Iron in PDB 5g5h: Escherichia Coli Periplasmic Aldehyde Oxidase R440H Mutant
Enzymatic activity of Escherichia Coli Periplasmic Aldehyde Oxidase R440H Mutant
All present enzymatic activity of Escherichia Coli Periplasmic Aldehyde Oxidase R440H Mutant:
1.17.1.4;
Protein crystallography data
The structure of Escherichia Coli Periplasmic Aldehyde Oxidase R440H Mutant, PDB code: 5g5h
was solved by
M.A.S.Correia,
A.R.Otrelo-Cardoso,
M.J.Romao,
T.Santos-Silva,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
48.27 /
2.30
|
Space group
|
C 1 2 1
|
Cell size a, b, c (Å), α, β, γ (°)
|
109.839,
78.263,
151.732,
90.00,
99.93,
90.00
|
R / Rfree (%)
|
16.4 /
22
|
Other elements in 5g5h:
The structure of Escherichia Coli Periplasmic Aldehyde Oxidase R440H Mutant also contains other interesting chemical elements:
Iron Binding Sites:
The binding sites of Iron atom in the Escherichia Coli Periplasmic Aldehyde Oxidase R440H Mutant
(pdb code 5g5h). This binding sites where shown within
5.0 Angstroms radius around Iron atom.
In total 8 binding sites of Iron where determined in the
Escherichia Coli Periplasmic Aldehyde Oxidase R440H Mutant, PDB code: 5g5h:
Jump to Iron binding site number:
1;
2;
3;
4;
5;
6;
7;
8;
Iron binding site 1 out
of 8 in 5g5h
Go back to
Iron Binding Sites List in 5g5h
Iron binding site 1 out
of 8 in the Escherichia Coli Periplasmic Aldehyde Oxidase R440H Mutant
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 1 of Escherichia Coli Periplasmic Aldehyde Oxidase R440H Mutant within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe1226
b:15.9
occ:1.00
|
FE1
|
A:FES1226
|
0.0
|
15.9
|
1.0
|
SG
|
A:CYS161
|
2.0
|
15.6
|
1.0
|
S2
|
A:FES1226
|
2.2
|
21.1
|
1.0
|
S1
|
A:FES1226
|
2.2
|
18.4
|
1.0
|
SG
|
A:CYS208
|
2.3
|
15.6
|
1.0
|
CB
|
A:CYS208
|
3.1
|
16.2
|
1.0
|
CB
|
A:CYS161
|
3.1
|
16.6
|
1.0
|
FE2
|
A:FES1226
|
3.1
|
17.0
|
1.0
|
CA
|
A:CYS208
|
3.4
|
15.9
|
1.0
|
O
|
A:HOH2076
|
4.0
|
14.1
|
1.0
|
CA
|
A:CYS161
|
4.1
|
16.7
|
1.0
|
N
|
A:CYS161
|
4.2
|
17.1
|
1.0
|
C
|
A:CYS208
|
4.3
|
16.4
|
1.0
|
CB
|
A:CYS210
|
4.4
|
18.3
|
1.0
|
N
|
A:ARG209
|
4.4
|
16.7
|
1.0
|
O
|
A:ILE207
|
4.6
|
15.9
|
1.0
|
N
|
A:CYS208
|
4.6
|
15.7
|
1.0
|
N
|
A:CYS210
|
4.7
|
18.4
|
1.0
|
SG
|
A:CYS210
|
4.7
|
19.9
|
1.0
|
C
|
A:CYS161
|
4.7
|
16.9
|
1.0
|
NE2
|
A:GLN165
|
4.9
|
17.2
|
1.0
|
SG
|
