Homo sapiens Protein: DPYD
Summary
InnateDB Protein IDBP-100419.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol DPYD
Protein Name dihydropyrimidine dehydrogenase
Synonyms DHP; DHPDHASE; DPD;
Species Homo sapiens
Ensembl Protein ENSP00000359211
InnateDB Gene IDBG-100417 (DPYD)
Protein Structure
UniProt Annotation
Function Involved in pyrimidine base degradation. Catalyzes the reduction of uracil and thymine. Also involved the degradation of the chemotherapeutic drug 5-fluorouracil.
Subcellular Localization Cytoplasm.
Disease Associations Dihydropyrimidine dehydrogenase deficiency (DPYDD) [MIM:274270]: A metabolic disorder with large phenotypic variability, ranging from no symptoms to a convulsive disorder with motor and mental retardation. It is characterized by persistent urinary excretion of excessive amounts of uracil, thymine and 5-hydroxymethyluracil. Patients suffering from this disease show a severe reaction to the anticancer drug 5- fluorouracil. {ECO:0000269PubMed:14702039, ECO:0000269PubMed:16710414, ECO:0000269PubMed:9266349, ECO:0000269PubMed:9439663}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Found in most tissues with greatest activity found in liver and peripheral blood mononuclear cells.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 3 experimentally validated interaction(s) in this database.
Experimentally validated
Total 3 [view]
Protein-Protein 3 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0004152 dihydroorotate dehydrogenase activity
GO:0004158 dihydroorotate oxidase activity
GO:0016491 oxidoreductase activity
GO:0016627 oxidoreductase activity, acting on the CH-CH group of donors
GO:0017113 dihydropyrimidine dehydrogenase (NADP+) activity
GO:0017150 tRNA dihydrouridine synthase activity
GO:0042803 protein homodimerization activity
GO:0046872 metal ion binding
GO:0050660 flavin adenine dinucleotide binding
GO:0050661 NADP binding
GO:0051536 iron-sulfur cluster binding
GO:0051539 4 iron, 4 sulfur cluster binding
Biological Process
GO:0006145 purine nucleobase catabolic process
GO:0006206 pyrimidine nucleobase metabolic process
GO:0006208 pyrimidine nucleobase catabolic process
GO:0006210 thymine catabolic process
GO:0006212 uracil catabolic process
GO:0006214 thymidine catabolic process
GO:0006222 UMP biosynthetic process
GO:0008033 tRNA processing
GO:0019483 beta-alanine biosynthetic process
GO:0044281 small molecule metabolic process
GO:0046135 pyrimidine nucleoside catabolic process
GO:0055086 nucleobase-containing small molecule metabolic process
GO:0055114 oxidation-reduction process
Cellular Component
GO:0005737 cytoplasm
GO:0005829 cytosol
Protein Structure and Domains
PDB ID
InterPro IPR001269 tRNA-dihydrouridine synthase
IPR005720 Dihydroorotate dehydrogenase domain
IPR009051 Alpha-helical ferredoxin
IPR012135 Dihydroorotate dehydrogenase, class 1/ 2
IPR013027 FAD-dependent pyridine nucleotide-disulphide oxidoreductase
IPR023753 Pyridine nucleotide-disulphide oxidoreductase, FAD/NAD(P)-binding domain
PFAM PF01207
PF01180
PF07992
PRINTS PR00368
PIRSF PIRSF006621
PIRSF000164
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q12882
PhosphoSite PhosphoSite-Q12882
TrEMBL
UniProt Splice Variant
Entrez Gene 1806
UniGene Hs.613866
RefSeq NP_000101
HUGO HGNC:3012
OMIM 612779
CCDS CCDS30777
HPRD 02036
IMGT
EMBL AB003063 AC091608 AC093576 AC099787 AC114878 AC138135 AK291217 AL356457 BC008379 BC064027 BC108742 BC131777 BC131778 BT006740 BX908805 CH471097 U09178 U20938 U57655 X95670
GenPept AAA57474 AAB07049 AAB51366 AAH08379 AAH64027 AAI08743 AAI31778 AAI31779 AAP35386 BAA89789 BAF83906 CAA64973 CAH70570 CAI15125 EAW73002