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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 name
aminomethyltransferase, 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 Category
organism-gene
Parent
PR:000004005
PR:000029067
Gene Template
HGNC:473
AMT (human)
Taxon
NCBITaxon:9606
Homo sapiens
Terms by PRO Category
Organism-Independent
Organism-Specific
Category
Number of Terms
Category
Number of Terms
Gene
0
Organism-Gene
1
Sequence
0
Organism-Sequence
4
Modification
0
Organism-Modification
1
Term Hierarchy
Visualization
DAG:
OLS:
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Related Cross References
Db identifiers
UniProtKB:P48728
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Protein Forms
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Extended View
Category
PRO Form Name
Ann.
Has Annotation?
Comp.
In Complex?
organism-gene
PR:P48728
aminomethyltransferase, mitochondrial (human), hAMT
organism-sequence
PR:P48728-1
aminomethyltransferase, mitochondrial isoform 1 (human), hAMT/iso:1
organism-sequence
PR:P48728-2
aminomethyltransferase, mitochondrial isoform h2 (human), hAMT/iso:h2
organism-sequence
PR:P48728-3
aminomethyltransferase, mitochondrial isoform h3 (human), hAMT/iso:h3
organism-sequence
PR:P48728-4
aminomethyltransferase, mitochondrial isoform h4 (human), hAMT/iso:h4
organism-modification
PR:000063470
aminomethyltransferase, mitochondrial, transit peptide removed form (human), hAMT/TransPep-