Molecular analysis of human solute carrier SLC26 anion transporter disease-causing mutations using 3-dimensional homology modeling. [electronic resource]
Producer: 20180208Description: 2420-2434 p. digitalISSN:- 0005-2736
- Amino Acid Sequence
- Anion Transport Proteins -- chemistry
- Bacterial Proteins -- chemistry
- Binding Sites
- Chloride-Bicarbonate Antiporters -- chemistry
- Computational Biology
- Deinococcus -- genetics
- Diarrhea -- congenital
- Gene Expression
- Goiter, Nodular -- genetics
- Hearing Loss, Sensorineural -- genetics
- Humans
- Ion Transport
- Membrane Transport Proteins -- chemistry
- Metabolism, Inborn Errors -- genetics
- Models, Molecular
- Mutation
- Osteochondrodysplasias -- genetics
- Protein Binding
- Protein Conformation, alpha-Helical
- Protein Conformation, beta-Strand
- Protein Interaction Domains and Motifs
- Structural Homology, Protein
- Substrate Specificity
- Sulfate Transporters
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Publication Type: Journal Article
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