A:CYS158
|
5.0
|
15.6
|
1.0
|
OG1
|
A:THR162
|
5.0
|
16.3
|
1.0
|
|
Iron binding site 2 out
of 8 in 5g5h
Go back to
Iron Binding Sites List in 5g5h
Iron binding site 2 out
of 8 in the Escherichia Coli Periplasmic Aldehyde Oxidase R440H Mutant
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 2 of Escherichia Coli Periplasmic Aldehyde Oxidase R440H Mutant within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe1226
b:17.0
occ:1.00
|
FE2
|
A:FES1226
|
0.0
|
17.0
|
1.0
|
S2
|
A:FES1226
|
2.2
|
21.1
|
1.0
|
S1
|
A:FES1226
|
2.2
|
18.4
|
1.0
|
SG
|
A:CYS210
|
2.2
|
19.9
|
1.0
|
SG
|
A:CYS158
|
2.3
|
15.6
|
1.0
|
FE1
|
A:FES1226
|
3.1
|
15.9
|
1.0
|
CB
|
A:CYS210
|
3.2
|
18.3
|
1.0
|
CB
|
A:CYS158
|
3.2
|
16.7
|
1.0
|
N
|
A:CYS158
|
3.4
|
16.6
|
1.0
|
CA
|
A:CYS158
|
3.7
|
16.7
|
1.0
|
O
|
A:HOH2079
|
3.8
|
11.2
|
1.0
|
N
|
A:GLY159
|
4.0
|
16.4
|
1.0
|
N
|
A:CYS210
|
4.1
|
18.4
|
1.0
|
CA
|
A:CYS210
|
4.2
|
18.3
|
1.0
|
SG
|
A:CYS208
|
4.3
|
15.6
|
1.0
|
C
|
A:CYS158
|
4.3
|
16.5
|
1.0
|
C
|
A:GLN157
|
4.5
|
16.7
|
1.0
|
N
|
A:TYR160
|
4.5
|
16.2
|
1.0
|
N
|
A:GLN157
|
4.7
|
16.7
|
1.0
|
SG
|
A:CYS161
|
4.8
|
15.6
|
1.0
|
CB
|
A:GLN157
|
4.8
|
17.3
|
1.0
|
N
|
A:CYS161
|
4.8
|
17.1
|
1.0
|
CA
|
A:GLN157
|
4.9
|
16.9
|
1.0
|
|
Iron binding site 3 out
of 8 in 5g5h
Go back to
Iron Binding Sites List in 5g5h
Iron binding site 3 out
of 8 in the Escherichia Coli Periplasmic Aldehyde Oxidase R440H Mutant
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 3 of Escherichia Coli Periplasmic Aldehyde Oxidase R440H Mutant within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe1227
b:17.1
occ:1.00
|
FE1
|
A:FES1227
|
0.0
|
17.1
|
1.0
|
SG
|
A:CYS107
|
2.2
|
18.5
|
1.0
|
S2
|
A:FES1227
|
2.2
|
14.8
|
1.0
|
S1
|
A:FES1227
|
2.2
|
13.5
|
1.0
|
SG
|
A:CYS119
|
2.3
|
18.0
|
1.0
|
FE2
|
A:FES1227
|
3.0
|
15.8
|
1.0
|
CB
|
A:CYS119
|
3.1
|
17.8
|
1.0
|
CB
|
A:CYS107
|
3.3
|
18.1
|
1.0
|
N
|
A:CYS119
|
4.1
|
18.2
|
1.0
|
CA
|
A:CYS119
|
4.2
|
18.9
|
1.0
|
N
|
A:CYS107
|
4.2
|
17.9
|
1.0
|
N
|
A:GLY102
|
4.3
|
17.6
|
1.0
|
CB
|
A:ASN117
|
4.3
|
15.6
|
1.0
|
CA
|
A:CYS107
|
4.4
|
17.6
|
1.0
|
SG
|
A:CYS99
|
4.5
|
15.2
|
1.0
|
CA
|
A:GLY102
|
4.5
|
17.4
|
1.0
|
N
|
A:ASP100
|
4.5
|
16.6
|
1.0
|
CG
|
A:ASN117
|
4.6
|
15.3
|
1.0
|
CD2
|
A:LEU83
|
4.7
|
17.3
|
1.0
|
CA
|
A:ASP100
|
4.7
|
16.9
|
1.0
|
SG
|
A:CYS104
