Homo sapiens Protein: CYB5R3 | |||||||||||||||||||||||
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Summary | |||||||||||||||||||||||
InnateDB Protein | IDBP-10151.6 | ||||||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||||||
Gene Symbol | CYB5R3 | ||||||||||||||||||||||
Protein Name | cytochrome b5 reductase 3 | ||||||||||||||||||||||
Synonyms | B5R; DIA1; | ||||||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||||||
Ensembl Protein | ENSP00000338461 | ||||||||||||||||||||||
InnateDB Gene | IDBG-10149 (CYB5R3) | ||||||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||||||
Function | Desaturation and elongation of fatty acids, cholesterol biosynthesis, drug metabolism, and, in erythrocyte, methemoglobin reduction. | ||||||||||||||||||||||
Subcellular Localization | Isoform 1: Endoplasmic reticulum membrane; Lipid-anchor; Cytoplasmic side. Mitochondrion outer membrane; Lipid-anchor; Cytoplasmic side.Isoform 2: Cytoplasm. Note=Produces the soluble form found in erythrocytes. | ||||||||||||||||||||||
Disease Associations | Methemoglobinemia CYB5R3-related (METHB-CYB5R3) [MIM:250800]: A form of methemoglobinemia, a hematologic disease characterized by the presence of excessive amounts of methemoglobin in blood cells, resulting in decreased oxygen carrying capacity of the blood, cyanosis and hypoxia. There are two types of methemoglobinemia CYB5R3-related. In type 1, the defect affects the soluble form of the enzyme, is restricted to red blood cells, and causes well-tolerated methemoglobinemia. In type 2, the defect affects both the soluble and microsomal forms of the enzyme and is thus generalized, affecting red cells, leukocytes and all body tissues. Type 2 methemoglobinemia is associated with mental deficiency and other neurologic symptoms. {ECO:0000269PubMed:10807796, ECO:0000269PubMed:12393396, ECO:0000269PubMed:1400360, ECO:0000269PubMed:15622768, ECO:0000269PubMed:1707593, ECO:0000269PubMed:1898726, ECO:0000269PubMed:7718898, ECO:0000269PubMed:8119939, ECO:0000269PubMed:9695975, ECO:0000269PubMed:9886302}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||||||
Tissue Specificity | Isoform 2 is expressed at late stages of erythroid maturation. | ||||||||||||||||||||||
Comments | |||||||||||||||||||||||
Interactions | |||||||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 10 experimentally validated interaction(s) in this database.
They are also associated with 3 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 |
IPR001433
Oxidoreductase FAD/NAD(P)-binding IPR001709 Flavoprotein pyridine nucleotide cytochrome reductase IPR001834 NADH:cytochrome b5 reductase (CBR) IPR008333 Oxidoreductase, FAD-binding domain IPR017938 Riboflavin synthase-like beta-barrel |
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PFAM |
PF00175
PF00970 |
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PRINTS |
PR00371
PR00406 |
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PIRSF | |||||||||||||||||||||||
SMART | |||||||||||||||||||||||
TIGRFAMs | |||||||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||||||
Modification | |||||||||||||||||||||||
Cross-References | |||||||||||||||||||||||
SwissProt | P00387 | ||||||||||||||||||||||
PhosphoSite | PhosphoSite-P00387 | ||||||||||||||||||||||
TrEMBL | B1AHF3 | ||||||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||||||
Entrez Gene | 1727 | ||||||||||||||||||||||
UniGene | Hs.561064 | ||||||||||||||||||||||
RefSeq | NP_000389 | ||||||||||||||||||||||
HUGO | HGNC:2873 | ||||||||||||||||||||||
OMIM | 613213 | ||||||||||||||||||||||
CCDS | CCDS33658 | ||||||||||||||||||||||
HPRD | 08942 | ||||||||||||||||||||||
IMGT | |||||||||||||||||||||||
EMBL | AF061830 AF061831 AF361370 AJ010116 AJ010117 AJ010118 AJ310899 AJ310900 AK302204 AY341030 BC004821 BT009821 CH471138 CR456435 M16461 M16462 M28705 M28706 M28707 M28708 M28709 M28710 M28711 M28713 Y09501 Z93241 | ||||||||||||||||||||||
GenPept | AAA52306 AAA52307 AAA59900 AAF06818 AAF06819 AAH04821 AAL87744 AAP88823 AAP88936 BAH13649 CAA09006 CAA09007 CAA09008 CAA70696 CAB42843 CAC84523 CAC84524 CAG30321 CAQ08414 EAW73268 EAW73272 EAW73273 | ||||||||||||||||||||||