Homo sapiens Protein: ALDH3A2 | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-34853.7 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | ALDH3A2 | ||||||||||||||||||
Protein Name | aldehyde dehydrogenase 3 family, member A2 | ||||||||||||||||||
Synonyms | ALDH10; FALDH; SLS; | ||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000345774 | ||||||||||||||||||
InnateDB Gene | IDBG-34849 (ALDH3A2) | ||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||
Function | Catalyzes the oxidation of long-chain aliphatic aldehydes to fatty acids. Active on a variety of saturated and unsaturated aliphatic aldehydes between 6 and 24 carbons in length. Responsible for conversion of the sphingosine 1-phosphate (S1P) degradation product hexadecenal to hexadecenoic acid. {ECO:0000269PubMed:22633490}. | ||||||||||||||||||
Subcellular Localization | Endoplasmic reticulum membrane; Single-pass membrane protein; Cytoplasmic side. | ||||||||||||||||||
Disease Associations | Sjoegren-Larsson syndrome (SLS) [MIM:270200]: An autosomal recessive neurocutaneous disorder characterized by a combination of severe mental retardation, spastic di- or tetraplegia and congenital ichthyosis. Ichthyosis is usually evident at birth with varying degrees of erythema and scaling, neurologic symptoms appear in the first or second year of life. Most patients have an IQ of less than 60. Additional clinical features include glistening white spots on the retina, seizures, short stature and speech defects. {ECO:0000269PubMed:10577908, ECO:0000269PubMed:10792573, ECO:0000269PubMed:8528251, ECO:0000269PubMed:9254849, ECO:0000269PubMed:9829906}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||
Tissue Specificity | |||||||||||||||||||
Comments | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 22 experimentally validated interaction(s) in this database.
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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 |
IPR008670
Acyl-CoA reductase, LuxC IPR012394 Aldehyde dehydrogenase NAD(P)-dependent IPR015590 Aldehyde dehydrogenase domain IPR016161 Aldehyde/histidinol dehydrogenase |
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PFAM |
PF05893
PF00171 |
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PRINTS | |||||||||||||||||||
PIRSF |
PIRSF009414
PIRSF036492 |
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SMART | |||||||||||||||||||
TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | P51648 | ||||||||||||||||||
PhosphoSite | PhosphoSite-P51648 | ||||||||||||||||||
TrEMBL | K7EN73 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 224 | ||||||||||||||||||
UniGene | Hs.737600 | ||||||||||||||||||
RefSeq | NP_001026976 | ||||||||||||||||||
HUGO | HGNC:403 | ||||||||||||||||||
OMIM | 609523 | ||||||||||||||||||
CCDS | CCDS32589 | ||||||||||||||||||
HPRD | 07188 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AC005722 AC115989 AK292381 AK315096 BC002430 CH471212 CR457422 L47162 U46689 U75286 U75287 U75288 U75289 U75290 U75291 U75292 U75293 U75294 U75295 U75296 | ||||||||||||||||||
GenPept | AAB01003 AAC50965 AAC50966 AAC51121 AAH02430 BAF85070 BAG37560 CAG33703 EAW50898 | ||||||||||||||||||