ReDisulphID

a tool for identifying drug-targetable redox-active disulphides

N-lysine methyltransferase KMT5A

Intermolecular
Cysteine 311 and cysteine 311
Intramolecular
Cysteine 311 and cysteine 324 L
A redox-regulated disulphide may form between two units of N-lysine methyltransferase KMT5A at cysteines 311 and 311.

Details

Redox score ?
73
PDB code
5w1y
Structure name
setd8 in complex with a covalent inhibitor
Structure deposition date
2017-06-05
Thiol separation (Å)
3
Half-sphere exposure sum ?
62
Minimum pKa ?
nan
% buried
nan
Peptide A name
N-lysine methyltransferase KMT5A
Peptide B name
N-lysine methyltransferase KMT5A
Peptide A accession
Q9NQR1
Peptide B accession
Q9NQR1
Peptide A residue number
311
Peptide B residue number
311

Ligandability

A redox-regulated disulphide may form within N-lysine methyltransferase KMT5A between cysteines 311 and 324. However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?

Details

Redox score ?
54
PDB code
5th7
Structure name
complex of setd8 with ms453
Structure deposition date
2016-09-29
Thiol separation (Å)
7
Half-sphere exposure sum ?
67
Minimum pKa ?
nan
% buried
nan
Peptide accession
Q9NQR1
Residue number A
311
Residue number B
324
Peptide name
N-lysine methyltransferase KMT5A

Ligandability

Cysteine 311 of N-lysine methyltransferase KMT5A

Cysteine 324 of N-lysine methyltransferase KMT5A

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