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EIF-W2 protein domain

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Protein family
W2
crystal structure of the catalytic fragment of eukaryotic initiation factor 2b epsilon
Identifiers
SymbolW2
PfamPF02020
Pfam clanCL0020
InterProIPR003307
SCOP21paq / SCOPe / SUPFAM
Available protein structures:
Pfam  structures / ECOD  
PDBRCSB PDB; PDBe; PDBj
PDBsumstructure summary

In molecular biology, the protein domain eIF4-gamma/eIF5/eIF2-epsilon is a family of evolutionarily related proteins. This domain is found at the C-terminus of several translation Initiation factors. It was first detected at the very C-termini of the yeast protein GCD6, eIF-2B epsilon, and two other eukaryotic translation initiation factors, eIF-4 gamma and eIF-5 and it may be involved in the interaction of eIF-2B, eIF-4 gamma, and eIF-5 with eIF-2.

Function

In molecular biology, the eIF-W2 domain functions as the binding site for Mnk eIF4E kinase, an enzyme that phosphorylates eukaryotic initiation factor 4E (eIF4E). For eIF2B-epsilon, the W2 C-terminal domain functions in guanine nucleotide exchange on eIF2. For eIF5, the W2 domain functions in mediating the multifactor complex (MFC) formation with eIF1, eIF2-GTP, eIF3 and Met-tRNAiMet. The eIF5 W2 C-terminal domain and the adjacent N-terminal linker region are responsible for the GDI activity against eIF2-GDP.

Domain Structure

The W2 domain has a globular fold and is exclusively composed out of alpha-helices. The structure can be divided into a structural C-terminal core onto which the two N-terminal helices are attached. The core contains two aromatic/acidic residue-rich regions (AA boxes), important for mediating protein-protein interactions.

This entry covers the entire W2 domain, part of the TPR clan.

Translation

Translation initiation is a well regulated and highly coordinated cellular process in eukaryotes, in which at least 11 eukaryotic initiation factors (eIFs) are included. These factors come together to form the pre-initiation complex.

Eukaryotic initiation factors

The W2 domain (two invariant tryptophans) is a region of approximately 165 amino acids which is found in the C-terminus of the following eukaryotic initiation factors(eIFs):

  • Eukaryotic translation initiation factor 2B epsilon (eIF-2B-epsilon)
  • Eukaryotic translation initiation factor 4 gamma (eIF-4-gamma)
  • Eukaryotic translation initiation factor 5 (eIF-5), a GTPase-activating protein (GAP) specific for eIF2

Examples

Genes encoding proteins containing this domain include AAG1, BZW1, BZW2, EIF2B5, EIF4G1, EIF4G2, EIF4G3, and EIF5.

References

  1. ^ Koonin EV (1995). "Multidomain organization of eukaryotic guanine nucleotide exchange translation initiation factor eIF-2B subunits revealed by analysis of conserved sequence motifs". Protein Sci. 4 (8): 1608–1617. doi:10.1002/pro.5560040819. PMC 2143190. PMID 8520487.
  2. Singh CR, Watanabe R, Zhou D, Jennings MD, Fukao A, Lee B, et al. (2011). "Mechanisms of translational regulation by a human eIF5-mimic protein". Nucleic Acids Res. 39 (19): 8314–28. doi:10.1093/nar/gkr339. PMC 3201852. PMID 21745818.
  3. Fukunaga R, Hunter T (1997). "MNK1, a new MAP kinase-activated protein kinase, isolated by a novel expression screening method for identifying protein kinase substrates". EMBO J. 16 (8): 1921–33. doi:10.1093/emboj/16.8.1921. PMC 1169795. PMID 9155018.
  4. Boesen T, Mohammad SS, Pavitt GD, Andersen GR (March 2004). "Structure of the catalytic fragment of translation initiation factor 2B and identification of a critically important catalytic residue". J. Biol. Chem. 279 (11): 10584–92. doi:10.1074/jbc.M311055200. PMID 14681227.
  5. Wei Z, Xue Y, Xu H, Gong W (May 2006). "Crystal structure of the C-terminal domain of S.cerevisiae eIF5". J. Mol. Biol. 359 (1): 1–9. doi:10.1016/j.jmb.2006.03.037. PMID 16616930.
  6. Bieniossek C, Schütz P, Bumann M, Limacher A, Uson I, Baumann U (July 2006). "The crystal structure of the carboxy-terminal domain of human translation initiation factor eIF5". J. Mol. Biol. 360 (2): 457–65. doi:10.1016/j.jmb.2006.05.021. PMID 16781736.
  7. Koonin EV (August 1995). "Multidomain organization of eukaryotic guanine nucleotide exchange translation initiation factor eIF-2B subunits revealed by analysis of conserved sequence motifs". Protein Sci. 4 (8): 1608–17. doi:10.1002/pro.5560040819. PMC 2143190. PMID 8520487.
This article incorporates text from the public domain Pfam and InterPro: IPR003307 Category: