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Manganese in PDB 2alx: Ribonucleotide Reductase R2 From Escherichia Coli in Space Group P6(1)22

Enzymatic activity of Ribonucleotide Reductase R2 From Escherichia Coli in Space Group P6(1)22

All present enzymatic activity of Ribonucleotide Reductase R2 From Escherichia Coli in Space Group P6(1)22:
1.17.4.1;

Protein crystallography data

The structure of Ribonucleotide Reductase R2 From Escherichia Coli in Space Group P6(1)22, PDB code: 2alx was solved by M.Sommerhalter, L.Saleh, J.M.Bollinger Jr., A.C.Rosenzweig, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 19.27 / 2.60
Space group P 61 2 2
Cell size a, b, c (Å), α, β, γ (°) 92.940, 92.940, 200.930, 90.00, 90.00, 120.00
R / Rfree (%) 22.7 / 27.6

Other elements in 2alx:

The structure of Ribonucleotide Reductase R2 From Escherichia Coli in Space Group P6(1)22 also contains other interesting chemical elements:

Mercury (Hg) 4 atoms

Manganese Binding Sites:

The binding sites of Manganese atom in the Ribonucleotide Reductase R2 From Escherichia Coli in Space Group P6(1)22 (pdb code 2alx). This binding sites where shown within 5.0 Angstroms radius around Manganese atom.
In total 2 binding sites of Manganese where determined in the Ribonucleotide Reductase R2 From Escherichia Coli in Space Group P6(1)22, PDB code: 2alx:
Jump to Manganese binding site number: 1; 2;

Manganese binding site 1 out of 2 in 2alx

Go back to Manganese Binding Sites List in 2alx
Manganese binding site 1 out of 2 in the Ribonucleotide Reductase R2 From Escherichia Coli in Space Group P6(1)22


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 1 of Ribonucleotide Reductase R2 From Escherichia Coli in Space Group P6(1)22 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mn401

b:41.3
occ:1.00
OE1 A:GLU115 1.9 47.8 1.0
OE2 A:GLU238 1.9 50.6 1.0
OD1 A:ASP84 2.1 39.0 1.0
ND1 A:HIS118 2.3 36.2 1.0
OD2 A:ASP84 2.6 39.8 1.0
CG A:ASP84 2.7 40.9 1.0
CD A:GLU238 3.0 51.0 1.0
CD A:GLU115 3.0 43.2 1.0
CE1 A:HIS118 3.1 37.5 1.0
OE1 A:GLU238 3.3 55.0 1.0
CG A:HIS118 3.3 34.1 1.0
OE2 A:GLU115 3.5 42.1 1.0
CB A:HIS118 3.7 34.4 1.0
MN A:MN402 3.8 41.3 1.0
CZ A:PHE208 3.9 56.8 1.0
CB A:ASP84 4.1 40.2 1.0
CG2 A:ILE234 4.1 36.5 1.0
CG A:GLU115 4.2 42.5 1.0
NE2 A:HIS118 4.3 36.1 1.0
CG A:GLU238 4.3 48.8 1.0
CE2 A:PHE208 4.3 57.7 1.0
CA A:GLU115 4.3 41.3 1.0
CB A:GLU115 4.4 40.7 1.0
CD2 A:HIS118 4.4 35.6 1.0
CE1 A:PHE208 4.4 56.5 1.0
CE1 A:HIS241 4.7 35.1 1.0
OH A:TYR122 4.7 35.4 1.0
CA A:ASP84 4.9 36.5 1.0
ND1 A:HIS241 4.9 34.6 1.0
O A:GLU115 4.9 43.5 1.0

Manganese binding site 2 out of 2 in 2alx

Go back to Manganese Binding Sites List in 2alx
Manganese binding site 2 out of 2 in the Ribonucleotide Reductase R2 From Escherichia Coli in Space Group P6(1)22


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 2 of Ribonucleotide Reductase R2 From Escherichia Coli in Space Group P6(1)22 within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mn402

b:41.3
occ:1.00
OE2 A:GLU115 1.8 42.1 1.0
OE1 A:GLU238 1.9 55.0 1.0
OE1 A:GLU204 2.0 47.7 1.0
ND1 A:HIS241 2.2 34.6 1.0
OE2 A:GLU204 2.5 47.2 1.0
CD A:GLU204 2.6 47.9 1.0
CD A:GLU115 2.9 43.2 1.0
CD A:GLU238 3.1 51.0 1.0
CE1 A:HIS241 3.1 35.1 1.0
CG A:HIS241 3.3 36.1 1.0
OE1 A:GLU115 3.3 47.8 1.0
OE2 A:GLU238 3.6 50.6 1.0
CB A:HIS241 3.6 38.9 1.0
NE1 A:TRP111 3.8 39.3 1.0
MN A:MN401 3.8 41.3 1.0
CG A:GLU204 4.1 51.1 1.0
CG A:GLU115 4.2 42.5 1.0
NE2 A:HIS241 4.2 37.2 1.0
CG A:GLU238 4.3 48.8 1.0
CA A:GLU238 4.3 41.1 1.0
CD2 A:HIS241 4.3 36.3 1.0
CD1 A:TRP111 4.4 39.3 1.0
CB A:GLU238 4.5 47.7 1.0
OD1 A:ASP84 4.6 39.0 1.0
CE2 A:PHE208 4.7 57.7 1.0
NE2 A:GLN87 4.7 39.1 1.0
CB A:GLU204 4.8 50.5 1.0
CG A:GLN87 4.9 40.9 1.0
CE2 A:TRP111 4.9 43.2 1.0
CD2 A:PHE208 4.9 56.5 1.0

Reference:

M.Sommerhalter, L.Saleh, J.M.Bollinger, A.C.Rosenzweig. Structure of Escherichia Coli Ribonucleotide Reductase R2 in Space Group P6122. Acta Crystallogr.,Sect.D V. 61 1649 2005.
ISSN: ISSN 0907-4449
PubMed: 16301799
DOI: 10.1107/S0907444905034062
Page generated: Sat Oct 5 13:26:36 2024

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