Iron in PDB 1fzi: Methane Monooxygenase Hydroxylase, Form I Pressurized with Xenon Gas
Enzymatic activity of Methane Monooxygenase Hydroxylase, Form I Pressurized with Xenon Gas
All present enzymatic activity of Methane Monooxygenase Hydroxylase, Form I Pressurized with Xenon Gas:
1.14.13.25;
Protein crystallography data
The structure of Methane Monooxygenase Hydroxylase, Form I Pressurized with Xenon Gas, PDB code: 1fzi
was solved by
D.A.Whittington,
A.C.Rosenzweig,
C.A.Frederick,
S.J.Lippard,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
12.00 /
3.30
|
Space group
|
P 21 21 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
61.700,
109.600,
330.200,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
22.3 /
25.3
|
Other elements in 1fzi:
The structure of Methane Monooxygenase Hydroxylase, Form I Pressurized with Xenon Gas also contains other interesting chemical elements:
Iron Binding Sites:
The binding sites of Iron atom in the Methane Monooxygenase Hydroxylase, Form I Pressurized with Xenon Gas
(pdb code 1fzi). This binding sites where shown within
5.0 Angstroms radius around Iron atom.
In total 4 binding sites of Iron where determined in the
Methane Monooxygenase Hydroxylase, Form I Pressurized with Xenon Gas, PDB code: 1fzi:
Jump to Iron binding site number:
1;
2;
3;
4;
Iron binding site 1 out
of 4 in 1fzi
Go back to
Iron Binding Sites List in 1fzi
Iron binding site 1 out
of 4 in the Methane Monooxygenase Hydroxylase, Form I Pressurized with Xenon Gas
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 1 of Methane Monooxygenase Hydroxylase, Form I Pressurized with Xenon Gas within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe5001
b:10.2
occ:1.00
|
OE1
|
A:GLU114
|
2.0
|
22.6
|
1.0
|
OE2
|
A:GLU144
|
2.0
|
19.9
|
1.0
|
ND1
|
A:HIS147
|
2.5
|
5.0
|
1.0
|
FE
|
A:FE5002
|
2.8
|
10.2
|
1.0
|
CD
|
A:GLU144
|
2.9
|
19.6
|
1.0
|
OE1
|
A:GLU144
|
3.1
|
19.5
|
1.0
|
CD
|
A:GLU114
|
3.1
|
22.6
|
1.0
|
CE1
|
A:HIS147
|
3.3
|
4.5
|
1.0
|
OE2
|
A:GLU114
|
3.5
|
23.6
|
1.0
|
CG
|
A:HIS147
|
3.6
|
5.1
|
1.0
|
OE2
|
A:GLU243
|
3.9
|
55.3
|
1.0
|
OE1
|
A:GLU243
|
3.9
|
47.8
|
1.0
|
CB
|
A:HIS147
|
3.9
|
7.0
|
1.0
|
OE2
|
A:GLU209
|
4.2
|
60.3
|
1.0
|
CE1
|
A:HIS246
|
4.3
|
58.5
|
1.0
|
ND1
|
A:HIS246
|
4.3
|
58.3
|
1.0
|
CD
|
A:GLU243
