ID:NP1L1_HUMAN DESCRIPTION: RecName: Full=Nucleosome assembly protein 1-like 1; AltName: Full=NAP-1-related protein; Short=hNRP; Flags: Precursor; FUNCTION: May be involved in modulating chromatin formation and contribute to regulation of cell proliferation. INTERACTION: Q92793:CREBBP; NbExp=3; IntAct=EBI-356392, EBI-81215; Q09472:EP300; NbExp=3; IntAct=EBI-356392, EBI-447295; P10588:NR2F6; NbExp=2; IntAct=EBI-356392, EBI-2681496; SUBCELLULAR LOCATION: Nucleus. Melanosome. Note=Identified by mass spectrometry in melanosome fractions from stage I to stage IV. TISSUE SPECIFICITY: Ubiquitously expressed. DOMAIN: The acidic domains are probably involved in the interaction with histones. PTM: Polyglutamylated by TTLL4, a modification that occurs exclusively on glutamate residues and results in polyglutamate chains on the gamma-carboxyl group. Some residues may also be monoglycylated but not polyglycylated due to the absence of functional TTLL10 in human (By similarity). SIMILARITY: Belongs to the nucleosome assembly protein (NAP) family.
The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.
ModBase Predicted Comparative 3D Structure on P55209
Front
Top
Side
The pictures above may be empty if there is no ModBase structure for the protein. The ModBase structure frequently covers just a fragment of the protein. You may be asked to log onto ModBase the first time you click on the pictures. It is simplest after logging in to just click on the picture again to get to the specific info on that model.
Orthologous Genes in Other Species
Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.