ReDisulphID

a tool for identifying drug-targetable redox-active disulphides

Nicotinamide/nicotinic acid mononucleotide adenylyltransferase 3

Intramolecular
Cysteine 134 and cysteine 164
Cysteine 12 and cysteine 134
A redox-regulated disulphide may form within Nicotinamide/nicotinic acid mononucleotide adenylyltransferase 3 between cysteines 134 and 164.

Details

Redox score ?
66
PDB code
1nur
Structure name
crystal structure of human cytosolic nmn/namn adenylyltransferase
Structure deposition date
2003-02-01
Thiol separation (Å)
4
Half-sphere exposure sum ?
79
Minimum pKa ?
9
% buried
100
Peptide accession
Q96T66
Residue number A
134
Residue number B
164
Peptide name
Nicotinamide/nicotinic acid mononucleotide adenylyltransferase 3

Ligandability

Cysteine 134 of Nicotinamide/nicotinic acid mononucleotide adenylyltransferase 3

Cysteine 164 of Nicotinamide/nicotinic acid mononucleotide adenylyltransferase 3

A redox-regulated disulphide may form within Nicotinamide/nicotinic acid mononucleotide adenylyltransferase 3 between cysteines 12 and 134. However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?

Details

Redox score ?
23
PDB code
1nur
Structure name
crystal structure of human cytosolic nmn/namn adenylyltransferase
Structure deposition date
2003-02-01
Thiol separation (Å)
10
Half-sphere exposure sum ?
78
Minimum pKa ?
14
% buried
100
Peptide accession
Q96T66
Residue number A
12
Residue number B
134
Peptide name
Nicotinamide/nicotinic acid mononucleotide adenylyltransferase 3

Ligandability

Cysteine 12 of Nicotinamide/nicotinic acid mononucleotide adenylyltransferase 3

Cysteine 134 of Nicotinamide/nicotinic acid mononucleotide adenylyltransferase 3

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