2V8U

Atomic resolution structure of Mn catalase from Thermus Thermophilus


Experimental Data Snapshot

  • Method: X-RAY DIFFRACTION
  • Resolution: 1.05 Å
  • R-Value Free: 0.121 
  • R-Value Work: 0.106 
  • R-Value Observed: 0.106 

wwPDB Validation   3D Report Full Report


This is version 1.3 of the entry. See complete history


Literature

Three-Dimentional Structure of the Enzyme Dimanganese Catalase from Thermus Thermophilus at 1 Angstrom Resolution

Antonyuk, S.V.Melik-Adamyan, W.R.Popov, A.N.Lamsin, V.S.Hempstead, P.D.Harrison, P.M.Artymyuk, P.J.Barynin, V.V.

(2000) Crystallogr Rep 45: 105


Macromolecules
Find similar proteins by:  (by identity cutoff)  |  3D Structure
Entity ID: 1
MoleculeChains Sequence LengthOrganismDetailsImage
MANGANESE-CONTAINING PSEUDOCATALASE
A, B
302Thermus thermophilus HB27Mutation(s): 0 
EC: 1.11.1.6
UniProt
Find proteins for Q84DB4 (Thermus thermophilus)
Explore Q84DB4 
Go to UniProtKB:  Q84DB4
Entity Groups  
Sequence Clusters30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity
UniProt GroupQ84DB4
Sequence Annotations
Expand
  • Reference Sequence
Small Molecules
Ligands 4 Unique
IDChains Name / Formula / InChI Key2D Diagram3D Interactions
SO4
Query on SO4

Download Ideal Coordinates CCD File 
AA [auth B]
BA [auth B]
L [auth A]
M [auth A]
O [auth A]
AA [auth B],
BA [auth B],
L [auth A],
M [auth A],
O [auth A],
P [auth A],
S [auth B]
SULFATE ION
O4 S
QAOWNCQODCNURD-UHFFFAOYSA-L
MN
Query on MN

Download Ideal Coordinates CCD File 
H [auth A],
I [auth A],
T [auth B],
U [auth B]
MANGANESE (II) ION
Mn
WAEMQWOKJMHJLA-UHFFFAOYSA-N
O
Query on O

Download Ideal Coordinates CCD File 
C [auth A]
D [auth A]
E [auth A]
F [auth A]
G [auth A]
C [auth A],
D [auth A],
E [auth A],
F [auth A],
G [auth A],
V [auth B],
W [auth B],
X [auth B],
Y [auth B],
Z [auth B]
OXYGEN ATOM
O
XLYOFNOQVPJJNP-UHFFFAOYSA-N
LI
Query on LI

Download Ideal Coordinates CCD File 
J [auth A],
K [auth A],
N [auth A],
Q [auth B],
R [auth B]
LITHIUM ION
Li
HBBGRARXTFLTSG-UHFFFAOYSA-N
Experimental Data & Validation

Experimental Data

  • Method: X-RAY DIFFRACTION
  • Resolution: 1.05 Å
  • R-Value Free: 0.121 
  • R-Value Work: 0.106 
  • R-Value Observed: 0.106 
  • Space Group: P 21 3
Unit Cell:
Length ( Å )Angle ( ˚ )
a = 132.3α = 90
b = 132.3β = 90
c = 132.3γ = 90
Software Package:
Software NamePurpose
REFMACrefinement
DENZOdata reduction
SCALEPACKdata scaling
MOLREPphasing

Structure Validation

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Entry History 

Deposition Data

Revision History  (Full details and data files)

  • Version 1.0: 2007-09-25
    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: Advisory, Data collection