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Protein Ontology report - methylmalonic aciduria type A protein, mitochondrial (human)
PR:Q8IVH4 - http://purl.obolibrary.org/obo/PR_Q8IVH4
 
  Protein Forms      
Ontology Information Show OBO stanza / GPI
  PRO ID
PR:Q8IVH4   
  PRO namemethylmalonic aciduria type A protein, mitochondrial (human) 
  Synonyms
PRO-Short-label: EXACT:hMMAA
Gene-based: RELATED:MMAA
  Definition"A methylmalonic aciduria type A, mitochondrial that is encoded in the genome of human." [PRO:DNx, UniProtKB:Q8IVH4] 
  PRO Categoryorganism-gene 
  ParentPR:000010912 methylmalonic aciduria type A, mitochondrial
PR:000029067 Homo sapiens protein
  Gene TemplateHGNC:18871 MMAA (human)
  TaxonNCBITaxon:9606 Homo sapiens
  Terms by PRO Category
Organism-Independent Organism-Specific
         Category          Number of Terms          Category          Number of Terms
         Gene0                                                  Organism-Gene 1                                        
         Sequence0                                                  Organism-Sequence 0                                        
         Modification0                                                  Organism-Modification 2                                        
  Term Hierarchy
  Visualization
DAG: OLS:
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Related Cross References

  Db identifiers
UniProtKB:Q8IVH4
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Protein Forms Switch to Compact View   

Category  
PRO ID
Name
Short Name
Definition
Ann. Has Annotation?

Comp. In Complex?
organism-gene


PR:Q8IVH4
methylmalonic aciduria type A protein, mitochondrial (human)
hMMAA
"A methylmalonic aciduria type A, mitochondrial that is encoded in the genome of human." [PRO:DNx, UniProtKB:Q8IVH4]

organism-modification


PR:000048389
methylmalonic aciduria type A protein, mitochondrial, transit peptide removed form (human)
hMMAA/TransPep-
"A methylmalonic aciduria type A protein, mitochondrial (human) that has had the transit peptide removed. UniProtKB:Q8IVH4, 66-418." [PRO:DNx, Reactome:R-HSA-2980907]

organism-modification


PR:000061613
methylmalonic aciduria type A protein, mitochondrial sequence variant Y207C, transit peptide removed form (human)
hMMAA/var:Y207C/TransPep-
"A methylmalonic aciduria type A protein, mitochondrial (human) that has a Cys residue at the position equivalent to Tyr-207 of the amino acid sequence represented by UniProtKB:Q8IVH4 and that has had the transit peptide removed. UniProtKB:Q8IVH4, 66-418, Tyr-207, CHEBI:29950." [PRO:DNx, Reactome:R-HSA-3322133]