The in-silico evaluation of important GLUT9 residue for uric acid transport based on renal hypouricemia type 2.
Ontology highlight
ABSTRACT: Uric acid is the end product of purine metabolism. Uric acid transporters in the renal proximal tubule plays a key role in uric acid transport. Functional abnormalities in these transporters could lead to high or low levels of uric acid in the blood plasma, known as hyperuricemia and hypouricemia, respectively. GLUT9 has been reported as a key transporter for uric acid reuptake in renal proximal tubule. GLUT9 mutation is known as causal gene for renal hypouricemia due to defective uric acid uptake, with more severe cases resulting in urolithiasis and exercise induced acute kidney injury (EIAKI). However, the effect of mutation is not fully investigated and hard to predict the change of binding affinity. We comprehensively described the effect of GLUT9 mutation for uric acid transport using
SUBMITTER: Cachau R
PROVIDER: S-EPMC10596759 | biostudies-literature | 2023 Mar
REPOSITORIES: biostudies-literature
ACCESS DATA