Zinc in PDB 1oez: Zn HIS46ARG Mutant of Human Cu, Zn Superoxide Dismutase
Enzymatic activity of Zn HIS46ARG Mutant of Human Cu, Zn Superoxide Dismutase
All present enzymatic activity of Zn HIS46ARG Mutant of Human Cu, Zn Superoxide Dismutase:
1.15.1.1;
Protein crystallography data
The structure of Zn HIS46ARG Mutant of Human Cu, Zn Superoxide Dismutase, PDB code: 1oez
was solved by
R.W.Strange,
S.Antonyuk,
M.A.Hough,
P.Doucette,
J.Rodriguez,
J.S.Elam,
P.J.Hart,
L.J.Hayward,
J.S.Valentine,
S.S.Hasnain,
with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:
Resolution Low / High (Å)
|
20.00 /
2.15
|
Space group
|
P 41 21 2
|
Cell size a, b, c (Å), α, β, γ (°)
|
190.812,
190.812,
34.666,
90.00,
90.00,
90.00
|
R / Rfree (%)
|
20.6 /
23.4
|
Zinc Binding Sites:
The binding sites of Zinc atom in the Zn HIS46ARG Mutant of Human Cu, Zn Superoxide Dismutase
(pdb code 1oez). This binding sites where shown within
5.0 Angstroms radius around Zinc atom.
In total 4 binding sites of Zinc where determined in the
Zn HIS46ARG Mutant of Human Cu, Zn Superoxide Dismutase, PDB code: 1oez:
Jump to Zinc binding site number:
1;
2;
3;
4;
Zinc binding site 1 out
of 4 in 1oez
Go back to
Zinc Binding Sites List in 1oez
Zinc binding site 1 out
of 4 in the Zn HIS46ARG Mutant of Human Cu, Zn Superoxide Dismutase
 Mono view
 Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 1 of Zn HIS46ARG Mutant of Human Cu, Zn Superoxide Dismutase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
W:Zn1154
b:19.2
occ:1.00
|
ND1
|
W:HIS80
|
1.8
|
9.2
|
1.0
|
ND1
|
W:HIS63
|
2.0
|
14.7
|
1.0
|
OD2
|
W:ASP83
|
2.2
|
12.7
|
1.0
|
OD1
|
W:ASP83
|
2.3
|
16.3
|
1.0
|
O
|
W:HOH2067
|
2.4
|
45.9
|
1.0
|
CG
|
W:ASP83
|
2.7
|
13.8
|
1.0
|
CE1
|
W:HIS80
|
2.7
|
13.5
|
1.0
|
CE1
|
W:HIS63
|
2.9
|
15.0
|
1.0
|
CG
|
W:HIS80
|
3.0
|
12.0
|
1.0
|
CG
|
W:HIS63
|
3.0
|
15.6
|
1.0
|
CB
|
W:HIS63
|
3.4
|
15.0
|
1.0
|
CB
|
W:HIS80
|
3.5
|
10.3
|
1.0
|
N
|
W:HIS80
|
3.8
|
10.7
|
1.0
|
NE2
|
W:HIS80
|
3.9
|
12.4
|
1.0
|
NE2
|
W:HIS63
|
4.0
|
15.4
|
1.0
|
CD2
|
W:HIS80
|
4.0
|
11.8
|
1.0
|
CD2
|
W:HIS63
|
4.1
|
14.3
|
1.0
|
CB
|
W:ASP83
|
4.2
|
14.8
|
1.0
|
CA
|
W:HIS80
|
4.3
|
10.8
|
1.0
|
NE
|
W:ARG46
|
4.5
|
24.1
