Cargando…

NAT/NCS2-hound: a webserver for the detection and evolutionary classification of prokaryotic and eukaryotic nucleobase-cation symporters of the NAT/NCS2 family

Nucleobase transporters are important for supplying the cell with purines and/or pyrimidines, for controlling the intracellular pool of nucleotides, and for obtaining exogenous nitrogen/carbon sources for metabolism. Nucleobase transporters are also evaluated as potential targets for antimicrobial t...

Descripción completa

Detalles Bibliográficos
Autores principales: Chaliotis, A, Vlastaridis, P, Ntountoumi, C, Botou, M, Yalelis, V, Lazou, P, Tatsaki, E, Mossialos, D, Frillingos, S, Amoutzias, G D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6308229/
https://www.ncbi.nlm.nih.gov/pubmed/30418564
http://dx.doi.org/10.1093/gigascience/giy133
_version_ 1783383149140508672
author Chaliotis, A
Vlastaridis, P
Ntountoumi, C
Botou, M
Yalelis, V
Lazou, P
Tatsaki, E
Mossialos, D
Frillingos, S
Amoutzias, G D
author_facet Chaliotis, A
Vlastaridis, P
Ntountoumi, C
Botou, M
Yalelis, V
Lazou, P
Tatsaki, E
Mossialos, D
Frillingos, S
Amoutzias, G D
author_sort Chaliotis, A
collection PubMed
description Nucleobase transporters are important for supplying the cell with purines and/or pyrimidines, for controlling the intracellular pool of nucleotides, and for obtaining exogenous nitrogen/carbon sources for metabolism. Nucleobase transporters are also evaluated as potential targets for antimicrobial therapies, since several pathogenic microorganisms rely on purine/pyrimidine salvage from their hosts. The majority of known nucleobase transporters belong to the evolutionarily conserved and ubiquitous nucleobase-ascorbate transporter/nucleobase-cation symporter-2 (NAT/NCS2) protein family. Based on a large-scale phylogenetic analysis that we performed on thousands of prokaryotic proteomes, we developed a webserver that can detect and distinguish this family of transporters from other homologous families that recognize different substrates. We can further categorize these transporters to certain evolutionary groups with distinct substrate preferences. The webserver scans whole proteomes and graphically displays which proteins are identified as NAT/NCS2, to which evolutionary groups and subgroups they belong to, and which conserved motifs they have. For key subgroups and motifs, the server displays annotated information from published crystal-structures and mutational studies pointing to key functional amino acids that may help experts assess the transport capability of the target sequences. The server is 100% accurate in detecting NAT/NCS2 family members. We also used the server to analyze 9,109 prokaryotic proteomes and identified Clostridia, Bacilli, β- and γ-Proteobacteria, Actinobacteria, and Fusobacteria as the taxa with the largest number of NAT/NCS2 transporters per proteome. An analysis of 120 representative eukaryotic proteomes also demonstrates the server's capability of correctly analyzing this major lineage, with plants emerging as the group with the highest number of NAT/NCS2 members per proteome.
format Online
Article
Text
id pubmed-6308229
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-63082292019-01-07 NAT/NCS2-hound: a webserver for the detection and evolutionary classification of prokaryotic and eukaryotic nucleobase-cation symporters of the NAT/NCS2 family Chaliotis, A Vlastaridis, P Ntountoumi, C Botou, M Yalelis, V Lazou, P Tatsaki, E Mossialos, D Frillingos, S Amoutzias, G D Gigascience Technical Note Nucleobase transporters are important for supplying the cell with purines and/or pyrimidines, for controlling the intracellular pool of nucleotides, and for obtaining exogenous nitrogen/carbon sources for metabolism. Nucleobase transporters are also evaluated as potential targets for antimicrobial therapies, since several pathogenic microorganisms rely on purine/pyrimidine salvage from their hosts. The majority of known nucleobase transporters belong to the evolutionarily conserved and ubiquitous nucleobase-ascorbate transporter/nucleobase-cation symporter-2 (NAT/NCS2) protein family. Based on a large-scale phylogenetic analysis that we performed on thousands of prokaryotic proteomes, we developed a webserver that can detect and distinguish this family of transporters from other homologous families that recognize