2CJ9

Crystal structure of Methanosarcina barkeri seryl-tRNA synthetase complexed with an analog of seryladenylate

Summary for 2CJ9

• Entry DOI: 10.2210/pdb2cj9/pdb
• Related: 2CIM 2CJA 2CJB
• Descriptor: SERYL-TRNA SYNTHETASE, ZINC ION, CHLORIDE ION, ... (5 entities in total)
• Functional Keywords: ligase, zinc ion, seryladenylate, trna synthetase
• Biological source: METHANOSARCINA BARKERI
• Total number of polymer chains: 2
• Total formula weight: 121221.48

Authors

Bilokapic, S.,Maier, T.,Ahel, D.,Gruic-Sovulj, I.,Soll, D.,Weygand-Durasevic, I.,Ban, N. (deposition date: 2006-03-29, release date: 2006-06-26, Last modification date: 2024-05-08)

Primary citation

Bilokapic, S.,Maier, T.,Ahel, D.,Gruic-Sovulj, I.,Soll, D.,Weygand-Durasevic, I.,Ban, N.
Structure of the Unusual Seryl-tRNA Synthetase Reveals a Distinct Zinc-Dependent Mode of Substrate Recognition
Embo J., 25:2498-, 2006

PubMed Abstract: Methanogenic archaea possess unusual seryl-tRNA synthetase (SerRS), evolutionarily distinct from the SerRSs found in other archaea, eucaryotes and bacteria. The two types of SerRSs show only minimal sequence similarity, primarily within class II conserved motifs 1, 2 and 3. Here, we report a 2.5 A resolution crystal structure of the atypical methanogenic Methanosarcina barkeri SerRS and its complexes with ATP, serine and the nonhydrolysable seryl-adenylate analogue 5'-O-(N-serylsulfamoyl)adenosine. The structures reveal two idiosyncratic features of methanogenic SerRSs: a novel N-terminal tRNA-binding domain and an active site zinc ion. The tetra-coordinated Zn2+ ion is bound to three conserved protein ligands (Cys306, Glu355 and Cys461) and binds the amino group of the serine substrate. The absolute requirement of the metal ion for enzymatic activity was confirmed by mutational analysis of the direct zinc ion ligands. This zinc-dependent serine recognition mechanism differs fundamentally from the one employed by the bacterial-type SerRSs. Consequently, SerRS represents the only known aminoacyl-tRNA synthetase system that evolved two distinct mechanisms for the recognition of the same amino-acid substrate.

PubMed: 16675947
DOI: 10.1038/SJ.EMBOJ.7601129

Experimental method

X-RAY DIFFRACTION (2.3 Å)