Manganese in PDB 9bwm: Neutron Structure of Oxidized TYR34PHE Mnsod
Enzymatic activity of Neutron Structure of Oxidized TYR34PHE Mnsod
All present enzymatic activity of Neutron Structure of Oxidized TYR34PHE Mnsod:
1.15.1.1;
Manganese Binding Sites:
The binding sites of Manganese atom in the Neutron Structure of Oxidized TYR34PHE Mnsod
(pdb code 9bwm). This binding sites where shown within
5.0 Angstroms radius around Manganese atom.
In total 2 binding sites of Manganese where determined in the
Neutron Structure of Oxidized TYR34PHE Mnsod, PDB code: 9bwm:
Jump to Manganese binding site number:
1;
2;
Manganese binding site 1 out
of 2 in 9bwm
Go back to
Manganese Binding Sites List in 9bwm
Manganese binding site 1 out
of 2 in the Neutron Structure of Oxidized TYR34PHE Mnsod
 Mono view
 Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 1 of Neutron Structure of Oxidized TYR34PHE Mnsod within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
A:Mn201
b:52.5
occ:1.00
|
O
|
A:HOH314
|
1.9
|
26.9
|
1.0
|
NE2
|
A:HIS26
|
2.1
|
31.4
|
1.0
|
NE2
|
A:HIS74
|
2.1
|
29.4
|
1.0
|
NE2
|
A:HIS163
|
2.1
|
26.7
|
1.0
|
OD2
|
A:ASP159
|
2.2
|
30.4
|
1.0
|
D1
|
A:HOH314
|
2.4
|
26.9
|
1.0
|
CE1
|
A:HIS163
|
3.0
|
27.1
|
1.0
|
CE1
|
A:HIS74
|
3.0
|
30.9
|
1.0
|
CD2
|
A:HIS26
|
3.0
|
28.9
|
1.0
|
CE1
|
A:HIS26
|
3.1
|
30.5
|
1.0
|
CD2
|
A:HIS74
|
3.1
|
26.4
|
1.0
|
CD2
|
A:HIS163
|
3.2
|
29.7
|
1.0
|
DE1
|
A:HIS163
|
3.2
|
29.7
|
1.0
|
DE1
|
A:HIS74
|
3.2
|
28.2
|
1.0
|
CG
|
A:ASP159
|
3.3
|
28.0
|
1.0
|
DD2
|
A:HIS26
|
3.3
|
30.0
|
1.0
|
DE1
|
A:HIS26
|
3.3
|
29.2
|
1.0
|
DD2
|
A:HIS74
|
3.4
|
27.8
|
1.0
|
DD2
|
A:HIS163
|
3.5
|
28.4
|
1.0
|
DE22
|
A:GLN143
|
3.5
|
28.0
|
1.0
|
DB2
|
A:TRP161
|
3.6
|
28.5
|
1.0
|
DZ2
|
A:TRP123
|
3.7
|
27.9
|
1.0
|
OD1
|
A:ASP159
|
3.7
|
24.5
|
1.0
|
DB2
|
A:ALA164
|
4.0
|
25.3
|
1.0
|
ND1
|
A:HIS26
|
4.1
|
29.3
|
1.0
|
ND1
|
A:HIS74
|
4.2
|
26.4
|
1.0
|
CG
|
A:HIS26
|
4.2
|
31.5
|
1.0
|
ND1
|
A:HIS163
|
4.2
|
25.0
|
1.0
|
CG
|
A:HIS74
|
4.2
|
28.8
|
1.0
|
CG
|
A:HIS163
|
4.3
|
28.4
|
1.0
|
CZ2
|
A:TRP123
|
4.4
|
28.3
|
1.0
|
CB
|
A:TRP161
|
4.4
|
27.0
|
1.0
|
DE2
|
A:PHE34
|
4.5
|
29.6
|
1.0
|
NE2
|
A:GLN143
|
4.5
|
27.2
|
1.0
|
CB
|
A:ASP159
|
4.5
|
27.5
|
1.0
|
CG
|
A:TRP161
|
4.5
|
27.1
|
1.0
|
DB2
|
A:ASP159
|
4.6
|
28.7
|
1.0
|
DB3
|
A:TRP161
|
4.6
|
24.4
|
1.0
|
DB3
|
A:HIS30
|
4.7
|
30.4
|
1.0
|
DH2
|
A:TRP123
|
4.7
|
27.4
|
1.0
|
DB3
|
A:ASP159
|
4.8
|
26.0
|
1.0
|
CD1
|
A:TRP161
|
4.8
|
27.6
|
1.0
|
CH2
|
A:TRP123
|
4.9
|
26.2
|
1.0
|
DE21
|
A:GLN143
|
4.9
|
25.7
|
1.0
|
DD1
|
A:TRP161