|
1.0
|
C
|
W:ARG79
|
4.6
|
12.5
|
1.0
|
CD
|
W:ARG46
|
4.6
|
23.1
|
1.0
|
CA
|
W:ARG79
|
4.7
|
14.4
|
1.0
|
O
|
W:GLU78
|
4.9
|
19.5
|
1.0
|
CA
|
W:HIS63
|
4.9
|
15.3
|
1.0
|
N
|
W:ARG79
|
5.0
|
16.8
|
1.0
|
|
Zinc binding site 2 out
of 4 in 1oez
Go back to
Zinc Binding Sites List in 1oez
Zinc binding site 2 out
of 4 in the Zn HIS46ARG Mutant of Human Cu, Zn Superoxide Dismutase
 Mono view
 Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 2 of Zn HIS46ARG Mutant of Human Cu, Zn Superoxide Dismutase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
X:Zn1154
b:18.6
occ:1.00
|
ND1
|
X:HIS63
|
1.9
|
15.0
|
1.0
|
ND1
|
X:HIS80
|
1.9
|
13.5
|
1.0
|
OD1
|
X:ASP83
|
2.4
|
19.2
|
1.0
|
OD2
|
X:ASP83
|
2.4
|
21.1
|
1.0
|
O
|
X:HOH2066
|
2.6
|
39.4
|
1.0
|
CG
|
X:ASP83
|
2.8
|
19.0
|
1.0
|
CE1
|
X:HIS80
|
2.8
|
19.1
|
1.0
|
CE1
|
X:HIS63
|
2.8
|
15.6
|
1.0
|
CG
|
X:HIS63
|
3.0
|
15.4
|
1.0
|
CG
|
X:HIS80
|
3.0
|
16.5
|
1.0
|
CB
|
X:HIS63
|
3.4
|
15.1
|
1.0
|
CB
|
X:HIS80
|
3.5
|
14.7
|
1.0
|
N
|
X:HIS80
|
3.8
|
14.7
|
1.0
|
NE2
|
X:HIS63
|
4.0
|
16.5
|
1.0
|
NE2
|
X:HIS80
|
4.0
|
17.4
|
1.0
|
CD2
|
X:HIS63
|
4.1
|
13.4
|
1.0
|
CD2
|
X:HIS80
|
4.1
|
17.8
|
1.0
|
CA
|
X:HIS80
|
4.3
|
15.1
|
1.0
|
CB
|
X:ASP83
|
4.3
|
18.9
|
1.0
|
NE
|
X:ARG46
|
4.5
|
23.8
|
1.0
|
C
|
X:ARG79
|
4.6
|
15.1
|
1.0
|
CD
|
X:ARG46
|
4.8
|
20.5
|
1.0
|
O
|
X:GLU78
|
4.8
|
21.4
|
1.0
|
CA
|
X:ARG79
|
4.8
|
16.3
|
1.0
|
CA
|
X:HIS63
|
4.9
|
15.2
|
1.0
|
|
Zinc binding site 3 out
of 4 in 1oez
Go back to
Zinc Binding Sites List in 1oez
Zinc binding site 3 out
of 4 in the Zn HIS46ARG Mutant of Human Cu, Zn Superoxide Dismutase
 Mono view
 Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 3 of Zn HIS46ARG Mutant of Human Cu, Zn Superoxide Dismutase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
Y:Zn1154
b:17.7
occ:1.00
|
ND1
|
Y:HIS80
|
1.8
|
9.5
|
1.0
|
ND1
|
Y:HIS63
|
2.0
|
13.1
|
1.0
|
OD2
|
Y:ASP83
|
2.1
|
16.4
|
1.0
|
O
|
Y:HOH2067
|
2.4
|
46.6
|
1.0
|
OD1
|
Y:ASP83
|
2.5
|
20.8
|
1.0
|
CE1
|
Y:HIS80
|
2.7
|
15.5
|
1.0
|
CG
|
Y:ASP83
|
2.7
|
15.8
|
1.0
|
CE1
|
Y:HIS63
|
2.9
|
13.7
|
1.0
|
CG
|
Y:HIS80
|
2.9
|
11.0
|
1.0
|
CG
|
Y:HIS63
|
3.0
|
13.3
|
1.0
|
CB
|
Y:HIS80
|
3.4
|
