| InnateDB Protein | IDBP-596629.3 | 
                            
                                | Last Modified | 2014-10-13  [Report errors or provide feedback] | 
  
                            
                                | Gene Symbol | CPT1A | 
                            
                                | Protein Name | carnitine palmitoyltransferase 1A (liver) | 
                            
                                | Synonyms | CPT1; CPT1-L; L-CPT1; | 
                            
                                | Species | Homo sapiens | 
                            
                                | Ensembl Protein | ENSP00000439084 | 
                            
                                | InnateDB Gene | IDBG-61582 (CPT1A) | 
                            
                                | Protein Structure |   | 
                            
                                
                            
   
                            
                                | Function | Catalyzes the transfer of the acyl group of long-chain fatty acid-CoA conjugates onto carnitine, an essential step for the mitochondrial uptake of long-chain fatty acids and their subsequent beta-oxidation in the mitochondrion. Plays an important role in triglyceride metabolism. | 
                            
                                | Subcellular Localization | Mitochondrion outer membrane {ECO:0000269PubMed:11350182, ECO:0000269PubMed:14517221}; Multi- pass membrane protein {ECO:0000269PubMed:11350182, ECO:0000269PubMed:14517221}. | 
                            
                                | Disease Associations | Carnitine palmitoyltransferase 1A deficiency (CPT1AD) [MIM:255120]: Rare autosomal recessive metabolic disorder of long- chain fatty acid oxidation characterized by severe episodes of hypoketotic hypoglycemia usually occurring after fasting or illness. Onset is in infancy or early childhood. {ECO:0000269PubMed:11350182, ECO:0000269PubMed:11441142, ECO:0000269PubMed:12189492, ECO:0000269PubMed:14517221, ECO:0000269PubMed:15110323, ECO:0000269PubMed:15669684, ECO:0000269PubMed:9691089}. Note=The disease is caused by mutations affecting the gene represented in this entry. | 
                            
                                | Tissue Specificity | Strong expression in kidney and heart, and lower in liver and skeletal muscle. | 
                            
                                | Comments |  | 
                            
                                
                            
                            
                                | Number of Interactions | This gene and/or its encoded proteins are associated with 31 experimentally validated interaction(s) in this database. 
                                        
                                            | 
                                                    | Experimentally validated |  
                                                        | Total | 31
                                                            
                                                            [view] |  
                                                        | Protein-Protein | 31
                                                            
                                                            [view] |  
                                                        | Protein-DNA | 0 |  
                                                        | Protein-RNA | 0 |  
                                                        | DNA-DNA | 0 |  
                                                        | RNA-RNA | 0 |  
                                                        | DNA-RNA | 0 |  |  |  | 
                            
                             
                            
                            
                                | Molecular Function
 | 
                                          
                                            | Accession | GO Term |  
                                            
                                        
                                        
                                        
                                        
                                        
                                        
                                        
                                        
                                        
                                        
                                        
                                           
                                            | GO:0004095 | carnitine O-palmitoyltransferase activity |    
                                            | GO:0016746 | transferase activity, transferring acyl groups |  | 
                            
                                | Biological Process |  | 
                            
                                | Cellular Component |  | 
                            
                            
                                
                            
                            | PDB ID |  | 
                            | InterPro | IPR000542 
                                    Acyltransferase ChoActase/COT/CPT 
 | 
                            | PFAM | PF00755 
 | 
                            | PRINTS |  | 
                            | PIRSF |  | 
                            | SMART |  | 
                            | TIGRFAMs |  | 
                            
                                
                            
   
                            
                                | Modification |  | 
                            
                                
                            
    
                            | SwissProt | P50416 | 
                            | PhosphoSite | PhosphoSite-P50416 | 
                            | TrEMBL | H3BUV7 | 
                            | UniProt Splice Variant |  | 
                            | Entrez Gene | 1374 | 
                            | UniGene | Hs.717370 | 
                            | RefSeq | XP_005273820 | 
            
                            
                            | HUGO | HGNC:2328 | 
                            
                            | OMIM | 600528 | 
                            | CCDS | CCDS31624 | 
           
                            | HPRD | 02755 | 
            
                            | IMGT |  | 
            
                            | EMBL | AJ420747
                                     
                                     
                                    
                                        AJ420748
                                     
                                     
                                    
                                        AP000808
                                     
                                     
                                    
                                        AP003732
                                     
                                     
                                    
                                        BC000185
                                     
                                     
                                    
                                        BT009791
                                     
                                     
                                    
                                        L39211 | 
                            | GenPept | AAC41748
                                     
                                     
                                    
                                        AAH00185
                                     
                                     
                                    
                                        AAP88793
                                     
                                     
                                    
                                        CAD12625
                                     
                                     
                                    
                                        CAD59673 | 
                            
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