different substrates. We can further categorize these transporters to certain evolutionary groups with distinct substrate preferences. The webserver scans whole proteomes and graphically displays which proteins are identified as NAT/NCS2, to which evolutionary groups and subgroups they belong to, and which conserved motifs they have. For key subgroups and motifs, the server displays annotated information from published crystal-structures and mutational studies pointing to key functional amino acids that may help experts assess the transport capability of the target sequences. The server is 100% accurate in detecting NAT/NCS2 family members. We also used the server to analyze 9,109 prokaryotic proteomes and identified Clostridia, Bacilli, β- and γ-Proteobacteria, Actinobacteria, and Fusobacteria as the taxa with the largest number of NAT/NCS2 transporters per proteome. An analysis of 120 representative eukaryotic proteomes also demonstrates the server's capability of correctly analyzing this major lineage, with plants emerging as the group with the highest number of NAT/NCS2 members per proteome. Oxford University Press 2018-11-10 /pmc/articles/PMC6308229/ /pubmed/30418564 http://dx.doi.org/10.1093/gigascience/giy133 Text en © The Author(s) 2018. Published by Oxford University Press. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Technical Note
Chaliotis, A
Vlastaridis, P
Ntountoumi, C
Botou, M
Yalelis, V
Lazou, P
Tatsaki, E
Mossialos, D
Frillingos, S
Amoutzias, G D
NAT/NCS2-hound: a webserver for the detection and evolutionary classification of prokaryotic and eukaryotic nucleobase-cation symporters of the NAT/NCS2 family
title NAT/NCS2-hound: a webserver for the detection and evolutionary classification of prokaryotic and eukaryotic nucleobase-cation symporters of the NAT/NCS2 family
title_full NAT/NCS2-hound: a webserver for the detection and evolutionary classification of prokaryotic and eukaryotic nucleobase-cation symporters of the NAT/NCS2 family
title_fullStr NAT/NCS2-hound: a webserver for the detection and evolutionary classification of prokaryotic and eukaryotic nucleobase-cation symporters of the NAT/NCS2 family
title_full_unstemmed NAT/NCS2-hound: a webserver for the detection and evolutionary classification of prokaryotic and eukaryotic nucleobase-cation symporters of the NAT/NCS2 family
title_short NAT/NCS2-hound: a webserver for the detection and evolutionary classification of prokaryotic and eukaryotic nucleobase-cation symporters of the NAT/NCS2 family
title_sort nat/ncs2-hound: a webserver for the detection and evolutionary classification of prokaryotic and eukaryotic nucleobase-cation symporters of the nat/ncs2 family
topic Technical Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6308229/
https://www.ncbi.nlm.nih.gov/pubmed/30418564
http://dx.doi.org/10.1093/gigascience/giy133
work_keys_str_mv AT chaliotisa natncs2houndawebserverforthedetectionandevolutionaryclassificationofprokaryoticandeukaryoticnucleobasecationsymportersofthenatncs2family
AT vlastaridisp natncs2houndawebserverforthedetectionandevolutionaryclassificationofprokaryoticandeukaryoticnucleobasecationsymportersofthenatncs2family
AT ntountoumic natncs2houndawebserverforthedetectionandevolutionaryclassificationofprokaryoticandeukaryoticnucleobasecationsymportersofthenatncs2family
AT botoum natncs2houndawebserverforthedetectionandevolutionaryclassificationofprokaryoticandeukaryoticnucleobasecationsymportersofthenatncs2family
AT yalelisv natncs2houndawebserverforthedetectionandevolutionaryclassificationofprokaryoticandeukaryoticnucleobasecationsymportersofthenatncs2family
AT lazoup natncs2houndawebserverforthedetectionandevolutionaryclassificationofprokaryoticandeukaryoticnucleobasecationsymportersofthenatncs2family
AT tatsakie natncs2houndawebserverforthedetectionandevolutionaryclassificationofprokaryoticandeukaryoticnucleobasecationsymportersofthenatncs2family
AT mossialosd natncs2houndawebserverforthedetectionandevolutionaryclassificationofprokaryoticandeukaryoticnucleobasecationsymportersofthenatncs2family
AT frillingoss natncs2houndawebserverforthedetectionandevolutionaryclassificationofprokaryoticandeukaryoticnucleobasecationsymportersofthenatncs2family
AT amoutziasgd natncs2houndawebserverforthedetectionandevolutionaryclassificationofprokaryoticandeukaryoticnucleobasecationsymportersofthenatncs2family