ReDisulphID

a tool for identifying drug-targetable redox-active disulphides

AP-2 complex subunit sigma

Intermolecular
Cysteine 193 of Protein Nef and cysteine 97
Intramolecular
Cysteine 68 and cysteine 70
A redox-regulated disulphide may form between cysteine 193 of Protein Nef and cysteine 97 of AP-2 complex subunit sigma.

Details

Redox score ?
81
PDB code
6owt
Structure name
structure of sivsmm nef and smm tetherin bound to the clathrin adaptor ap-2 complex
Structure deposition date
2019-05-10
Thiol separation (Å)
2
Half-sphere exposure sum ?
74
Minimum pKa ?
nan
% buried
nan
Peptide A name
Protein Nef
Peptide B name
AP-2 complex subunit sigma
Peptide A accession
Q4JGV0
Peptide B accession
P62744
Peptide A residue number
193
Peptide B residue number
97

Ligandability

Cysteine 193 of Protein Nef

Cysteine 97 of AP-2 complex subunit sigma

Cysteine 97 in protein B could not be asigned to a Uniprot residue.
A redox-regulated disulphide may form within AP-2 complex subunit sigma between cysteines 68 and 70. However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?

Details

Redox score ?
28
PDB code
2jkt
Structure name
ap2 clathrin adaptor core with cd4 dileucine peptide rm( phosphos)eikrllse q to e mutant
Structure deposition date
2008-08-29
Thiol separation (Å)
9
Half-sphere exposure sum ?
90
Minimum pKa ?
12
% buried
100
Peptide accession
P62743
Residue number A
68
Residue number B
70
Peptide name
AP-2 complex subunit sigma

Ligandability

Cysteine 68 of AP-2 complex subunit sigma

Cysteine 70 of AP-2 complex subunit sigma

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