11.0
|
1.0
|
CB
|
Y:HIS63
|
3.4
|
14.4
|
1.0
|
N
|
Y:HIS80
|
3.8
|
12.7
|
1.0
|
NE2
|
Y:HIS80
|
3.8
|
13.7
|
1.0
|
O
|
Y:GLU78
|
3.9
|
24.3
|
1.0
|
CD2
|
Y:HIS80
|
4.0
|
9.6
|
1.0
|
NE2
|
Y:HIS63
|
4.0
|
13.8
|
1.0
|
CD2
|
Y:HIS63
|
4.1
|
12.0
|
1.0
|
CB
|
Y:ASP83
|
4.2
|
15.5
|
1.0
|
CA
|
Y:HIS80
|
4.2
|
11.7
|
1.0
|
C
|
Y:GLU78
|
4.6
|
22.0
|
1.0
|
NE
|
Y:ARG46
|
4.6
|
24.8
|
1.0
|
C
|
Y:ARG79
|
4.6
|
14.4
|
1.0
|
CA
|
Y:ARG79
|
4.9
|
16.3
|
1.0
|
CD
|
Y:ARG46
|
4.9
|
20.2
|
1.0
|
CA
|
Y:HIS63
|
5.0
|
15.0
|
1.0
|
|
Zinc binding site 4 out
of 4 in 1oez
Go back to
Zinc Binding Sites List in 1oez
Zinc binding site 4 out
of 4 in the Zn HIS46ARG Mutant of Human Cu, Zn Superoxide Dismutase
 Mono view
 Stereo pair view
|
A full contact list of Zinc with other atoms in the Zn binding
site number 4 of Zn HIS46ARG Mutant of Human Cu, Zn Superoxide Dismutase within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
Z:Zn1154
b:17.6
occ:1.00
|
ND1
|
Z:HIS80
|
1.8
|
12.8
|
1.0
|
ND1
|
Z:HIS63
|
1.8
|
13.4
|
1.0
|
OD2
|
Z:ASP83
|
2.2
|
16.4
|
1.0
|
O
|
Z:HOH2076
|
2.4
|
44.7
|
1.0
|
OD1
|
Z:ASP83
|
2.5
|
13.8
|
1.0
|
CE1
|
Z:HIS80
|
2.7
|
17.6
|
1.0
|
CG
|
Z:ASP83
|
2.8
|
14.8
|
1.0
|
CE1
|
Z:HIS63
|
2.8
|
12.2
|
1.0
|
CG
|
Z:HIS80
|
2.9
|
13.9
|
1.0
|
CG
|
Z:HIS63
|
2.9
|
15.7
|
1.0
|
CB
|
Z:HIS63
|
3.3
|
14.3
|
1.0
|
CB
|
Z:HIS80
|
3.4
|
14.3
|
1.0
|
NE2
|
Z:HIS80
|
3.8
|
16.6
|
1.0
|
N
|
Z:HIS80
|
3.8
|
15.5
|
1.0
|
NE2
|
Z:HIS63
|
3.9
|
14.6
|
1.0
|
CD2
|
Z:HIS80
|
3.9
|
15.6
|
1.0
|
CD2
|
Z:HIS63
|
4.0
|
15.1
|
1.0
|
CA
|
Z:HIS80
|
4.3
|
14.8
|
1.0
|
CB
|
Z:ASP83
|
4.3
|
16.5
|
1.0
|
NH1
|
Z:ARG46
|
4.6
|
36.9
|
1.0
|
C
|
Z:ARG79
|
4.7
|
16.6
|
1.0
|
CA
|
Z:ARG79
|
4.8
|
18.0
|
1.0
|
CD
|
Z:ARG46
|
4.9
|
24.7
|
1.0
|
CA
|
Z:HIS63
|
4.9
|
14.8
|
1.0
|
O
|
Z:GLU78
|
4.9
|
22.6
|
1.0
|
|
Reference:
J.S.Elam,
A.B.Taylor,
R.W.Strange,
S.Antonyuk,
P.Doucette,
J.Rodriguez,
S.S.Hasnain,
L.J.Hayward,
J.S.Valentine,
T.O.Yeates,
P.J.Hart.
Amyloid-Like Filaments and Water-Filled Nanotubes Formed By SOD1 Mutant Proteins Linked to Familial Als Nat.Struct.Biol. V. 10 461 2003.
ISSN: ISSN 1072-8368
PubMed: 12754496
DOI: 10.1038/NSB935
Page generated: Wed Oct 16 17:30:10 2024
|