The cytoplasmic domain is essential for transport function of the integral membrane transport protein SLC4A11

Human SLC4A11-C functions as a DIDS-stimulatable H+(OH−) permeation pathway: partial correction of R109H mutant transport

(2015) Liyo Kao et al.   AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY

A Call for Systematic Research on Solute Carriers

(2015) Adrián César-Razquin et al.   CELL

Functional Architecture of the Cytoplasmic Entrance to the Cystic Fibrosis Transmembrane Conductance Regulator Chloride Channel Pore

(2015) Yassine El Hiani et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Human SLC4A11 Is a Novel NH3/H+Co-transporter

(2015) Wenlin Zhang et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Two novel mutations including a large deletion of theSLC4A11gene causing autosomal recessive hereditary endothelial dystrophy

(2014) Vilavun Puangsricharern et al.   BRITISH JOURNAL OF OPHTHALMOLOGY

Corneal Dystrophy-Causing SLC4A11 Mutants: Suitability for Folding-Correction Therapy

(2014) Sampath K. Loganathan et al.   HUMAN MUTATION

Bicarbonate transport in health and disease

(2014) Kumari Alka et al.   IUBMB LIFE

Biosynthetic and functional defects in newly identified SLC4A11 mutants and absence of COL8A2 mutations in Fuchs endothelial corneal dystrophy

(2014) Nagasamy Soumittra et al.   JOURNAL OF HUMAN GENETICS

SLC4A11 is an EIPA-sensitive Na+ permeable pHi regulator

(2013) Diego G. Ogando et al.   AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY

Transmembrane water-flux through SLC4A11: a route defective in genetic corneal diseases

(2013) Gonzalo L. Vilas et al.   HUMAN MOLECULAR GENETICS

A Substrate Access Tunnel in the Cytosolic Domain Is Not an Essential Feature of the Solute Carrier 4 (SLC4) Family of Bicarbonate Transporters

(2013) Volodymyr Shnitsar et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Three-Dimensional Model for the Human Cl−/HCO3− Exchanger, AE1, by Homology to the E. coli ClC Protein

(2013) Pamela Bonar et al.   JOURNAL OF MOLECULAR BIOLOGY

A Biochemical Framework for SLC4A11, the Plasma Membrane Protein Defective in Corneal Dystrophies

(2011) Gonzalo L. Vilas et al.   BIOCHEMISTRY

Oligomerization of SLC4A11 protein and the severity of FECD and CHED2 corneal dystrophies caused bySLC4A11mutations

(2011) Gonzalo L. Vilas et al.   HUMAN MUTATION

Distance Measurements within a Concatamer of the Plasma Membrane Cl−/HCO3−Exchanger, AE1

(2010) Arghya Basu et al.   BIOCHEMISTRY

A new bright green-emitting fluorescent protein - engineered monomeric and dimeric forms

(2010) Robielyn P. Ilagan et al.   FEBS Journal

SLC4A11 Prevents Osmotic Imbalance Leading to Corneal Endothelial Dystrophy, Deafness, and Polyuria

(2010) Nicole Gröger et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Purification of functional human exchanger, AE1, over-expressed in Saccharomyces cerevisiae

(2010) Pamela Bonar et al.   PROTEIN EXPRESSION AND PURIFICATION

Red Fluorescent Protein pH Biosensor to Detect Concentrative Nucleoside Transport

(2009) Danielle E. Johnson et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Protein structure prediction on the Web: a case study using the Phyre server

(2009) Lawrence A Kelley et al.   Nature Protocols

Identification of Mutations in the SLC4A11 Gene in Patients With Recessive Congenital Hereditary Endothelial Dystrophy

(2008) Boomiraj Hemadevi   ARCHIVES OF OPHTHALMOLOGY

Entry to “ Tunnel” Revealed by SLC4A4 Human Mutation and Structural Model

(2008) Min-Hwang Chang et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Congenital hereditary endothelial dystrophy with progressive sensorineural deafness (Harboyan syndrome)

(2008) Julie Desir et al.   Orphanet Journal of Rare Diseases