Atomistry » Iron » PDB 3qjt-3r0g » 3qzz
Atomistry »
  Iron »
    PDB 3qjt-3r0g »
      3qzz »

Iron in PDB 3qzz: 3D Structure of Ferric Methanosarcina Acetivorans Protoglobin Y61W Mutant in Aquomet Form

Protein crystallography data

The structure of 3D Structure of Ferric Methanosarcina Acetivorans Protoglobin Y61W Mutant in Aquomet Form, PDB code: 3qzz was solved by A.Pesce, L.Tilleman, S.Dewilde, P.Ascenzi, M.Coletta, C.Ciaccio, S.Bruno, L.Moens, M.Bolognesi, M.Nardini, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 39.89 / 2.40
Space group C 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 81.296, 48.730, 50.925, 90.00, 101.10, 90.00
R / Rfree (%) 23.8 / 30.6

Iron Binding Sites:

The binding sites of Iron atom in the 3D Structure of Ferric Methanosarcina Acetivorans Protoglobin Y61W Mutant in Aquomet Form (pdb code 3qzz). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total only one binding site of Iron was determined in the 3D Structure of Ferric Methanosarcina Acetivorans Protoglobin Y61W Mutant in Aquomet Form, PDB code: 3qzz:

Iron binding site 1 out of 1 in 3qzz

Go back to Iron Binding Sites List in 3qzz
Iron binding site 1 out of 1 in the 3D Structure of Ferric Methanosarcina Acetivorans Protoglobin Y61W Mutant in Aquomet Form


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of 3D Structure of Ferric Methanosarcina Acetivorans Protoglobin Y61W Mutant in Aquomet Form within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe200

b:16.9
occ:1.00
FE A:HEM200 0.0 16.9 1.0
ND A:HEM200 2.0 17.1 1.0
NA A:HEM200 2.0 10.9 1.0
NB A:HEM200 2.0 7.0 1.0
NC A:HEM200 2.1 6.9 1.0
NE2 A:HIS120 2.3 8.0 1.0
O A:HOH196 2.6 15.5 1.0
C4D A:HEM200 2.9 25.4 1.0
C1A A:HEM200 2.9 11.4 1.0
C4B A:HEM200 3.0 16.4 1.0
C1C A:HEM200 3.0 2.8 1.0
C1D A:HEM200 3.1 21.8 1.0
C4A A:HEM200 3.1 12.0 1.0
C4C A:HEM200 3.1 14.5 1.0
C1B A:HEM200 3.1 15.4 1.0
CE1 A:HIS120 3.2 22.3 1.0
CHA A:HEM200 3.2 20.1 1.0
CD2 A:HIS120 3.3 19.4 1.0
CHC A:HEM200 3.3 8.4 1.0
CHD A:HEM200 3.5 19.4 1.0
CHB A:HEM200 3.5 14.4 1.0
C3D A:HEM200 4.1 26.2 1.0
C2A A:HEM200 4.2 20.5 1.0
C2D A:HEM200 4.2 24.7 1.0
C2C A:HEM200 4.3 10.8 1.0
C3B A:HEM200 4.3 14.8 1.0
C3A A:HEM200 4.3 20.4 1.0
C2B A:HEM200 4.3 16.1 1.0
C3C A:HEM200 4.3 13.6 1.0
ND1 A:HIS120 4.4 24.5 1.0
CG A:HIS120 4.4 26.1 1.0

Reference:

A.Pesce, L.Tilleman, S.Dewilde, P.Ascenzi, M.Coletta, C.Ciaccio, S.Bruno, L.Moens, M.Bolognesi, M.Nardini. Structural Heterogeneity and Ligand Gating in Ferric Methanosarcina Acetivorans Protoglobin Mutants. Iubmb Life V. 63 287 2011.
ISSN: ISSN 1521-6543
PubMed: 21618401
DOI: 10.1002/IUB.484
Page generated: Sun Aug 4 19:00:12 2024

Last articles

Zn in 9JPJ
Zn in 9JP7
Zn in 9JPK
Zn in 9JPL
Zn in 9GN6
Zn in 9GN7
Zn in 9GKU
Zn in 9GKW
Zn in 9GKX
Zn in 9GL0
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy