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Sodium in PDB 7za4: Gstf SH155 Mutant

Enzymatic activity of Gstf SH155 Mutant

All present enzymatic activity of Gstf SH155 Mutant:
2.5.1.18;

Protein crystallography data

The structure of Gstf SH155 Mutant, PDB code: 7za4 was solved by A.C.Papageorgiou, with X-Ray Crystallography technique. A brief refinement statistics is given in the table below:

Resolution Low / High (Å) 45.31 / 2.05
Space group I 1 2 1
Cell size a, b, c (Å), α, β, γ (°) 46.478, 99.003, 153.212, 90, 93.73, 90
R / Rfree (%) 21.6 / 25.2

Sodium Binding Sites:

The binding sites of Sodium atom in the Gstf SH155 Mutant (pdb code 7za4). This binding sites where shown within 5.0 Angstroms radius around Sodium atom.
In total 2 binding sites of Sodium where determined in the Gstf SH155 Mutant, PDB code: 7za4:
Jump to Sodium binding site number: 1; 2;

Sodium binding site 1 out of 2 in 7za4

Go back to Sodium Binding Sites List in 7za4
Sodium binding site 1 out of 2 in the Gstf SH155 Mutant


Mono view


Stereo pair view

A full contact list of Sodium with other atoms in the Na binding site number 1 of Gstf SH155 Mutant within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Na301

b:38.1
occ:1.00
O A:HOH321 2.3 31.8 1.0
OE1 B:GLU103 2.6 34.3 1.0
O A:HOH352 2.7 38.3 1.0
NE2 B:HIS107 2.9 42.4 1.0
CD B:GLU103 3.4 38.5 1.0
OE2 B:GLU103 3.5 38.1 1.0
CD2 B:HIS107 3.5 34.1 1.0
CB A:ALA106 3.5 29.8 1.0
CE1 B:HIS107 4.0 41.1 1.0
CD A:ARG69 4.0 33.8 1.0
NE2 A:HIS107 4.1 38.6 1.0
O B:HOH433 4.1 40.7 1.0
OE1 A:GLU103 4.2 34.3 1.0
CB B:ALA106 4.3 34.3 1.0
NE A:ARG69 4.3 30.3 1.0
O A:HOH319 4.4 33.5 1.0
OE2 A:GLU103 4.4 30.4 1.0
NH1 A:ARG69 4.5 33.9 1.0
CZ A:ARG69 4.6 34.6 1.0
CD A:GLU103 4.7 36.8 1.0
CE1 A:HIS107 4.7 41.2 1.0
CG B:HIS107 4.8 36.0 1.0
CG B:GLU103 4.8 36.9 1.0
CD2 A:HIS107 4.8 35.7 1.0
ND1 B:HIS107 5.0 38.7 1.0

Sodium binding site 2 out of 2 in 7za4

Go back to Sodium Binding Sites List in 7za4
Sodium binding site 2 out of 2 in the Gstf SH155 Mutant


Mono view


Stereo pair view

A full contact list of Sodium with other atoms in the Na binding site number 2 of Gstf SH155 Mutant within 5.0Å range:
probe atom residue distance (Å) B Occ
B:Na302

b:55.5
occ:1.00
O B:HOH443 2.1 58.9 1.0
ND1 B:HIS107 2.6 38.7 1.0
O A:HOH343 2.8 51.5 1.0
CE1 B:HIS107 3.5 41.1 1.0
CG B:HIS107 3.7 36.0 1.0
CB B:HIS107 4.0 34.5 1.0
CA B:HIS107 4.2 32.3 1.0
O A:HOH315 4.2 41.8 1.0
O B:HIS107 4.6 40.5 1.0
NE2 B:HIS107 4.7 42.4 1.0
CD2 B:HIS107 4.8 34.1 1.0
O A:ALA106 4.8 34.9 1.0
O B:ALA106 4.9 39.2 1.0
C B:HIS107 5.0 37.4 1.0
ND1 A:HIS107 5.0 38.0 1.0

Reference:

E.Ioannou, A.C.Papageorgiou, N.E.Labrou. Directed Evolution of Phi Class Glutathione Transferases Involved in Multiple-Herbicide Resistance of Grass Weeds and Crops. Int J Mol Sci V. 23 2022.
ISSN: ESSN 1422-0067
PubMed: 35806486
DOI: 10.3390/IJMS23137469
Page generated: Mon Aug 18 12:45:57 2025

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