Iron in PDB 6hqg: Cytochrome P450-153 From Phenylobacterium Zucineum
Protein crystallography data
The structure of Cytochrome P450-153 From Phenylobacterium Zucineum, PDB code: 6hqg
was solved by
F.Fiorentini,
A.Mattevi,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
49.31 /
2.90
|
Space group
|
C 1 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
105.464,
89.207,
201.820,
90.00,
96.60,
90.00
|
R / Rfree (%)
|
21.2 /
27.2
|
Iron Binding Sites:
The binding sites of Iron atom in the Cytochrome P450-153 From Phenylobacterium Zucineum
(pdb code 6hqg). This binding sites where shown within
5.0 Angstroms radius around Iron atom.
In total 4 binding sites of Iron where determined in the
Cytochrome P450-153 From Phenylobacterium Zucineum, PDB code: 6hqg:
Jump to Iron binding site number:
1;
2;
3;
4;
Iron binding site 1 out
of 4 in 6hqg
Go back to
Iron Binding Sites List in 6hqg
Iron binding site 1 out
of 4 in the Cytochrome P450-153 From Phenylobacterium Zucineum
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 1 of Cytochrome P450-153 From Phenylobacterium Zucineum within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe501
b:29.1
occ:1.00
|
FE
|
A:HEM501
|
0.0
|
29.1
|
1.0
|
ND
|
A:HEM501
|
1.9
|
32.7
|
1.0
|
NA
|
A:HEM501
|
2.0
|
32.5
|
1.0
|
NC
|
A:HEM501
|
2.1
|
31.4
|
1.0
|
NB
|
A:HEM501
|
2.1
|
33.1
|
1.0
|
SG
|
A:CYS373
|
2.2
|
25.5
|
1.0
|
C1D
|
A:HEM501
|
2.9
|
33.7
|
1.0
|
C4D
|
A:HEM501
|
2.9
|
33.9
|
1.0
|
C1A
|
A:HEM501
|
3.0
|
33.2
|
1.0
|
C4C
|
A:HEM501
|
3.0
|
34.0
|
1.0
|
C4A
|
A:HEM501
|
3.0
|
32.5
|
1.0
|
C1B
|
A:HEM501
|
3.1
|
32.9
|
1.0
|
C4B
|
A:HEM501
|
3.1
|
31.4
|
1.0
|
C1C
|
A:HEM501
|
3.1
|
29.4
|
1.0
|
CB
|
A:CYS373
|
3.3
|
31.1
|
1.0
|
CHD
|
A:HEM501
|
3.3
|
35.3
|
1.0
|
CHA
|
A:HEM501
|
3.4
|
33.9
|
1.0
|
O
|
A:GLY262
|
3.4
|
34.4
|
1.0
|
CHB
|
A:HEM501
|
3.5
|
32.3
|
1.0
|
CHC
|
A:HEM501
|
3.5
|
31.0
|
1.0
|
CA
|
A:CYS373
|
4.1
|
32.3
|
1.0
|
C2D
|
A:HEM501
|
4.2
|
32.5
|
1.0
|
C3D
|
A:HEM501
|
4.2
|
33.4
|
1.0
|
C2A
|
A:HEM501
|
4.2
|
33.7
|
1.0
|
C3A
|
A:HEM501
|
4.2
|
33.6
|
1.0
|
C3C
|
A:HEM501
|
4.3
|
32.0
|
1.0
|
C2C
|
A:HEM501
|
4.3
|
29.0
|
1.0
|
C2B
|
A:HEM501
|
4.3
|
32.5
|
1.0
|
C
|
A:GLY262
|
4.3
|
32.3
|
1.0
|
C3B
|
A:HEM501
|
4.4
|
31.6
|
1.0
|
CA
|
A:GLY262
|
4.8
|
32.8
|
1.0
|
C
|
A:CYS373
|
4.9
|
33.9
|
1.0
|
|
Iron binding site 2 out
of 4 in 6hqg
Go back to
