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Manganese in PDB 5kfc: Human Dna Polymerase Eta-Dna Ternary Complex: Reaction with 1 Mm MN2+ For 180S

Enzymatic activity of Human Dna Polymerase Eta-Dna Ternary Complex: Reaction with 1 Mm MN2+ For 180S

All present enzymatic activity of Human Dna Polymerase Eta-Dna Ternary Complex: Reaction with 1 Mm MN2+ For 180S:
2.7.7.7;

Protein crystallography data

The structure of Human Dna Polymerase Eta-Dna Ternary Complex: Reaction with 1 Mm MN2+ For 180S, PDB code: 5kfc was solved by Y.Gao, W.Yang, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 19.95 / 1.50
Space group P 61
Cell size a, b, c (Å), α, β, γ (°) 98.150, 98.150, 82.090, 90.00, 90.00, 120.00
R / Rfree (%) 18 / 21

Other elements in 5kfc:

The structure of Human Dna Polymerase Eta-Dna Ternary Complex: Reaction with 1 Mm MN2+ For 180S also contains other interesting chemical elements:

Calcium (Ca) 1 atom

Manganese Binding Sites:

The binding sites of Manganese atom in the Human Dna Polymerase Eta-Dna Ternary Complex: Reaction with 1 Mm MN2+ For 180S (pdb code 5kfc). This binding sites where shown within 5.0 Angstroms radius around Manganese atom.
In total 2 binding sites of Manganese where determined in the Human Dna Polymerase Eta-Dna Ternary Complex: Reaction with 1 Mm MN2+ For 180S, PDB code: 5kfc:
Jump to Manganese binding site number: 1; 2;

Manganese binding site 1 out of 2 in 5kfc

Go back to Manganese Binding Sites List in 5kfc
Manganese binding site 1 out of 2 in the Human Dna Polymerase Eta-Dna Ternary Complex: Reaction with 1 Mm MN2+ For 180S


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 1 of Human Dna Polymerase Eta-Dna Ternary Complex: Reaction with 1 Mm MN2+ For 180S within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mn501

b:13.2
occ:0.85
OD2 A:ASP13 2.1 14.8 0.8
OE2 A:GLU116 2.2 15.2 1.0
O A:HOH791 2.2 16.0 1.0
O1A A:DTP506 2.2 11.1 1.0
OD1 A:ASP115 2.2 12.3 1.0
O3' P:DT8 2.4 13.2 1.0
OD2 A:ASP13 2.6 11.2 0.1
OD1 A:ASP13 3.0 11.1 0.1
CG A:ASP13 3.1 12.8 0.1
CG A:ASP115 3.2 9.7 1.0
CD A:GLU116 3.2 17.6 1.0
CG A:ASP13 3.2 12.8 0.8
C3' P:DT8 3.3 13.8 1.0
OD2 A:ASP115 3.4 12.0 1.0
PA A:DTP506 3.5 11.5 1.0
MN A:MN503 3.6 11.9 0.8
CA A:CA502 3.6 11.8 0.2
OD1 A:ASP13 3.7 13.3 0.8
OG A:SER113 3.8 15.6 1.0
OE1 A:GLU116 3.9 18.2 1.0
O2A A:DTP506 4.0 13.7 1.0
O5' A:DTP506 4.0 11.6 1.0
CB A:GLU116 4.1 12.8 1.0
CG A:GLU116 4.1 11.4 1.0
C4' P:DT8 4.2 15.6 1.0
C5' A:DTP506 4.2 12.8 1.0
NZ A:LYS224 4.2 14.6 0.7
O A:HOH702 4.3 18.6 1.0
O P:HOH103 4.4 13.1 0.7
CB A:ASP13 4.4 11.4 0.8
C2' P:DT8 4.6 16.3 1.0
CB A:ASP13 4.6 11.4 0.1
C5' P:DT8 4.6 19.0 0.5
CB A:ASP115 4.6 10.1 1.0
C A:ASP115 4.6 11.6 1.0
O A:ASP115 4.7 12.6 1.0
C5' P:DT8 4.7 18.8 0.5
CB A:SER113 4.8 13.2 1.0
O1G A:DTP506 4.8 11.0 1.0
O3A A:DTP506 4.8 11.7 1.0
N A:GLU116 4.8 9.4 1.0

Manganese binding site 2 out of 2 in 5kfc

Go back to Manganese Binding Sites List in 5kfc
Manganese binding site 2 out of 2 in the Human Dna Polymerase Eta-Dna Ternary Complex: Reaction with 1 Mm MN2+ For 180S


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 2 of Human Dna Polymerase Eta-Dna Ternary Complex: Reaction with 1 Mm MN2+ For 180S within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mn503

b:11.9
occ:0.75
CA A:CA502 0.0 11.8 0.2
OD1 A:ASP13 2.1 11.1 0.1
OD1 A:ASP13 2.2 13.3 0.8
O A:MET14 2.2 11.4 1.0
OD2 A:ASP115 2.2 12.0 1.0
O1G A:DTP506 2.2 11.0 1.0
O1B A:DTP506 2.3 10.1 1.0
O1A A:DTP506 2.4 11.1 1.0
CG A:ASP13 3.0 12.8 0.8
OD2 A:ASP13 3.1 14.8 0.8
CG A:ASP115 3.3 9.7 1.0
PB A:DTP506 3.3 10.9 1.0
C A:MET14 3.4 9.3 1.0
CG A:ASP13 3.4 12.8 0.1
PG A:DTP506 3.5 11.0 1.0
PA A:DTP506 3.5 11.5 1.0
MN A:MN501 3.6 13.2 0.8
O3A A:DTP506 3.6 11.7 1.0
OD1 A:ASP115 3.7 12.3 1.0
NZ A:LYS231 3.7 10.2 0.5
O3B A:DTP506 3.8 9.6 1.0
N A:MET14 3.9 9.3 1.0
O A:HOH702 3.9 18.6 1.0
O2G A:DTP506 4.0 10.5 1.0
CA A:MET14 4.1 9.5 1.0
OD2 A:ASP13 4.1 11.2 0.1
C5' A:DTP506 4.1 12.8 1.0
C A:ASP13 4.2 9.5 1.0
O5' A:DTP506 4.3 11.6 1.0
CB A:ASP13 4.3 11.4 0.8
O A:HOH791 4.4 16.0 1.0
CB A:ASP13 4.4 11.4 0.1
N A:ASP15 4.4 7.5 1.0
N A:CYS16 4.5 8.9 1.0
CE A:LYS231 4.6 11.1 0.5
CB A:ASP115 4.6 10.1 1.0
CA A:ASP15 4.6 8.2 1.0
O A:ASP13 4.6 11.3 1.0
CB A:MET14 4.6 10.8 1.0
O2B A:DTP506 4.7 11.5 1.0
O3G A:DTP506 4.7 12.7 1.0
O2A A:DTP506 4.7 13.7 1.0
C A:ASP15 4.7 10.0 1.0
CA A:ASP13 4.7 11.2 0.1
CA A:ASP13 4.8 11.1 0.8
N A:PHE17 4.8 9.5 1.0
O A:ASP115 4.9 12.6 1.0
CB A:PHE17 4.9 7.9 1.0

Reference:

Y.Gao, W.Yang. Capture of A Third MG2+ Is Essential For Catalyzing Dna Synthesis. Science V. 352 1334 2016.
ISSN: ESSN 1095-9203
PubMed: 27284197
DOI: 10.1126/SCIENCE.AAD9633
Page generated: Sun Oct 6 01:38:05 2024

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