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Manganese in PDB 8qfn: Ergothioneine Dioxygenase From Thermocatellispora Tengchongensis in Complex with Manganese and in Presence of Catalase Aerobic

Protein crystallography data

The structure of Ergothioneine Dioxygenase From Thermocatellispora Tengchongensis in Complex with Manganese and in Presence of Catalase Aerobic, PDB code: 8qfn was solved by C.M.Vasseur, F.P.Seebeck, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 44.45 / 1.75
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 44.507, 59.209, 134.572, 90, 90, 90
R / Rfree (%) 18.8 / 22.5

Other elements in 8qfn:

The structure of Ergothioneine Dioxygenase From Thermocatellispora Tengchongensis in Complex with Manganese and in Presence of Catalase Aerobic also contains other interesting chemical elements:

Magnesium (Mg) 1 atom

Manganese Binding Sites:

The binding sites of Manganese atom in the Ergothioneine Dioxygenase From Thermocatellispora Tengchongensis in Complex with Manganese and in Presence of Catalase Aerobic (pdb code 8qfn). This binding sites where shown within 5.0 Angstroms radius around Manganese atom.
In total 2 binding sites of Manganese where determined in the Ergothioneine Dioxygenase From Thermocatellispora Tengchongensis in Complex with Manganese and in Presence of Catalase Aerobic, PDB code: 8qfn:
Jump to Manganese binding site number: 1; 2;

Manganese binding site 1 out of 2 in 8qfn

Go back to Manganese Binding Sites List in 8qfn
Manganese binding site 1 out of 2 in the Ergothioneine Dioxygenase From Thermocatellispora Tengchongensis in Complex with Manganese and in Presence of Catalase Aerobic


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 1 of Ergothioneine Dioxygenase From Thermocatellispora Tengchongensis in Complex with Manganese and in Presence of Catalase Aerobic within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mn207

b:21.1
occ:1.00
NE2 A:HIS134 2.1 25.3 1.0
NE2 A:HIS90 2.1 22.3 1.0
O A:HOH337 2.1 26.1 1.0
NE2 A:HIS88 2.1 25.2 1.0
O A:ACT201 2.1 26.4 0.9
O A:HOH342 2.3 24.4 1.0
CE1 A:HIS134 3.0 24.7 1.0
CE1 A:HIS90 3.0 24.0 1.0
CE1 A:HIS88 3.1 25.1 1.0
HE1 A:HIS134 3.1 29.6 1.0
HE1 A:HIS90 3.1 28.9 1.0
CD2 A:HIS88 3.1 25.9 1.0
CD2 A:HIS90 3.2 23.3 1.0
CD2 A:HIS134 3.2 25.7 1.0
C A:ACT201 3.2 27.9 0.9
HE1 A:HIS88 3.2 30.1 1.0
HD2 A:HIS88 3.3 31.2 1.0
HD2 A:HIS90 3.4 28.0 1.0
HD2 A:HIS134 3.4 30.9 1.0
O A:HOH385 3.4 39.0 1.0
OXT A:ACT201 3.5 27.4 0.9
HE1 A:TYR149 3.8 29.5 1.0
HZ A:PHE128 4.0 32.3 1.0
OH A:TYR149 4.0 26.6 1.0
ND1 A:HIS134 4.1 24.1 1.0
ND1 A:HIS90 4.1 25.6 1.0
ND1 A:HIS88 4.2 25.8 1.0
CG A:HIS134 4.2 20.6 1.0
CG A:HIS88 4.2 24.8 1.0
CG A:HIS90 4.3 24.3 1.0
CH3 A:ACT201 4.5 25.9 0.9
CE1 A:TYR149 4.6 24.5 1.0
HH A:TYR149 4.6 32.0 1.0
CZ A:PHE128 4.7 26.9 1.0
HD12 A:LEU136 4.7 32.2 1.0
H2 A:ACT201 4.8 31.1 0.9
CZ A:TYR149 4.8 26.0 1.0
HG A:LEU136 4.8 33.9 1.0
HD11 A:LEU136 4.9 32.2 1.0
HD1 A:HIS134 4.9 28.9 1.0
HG21 A:THR85 4.9 35.7 1.0
HD1 A:HIS90 4.9 30.8 1.0
HD1 A:HIS88 5.0 30.9 1.0

Manganese binding site 2 out of 2 in 8qfn

Go back to Manganese Binding Sites List in 8qfn
Manganese binding site 2 out of 2 in the Ergothioneine Dioxygenase From Thermocatellispora Tengchongensis in Complex with Manganese and in Presence of Catalase Aerobic


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 2 of Ergothioneine Dioxygenase From Thermocatellispora Tengchongensis in Complex with Manganese and in Presence of Catalase Aerobic within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Mn202

b:21.5
occ:1.00
O B:HOH352 2.0 30.5 1.0
NE2 B:HIS90 2.1 21.7 1.0
NE2 B:HIS134 2.1 26.1 1.0
O B:ACT201 2.1 28.7 1.0
NE2 B:HIS88 2.1 22.7 1.0
O B:HOH326 2.2 26.3 1.0
CE1 B:HIS90 3.0 25.5 1.0
CE1 B:HIS134 3.0 28.3 1.0
CD2 B:HIS88 3.1 25.2 1.0
CD2 B:HIS90 3.1 24.1 1.0
CE1 B:HIS88 3.1 27.7 1.0
HE1 B:HIS134 3.2 33.9 1.0
C B:ACT201 3.2 31.1 1.0
HE1 B:HIS90 3.2 30.6 1.0
CD2 B:HIS134 3.2 24.6 1.0
HD2 B:HIS88 3.3 30.2 1.0
HE1 B:HIS88 3.3 33.2 1.0
HD2 B:HIS90 3.3 29.0 1.0
HD2 B:HIS134 3.4 29.6 1.0
O B:HOH381 3.5 44.8 1.0
OXT B:ACT201 3.5 27.8 1.0
HE1 B:TYR149 3.7 28.5 1.0
HZ B:PHE128 3.9 31.8 1.0
OH B:TYR149 4.1 29.9 1.0
ND1 B:HIS90 4.2 25.4 1.0
ND1 B:HIS134 4.2 25.5 1.0
ND1 B:HIS88 4.2 26.5 1.0
CG B:HIS90 4.2 24.3 1.0
CG B:HIS88 4.3 25.1 1.0
CG B:HIS134 4.3 24.2 1.0
HD12 B:LEU136 4.5 36.1 1.0
CE1 B:TYR149 4.5 23.7 1.0
CH3 B:ACT201 4.5 27.3 1.0
CZ B:PHE128 4.7 26.4 1.0
HH B:TYR149 4.7 35.9 1.0
H2 B:ACT201 4.8 32.8 1.0
CZ B:TYR149 4.8 29.9 1.0
H1 B:ACT201 4.9 32.8 1.0
HG21 B:THR85 4.9 41.4 1.0
HD1 B:HIS90 4.9 30.6 1.0
HD1 B:HIS134 4.9 30.6 1.0
HG B:LEU136 5.0 39.4 1.0

Reference:

E.Nalivaiko, C.M.Vasseur, F.P.Seebeck. Enzyme-Catalyzed Oxidative Degradation of Ergothioneine. Angew.Chem.Int.Ed.Engl. 18445 2023.
ISSN: ESSN 1521-3773
PubMed: 38095354
DOI: 10.1002/ANIE.202318445
Page generated: Sun Oct 6 13:40:48 2024

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