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1y4j

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(New page: 200px<br /> <applet load="1y4j" size="450" color="white" frame="true" align="right" spinBox="true" caption="1y4j, resolution 1.864&Aring;" /> '''Crystal structure ...)
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<applet load="1y4j" size="450" color="white" frame="true" align="right" spinBox="true"
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caption="1y4j, resolution 1.864&Aring;" />
'''Crystal structure of the paralogue of the human formylglycine generating enzyme'''<br />
'''Crystal structure of the paralogue of the human formylglycine generating enzyme'''<br />
==Overview==
==Overview==
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In eukaryotes, sulfate esters are degraded by sulfatases, which possess a, unique Calpha-formylglycine residue in their active site. The defect in, post-translational formation of the Calpha-formylglycine residue causes a, severe lysosomal storage disorder in humans. Recently, FGE, (formylglycine-generating enzyme) has been identified as the protein, required for this specific modification. Using sequence comparisons, a, protein homologous to FGE was found and denoted pFGE (paralog of FGE)., pFGE binds a sulfatase-derived peptide bearing the FGE recognition motif, but it lacks formylglycine-generating activity. Both proteins belong to a, large family of pro- and eukaryotic proteins containing the DUF323 domain, a formylglycine-generating enzyme domain of unknown three-dimensional, structure. We have crystallized the glycosylated human pFGE and determined, its crystal structure at a resolution of 1.86 A. The structure reveals a, novel fold, which we denote the FGE fold and which therefore serves as a, paradigm for the DUF323 domain. It is characterized by an asymmetric, partitioning of secondary structure elements and is stabilized by two, calcium cations. A deep cleft on the surface of pFGE most likely, represents the sulfatase polypeptide binding site. The asymmetric unit of, the pFGE crystal contains a homodimer. The putative peptide binding site, is buried between the monomers, indicating a biological significance of, the dimer. The structure suggests the capability of pFGE to form a, heterodimer with FGE.
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In eukaryotes, sulfate esters are degraded by sulfatases, which possess a unique Calpha-formylglycine residue in their active site. The defect in post-translational formation of the Calpha-formylglycine residue causes a severe lysosomal storage disorder in humans. Recently, FGE (formylglycine-generating enzyme) has been identified as the protein required for this specific modification. Using sequence comparisons, a protein homologous to FGE was found and denoted pFGE (paralog of FGE). pFGE binds a sulfatase-derived peptide bearing the FGE recognition motif, but it lacks formylglycine-generating activity. Both proteins belong to a large family of pro- and eukaryotic proteins containing the DUF323 domain, a formylglycine-generating enzyme domain of unknown three-dimensional structure. We have crystallized the glycosylated human pFGE and determined its crystal structure at a resolution of 1.86 A. The structure reveals a novel fold, which we denote the FGE fold and which therefore serves as a paradigm for the DUF323 domain. It is characterized by an asymmetric partitioning of secondary structure elements and is stabilized by two calcium cations. A deep cleft on the surface of pFGE most likely represents the sulfatase polypeptide binding site. The asymmetric unit of the pFGE crystal contains a homodimer. The putative peptide binding site is buried between the monomers, indicating a biological significance of the dimer. The structure suggests the capability of pFGE to form a heterodimer with FGE.
==About this Structure==
==About this Structure==
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1Y4J is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with CA and MPD as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1Y4J OCA].
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1Y4J is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=CA:'>CA</scene> and <scene name='pdbligand=MPD:'>MPD</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1Y4J OCA].
==Reference==
==Reference==
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[[Category: Dickmanns, A.]]
[[Category: Dickmanns, A.]]
[[Category: Ficner, R.]]
[[Category: Ficner, R.]]
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[[Category: Rudolph, M.G.]]
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[[Category: Rudolph, M G.]]
[[Category: CA]]
[[Category: CA]]
[[Category: MPD]]
[[Category: MPD]]
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[[Category: sulfatases]]
[[Category: sulfatases]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 20:14:47 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 16:01:48 2008''

Revision as of 14:01, 21 February 2008


1y4j, resolution 1.864Å

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Crystal structure of the paralogue of the human formylglycine generating enzyme

Overview

In eukaryotes, sulfate esters are degraded by sulfatases, which possess a unique Calpha-formylglycine residue in their active site. The defect in post-translational formation of the Calpha-formylglycine residue causes a severe lysosomal storage disorder in humans. Recently, FGE (formylglycine-generating enzyme) has been identified as the protein required for this specific modification. Using sequence comparisons, a protein homologous to FGE was found and denoted pFGE (paralog of FGE). pFGE binds a sulfatase-derived peptide bearing the FGE recognition motif, but it lacks formylglycine-generating activity. Both proteins belong to a large family of pro- and eukaryotic proteins containing the DUF323 domain, a formylglycine-generating enzyme domain of unknown three-dimensional structure. We have crystallized the glycosylated human pFGE and determined its crystal structure at a resolution of 1.86 A. The structure reveals a novel fold, which we denote the FGE fold and which therefore serves as a paradigm for the DUF323 domain. It is characterized by an asymmetric partitioning of secondary structure elements and is stabilized by two calcium cations. A deep cleft on the surface of pFGE most likely represents the sulfatase polypeptide binding site. The asymmetric unit of the pFGE crystal contains a homodimer. The putative peptide binding site is buried between the monomers, indicating a biological significance of the dimer. The structure suggests the capability of pFGE to form a heterodimer with FGE.

About this Structure

1Y4J is a Single protein structure of sequence from Homo sapiens with and as ligands. Full crystallographic information is available from OCA.

Reference

Crystal structure of human pFGE, the paralog of the Calpha-formylglycine-generating enzyme., Dickmanns A, Schmidt B, Rudolph MG, Mariappan M, Dierks T, von Figura K, Ficner R, J Biol Chem. 2005 Apr 15;280(15):15180-7. Epub 2005 Feb 1. PMID:15687489

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