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Human seryl-tRNA synthetase dimer complexed with one molecule of trnasec

Analyse Human seryl-tRNA synthetase dimer complexed with one molecule of trnasec in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4RQF
Type
protein + RNA
Length
988 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Selenocysteine tRNA; Serine--tRNA ligase, cytoplasmic
EC
6.1.1.11
UniProt
P49591
Ligands
ANP, SER
Pockets
14 · best druggability 0.77

Structure

x-ray diffraction · 3 distinct chains · 40% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
CSelenocysteine tRNArna63——
ASerine--tRNA ligase, cytoplasmic (EC 6.1.1.11)protein45139% helix, 20% strandP49591
BSerine--tRNA ligase, cytoplasmic (EC 6.1.1.11)protein47441% helix, 20% strandP49591

Ligands and binding sites

  • ANP · Phosphoaminophosphonic acid-adenylate ester · ligand · 2 copies · chains A, B
  • SER · Serine · ligand · 2 copies · chains A, B

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

14 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1820.770.9918empty
28350.740.7968SER, ANP
37640.730.7949ANP, SER
45250.690.8036empty
5570.680.9717empty

Interfaces

2 interfaces between chains.

  • A–B · 3040 Ų buried · 45 hydrogen bonds · protein-protein
  • C–A · 622 Ų buried · 6 hydrogen bonds · protein-nucleic

Compared structures

  • 4RQF · human Seryl-tRNA synthetase dimer complexed with one molecule of tRNAsec · the same entry in another collection · chain C against C, TM-score 1.00
  • P49591 · AlphaFold monomer V2.0 prediction for serine--tRNA ligase, cytoplasmic (P49591) · a predicted model of the same protein · chain A against A, TM-score 0.98

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