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Protein Page:
UGT1A10 (human)

UGT1A10 UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. Belongs to the UDP-glycosyltransferase family. 1 isoforms of the human protein are produced by alternative splicing. Note: This description may include information from UniProtKB.
Protein type: Cofactor and Vitamin Metabolism - porphyrin and chlorophyll; EC; Xenobiotic Metabolism - drug metabolism - other enzymes; Carbohydrate Metabolism - pentose and glucuronate interconversions; Lipid Metabolism - androgen and estrogen; Xenobiotic Metabolism - drug metabolism - cytochrome P450; Carbohydrate Metabolism - starch and sucrose; Cofactor and Vitamin Metabolism - retinol; Carbohydrate Metabolism - ascorbate and aldarate; Transferase; Xenobiotic Metabolism - metabolism by cytochrome P450; Membrane protein, integral
Cellular Component: endoplasmic reticulum membrane; endoplasmic reticulum; integral to membrane
Molecular Function: protein homodimerization activity; retinoic acid binding; enzyme binding; protein kinase C binding; glucuronosyltransferase activity; protein heterodimerization activity
Biological Process: flavone metabolic process
Reference #:  Q9HAW8 (UniProtKB)
Alt. Names/Synonyms: GNT1; UD110; UDP glucuronosyltransferase 1 family, polypeptide A10; UDP glycosyltransferase 1 family, polypeptide A10; UDP-glucuronosyltransferase 1-10; UDP-glucuronosyltransferase 1-J; UDP-glucuronosyltransferase 1A10; UDPGT; UDPGT 1-10; UGT-1J; UGT1; UGT1*10; UGT1-10; UGT1.10; UGT1A10; UGT1J
Gene Symbols: UGT1A10
Molecular weight: 59,810 Da
Basal Isoelectric point: 6.88  Predict pI for various phosphorylation states
Select Structure to View Below


Protein Structure Not Found.

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Modification Sites and Domains  

Modification Sites in Parent Protein, Orthologs, and Isoforms  

Show Multiple Sequence Alignment


SS: The number of records in which this modification site was determined using site-specific methods. SS methods include amino acid sequencing, site-directed mutagenesis, modification site-specific antibodies, specific MS strategies, etc.


MS: The number of records in which this modification site was assigned using ONLY proteomic discovery-mode mass spectrometry.



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