Manganese in PDB 4hov: Dypb N246A in Complex with Manganese

The structure of Dypb N246A in Complex with Manganese, PDB code: 4hov was solved by J.C.Grigg, R.Singh, L.D.Eltis, M.E.P.Murphy, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å)	41.56 / 2.20
Space group	P 32 2 1
Cell size a, b, c (Å), α, β, γ (°)	132.960, 132.960, 159.502, 90.00, 90.00, 120.00
R / Rfree (%)	16.7 / 19.5

The structure of Dypb N246A in Complex with Manganese also contains other interesting chemical elements:

Iron	(Fe)	3 atoms
Chlorine	(Cl)	3 atoms

The binding sites of Manganese atom in the Dypb N246A in Complex with Manganese (pdb code 4hov). This binding sites where shown within 5.0 Angstroms radius around Manganese atom.
In total 3 binding sites of Manganese where determined in the Dypb N246A in Complex with Manganese, PDB code: 4hov:
Jump to Manganese binding site number: 1; 2; 3;

Manganese binding site 1 out of 3 in the Dypb N246A in Complex with Manganese


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 1 of Dypb N246A in Complex with Manganese within 5.0Å range: probe atom residue distance (Å) B Occ A:Mn404 b:43.7 occ:0.60 O A:HOH643 1.8 47.5 1.0 O A:HOH645 1.9 45.2 1.0 O A:HOH642 2.1 26.9 1.0 O A:HOH644 2.3 49.0 1.0 O A:HOH646 2.4 41.0 1.0 OE1 A:GLU215 4.0 47.6 1.0 O2D A:HEM401 4.0 28.1 1.0 O1D A:HEM401 4.1 27.5 1.0 OE2 A:GLU239 4.2 44.5 1.0 O A:HOH654 4.3 48.8 1.0 OE2 A:GLU215 4.5 48.7 1.0 CGD A:HEM401 4.5 28.1 1.0 OE1 A:GLU239 4.5 40.9 1.0 OG1 A:THR231 4.6 29.9 1.0 CD A:GLU215 4.6 42.5 1.0 OE1 A:GLU156 4.7 46.4 1.0 O A:HOH722 4.7 63.9 1.0 CD A:GLU239 4.8 43.2 1.0 CD A:GLU156 5.0 38.8 1.0

Manganese binding site 2 out of 3 in the Dypb N246A in Complex with Manganese


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 2 of Dypb N246A in Complex with Manganese within 5.0Å range: probe atom residue distance (Å) B Occ B:Mn403 b:49.8 occ:0.60 O B:HOH648 2.0 47.9 0.6 O B:HOH645 2.0 41.7 0.6 O B:HOH643 2.2 53.6 1.0 O B:HOH644 2.2 60.3 1.0 O B:HOH642 2.3 36.3 1.0 O B:HOH673 3.4 58.8 1.0 OE2 B:GLU239 4.2 56.1 1.0 O1D B:HEM401 4.2 27.6 1.0 O2D B:HEM401 4.2 28.1 1.0 OE1 B:GLU215 4.3 56.3 1.0 OE1 B:GLU156 4.5 47.6 1.0 OE2 B:GLU215 4.5 58.3 1.0 OE1 B:GLU239 4.6 50.1 1.0 CGD B:HEM401 4.7 27.5 1.0 OG1 B:THR231 4.7 37.5 1.0 CD B:GLU239 4.8 52.5 1.0 CD B:GLU215 4.8 52.0 1.0 CD B:GLU156 4.9 38.5 1.0 CG2 B:THR231 4.9 34.8 1.0

Manganese binding site 3 out of 3 in the Dypb N246A in Complex with Manganese


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 3 of Dypb N246A in Complex with Manganese within 5.0Å range: probe atom residue distance (Å) B Occ C:Mn403 b:53.0 occ:0.60 O C:HOH590 1.9 48.9 0.6 O C:HOH588 2.2 53.7 1.0 O C:HOH587 2.2 35.8 1.0 O C:HOH589 2.2 43.4 0.6 O C:HOH586 2.4 53.3 1.0 OE1 C:GLU215 4.0 53.5 1.0 O1D C:HEM401 4.2 32.5 1.0 O2D C:HEM401 4.3 31.8 1.0 OE2 C:GLU239 4.3 65.3 1.0 OE2 C:GLU215 4.3 59.0 1.0 CD C:GLU215 4.6 51.7 1.0 OE1 C:GLU156 4.6 54.4 1.0 CGD C:HEM401 4.7 31.4 1.0 OG1 C:THR231 4.8 40.6 1.0 OE1 C:GLU239 4.8 59.9 1.0 CD C:GLU156 4.9 44.4 1.0 CD C:GLU239 5.0 60.6 1.0

R.Singh, J.C.Grigg, W.Qin, J.F.Kadla, M.E.Murphy, L.D.Eltis. Improved Manganese-Oxidizing Activity of Dypb, A Peroxidase From A Lignolytic Bacterium. Acs Chem.Biol. V. 8 700 2013.
ISSN: ISSN 1554-8929
PubMed: 23305326
DOI: 10.1021/CB300608X