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4WZ2

Crystal structure of U-box 2 of LubX / LegU2 / Lpp2887 from Legionella pneumophila str. Paris, Ile175Met mutant

Summary for 4WZ2
Entry DOI10.2210/pdb4wz2/pdb
Related4WZ0 4WZ1 4WZ3
DescriptorE3 ubiquitin-protein ligase LubX, HEXANE-1,6-DIOL, CHLORIDE ION, ... (4 entities in total)
Functional Keywordsalpha/beta protein, effector, structural genomics, psi-biology, midwest center for structural genomics, mcsg, ligase
Biological sourceLegionella pneumophila
Total number of polymer chains3
Total formula weight36061.88
Authors
Stogios, P.J.,Qualie, A.T.,Skarina, T.,Nocek, B.,Di Leo, R.,Yim, V.,Savchenko, A.,Joachimiak, A.,Midwest Center for Structural Genomics (MCSG) (deposition date: 2014-11-18, release date: 2015-01-28, Last modification date: 2019-12-04)
Primary citationQuaile, A.T.,Urbanus, M.L.,Stogios, P.J.,Nocek, B.,Skarina, T.,Ensminger, A.W.,Savchenko, A.
Molecular Characterization of LubX: Functional Divergence of the U-Box Fold by Legionella pneumophila.
Structure, 23:1459-1469, 2015
Cited by
PubMed Abstract: LubX is part of the large arsenal of effectors in Legionella pneumophila that are translocated into the host cytosol during infection. Despite such unique features as the presence of two U-box motifs and its targeting of another effector SidH, the molecular basis of LubX activity remains poorly understood. Here we show that the N terminus of LubX is able to activate an extended number of ubiquitin-conjugating (E2) enzymes including UBE2W, UBEL6, and all tested members of UBE2D and UBE2E families. Crystal structures of LubX alone and in complex with UBE2D2 revealed drastic molecular diversification between the two U-box domains, with only the N-terminal U-box retaining E2 recognition features typical for its eukaryotic counterparts. Extensive mutagenesis followed by functional screening in a yeast model system captured functionally important LubX residues including Arg121, critical for interactions with SidH. Combined, these data provide a new molecular insight into the function of this unique pathogenic factor.
PubMed: 26146184
DOI: 10.1016/j.str.2015.05.020
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.408 Å)
Structure validation

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数据于2024-10-30公开中

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