Magnesium in PDB 7m46: Dna Polymerase Lambda, Ttp:at MG2+ Product State Ternary Complex, 5 Min

Enzymatic activity of Dna Polymerase Lambda, Ttp:at MG2+ Product State Ternary Complex, 5 Min

All present enzymatic activity of Dna Polymerase Lambda, Ttp:at MG2+ Product State Ternary Complex, 5 Min:
2.7.7.7;

Protein crystallography data

The structure of Dna Polymerase Lambda, Ttp:at MG2+ Product State Ternary Complex, 5 Min, PDB code: 7m46 was solved by J.A.Jamsen, S.H.Wilson, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 23.62 / 1.92
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 56.263, 62.808, 139.452, 90, 90, 90
R / Rfree (%) 18.6 / 21.7

Other elements in 7m46:

The structure of Dna Polymerase Lambda, Ttp:at MG2+ Product State Ternary Complex, 5 Min also contains other interesting chemical elements:

Sodium (Na) 4 atoms

Magnesium Binding Sites:

The binding sites of Magnesium atom in the Dna Polymerase Lambda, Ttp:at MG2+ Product State Ternary Complex, 5 Min (pdb code 7m46). 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 Dna Polymerase Lambda, Ttp:at MG2+ Product State Ternary Complex, 5 Min, PDB code: 7m46:

Magnesium binding site 1 out of 1 in 7m46

Go back to Magnesium Binding Sites List in 7m46
Magnesium binding site 1 out of 1 in the Dna Polymerase Lambda, Ttp:at MG2+ Product State Ternary Complex, 5 Min


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 1 of Dna Polymerase Lambda, Ttp:at MG2+ Product State Ternary Complex, 5 Min within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg601

b:28.0
occ:1.00
 OD1 A:ASP427 2.0 28.4 1.0
OD2 A:ASP429 2.0 29.6 1.0
OP1 P:DT7 2.0 28.9 1.0
O A:HOH701 2.0 37.9 1.0
O11 A:PPV610 2.1 32.6 0.8
O22 A:PPV610 2.3 34.0 0.8
CG A:ASP427 2.9 43.0 1.0
CG A:ASP429 2.9 31.4 1.0
P1 A:PPV610 3.2 42.0 0.8
OD1 A:ASP429 3.2 27.1 1.0
OD2 A:ASP427 3.2 43.3 1.0
O31 A:PPV610 3.3 58.9 0.8
P2 A:PPV610 3.4 53.1 0.8
P P:DT7 3.4 30.5 1.0
NA A:NA603 3.5 31.6 1.0
O32 A:PPV610 3.7 36.3 0.8
OPP A:PPV610 3.8 44.2 0.8
O5' P:DT7 3.9 27.5 1.0
C5' P:DT7 4.0 28.6 1.0
OP2 P:DT7 4.2 25.7 1.0
O A:ASP427 4.3 27.2 1.0
CB A:ASP427 4.3 29.9 1.0
CB A:ASP429 4.3 29.0 1.0
O A:HOH767 4.4 44.4 1.0
CA A:GLY416 4.4 31.1 1.0
O3' P:DC6 4.4 30.3 1.0
C A:ASP427 4.5 31.6 1.0
O21 A:PPV610 4.5 32.3 0.8
O12 A:PPV610 4.7 57.3 0.8
N A:SER417 4.7 32.0 1.0
N A:ASP427 4.7 31.2 1.0
CA A:ASP427 4.7 28.6 1.0
O A:HOH824 4.8 41.1 1.0
N A:VAL428 5.0 27.0 1.0

Reference:

J.A.Jamsen, D.D.Shock, S.H.Wilson. Watching Right and Wrong Nucleotide Insertion Captures Hidden Polymerase Fidelity Checkpoints. Nat Commun V. 13 3193 2022.
ISSN: ESSN 2041-1723
PubMed: 35680862
DOI: 10.1038/S41467-022-30141-W
Page generated: Wed Oct 2 23:41:32 2024

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