ENSGALG00000016697


Gallus gallus

Features
Gene ID: ENSGALG00000016697
  
Biological name :MUT
  
Synonyms : methylmalonyl-CoA mutase / MUT
  
Possible biological names infered from orthology : Methylmalonyl-CoA mutase, mitochondrial / P16332 / P22033
  
Species: Gallus gallus
  
Chr. number: 3
Strand: 1
Band:
Gene start: 109275576
Gene end: 109293110
  
Corresponding Affymetrix probe sets: GgaAffx.10684.1.S1_at (Chicken Array)   GgaAffx.10684.2.S1_at (Chicken Array)   
  
Cross references: Ensembl peptide - ENSGALP00000026895
NCBI entrez gene - 422049     See in Manteia.
RefSeq - XM_004935917
RefSeq - XM_420055
RefSeq - XM_004935918
RefSeq - XM_004935919
swissprot - E1BY22
Ensembl - ENSGALG00000016697
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 mutENSDARG00000060554Danio rerio
 MUTENSG00000146085Homo sapiens
 MutENSMUSG00000023921Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
No match


Protein motifs (from Interpro)
Interpro ID Name
 IPR006098  Methylmalonyl-CoA mutase, alpha chain, catalytic
 IPR006099  Methylmalonyl-CoA mutase, alpha/beta chain, catalytic
 IPR006158  Cobalamin (vitamin B12)-binding domain
 IPR006159  Methylmalonyl-CoA mutase, C-terminal
 IPR016176  Cobalamin (vitamin B12)-dependent enzyme, catalytic


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0008152 metabolic process IEA
 biological_processGO:0009791 post-embryonic development IEA
 biological_processGO:0043547 positive regulation of GTPase activity IEA
 biological_processGO:0050667 homocysteine metabolic process IEA
 cellular_componentGO:0005739 mitochondrion IEA
 molecular_functionGO:0003824 catalytic activity IEA
 molecular_functionGO:0003924 GTPase activity IEA
 molecular_functionGO:0004494 methylmalonyl-CoA mutase activity IEA
 molecular_functionGO:0016853 isomerase activity IEA
 molecular_functionGO:0016866 intramolecular transferase activity IEA
 molecular_functionGO:0031419 cobalamin binding IEA
 molecular_functionGO:0042802 identical protein binding IEA
 molecular_functionGO:0042803 protein homodimerization activity IEA
 molecular_functionGO:0046872 metal ion binding IEA
 molecular_functionGO:0072341 modified amino acid binding IEA


Pathways (from Reactome)
Pathway description
Cobalamin (Cbl, vitamin B12) transport and metabolism
Propionyl-CoA catabolism


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
No match
  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSGALG00000009974 MMAA / methylmalonic aciduria (cobalamin deficiency) cblA type / Q8C7H1* / Q8IVH4* / Methylmalonic aciduria type A homolog, mitochondrial *  / complex
 ENSGALG00000016697 MUT / methylmalonyl-CoA mutase / P16332* / P22033* / Methylmalonyl-CoA mutase, mitochondrial *  / complex






 

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