6SOZ
Glycosylated Trypanosoma brucei transferrin receptor in complex with human transferrin
Summary for 6SOZ
| Entry DOI | 10.2210/pdb6soz/pdb |
| Related | 6SOY |
| Descriptor | ESAG6, subunit of heterodimeric transferrin receptor, ESAG7, subunit of heterodimeric transferrin receptor, Serotransferrin, ... (7 entities in total) |
| Functional Keywords | trypanosoma brucei trypanosome transferrin receptor transferrrin cell surface, protein binding |
| Biological source | Trypanosoma brucei More |
| Total number of polymer chains | 3 |
| Total formula weight | 159196.75 |
| Authors | Trevor, C.,Carrington, M.,Higgins, M.K. (deposition date: 2019-08-30, release date: 2019-11-06, Last modification date: 2024-10-16) |
| Primary citation | Trevor, C.E.,Gonzalez-Munoz, A.L.,Macleod, O.J.S.,Woodcock, P.G.,Rust, S.,Vaughan, T.J.,Garman, E.F.,Minter, R.,Carrington, M.,Higgins, M.K. Structure of the trypanosome transferrin receptor reveals mechanisms of ligand recognition and immune evasion. Nat Microbiol, 4:2074-2081, 2019 Cited by PubMed Abstract: To maintain prolonged infection of mammals, African trypanosomes have evolved remarkable surface coats and a system of antigenic variation. Within these coats are receptors for macromolecular nutrients such as transferrin. These must be accessible to their ligands but must not confer susceptibility to immunoglobulin-mediated attack. Trypanosomes have a wide host range and their receptors must also bind ligands from diverse species. To understand how these requirements are achieved, in the context of transferrin uptake, we determined the structure of a Trypanosoma brucei transferrin receptor in complex with human transferrin, showing how this heterodimeric receptor presents a large asymmetric ligand-binding platform. The trypanosome genome contains a family of around 14 transferrin receptors, which has been proposed to allow binding to transferrin from different mammalian hosts. However, we find that a single receptor can bind transferrin from a broad range of mammals, indicating that receptor variation is unlikely to be necessary for promiscuity of host infection. In contrast, polymorphic sites and N-linked glycans are preferentially found in exposed positions on the receptor surface, not contacting transferrin, suggesting that transferrin receptor diversification is driven by a need for antigenic variation in the receptor to prolong survival in a host. PubMed: 31636418DOI: 10.1038/s41564-019-0589-0 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (3.42 Å) |
Structure validation
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