1FRV

CRYSTAL STRUCTURE OF THE OXIDIZED FORM OF NI-FE HYDROGENASE


Experimental Data Snapshot

  • Method: X-RAY DIFFRACTION
  • Resolution: 2.85 Å

wwPDB Validation   3D Report Full Report


This is version 1.2 of the entry. See complete history


Literature

Crystal structure of the nickel-iron hydrogenase from Desulfovibrio gigas.

Volbeda, A.Charon, M.H.Piras, C.Hatchikian, E.C.Frey, M.Fontecilla-Camps, J.C.

(1995) Nature 373: 580-587

  • DOI: https://doi.org/10.1038/373580a0
  • Primary Citation of Related Structures:  
    1FRV

  • PubMed Abstract: 

    The X-ray structure of the heterodimeric Ni-Fe hydrogenase from Desulfovibrio gigas, the enzyme responsible for the metabolism of molecular hydrogen, has been solved at 2.85 A resolution. The active site, which appears to contain, besides nickel, a second metal ion, is buried in the 60K subunit. The 28K subunit, which coordinates one [3Fe-4S] and two [4Fe-4S] clusters, contains an amino-terminal domain with similarities to the redox protein flavodoxin. The structure suggests plausible electron and proton transfer pathways.


  • Organizational Affiliation

    Laboratoire de Cristallographie et de Cristallogénèse des Protéines, Institut de Biologie Structurale J. P. Ebel (CEA, CNRS), Grenoble, France.


Macromolecules
Find similar proteins by:  (by identity cutoff)  |  3D Structure
Entity ID: 1
MoleculeChains Sequence LengthOrganismDetailsImage
HYDROGENASE
A, C
264Megalodesulfovibrio gigasMutation(s): 0 
EC: 1.12.2.1
UniProt
Find proteins for P12943 (Megalodesulfovibrio gigas)
Explore P12943 
Go to UniProtKB:  P12943
Entity Groups  
Sequence Clusters30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity
UniProt GroupP12943
Sequence Annotations
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  • Reference Sequence
Find similar proteins by:  (by identity cutoff)  |  3D Structure
Entity ID: 2
MoleculeChains Sequence LengthOrganismDetailsImage
HYDROGENASE
B, D
536Megalodesulfovibrio gigasMutation(s): 0 
EC: 1.12.2.1
UniProt
Find proteins for P12944 (Megalodesulfovibrio gigas)
Explore P12944 
Go to UniProtKB:  P12944
Entity Groups  
Sequence Clusters30% Identity50% Identity70% Identity90% Identity95% Identity100% Identity
UniProt GroupP12944
Sequence Annotations
Expand
  • Reference Sequence
Small Molecules
Ligands 4 Unique
IDChains Name / Formula / InChI Key2D Diagram3D Interactions
SF4
Query on SF4

Download Ideal Coordinates CCD File 
E [auth A],
G [auth A],
J [auth C],
L [auth C]
IRON/SULFUR CLUSTER
Fe4 S4
LJBDFODJNLIPKO-UHFFFAOYSA-N
F3S
Query on F3S

Download Ideal Coordinates CCD File 
F [auth A],
K [auth C]
FE3-S4 CLUSTER
Fe3 S4
FCXHZBQOKRZXKS-UHFFFAOYSA-N
FEL
Query on FEL

Download Ideal Coordinates CCD File 
I [auth B],
N [auth D]
HYDRATED FE
Fe H6 O3
MSNWSDPPULHLDL-UHFFFAOYSA-N
NI
Query on NI

Download Ideal Coordinates CCD File 
H [auth B],
M [auth D]
NICKEL (II) ION
Ni
VEQPNABPJHWNSG-UHFFFAOYSA-N
Experimental Data & Validation

Experimental Data

  • Method: X-RAY DIFFRACTION
  • Resolution: 2.85 Å
  • Space Group: P 1
Unit Cell:
Length ( Å )Angle ( ˚ )
a = 63.6α = 89.8
b = 93.9β = 102.9
c = 69.2γ = 90.8
Software Package:
Software NamePurpose
MOSFLMdata reduction
SCALKB/KBAPLYdata reduction
X-PLORmodel building
PROLSQrefinement
X-PLORrefinement
BIOMOLdata scaling
X-PLORphasing

Structure Validation

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Entry History 

Deposition Data

Revision History  (Full details and data files)

  • Version 1.0: 1996-11-08
    Type: Initial release
  • Version 1.1: 2008-03-03
    Changes: Version format compliance
  • Version 1.2: 2011-07-13
    Changes: Version format compliance