Atomistry » Calcium » PDB 1m9i-1mr8 » 1mn2
Atomistry »
  Calcium »
    PDB 1m9i-1mr8 »
      1mn2 »

Calcium in PDB 1mn2: Manganese Peroxidase Substrate Binding Site Mutant E35Q, D179N

Enzymatic activity of Manganese Peroxidase Substrate Binding Site Mutant E35Q, D179N

All present enzymatic activity of Manganese Peroxidase Substrate Binding Site Mutant E35Q, D179N:
1.11.1.13;

Protein crystallography data

The structure of Manganese Peroxidase Substrate Binding Site Mutant E35Q, D179N, PDB code: 1mn2 was solved by M.Sundaramoorthy, T.L.Poulos, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 8.00 / 2.00
Space group C 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 163.240, 45.970, 53.570, 90.00, 97.16, 90.00
R / Rfree (%) 18.7 / n/a

Other elements in 1mn2:

The structure of Manganese Peroxidase Substrate Binding Site Mutant E35Q, D179N also contains other interesting chemical elements:

Iron (Fe) 1 atom

Calcium Binding Sites:

The binding sites of Calcium atom in the Manganese Peroxidase Substrate Binding Site Mutant E35Q, D179N (pdb code 1mn2). This binding sites where shown within 5.0 Angstroms radius around Calcium atom.
In total 2 binding sites of Calcium where determined in the Manganese Peroxidase Substrate Binding Site Mutant E35Q, D179N, PDB code: 1mn2:
Jump to Calcium binding site number: 1; 2;

Calcium binding site 1 out of 2 in 1mn2

Go back to Calcium Binding Sites List in 1mn2
Calcium binding site 1 out of 2 in the Manganese Peroxidase Substrate Binding Site Mutant E35Q, D179N


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 1 of Manganese Peroxidase Substrate Binding Site Mutant E35Q, D179N within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Ca371

b:6.5
occ:1.00
O A:THR193 2.3 5.8 1.0
O A:SER174 2.3 4.5 1.0
OG A:SER174 2.4 7.6 1.0
OG1 A:THR193 2.4 4.9 1.0
O A:THR196 2.4 8.9 1.0
OD2 A:ASP191 2.5 3.5 1.0
OD1 A:ASP198 2.6 10.2 1.0
OD1 A:ASP191 2.9 6.4 1.0
CG A:ASP191 3.1 3.8 1.0
C A:THR193 3.2 6.2 1.0
C A:SER174 3.3 4.6 1.0
CB A:THR193 3.4 5.3 1.0
CB A:SER174 3.5 4.2 1.0
CG A:ASP198 3.6 9.3 1.0
C A:THR196 3.6 6.0 1.0
CA A:SER174 3.7 5.5 1.0
CA A:THR193 3.8 6.4 1.0
OD2 A:ASP198 4.1 8.4 1.0
N A:ASP198 4.1 7.6 1.0
N A:THR193 4.2 5.7 1.0
N A:PRO194 4.2 6.6 1.0
N A:THR196 4.4 6.0 1.0
CA A:THR196 4.4 8.2 1.0
N A:VAL175 4.5 6.6 1.0
CB A:THR196 4.5 8.2 1.0
O A:HOH424 4.5 9.9 1.0
O A:ASP198 4.6 7.6 1.0
CB A:ASP191 4.6 3.7 1.0
CB A:GLN200 4.6 7.1 1.0
CA A:PRO194 4.6 6.2 1.0
N A:PHE197 4.7 6.5 1.0
CG2 A:THR193 4.8 6.6 1.0
CB A:ASP198 4.8 7.3 1.0
CA A:ASP198 4.8 6.6 1.0
CA A:PHE197 4.9 6.1 1.0
CG1 A:VAL175 4.9 5.8 1.0
C A:ASP198 4.9 7.3 1.0
C A:PRO194 5.0 6.3 1.0

Calcium binding site 2 out of 2 in 1mn2

Go back to Calcium Binding Sites List in 1mn2
Calcium binding site 2 out of 2 in the Manganese Peroxidase Substrate Binding Site Mutant E35Q, D179N


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 2 of Manganese Peroxidase Substrate Binding Site Mutant E35Q, D179N within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Ca372

b:6.9
occ:1.00
O A:HOH545 2.2 9.9 1.0
O A:HOH493 2.3 4.8 1.0
O A:GLY62 2.5 6.4 1.0
OG A:SER66 2.5 8.0 1.0
O A:ASP47 2.5 4.8 1.0
OD1 A:ASP47 2.5 7.3 1.0
OD1 A:ASP64 2.6 7.2 1.0
C A:ASP47 3.4 5.7 1.0
CG A:ASP64 3.5 9.8 1.0
CG A:ASP47 3.6 8.4 1.0
C A:GLY62 3.6 6.6 1.0
CB A:SER66 3.7 5.4 1.0
CA A:ASP47 3.9 5.6 1.0
OD2 A:ASP64 3.9 10.3 1.0
O A:HOH495 4.0 9.2 1.0
N A:SER66 4.2 7.5 1.0
N A:ASP64 4.2 10.3 1.0
N A:GLY62 4.3 5.4 1.0
CB A:ALA50 4.3 6.3 1.0
CA A:GLY62 4.3 7.9 1.0
CB A:ASP47 4.4 6.0 1.0
O A:ALA50 4.4 8.1 1.0
OD2 A:ASP47 4.5 8.0 1.0
OE1 A:GLU74 4.5 9.3 1.0
CA A:SER66 4.6 7.8 1.0
OE2 A:GLU74 4.6 10.4 1.0
N A:ALA48 4.6 5.8 1.0
N A:GLY65 4.7 8.9 1.0
N A:ALA63 4.7 7.9 1.0
CB A:ASP64 4.8 9.7 1.0
CA A:ASP64 4.9 9.3 1.0
O A:HIS46 4.9 4.8 1.0
CA A:ALA63 5.0 9.0 1.0
C A:GLY61 5.0 6.4 1.0

Reference:

M.Sundaramoorthy, K.Kishi, M.H.Gold, T.L.Poulos. Crystal Structures of Substrate Binding Site Mutants of Manganese Peroxidase. J.Biol.Chem. V. 272 17574 1997.
ISSN: ISSN 0021-9258
PubMed: 9211904
DOI: 10.1074/JBC.272.28.17574
Page generated: Thu Jul 11 12:34:12 2024

Last articles

Zn in 9JPJ
Zn in 9JP7
Zn in 9JPK
Zn in 9JPL
Zn in 9GN6
Zn in 9GN7
Zn in 9GKU
Zn in 9GKW
Zn in 9GKX
Zn in 9GL0
© Copyright 2008-2020 by atomistry.com
Home   |    Site Map   |    Copyright   |    Contact us   |    Privacy