Iron in PDB 6e0z: A131Q Mutant of Cyt P460 of Nitrosomonas Sp. AL212
Protein crystallography data
The structure of A131Q Mutant of Cyt P460 of Nitrosomonas Sp. AL212, PDB code: 6e0z
was solved by
M.Smith,
K.Lancaster,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
67.09 /
2.30
|
Space group
|
P 1 21 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
48.031,
80.941,
120.598,
90.00,
96.03,
90.00
|
R / Rfree (%)
|
24.2 /
29.9
|
Iron Binding Sites:
The binding sites of Iron atom in the A131Q Mutant of Cyt P460 of Nitrosomonas Sp. AL212
(pdb code 6e0z). This binding sites where shown within
5.0 Angstroms radius around Iron atom.
In total 4 binding sites of Iron where determined in the
A131Q Mutant of Cyt P460 of Nitrosomonas Sp. AL212, PDB code: 6e0z:
Jump to Iron binding site number:
1;
2;
3;
4;
Iron binding site 1 out
of 4 in 6e0z
Go back to
Iron Binding Sites List in 6e0z
Iron binding site 1 out
of 4 in the A131Q Mutant of Cyt P460 of Nitrosomonas Sp. AL212
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 1 of A131Q Mutant of Cyt P460 of Nitrosomonas Sp. AL212 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe201
b:36.5
occ:1.00
|
FE
|
A:HEC201
|
0.0
|
36.5
|
1.0
|
NB
|
A:HEC201
|
2.0
|
36.1
|
1.0
|
ND
|
A:HEC201
|
2.1
|
38.3
|
1.0
|
NC
|
A:HEC201
|
2.1
|
54.8
|
1.0
|
NA
|
A:HEC201
|
2.2
|
59.9
|
1.0
|
NE2
|
A:HIS172
|
2.5
|
41.5
|
1.0
|
C1D
|
A:HEC201
|
3.0
|
31.0
|
1.0
|
C4C
|
A:HEC201
|
3.0
|
35.1
|
1.0
|
C1B
|
A:HEC201
|
3.0
|
36.6
|
1.0
|
C4A
|
A:HEC201
|
3.1
|
35.4
|
1.0
|
C4B
|
A:HEC201
|
3.1
|
40.7
|
1.0
|
C1C
|
A:HEC201
|
3.1
|
36.6
|
1.0
|
C4D
|
A:HEC201
|
3.1
|
41.1
|
1.0
|
C1A
|
A:HEC201
|
3.2
|
37.5
|
1.0
|
CHD
|
A:HEC201
|
3.3
|
29.4
|
1.0
|
CHB
|
A:HEC201
|
3.4
|
48.3
|
1.0
|
CD2
|
A:HIS172
|
3.4
|
34.6
|
1.0
|
CE1
|
A:HIS172
|
3.4
|
36.3
|
1.0
|
CHC
|
A:HEC201
|
3.5
|
47.4
|
1.0
|
CHA
|
A:HEC201
|
3.5
|
52.2
|
1.0
|
O
|
A:HOH343
|
4.1
|
36.3
|
1.0
|
C3A
|
A:HEC201
|
4.2
|
26.9
|
1.0
|
C2D
|
A:HEC201
|
4.3
|
35.6
|
1.0
|
C3C
|
A:HEC201
|
4.3
|
43.0
|
1.0
|
C2B
|
A:HEC201
|
4.3
|
49.4
|
1.0
|
C2C
|
A:HEC201
|
4.3
|
42.0
|
1.0
|
C2A
|
A:HEC201
|
4.3
|
31.7
|
1.0
|
C3B
|
A:HEC201
|
4.3
|
43.3
|
1.0
|
C3D
|
A:HEC201
|
4.3
|
32.3
|
1.0
|
ND1
|
A:HIS172
|
4.5
|
49.0
|
1.0
|
CG
|
A:HIS172
|
4.6
|
45.0
|
1.0
|
NZ
|
A:LYS106
|
4.6
|
54.7
|
1.0
|
NE2
|
A:GLN131
|
4.8
|
57.7
|
1.0
|
|
Iron binding site 2 out
of 4 in 6e0z
Go back to
Iron Binding Sites List in 6e0z
Iron binding site 2 out
