1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-2
Intramolecular
Cysteine 353 and cysteine 355
Cysteine 296 and cysteine 781
Cysteine 360 and cysteine 424
Cysteine 216 and cysteine 296
2fju B 353 B 355
A redox-regulated disulphide may form within 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-2 between cysteines 353 and 355. However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?
Details
Redox score ?
43
PDB code
2fju
Structure name
activated rac1 bound to its effector phospholipase c beta 2
Structure deposition date
2006-01-03
Thiol separation (Å)
7
Half-sphere exposure sum ?
95
Minimum pKa ?
11
% buried
100
Peptide accession
Q00722
Residue number A
353
Residue number B
355
Peptide name
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-2
Ligandability
Cysteine 353 of 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-2
Cysteine 355 of 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-2
2fju B 296 B 777
A redox-regulated disulphide may form within 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-2 between cysteines 296 and 781 (296 and 777 respectively in this structure). However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?
Details
Redox score ?
40
PDB code
2fju
Structure name
activated rac1 bound to its effector phospholipase c beta 2
Structure deposition date
2006-01-03
Thiol separation (Å)
8
Half-sphere exposure sum ?
76
Minimum pKa ?
11
% buried
100
Peptide accession
Q00722
Residue number A
296
Residue number B
781
Peptide name
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-2
Ligandability
Cysteine 296 of 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-2
Cysteine 781 of 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-2
2fju B 360 B 424
A redox-regulated disulphide may form within 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-2 between cysteines 360 and 424. However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?
Details
Redox score ?
37
PDB code
2fju
Structure name
activated rac1 bound to its effector phospholipase c beta 2
Structure deposition date
2006-01-03
Thiol separation (Å)
8
Half-sphere exposure sum ?
75
Minimum pKa ?
13
% buried
100
Peptide accession
Q00722
Residue number A
360
Residue number B
424
Peptide name
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-2
Ligandability
Cysteine 360 of 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-2
Cysteine 424 of 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-2
2fju B 216 B 296
A redox-regulated disulphide may form within 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-2 between cysteines 216 and 296. However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?
Details
Redox score ?
37
PDB code
2fju
Structure name
activated rac1 bound to its effector phospholipase c beta 2
Structure deposition date
2006-01-03
Thiol separation (Å)
9
Half-sphere exposure sum ?
66
Minimum pKa ?
11
% buried
100
Peptide accession
Q00722
Residue number A
216
Residue number B
296
Peptide name
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-2
Ligandability
Cysteine 216 of 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-2
Cysteine 296 of 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-2
If this tool was useful for finding a disulphide, please cite: