The SLC3 and SLC7 families of amino acid transporters

D Fotiadis, Y Kanai, M Palacín - Molecular aspects of medicine, 2013 - Elsevier
Amino acids are necessary for all living cells and organisms. Specialized transporters
mediate the transfer of amino acids across plasma membranes. Malfunction of these …

CATs and HATs: the SLC7 family of amino acid transporters

F Verrey, EI Closs, CA Wagner, M Palacin, H Endou… - Pflügers Archiv, 2004 - Springer
The SLC7 family is divided into two subgroups, the cationic amino acid transporters (the
CAT family, SLC7A1–4) and the glycoprotein-associated amino acid transporters (the gpaAT …

Fourteen monogenic genes account for 15% of nephrolithiasis/nephrocalcinosis

J Halbritter, M Baum, AM Hynes, SJ Rice… - Journal of the …, 2015 - journals.lww.com
Nephrolithiasis is a prevalent condition with a high morbidity. Although dozens of
monogenic causes have been identified, the fraction of single-gene disease has not been …

Cryo-EM structure of the human L-type amino acid transporter 1 in complex with glycoprotein CD98hc

Y Lee, P Wiriyasermkul, C Jin, L Quan… - Nature structural & …, 2019 - nature.com
The L-type amino acid transporter 1 (LAT1 or SLC7A5) transports large neutral amino acids
across the membrane and is crucial for brain drug delivery and tumor growth. LAT1 forms a …

The Cα—H⋅⋅⋅ O hydrogen bond: A determinant of stability and specificity in transmembrane helix interactions

A Senes, I Ubarretxena-Belandia… - Proceedings of the …, 2001 - National Acad Sciences
The Cα—H⋅⋅⋅ O hydrogen bond has been given little attention as a determinant of
transmembrane helix association. Stimulated by recent calculations suggesting that such …

Function and structure of heterodimeric amino acid transporters

CA Wagner, F Lang, S Bröer - American Journal of …, 2001 - journals.physiology.org
Heterodimeric amino acid transporters are comprised of two subunits, a polytopic membrane
protein (light chain) and an associated type II membrane protein (heavy chain). The heavy …

Comparison between SLC3A1 and SLC7A9 cystinuria patients and carriers: a need for a new classification

LD Strologo, E Pras, C Pontesilli, E Beccia… - Journal of the …, 2002 - journals.lww.com
Recent developments in the genetics and physiology of cystinuria do not support the
traditional classification, which is based on the excretion of cystine and dibasic amino acids …

Pathophysiology and treatment of cystinuria

J Chillarón, M Font-Llitjós, J Fort, A Zorzano… - Nature Reviews …, 2010 - nature.com
Cystinuria is a primary inherited aminoaciduria caused by mutations in the genes that
encode the two subunits (neutral and basic amino acid transport protein rBAT and b (0,+) …

The role of amino acid transporters in inherited and acquired diseases

S Broeer, M Palacin - Biochemical Journal, 2011 - portlandpress.com
Amino acids are essential building blocks of all mammalian cells. In addition to their role in
protein synthesis, amino acids play an important role as energy fuels, precursors for a …

Heteromeric amino acid transporters: biochemistry, genetics, and physiology

J Chillarón, R Roca, A Valencia… - American Journal of …, 2001 - journals.physiology.org
The heteromeric amino acid transporters (HATs) are composed of two polypeptides: a heavy
subunit (HSHAT) and a light subunit (LSHAT) linked by a disulfide bridge. HSHATs are N …