|
4.3
|
54.3
|
1.0
|
CG
|
A:GLU144
|
4.4
|
16.6
|
1.0
|
CG
|
A:GLU114
|
4.4
|
21.5
|
1.0
|
NE2
|
A:HIS147
|
4.5
|
5.4
|
1.0
|
CD2
|
A:HIS147
|
4.7
|
7.0
|
1.0
|
CA
|
A:GLU114
|
4.7
|
6.4
|
1.0
|
CB
|
A:GLU114
|
4.7
|
18.3
|
1.0
|
CA
|
A:GLU144
|
4.8
|
0.0
|
1.0
|
CG2
|
A:ILE239
|
4.8
|
4.2
|
1.0
|
CB
|
A:GLU144
|
4.9
|
16.6
|
1.0
|
|
Iron binding site 2 out
of 4 in 1fzi
Go back to
Iron Binding Sites List in 1fzi
Iron binding site 2 out
of 4 in the Methane Monooxygenase Hydroxylase, Form I Pressurized with Xenon Gas
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 2 of Methane Monooxygenase Hydroxylase, Form I Pressurized with Xenon Gas within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe5002
b:10.2
occ:1.00
|
OE1
|
A:GLU243
|
2.0
|
47.8
|
1.0
|
OE2
|
A:GLU209
|
2.1
|
60.3
|
1.0
|
ND1
|
A:HIS246
|
2.1
|
58.3
|
1.0
|
OE1
|
A:GLU144
|
2.4
|
19.5
|
1.0
|
FE
|
A:FE5001
|
2.8
|
10.2
|
1.0
|
CE1
|
A:HIS246
|
2.8
|
58.5
|
1.0
|
CD
|
A:GLU209
|
3.0
|
61.5
|
1.0
|
CD
|
A:GLU243
|
3.0
|
54.3
|
1.0
|
CG
|
A:HIS246
|
3.3
|
59.4
|
1.0
|
CD
|
A:GLU144
|
3.3
|
19.6
|
1.0
|
OE2
|
A:GLU243
|
3.4
|
55.3
|
1.0
|
OE2
|
A:GLU144
|
3.5
|
19.9
|
1.0
|
NE2
|
A:GLN140
|
3.6
|
19.4
|
1.0
|
CG
|
A:GLU209
|
3.8
|
59.3
|
1.0
|
CB
|
A:HIS246
|
3.8
|
60.1
|
1.0
|
OE1
|
A:GLU209
|
3.9
|
58.7
|
1.0
|
NE2
|
A:HIS246
|
4.1
|
57.6
|
1.0
|
CD2
|
A:HIS246
|
4.3
|
59.2
|
1.0
|
CG
|
A:GLU243
|
4.4
|
52.8
|
1.0
|
ND1
|
A:HIS147
|
4.4
|
5.0
|
1.0
|
CE1
|
A:HIS147
|
4.5
|
4.5
|
1.0
|
CD
|
A:GLN140
|
4.5
|
20.3
|
1.0
|
CG
|
A:GLU144
|
4.7
|
16.6
|
1.0
|
OE1
|
A:GLU114
|
4.7
|
22.6
|
1.0
|
CG
|
A:GLN140
|
4.8
|
20.5
|
1.0
|
CB
|
A:GLU209
|
5.0
|
60.8
|
1.0
|
|
Iron binding site 3 out
of 4 in 1fzi
Go back to
Iron Binding Sites List in 1fzi
Iron binding site 3 out
of 4 in the Methane Monooxygenase Hydroxylase, Form I Pressurized with Xenon Gas
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 3 of Methane Monooxygenase Hydroxylase, Form I Pressurized with Xenon Gas within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe5003
b:15.2
occ:1.00
|
OE1
|
B:GLU114
|
2.0
|
28.5
|
1.0
|
OE2
|
B:GLU144
|
2.1
|
11.8
|
1.0
|
ND1
|
B:HIS147
|
2.1
|
5.2
|
1.0
|
FE
|
B:FE5004
|
2.7
|
15.2
|
1.0
|
CD
|
B:GLU144
|
3.0
|
9.9
|
1.0
|
CE1
|
B:HIS147
|
3.0
|
5.9
|
1.0
|
CD
|
B:GLU114
|
3.1
|
