ReDisulphID

a tool for identifying drug-targetable redox-active disulphides

Kanadaptin

Intramolecular
Cysteine 197 and cysteine 200
Cysteine 189 and cysteine 197
A redox-regulated disulphide may form within Kanadaptin between cysteines 197 and 200.

Details

Redox score ?
66
PDB code
4h87
Structure name
crystal structure of a fha domain of kanadaptin (slc4a1ap) from homo sapiens at 1
Structure deposition date
2012-09-21
Thiol separation (Å)
6
Half-sphere exposure sum ?
50
Minimum pKa ?
10
% buried
22
Peptide accession
Q9BWU0
Residue number A
197
Residue number B
200
Peptide name
Kanadaptin

Ligandability

Cysteine 197 of Kanadaptin

Cysteine 200 of Kanadaptin

A redox-regulated disulphide may form within Kanadaptin between cysteines 189 and 197. However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?

Details

Redox score ?
41
PDB code
4h87
Structure name
crystal structure of a fha domain of kanadaptin (slc4a1ap) from homo sapiens at 1
Structure deposition date
2012-09-21
Thiol separation (Å)
9
Half-sphere exposure sum ?
61
Minimum pKa ?
11
% buried
62
Peptide accession
Q9BWU0
Residue number A
189
Residue number B
197
Peptide name
Kanadaptin

Ligandability

Cysteine 189 of Kanadaptin

Cysteine 197 of Kanadaptin

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