|
5.0
|
28.9
|
1.0
|
DB2
|
A:HIS30
|
5.0
|
29.4
|
1.0
|
|
Manganese binding site 2 out
of 2 in 9bwm
Go back to
Manganese Binding Sites List in 9bwm
Manganese binding site 2 out
of 2 in the Neutron Structure of Oxidized TYR34PHE Mnsod
 Mono view
 Stereo pair view
|
A full contact list of Manganese with other atoms in the Mn binding
site number 2 of Neutron Structure of Oxidized TYR34PHE Mnsod within 5.0Å range:
probe
|
atom
|
residue
|
distance (Å)
|
B
|
Occ
|
B:Mn201
b:33.4
occ:1.00
|
O
|
B:HOH314
|
1.9
|
24.8
|
1.0
|
NE2
|
B:HIS26
|
2.1
|
27.5
|
1.0
|
NE2
|
B:HIS74
|
2.1
|
26.5
|
1.0
|
NE2
|
B:HIS163
|
2.1
|
24.2
|
1.0
|
OD2
|
B:ASP159
|
2.2
|
24.5
|
1.0
|
D1
|
B:HOH314
|
2.4
|
23.0
|
1.0
|
CE1
|
B:HIS26
|
3.0
|
25.8
|
1.0
|
CD2
|
B:HIS26
|
3.0
|
25.3
|
1.0
|
CE1
|
B:HIS74
|
3.0
|
26.4
|
1.0
|
CE1
|
B:HIS163
|
3.1
|
25.6
|
1.0
|
CD2
|
B:HIS74
|
3.1
|
26.1
|
1.0
|
CD2
|
B:HIS163
|
3.2
|
27.3
|
1.0
|
DE1
|
B:HIS163
|
3.2
|
28.0
|
1.0
|
DE1
|
B:HIS74
|
3.2
|
27.9
|
1.0
|
DD2
|
B:HIS26
|
3.3
|
25.5
|
1.0
|
CG
|
B:ASP159
|
3.3
|
24.3
|
1.0
|
DE1
|
B:HIS26
|
3.3
|
25.0
|
1.0
|
DD2
|
B:HIS74
|
3.4
|
24.9
|
1.0
|
DD2
|
B:HIS163
|
3.4
|
27.0
|
1.0
|
DB2
|
B:TRP161
|
3.5
|
25.0
|
1.0
|
DE22
|
B:GLN143
|
3.5
|
24.6
|
1.0
|
OD1
|
B:ASP159
|
3.7
|
24.7
|
1.0
|
DZ2
|
B:TRP123
|
3.7
|
25.6
|
1.0
|
DB2
|
B:ALA164
|
4.0
|
23.2
|
1.0
|
ND1
|
B:HIS26
|
4.1
|
25.1
|
1.0
|
CG
|
B:HIS26
|
4.1
|
24.2
|
1.0
|
ND1
|
B:HIS74
|
4.2
|
24.3
|
1.0
|
ND1
|
B:HIS163
|
4.2
|
22.8
|
1.0
|
CG
|
B:HIS74
|
4.2
|
25.6
|
1.0
|
CG
|
B:HIS163
|
4.3
|
25.2
|
1.0
|
CB
|
B:TRP161
|
4.4
|
23.6
|
1.0
|
CZ2
|
B:TRP123
|
4.4
|
25.2
|
1.0
|
DE2
|
B:PHE34
|
4.4
|
26.7
|
1.0
|
NE2
|
B:GLN143
|
4.5
|
25.7
|
1.0
|
CG
|
B:TRP161
|
4.5
|
23.8
|
1.0
|
CB
|
B:ASP159
|
4.5
|
25.3
|
1.0
|
DB3
|
B:TRP161
|
4.6
|
22.2
|
1.0
|
DB2
|
B:ASP159
|
4.6
|
24.6
|
1.0
|
DB3
|
B:HIS30
|
4.7
|
29.5
|
1.0
|
DH2
|
B:TRP123
|
4.7
|
22.8
|
1.0
|
DB2
|
B:HIS30
|
4.8
|
28.3
|
1.0
|
CD1
|
B:TRP161
|
4.8
|
23.2
|
1.0
|
DB3
|
B:ASP159
|
4.8
|
24.4
|
1.0
|
DE21
|
B:GLN143
|
4.9
|
25.9
|
1.0
|
CH2
|
B:TRP123
|
4.9
|
22.2
|
1.0
|
DD1
|
B:TRP161
|
4.9
|
25.4
|
1.0
|
|
Reference:
J.Azadmanesh,
K.Slobodnik,
L.R.Struble,
J.J.Lovelace,
E.A.Cone,
M.Dasgupta,
W.E.Lutz,
S.Kumar,
A.Natarajan,
L.Coates,
K.L.Weiss,
D.A.A.Myles,
T.Kroll,
G.E.O.Borgstahl.
The Role of TYR34 in Proton Coupled Electron Transfer and Product Inhibition of Manganese Superoxide Dismutase. Nat Commun V. 16 1887 2025.
ISSN: ESSN 2041-1723
PubMed: 39987263
DOI: 10.1038/S41467-025-57180-3
Page generated: Sun Aug 17 02:10:27 2025
|