TY  - JOUR 
AU  - Neira, José L.
AU  - Mesa Torres, Noel
AU  - Pey Rodríguez, Ángel Luis
PY  - 2022
UR  - https://hdl.handle.net/10481/79282
AB  - The mutations G170R and I244T are the most common disease cause in primary hyperoxaluria
type I (PH1). These mutations cause the misfolding of the AGT protein in the minor allele
AGT-LM that contains the P11L polymorphism, which may affect the...
LA  - eng
PB  - MDPI
KW  - Conformational landscape
KW  - Spectroscopy
KW  - Circular dichroism
KW  - NMR
KW  - Phosphorylation
KW  - Mutation
KW  - Genetic disease
KW  - Protein misfolding
KW  - Primary hyperoxaluria type I
KW  - Statistical mechanics
TI  - Phosphorylation of Thr9 Affects the Folding Landscape of the N-Terminal Segment of Human AGT Enhancing Protein Aggregation of Disease-Causing Mutants
DO  - 10.3390/molecules27248762
ER  -