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NSUN5P2
May have S-adenosyl-L-methionine-dependent methyl-transferase activity. Belongs to the class I-like SAM-binding methyltransferase superfamily. RsmB/NOP family. Ubiquitous. 5 alternatively spliced human isoforms have been reported. Note: This description may include information from UniProtKB.
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| Protein type: EC 2.1.1.-; Methyltransferase |
| Chromosomal Location of human Ortholog: 7q11.23 |
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Cellular Component:
nucleolus
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Molecular Function:
methyltransferase activity; RNA binding
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Biological Process:
rRNA base methylation
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Reference #:
Q63ZY6
(UniProtKB)
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Alt. Names/Synonyms: DKFZp434K058; DKFZp666P104; FLJ11626; MGC129801; MGC15057; NOL1/NOP2/Sun domain family member 5C; NOL1/NOP2/Sun domain family, member 5C; NOL1R2; NOP2/Sun domain family, member 5 pseudogene 2; NOP2/Sun domain family, member 5C (pseudogene); NOP2/Sun RNA methyltransferase family member 5 pseudogene 2; NSN5C; NSUN5 pseudogene 2; NSUN5C; NSUN5P2; Putative methyltransferase NSUN5C; WBSCR20B; WBSCR20C; Williams Beuren syndrome chromosome region 20C; Williams-Beuren syndrome chromosomal region 20C protein
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Gene Symbols: NSUN5P2
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Molecular weight:
34,347 Da
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Basal Isoelectric point:
9.01
Predict pI for various phosphorylation states
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