1y1j: Difference between revisions

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[[Image:1y1j.gif|left|200px]]
[[Image:1y1j.gif|left|200px]]


{{Structure
<!--
|PDB= 1y1j |SIZE=350|CAPTION= <scene name='initialview01'>1y1j</scene>, resolution 1.55&Aring;
The line below this paragraph, containing "STRUCTURE_1y1j", creates the "Structure Box" on the page.
|SITE=
You may change the PDB parameter (which sets the PDB file loaded into the applet)
|LIGAND= <scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=CXS:3-CYCLOHEXYL-1-PROPYLSULFONIC+ACID'>CXS</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>, <scene name='pdbligand=OCS:CYSTEINESULFONIC+ACID'>OCS</scene>
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
|ACTIVITY=  
or leave the SCENE parameter empty for the default display.
|GENE=  
-->
|DOMAIN=
{{STRUCTURE_1y1j| PDB=1y1j  | SCENE= }}  
|RELATEDENTRY=[[1y1e|1Y1E]], [[1y1f|1Y1F]], [[1y1g|1Y1G]], [[1y1h|1Y1H]], [[1y1i|1Y1I]]
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1y1j FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1y1j OCA], [http://www.ebi.ac.uk/pdbsum/1y1j PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1y1j RCSB]</span>
}}


'''human formylglycine generating enzyme, sulfonic acid/desulfurated form'''
'''human formylglycine generating enzyme, sulfonic acid/desulfurated form'''
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[[Category: Ficner, R.]]
[[Category: Ficner, R.]]
[[Category: Rudolph, M G.]]
[[Category: Rudolph, M G.]]
[[Category: cysteine sulfenic acid]]
[[Category: Cysteine sulfenic acid]]
[[Category: formylglycine]]
[[Category: Formylglycine]]
[[Category: multiple sulfatase deficiency]]
[[Category: Multiple sulfatase deficiency]]
 
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Revision as of 15:46, 3 May 2008

File:1y1j.gif

Template:STRUCTURE 1y1j

human formylglycine generating enzyme, sulfonic acid/desulfurated form


OverviewOverview

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.

About this StructureAbout this Structure

1Y1J is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

ReferenceReference

Molecular basis for multiple sulfatase deficiency and mechanism for formylglycine generation of the human formylglycine-generating enzyme., Dierks T, Dickmanns A, Preusser-Kunze A, Schmidt B, Mariappan M, von Figura K, Ficner R, Rudolph MG, Cell. 2005 May 20;121(4):541-52. PMID:15907468 Page seeded by OCA on Sat May 3 15:46:25 2008

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