reaction cycle in which the enzyme repeatedly binds and releases Ca 2+ . Here, we report crystal structures of Cut190 mutants with high thermal stability complexed with PET-like ligands that contain aromatic rings. The structural information has allowed us to perform further computational analyses using a PET-trimer bound model. Our multicanonical molecular dynamics simulations and subsequent analyses of the free energy landscapes revealed a novel intermediate form that occurs during the enzymatic reaction cycle. Furthermore, the computational analyses were used to investigate the effect of the point mutations F77L and F81L in the Ca 2+ -binding site, which showed that the former stabilizes the engaged and open forms to improve transition between the open and active forms, while the latter extremely increases the open form. Subsequent experiments showed that the F77L mutation increased the activity, while the F81L mutation decreased the activity. Our computational analysis has enabled us to explore the dynamics of Cut190 on a completely new level, providing key insights into how the balance between the various conformations influences the reaction cycle and ultimately how to improve the reaction cycle.


  • Organizational Affiliation

    Medical Research Laboratory, Institute of Integrated Research, Institute of Science Tokyo, 1-5-45 Yushima Bunkyo-ku, Tokyo 113-8510, Japan; International Center for Structural Biology, Research Institute for Interdisciplinary Science, Okayama University, 3-1-1 Tsushima-naka, Kita-ku, Okayama 700-8530, Japan.


Macromolecules
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Entity ID: 1
MoleculeChains Sequence LengthOrganismDetailsImage
Alpha/beta hydrolase family protein
A, B
260Saccharomonospora viridisMutation(s): 8 
Gene Names: Cut190MINT15_00360
EC: 3.1.1.74
UniProt
Find proteins for W0TJ64 (Saccharomonospora viridis)
Explore W0TJ64 
Go to UniProtKB:  W0TJ64
Entity Groups  
Sequence Clusters30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity
UniProt GroupW0TJ64
Sequence Annotations
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  • Reference Sequence
Experimental Data & Validation

Experimental Data

  • Method: X-RAY DIFFRACTION
  • Resolution: 1.38 Å
  • R-Value Free: 0.168 
  • R-Value Work: 0.144 
  • R-Value Observed: 0.155 
  • Space Group: P 3
Unit Cell:
Length ( Å )Angle ( ˚ )
a = 84.33α = 90
b = 84.33β = 90
c = 64.86γ = 120
Software Package:
Software NamePurpose
PHENIXrefinement
XDSdata reduction
XSCALEdata scaling
PHASERphasing

Structure Validation

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Ligand Structure Quality Assessment 


Entry History & Funding Information

Deposition Data


Funding OrganizationLocationGrant Number
Japan Society for the Promotion of Science (JSPS)JapanJP21H02120

Revision History  (Full details and data files)

  • Version 1.0: 2024-11-06
    Type: Initial release