Iron in PDB 1mhy: Methane Monooxygenase Hydroxylase
Enzymatic activity of Methane Monooxygenase Hydroxylase
All present enzymatic activity of Methane Monooxygenase Hydroxylase:
1.14.13.25;
Protein crystallography data
The structure of Methane Monooxygenase Hydroxylase, PDB code: 1mhy
was solved by
N.Elango,
R.Radhakrishnan,
W.A.Froland,
B.J.Waller,
C.A.Earhart,
J.D.Lipscomb,
D.H.Ohlendorf,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
5.00 /
2.00
|
Space group
|
C 2 2 21
|
Cell size a, b, c (Å), α, β, γ (°)
|
264.490,
71.190,
139.440,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
13.7 /
n/a
|
Iron Binding Sites:
The binding sites of Iron atom in the Methane Monooxygenase Hydroxylase
(pdb code 1mhy). This binding sites where shown within
5.0 Angstroms radius around Iron atom.
In total 2 binding sites of Iron where determined in the
Methane Monooxygenase Hydroxylase, PDB code: 1mhy:
Jump to Iron binding site number:
1;
2;
Iron binding site 1 out
of 2 in 1mhy
Go back to
Iron Binding Sites List in 1mhy
Iron binding site 1 out
of 2 in the Methane Monooxygenase Hydroxylase
 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 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Fe801
b:14.1
occ:1.00
|
H2
|
D:HOH803
|
1.2
|
0.0
|
1.0
|
HD1
|
D:HIS147
|
1.3
|
0.0
|
1.0
|
H1
|
D:HOH803
|
1.7
|
0.0
|
1.0
|
O
|
D:HOH803
|
1.7
|
11.5
|
1.0
|
OE1
|
D:GLU114
|
1.9
|
12.8
|
1.0
|
OE1
|
D:GLU144
|
2.0
|
12.5
|
1.0
|
O
|
D:HOH804
|
2.2
|
14.8
|
1.0
|
ND1
|
D:HIS147
|
2.2
|
8.7
|
1.0
|
O
|
D:HOH805
|
2.2
|
13.0
|
1.0
|
H1
|
D:HOH805
|
2.5
|
0.0
|
1.0
|
H1
|
D:HOH804
|
2.7
|
0.0
|
1.0
|
CD
|
D:GLU114
|
2.9
|
16.4
|
1.0
|
H2
|
D:HOH804
|
3.0
|
0.0
|
1.0
|
CD
|
D:GLU144
|
3.0
|
15.3
|
1.0
|
FE
|
D:FE802
|
3.0
|
21.1
|
1.0
|
CE1
|
D:HIS147
|
3.1
|
9.4
|
1.0
|
H2
|
D:HOH805
|
3.2
|
0.0
|
1.0
|
OE2
|
D:GLU144
|
3.2
|
12.0
|
1.0
|
CG
|
D:HIS147
|
3.3
|
10.1
|
1.0
|
OE2
|
D:GLU114
|
3.4
|
17.8
|
1.0
|
CB
|
D:HIS147
|
3.7
|
9.6
|
1.0
|
OE1
|
D:GLU243
|
3.7
|
31.2
|
1.0
|
H1
|
D:HOH806
|
3.8
|
0.0
|
1.0
|
HD1
|
D:HIS246
|
3.9
|
0.0
|
1.0
|
OE2
|
D:GLU243
|
4.2
|
18.1
|
1.0
|
CG
|
D:GLU114
|
4.2
|
13.2
|
1.0
|
O
|
D:HOH806
|
4.2
|
27.8
|
1.0
|
NE2
|
D:HIS147
|
4.3
|
9.7
|
1.0
|
CE1
|
D:HIS246
|
4.4
|
17.5
|
1.0
|
CD2
|
D:HIS147
|
4.4
|
8.6
|
1.0
|
O
|
D:HOH807
|
4.4
|
59.0
|
1.0
|
CD
|
D:GLU243
|
4.4
|
28.3
|
1.0
|
H2
|
D:HOH807
|
4.4
|
0.0
|
1.0
|
CG
|
D:GLU144
|
4.4
|
8.9
|
