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Magnesium in PDB 5egy: Structure of Ligand Free Human DPP3 in Closed Form.

Enzymatic activity of Structure of Ligand Free Human DPP3 in Closed Form.

All present enzymatic activity of Structure of Ligand Free Human DPP3 in Closed Form.:
3.4.14.4;

Protein crystallography data

The structure of Structure of Ligand Free Human DPP3 in Closed Form., PDB code: 5egy was solved by P.Kumar, V.Reithofer, M.Reisinger, T.Pavkov-Keller, S.Wallner, P.Macheroux, K.Gruber, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 43.83 / 2.74
Space group C 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 119.190, 106.206, 62.572, 90.00, 91.81, 90.00
R / Rfree (%) 20.7 / 25.4

Other elements in 5egy:

The structure of Structure of Ligand Free Human DPP3 in Closed Form. also contains other interesting chemical elements:

Zinc (Zn) 1 atom

Magnesium Binding Sites:

The binding sites of Magnesium atom in the Structure of Ligand Free Human DPP3 in Closed Form. (pdb code 5egy). This binding sites where shown within 5.0 Angstroms radius around Magnesium atom.
In total only one binding site of Magnesium was determined in the Structure of Ligand Free Human DPP3 in Closed Form., PDB code: 5egy:

Magnesium binding site 1 out of 1 in 5egy

Go back to Magnesium Binding Sites List in 5egy
Magnesium binding site 1 out of 1 in the Structure of Ligand Free Human DPP3 in Closed Form.


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 1 of Structure of Ligand Free Human DPP3 in Closed Form. within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg802

b:65.8
occ:1.00
O A:GLY164 2.4 81.0 1.0
O A:GLY167 2.9 71.0 1.0
O A:GLY162 3.2 68.3 1.0
C A:GLY167 3.5 72.1 1.0
C A:GLY164 3.5 80.7 1.0
N A:GLY164 3.6 75.7 1.0
C A:LEU163 3.9 72.3 1.0
O A:GLY174 4.0 78.2 1.0
N A:ILE168 4.1 74.8 1.0
CA A:LEU163 4.1 69.5 1.0
CA A:GLY164 4.1 79.0 1.0
CA A:ILE168 4.1 68.8 1.0
C A:GLY162 4.3 68.9 1.0
CA A:GLY167 4.3 72.1 1.0
N A:GLY167 4.4 83.0 1.0
N A:THR169 4.5 69.8 1.0
CG2 A:THR169 4.6 69.5 1.0
N A:LYS165 4.6 81.5 1.0
C A:ILE168 4.6 68.3 1.0
O A:LEU163 4.6 77.0 1.0
N A:LEU163 4.7 79.9 1.0
C A:GLY174 4.7 72.7 1.0
CA A:GLY174 4.7 69.6 1.0
O A:CYS176 4.8 78.9 1.0
CA A:LYS165 4.9 81.9 1.0

Reference:

P.Kumar, V.Reithofer, M.Reisinger, S.Wallner, T.Pavkov-Keller, P.Macheroux, K.Gruber. Substrate Complexes of Human Dipeptidyl Peptidase III Reveal the Mechanism of Enzyme Inhibition. Sci Rep V. 6 23787 2016.
ISSN: ESSN 2045-2322
PubMed: 27025154
DOI: 10.1038/SREP23787
Page generated: Tue Aug 12 07:46:36 2025

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