PRMT4B
Gene Ontology Biological Process
Gene Ontology Molecular Function- [myelin basic protein]-arginine N-methyltransferase activity [IDA]
- histone-arginine N-methyltransferase activity [IDA]
- methyltransferase activity [ISS]
- protein heterodimerization activity [IPI]
- protein homodimerization activity [IPI]
- protein-arginine omega-N asymmetric methyltransferase activity [IDA]
- protein-arginine omega-N monomethyltransferase activity [IDA]
- [myelin basic protein]-arginine N-methyltransferase activity [IDA]
- histone-arginine N-methyltransferase activity [IDA]
- methyltransferase activity [ISS]
- protein heterodimerization activity [IPI]
- protein homodimerization activity [IPI]
- protein-arginine omega-N asymmetric methyltransferase activity [IDA]
- protein-arginine omega-N monomethyltransferase activity [IDA]
PRMT4A
Gene Ontology Biological Process
Gene Ontology Molecular Function- [myelin basic protein]-arginine N-methyltransferase activity [IDA]
- histone-arginine N-methyltransferase activity [IDA]
- methyltransferase activity [ISS]
- protein heterodimerization activity [IPI]
- protein homodimerization activity [IPI]
- protein-arginine omega-N asymmetric methyltransferase activity [IDA]
- protein-arginine omega-N monomethyltransferase activity [IDA]
- [myelin basic protein]-arginine N-methyltransferase activity [IDA]
- histone-arginine N-methyltransferase activity [IDA]
- methyltransferase activity [ISS]
- protein heterodimerization activity [IPI]
- protein homodimerization activity [IPI]
- protein-arginine omega-N asymmetric methyltransferase activity [IDA]
- protein-arginine omega-N monomethyltransferase activity [IDA]
Co-fractionation
Interaction inferred from the presence of two or more protein subunits in a partially purified protein preparation. If co-fractionation is demonstrated between 3 or more proteins, then add them as a complex.
Publication
A proteomic strategy for global analysis of plant protein complexes.
Global analyses of protein complex assembly, composition, and location are needed to fully understand how cells coordinate diverse metabolic, mechanical, and developmental activities. The most common methods for proteome-wide analysis of protein complexes rely on affinity purification-mass spectrometry or yeast two-hybrid approaches. These methods are time consuming and are not suitable for many plant species that are refractory to transformation ... [more]
Throughput
- High Throughput
Related interactions
| Interaction | Experimental Evidence Code | Dataset | Throughput | Score | Curated By | Notes |
|---|---|---|---|---|---|---|
| PRMT4A PRMT4B | Reconstituted Complex Reconstituted Complex An interaction is inferred between proteins in vitro. This can include proteins in recombinant form or proteins isolated directly from cells with recombinant or purified bait. For example, GST pull-down assays where a GST-tagged protein is first isolated and then used to fish interactors from cell lysates are considered reconstituted complexes (e.g. PUBMED: 14657240, Fig. 4A or PUBMED: 14761940, Fig. 5). This can also include gel-shifts, surface plasmon resonance, isothermal titration calorimetry (ITC) and bio-layer interferometry (BLI) experiments. The bait-hit directionality may not be clear for 2 interacting proteins. In these cases the directionality is up to the discretion of the curator. | Low | - | BioGRID | - |
Curated By
- BioGRID