1.14.99.54	A143C/P183C/S73C/A115C	introduction of addtitional disulfide bridges A143C-P183C and S73C-A115C, increase in melting temperature by 12 degrees	-, 746362	
1.14.99.54	A143C/P183C/S73C/A115C	introduction of two additional disulfide bridges, mutant displays a 12°C increase in melting temperature and is able to retain 60% of its activity after heat treatment	-, 741358	
1.14.99.54	A148G	mutation leads to loss of C4 oxidation, i.e to the activity of EC 1.14.99.54	-, 745380	
1.14.99.54	A148S	mutation leads to loss of C4 oxidation, i.e to the activity of EC 1.14.99.54	-, 745380	
1.14.99.54	D140A	mutant shows moderately reduced activity and essentially unchanged oxidative regioselectivity	-, 745380	
1.14.99.54	additional information	construction of a C-terminally truncated variant containing 21 residues of the predicted linker domain. The truncated variant exhibits reduced binding to cellulose and about 50% of wild-type activity on cellulose	-, 745374	
1.14.99.54	additional information	introduction of additional disulfide bridges. Four out of 16 variants display an improvement in melting temperature, ranging from 2°C to 9°C	-, 741358	
1.14.99.54	additional information	isotopical labeling of the apo-form of the 21.4 kDa catalytic domain and the 10.7 kDa carbohydrate binding domain of LPMO10C and recombinant expression in Escherichia coli and assignment of the backbone of full-length LPMO10C	-, 744472	
1.14.99.54	additional information	neither truncation of the LPMO10B family 2 carbohydrate-binding module nor mutations altering access to the solvent-exposed axial copper coordination site significantly change the C1:C4 oxidation ratio	-, 745380	
1.14.99.54	N85F	mutation changes the C1:C4 oxidation ratio from 0.9 (for the wild-type) to 5.9	-, 745380