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Calcium in PDB 5al9: Structure of Leishmania Major Peroxidase D211R Mutant (High Res)

Enzymatic activity of Structure of Leishmania Major Peroxidase D211R Mutant (High Res)

All present enzymatic activity of Structure of Leishmania Major Peroxidase D211R Mutant (High Res):
1.11.1.5;

Protein crystallography data

The structure of Structure of Leishmania Major Peroxidase D211R Mutant (High Res), PDB code: 5al9 was solved by G.Chreifi, S.A.Hollingsworth, H.Li, S.Tripathi, A.P.Arce, H.I.Magana-Garcia, T.L.Poulos, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 36.511 / 1.37
Space group C 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 142.439, 57.860, 36.620, 90.00, 97.59, 90.00
R / Rfree (%) 18.48 / 20.37

Other elements in 5al9:

The structure of Structure of Leishmania Major Peroxidase D211R Mutant (High Res) also contains other interesting chemical elements:

Potassium (K) 1 atom
Iron (Fe) 1 atom

Calcium Binding Sites:

The binding sites of Calcium atom in the Structure of Leishmania Major Peroxidase D211R Mutant (High Res) (pdb code 5al9). This binding sites where shown within 5.0 Angstroms radius around Calcium atom.
In total only one binding site of Calcium was determined in the Structure of Leishmania Major Peroxidase D211R Mutant (High Res), PDB code: 5al9:

Calcium binding site 1 out of 1 in 5al9

Go back to Calcium Binding Sites List in 5al9
Calcium binding site 1 out of 1 in the Structure of Leishmania Major Peroxidase D211R Mutant (High Res)


Mono view


Stereo pair view

A full contact list of Calcium with other atoms in the Ca binding site number 1 of Structure of Leishmania Major Peroxidase D211R Mutant (High Res) within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Ca307

b:46.5
occ:1.00
O A:HOH2059 2.3 24.5 1.0
O A:HOH2060 2.4 25.4 1.0
OG A:SER72 2.6 23.6 1.0
OE2 A:GLU92 2.7 20.4 1.0
O A:GLU69 2.7 11.1 1.0
OE2 A:GLU69 3.2 12.7 1.0
OG A:SER86 3.2 17.0 1.0
CB A:SER72 3.4 23.3 1.0
CD A:GLU69 3.4 12.5 1.0
O A:HOH2061 3.4 27.0 1.0
OE1 A:GLU69 3.4 13.4 1.0
C A:GLU69 3.5 8.9 1.0
CD A:GLU92 3.5 18.7 1.0
OE1 A:GLU92 3.7 20.8 1.0
O A:SER81 3.7 14.7 1.0
CA A:GLU69 3.8 7.7 1.0
O A:GLY80 3.8 19.1 1.0
O A:HIS68 4.1 9.6 1.0
O A:HOH2056 4.2 15.4 1.0
CA A:PRO82 4.2 11.5 1.0
CG A:GLU69 4.3 10.6 1.0
C A:SER81 4.4 14.9 1.0
N A:SER72 4.6 13.7 1.0
CB A:SER86 4.6 15.1 1.0
CA A:SER72 4.6 17.3 1.0
N A:PRO82 4.6 12.0 1.0
CB A:GLU69 4.6 9.4 1.0
N A:ALA70 4.7 8.7 1.0
N A:ASN83 4.8 9.7 1.0
OG A:SER81 4.9 28.0 1.0
N A:GLU69 4.9 6.8 1.0
C A:PRO82 4.9 9.9 1.0
C A:HIS68 4.9 7.5 1.0
CG A:GLU92 5.0 15.0 1.0
N A:MET87 5.0 11.0 1.0

Reference:

G.Chreifi, S.A.Hollingsworth, H.Li, S.Tripathi, A.P.Arce, H.I.Magana-Garcia, T.L.Poulos. Enzymatic Mechanism of Leishmania Major Peroxidase and the Critical Role of Specific Ionic Interactions. Biochemistry 2015.
ISSN: ESSN 1520-4995
PubMed: 25941976
DOI: 10.1021/ACS.BIOCHEM.5B00338
Page generated: Sat Dec 12 05:17:30 2020

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