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The Evolutionary History of Topological Variations in the CPA/AT Transporters

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Specialty Biology
Date 2021 Aug 17
PMID 34403419
Citations 2
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Abstract

CPA/AT transporters are made up of scaffold and a core domain. The core domain contains two non-canonical helices (broken or reentrant) that mediate the transport of ions, amino acids or other charged compounds. During evolution, these transporters have undergone substantial changes in structure, topology and function. To shed light on these structural transitions, we create models for all families using an integrated topology annotation method. We find that the CPA/AT transporters can be classified into four fold-types based on their structure; (1) the CPA-broken fold-type, (2) the CPA-reentrant fold-type, (3) the BART fold-type, and (4) a previously not described fold-type, the Reentrant-Helix-Reentrant fold-type. Several topological transitions are identified, including the transition between a broken and reentrant helix, one transition between a loop and a reentrant helix, complete changes of orientation, and changes in the number of scaffold helices. These transitions are mainly caused by gene duplication and shuffling events. Structural models, topology information and other details are presented in a searchable database, CPAfold (cpafold.bioinfo.se).

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The evolutionary history of topological variations in the CPA/AT transporters.

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References
1.
Garaeva A, Oostergetel G, Gati C, Guskov A, Paulino C, Slotboom D . Cryo-EM structure of the human neutral amino acid transporter ASCT2. Nat Struct Mol Biol. 2018; 25(6):515-521. DOI: 10.1038/s41594-018-0076-y. View

2.
Sonnhammer E, von Heijne G, KROGH A . A hidden Markov model for predicting transmembrane helices in protein sequences. Proc Int Conf Intell Syst Mol Biol. 1998; 6:175-82. View

3.
Mirdita M, von den Driesch L, Galiez C, Martin M, Soding J, Steinegger M . Uniclust databases of clustered and deeply annotated protein sequences and alignments. Nucleic Acids Res. 2016; 45(D1):D170-D176. PMC: 5614098. DOI: 10.1093/nar/gkw1081. View

4.
Pornillos O, Chang G . Inverted repeat domains in membrane proteins. FEBS Lett. 2006; 580(2):358-62. DOI: 10.1016/j.febslet.2005.12.054. View

5.
Mesdaghi S, Murphy D, Sanchez Rodriguez F, Burgos-Marmol J, Rigden D . In silico prediction of structure and function for a large family of transmembrane proteins that includes human Tmem41b. F1000Res. 2021; 9:1395. PMC: 7818093. DOI: 10.12688/f1000research.27676.2. View