2agc: Difference between revisions

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[[Image:2agc.gif|left|200px]]
[[Image:2agc.gif|left|200px]]


{{Structure
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The line below this paragraph, containing "STRUCTURE_2agc", 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=DAO:LAURIC+ACID'>DAO</scene>, <scene name='pdbligand=MYR:MYRISTIC+ACID'>MYR</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= Gm2a ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=10090 Mus musculus])
-->
|DOMAIN=
{{STRUCTURE_2agc| PDB=2agc  | SCENE= }}  
|RELATEDENTRY=[[1g13|1G13]]
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2agc FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2agc OCA], [http://www.ebi.ac.uk/pdbsum/2agc PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2agc RCSB]</span>
}}


'''Crystal Structure of mouse GM2- activator Protein'''
'''Crystal Structure of mouse GM2- activator Protein'''
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[[Category: Rastinejad, F.]]
[[Category: Rastinejad, F.]]
[[Category: Wright, C S.]]
[[Category: Wright, C S.]]
[[Category: constricted lipid binding pocket]]
[[Category: Constricted lipid binding pocket]]
 
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Revision as of 19:01, 3 May 2008

File:2agc.gif

Template:STRUCTURE 2agc

Crystal Structure of mouse GM2- activator Protein


OverviewOverview

GM2-activator protein (GM2AP) is a lysosomal lipid transfer protein with important biological roles in ganglioside catabolism, phospholipid metabolism, and T-cell activation. Previous studies of crystal structures of GM2AP complexed with the physiological ligand GM2 and platelet activating factor (PAF) have shown binding at two specific locations within the spacious apolar pocket and an ordering effect of endogenous resident lipids. To investigate the structural basis of phospholipid binding further, GM2AP was cocrystallized with phosphatidylcholine (PC), known to interact with GM2AP. Analysis of three crystal forms revealed binding of single chain lipids and fatty acids only and surprisingly not intact PC. The regions of best defined electron density are consistent with the presence of lyso-PC and oleic acid, which constitute deacylation products of PC. Their acyl tails are in stacking contact with shorter, less well-defined stretches of electron density that may represent resident fatty acids. The GM2AP associated hydrolytic activity that generates lyso-PC was further confirmed by mass spectrometry and enzymatic assays. In addition, we report the structures of (i) mutant Y137S, assessing the role of Tyr137 in lipid transfer via the hydrophobic cleft, and (ii) apo-mouse GM2AP, revealing a hydrophobic pocket with a constricted opening. Our structural results provide new insights into the biological functions of GM2AP. The combined effect of hydrolytic and lipid transfer properties has profound implications in cellular signaling.

About this StructureAbout this Structure

2AGC is a Single protein structure of sequence from Mus musculus. Full crystallographic information is available from OCA.

ReferenceReference

Crystal structure analysis of phosphatidylcholine-GM2-activator product complexes: evidence for hydrolase activity., Wright CS, Mi LZ, Lee S, Rastinejad F, Biochemistry. 2005 Oct 18;44(41):13510-21. PMID:16216074 Page seeded by OCA on Sat May 3 19:01:04 2008

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