1pu5: Difference between revisions

New page: left|200px<br /> <applet load="1pu5" size="450" color="white" frame="true" align="right" spinBox="true" caption="1pu5, resolution 1.90Å" /> '''GM2-activator Prote...
 
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[[Image:1pu5.gif|left|200px]]<br />
[[Image:1pu5.gif|left|200px]]<br /><applet load="1pu5" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="1pu5" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="1pu5, resolution 1.90&Aring;" />
caption="1pu5, resolution 1.90&Aring;" />
'''GM2-activator Protein crystal structure'''<br />
'''GM2-activator Protein crystal structure'''<br />


==Overview==
==Overview==
The GM2-activator protein (GM2-AP) is a small lysosomal lipid transfer, protein essential for the hydrolytic conversion of ganglioside GM2 to GM3, by beta-hexosaminidase A. The crystal structure of human apo-GM2-AP is, known to consist of a novel beta-cup fold with a spacious hydrophobic, interior. Here, we present two new structures of GM2-AP with bound lipids, showing two different lipid-binding modes within the apolar pocket. The, 1.9A structure with GM2 bound shows the position of the ceramide tail and, significant conformational differences among the three molecular copies in, the asymmetric unit. The tetrasaccharide head group is not visible and is, presumed to be disordered. However, its general position could be, established through modeling. The structure of a low-pH crystal, determined at 2.5A resolution, has a significantly enlarged hydrophobic, channel that merges with the apolar pocket. Electron density inside the, pocket and channel suggests the presence of a trapped phospholipid, molecule. Structure alignments among the four crystallographically unique, monomers provide information on the potential role for lipid binding of, flexible chain segments at the rim of the cavity opening. Two discrete, orientations of the S130-T133 loop define an open and a closed, configuration of the hydrophobic channel that merges with the apolar, pocket. We propose: (i) that the low-pH structure represents an active, membrane-binding conformation; (ii) that the mobile S130-T133 loop serves, as a gate for passage of ligand into the apolar pocket; and (iii) that, this loop and the adjacent apolar V59-W63 loop form a surface patch with, two exposed tryptophan residues that could interface with lipid bilayers.
The GM2-activator protein (GM2-AP) is a small lysosomal lipid transfer protein essential for the hydrolytic conversion of ganglioside GM2 to GM3 by beta-hexosaminidase A. The crystal structure of human apo-GM2-AP is known to consist of a novel beta-cup fold with a spacious hydrophobic interior. Here, we present two new structures of GM2-AP with bound lipids, showing two different lipid-binding modes within the apolar pocket. The 1.9A structure with GM2 bound shows the position of the ceramide tail and significant conformational differences among the three molecular copies in the asymmetric unit. The tetrasaccharide head group is not visible and is presumed to be disordered. However, its general position could be established through modeling. The structure of a low-pH crystal, determined at 2.5A resolution, has a significantly enlarged hydrophobic channel that merges with the apolar pocket. Electron density inside the pocket and channel suggests the presence of a trapped phospholipid molecule. Structure alignments among the four crystallographically unique monomers provide information on the potential role for lipid binding of flexible chain segments at the rim of the cavity opening. Two discrete orientations of the S130-T133 loop define an open and a closed configuration of the hydrophobic channel that merges with the apolar pocket. We propose: (i) that the low-pH structure represents an active membrane-binding conformation; (ii) that the mobile S130-T133 loop serves as a gate for passage of ligand into the apolar pocket; and (iii) that this loop and the adjacent apolar V59-W63 loop form a surface patch with two exposed tryptophan residues that could interface with lipid bilayers.


==Disease==
==Disease==
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==About this Structure==
==About this Structure==
1PU5 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 EPE as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1PU5 OCA].  
1PU5 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=EPE:'>EPE</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1PU5 OCA].  


==Reference==
==Reference==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Rastinejad, F.]]
[[Category: Rastinejad, F.]]
[[Category: Wright, C.S.]]
[[Category: Wright, C S.]]
[[Category: Zhao, Q.]]
[[Category: Zhao, Q.]]
[[Category: EPE]]
[[Category: EPE]]
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[[Category: protein dynamics]]
[[Category: protein dynamics]]


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