Zinc in PDB 7aq5: Pseudomonas Stutzeri Nitrous Oxide Reductase Mutant, H583N

All present enzymatic activity of Pseudomonas Stutzeri Nitrous Oxide Reductase Mutant, H583N:
1.7.2.4;

The structure of Pseudomonas Stutzeri Nitrous Oxide Reductase Mutant, H583N, PDB code: 7aq5 was solved by L.Zhang, E.Bill, P.M.H.Kroneck, O.Einsle, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	62.65 / 1.70
Space group	P 1 21 1
Cell size a, b, c (Å), α, β, γ (°)	69.289, 76.452, 109.485, 90, 93.38, 90
R / Rfree (%)	16.1 / 19.9

The structure of Pseudomonas Stutzeri Nitrous Oxide Reductase Mutant, H583N also contains other interesting chemical elements:

Chlorine	(Cl)	3 atoms
Copper	(Cu)	8 atoms
Sodium	(Na)	2 atoms
Potassium	(K)	1 atom
Calcium	(Ca)	2 atoms

The binding sites of Zinc atom in the Pseudomonas Stutzeri Nitrous Oxide Reductase Mutant, H583N (pdb code 7aq5). This binding sites where shown within 5.0 Angstroms radius around Zinc atom.
In total 2 binding sites of Zinc where determined in the Pseudomonas Stutzeri Nitrous Oxide Reductase Mutant, H583N, PDB code: 7aq5:
Jump to Zinc binding site number: 1; 2;

Zinc binding site 1 out of 2 in the Pseudomonas Stutzeri Nitrous Oxide Reductase Mutant, H583N


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 1 of Pseudomonas Stutzeri Nitrous Oxide Reductase Mutant, H583N within 5.0Å range: probe atom residue distance (Å) B Occ A:Zn709 b:82.3 occ:1.00 NE2 A:HIS326 2.2 53.6 1.0 NE2 A:HIS382 2.3 37.9 1.0 O A:HOH1033 2.6 40.6 1.0 O A:HOH1154 2.6 54.9 1.0 CD2 A:HIS326 3.0 44.8 1.0 CE1 A:HIS326 3.2 47.3 1.0 CD2 A:HIS382 3.2 38.7 1.0 CE1 A:HIS382 3.2 38.3 1.0 ZN A:ZN711 3.3 50.9 1.0 NE2 A:HIS433 3.4 43.6 1.0 CD2 A:HIS433 3.6 47.5 1.0 CE1 A:HIS494 3.7 53.0 1.0 NE2 A:HIS494 3.7 39.7 1.0 CG A:HIS326 4.2 39.8 1.0 ND1 A:HIS326 4.3 49.0 1.0 CE1 A:HIS433 4.3 42.1 1.0 ND1 A:HIS382 4.3 39.2 1.0 CG A:HIS382 4.4 39.4 1.0 ND2 A:ASN241 4.5 41.4 1.0 CE B:MET627 4.5 97.3 1.0 CG A:HIS433 4.6 38.3 1.0 ND1 A:HIS494 4.9 52.3 1.0 ND1 A:HIS433 4.9 41.1 1.0 CD2 A:HIS494 5.0 53.5 1.0

Zinc binding site 2 out of 2 in the Pseudomonas Stutzeri Nitrous Oxide Reductase Mutant, H583N


Mono view


Stereo pair view

A full contact list of Zinc with other atoms in the Zn binding site number 2 of Pseudomonas Stutzeri Nitrous Oxide Reductase Mutant, H583N within 5.0Å range: probe atom residue distance (Å) B Occ A:Zn711 b:50.9 occ:1.00 NE2 A:HIS433 2.2 43.6 1.0 NE2 A:HIS130 2.2 32.4 1.0 O A:HOH1033 2.4 40.6 1.0 NE2 A:HIS494 2.4 39.7 1.0 CD2 A:HIS494 3.0 53.5 1.0 CD2 A:HIS433 3.0 47.5 1.0 CE1 A:HIS130 3.2 26.6 1.0 CD2 A:HIS130 3.2 23.5 1.0 CE1 A:HIS433 3.3 42.1 1.0 ZN A:ZN709 3.3 82.3 1.0 CE1 A:HIS494 3.4 53.0 1.0 OD1 A:ASN241 4.0 42.7 1.0 CG A:HIS494 4.1 46.5 1.0 CE1 A:HIS178 4.1 54.1 1.0 NE2 A:HIS178 4.1 53.7 1.0 NE2 A:HIS382 4.1 37.9 1.0 CG A:HIS433 4.2 38.3 1.0 ND1 A:HIS494 4.3 52.3 1.0 ND1 A:HIS130 4.3 29.0 1.0 ND1 A:HIS433 4.3 41.1 1.0 CG A:HIS130 4.3 30.6 1.0 CE1 A:HIS382 4.4 38.3 1.0 CB A:HIS129 4.4 23.9 1.0 O A:HOH881 4.5 58.6 1.0 CG A:ASN241 4.8 33.8 1.0 NE2 A:HIS326 4.8 53.6 1.0 ND2 A:ASN241 4.8 41.4 1.0 CE B:MET627 4.9 97.3 1.0 O A:HOH1154 4.9 54.9 1.0 CD2 A:HIS129 5.0 32.5 1.0

L.Zhang, E.Bill, P.M.H.Kroneck, O.Einsle. Histidine-Gated Proton-Coupled Electron Transfer to the Cu A Site of Nitrous Oxide Reductase. J.Am.Chem.Soc. 2020.
ISSN: ESSN 1520-5126
PubMed: 33377777
DOI: 10.1021/JACS.0C10057