|
4.8
|
21.9
|
1.0
|
N
|
A:GLY105
|
4.8
|
16.6
|
1.0
|
N
|
A:HIS101
|
4.9
|
18.1
|
1.0
|
CA
|
A:ASN117
|
4.9
|
16.2
|
1.0
|
C
|
A:ASN117
|
5.0
|
16.9
|
1.0
|
OD1
|
A:ASN117
|
5.0
|
15.1
|
1.0
|
N
|
A:ALA118
|
5.0
|
17.2
|
1.0
|
N
|
A:ALA106
|
5.0
|
16.0
|
1.0
|
|
Iron binding site 4 out
of 8 in 5g5h
Go back to
Iron Binding Sites List in 5g5h
Iron binding site 4 out
of 8 in the Escherichia Coli Periplasmic Aldehyde Oxidase R440H Mutant
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 4 of Escherichia Coli Periplasmic Aldehyde Oxidase R440H Mutant within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Fe1227
b:15.8
occ:1.00
|
FE2
|
A:FES1227
|
0.0
|
15.8
|
1.0
|
S1
|
A:FES1227
|
2.2
|
13.5
|
1.0
|
S2
|
A:FES1227
|
2.2
|
14.8
|
1.0
|
SG
|
A:CYS104
|
2.3
|
21.9
|
1.0
|
SG
|
A:CYS99
|
2.3
|
15.2
|
1.0
|
FE1
|
A:FES1227
|
3.0
|
17.1
|
1.0
|
N
|
A:CYS99
|
3.2
|
17.3
|
1.0
|
CB
|
A:CYS104
|
3.3
|
19.4
|
1.0
|
CB
|
A:CYS99
|
3.4
|
16.1
|
1.0
|
N
|
A:CYS104
|
3.6
|
18.8
|
1.0
|
CA
|
A:CYS99
|
3.7
|
16.7
|
1.0
|
N
|
A:ASP100
|
3.8
|
16.6
|
1.0
|
N
|
A:GLY105
|
3.8
|
16.6
|
1.0
|
CA
|
A:CYS104
|
3.9
|
18.7
|
1.0
|
C
|
A:GLY98
|
4.1
|
17.9
|
1.0
|
N
|
A:GLN103
|
4.2
|
17.8
|
1.0
|
C
|
A:CYS99
|
4.2
|
17.2
|
1.0
|
N
|
A:GLY98
|
4.2
|
17.4
|
1.0
|
C
|
A:CYS104
|
4.3
|
18.2
|
1.0
|
CA
|
A:GLY98
|
4.3
|
17.3
|
1.0
|
N
|
A:ALA106
|
4.4
|
16.0
|
1.0
|
N
|
A:GLY102
|
4.5
|
17.6
|
1.0
|
SG
|
A:CYS119
|
4.5
|
18.0
|
1.0
|
N
|
A:HIS101
|
4.6
|
18.1
|
1.0
|
C
|
A:GLN103
|
4.7
|
19.7
|
1.0
|
SG
|
A:CYS107
|
4.7
|
18.5
|
1.0
|
CA
|
A:ASP100
|
4.8
|
16.9
|
1.0
|
C
|
A:GLY102
|
4.9
|
17.2
|
1.0
|
CA
|
A:GLY102
|
4.9
|
17.4
|
1.0
|
CA
|
A:GLY105
|
4.9
|
16.8
|
1.0
|
CA
|
A:GLN103
|
4.9
|
19.8
|
1.0
|
|
Iron binding site 5 out
of 8 in 5g5h
Go back to
Iron Binding Sites List in 5g5h
Iron binding site 5 out
of 8 in the Escherichia Coli Periplasmic Aldehyde Oxidase R440H Mutant
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 5 of Escherichia Coli Periplasmic Aldehyde Oxidase R440H Mutant within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe1317
b:30.6
occ:1.00
|
FE1
|
B:SF41317
|
0.0
|
30.6
|
1.0
|
S4
|
B:SF41317
|
2.1
|
26.0
|
1.0
|
S3
|
B:SF41317
|
2.1
|
26.3
|
1.0
|
S2
|
B:SF41317
|
2.1
|
26.7
|
1.0
|
SG
|
B:CYS157
|
2.2
|
23.8
|
1.0
|
FE4
|
B:SF41317
|
3.0
|
30.9
|
1.0
|
FE2
|
B:SF41317
|
3.0
|
28.8
