Exportin-4
Intramolecular
Cysteine 134 and cysteine 186
Cysteine 1022 and cysteine 1025
Cysteine 380 and cysteine 439 L
Cysteine 988 and cysteine 1025
Cysteine 977 and cysteine 1025
Cysteine 813 and cysteine 838
5dlq B 134 B 186
A redox-regulated disulphide may form within Exportin-4 between cysteines 134 and 186. However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?
Details
Redox score ?
53
PDB code
5dlq
Structure name
crystal structure of rangtp-exportin 4-eif5a complex
Structure deposition date
2015-09-07
Thiol separation (Å)
7
Half-sphere exposure sum ?
61
Minimum pKa ?
10
% buried
60
Peptide accession
Q9ESJ0
Residue number A
134
Residue number B
186
Peptide name
Exportin-4
Ligandability
Cysteine 134 of Exportin-4
Cysteine 186 of Exportin-4
5dlq A 1022 A 1025
A redox-regulated disulphide may form within Exportin-4 between cysteines 1022 and 1025. However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?
Details
Redox score ?
51
PDB code
5dlq
Structure name
crystal structure of rangtp-exportin 4-eif5a complex
Structure deposition date
2015-09-07
Thiol separation (Å)
7
Half-sphere exposure sum ?
77
Minimum pKa ?
10
% buried
62
Peptide accession
Q9ESJ0
Residue number A
1022
Residue number B
1025
Peptide name
Exportin-4
Ligandability
Cysteine 1022 of Exportin-4
Cysteine 1025 of Exportin-4
5dlq A 380 A 439
A redox-regulated disulphide may form within Exportin-4 between cysteines 380 and 439. However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?
Details
Redox score ?
42
PDB code
5dlq
Structure name
crystal structure of rangtp-exportin 4-eif5a complex
Structure deposition date
2015-09-07
Thiol separation (Å)
8
Half-sphere exposure sum ?
69
Minimum pKa ?
10
% buried
72
Peptide accession
Q9ESJ0
Residue number A
380
Residue number B
439
Peptide name
Exportin-4
Ligandability
Cysteine 380 of Exportin-4
Cysteine 439 of Exportin-4
5dlq A 988 A 1025
A redox-regulated disulphide may form within Exportin-4 between cysteines 988 and 1025. However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?
Details
Redox score ?
39
PDB code
5dlq
Structure name
crystal structure of rangtp-exportin 4-eif5a complex
Structure deposition date
2015-09-07
Thiol separation (Å)
9
Half-sphere exposure sum ?
75
Minimum pKa ?
11
% buried
73
Peptide accession
Q9ESJ0
Residue number A
988
Residue number B
1025
Peptide name
Exportin-4
Ligandability
Cysteine 988 of Exportin-4
Cysteine 1025 of Exportin-4
5dlq B 977 B 1025
A redox-regulated disulphide may form within Exportin-4 between cysteines 977 and 1025. However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?
Details
Redox score ?
38
PDB code
5dlq
Structure name
crystal structure of rangtp-exportin 4-eif5a complex
Structure deposition date
2015-09-07
Thiol separation (Å)
9
Half-sphere exposure sum ?
78
Minimum pKa ?
11
% buried
80
Peptide accession
Q9ESJ0
Residue number A
977
Residue number B
1025
Peptide name
Exportin-4
Ligandability
Cysteine 977 of Exportin-4
Cysteine 1025 of Exportin-4
5dlq A 813 A 838
A redox-regulated disulphide may form within Exportin-4 between cysteines 813 and 838. However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?
Details
Redox score ?
28
PDB code
5dlq
Structure name
crystal structure of rangtp-exportin 4-eif5a complex
Structure deposition date
2015-09-07
Thiol separation (Å)
9
Half-sphere exposure sum ?
78
Minimum pKa ?
12
% buried
96
Peptide accession
Q9ESJ0
Residue number A
813
Residue number B
838
Peptide name
Exportin-4
Ligandability
Cysteine 813 of Exportin-4
Cysteine 838 of Exportin-4
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