30.1
|
1.0
|
CG
|
B:HIS147
|
3.2
|
4.9
|
1.0
|
OE1
|
B:GLU144
|
3.2
|
11.2
|
1.0
|
OE2
|
B:GLU114
|
3.6
|
34.8
|
1.0
|
CB
|
B:HIS147
|
3.6
|
5.2
|
1.0
|
OE2
|
B:GLU243
|
4.0
|
45.6
|
1.0
|
CE1
|
B:HIS246
|
4.2
|
8.3
|
1.0
|
NE2
|
B:HIS147
|
4.2
|
6.9
|
1.0
|
CD2
|
B:HIS147
|
4.3
|
6.4
|
1.0
|
ND1
|
B:HIS246
|
4.3
|
11.7
|
1.0
|
CG
|
B:GLU144
|
4.4
|
7.1
|
1.0
|
OE1
|
B:GLU243
|
4.4
|
37.7
|
1.0
|
CG
|
B:GLU114
|
4.4
|
26.7
|
1.0
|
OE2
|
B:GLU209
|
4.5
|
0.0
|
1.0
|
CD
|
B:GLU243
|
4.6
|
41.2
|
1.0
|
CA
|
B:GLU144
|
4.6
|
19.3
|
1.0
|
CB
|
B:GLU114
|
4.7
|
25.6
|
1.0
|
CA
|
B:GLU114
|
4.7
|
13.3
|
1.0
|
CG2
|
B:ILE239
|
4.8
|
0.0
|
1.0
|
CB
|
B:GLU144
|
4.8
|
5.2
|
1.0
|
|
Iron binding site 4 out
of 4 in 1fzi
Go back to
Iron Binding Sites List in 1fzi
Iron binding site 4 out
of 4 in the Methane Monooxygenase Hydroxylase, Form I Pressurized with Xenon Gas
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 4 of Methane Monooxygenase Hydroxylase, Form I Pressurized with Xenon Gas within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe5004
b:15.2
occ:1.00
|
OE2
|
B:GLU209
|
2.2
|
0.0
|
1.0
|
ND1
|
B:HIS246
|
2.2
|
11.7
|
1.0
|
OE1
|
B:GLU144
|
2.2
|
11.2
|
1.0
|
OE1
|
B:GLU243
|
2.4
|
37.7
|
1.0
|
FE
|
B:FE5003
|
2.7
|
15.2
|
1.0
|
CE1
|
B:HIS246
|
2.8
|
8.3
|
1.0
|
CD
|
B:GLU144
|
3.1
|
9.9
|
1.0
|
OE2
|
B:GLU144
|
3.2
|
11.8
|
1.0
|
CD
|
B:GLU243
|
3.3
|
41.2
|
1.0
|
CD
|
B:GLU209
|
3.3
|
0.5
|
1.0
|
OE2
|
B:GLU243
|
3.4
|
45.6
|
1.0
|
CG
|
B:HIS246
|
3.4
|
10.8
|
1.0
|
NE2
|
B:GLN140
|
3.7
|
28.7
|
1.0
|
NE2
|
B:HIS246
|
4.1
|
13.6
|
1.0
|
CB
|
B:HIS246
|
4.1
|
11.8
|
1.0
|
ND1
|
B:HIS147
|
4.1
|
5.2
|
1.0
|
CG
|
B:GLU209
|
4.2
|
0.4
|
1.0
|
OE1
|
B:GLU209
|
4.2
|
0.7
|
1.0
|
CE1
|
B:HIS147
|
4.3
|
5.9
|
1.0
|
CD2
|
B:HIS246
|
4.4
|
12.3
|
1.0
|
OE1
|
B:GLU114
|
4.4
|
28.5
|
1.0
|
CG
|
B:GLU144
|
4.5
|
7.1
|
1.0
|
CD
|
B:GLN140
|
4.6
|
29.1
|
1.0
|
CG
|
B:GLU243
|
4.7
|
38.4
|
1.0
|
CG
|
B:GLN140
|
4.8
|
29.3
|
1.0
|
|
Reference:
D.A.Whittington,
A.C.Rosenzweig,
C.A.Frederick,
S.J.Lippard.
Xenon and Halogenated Alkanes Track Putative Substrate Binding Cavities in the Soluble Methane Monooxygenase Hydroxylase. Biochemistry V. 40 3476 2001.
ISSN: ISSN 0006-2960
PubMed: 11297413
DOI: 10.1021/BI0022487
Page generated: Sat Aug 3 05:40:34 2024
|