1UQR

Type II 3-dehydroquinate dehydratase (DHQase) from Actinobacillus pleuropneumoniae


Experimental Data Snapshot

  • Method: X-RAY DIFFRACTION
  • Resolution: 1.70 Å
  • R-Value Free: 0.199 
  • R-Value Work: 0.178 
  • R-Value Observed: 0.178 

wwPDB Validation   3D Report Full Report


This is version 1.4 of the entry. See complete history


Literature

Structural Study of the Type II 3-Dehydroquinate Dehydratase from Actinobacillus Pleuropneumoniae

Maes, D.Gonzalez-Ramirez, L.A.Lopez-Jaramillo, J.Yu, B.De Bondt, H.Zegers, I.Afonina, E.Garcia-Ruiz, J.M.Gulnik, S.

(2004) Acta Crystallogr D Biol Crystallogr 60: 463

  • DOI: https://doi.org/10.1107/S090744490302969X
  • Primary Citation of Related Structures:  
    1UQR

  • PubMed Abstract: 

    The structure of the type II dehydroquinate dehydratase (DHQase) from Actinobacillus pleuropneumoniae, the third enzyme of the shikimate pathway, has been determined. Crystals diffracting to 1.7 A were obtained in space and on earth using the counter-diffusion technique. The structure was solved using molecular replacement and refined to high resolution. The overall structure of the dodecameric enzyme is described and compared with structures of DHQases from other bacteria. DHQases contain a flexible loop that presumably closes over the active site upon substrate binding. The enzyme can exist in an open or closed conformation. The present structure displays the open conformation, with a sulfate anion bound in the active site. The availability of this structure opens a route to structure-based antibiotics targetting this pathogenic bacterium.


  • Organizational Affiliation

    ULTR, Vrije Universiteit Brussel, Vlaams Interuniversitair Instituut voor Biotechnologie (VIB), Pleinlaan 2, 1050 Brussels, Belgium. dominique.maes@vub.ac.be


Macromolecules
Find similar proteins by:  (by identity cutoff)  |  3D Structure
Entity ID: 1
MoleculeChains Sequence LengthOrganismDetailsImage
3-DEHYDROQUINATE DEHYDRATASE
A, B, C, D, E
A, B, C, D, E, F, G, H, I, J, K, L
154Actinobacillus pleuropneumoniaeMutation(s): 0 
EC: 4.2.1.10
UniProt
Find proteins for P43877 (Actinobacillus pleuropneumoniae)
Explore P43877 
Go to UniProtKB:  P43877
Entity Groups  
Sequence Clusters30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity
UniProt GroupP43877
Sequence Annotations
Expand
  • Reference Sequence
Small Molecules
Ligands 2 Unique
IDChains Name / Formula / InChI Key2D Diagram3D Interactions
TRS
Query on TRS

Download Ideal Coordinates CCD File 
AA [auth E],
KA [auth H],
Q [auth B],
SA [auth K]
2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL
C4 H12 N O3
LENZDBCJOHFCAS-UHFFFAOYSA-O
SO4
Query on SO4

Download Ideal Coordinates CCD File 
BA [auth F]
CA [auth F]
DA [auth F]
EA [auth F]
FA [auth G]
BA [auth F],
CA [auth F],
DA [auth F],
EA [auth F],
FA [auth G],
GA [auth H],
HA [auth H],
IA [auth H],
JA [auth H],
LA [auth I],
M [auth A],
MA [auth J],
N [auth A],
NA [auth J],
O [auth B],
OA [auth J],
P [auth B],
PA [auth K],
QA [auth K],
R [auth C],
RA [auth K],
S [auth C],
T [auth C],
TA [auth L],
U [auth D],
UA [auth L],
V [auth D],
W [auth D],
X [auth E],
Y [auth E],
Z [auth E]
SULFATE ION
O4 S
QAOWNCQODCNURD-UHFFFAOYSA-L
Experimental Data & Validation

Experimental Data

  • Method: X-RAY DIFFRACTION
  • Resolution: 1.70 Å
  • R-Value Free: 0.199 
  • R-Value Work: 0.178 
  • R-Value Observed: 0.178 
  • Space Group: P 21 21 21
Unit Cell:
Length ( Å )Angle ( ˚ )
a = 129.095α = 90
b = 131.333β = 90
c = 161.619γ = 90
Software Package:
Software NamePurpose
CNSrefinement
XDSdata reduction
XSCALEdata scaling

Structure Validation

View Full Validation Report



Entry History 

Deposition Data

Revision History  (Full details and data files)

  • Version 1.0: 2003-10-30
    Type: Initial release
  • Version 1.1: 2011-05-08
    Changes: Version format compliance
  • Version 1.2: 2011-07-13
    Changes: Version format compliance
  • Version 1.3: 2019-07-24
    Changes: Data collection
  • Version 1.4: 2024-05-08
    Changes: Data collection, Database references, Other