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Manganese in PDB 4my4: Crystal Structure of Phosphoglycerate Mutase From Staphylococcus Aureus.

Enzymatic activity of Crystal Structure of Phosphoglycerate Mutase From Staphylococcus Aureus.

All present enzymatic activity of Crystal Structure of Phosphoglycerate Mutase From Staphylococcus Aureus.:
5.4.2.1;

Protein crystallography data

The structure of Crystal Structure of Phosphoglycerate Mutase From Staphylococcus Aureus., PDB code: 4my4 was solved by A.Roychowdhury, A.Kundu, A.Gujar, M.Bose, A.K.Das, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 19.69 / 2.00
Space group P 21 21 21
Cell size a, b, c (Å), α, β, γ (°) 73.206, 81.747, 89.184, 90.00, 90.00, 90.00
R / Rfree (%) 16.4 / 21.6

Manganese Binding Sites:

The binding sites of Manganese atom in the Crystal Structure of Phosphoglycerate Mutase From Staphylococcus Aureus. (pdb code 4my4). This binding sites where shown within 5.0 Angstroms radius around Manganese atom.
In total 2 binding sites of Manganese where determined in the Crystal Structure of Phosphoglycerate Mutase From Staphylococcus Aureus., PDB code: 4my4:
Jump to Manganese binding site number: 1; 2;

Manganese binding site 1 out of 2 in 4my4

Go back to Manganese Binding Sites List in 4my4
Manganese binding site 1 out of 2 in the Crystal Structure of Phosphoglycerate Mutase From Staphylococcus Aureus.


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 1 of Crystal Structure of Phosphoglycerate Mutase From Staphylococcus Aureus. within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mn601

b:15.4
occ:1.00
O A:HOH703 2.1 12.8 1.0
OD1 A:ASP397 2.2 12.3 1.0
O A:HOH701 2.2 18.3 1.0
NE2 A:HIS401 2.2 20.2 1.0
O A:HOH702 2.3 16.0 1.0
NE2 A:HIS456 2.3 17.4 1.0
CG A:ASP397 3.0 13.4 1.0
OD2 A:ASP397 3.1 14.9 1.0
CE1 A:HIS456 3.2 17.2 1.0
CE1 A:HIS401 3.2 18.0 1.0
CD2 A:HIS401 3.2 18.8 1.0
CD2 A:HIS456 3.4 17.6 1.0
NZ A:LYS330 4.0 13.8 1.0
O A:HOH986 4.3 33.4 1.0
ND1 A:HIS401 4.3 19.5 1.0
ND1 A:HIS456 4.3 16.4 1.0
O A:HOH742 4.3 18.1 1.0
CG A:HIS401 4.4 18.6 1.0
CB A:ASP397 4.4 13.3 1.0
CG A:HIS456 4.5 17.6 1.0
O A:HOH745 4.5 19.6 1.0
OG A:SER62 4.5 13.7 1.0
CE1 A:HIS439 4.5 15.3 1.0
ND2 A:ASN441 4.6 12.4 1.0
O A:HOH762 4.8 32.7 1.0
NE2 A:HIS439 4.9 15.3 1.0
SD A:MET398 4.9 16.7 1.0
O A:ASP397 5.0 14.6 1.0

Manganese binding site 2 out of 2 in 4my4

Go back to Manganese Binding Sites List in 4my4
Manganese binding site 2 out of 2 in the Crystal Structure of Phosphoglycerate Mutase From Staphylococcus Aureus.


Mono view


Stereo pair view

A full contact list of Manganese with other atoms in the Mn binding site number 2 of Crystal Structure of Phosphoglycerate Mutase From Staphylococcus Aureus. within 5.0Å range:
probe atom residue distance (Å) B Occ
A:Mn602

b:10.2
occ:1.00
OD1 A:ASP12 1.9 13.4 1.0
OD1 A:ASP438 1.9 15.2 1.0
OG A:SER62 1.9 13.7 1.0
NE2 A:HIS439 2.0 15.3 1.0
CG A:ASP12 2.6 13.0 1.0
CG A:ASP438 2.7 14.4 1.0
OD2 A:ASP12 2.8 13.7 1.0
OD2 A:ASP438 2.8 14.5 1.0
CD2 A:HIS439 2.9 15.8 1.0
CB A:SER62 3.0 12.9 1.0
CE1 A:HIS439 3.0 15.3 1.0
CA A:SER62 3.3 13.0 1.0
NZ A:LYS330 3.7 13.8 1.0
N A:SER62 3.7 14.2 1.0
CB A:ASP12 4.0 13.0 1.0
CG A:HIS439 4.1 15.4 1.0
O A:HOH703 4.1 12.8 1.0
ND1 A:HIS439 4.1 15.5 1.0
OD1 A:ASP397 4.1 12.3 1.0
CB A:ASP438 4.2 13.4 1.0
CG A:ASP397 4.3 13.4 1.0
C A:ASN61 4.3 14.7 1.0
CE A:LYS330 4.3 13.6 1.0
N A:GLY13 4.3 14.1 1.0
CE1 A:HIS66 4.5 12.8 1.0
CA A:ASP12 4.5 13.3 1.0
OD2 A:ASP397 4.6 14.9 1.0
C A:SER62 4.6 12.9 1.0
O A:ASN61 4.7 12.7 1.0
CB A:ASP397 4.8 13.3 1.0
C A:ASP12 4.8 13.9 1.0
CD A:LYS330 4.8 13.7 1.0
ND1 A:HIS66 4.9 12.9 1.0

Reference:

A.Roychowdhury, A.Kundu, A.Gujar, M.Bose, S.Mukherjee, A.K.Das. Structural and Funcctional Analysis of Phosphoglycerate Mutase From Staphylococcus Aureus. To Be Published.
Page generated: Sat Oct 5 20:28:44 2024

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