3ENR
ZINC-CALCIUM CONCANAVALIN A AT PH 6.15
Summary for 3ENR
Entry DOI | 10.2210/pdb3enr/pdb |
Descriptor | Concanavalin-A, ZINC ION, CALCIUM ION, ... (4 entities in total) |
Functional Keywords | concanavalin a, lectin, metal binding, ph |
Biological source | Canavalia ensiformis (Jack bean) More |
Total number of polymer chains | 2 |
Total formula weight | 51586.56 |
Authors | Bouckaert, J.,Loris, R.,Wyns, L. (deposition date: 1999-02-11, release date: 2000-09-18, Last modification date: 2023-09-06) |
Primary citation | Bouckaert, J.,Loris, R.,Wyns, L. Zinc/calcium- and cadmium/cadmium-substituted concanavalin A: interplay of metal binding, pH and molecular packing. Acta Crystallogr.,Sect.D, 56:1569-1576, 2000 Cited by PubMed Abstract: The crystal structures of cadmium/cadmium and zinc/calcium concanavalin A (con A) at pH 5.0 and pH 6.15, respectively, were determined. The structure of cadmium/cadmium con A confirms that the secondary Cd(2+)-binding site S3 is empty at pH 5. The metal-binding sites S1 and S2 are only very slightly affected by the substitution with cadmium. On the other hand, S1 and S2 and most of the protein surface of zinc/calcium con A at pH 6.15 differ from other fully metal-bound and carbohydrate-free structures. Most of these structural differences at the protein surface are a result of the interplay between metal binding, protonation and crystal packing. This interplay is expressed by relative rotations and translations of the con A units in alternative crystal packings and participation in space-group conversions inside crystals in situ. The particular crystal packing of zinc/calcium con A creates a novel zinc-binding site S4. The Zn(2+) ion in S4 ligates two aspartates from one tetramer and a histidine from a symmetry-related tetramer. PubMed: 11092923DOI: 10.1107/S0907444900013342 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.4 Å) |
Structure validation
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