of 4 in the A131Q Mutant of Cyt P460 of Nitrosomonas Sp. AL212
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 2 of A131Q Mutant of Cyt P460 of Nitrosomonas Sp. AL212 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe201
b:46.3
occ:1.00
|
FE
|
B:HEC201
|
0.0
|
46.3
|
1.0
|
NA
|
B:HEC201
|
2.0
|
49.3
|
1.0
|
ND
|
B:HEC201
|
2.0
|
55.8
|
1.0
|
NC
|
B:HEC201
|
2.1
|
50.4
|
1.0
|
NB
|
B:HEC201
|
2.2
|
39.4
|
1.0
|
NE2
|
B:HIS172
|
2.5
|
30.9
|
1.0
|
C1A
|
B:HEC201
|
3.0
|
42.4
|
1.0
|
C4A
|
B:HEC201
|
3.0
|
55.7
|
1.0
|
C4D
|
B:HEC201
|
3.0
|
45.0
|
1.0
|
C1D
|
B:HEC201
|
3.0
|
48.6
|
1.0
|
C4C
|
B:HEC201
|
3.1
|
51.6
|
1.0
|
C1B
|
B:HEC201
|
3.1
|
40.4
|
1.0
|
C1C
|
B:HEC201
|
3.2
|
49.5
|
1.0
|
C4B
|
B:HEC201
|
3.2
|
43.0
|
1.0
|
CHA
|
B:HEC201
|
3.3
|
42.5
|
1.0
|
CHD
|
B:HEC201
|
3.4
|
53.0
|
1.0
|
CHB
|
B:HEC201
|
3.4
|
44.0
|
1.0
|
CD2
|
B:HIS172
|
3.5
|
31.2
|
1.0
|
CE1
|
B:HIS172
|
3.5
|
37.0
|
1.0
|
CHC
|
B:HEC201
|
3.6
|
48.1
|
1.0
|
O
|
B:HOH332
|
3.7
|
54.0
|
1.0
|
C2A
|
B:HEC201
|
4.2
|
35.0
|
1.0
|
C3A
|
B:HEC201
|
4.2
|
45.2
|
1.0
|
C3D
|
B:HEC201
|
4.3
|
47.1
|
1.0
|
C2D
|
B:HEC201
|
4.3
|
47.0
|
1.0
|
C2B
|
B:HEC201
|
4.4
|
47.4
|
1.0
|
C3C
|
B:HEC201
|
4.4
|
51.1
|
1.0
|
C2C
|
B:HEC201
|
4.4
|
44.8
|
1.0
|
C3B
|
B:HEC201
|
4.4
|
51.0
|
1.0
|
NZ
|
B:LYS106
|
4.5
|
40.3
|
1.0
|
OE1
|
B:GLN131
|
4.6
|
53.6
|
1.0
|
ND1
|
B:HIS172
|
4.6
|
31.3
|
1.0
|
CG
|
B:HIS172
|
4.6
|
35.9
|
1.0
|
CE2
|
B:PHE182
|
5.0
|
37.8
|
1.0
|
|
Iron binding site 3 out
of 4 in 6e0z
Go back to
Iron Binding Sites List in 6e0z
Iron binding site 3 out
of 4 in the A131Q Mutant of Cyt P460 of Nitrosomonas Sp. AL212
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 3 of A131Q Mutant of Cyt P460 of Nitrosomonas Sp. AL212 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Fe201
b:54.6
occ:1.00
|
FE
|
C:HEC201
|
0.0
|
54.6
|
1.0
|
NC
|
C:HEC201
|
2.0
|
47.4
|
1.0
|
ND
|
C:HEC201
|
2.0
|
47.0
|
1.0
|
NB
|
C:HEC201
|
2.1
|
45.3
|
1.0
|
NA
|
C:HEC201
|
2.2
|
46.1
|
1.0
|
CE1
|
C:HIS172
|
2.8
|
49.0
|
1.0
|
C1C
|
C:HEC201
|
3.0
|
40.7
|
1.0
|
C4D
|
C:HEC201
|
3.0
|
51.2
|
1.0
|
C4C
|
C:HEC201
|
3.0
|
43.8
|
1.0
|
C1D
|
C:HEC201
|
3.0
|
49.9
|
1.0
|
NE2
|
C:HIS172
|
3.0
|
43.2
|
1.0
|
C4B
|
C:HEC201
|
3.1
|
55.7
|
1.0
|
C1A
|
C:HEC201
|
3.1
|
46.7
|
1.0
|
C1B
|
C:HEC201
|
3.1
|
51.9
|
1.0
|
C4A
|
C:HEC201
|
3.2
|
39.6
|
1.0
|
CHA
|
C:HEC201
|
3.4
|
49.5
|
1.0
|
CHD
|
C:HEC201
|
3.4
|
43.1
|
1.0
|
CHC
|
C:HEC201
|
3.4
|
