5AMT
Intracellular growth locus protein E
Summary for 5AMT
| Entry DOI | 10.2210/pdb5amt/pdb |
| Related | 5AMU |
| Descriptor | IGLE, 1,2-ETHANEDIOL, BROMIDE ION, ... (4 entities in total) |
| Functional Keywords | transport protein, bacterial secretion system, lipoprotein, igle, tssj, francisella novicida |
| Biological source | FRANCISELLA NOVICIDA |
| Total number of polymer chains | 2 |
| Total formula weight | 29781.32 |
| Authors | Robb, C.S.,Nano, F.E.,Boraston, A.B. (deposition date: 2015-09-01, release date: 2016-10-05, Last modification date: 2024-05-08) |
| Primary citation | Robb, C.S.,Nano, F.E.,Boraston, A.B. Cloning, Expression, Purification, Crystallization and Preliminary X-Ray Diffraction Analysis of Intracellular Growth Locus E (Igle) Protein from Francisella Tularensis Subsp. Novicida. Acta Crystallogr.,Sect.F, 66:1596-1598, 2010 Cited by PubMed Abstract: Tularaemia is an uncommon but potentially dangerous zoonotic disease caused by the bacterium Francisella tularensis. As few as ten bacterial cells are sufficient to cause disease in a healthy human, making this one of the most infectious disease agents known. The virulence of this organism is dependent upon a genetic locus known as the Francisella pathogenicity island (FPI), which encodes components of a secretion system that is related to the type VI secretion system. Here, the cloning, expression, purification and preliminary X-ray diffraction statistics of the FPI-encoded protein IglE are presented. This putative lipoprotein is required for intra-macrophage growth and is thought to be a constituent of the periplasmic portion of the type VI-like protein complex that is responsible for the secretion of critical virulence factors in Francisella. PubMed: 21139203DOI: 10.1107/S1744309110034378 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.62 Å) |
Structure validation
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