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Magnesium in PDB 8e87: Human Dna Polymerase Eta-Dna-Ra-Ended Primer-Dgmpnpp Ternary Mismatch Complex with MG2+

Enzymatic activity of Human Dna Polymerase Eta-Dna-Ra-Ended Primer-Dgmpnpp Ternary Mismatch Complex with MG2+

All present enzymatic activity of Human Dna Polymerase Eta-Dna-Ra-Ended Primer-Dgmpnpp Ternary Mismatch Complex with MG2+:
2.7.7.7;

Protein crystallography data

The structure of Human Dna Polymerase Eta-Dna-Ra-Ended Primer-Dgmpnpp Ternary Mismatch Complex with MG2+, PDB code: 8e87 was solved by C.Chang, Y.Gao, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 42.32 / 2.19
Space group P 61
Cell size a, b, c (Å), α, β, γ (°) 97.728, 97.728, 81.881, 90, 90, 120
R / Rfree (%) 20 / 24.9

Magnesium Binding Sites:

The binding sites of Magnesium atom in the Human Dna Polymerase Eta-Dna-Ra-Ended Primer-Dgmpnpp Ternary Mismatch Complex with MG2+ (pdb code 8e87). This binding sites where shown within 5.0 Angstroms radius around Magnesium atom.
In total 2 binding sites of Magnesium where determined in the Human Dna Polymerase Eta-Dna-Ra-Ended Primer-Dgmpnpp Ternary Mismatch Complex with MG2+, PDB code: 8e87:
Jump to Magnesium binding site number: 1; 2;

Magnesium binding site 1 out of 2 in 8e87

Go back to Magnesium Binding Sites List in 8e87
Magnesium binding site 1 out of 2 in the Human Dna Polymerase Eta-Dna-Ra-Ended Primer-Dgmpnpp Ternary Mismatch Complex with MG2+


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 1 of Human Dna Polymerase Eta-Dna-Ra-Ended Primer-Dgmpnpp Ternary Mismatch Complex with MG2+ within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg501

b:29.4
occ:1.00
O2G A:XG4503 1.9 22.4 1.0
OD1 A:ASP13 2.0 27.4 1.0
O1B A:XG4503 2.1 26.1 1.0
OD2 A:ASP115 2.1 24.4 1.0
O1A A:XG4503 2.2 27.1 1.0
O A:MET14 2.2 24.8 1.0
CG A:ASP13 3.0 27.7 1.0
PB A:XG4503 3.1 27.4 1.0
PG A:XG4503 3.2 29.5 1.0
CG A:ASP115 3.2 30.5 1.0
PA A:XG4503 3.3 31.2 1.0
C A:MET14 3.4 24.2 1.0
O3B A:XG4503 3.4 30.8 1.0
N3A A:XG4503 3.4 26.4 1.0
OD2 A:ASP13 3.4 32.0 1.0
MG A:MG502 3.5 25.4 1.0
OD1 A:ASP115 3.7 28.5 1.0
O3G A:XG4503 3.8 31.9 1.0
NZ A:LYS231 3.9 22.7 1.0
N A:MET14 4.0 32.8 1.0
C5' A:XG4503 4.1 26.5 1.0
CA A:MET14 4.2 27.1 1.0
O5' A:XG4503 4.2 30.4 1.0
C A:ASP13 4.3 27.8 1.0
CB A:ASP13 4.3 34.8 1.0
O A:HOH604 4.3 28.5 1.0
N A:ASP15 4.4 22.1 1.0
O1G A:XG4503 4.4 26.8 1.0
CB A:ASP115 4.5 22.1 1.0
O2B A:XG4503 4.5 27.8 1.0
N A:CYS16 4.5 28.3 1.0
O2A A:XG4503 4.5 28.6 1.0
CE A:LYS231 4.5 32.1 1.0
CA A:ASP15 4.6 30.6 1.0
O A:ASP13 4.6 24.3 1.0
N A:PHE17 4.7 25.8 1.0
C A:ASP15 4.7 30.2 1.0
CB A:MET14 4.8 30.9 1.0
CA A:ASP13 4.8 29.7 1.0
CB A:PHE17 4.8 21.1 1.0

Magnesium binding site 2 out of 2 in 8e87

Go back to Magnesium Binding Sites List in 8e87
Magnesium binding site 2 out of 2 in the Human Dna Polymerase Eta-Dna-Ra-Ended Primer-Dgmpnpp Ternary Mismatch Complex with MG2+


Mono view


Stereo pair view

A full contact list of Magnesium with other atoms in the Mg binding site number 2 of Human Dna Polymerase Eta-Dna-Ra-Ended Primer-Dgmpnpp Ternary Mismatch Complex with MG2+ within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mg502

b:25.4
occ:1.00
OD2 A:ASP13 2.1 32.0 1.0
O A:HOH604 2.1 28.5 1.0
O3' P:A9 2.2 30.4 1.0
O1A A:XG4503 2.2 27.1 1.0
OD1 A:ASP115 2.2 28.5 1.0
OE1 A:GLU116 2.3 33.2 1.0
CG A:ASP115 3.1 30.5 1.0
CG A:ASP13 3.1 27.7 1.0
PA A:XG4503 3.2 31.2 1.0
C3' P:A9 3.2 35.0 1.0
CD A:GLU116 3.3 36.8 1.0
OD2 A:ASP115 3.3 24.4 1.0
OD1 A:ASP13 3.4 27.4 1.0
MG A:MG501 3.5 29.4 1.0
O2A A:XG4503 3.6 28.6 1.0
O5' A:XG4503 3.7 30.4 1.0
OG A:SER113 3.8 33.6 1.0
C5' A:XG4503 3.9 26.5 1.0
OE2 A:GLU116 3.9 35.7 1.0
C4' P:A9 3.9 38.5 1.0
C5' P:A9 4.1 30.5 1.0
CB A:GLU116 4.2 25.2 1.0
CG A:GLU116 4.3 35.5 1.0
NZ A:LYS224 4.3 31.5 1.0
CB A:ASP13 4.4 34.8 1.0
O2G A:XG4503 4.5 22.4 1.0
CB A:ASP115 4.5 22.1 1.0
C2' P:A9 4.5 40.6 1.0
N3A A:XG4503 4.6 26.4 1.0
C A:ASP115 4.7 31.0 1.0
O2' P:A9 4.7 36.3 1.0
O1B A:XG4503 4.8 26.1 1.0
O5' P:A9 4.8 41.6 1.0
O A:ASP115 4.8 31.6 1.0
N A:GLU116 4.9 28.9 1.0
CB A:SER113 5.0 28.7 1.0

Reference:

C.Chang, C.Lee Luo, S.Eleraky, A.Lin, G.Zhou, Y.Gao. Primer Terminal Ribonucleotide Alters the Active Site Dynamics of Dna Polymerase Eta and Reduce Dna Synthesis Fidelity J.Biol.Chem. 02938 2023.
ISSN: ESSN 1083-351X
DOI: 10.1016/J.JBC.2023.102938
Page generated: Fri Oct 4 01:05:03 2024

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