Membrane integration and topology of the first transmembrane segment in normal and Southeast Asian ovalocytosis human erythrocyte anion exchanger 1.

scientific article published on May 2005

Membrane integration and topology of the first transmembrane segment in normal and Southeast Asian ovalocytosis human erythrocyte anion exchanger 1. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1080/09687860500093115
P8608Fatcat IDrelease_n5mfvhn5ynbcdgvpqvcrsfi74e
P698PubMed publication ID16096263

P2093author name stringReinhart A F Reithmeier
Joanne C Cheung
P2860cites workDeletion in erythrocyte band 3 gene in malaria-resistant Southeast Asian ovalocytosisQ24559966
A simple method for displaying the hydropathic character of a proteinQ26778481
Structural studies on the effects of the deletion in the red cell anion exchanger (band 3, AE1) associated with South East Asian ovalocytosisQ27766488
A new technique for the assay of infectivity of human adenovirus 5 DNAQ27860797
Coordination of N-glycosylation and protein translocation across the endoplasmic reticulum membrane by Sss1 protein.Q27932024
Electrogenic Na+/HCO3- cotransporters: cloning and physiologyQ28140080
Localization of the Cl-/HCO3- anion exchanger binding site to the amino-terminal region of carbonic anhydrase IIQ28143034
Identification of the carbonic anhydrase II binding site in the Cl(-)/HCO(3)(-) anion exchanger AE1Q28144854
Band 3 anion exchanger and its involvement in erythrocyte and kidney disordersQ28201311
Membrane topology of the human Na+/glucose cotransporter SGLT1Q28273665
Carbonic anhydrase II binds to the carboxyl terminus of human band 3, the erythrocyte C1-/HCO3- exchangerQ28285560
Cloning and characterization of band 3, the human erythrocyte anion-exchange protein (AE1)Q28609272
Membrane topology and insertion of membrane proteins: search for topogenic signalsQ30326361
Molecular defect of the band 3 protein in southeast Asian ovalocytosisQ34175832
A membrane metabolon linking carbonic anhydrase with chloride/bicarbonate anion exchangersQ34254361
Molecular basis for membrane rigidity of hereditary ovalocytosis. A novel mechanism involving the cytoplasmic domain of band 3Q35598418
The COOH-terminal ends of internal signal and signal-anchor sequences are positioned differently in the ER translocaseQ36234592
Twenty seven nucleotide deletion within exon 11 of the erythrocyte band 3 gene in Indonesian ovalocytosisQ36733660
Coupled cell-free synthesis, segregation, and core glycosylation of a secretory proteinQ37586525
Structure and function of the cytoplasmic domain of band 3: center of erythrocyte membrane-peripheral protein interactionsQ39479426
Oligomeric structure and the anion transport function of human erythrocyte band 3 proteinQ40077925
High level transient expression of a chloramphenicol acetyl transferase gene by DEAE-dextran mediated DNA transfection coupled with a dimethyl sulfoxide or glycerol shock treatment.Q40461112
The complete amino acid sequence of the human erythrocyte membrane anion-transport protein deduced from the cDNA sequenceQ42068548
Asparagine-linked oligosaccharides are localized to single extracytosolic segments in multi-span membrane glycoproteinsQ42828786
Molecular basis and functional consequences of the dominant effects of the mutant band 3 on the structure of normal band 3 in Southeast Asian ovalocytosisQ43904199
Transmembrane topology of the secretory Na+-K+-2Cl- cotransporter NKCC1 studied by in vitro translationQ45871253
Defective anion transport activity of the abnormal band 3 in hereditary ovalocytic red blood cellsQ47858863
Ovalocytosis and cerebral malariaQ48024505
The N-terminal region of the transmembrane domain of human erythrocyte band 3. Residues critical for membrane insertion and transport activityQ48842337
The expression of the abnormal human red cell anion transporter from South-East Asian ovalocytes (band 3 SAO) in Xenopus oocytesQ49133467
Interactions between mutant and wild-type band 3 subunits in hereditary Southeast Asian ovalocytic red blood cell membranes.Q52312864
Proline-induced disruption of a transmembrane alpha-helix in its natural environment.Q52532824
P433issue3
P921main subjecttransmembrane proteinQ424204
human erythrocyteQ111535219
P304page(s)203-214
P577publication date2005-05-01
P1433published inMolecular Membrane BiologyQ6895964
P1476titleMembrane integration and topology of the first transmembrane segment in normal and Southeast Asian ovalocytosis human erythrocyte anion exchanger 1.
P478volume22

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cites work (P2860)
Q35579788Alteration of CFTR transmembrane span integration by disease-causing mutations
Q42173367Effect of the Southeast Asian Ovalocytosis Deletion on the Conformational Dynamics of Signal-Anchor Transmembrane Segment 1 of Red Cell Anion Exchanger 1 (AE1, Band 3, or SLC4A1).
Q37241873Molecular mechanisms of autosomal dominant and recessive distal renal tubular acidosis caused by SLC4A1 (AE1) mutations
Q24642152Molecular physiology and genetics of Na+-independent SLC4 anion exchangers
Q52604794Protein 4.2 interaction with hereditary spherocytosis mutants of the cytoplasmic domain of human anion exchanger 1
Q40501505The Stalk Domain of NKp30 Contributes to Ligand Binding and Signaling of a Preassembled NKp30-CD3ζ Complex.
Q40440078Topology of transmembrane segments 1-4 in the human chloride/bicarbonate anion exchanger 1 (AE1) by scanning N-glycosylation mutagenesis
Q40384079Trafficking defects of the Southeast Asian ovalocytosis deletion mutant of anion exchanger 1 membrane proteins