Atomistry » Iron » PDB 6rr4-6soq » 6son
Atomistry »
  Iron »
    PDB 6rr4-6soq »
      6son »

Iron in PDB 6son: 2 Minute FE2+ Soak Structure of Synftn Variant D137A

Enzymatic activity of 2 Minute FE2+ Soak Structure of Synftn Variant D137A

All present enzymatic activity of 2 Minute FE2+ Soak Structure of Synftn Variant D137A:
1.16.3.2;

Protein crystallography data

The structure of 2 Minute FE2+ Soak Structure of Synftn Variant D137A, PDB code: 6son was solved by A.M.Hemmings, J.M.Bradley, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 51.07 / 1.60
Space group F 4 3 2
Cell size a, b, c (Å), α, β, γ (°) 176.900, 176.900, 176.900, 90.00, 90.00, 90.00
R / Rfree (%) 15.8 / 18.9

Other elements in 6son:

The structure of 2 Minute FE2+ Soak Structure of Synftn Variant D137A also contains other interesting chemical elements:

Chlorine (Cl) 1 atom

Iron Binding Sites:

The binding sites of Iron atom in the 2 Minute FE2+ Soak Structure of Synftn Variant D137A (pdb code 6son). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total 2 binding sites of Iron where determined in the 2 Minute FE2+ Soak Structure of Synftn Variant D137A, PDB code: 6son:
Jump to Iron binding site number: 1; 2;

Iron binding site 1 out of 2 in 6son

Go back to Iron Binding Sites List in 6son
Iron binding site 1 out of 2 in the 2 Minute FE2+ Soak Structure of Synftn Variant D137A


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of 2 Minute FE2+ Soak Structure of Synftn Variant D137A within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe201

b:48.2
occ:0.50
OE1 A:GLU33 2.0 34.1 0.6
O A:HOH364 2.1 75.3 1.0
OE1 A:GLU66 2.1 43.9 1.0
OE2 A:GLU66 2.4 47.0 1.0
CD A:GLU66 2.6 43.7 1.0
ND1 A:HIS69 2.7 39.6 1.0
CD A:GLU33 3.0 34.1 0.6
OE2 A:GLU33 3.3 34.8 0.6
OE2 A:GLU33 3.4 39.3 0.4
CD A:GLU33 3.5 38.2 0.4
FE A:FE202 3.5 70.7 0.4
CG A:HIS69 3.6 35.6 1.0
CG A:GLU33 3.6 35.6 0.4
CB A:HIS69 3.7 32.0 1.0
CE1 A:HIS69 3.7 40.9 1.0
CG2 A:THR113 3.8 35.7 1.0
O A:HOH304 4.0 50.9 1.0
OE1 A:GLN143 4.0 35.8 1.0
CG A:GLU66 4.0 39.3 1.0
O A:HOH334 4.2 40.9 1.0
OE1 A:GLU33 4.2 39.3 0.4
O A:HOH345 4.3 34.0 1.0
CG A:GLU33 4.3 32.2 0.6
CB A:GLU33 4.4 33.9 0.4
CA A:GLU66 4.5 29.6 1.0
CB A:GLU66 4.6 33.7 1.0
CB A:GLU33 4.6 31.1 0.6
OE2 A:GLU110 4.7 40.8 1.0
O A:HOH428 4.8 41.2 1.0
CD A:GLN143 4.8 33.3 1.0
O A:GLU66 4.8 28.4 1.0
CD2 A:HIS69 4.8 37.5 1.0
NE2 A:HIS69 4.8 39.2 1.0
CB A:THR113 4.9 35.0 1.0
OG1 A:THR113 5.0 36.4 1.0

Iron binding site 2 out of 2 in 6son

Go back to Iron Binding Sites List in 6son
Iron binding site 2 out of 2 in the 2 Minute FE2+ Soak Structure of Synftn Variant D137A


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 2 of 2 Minute FE2+ Soak Structure of Synftn Variant D137A within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe202

b:70.7
occ:0.36
OE2 A:GLU110 2.0 40.8 1.0
O A:HOH334 2.1 40.9 1.0
O A:HOH304 2.3 50.9 1.0
OE2 A:GLU66 2.3 47.0 1.0
OE1 A:GLU110 2.5 44.4 1.0
CD A:GLU110 2.5 40.9 1.0
CD A:GLU66 3.0 43.7 1.0
OE1 A:GLU66 3.5 43.9 1.0
FE A:FE201 3.5 48.2 0.5
OH A:TYR40 3.7 41.4 1.0
CG A:GLU66 3.9 39.3 1.0
CG A:GLU110 4.0 39.6 1.0
CE2 A:TYR40 4.1 34.1 1.0
OE1 A:GLN143 4.1 35.8 1.0
NE2 A:GLN143 4.2 33.4 1.0
OG1 A:THR113 4.3 36.4 1.0
CZ A:TYR40 4.4 38.1 1.0
CA A:GLU110 4.5 32.4 1.0
CG2 A:THR113 4.5 35.7 1.0
CB A:GLU110 4.5 35.0 1.0
CB A:THR113 4.5 35.0 1.0
CD A:GLN143 4.6 33.3 1.0
O A:HOH364 4.6 75.3 1.0
O A:HOH466 5.0 64.4 1.0

Reference:

J.M.Bradley, J.Pullin, G.R.Moore, D.A.Svistunenko, A.M.Hemmings, N.E.Le Brun. Routes of Iron Entry Into, and Exit From, the Catalytic Ferroxidase Sites of the Prokaryotic Ferritin Synftn. Dalton Trans 2020.
ISSN: ESSN 1477-9234
PubMed: 31930254
DOI: 10.1039/C9DT03570B
Page generated: Wed Aug 7 09:57:14 2024

Last articles

Zn in 9JYW
Zn in 9IR4
Zn in 9IR3
Zn in 9GMX
Zn in 9GMW
Zn in 9JEJ
Zn in 9ERF
Zn in 9ERE
Zn in 9EGV
Zn in 9EGW
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy