Our recent progress and ongoing work: We have identified a novel family of lysine-specific protein methyltransferases (KMTs) (Fig. A) encoded in the human genome (Kernstock et al., 2012). We have so far identified the targets for several of these KMTs, and these targets encompass proteins involved in a wide range of cellular process, including protein folding, protein translation, mitochondrial metabolism and DNA repair (Reviewed in Falnes et al. 2016). For example, we found that the previously uncharacterized human MTase METTL21D (now named VCP-KMT) methylates Lys-315 in the essential chaperone protein VCP (Fig. B), and this MTase is important for cancer metastasisr cancer metastasis. 
Figure: A, Methylation of proteins by lysine (K) methyltransferases (KMTs). B, Trimethylation of VCP on Lys315 by the novel methyltransferase VCP-KMT (Kernstock et al., 2012)
Currently, the group focuses on unravelling the function of additional, yet uncharacterized, human MTases, many of which are involved in protein lysine methylation, but we are also studying MTases that target other substrates, e.g. DNA and RNA.
The actual project: In the proposed master project, you will be investigating a novel human MTase. The project will involve a characterization of the enzymatic activity of the MTase on candidate substrates, and the identification (by mutagenesis) of regions/residues in the MTase that are particularly important for function. Moreover, the study will use gene knock-out (CRISPR/Cas9 technology) in human cell culture to address the functional significance of the MTase.
The practical part of the project will be supervised by experienced postdocs/researchers who are focusing their research on various MTases, thus providing an good environment for capable supervision. During this project you will gain work experience in a wide variety of practical techniques, including recombinant DNA technology and mutagenesis, PCR, protein expression and purification, protein biochemistry, enzymatic assays, Western blotting and mammalian cell culture (including gene knock-out cells).
Some relevant recent references:
Kernstock,S., Davydova,E., Jakobsson,M., Moen,A., Pettersen,S., Maelandsmo,G.M., Egge-Jacobsen,W. and Falnes§,P.Ø. (2012) Lysine methylation of VCP by a member of a novel human protein methyltransferase family. Nat.Commun., 3, #1038
Falnes§, P.Ø., Jakobsson, M.E., Davydova, E., Ho, A.Y., and Małecki, J. (2016) Protein lysine methylation by seven-β-strand methyltransferases (2016) J. Biochem. J., 473, 1995-2009 (Review article)
Jakobsson, M.E., Moen, A., and Falnes§, P.Ø. (2016) Correspondence: On the enzymology and significance of HSPA1 lysine methylation, Nat.Commun., 7, #11464
Malecki, J., Aileni V.K.,†, Ho, A.Y.Y., Schwarz, J., Moen A., Sørensen, V., Nilges, B.S., Jakobsson, M.E., Leidel, S.A., Falnes, P.Ø. (2017) The novel lysine specific methyltransferase METTL21B affects mRNA translation through inducible and dynamic methylation of Lys-165 in human eukaryotic elongation factor 1 alpha (eEF1A). Nucl. Acids Res., 45, 4370-4389.