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Iron in PDB 4enp: Structure of E530A Variant E. Coli Kate

Enzymatic activity of Structure of E530A Variant E. Coli Kate

All present enzymatic activity of Structure of E530A Variant E. Coli Kate:
1.11.1.6;

Protein crystallography data

The structure of Structure of E530A Variant E. Coli Kate, PDB code: 4enp was solved by P.C.Loewen, V.Jha, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 35.24 / 1.50
Space group P 1 21 1
Cell size a, b, c (Å), α, β, γ (°) 93.330, 133.110, 122.740, 90.00, 109.41, 90.00
R / Rfree (%) 13.8 / 16.2

Iron Binding Sites:

The binding sites of Iron atom in the Structure of E530A Variant E. Coli Kate (pdb code 4enp). This binding sites where shown within 5.0 Angstroms radius around Iron atom.
In total 4 binding sites of Iron where determined in the Structure of E530A Variant E. Coli Kate, PDB code: 4enp:
Jump to Iron binding site number: 1; 2; 3; 4;

Iron binding site 1 out of 4 in 4enp

Go back to Iron Binding Sites List in 4enp
Iron binding site 1 out of 4 in the Structure of E530A Variant E. Coli Kate


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 1 of Structure of E530A Variant E. Coli Kate within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Fe801

b:8.2
occ:1.00
FE A:HEM801 0.0 8.2 1.0
OH A:TYR415 2.0 7.6 1.0
NC A:HEM801 2.0 7.3 1.0
NA A:HEM801 2.0 6.8 1.0
ND A:HEM801 2.0 7.4 1.0
NB A:HEM801 2.0 7.0 1.0
CZ A:TYR415 2.9 6.7 1.0
C1B A:HEM801 3.0 7.5 1.0
C4A A:HEM801 3.0 7.5 1.0
C4C A:HEM801 3.0 8.0 1.0
C1D A:HEM801 3.1 7.8 1.0
C4D A:HEM801 3.1 7.2 1.0
C1A A:HEM801 3.1 7.5 1.0
C1C A:HEM801 3.1 7.5 1.0
C4B A:HEM801 3.1 7.5 1.0
CHD A:HEM801 3.4 8.6 1.0
CHA A:HEM801 3.5 7.7 1.0
CHB A:HEM801 3.5 7.7 1.0
CHC A:HEM801 3.5 7.7 1.0
CE1 A:TYR415 3.7 6.4 1.0
CE2 A:TYR415 3.9 7.8 1.0
NE A:ARG411 4.0 6.2 1.0
NH2 A:ARG411 4.1 7.9 1.0
C2B A:HEM801 4.3 8.3 1.0
C2D A:HEM801 4.3 8.9 1.0
C3B A:HEM801 4.3 8.1 1.0
C3A A:HEM801 4.3 7.0 1.0
C2A A:HEM801 4.3 7.6 1.0
C3D A:HEM801 4.3 8.0 1.0
C3C A:HEM801 4.3 8.1 1.0
C2C A:HEM801 4.3 7.9 1.0
CZ A:ARG411 4.5 7.4 1.0
O A:HOH1174 4.6 16.4 1.0
CG2 A:VAL127 4.7 8.7 1.0
CZ A:PHE214 4.7 9.0 1.0
NE2 A:HIS128 4.8 9.5 1.0
CD2 A:HIS128 4.8 8.6 1.0
CD1 A:TYR415 4.9 7.4 1.0

Iron binding site 2 out of 4 in 4enp

Go back to Iron Binding Sites List in 4enp
Iron binding site 2 out of 4 in the Structure of E530A Variant E. Coli Kate


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 2 of Structure of E530A Variant E. Coli Kate within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Fe801

b:8.9
occ:1.00
FE B:HEM801 0.0 8.9 1.0
OH B:TYR415 2.0 9.1 1.0
NA B:HEM801 2.0 8.7 1.0
ND B:HEM801 2.0 8.2 1.0
NC B:HEM801 2.0 8.9 1.0
NB B:HEM801 2.1 8.9 1.0
CZ B:TYR415 2.9 7.6 1.0
C4C B:HEM801 3.0 9.3 1.0
C4A B:HEM801 3.0 7.8 1.0
C4D B:HEM801 3.1 8.3 1.0
C1D B:HEM801 3.1 9.2 1.0
C1B B:HEM801 3.1 9.0 1.0
C4B B:HEM801 3.1 9.1 1.0
C1A B:HEM801 3.1 7.8 1.0
C1C B:HEM801 3.1 9.2 1.0
CHB B:HEM801 3.4 8.4 1.0
CHD B:HEM801 3.4 9.8 1.0
CHC B:HEM801 3.5 10.0 1.0
CHA B:HEM801 3.5 7.8 1.0
CE1 B:TYR415 3.6 8.8 1.0
CE2 B:TYR415 3.9 8.3 1.0
NE B:ARG411 4.1 8.4 1.0
NH2 B:ARG411 4.2 8.6 1.0
C2D B:HEM801 4.3 9.8 1.0
C3B B:HEM801 4.3 8.8 1.0
C3C B:HEM801 4.3 10.0 1.0
C3D B:HEM801 4.3 9.8 1.0
C3A B:HEM801 4.3 8.0 1.0
C2A B:HEM801 4.3 7.7 1.0
C2B B:HEM801 4.3 9.4 1.0
C2C B:HEM801 4.4 10.0 1.0
O B:HOH1218 4.5 19.8 1.0
CZ B:ARG411 4.5 8.6 1.0
CG2 B:VAL127 4.7 9.6 1.0
CZ B:PHE214 4.7 10.0 1.0
NE2 B:HIS128 4.8 10.1 1.0
CD2 B:HIS128 4.8 9.2 1.0
CD1 B:TYR415 4.9 8.4 1.0