48.8
|
1.0
|
CHB
|
C:HEC201
|
3.6
|
54.3
|
1.0
|
CE2
|
C:PHE76
|
3.9
|
76.6
|
1.0
|
ND1
|
C:HIS172
|
4.0
|
52.7
|
1.0
|
NZ
|
C:LYS106
|
4.1
|
41.9
|
1.0
|
C2C
|
C:HEC201
|
4.2
|
45.3
|
1.0
|
C3C
|
C:HEC201
|
4.3
|
39.7
|
1.0
|
C2D
|
C:HEC201
|
4.3
|
47.1
|
1.0
|
C3D
|
C:HEC201
|
4.3
|
43.5
|
1.0
|
C2A
|
C:HEC201
|
4.3
|
45.8
|
1.0
|
C3B
|
C:HEC201
|
4.3
|
51.0
|
1.0
|
C3A
|
C:HEC201
|
4.3
|
45.1
|
1.0
|
C2B
|
C:HEC201
|
4.3
|
47.5
|
1.0
|
CD2
|
C:HIS172
|
4.4
|
52.9
|
1.0
|
OE1
|
C:GLN131
|
4.5
|
44.6
|
1.0
|
CZ
|
C:PHE76
|
4.6
|
60.4
|
1.0
|
CD2
|
C:PHE76
|
4.6
|
74.9
|
1.0
|
CG
|
C:HIS172
|
4.8
|
53.6
|
1.0
|
|
Iron binding site 4 out
of 4 in 6e0z
Go back to
Iron Binding Sites List in 6e0z
Iron binding site 4 out
of 4 in the A131Q Mutant of Cyt P460 of Nitrosomonas Sp. AL212
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 4 of A131Q Mutant of Cyt P460 of Nitrosomonas Sp. AL212 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Fe201
b:50.4
occ:1.00
|
FE
|
D:HEC201
|
0.0
|
50.4
|
1.0
|
NC
|
D:HEC201
|
2.1
|
61.7
|
1.0
|
NB
|
D:HEC201
|
2.1
|
58.2
|
1.0
|
NA
|
D:HEC201
|
2.1
|
59.4
|
1.0
|
ND
|
D:HEC201
|
2.1
|
47.9
|
1.0
|
NE2
|
D:HIS172
|
2.4
|
39.5
|
1.0
|
C4A
|
D:HEC201
|
3.0
|
48.6
|
1.0
|
C1A
|
D:HEC201
|
3.0
|
57.3
|
1.0
|
C4C
|
D:HEC201
|
3.1
|
65.3
|
1.0
|
C1B
|
D:HEC201
|
3.1
|
56.9
|
1.0
|
C1C
|
D:HEC201
|
3.1
|
55.0
|
1.0
|
C1D
|
D:HEC201
|
3.1
|
53.6
|
1.0
|
C4D
|
D:HEC201
|
3.1
|
45.6
|
1.0
|
C4B
|
D:HEC201
|
3.2
|
53.3
|
1.0
|
CE1
|
D:HIS172
|
3.3
|
45.6
|
1.0
|
CD2
|
D:HIS172
|
3.4
|
42.6
|
1.0
|
CHB
|
D:HEC201
|
3.4
|
51.0
|
1.0
|
CHA
|
D:HEC201
|
3.4
|
45.0
|
1.0
|
CHD
|
D:HEC201
|
3.4
|
63.4
|
1.0
|
CHC
|
D:HEC201
|
3.5
|
47.4
|
1.0
|
C3A
|
D:HEC201
|
4.1
|
41.1
|
1.0
|
C2A
|
D:HEC201
|
4.1
|
37.2
|
1.0
|
C2C
|
D:HEC201
|
4.3
|
51.6
|
1.0
|
C3C
|
D:HEC201
|
4.3
|
64.1
|
1.0
|
C2B
|
D:HEC201
|
4.3
|
64.0
|
1.0
|
C2D
|
D:HEC201
|
4.4
|
57.0
|
1.0
|
C3D
|
D:HEC201
|
4.4
|
40.7
|
1.0
|
C3B
|
D:HEC201
|
4.4
|
60.8
|
1.0
|
ND1
|
D:HIS172
|
4.4
|
45.1
|
1.0
|
CG
|
D:HIS172
|
4.5
|
46.8
|
1.0
|
NZ
|
D:LYS106
|
4.6
|
47.7
|
1.0
|
OE1
|
D:GLN131
|
4.8
|
53.9
|
1.0
|
CE2
|
D:PHE182
|
5.0
|
63.4
|
1.0
|
|
Reference:
M.A.Smith,
S.H.Majer,
A.C.Vilbert,
K.M.Lancaster.
Controlling A Burn: Outer-Sphere Gating of Hydroxylamine Oxidation By A Distal Base in Cytochrome P460. Chem Sci V. 10 3756 2019.
ISSN: ISSN 2041-6520
PubMed: 31015919
DOI: 10.1039/C9SC00195F
Page generated: Tue Aug 6 17:12:17 2024
|