Iron Binding Sites List in 6hqg
Iron binding site 2 out
of 4 in the Cytochrome P450-153 From Phenylobacterium Zucineum
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 2 of Cytochrome P450-153 From Phenylobacterium Zucineum within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe501
b:30.5
occ:1.00
|
FE
|
B:HEM501
|
0.0
|
30.5
|
1.0
|
ND
|
B:HEM501
|
1.9
|
26.2
|
1.0
|
SG
|
B:CYS373
|
1.9
|
31.1
|
1.0
|
NA
|
B:HEM501
|
2.0
|
27.1
|
1.0
|
NC
|
B:HEM501
|
2.1
|
28.6
|
1.0
|
NB
|
B:HEM501
|
2.1
|
29.6
|
1.0
|
C1D
|
B:HEM501
|
2.8
|
26.1
|
1.0
|
C4D
|
B:HEM501
|
2.9
|
26.2
|
1.0
|
C1A
|
B:HEM501
|
3.0
|
26.4
|
1.0
|
C4A
|
B:HEM501
|
3.0
|
27.1
|
1.0
|
C4C
|
B:HEM501
|
3.0
|
28.1
|
1.0
|
C1B
|
B:HEM501
|
3.1
|
27.9
|
1.0
|
C4B
|
B:HEM501
|
3.1
|
28.7
|
1.0
|
C1C
|
B:HEM501
|
3.2
|
28.0
|
1.0
|
CHD
|
B:HEM501
|
3.3
|
27.1
|
1.0
|
CHA
|
B:HEM501
|
3.3
|
26.4
|
1.0
|
CB
|
B:CYS373
|
3.3
|
26.7
|
1.0
|
CHB
|
B:HEM501
|
3.4
|
28.2
|
1.0
|
O
|
B:GLY262
|
3.6
|
33.8
|
1.0
|
CHC
|
B:HEM501
|
3.6
|
28.6
|
1.0
|
CA
|
B:CYS373
|
4.0
|
27.2
|
1.0
|
C2D
|
B:HEM501
|
4.1
|
27.7
|
1.0
|
C3D
|
B:HEM501
|
4.1
|
28.1
|
1.0
|
C2A
|
B:HEM501
|
4.2
|
24.0
|
1.0
|
C3A
|
B:HEM501
|
4.2
|
24.4
|
1.0
|
C3C
|
B:HEM501
|
4.3
|
27.7
|
1.0
|
C2B
|
B:HEM501
|
4.3
|
26.3
|
1.0
|
C2C
|
B:HEM501
|
4.4
|
27.2
|
1.0
|
C3B
|
B:HEM501
|
4.4
|
27.1
|
1.0
|
C
|
B:GLY262
|
4.4
|
31.9
|
1.0
|
CA
|
B:GLY262
|
4.8
|
29.6
|
1.0
|
C
|
B:CYS373
|
4.9
|
26.0
|
1.0
|
|
Iron binding site 3 out
of 4 in 6hqg
Go back to
Iron Binding Sites List in 6hqg
Iron binding site 3 out
of 4 in the Cytochrome P450-153 From Phenylobacterium Zucineum
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 3 of Cytochrome P450-153 From Phenylobacterium Zucineum within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
C:Fe501
b:34.5
occ:1.00
|
FE
|
C:HEM501
|
0.0
|
34.5
|
1.0
|
ND
|
C:HEM501
|
1.9
|
34.9
|
1.0
|
NA
|
C:HEM501
|
2.0
|
36.0
|
1.0
|
NC
|
C:HEM501
|
2.1
|
34.3
|
1.0
|
NB
|
C:HEM501
|
2.1
|
33.2
|
1.0
|
SG
|
C:CYS373
|
2.4
|
46.0
|
1.0
|
C1D
|
C:HEM501
|
2.9
|
34.5
|
1.0
|
C4D
|
C:HEM501
|
2.9
|
34.3
|
1.0
|
C1A
|
C:HEM501
|
3.0
|
36.9
|
1.0
|
C4C
|
C:HEM501
|
3.0
|
35.5
|
1.0
|
C4A
|
C:HEM501
|
3.0
|
35.2
|
1.0
|
C4B
|
C:HEM501
|
3.1
|
33.2
|
1.0
|
C1B
|
C:HEM501
|
3.1
|
32.5
|
1.0
|
C1C
|
C:HEM501
|
3.1
|
34.9
|
1.0
|
CHD
|
C:HEM501
|
3.3
|
35.3
|
1.0
|
CHA
|
C:HEM501
|
3.4
|
35.2
|
1.0
