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2CIM

Crystal structure of Methanosarcina barkeri seryl-tRNA synthetase

Summary for 2CIM
Entry DOI10.2210/pdb2cim/pdb
DescriptorSERYL-TRNA SYNTHETASE, ZINC ION, CHLORIDE ION, ... (5 entities in total)
Functional Keywordsligase, trna synthetase, zinc ion
Biological sourceMETHANOSARCINA BARKERI
Total number of polymer chains2
Total formula weight120549.76
Authors
Bilokapic, S.,Maier, T.,Ahel, D.,Gruic-Sovulj, I.,Soll, D.,Weygand-Durasevic, I.,Ban, N. (deposition date: 2006-03-24, release date: 2006-06-26, Last modification date: 2024-05-08)
Primary citationBilokapic, 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
Cited by
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
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.51 Å)
Structure validation

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