Iron binding site 3 out of 4 in 4enp

Go back to Iron Binding Sites List in 4enp
Iron binding site 3 out of 4 in the Structure of E530A Variant E. Coli Kate


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 3 of Structure of E530A Variant E. Coli Kate within 5.0Å range:
probe atom residue distance (Å) B Occ
C:Fe801

b:8.9
occ:1.00
FE C:HEM801 0.0 8.9 1.0
NC C:HEM801 2.0 7.7 1.0
NA C:HEM801 2.0 7.5 1.0
ND C:HEM801 2.0 8.5 1.0
OH C:TYR415 2.0 8.4 1.0
NB C:HEM801 2.1 7.9 1.0
CZ C:TYR415 3.0 7.8 1.0
C4C C:HEM801 3.0 8.0 1.0
C1D C:HEM801 3.0 9.0 1.0
C4A C:HEM801 3.0 7.3 1.0
C4D C:HEM801 3.0 8.1 1.0
C1B C:HEM801 3.0 8.4 1.0
C4B C:HEM801 3.1 9.0 1.0
C1A C:HEM801 3.1 7.6 1.0
C1C C:HEM801 3.1 9.3 1.0
CHD C:HEM801 3.4 8.8 1.0
CHB C:HEM801 3.4 8.4 1.0
CHA C:HEM801 3.5 7.7 1.0
CHC C:HEM801 3.5 9.6 1.0
CE1 C:TYR415 3.6 8.0 1.0
CE2 C:TYR415 3.9 9.4 1.0
NE C:ARG411 4.0 7.4 1.0
NH2 C:ARG411 4.2 7.5 1.0
C3B C:HEM801 4.3 8.8 1.0
C3C C:HEM801 4.3 8.9 1.0
C3D C:HEM801 4.3 9.1 1.0
C2D C:HEM801 4.3 9.9 1.0
C2C C:HEM801 4.3 8.8 1.0
C2B C:HEM801 4.3 10.0 1.0
C2A C:HEM801 4.3 7.3 1.0
C3A C:HEM801 4.3 7.6 1.0
CZ C:ARG411 4.5 8.6 1.0
O C:HOH1707 4.5 17.6 1.0
CG2 C:VAL127 4.7 11.0 1.0
CZ C:PHE214 4.7 10.2 1.0
NE2 C:HIS128 4.8 9.8 1.0
CD2 C:HIS128 4.8 7.9 1.0
CD1 C:TYR415 4.9 8.3 1.0

Iron binding site 4 out of 4 in 4enp

Go back to Iron Binding Sites List in 4enp
Iron binding site 4 out of 4 in the Structure of E530A Variant E. Coli Kate


Mono view


Stereo pair view

A full contact list of Iron with other atoms in the Fe binding site number 4 of Structure of E530A Variant E. Coli Kate within 5.0Å range:
probe atom residue distance (Å) B Occ
D:Fe801

b:8.3
occ:1.00
FE D:HEM801 0.0 8.3 1.0
OH D:TYR415 2.0 7.8 1.0
NC D:HEM801 2.0 7.7 1.0
ND D:HEM801 2.0 7.9 1.0
NA D:HEM801 2.1 7.7 1.0
NB D:HEM801 2.1 8.2 1.0
CZ D:TYR415 2.9 6.8 1.0
C4C D:HEM801 3.0 8.6 1.0
C4A D:HEM801 3.1 8.0 1.0
C1B D:HEM801 3.1 7.7 1.0
C1D D:HEM801 3.1 8.6 1.0
C4D D:HEM801 3.1 7.9 1.0
C1C D:HEM801 3.1 7.7 1.0
C4B D:HEM801 3.1 8.0 1.0
C1A D:HEM801 3.1 7.2 1.0
CHD D:HEM801 3.4 8.4 1.0
CHB D:HEM801 3.5 7.9 1.0
CHC D:HEM801 3.5 8.3 1.0
CHA D:HEM801 3.5 7.5 1.0
CE1 D:TYR415 3.6 7.5 1.0
CE2 D:TYR415 3.8 7.5 1.0
NE D:ARG411 4.0 7.5 1.0
NH2 D:ARG411 4.1 8.2 1.0
C3B D:HEM801 4.3 9.0 1.0
C3C D:HEM801 4.3 8.6 1.0
C3A D:HEM801 4.3 7.4 1.0
C2D D:HEM801 4.3 8.6 1.0
C2A D:HEM801 4.3 7.3 1.0
C2B D:HEM801 4.3 7.8 1.0
C3D D:HEM801 4.3 9.5 1.0
C2C D:HEM801 4.3 8.3 1.0
CZ D:ARG411 4.5 7.8 1.0
O D:HOH1047 4.6 16.2 1.0
CG2 D:VAL127 4.7 8.9 1.0
CZ D:PHE214 4.7 9.2 1.0
NE2 D:HIS128 4.8 9.7 1.0
CD2 D:HIS128 4.9 8.2 1.0
CD1 D:TYR415 4.9 8.7 1.0

Reference:

V.Jha, P.Chelikani, X.Carpena, I.Fita, P.C.Loewen. Influence of Main Channel Structure on H(2)O(2) Access to the Heme Cavity of Catalase Kate of Escherichia Coli. Arch.Biochem.Biophys. V. 526 54 2012.
ISSN: ISSN 0003-9861
PubMed: 22820098
DOI: 10.1016/J.ABB.2012.06.010
Page generated: Sun Dec 13 15:33:06 2020

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