Dual specificity tyrosine-phosphorylation-regulated kinase 2
7dg4 A 347 A 373
A redox-regulated disulphide may form within Dual specificity tyrosine-phosphorylation-regulated kinase 2 between cysteines 347 and 373.
Details
Redox score ?
69
PDB code
7dg4
Structure name
the co-crystal structure of dyrk2 with a small molecule inhibitor 6
Structure deposition date
2020-11-10
Thiol separation (Å)
4
Half-sphere exposure sum ?
77
Minimum pKa ?
8
% buried
81
Peptide accession
Q92630
Residue number A
347
Residue number B
373
Peptide name
Dual specificity tyrosine-phosphorylation-regulated kinase 2
Ligandability
Cysteine 347 of Dual specificity tyrosine-phosphorylation-regulated kinase 2
Cysteine 373 of Dual specificity tyrosine-phosphorylation-regulated kinase 2
7dhc A 410 A 515
A redox-regulated disulphide may form within Dual specificity tyrosine-phosphorylation-regulated kinase 2 between cysteines 410 and 515. However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?
Details
Redox score ?
31
PDB code
7dhc
Structure name
the co-crystal structure of dyrk2 with a small molecule inhibitor 10
Structure deposition date
2020-11-13
Thiol separation (Å)
9
Half-sphere exposure sum ?
79
Minimum pKa ?
12
% buried
100
Peptide accession
Q92630
Residue number A
410
Residue number B
515
Peptide name
Dual specificity tyrosine-phosphorylation-regulated kinase 2
Ligandability
Cysteine 410 of Dual specificity tyrosine-phosphorylation-regulated kinase 2
Cysteine 515 of Dual specificity tyrosine-phosphorylation-regulated kinase 2
If this tool was useful for finding a disulphide, please cite: