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FLASH GENE
Symbol DLAT contributors: mct - updated : 23-06-2021
HGNC name dihydrolipoamide S-acetyltransferase (E2 component of pyruvate dehydrogenase complex)
HGNC id 2896
RNA
TRANSCRIPTS type messenger
identificationnb exonstypebpproduct
ProteinkDaAAspecific expressionYearPubmed
14 - 3882 - 493 - 1988 3191998
14 - 3896 - 653 - 1988 3191998
14 - 3878 - 647 - 1988 3191998
14 - 3857 - 640 - 1988 3191998
13 - 3770 - 611 - 1988 3191998
12 - 3563 - 542 - 1988 3191998
11 - 3455 - 506 - 1988 3191998
12 - 3599 - 554 - 1988 3191998
12 - 3497 - 520 - 1988 3191998
14 - 3845 - 636 - 1988 3191998
14 - 3793 - 605 - 1988 3191998
14 - 3751 - 591 - 1988 3191998
14 - 3872 - 645 - 1988 3191998
EXPRESSION
Type ubiquitous
   expressed in (based on citations)
organ(s)
SystemOrgan level 1Organ level 2Organ level 3Organ level 4LevelPubmedSpeciesStageRna symbol
Digestivemouth   highly
Lymphoid/Immunelymph node   highly
Nervousbrain    
Reproductivemale systemtestis  highly
Respiratoryrespiratory tracttrachea  highly
cell lineage
cell lines
fluid/secretion
at STAGE
PROTEIN
PHYSICAL PROPERTIES
STRUCTURE
motifs/domains
  • two lipoyl-binding domains
  • E3 binding domain
  • a catalytic domain
  • HOMOLOGY
    intraspecies homolog to 2 oxoacid dehydrogenases acetyl-transferase
    Homologene
    FAMILY 2-oxoacid dehydrogenase family
    CATEGORY enzyme
    SUBCELLULAR LOCALIZATION     intracellular
    intracellular,cytoplasm,organelle,mitochondria,matrix
    basic FUNCTION
  • conversion of pyruvate to involved in the production of acetyl-CoA and carbone dioxide
  • novel function of DLAT in the nucleus, suggesting nuclear-mitochondrial crosstalk through the interaction between STAT5 and DLAT
  • radiation-induced blockade of autophagic flux stimulates redirection of intracellular molecules such as PDCE2 to the cell surface via a non-canonical secretory autophagy pathway
  • CELLULAR PROCESS
    PHYSIOLOGICAL PROCESS
    PATHWAY
    metabolism energetic
    signaling
    a component
  • E2 component of pyruvate dehydrogenase complex
  • multiple copies of three enzymatic components: pyruvate dehydrogenase (E1), dihydrolipoamide acetyltransferase (E2) and lipoamide dehydrogenase (E3)
  • INTERACTION
    DNA
    RNA
    small molecule metal binding,
  • biotin
  • lipoate CoA
  • binds 2 lipoyl cofactors covalently
  • protein
  • binding HLA-A*0201
  • STAT5A-mediated repression of mtDNA expression also positively correlated with STAT5A binding to DLAT, both a gate-keeping metabolic enzyme and a component of mtDNA nucleoid in mitochondrial matrix
  • cell & other
    REGULATION
    ASSOCIATED DISORDERS
    corresponding disease(s) DLATD
    related resource MITOP database
    Other morbid association(s)
    TypeGene ModificationChromosome rearrangementProtein expressionProtein Function
    constitutional     --over  
    in placentas from pregnancies with IUGR
    constitutional     --over  
    of DLAT was seen in the damaged small bile ducts (SBDs) in primary biliary cirrhosis (PBC) and the expression was significantly more frequent in PBC than in control livers
    Susceptibility
    Variant & Polymorphism
    Candidate gene
    Marker
    Therapy target
    ANIMAL & CELL MODELS