ReDisulphID

a tool for identifying drug-targetable redox-active disulphides

Rho guanine nucleotide exchange factor 6

Intramolecular
Cysteine 57 and cysteine 66
Cysteine 42 and cysteine 57
Cysteine 42 and cysteine 77
Cysteine 42 and cysteine 66
A redox-regulated disulphide may form within Rho guanine nucleotide exchange factor 6 between cysteines 57 and 66 (61 and 70 respectively in this structure). However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?

Details

Redox score ?
55
PDB code
1wyr
Structure name
solution structure of the ch domain of human rho guanine nucleotide exchange factor 6
Structure deposition date
2005-02-15
Thiol separation (Å)
7
Half-sphere exposure sum ?
59
Minimum pKa ?
10
% buried
6
Peptide accession
Q15052
Residue number A
57
Residue number B
66
Peptide name
Rho guanine nucleotide exchange factor 6

Ligandability

Cysteine 57 of Rho guanine nucleotide exchange factor 6

Cysteine 66 of Rho guanine nucleotide exchange factor 6

A redox-regulated disulphide may form within Rho guanine nucleotide exchange factor 6 between cysteines 42 and 57 (46 and 61 respectively in this structure). However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?

Details

Redox score ?
43
PDB code
1wyr
Structure name
solution structure of the ch domain of human rho guanine nucleotide exchange factor 6
Structure deposition date
2005-02-15
Thiol separation (Å)
9
Half-sphere exposure sum ?
64
Minimum pKa ?
10
% buried
30
Peptide accession
Q15052
Residue number A
42
Residue number B
57
Peptide name
Rho guanine nucleotide exchange factor 6

Ligandability

Cysteine 42 of Rho guanine nucleotide exchange factor 6

Cysteine 57 of Rho guanine nucleotide exchange factor 6

A redox-regulated disulphide may form within Rho guanine nucleotide exchange factor 6 between cysteines 42 and 77 (46 and 81 respectively in this structure). However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?

Details

Redox score ?
37
PDB code
1wyr
Structure name
solution structure of the ch domain of human rho guanine nucleotide exchange factor 6
Structure deposition date
2005-02-15
Thiol separation (Å)
9
Half-sphere exposure sum ?
71
Minimum pKa ?
11
% buried
54
Peptide accession
Q15052
Residue number A
42
Residue number B
77
Peptide name
Rho guanine nucleotide exchange factor 6

Ligandability

Cysteine 42 of Rho guanine nucleotide exchange factor 6

Cysteine 77 of Rho guanine nucleotide exchange factor 6

A redox-regulated disulphide may form within Rho guanine nucleotide exchange factor 6 between cysteines 42 and 66 (46 and 70 respectively in this structure). However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?

Details

Redox score ?
36
PDB code
1wyr
Structure name
solution structure of the ch domain of human rho guanine nucleotide exchange factor 6
Structure deposition date
2005-02-15
Thiol separation (Å)
10
Half-sphere exposure sum ?
70
Minimum pKa ?
10
% buried
36
Peptide accession
Q15052
Residue number A
42
Residue number B
66
Peptide name
Rho guanine nucleotide exchange factor 6

Ligandability

Cysteine 42 of Rho guanine nucleotide exchange factor 6

Cysteine 66 of Rho guanine nucleotide exchange factor 6

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