2d4q

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Revision as of 19:19, 12 November 2007

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spinqualitylabelsall models 2d4q, resolution 2.30Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image

Crystal structure of the Sec-PH domain of the human neurofibromatosis type 1 protein

Contents 1 Overview 2 Disease 3 About this Structure 4 Reference

Overview

Neurofibromatosis type 1 (NF1) is a common tumour predisposition syndrome, associated with numerous clinical complications. Mutations in the tumour, suppressor gene NF1 are responsible for disease pathogenesis. This gene, encodes the 320 kDa protein neurofibromin, the only clearly defined, function of which is to act as a Ras-specific GTPase-activating protein, (RasGAP). Here we report the structural discovery of a novel module in, neurofibromin, composed of a Sec14p homologous segment and a previously, undetected pleckstrin homology (PH)-like domain of potentially novel, function. We show phospholipid binding by this bipartite module and, identify residues that are involved in this activity; we also show that, the PH-like domain is not sufficient for lipid binding. The unique, architecture of the domain interface points to a model of how the PH-like, domain may regulate binding of a ligand by the Sec14 module.

Disease

Known diseases associated with this structure: Leukemia, juvenile myelomonocytic OMIM:[162200], Melanoma, desmoplastic neurotropic OMIM:[162200], Neurofibromatosis, familial spinal OMIM:[162200], Neurofibromatosis, type 1 OMIM:[162200], Neurofibromatosis-Noonan syndrome OMIM:[162200], Pseudarthrosis, tibial, in NF1 OMIM:[162200], Watson syndrome OMIM:[162200]

About this Structure

2D4Q is a Single protein structure of sequence from Homo sapiens with OXN and POP as ligands. Full crystallographic information is available from OCA.

Reference

A novel bipartite phospholipid-binding module in the neurofibromatosis type 1 protein., D'Angelo I, Welti S, Bonneau F, Scheffzek K, EMBO Rep. 2006 Feb;7(2):174-9. PMID:16397625

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