|
1.0
|
FE3
|
B:SF41317
|
3.0
|
28.2
|
1.0
|
CB
|
B:CYS157
|
3.3
|
25.7
|
1.0
|
S1
|
B:SF41317
|
3.7
|
27.4
|
1.0
|
CA
|
B:CYS157
|
3.8
|
26.6
|
1.0
|
CB
|
B:ALA159
|
3.8
|
22.7
|
1.0
|
N
|
B:ILE158
|
4.0
|
24.9
|
1.0
|
N
|
B:ALA159
|
4.1
|
23.8
|
1.0
|
C
|
B:CYS157
|
4.4
|
25.6
|
1.0
|
CE
|
B:LYS131
|
4.4
|
27.8
|
1.0
|
CB
|
B:LYS131
|
4.4
|
27.5
|
1.0
|
CA
|
B:ALA159
|
4.5
|
22.8
|
1.0
|
SG
|
B:CYS138
|
4.7
|
28.6
|
1.0
|
O
|
B:ALA156
|
4.8
|
29.7
|
1.0
|
CD
|
B:LYS131
|
4.9
|
27.3
|
1.0
|
C
|
B:ILE158
|
4.9
|
24.4
|
1.0
|
SG
|
B:CYS129
|
5.0
|
24.7
|
1.0
|
|
Iron binding site 6 out
of 8 in 5g5h
Go back to
Iron Binding Sites List in 5g5h
Iron binding site 6 out
of 8 in the Escherichia Coli Periplasmic Aldehyde Oxidase R440H Mutant
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 6 of Escherichia Coli Periplasmic Aldehyde Oxidase R440H Mutant within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe1317
b:28.8
occ:1.00
|
FE2
|
B:SF41317
|
0.0
|
28.8
|
1.0
|
S4
|
B:SF41317
|
2.1
|
26.0
|
1.0
|
S3
|
B:SF41317
|
2.1
|
26.3
|
1.0
|
S1
|
B:SF41317
|
2.1
|
27.4
|
1.0
|
SG
|
B:CYS138
|
2.3
|
28.6
|
1.0
|
FE1
|
B:SF41317
|
3.0
|
30.6
|
1.0
|
FE4
|
B:SF41317
|
3.0
|
30.9
|
1.0
|
FE3
|
B:SF41317
|
3.0
|
28.2
|
1.0
|
CB
|
B:CYS138
|
3.1
|
29.4
|
1.0
|
CA
|
B:CYS138
|
3.3
|
29.1
|
1.0
|
S2
|
B:SF41317
|
3.7
|
26.7
|
1.0
|
C
|
B:CYS138
|
3.9
|
29.2
|
1.0
|
N
|
B:ALA139
|
4.0
|
27.3
|
1.0
|
CB
|
B:ALA140
|
4.1
|
24.7
|
1.0
|
N
|
B:ALA140
|
4.2
|
26.0
|
1.0
|
O
|
B:ALA156
|
4.4
|
29.7
|
1.0
|
CA
|
B:CYS157
|
4.5
|
26.6
|
1.0
|
N
|
B:CYS138
|
4.6
|
29.8
|
1.0
|
O
|
B:CYS138
|
4.6
|
30.6
|
1.0
|
SG
|
B:CYS157
|
4.7
|
23.8
|
1.0
|
CA
|
B:ALA140
|
4.8
|
25.6
|
1.0
|
N
|
B:ILE158
|
4.8
|
24.9
|
1.0
|
CB
|
B:CYS157
|
4.8
|
25.7
|
1.0
|
O
|
B:GLY137
|
4.8
|
29.1
|
1.0
|
CA
|
B:CYS129
|
4.9
|
26.2
|
1.0
|
|
Iron binding site 7 out
of 8 in 5g5h
Go back to
Iron Binding Sites List in 5g5h
Iron binding site 7 out
of 8 in the Escherichia Coli Periplasmic Aldehyde Oxidase R440H Mutant
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 7 of Escherichia Coli Periplasmic Aldehyde Oxidase R440H Mutant within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe1317
b:28.2
occ:1.00
|
FE3
|
B:SF41317
|
0.0
|
28.2
|
1.0
|
S4
|
B:SF41317
|
2.1
|
26.0
|
1.0
|
S2
|
B:SF41317
|
2.1
|
26.7
|
1.0
|
S1
|
B:SF41317
|
2.1
|
