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We are deeply saddened by the passing of Amos Bairoch (1957–2025), the creator of PROSITE. We wish to dedicate our latest paper, published shortly before his death, to him. He will always be a source of inspiration to us.
Our deepest condolences go out to his family and friends, and to all those who had the privilege of working with him. Rest in peace, Amos. Your work will live on long after you are gone.
Amos Bairoch

PROSITE documentation PDOC51709
TrmE-type guanine nucleotide-binding (G) domain profile


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PURL: https://purl.expasy.org/prosite/documentation/PDOC51709

Description

The P-loop (see <PDOC00017>) guanosine triphosphatases (GTPases) control a multitude of biological processes, ranging from cell division, cell cycling, and signal transduction, to ribosome assembly and protein synthesis. GTPases exert their control by interchanging between an inactive GDP-bound state and an active GTP-bound state, thereby acting as molecular switches. The common denominator of GTPases is the highly conserved guanine nucleotide-binding (G) domain that is responsible for binding and hydrolysis of guanine nucleotides.

TrmE (also called MnmE) contains a canonical G domain and is conserved in all three kingdoms of life. It is involved in the modification of uridine bases (U34) at the first anticodon (wobble) position of tRNAs decoding two-family box triplets. TrmE is organized as a multidomain protein consisting of an ~220-amino acid N-terminal domain, probably required for self-assembly, a middle GTPase domain, of about 160 residues, and an ~75-amino acid C-terminal domain, which contains a highly conserved CxGK motif. TrmE contains at least four of the five conserved nucleotide-binding motifs G1 (GxxxxGK[ST] or P-loop), G2 (T), G3 (DxxG) and G4 ([NT]KxD). The totally invariant alanine in the SA[KL] (G5) motif of Ras anGalph proteins is less well conserved [1,2,3,4,5].

The structure of the TrmE-type G domain consists of a central four-stranded β-sheet flanked by five α-helices (see <PDB:1XZP>). It dimerises in a potassium-dependent manner [4,5].

The profile we developed covers the entire TmrE-type G domain.

Last update:

March 2014 / First entry.

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Technical section

PROSITE method (with tools and information) covered by this documentation:

G_TRME, PS51709; TrmE-type guanine nucleotide-binding (G) domain profile  (MATRIX)


References

1AuthorsLeipe D.D. Wolf Y.I. Koonin E.V. Aravind L.
TitleClassification and evolution of P-loop GTPases and related ATPases.
SourceJ. Mol. Biol. 317:41-72(2002).
PubMed ID11916378
DOI10.1006/jmbi.2001.5378

2AuthorsYamanaka K. Hwang J. Inouye M.
TitleCharacterization of GTPase activity of TrmE, a member of a novel GTPase superfamily, from Thermotoga maritima.
SourceJ. Bacteriol. 182:7078-7082(2000).
PubMed ID11092873

3AuthorsYim L. Martinez-Vicente M. Villarroya M. Aguado C. Knecht E.
TitleArmengod M.-E. The GTPase activity and C-terminal cysteine of the Escherichia coli MnmE protein are essential for its tRNA modifying function.
SourceJ. Biol. Chem. 278:28378-28387(2003).
PubMed ID12730230
DOI10.1074/jbc.M301381200

4AuthorsScrima A. Vetter I.R. Armengod M.E. Wittinghofer A.
TitleThe structure of the TrmE GTP-binding protein and its implications for tRNA modification.
SourceEMBO J. 24:23-33(2005).
PubMed ID15616586
DOI10.1038/sj.emboj.7600507

5AuthorsMonleon D. Martinez-Vicente M. Esteve V. Yim L. Prado S. Armengod M.-E. Celda B.
TitleStructural insights into the GTPase domain of Escherichia coli MnmE protein.
SourceProteins 66:726-739(2007).
PubMed ID17143896
DOI10.1002/prot.21186



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