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Potassium in PDB 5amm: Structure of Leishmania Major Peroxidase D211N Mutant

Enzymatic activity of Structure of Leishmania Major Peroxidase D211N Mutant

All present enzymatic activity of Structure of Leishmania Major Peroxidase D211N Mutant:
1.11.1.11; 1.11.1.5;

Protein crystallography data

The structure of Structure of Leishmania Major Peroxidase D211N Mutant, PDB code: 5amm was solved by G.Chreifi, J.B.Fields, S.A.Hollingsworth, M.Heyden, A.P.Arce, H.I.Magana-Garcia, T.L.Poulos, D.J.Tobias, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 50.00 / 2.09
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 46.249, 78.310, 160.977, 90.00, 90.00, 90.00
R / Rfree (%) 18.418 / 24.455

Other elements in 5amm:

The structure of Structure of Leishmania Major Peroxidase D211N Mutant also contains other interesting chemical elements:

Iron (Fe) 2 atoms
Calcium (Ca) 2 atoms

Potassium Binding Sites:

The binding sites of Potassium atom in the Structure of Leishmania Major Peroxidase D211N Mutant (pdb code 5amm). This binding sites where shown within 5.0 Angstroms radius around Potassium atom.
In total 2 binding sites of Potassium where determined in the Structure of Leishmania Major Peroxidase D211N Mutant, PDB code: 5amm:
Jump to Potassium binding site number: 1; 2;

Potassium binding site 1 out of 2 in 5amm

Go back to Potassium Binding Sites List in 5amm
Potassium binding site 1 out of 2 in the Structure of Leishmania Major Peroxidase D211N Mutant


Mono view


Stereo pair view

A full contact list of Potassium with other atoms in the K binding site number 1 of Structure of Leishmania Major Peroxidase D211N Mutant within 5.0Å range:
probe atom residue distance (Å) B Occ
A:K306

b:68.1
occ:1.00
O A:THR193 2.3 49.4 1.0
O A:ASN211 2.4 59.8 1.0
O A:GLY214 2.5 56.1 1.0
OG1 A:THR193 2.7 52.2 1.0
OG1 A:THR209 2.9 56.3 1.0
C A:THR193 3.2 50.6 1.0
C A:ASN211 3.4 60.9 1.0
OG A:SER218 3.5 73.4 1.0
C A:GLY214 3.6 54.7 1.0
CB A:THR193 3.7 49.9 1.0
CA A:THR193 3.8 48.1 1.0
CB A:THR209 3.9 57.3 1.0
CG2 A:THR209 4.1 54.4 1.0
OD1 A:ASP216 4.1 57.1 1.0
N A:GLY214 4.1 60.2 1.0
N A:CYS194 4.2 45.3 1.0
CA A:GLY214 4.2 58.1 1.0
CG2 A:THR193 4.3 50.3 1.0
N A:LYS212 4.3 61.0 1.0
CA A:ASN211 4.3 65.3 1.0
CB A:ASN211 4.4 71.8 1.0
CA A:CYS194 4.4 47.8 1.0
CA A:LYS212 4.4 58.1 1.0
N A:ASN211 4.6 65.7 1.0
N A:PHE215 4.6 50.4 1.0
C A:LYS212 4.7 55.7 1.0
CB A:CYS194 4.8 49.4 1.0
N A:ASP216 4.9 50.8 1.0
CB A:SER218 4.9 60.4 1.0
CA A:PHE215 4.9 52.6 1.0
N A:ASN213 4.9 58.0 1.0
CG A:ASN211 5.0 75.7 1.0

Potassium binding site 2 out of 2 in 5amm

Go back to Potassium Binding Sites List in 5amm
Potassium binding site 2 out of 2 in the Structure of Leishmania Major Peroxidase D211N Mutant


Mono view


Stereo pair view

A full contact list of Potassium with other atoms in the K binding site number 2 of Structure of Leishmania Major Peroxidase D211N Mutant within 5.0Å range:
probe atom residue distance (Å) B Occ
B:K307

b:85.5
occ:1.00
O B:THR193 2.4 62.9 1.0
O B:ASN211 2.4 69.2 1.0
O B:GLY214 2.7 72.8 1.0
OG1 B:THR209 3.0 63.8 1.0
OG1 B:THR193 3.1 64.3 1.0
C B:THR193 3.4 61.9 1.0
C B:ASN211 3.5 74.5 1.0
C B:GLY214 3.7 72.1 1.0
OG B:SER218 3.7 84.5 1.0
CB B:THR209 3.9 63.3 1.0
CB B:THR193 4.0 58.8 1.0
CA B:THR193 4.1 55.5 1.0
OD1 B:ASP216 4.2 74.6 1.0
N B:GLY214 4.2 74.0 1.0
CA B:ASN211 4.3 78.2 1.0
N B:CYS194 4.3 56.9 1.0
CG2 B:THR209 4.3 62.9 1.0
CA B:GLY214 4.3 73.9 1.0
CB B:ASN211 4.4 83.2 1.0
CG2 B:THR193 4.4 58.4 1.0
CA B:CYS194 4.4 61.7 1.0
N B:LYS212 4.4 71.2 1.0
N B:ASN211 4.5 73.0 1.0
CA B:LYS212 4.6 69.4 1.0
N B:PHE215 4.6 68.7 1.0
N B:ASP216 4.7 69.5 1.0
C B:LYS212 4.7 68.1 1.0
CA B:PHE215 4.8 69.2 1.0
CB B:CYS194 4.8 66.0 1.0
CG B:ASP216 4.9 73.4 1.0
O B:LYS212 5.0 67.9 1.0

Reference:

J.B.Fields, S.A.Hollingsworth, G.Chreifi, M.Heyden, A.P.Arce, H.I.Magana-Garcia, T.L.Poulos, D.J.Tobias. "Bind and Crawl" Association Mechanism of Leishmania Major Peroxidase and Cytochrome C Revealed By Brownian and Molecular Dynamics Simulations. Biochemistry V. 54 7272 2015.
ISSN: ISSN 0006-2960
PubMed: 26598276
DOI: 10.1021/ACS.BIOCHEM.5B00569
Page generated: Mon Aug 12 12:54:50 2024

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