3cy4: Difference between revisions

Revision as of 20:09, 27 July 2008

This article has been automatically seeded. Changes to this page should pertain to the PDB entry only and not to the protein or biomolecule in general.

File:3cy4.png

Template:STRUCTURE 3cy4

Crystal Structure cation-dependent mannose 6-phosphate receptor at pH 7.4Crystal Structure cation-dependent mannose 6-phosphate receptor at pH 7.4

Template:ABSTRACT PUBMED 18272523

About this StructureAbout this Structure

3CY4 is a Single protein structure of sequence from Bos taurus. This structure supersedes the now removed PDB entry 2rl6. Full crystallographic information is available from OCA.

ReferenceReference

Structural Insights into the mechanism of pH-dependent ligand binding and release by the cation-dependent mannose 6-phosphate receptor., Olson LJ, Hindsgaul O, Dahms NM, Kim JJ, J Biol Chem. 2008 Feb 13;. PMID:18272523

Page seeded by OCA on Sun Jul 27 20:09:13 2008

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OCA

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-'''Crystal Structure cation-dependent mannose 6-phosphate receptor at pH 7.4'''
+===Crystal Structure cation-dependent mannose 6-phosphate receptor at pH 7.4===
-==Overview==
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-The cation-dependent mannose 6-phosphate receptor (CD-MPR) is a key component of the lysosomal enzyme targeting system that binds newly synthesized mannose 6-phosphate (Man-6-P)-containing acid hydrolases and transports them to endosomal compartments. The interaction between the MPRs and its ligands is pH-dependent: the homodimeric CD-MPR binds lysosomal enzymes optimally in the pH environment of the trans Golgi network (TGN) (~pH 6.5) and releases its cargo in acidic endosomal compartments (&lt; pH 5.5) and at the cell surface. In addition, CD-MPR binding affinities are modulated by divalent cations. Our previous crystallographic studies have shown that at pH 6.5, the CD-MPR bound to Man-6-P adopts a significantly different quaternary conformation than the CD-MPR in a ligand-unbound state, a feature unique among known lectin structures. To determine whether different pH conditions elicit conformational changes in the receptor that alters ligand binding affinities, we have obtained additional crystal structures representative of the various environments encountered by the receptor including: 1) the CD-MPR bound at pH 6.5 (i.e., TGN) to a high affinity ligand (the terminally phosphorylated trisaccharide P-Man(a1,2)Man(a1,2)Man-O-(CH(2))(8)COOMe), 2) the CD-MPR at pH 4.8 in an unbound state (i.e., endosome), and 3) the CD-MPR at pH 7.4 (i.e., cell surface). A detailed comparison of the available CD-MPR structures reveals the positional invariability of specific binding pocket residues and implicates inter-monomer contact(s), as well as the protonation state of Man-6-P, as regulators of pH-dependent carbohydrate binding.
+The line below this paragraph, {{ABSTRACT_PUBMED_18272523}}, adds the Publication Abstract to the page
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+{{ABSTRACT_PUBMED_18272523}}
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 [[Category: Transmembrane]]
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