6TMS neutral amino acid transporter family

The 6TMS Neutral Amino Acid Transporter (NAAT) Family (TC# 2.A.95) is a family of transporters belonging to the Lysine Exporter (LysE) Superfamily. Homologues are found in numerous Gram-negative and Gram-positive bacteria including many human pathogens. Several archaea also encode MarC (see below) homologues. Some of these organisms have 2 or more paralogues. Most of these proteins are of about the same size (180-230 aas) although a few are larger. They exhibit 6 (or in some cases, possibly 5) putative TMSs. A representative list of members belonging to the NAAT family can be found in the Transporter Classification Database.

SnatA

A gene encoding a small neutral amino acid transporter was cloned from the genome of the hyperthermophilic archaeon Thermococcus sp. KS-1. The cloned gene, snatA, encodes a protein of 216 amino acid residues, SnatA (TC# 2.A.95.1.4), with six membrane-spanning segments (TMSs). Competition studies indicated that SnatA transports various L-type neutral amino acids. It has also been noted that glycine transport is inhibited by a protonophore, FCCP, or valinomycin plus nigericin, indicating that the process is dependent on an electrochemical potential of H+.[1]

The generalized reaction catalyzed by SnatA is:[2]

Amino acid (in) → Amino acid (out)

MarC

MarC is encoded by a gene at the multiple antibiotic resistance (mar) locus. The mar locus consists of two divergently positioned transcriptional units that flank the operator, marO, in both E. coli and Salmonella typhimurium. One transcription unit encodes MarC, an integral inner membrane protein with 6 established TMSs with the N- and C-termini in the cytoplasm.[3] Its function is unknown. The other unit consists of an operon, marRAB, encoding (1) the MarR repressor which binds marO and negatively regulates marRAB expression, (2) MarA, a transcriptional activator that activates expression of other genes such as acrAB (encoding the principal E. coli multidrug efflux pump of the RND superfamily (TC #2.A.6.2)) and the mar regulon itself, and (3) MarB, a small protein of 71 amino acyl residues of unknown function. A periplasmic binding protein, MppA, essential for the uptake of the cell wall murein tripeptide, L-alanyl-γ-D-glutamyl-meso-diaminopimelate via the Opp permease, regulates mar regulon expression. Loss of MppA causes overproduction of MarA which activates acrAB, causing pleiotropic drug resistance. MppA probably functions upstream of MarA in a signal transduction pathway that negatively controls expression of the marRAB operon.

gollark: Faster, though.
gollark: If I was forced to write all osmarks.net backend services as highly optimized C or something, they would probably be buggier, slower, less maintainable and lacking features.
gollark: Ah, but people have to make computers faster to make the continually worsening code keep running.
gollark: Well, the pay is good.
gollark: I occasionally write surprisingly good code which ends up continuing to function properly without any maintenance, but this is quite rare.

References
  1. Akahane, Shohei; Kamata, Hideaki; Yagisawa, Hitoshi; Hirata, Hajime (2003-02-01). "A novel neutral amino acid transporter from the hyperthermophilic archaeon Thermococcus sp. KS-1". Journal of Biochemistry. 133 (2): 173–180. doi:10.1093/jb/mvg021. ISSN 0021-924X. PMID 12761179.
  2. "2.A.95 The 6TMS Neutral Amino Acid Transporter (NAAT) Family". Transporter Classification Database. Retrieved 2016-02-25.
  3. Drew, David; Sjöstrand, Dan; Nilsson, Johan; Urbig, Thomas; Chin, Chen-ni; de Gier, Jan-Willem; von Heijne, Gunnar (2002-03-05). "Rapid topology mapping of Escherichia coli inner-membrane proteins by prediction and PhoA/GFP fusion analysis". Proceedings of the National Academy of Sciences of the United States of America. 99 (5): 2690–2695. doi:10.1073/pnas.052018199. ISSN 0027-8424. PMC 122409. PMID 11867724.

As of this edit, this article uses content from "2.A.95 The 6TMS Neutral Amino Acid Transporter (NAAT) Family", which is licensed in a way that permits reuse under the Creative Commons Attribution-ShareAlike 3.0 Unported License, but not under the GFDL. All relevant terms must be followed.


This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.