Crystal structure of the N-terminal methyltransferase-like domain of anamorsin

Proteins. 2014 Jun;82(6):1066-71. doi: 10.1002/prot.24443. Epub 2013 Nov 22.

Abstract

Anamorsin is a recently identified molecule that inhibits apoptosis during hematopoiesis. It contains an N-terminal methyltransferase-like domain and a C-terminal Fe-S cluster motif. Not much is known about the function of the protein. To better understand the function of anamorsin, we have solved the crystal structure of the N-terminal domain at 1.8 Å resolution. Although the overall structure resembles a typical S-adenosylmethionine (SAM) dependent methyltransferase fold, it lacks one α-helix and one β-strand. As a result, the N-terminal domain as well as the full-length anamorsin did not show S-adenosyl-L-methionine (AdoMet) dependent methyltransferase activity. Structural comparisons with known AdoMet dependent methyltransferases reveals subtle differences in the SAM binding pocket that preclude the N-terminal domain from binding to AdoMet. The N-terminal methyltransferase-like domain of anamorsin probably functions as a structural scaffold to inhibit methyl transfers by out-competing other AdoMet dependant methyltransferases or acts as bait for protein-protein interactions.

Keywords: CIAPIN1; anamorsin; crystal structure; methyltransferase-like fold.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Catalytic Domain
  • Crystallography, X-Ray
  • Humans
  • Intracellular Signaling Peptides and Proteins / chemistry*
  • Methyltransferases / chemistry*
  • Models, Molecular
  • Molecular Sequence Data
  • Protein Structure, Secondary

Substances

  • CIAPIN1 protein, human
  • Intracellular Signaling Peptides and Proteins
  • Methyltransferases

Associated data

  • PDB/4M7R