|
CHB
|
C:HEM501
|
3.4
|
33.1
|
1.0
|
CB
|
C:CYS373
|
3.4
|
43.0
|
1.0
|
CHC
|
C:HEM501
|
3.5
|
35.0
|
1.0
|
O
|
C:GLY262
|
3.7
|
45.4
|
1.0
|
C2D
|
C:HEM501
|
4.2
|
35.0
|
1.0
|
C3D
|
C:HEM501
|
4.2
|
32.7
|
1.0
|
C3A
|
C:HEM501
|
4.2
|
36.9
|
1.0
|
C2A
|
C:HEM501
|
4.2
|
37.2
|
1.0
|
C3C
|
C:HEM501
|
4.2
|
35.8
|
1.0
|
CA
|
C:CYS373
|
4.2
|
41.2
|
1.0
|
C2C
|
C:HEM501
|
4.3
|
34.0
|
1.0
|
C2B
|
C:HEM501
|
4.3
|
32.7
|
1.0
|
C
|
C:GLY262
|
4.3
|
41.7
|
1.0
|
C3B
|
C:HEM501
|
4.3
|
32.4
|
1.0
|
CA
|
C:GLY262
|
4.8
|
43.3
|
1.0
|
|
Iron binding site 4 out
of 4 in 6hqg
Go back to
Iron Binding Sites List in 6hqg
Iron binding site 4 out
of 4 in the Cytochrome P450-153 From Phenylobacterium Zucineum
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 4 of Cytochrome P450-153 From Phenylobacterium Zucineum within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Fe501
b:26.6
occ:1.00
|
FE
|
D:HEM501
|
0.0
|
26.6
|
1.0
|
ND
|
D:HEM501
|
1.9
|
27.2
|
1.0
|
NA
|
D:HEM501
|
2.0
|
27.2
|
1.0
|
NB
|
D:HEM501
|
2.1
|
27.9
|
1.0
|
NC
|
D:HEM501
|
2.1
|
27.7
|
1.0
|
SG
|
D:CYS373
|
2.4
|
30.3
|
1.0
|
C1D
|
D:HEM501
|
2.9
|
26.2
|
1.0
|
C4D
|
D:HEM501
|
2.9
|
26.4
|
1.0
|
C1A
|
D:HEM501
|
3.0
|
26.3
|
1.0
|
C4A
|
D:HEM501
|
3.0
|
28.1
|
1.0
|
C4C
|
D:HEM501
|
3.0
|
27.2
|
1.0
|
C1B
|
D:HEM501
|
3.1
|
28.1
|
1.0
|
C4B
|
D:HEM501
|
3.1
|
26.3
|
1.0
|
C1C
|
D:HEM501
|
3.2
|
25.8
|
1.0
|
CHD
|
D:HEM501
|
3.3
|
26.3
|
1.0
|
CHA
|
D:HEM501
|
3.4
|
25.4
|
1.0
|
CHB
|
D:HEM501
|
3.5
|
26.9
|
1.0
|
CB
|
D:CYS373
|
3.5
|
29.0
|
1.0
|
CHC
|
D:HEM501
|
3.5
|
24.7
|
1.0
|
O
|
D:GLY262
|
3.7
|
31.0
|
1.0
|
C2D
|
D:HEM501
|
4.1
|
27.5
|
1.0
|
C3D
|
D:HEM501
|
4.1
|
26.6
|
1.0
|
C2A
|
D:HEM501
|
4.2
|
26.2
|
1.0
|
C3A
|
D:HEM501
|
4.2
|
26.9
|
1.0
|
CA
|
D:CYS373
|
4.2
|
28.4
|
1.0
|
C3C
|
D:HEM501
|
4.3
|
25.8
|
1.0
|
C2B
|
D:HEM501
|
4.3
|
27.4
|
1.0
|
C3B
|
D:HEM501
|
4.4
|
26.9
|
1.0
|
C2C
|
D:HEM501
|
4.4
|
25.8
|
1.0
|
C
|
D:GLY262
|
4.4
|
28.5
|
1.0
|
CA
|
D:GLY262
|
4.8
|
27.2
|
1.0
|
C
|
D:CYS373
|
5.0
|
27.6
|
1.0
|
|
Reference:
F.Fiorentini,
A.M.Hatzl,
S.Schmidt,
S.Savino,
A.Glieder,
A.Mattevi.
The Extreme Structural Plasticity in the CYP153 Subfamily of P450S Directs Development of Designer Hydroxylases. Biochemistry V. 57 6701 2018.
ISSN: ISSN 0006-2960
PubMed: 30398864
DOI: 10.1021/ACS.BIOCHEM.8B01052
Page generated: Tue Aug 6 21:34:08 2024
|