2evt
From Proteopedia
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Crystal structure of D48V mutant of human Glycolipid Transfer Protein
Overview
Lipid transfer proteins are important in membrane vesicle biogenesis and, trafficking, signal transduction and immunological presentation processes., The conserved and ubiquitous mammalian glycolipid transfer proteins, (GLTPs) serve as potential regulators of cell processes mediated by, glycosphingolipids, ranging from differentiation and proliferation to, invasive adhesion, neurodegeneration and apoptosis. Here we report crystal, structures of apo-GLTP (1.65 A resolution) and lactosylceramide-bound, (1.95 A) GLTP, in which the bound glycosphingolipid is sandwiched, after, adaptive recognition, within a previously unknown two-layer, all-alpha-helical topology. Glycosphingolipid binding specificity is, achieved through recognition and anchoring of the sugar-amide headgroup to, the GLTP recognition centre by hydrogen bond networks and hydrophobic, contacts, and encapsulation of both lipid chains, in a precisely oriented, manner within a 'moulded-to-fit' hydrophobic tunnel. A cleft-like, conformational gating mechanism, involving two interhelical loops and one, alpha-helix of GLTP, could enable the glycolipid chains to enter and leave, the tunnel in the membrane-associated state. Mutation and functional, analyses of residues in the glycolipid recognition centre and within the, hydrophobic tunnel support a framework for understanding how GLTPs acquire, and release glycosphingolipids during lipid intermembrane transfer and, presentation processes.
About this Structure
2EVT is a Single protein structure of sequence from Homo sapiens with HEX as ligand. Full crystallographic information is available from OCA.
Reference
Structural basis for glycosphingolipid transfer specificity., Malinina L, Malakhova ML, Teplov A, Brown RE, Patel DJ, Nature. 2004 Aug 26;430(7003):1048-53. PMID:15329726
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