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1Y1G

Human formylglycine generating enzyme, double sulfonic acid form

Summary for 1Y1G
Entry DOI10.2210/pdb1y1g/pdb
Related1Y1E 1Y1F 1Y1H 1Y1I 1Y1J
DescriptorC-alpha-formyglycine-generating enzyme, 2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, CALCIUM ION, ... (4 entities in total)
Functional Keywordsformylglycine, multiple sulfatase deficiency, cysteine sulfenic acid, oxidoreductase
Biological sourceHomo sapiens (human)
Total number of polymer chains1
Total formula weight35509.20
Authors
Rudolph, M.G.,Dickmanns, A.,Ficner, R. (deposition date: 2004-11-18, release date: 2005-05-31, Last modification date: 2020-07-29)
Primary citationDierks, T.,Dickmanns, A.,Preusser-Kunze, A.,Schmidt, B.,Mariappan, M.,von Figura, K.,Ficner, R.,Rudolph, M.G.
Molecular basis for multiple sulfatase deficiency and mechanism for formylglycine generation of the human formylglycine-generating enzyme.
Cell(Cambridge,Mass.), 121:541-552, 2005
Cited by
PubMed Abstract: Sulfatases are enzymes essential for degradation and remodeling of sulfate esters. Formylglycine (FGly), the key catalytic residue in the active site, is unique to sulfatases. In higher eukaryotes, FGly is generated from a cysteine precursor by the FGly-generating enzyme (FGE). Inactivity of FGE results in multiple sulfatase deficiency (MSD), a fatal autosomal recessive syndrome. Based on the crystal structure, we report that FGE is a single-domain monomer with a surprising paucity of secondary structure and adopts a unique fold. The effect of all 18 missense mutations found in MSD patients is explained by the FGE structure, providing a molecular basis of MSD. The catalytic mechanism of FGly generation was elucidated by six high-resolution structures of FGE in different redox environments. The structures allow formulation of a novel oxygenase mechanism whereby FGE utilizes molecular oxygen to generate FGly via a cysteine sulfenic acid intermediate.
PubMed: 15907468
DOI: 10.1016/j.cell.2005.03.001
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.67 Å)
Structure validation

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