ReDisulphID

a tool for identifying drug-targetable redox-active disulphides

C-C motif chemokine 27

Intramolecular
Cysteine 33 and cysteine 62
Cysteine 34 and cysteine 77
Cysteine 34 and cysteine 62
Cysteine 33 and cysteine 34
Cysteine 62 and cysteine 77
Cysteine 33 and cysteine 77
A redox-regulated disulphide may form within C-C motif chemokine 27 between cysteines 33 and 62 (9 and 38 respectively in this structure).

Details

Redox score ?
83
PDB code
2kum
Structure name
solution structure of the human chemokine ccl27
Structure deposition date
2010-02-22
Thiol separation (Å)
2
Half-sphere exposure sum ?
48
Minimum pKa ?
nan
% buried
nan
Peptide accession
Q9Y4X3
Residue number A
33
Residue number B
62
Peptide name
C-C motif chemokine 27

Ligandability

Cysteine 33 of C-C motif chemokine 27

Cysteine 62 of C-C motif chemokine 27

A redox-regulated disulphide may form within C-C motif chemokine 27 between cysteines 34 and 77 (10 and 53 respectively in this structure).

Details

Redox score ?
83
PDB code
2kum
Structure name
solution structure of the human chemokine ccl27
Structure deposition date
2010-02-22
Thiol separation (Å)
2
Half-sphere exposure sum ?
71
Minimum pKa ?
nan
% buried
nan
Peptide accession
Q9Y4X3
Residue number A
34
Residue number B
77
Peptide name
C-C motif chemokine 27

Ligandability

Cysteine 34 of C-C motif chemokine 27

Cysteine 77 of C-C motif chemokine 27

A redox-regulated disulphide may form within C-C motif chemokine 27 between cysteines 34 and 62 (10 and 38 respectively in this structure). However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?

Details

Redox score ?
57
PDB code
2kum
Structure name
solution structure of the human chemokine ccl27
Structure deposition date
2010-02-22
Thiol separation (Å)
7
Half-sphere exposure sum ?
51
Minimum pKa ?
nan
% buried
nan
Peptide accession
Q9Y4X3
Residue number A
34
Residue number B
62
Peptide name
C-C motif chemokine 27

Ligandability

Cysteine 34 of C-C motif chemokine 27

Cysteine 62 of C-C motif chemokine 27

A redox-regulated disulphide may form within C-C motif chemokine 27 between cysteines 33 and 34 (9 and 10 respectively in this structure). However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?

Details

Redox score ?
51
PDB code
2kum
Structure name
solution structure of the human chemokine ccl27
Structure deposition date
2010-02-22
Thiol separation (Å)
8
Half-sphere exposure sum ?
63
Minimum pKa ?
nan
% buried
nan
Peptide accession
Q9Y4X3
Residue number A
33
Residue number B
34
Peptide name
C-C motif chemokine 27

Ligandability

Cysteine 33 of C-C motif chemokine 27

Cysteine 34 of C-C motif chemokine 27

A redox-regulated disulphide may form within C-C motif chemokine 27 between cysteines 62 and 77 (38 and 53 respectively in this structure). However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?

Details

Redox score ?
42
PDB code
2kum
Structure name
solution structure of the human chemokine ccl27
Structure deposition date
2010-02-22
Thiol separation (Å)
9
Half-sphere exposure sum ?
56
Minimum pKa ?
nan
% buried
nan
Peptide accession
Q9Y4X3
Residue number A
62
Residue number B
77
Peptide name
C-C motif chemokine 27

Ligandability

Cysteine 62 of C-C motif chemokine 27

Cysteine 77 of C-C motif chemokine 27

A redox-regulated disulphide may form within C-C motif chemokine 27 between cysteines 33 and 77 (9 and 53 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
2kum
Structure name
solution structure of the human chemokine ccl27
Structure deposition date
2010-02-22
Thiol separation (Å)
9
Half-sphere exposure sum ?
68
Minimum pKa ?
nan
% buried
nan
Peptide accession
Q9Y4X3
Residue number A
33
Residue number B
77
Peptide name
C-C motif chemokine 27

Ligandability

Cysteine 33 of C-C motif chemokine 27

Cysteine 77 of C-C motif chemokine 27

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