1.0
|
ND1
|
D:HIS246
|
4.5
|
16.9
|
1.0
|
CB
|
D:GLU114
|
4.6
|
14.3
|
1.0
|
CA
|
D:GLU144
|
4.6
|
9.3
|
1.0
|
OE2
|
D:GLU209
|
4.6
|
26.3
|
1.0
|
CA
|
D:GLU114
|
4.7
|
12.7
|
1.0
|
CG1
|
D:VAL239
|
4.8
|
19.7
|
1.0
|
CB
|
D:GLU144
|
4.8
|
9.9
|
1.0
|
O
|
D:ASP143
|
4.9
|
13.2
|
1.0
|
|
Iron binding site 2 out
of 2 in 1mhy
Go back to
Iron Binding Sites List in 1mhy
Iron binding site 2 out
of 2 in the Methane Monooxygenase Hydroxylase
 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 within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
D:Fe802
b:21.1
occ:1.00
|
HD1
|
D:HIS246
|
1.3
|
0.0
|
1.0
|
H1
|
D:HOH804
|
1.7
|
0.0
|
1.0
|
H2
|
D:HOH803
|
1.8
|
0.0
|
1.0
|
OE2
|
D:GLU243
|
1.9
|
18.1
|
1.0
|
OE2
|
D:GLU209
|
2.0
|
26.3
|
1.0
|
O
|
D:HOH803
|
2.0
|
11.5
|
1.0
|
O
|
D:HOH804
|
2.2
|
14.8
|
1.0
|
ND1
|
D:HIS246
|
2.3
|
16.9
|
1.0
|
OE2
|
D:GLU144
|
2.3
|
12.0
|
1.0
|
H1
|
D:HOH803
|
2.4
|
0.0
|
1.0
|
CD
|
D:GLU243
|
2.8
|
28.3
|
1.0
|
H2
|
D:HOH804
|
2.9
|
0.0
|
1.0
|
FE
|
D:FE801
|
3.0
|
14.1
|
1.0
|
CD
|
D:GLU209
|
3.0
|
24.9
|
1.0
|
CE1
|
D:HIS246
|
3.0
|
17.5
|
1.0
|
OE1
|
D:GLU243
|
3.1
|
31.2
|
1.0
|
CD
|
D:GLU144
|
3.2
|
15.3
|
1.0
|
CG
|
D:HIS246
|
3.4
|
20.4
|
1.0
|
HE22
|
D:GLN140
|
3.5
|
0.0
|
1.0
|
OE1
|
D:GLU144
|
3.5
|
12.5
|
1.0
|
CG
|
D:GLU209
|
3.6
|
22.6
|
1.0
|
HD1
|
D:HIS147
|
3.9
|
0.0
|
1.0
|
CB
|
D:HIS246
|
3.9
|
19.9
|
1.0
|
NE2
|
D:GLN140
|
3.9
|
14.1
|
1.0
|
O
|
D:HOH805
|
4.0
|
13.0
|
1.0
|
OE1
|
D:GLU209
|
4.0
|
23.9
|
1.0
|
HE21
|
D:GLN140
|
4.2
|
0.0
|
1.0
|
NE2
|
D:HIS246
|
4.2
|
16.1
|
1.0
|
H1
|
D:HOH806
|
4.2
|
0.0
|
1.0
|
CG
|
D:GLU243
|
4.2
|
28.2
|
1.0
|
CD2
|
D:HIS246
|
4.4
|
15.0
|
1.0
|
ND1
|
D:HIS147
|
4.5
|
8.7
|
1.0
|
H2
|
D:HOH805
|
4.5
|
0.0
|
1.0
|
H1
|
D:HOH805
|
4.6
|
0.0
|
1.0
|
OE1
|
D:GLU114
|
4.6
|
12.8
|
1.0
|
CG
|
D:GLU144
|
4.6
|
8.9
|
1.0
|
CE1
|
D:HIS147
|
4.6
|
9.4
|
1.0
|
CD
|
D:GLN140
|
4.7
|
18.8
|
1.0
|
O
|
D:HOH806
|
4.8
|
27.8
|
1.0
|
O
|
D:HOH807
|
4.8
|
59.0
|
1.0
|
CB
|
D:GLU209
|
4.8
|
20.9
|
1.0
|
H2
|
D:HOH809
|
4.9
|
0.0
|
1.0
|
CG
|
D:GLN140
|
5.0
|
14.0
|
1.0
|
|
Reference:
N.Elango,
R.Radhakrishnan,
W.A.Froland,
B.J.Wallar,
C.A.Earhart,
J.D.Lipscomb,
D.H.Ohlendorf.
Crystal Structure of the Hydroxylase Component of Methane Monooxygenase From Methylosinus Trichosporium OB3B Protein Sci. V. 6 556 1997.
ISSN: ISSN 0961-8368
PubMed: 9070438
Page generated: Sat Aug 3 10:41:33 2024
|