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Manganese in PDB 8icp: Dna Polymerase Beta (Pol B) (E.C.2.7.7.7) Complexed with Seven Base Pairs of Dna; Soaked in the Presence of Datp (1 Millimolar) and MNCL2 (5 Millimolar)

Protein crystallography data

The structure of Dna Polymerase Beta (Pol B) (E.C.2.7.7.7) Complexed with Seven Base Pairs of Dna; Soaked in the Presence of Datp (1 Millimolar) and MNCL2 (5 Millimolar), PDB code: 8icp was solved by H.Pelletier, M.R.Sawaya, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 20.00 / 2.90
Space group P 21 21 2
Cell size a, b, c (Å), α, β, γ (°) 179.948, 57.626, 48.218, 90.00, 90.00, 90.00
R / Rfree (%) 16.7 / n/a

Other elements in 8icp:

The structure of Dna Polymerase Beta (Pol B) (E.C.2.7.7.7) Complexed with Seven Base Pairs of Dna; Soaked in the Presence of Datp (1 Millimolar) and MNCL2 (5 Millimolar) also contains other interesting chemical elements:

Sodium (Na) 2 atoms

Manganese Binding Sites:

The binding sites of Manganese atom in the Dna Polymerase Beta (Pol B) (E.C.2.7.7.7) Complexed with Seven Base Pairs of Dna; Soaked in the Presence of Datp (1 Millimolar) and MNCL2 (5 Millimolar) (pdb code 8icp). This binding sites where shown within 5.0 Angstroms radius around Manganese atom.
In total only one binding site of Manganese was determined in the Dna Polymerase Beta (Pol B) (E.C.2.7.7.7) Complexed with Seven Base Pairs of Dna; Soaked in the Presence of Datp (1 Millimolar) and MNCL2 (5 Millimolar), PDB code: 8icp:

Manganese binding site 1 out of 1 in 8icp

Go back to Manganese Binding Sites List in 8icp
Manganese binding site 1 out of 1 in the Dna Polymerase Beta (Pol B) (E.C.2.7.7.7) Complexed with Seven Base Pairs of Dna; Soaked in the Presence of Datp (1 Millimolar) and MNCL2 (5 Millimolar)


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 1 of Dna Polymerase Beta (Pol B) (E.C.2.7.7.7) Complexed with Seven Base Pairs of Dna; Soaked in the Presence of Datp (1 Millimolar) and MNCL2 (5 Millimolar) within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mn339

b:30.0
occ:0.49
OD2 A:ASP192 2.6 49.5 1.0
OP2 P:DA8 2.6 93.1 0.5
OD1 A:ASP190 2.6 49.1 1.0
O3G A:DTP338 2.8 69.3 0.5
OD2 A:ASP190 3.2 52.5 1.0
CG A:ASP190 3.3 46.5 1.0
O A:HOH522 3.4 23.4 1.0
CG A:ASP192 3.7 46.5 1.0
O3A A:DTP338 3.7 0.0 0.5
O3' P:DG7 3.7 88.6 1.0
P P:DA8 3.7 92.0 0.5
O2B A:DTP338 3.8 98.0 0.5
O3B A:DTP338 3.9 68.9 0.5
PG A:DTP338 3.9 48.0 0.5
OD1 A:ASP192 4.0 55.3 1.0
PB A:DTP338 4.1 0.0 0.5
O1G A:DTP338 4.2 10.9 0.5
O P:HOH587 4.2 50.2 1.0
O A:ASP190 4.6 24.4 1.0
OP1 P:DA8 4.7 90.3 0.5
CB A:ASP190 4.8 34.4 1.0
CB A:ASP192 4.9 29.7 1.0
O5' P:DA8 4.9 94.9 0.5
C3' P:DG7 5.0 83.0 1.0

Reference:

H.Pelletier, M.R.Sawaya, W.Wolfle, S.H.Wilson, J.Kraut. A Structural Basis For Metal Ion Mutagenicity and Nucleotide Selectivity in Human Dna Polymerase Beta. Biochemistry V. 35 12762 1996.
ISSN: ISSN 0006-2960
PubMed: 8841119
DOI: 10.1021/BI9529566
Page generated: Sun Oct 6 12:31:05 2024

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