ReDisulphID

a tool for identifying drug-targetable redox-active disulphides

Glutamine synthetase

Intermolecular
Cysteine 163 and cysteine 42
Intramolecular
Cysteine 252 and cysteine 346
A redox-regulated disulphide may form between two units of Glutamine synthetase at cysteines 163 and 42. However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?

Details

Redox score ?
42
PDB code
2qc8
Structure name
crystal structure of human glutamine synthetase in complex with adp and methionine sulfoximine phosphate
Structure deposition date
2007-06-19
Thiol separation (Å)
6
Half-sphere exposure sum ?
83
Minimum pKa ?
12
% buried
100
Peptide A name
Glutamine synthetase
Peptide B name
Glutamine synthetase
Peptide A accession
P15104
Peptide B accession
P15104
Peptide A residue number
163
Peptide B residue number
42

Ligandability

Cysteine 163 of Glutamine synthetase

Cysteine 42 of Glutamine synthetase

A redox-regulated disulphide may form within Glutamine synthetase between cysteines 252 and 346.

Details

Redox score ?
71
PDB code
2uu7
Structure name
crystal structure of apo glutamine synthetase from dog ( canis familiaris)
Structure deposition date
2007-02-28
Thiol separation (Å)
4
Half-sphere exposure sum ?
84
Minimum pKa ?
8
% buried
100
Peptide accession
Q8HZM5
Residue number A
252
Residue number B
346
Peptide name
Glutamine synthetase

Ligandability

Cysteine 252 of Glutamine synthetase

Cysteine 346 of Glutamine synthetase

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