ReDisulphID

a tool for identifying drug-targetable redox-active disulphides

Cyclin-K

Intramolecular
Cysteine 98 and cysteine 99
Cysteine 98 and cysteine 113
A redox-regulated disulphide may form within Cyclin-K between cysteines 98 and 99. However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?

Details

Redox score ?
41
PDB code
6b3e
Structure name
crystal structure of human cdk12/cyclink in complex with an inhibitor
Structure deposition date
2017-09-21
Thiol separation (Å)
6
Half-sphere exposure sum ?
98
Minimum pKa ?
13
% buried
100
Peptide accession
O75909
Residue number A
98
Residue number B
99
Peptide name
Cyclin-K

Ligandability

Cysteine 98 of Cyclin-K

Cysteine 99 of Cyclin-K

A redox-regulated disulphide may form within Cyclin-K between cysteines 98 and 113. However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?

Details

Redox score ?
40
PDB code
4cxa
Structure name
crystal structure of the human cdk12-cyclin k complex bound to amppnp
Structure deposition date
2014-04-04
Thiol separation (Å)
8
Half-sphere exposure sum ?
82
Minimum pKa ?
11
% buried
76
Peptide accession
O75909
Residue number A
98
Residue number B
113
Peptide name
Cyclin-K

Ligandability

Cysteine 98 of Cyclin-K

Cysteine 113 of Cyclin-K

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