5-aminolevulinate synthase, erythroid-specific, mitochondrial
5qqs B 338 B 344
A redox-regulated disulphide may form within 5-aminolevulinate synthase, erythroid-specific, mitochondrial between cysteines 338 and 344. However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?
Details
Redox score ?
43
PDB code
5qqs
Structure name
pandda analysis group deposition -- crystal structure of human alas2a in complex with z275151340
Structure deposition date
2019-05-22
Thiol separation (Å)
7
Half-sphere exposure sum ?
78
Minimum pKa ?
13
% buried
96
Peptide accession
P22557
Residue number A
338
Residue number B
344
Peptide name
5-aminolevulinate synthase, erythroid-specific, mitochondrial
Ligandability
Cysteine 338 of 5-aminolevulinate synthase, erythroid-specific, mitochondrial
Cysteine 344 of 5-aminolevulinate synthase, erythroid-specific, mitochondrial
6hrh A 195 A 490
A redox-regulated disulphide may form within 5-aminolevulinate synthase, erythroid-specific, mitochondrial between cysteines 195 and 490. However, the redox score of this cysteine pair is lower than any known redox-active intermolecular disulphide. ?
Details
Redox score ?
40
PDB code
6hrh
Structure name
structure of human erythroid-specific 5'-aminolevulinate synthase, alas2
Structure deposition date
2018-09-27
Thiol separation (Å)
7
Half-sphere exposure sum ?
82
Minimum pKa ?
12
% buried
97
Peptide accession
P22557
Residue number A
195
Residue number B
490
Peptide name
5-aminolevulinate synthase, erythroid-specific, mitochondrial
Ligandability
Cysteine 195 of 5-aminolevulinate synthase, erythroid-specific, mitochondrial
Cysteine 490 of 5-aminolevulinate synthase, erythroid-specific, mitochondrial
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