ReDisulphID

a tool for identifying drug-targetable redox-active disulphides

Citrate synthase, mitochondrial

Intramolecular
Cysteine 211 and cysteine 500
Cysteine 101 and cysteine 359
A redox-regulated disulphide may form within Citrate synthase, mitochondrial between cysteines 211 and 500 (184 and 500 respectively in this structure).

Details

Redox score ?
85
PDB code
3enj
Structure name
structure of pig heart citrate synthase at 1
Structure deposition date
2008-09-25
Thiol separation (Å)
2
Half-sphere exposure sum ?
nan
Minimum pKa ?
nan
% buried
nan
Peptide accession
P00889
Residue number A
211
Residue number B
500
Peptide name
Citrate synthase, mitochondrial

Ligandability

Cysteine 211 of Citrate synthase, mitochondrial

Cysteine 500 of Citrate synthase, mitochondrial

Cysteine 500 in protein B could not be asigned to a Uniprot residue.
A redox-regulated disulphide may form within Citrate synthase, mitochondrial between cysteines 101 and 359. However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?

Details

Redox score ?
34
PDB code
5uzr
Structure name
crystal structure of citrate synthase from homo sapiens
Structure deposition date
2017-02-27
Thiol separation (Å)
9
Half-sphere exposure sum ?
72
Minimum pKa ?
12
% buried
92
Peptide accession
O75390
Residue number A
101
Residue number B
359
Peptide name
Citrate synthase, mitochondrial

Ligandability

Cysteine 101 of Citrate synthase, mitochondrial

Cysteine 359 of Citrate synthase, mitochondrial

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