3WLU
Crystal Structure of human galectin-9 NCRD with Selenolactose
Summary for 3WLU
| Entry DOI | 10.2210/pdb3wlu/pdb |
| Related | 2EAK |
| Descriptor | Galectin-9, 2-(trimethylsilyl)ethyl 4-O-beta-D-galactopyranosyl-6-Se-methyl-6-seleno-beta-D-glucopyranoside (3 entities in total) |
| Functional Keywords | selenolactose, beta sandwich, galectin, carbohydrate binding, sugar binding protein |
| Biological source | Homo sapiens (human) |
| Cellular location | Cytoplasm : O00182 |
| Total number of polymer chains | 4 |
| Total formula weight | 65765.38 |
| Authors | Makyio, H.,Suzuki, T.,Ando, H.,Yamada, Y.,Ishida, H.,Kiso, M.,Wakatsuki, S.,Kato, R. (deposition date: 2013-11-14, release date: 2014-11-05, Last modification date: 2024-03-20) |
| Primary citation | Suzuki, T.,Makyio, H.,Ando, H.,Komura, N.,Menjo, M.,Yamada, Y.,Imamura, A.,Ishida, H.,Wakatsuki, S.,Kato, R.,Kiso, M. Expanded potential of seleno-carbohydrates as a molecular tool for X-ray structural determination of a carbohydrate-protein complex with single/multi-wavelength anomalous dispersion phasing Bioorg.Med.Chem., 22:2090-2101, 2014 Cited by PubMed Abstract: Seleno-lactoses have been successfully synthesized as candidates for mimicking carbohydrate ligands for human galectin-9 N-terminal carbohydrate recognition domain (NCRD). Selenium was introduced into the mono- or di-saccharides using p-methylselenobenzoic anhydride (Tol2Se) as a novel selenating reagent. The TolSe-substituted monosaccharides were converted into selenoglycosyl donors or acceptors, which were reacted with coupling partners to afford seleno-lactoses. The seleno-lactoses were converted to the target compounds. The structure of human galectin-9 NCRD co-crystallized with 6-MeSe-lactose was determined with single/multi-wavelength anomalous dispersion (SAD/MAD) phasing and was similar to that of the co-crystal with natural lactose. PubMed: 24631362DOI: 10.1016/j.bmc.2014.02.023 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (1.4 Å) |
Structure validation
Download full validation report






