ReDisulphID

a tool for identifying drug-targetable redox-active disulphides

UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase

Intermolecular
Cysteine 106 and cysteine 106
Cysteine 106 and cysteine 107
Cysteine 107 and cysteine 107
Intramolecular
Cysteine 81 and cysteine 87
A redox-regulated disulphide may form between two units of UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase at cysteines 106 and 106.

Details

Redox score ?
71
PDB code
6bw6
Structure name
human gpt (dpagt1) h129 variant in complex with tunicamycin
Structure deposition date
2017-12-14
Thiol separation (Å)
4
Half-sphere exposure sum ?
93
Minimum pKa ?
5
% buried
100
Peptide A name
UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase
Peptide B name
UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase
Peptide A accession
Q9H3H5
Peptide B accession
Q9H3H5
Peptide A residue number
106
Peptide B residue number
106

Ligandability

A redox-regulated disulphide may form between two units of UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase at cysteines 106 and 107. However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?

Details

Redox score ?
59
PDB code
6bw5
Structure name
human gpt (dpagt1) in complex with tunicamycin
Structure deposition date
2017-12-14
Thiol separation (Å)
4
Half-sphere exposure sum ?
98
Minimum pKa ?
13
% buried
nan
Peptide A name
UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase
Peptide B name
UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase
Peptide A accession
Q9H3H5
Peptide B accession
Q9H3H5
Peptide A residue number
106
Peptide B residue number
107

Ligandability

Cysteine 106 of UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase

Cysteine 107 of UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase

A redox-regulated disulphide may form between two units of UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase at cysteines 107 and 107. However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?

Details

Redox score ?
24
PDB code
6bw5
Structure name
human gpt (dpagt1) in complex with tunicamycin
Structure deposition date
2017-12-14
Thiol separation (Å)
9
Half-sphere exposure sum ?
100
Minimum pKa ?
13
% buried
100
Peptide A name
UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase
Peptide B name
UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase
Peptide A accession
Q9H3H5
Peptide B accession
Q9H3H5
Peptide A residue number
107
Peptide B residue number
107

Ligandability

A redox-regulated disulphide may form within UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase between cysteines 81 and 87.

Details

Redox score ?
70
PDB code
6bw6
Structure name
human gpt (dpagt1) h129 variant in complex with tunicamycin
Structure deposition date
2017-12-14
Thiol separation (Å)
7
Half-sphere exposure sum ?
nan
Minimum pKa ?
8
% buried
0
Peptide accession
Q9H3H5
Residue number A
81
Residue number B
87
Peptide name
UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase

Ligandability

Cysteine 81 of UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase

Cysteine 87 of UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase

If this tool was useful for finding a disulphide, please cite: