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Magnesium in PDB 4unf: Crystal Structure of Deinococcus Radiodurans Endonuclease III-1

Enzymatic activity of Crystal Structure of Deinococcus Radiodurans Endonuclease III-1

All present enzymatic activity of Crystal Structure of Deinococcus Radiodurans Endonuclease III-1:
4.2.99.18;

Protein crystallography data

The structure of Crystal Structure of Deinococcus Radiodurans Endonuclease III-1, PDB code: 4unf was solved by A.Sarre, M.Okvist, T.Klar, D.Hall, A.O.Smalas, S.Mcsweeney, J.Timmins, E.Moe, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 34.192 / 2.15
Space group C 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 181.380, 38.558, 37.094, 90.00, 89.34, 90.00
R / Rfree (%) 15.31 / 19.43

Other elements in 4unf:

The structure of Crystal Structure of Deinococcus Radiodurans Endonuclease III-1 also contains other interesting chemical elements:

Iron (Fe) 4 atoms

Magnesium Binding Sites:

The binding sites of Magnesium atom in the Crystal Structure of Deinococcus Radiodurans Endonuclease III-1 (pdb code 4unf). This binding sites where shown within 5.0 Angstroms radius around Magnesium atom.
In total 2 binding sites of Magnesium where determined in the Crystal Structure of Deinococcus Radiodurans Endonuclease III-1, PDB code: 4unf:
Jump to Magnesium binding site number: 1; 2;

Magnesium binding site 1 out of 2 in 4unf

Go back to Magnesium Binding Sites List in 4unf
Magnesium binding site 1 out of 2 in the Crystal Structure of Deinococcus Radiodurans Endonuclease III-1


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 1 of Crystal Structure of Deinococcus Radiodurans Endonuclease III-1 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg1249

b:60.5
occ:1.00
O A:ALA118 2.3 61.7 1.0
O A:GLY121 2.3 66.1 1.0
O A:ILE115 2.4 59.5 1.0
O A:HOH2067 2.5 86.5 1.0
O A:GLY120 2.6 59.4 1.0
O A:LYS116 2.7 60.5 1.0
C A:LYS116 3.1 59.2 1.0
C A:ALA118 3.1 63.2 1.0
C A:GLY120 3.2 62.7 1.0
CA A:LYS116 3.4 55.2 1.0
C A:GLY121 3.4 69.2 1.0
C A:ILE115 3.5 53.5 1.0
N A:ALA118 3.5 62.2 1.0
O A:HOH2068 3.5 55.5 1.0
CA A:ALA118 3.7 62.7 1.0
N A:GLY121 3.7 62.4 1.0
CA A:GLY121 3.8 68.2 1.0
N A:LYS116 3.9 54.3 1.0
C A:PRO119 4.0 65.8 1.0
CB A:ALA118 4.0 52.3 1.0
O A:PRO119 4.0 63.6 1.0
N A:GLY120 4.1 59.5 1.0
CA A:GLY120 4.1 59.8 1.0
N A:ALA117 4.1 60.8 1.0
N A:PRO119 4.2 67.1 1.0
C A:ALA117 4.3 63.7 1.0
CA A:PRO119 4.5 71.3 1.0
O A:ASP123 4.6 57.3 1.0
N A:TYR122 4.6 65.9 1.0
N A:ASP123 4.7 57.4 1.0
CB A:LYS116 4.8 51.8 1.0
CA A:ALA117 4.8 64.6 1.0
CG2 A:ILE115 4.8 47.0 1.0
CA A:ILE115 4.8 48.7 1.0
O A:ALA117 5.0 57.0 1.0

Magnesium binding site 2 out of 2 in 4unf

Go back to Magnesium Binding Sites List in 4unf
Magnesium binding site 2 out of 2 in the Crystal Structure of Deinococcus Radiodurans Endonuclease III-1


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 2 of Crystal Structure of Deinococcus Radiodurans Endonuclease III-1 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg1250

b:60.6
occ:1.00
O A:THR140 2.0 50.7 1.0
O A:HOH2077 2.6 63.8 1.0
O A:VAL145 2.6 47.8 1.0
O A:LEU142 2.7 53.3 1.0
O A:HOH2074 3.0 63.4 1.0
C A:THR140 3.2 47.5 1.0
C A:VAL145 3.7 49.9 1.0
C A:LEU142 3.7 54.8 1.0
N A:VAL145 3.9 49.3 1.0
CA A:THR140 4.0 43.9 1.0
C A:ASP141 4.1 51.8 1.0
N A:LEU142 4.1 45.7 1.0
N A:ASP141 4.2 45.2 1.0
CA A:VAL145 4.2 46.4 1.0
O A:ASP141 4.3 54.5 1.0
CA A:ASP141 4.4 52.3 1.0
N A:GLY144 4.4 52.0 1.0
CA A:LEU142 4.6 45.7 1.0
N A:PRO143 4.6 59.6 1.0
CB A:VAL145 4.6 47.2 1.0
CA A:PRO143 4.6 54.6 1.0
CB A:THR140 4.7 46.1 1.0
O A:HOH2043 4.7 56.2 1.0
C A:PRO143 4.8 55.1 1.0
N A:GLY146 4.8 48.5 1.0
O A:LEU139 4.8 41.7 1.0
C A:GLY144 4.9 54.5 1.0

Reference:

A.Sarre, M.Okvist, T.Klar, D.R.Hall, A.O.Smalas, S.Mcsweeney, J.Timmins, E.Moe. Structural and Functional Characterization of Two Unusual Endonuclease III Enzymes From Deinococcus Radiodurans. J.Struct.Biol. V. 191 87 2015.
ISSN: ISSN 1047-8477
PubMed: 26172070
DOI: 10.1016/J.JSB.2015.05.009
Page generated: Mon Dec 14 19:37:39 2020

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