Bos taurus Protein: WBSCR22 | |||||||||||||||
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Summary | |||||||||||||||
InnateDB Protein | IDBP-692248.2 | ||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||
Gene Symbol | WBSCR22 | ||||||||||||||
Protein Name | Uncharacterized methyltransferase WBSCR22 | ||||||||||||||
Synonyms | |||||||||||||||
Species | Bos taurus | ||||||||||||||
Ensembl Protein | ENSBTAP00000022697 | ||||||||||||||
InnateDB Gene | IDBG-640042 (WBSCR22) | ||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||
Function | S-adenosyl-L-methionine-dependent methyltransferase that specifically methylates the N(7) position of a guanine in 18S rRNA. Important for biogenesis end export of the 40S ribosomal subunit independent on its methyltransferase activity. Locus- specific steroid receptor coactivator. Potentiates transactivation by glucocorticoid (NR3C1), mineralocorticoid (NR3C2), androgen (AR) and progesterone (PGR) receptors. Required for the maintenance of open chromatin at the TSC22D3/GILZ locus to facilitate NR3C1 loading on the response elements. Required for maintenance of dimethylation on histone H3 'Lys-79' (H3K79me2) (By similarity). {ECO:0000250}. | ||||||||||||||
Subcellular Localization | Nucleus {ECO:0000250}. Cytoplasm {ECO:0000250}. Note=Localized diffusely throughout the nucleus and the cytoplasm. {ECO:0000250}. | ||||||||||||||
Disease Associations | |||||||||||||||
Tissue Specificity | |||||||||||||||
Comments | |||||||||||||||
Interactions | |||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 12 interaction(s) predicted by orthology.
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Gene Ontology | |||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||
PDB ID | |||||||||||||||
InterPro |
IPR013216
Methyltransferase type 11 IPR022238 Uncharacterised protein family, methyltransferase, Williams-Beuren syndrome IPR029063 S-adenosyl-L-methionine-dependent methyltransferase-like |
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PFAM |
PF08241
PF12589 |
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PRINTS | |||||||||||||||
PIRSF | |||||||||||||||
SMART | |||||||||||||||
TIGRFAMs | |||||||||||||||
Post-translational Modifications | |||||||||||||||
Modification | |||||||||||||||
Cross-References | |||||||||||||||
SwissProt | Q58DP0 | ||||||||||||||
PhosphoSite | PhosphoSite- | ||||||||||||||
TrEMBL | |||||||||||||||
UniProt Splice Variant | |||||||||||||||
Entrez Gene | 513878 | ||||||||||||||
UniGene | Bt.4845 | ||||||||||||||
RefSeq | NP_001029629 | ||||||||||||||
HUGO | |||||||||||||||
OMIM | |||||||||||||||
CCDS | |||||||||||||||
HPRD | |||||||||||||||
IMGT | |||||||||||||||
EMBL | BC109889 BT021557 | ||||||||||||||
GenPept | AAI09890 AAX46404 | ||||||||||||||