27.4
|
1.0
|
SG
|
B:CYS119
|
2.2
|
24.9
|
1.0
|
FE4
|
B:SF41317
|
3.0
|
30.9
|
1.0
|
FE1
|
B:SF41317
|
3.0
|
30.6
|
1.0
|
FE2
|
B:SF41317
|
3.0
|
28.8
|
1.0
|
CB
|
B:CYS119
|
3.1
|
23.6
|
1.0
|
S3
|
B:SF41317
|
3.7
|
26.3
|
1.0
|
NE2
|
B:HIS148
|
3.7
|
28.7
|
1.0
|
CB
|
B:ALA140
|
4.1
|
24.7
|
1.0
|
CD2
|
B:HIS148
|
4.3
|
29.3
|
1.0
|
N
|
B:PHE122
|
4.4
|
24.1
|
1.0
|
CB
|
B:PHE122
|
4.5
|
24.2
|
1.0
|
CA
|
B:CYS119
|
4.5
|
22.7
|
1.0
|
CB
|
B:TYR121
|
4.6
|
23.7
|
1.0
|
CB
|
B:ALA159
|
4.8
|
22.7
|
1.0
|
SG
|
B:CYS129
|
4.8
|
24.7
|
1.0
|
CE1
|
B:HIS148
|
4.9
|
29.2
|
1.0
|
SG
|
B:CYS138
|
4.9
|
28.6
|
1.0
|
|
Iron binding site 8 out
of 8 in 5g5h
Go back to
Iron Binding Sites List in 5g5h
Iron binding site 8 out
of 8 in the Escherichia Coli Periplasmic Aldehyde Oxidase R440H Mutant
Mono view
Stereo pair view
|
A full contact list of Iron with other atoms in the Fe binding
site number 8 of Escherichia Coli Periplasmic Aldehyde Oxidase R440H Mutant within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Fe1317
b:30.9
occ:1.00
|
FE4
|
B:SF41317
|
0.0
|
30.9
|
1.0
|
S1
|
B:SF41317
|
2.1
|
27.4
|
1.0
|
S2
|
B:SF41317
|
2.1
|
26.7
|
1.0
|
S3
|
B:SF41317
|
2.1
|
26.3
|
1.0
|
SG
|
B:CYS129
|
2.2
|
24.7
|
1.0
|
FE1
|
B:SF41317
|
3.0
|
30.6
|
1.0
|
FE2
|
B:SF41317
|
3.0
|
28.8
|
1.0
|
FE3
|
B:SF41317
|
3.0
|
28.2
|
1.0
|
CB
|
B:CYS129
|
3.1
|
25.2
|
1.0
|
CA
|
B:CYS129
|
3.3
|
26.2
|
1.0
|
S4
|
B:SF41317
|
3.7
|
26.0
|
1.0
|
C
|
B:CYS129
|
3.8
|
26.4
|
1.0
|
N
|
B:ASN130
|
3.9
|
27.5
|
1.0
|
N
|
B:LYS131
|
4.0
|
27.9
|
1.0
|
CB
|
B:LYS131
|
4.0
|
27.5
|
1.0
|
CB
|
B:PHE122
|
4.4
|
24.2
|
1.0
|
N
|
B:PHE122
|
4.6
|
24.1
|
1.0
|
CA
|
B:LYS131
|
4.6
|
27.9
|
1.0
|
CA
|
B:PHE122
|
4.6
|
24.2
|
1.0
|
O
|
B:CYS129
|
4.6
|
26.0
|
1.0
|
N
|
B:CYS129
|
4.6
|
27.6
|
1.0
|
SG
|
B:CYS119
|
4.7
|
24.9
|
1.0
|
O
|
B:PRO128
|
4.8
|
26.3
|
1.0
|
CA
|
B:ASN130
|
4.9
|
28.1
|
1.0
|
C
|
B:ASN130
|
4.9
|
28.6
|
1.0
|
|
Reference:
M.A.Correia,
A.R.Otrelo-Cardoso,
V.Schwuchow,
K.G.Sigfridsson Clauss,
M.Haumann,
M.J.Romao,
S.Leimkuhler,
T.Santos-Silva.
The Escherichia Coli Periplasmic Aldehyde Oxidoreductase Is An Exceptional Member of the Xanthine Oxidase Family of Molybdoenzymes. Acs Chem.Biol. V. 11 2923 2016.
ISSN: ISSN 1554-8929
PubMed: 27622978
DOI: 10.1021/ACSCHEMBIO.6B00572
Page generated: Tue Aug 6 01:25:14 2024
|