back to PRO homepage
  Home |   Linked Open Data |   Browse |  
Search

|   Statistics |   Download
 RACE-PRO
 PRO tracker
 Community
 PRO Consortium
 Publications
 Documentation

Protein Ontology report - aminomethyltransferase, mitochondrial (human)
PR:P48728 - http://purl.obolibrary.org/obo/PR_P48728
 
  Protein Forms      
Ontology Information Show OBO stanza / GPI
  PRO ID
PR:P48728   
  PRO nameaminomethyltransferase, mitochondrial (human) 
  Synonyms
PRO-Short-label: EXACT:hAMT
Gene-based: RELATED:AMT | GCST
Other: EXACT:GCVT (human) | glycine cleavage system T protein (human)
  Definition"An aminomethyltransferase, mitochondrial that is encoded in the genome of human." [PRO:DNx, UniProtKB:P48728
  PRO Categoryorganism-gene 
  ParentPR:000004005 aminomethyltransferase, mitochondrial
PR:000029067 Homo sapiens protein
  Gene TemplateHGNC:473 AMT (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 4                                        
         Modification0                                                  Organism-Modification 1                                        
  Term Hierarchy
  Visualization
DAG: OLS:
Back to top
Related Cross References

  Db identifiers
UniProtKB:P48728
Back to top
Protein Forms Switch to Compact View   

Category  

PRO ID

Name

Short Name

Definition

Ann. Has Annotation?

Comp. In Complex?
organism-gene



PR:P48728

aminomethyltransferase, mitochondrial (human)

hAMT


"An aminomethyltransferase, mitochondrial that is encoded in the genome of human." [PRO:DNx, UniProtKB:P48728]


organism-sequence



PR:P48728-1

aminomethyltransferase, mitochondrial isoform 1 (human)

hAMT/iso:1


"An aminomethyltransferase, mitochondrial isoform 1 that is encoded in the genome of human." [PRO:DNx]


organism-sequence



PR:P48728-2

aminomethyltransferase, mitochondrial isoform h2 (human)

hAMT/iso:h2


"An aminomethyltransferase, mitochondrial (human) that is a translation product of some mRNA whose exon structure and start site selection renders it capable of giving rise to a protein with the amino acid sequence represented by UniProtKB:P48728-2." [PRO:DNx, UniProtKB:P48728]


organism-sequence



PR:P48728-3

aminomethyltransferase, mitochondrial isoform h3 (human)

hAMT/iso:h3


"An aminomethyltransferase, mitochondrial (human) that is a translation product of some mRNA whose exon structure and start site selection renders it capable of giving rise to a protein with the amino acid sequence represented by UniProtKB:P48728-3." [PRO:DNx, UniProtKB:P48728]


organism-sequence



PR:P48728-4

aminomethyltransferase, mitochondrial isoform h4 (human)

hAMT/iso:h4


"An aminomethyltransferase, mitochondrial (human) that is a translation product of some mRNA whose exon structure and start site selection renders it capable of giving rise to a protein with the amino acid sequence represented by UniProtKB:P48728-4." [PRO:DNx, UniProtKB:P48728]


organism-modification



PR:000063470

aminomethyltransferase, mitochondrial, transit peptide removed form (human)

hAMT/TransPep-


"An aminomethyltransferase, mitochondrial (human) that has had the transit peptide removed. Example: UniProtKB:P48728-1, 29-403." [PRO:DNx, Reactome:R-HSA-5693981]