Glycyl-tRNA synthetase from Nanoarchaeum equitans: The first crystal structure of archaeal GlyRS and analysis of its tRNA glycylation

• Published in: Biochemical and biophysical research communications Vol. 511; no. 2; pp. 228 - 233
• Main Authors: Fujisawa, Alma, Toki, Risako, Miyake, Hideaki, Shoji, Tomoko, Doi, Hiromi, Hayashi, Hiromi, Hanabusa, Rina, Mutsuro-Aoki, Hiromi, Umehara, Takuya, Ando, Tadashi, Noguchi, Hiroki, Voet, Arnout, Park, Sam-Yong, Tamura, Koji
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 02.04.2019
• Subjects: Acceptor-stem recognition; Amino Acid Sequence; Aminoacylation; Archaeal Proteins - chemistry; Archaeal Proteins - metabolism; Crystal structure; Crystallography, X-Ray; Glycine-tRNA Ligase - chemistry; Glycine-tRNA Ligase - metabolism; Glycyl-tRNA synthetase; Models, Molecular; Nanoarchaeota - chemistry; Nanoarchaeota - enzymology; Nanoarchaeota - metabolism; Nanoarchaeum equitans; Protein Conformation; RNA, Transfer - chemistry; RNA, Transfer - metabolism; Sequence Alignment; tRNA; Glycyl-tRNA synthetase; Acceptor-stem recognition; Aminoacylation; tRNA; Nanoarchaeum equitans; Crystal structure
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2019.01.142

This study reports the X-ray crystallographic structure of the glycyl-tRNA synthetase (GlyRS) of Nanoarchaeum equitans — a hyperthermophilic archaeal species. This is the first archaeal GlyRS crystal structure elucidated. The GlyRS comprises an N-terminal catalytic domain and a C-terminal anticodon-binding domain with a long β-sheet inserted between these domains. An unmodified transcript of the wild-type N. equitans tRNAGly was successfully glycylated using GlyRS. Substitution of the discriminator base A73 of tRNAGly with any other nucleotide caused a significant decrease in glycylation activity. Mutational analysis of the second base-pair C2G71 of the acceptor stem of tRNAGly elucidated the importance of the base-pair, especially G71, as an identity element for recognition by GlyRS. Glycylation assays using tRNAGly G71 substitution mutants and a GlyRS mutant where Arg223 is mutated to alanine strengthen the possibility that the carbonyl oxygen at position 6 of G71 would hydrogen-bond with the guanidine nitrogen of Arg223 in N. equitans GlyRS. •The X-ray crystallographic structure of Nanoarchaeum equitans GlyRS has been solved in this study.•This is the first crystal structure of archaeal GlyRS.•The A73 and G71 residues of the tRNAGly acceptor stem are important for glycylation.•Arg223 of GlyRS possibly interacts with the carbonyl oxygen at position 6 of G71.