1x3z

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(New page: 200px<br /><applet load="1x3z" size="450" color="white" frame="true" align="right" spinBox="true" caption="1x3z, resolution 2.80&Aring;" /> '''Structure of a pepti...)
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'''Structure of a peptide:N-glycanase-Rad23 complex'''<br />
'''Structure of a peptide:N-glycanase-Rad23 complex'''<br />
==Overview==
==Overview==
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In eukaryotes, misfolded proteins must be distinguished from correctly, folded proteins during folding and transport processes by quality control, systems. Yeast peptide:N-glycanase (yPNGase) specifically deglycosylates, the denatured form of N-linked glycoproteins in the cytoplasm and assists, proteasome-mediated glycoprotein degradation by forming a complex with 26S, proteasome through DNA repair protein, yRad23. Here, we describe the, crystal structures of a yPNGase and XPC-binding domain of yRad23, (yRad23XBD, residues 238-309) complex and of a yPNGase-yRad23XBD complex, bound to a caspase inhibitor, Z-VAD-fmk. yPNGase is formed with three, domains, a core domain containing a Cys-His-Asp triad, a Zn-binding, domain, and a Rad23-binding domain. Both N- and C-terminal helices of, yPNGase interact with yRad23 through extensive hydrophobic interactions., The active site of yPNGase is located in a deep cleft that is formed with, residues conserved in all PNGase members, and three sugar molecules are, bound to this cleft. Complex structures in conjunction with mutational, analyses revealed that the walls of the cleft block access to the active, site of yPNGase by native glycoprotein, whereas the cleft is sufficiently, wide to accommodate denatured glycoprotein, thus explaining the, specificity of PNGase for denatured substrates.
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In eukaryotes, misfolded proteins must be distinguished from correctly folded proteins during folding and transport processes by quality control systems. Yeast peptide:N-glycanase (yPNGase) specifically deglycosylates the denatured form of N-linked glycoproteins in the cytoplasm and assists proteasome-mediated glycoprotein degradation by forming a complex with 26S proteasome through DNA repair protein, yRad23. Here, we describe the crystal structures of a yPNGase and XPC-binding domain of yRad23 (yRad23XBD, residues 238-309) complex and of a yPNGase-yRad23XBD complex bound to a caspase inhibitor, Z-VAD-fmk. yPNGase is formed with three domains, a core domain containing a Cys-His-Asp triad, a Zn-binding domain, and a Rad23-binding domain. Both N- and C-terminal helices of yPNGase interact with yRad23 through extensive hydrophobic interactions. The active site of yPNGase is located in a deep cleft that is formed with residues conserved in all PNGase members, and three sugar molecules are bound to this cleft. Complex structures in conjunction with mutational analyses revealed that the walls of the cleft block access to the active site of yPNGase by native glycoprotein, whereas the cleft is sufficiently wide to accommodate denatured glycoprotein, thus explaining the specificity of PNGase for denatured substrates.
==About this Structure==
==About this Structure==
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1X3Z is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Saccharomyces_cerevisiae Saccharomyces cerevisiae] with SUC and ZN as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine_amidase Peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine amidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.5.1.52 3.5.1.52] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1X3Z OCA].
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1X3Z is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Saccharomyces_cerevisiae Saccharomyces cerevisiae] with <scene name='pdbligand=SUC:'>SUC</scene> and <scene name='pdbligand=ZN:'>ZN</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine_amidase Peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine amidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.5.1.52 3.5.1.52] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1X3Z OCA].
==Reference==
==Reference==
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[[Category: Saccharomyces cerevisiae]]
[[Category: Saccharomyces cerevisiae]]
[[Category: Cho, Y.]]
[[Category: Cho, Y.]]
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[[Category: Choi, J.M.]]
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[[Category: Choi, J M.]]
[[Category: Lee, C.]]
[[Category: Lee, C.]]
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[[Category: Lee, J.H.]]
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[[Category: Lee, J H.]]
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[[Category: Yi, K.J.]]
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[[Category: Yi, K J.]]
[[Category: SUC]]
[[Category: SUC]]
[[Category: ZN]]
[[Category: ZN]]
[[Category: protein-protein-inhibitor complex]]
[[Category: protein-protein-inhibitor complex]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Wed Nov 21 05:49:42 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:50:47 2008''

Revision as of 13:50, 21 February 2008


1x3z, resolution 2.80Å

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Structure of a peptide:N-glycanase-Rad23 complex

Overview

In eukaryotes, misfolded proteins must be distinguished from correctly folded proteins during folding and transport processes by quality control systems. Yeast peptide:N-glycanase (yPNGase) specifically deglycosylates the denatured form of N-linked glycoproteins in the cytoplasm and assists proteasome-mediated glycoprotein degradation by forming a complex with 26S proteasome through DNA repair protein, yRad23. Here, we describe the crystal structures of a yPNGase and XPC-binding domain of yRad23 (yRad23XBD, residues 238-309) complex and of a yPNGase-yRad23XBD complex bound to a caspase inhibitor, Z-VAD-fmk. yPNGase is formed with three domains, a core domain containing a Cys-His-Asp triad, a Zn-binding domain, and a Rad23-binding domain. Both N- and C-terminal helices of yPNGase interact with yRad23 through extensive hydrophobic interactions. The active site of yPNGase is located in a deep cleft that is formed with residues conserved in all PNGase members, and three sugar molecules are bound to this cleft. Complex structures in conjunction with mutational analyses revealed that the walls of the cleft block access to the active site of yPNGase by native glycoprotein, whereas the cleft is sufficiently wide to accommodate denatured glycoprotein, thus explaining the specificity of PNGase for denatured substrates.

About this Structure

1X3Z is a Protein complex structure of sequences from Saccharomyces cerevisiae with and as ligands. Active as Peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine amidase, with EC number 3.5.1.52 Full crystallographic information is available from OCA.

Reference

Structure of a peptide:N-glycanase-Rad23 complex: insight into the deglycosylation for denatured glycoproteins., Lee JH, Choi JM, Lee C, Yi KJ, Cho Y, Proc Natl Acad Sci U S A. 2005 Jun 28;102(26):9144-9. Epub 2005 Jun 17. PMID:15964983

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