{"global_stoichiometry": "Monomer - A ", "ligstr": "", "uniprot_ac": "P61626", "inchi": "", "reference": "Nature. 1997 Feb 27;385(6619):787-93", "author": "Booth, D.R., Sunde, M., Bellotti, V., Robinson, C.V., Hutchinson, W.L., Fraser, P.E., Hawkins, P.N., Dobson, C.M., Radford, S.E., Blake, C.C., Pepys, M.B.", "type": "Protein", "ligand_id": "", "species": "Homo sapiens", "method": "X-RAY DIFFRACTION", "keyword": "LYSOZYME", "gene_names": "LYZ, LZM", "chain_id": "", "ligand_mw": "", "inchi_key": "", "secondary_structure": "KVFERCELARTLKRLGMDGYRGISLANWMCLAKWESGYNTRATNYNAGDRSTDYGTFQINSRYWCNDGKTPGAVNACHLSCSALLQDNIADAVACAKRVVRDPQGIRAWVAWRNRCQNRDVRQYVQGCGV#CBCCHHHHHHHHHHTTCTTBTTBCHHHHHHHHHHHHTTBTTCEEEETTTTEEEETTTTEETTTTCBCSCSTTCCCTTCCBGGGGGSSSTHHHHHHHHHHTTSTTGGGGCHHHHHHTTTSCCGGGTTTSCC", "amyloid_non_amyloid": "Amyloid", "length": "130", "remarks": "AMYLOIDOGENIC VARIANT (I56T) VARIANT OF HUMAN LYSOZYME", "protein_name": "Lysozyme C", "peptide_protein_sequence": "chain-ID A: KVFERCELARTLKRLGMDGYRGISLANWMCLAKWESGYNTRATNYNAGDRSTDYGTFQINSRYWCNDGKTPGAVNACHLSCSALLQDNIADAVACAKRVVRDPQGIRAWVAWRNRCQNRDVRQYVQGCGV", "ligand_name": "", "ligand_smiles": "", "pdb_id": "1LOZ", "ec_number": "3.2.1.17", "pdb_classification": "HYDROLASE", "mutation_s_field": "I56T", "ligand_formula": "", "r_value_free": "", "alternative_name": "1, 4-beta-N-acetylmuramidase C", "description": "The naturally occurring human lysozyme variants is amyloidogenic, and shown here to be unstable. This aggregates to form amyloid fibrils with transformation of the mainly helical native fold, observed in crystal structures, to the amyloid fibril cross-Beta fold. Biophysical studies suggest that partly folded intermediates are involved in fibrillogenesis", "resolution": "1.8", "pmid": "9039909", "entry": "S-0042"}