AGXT2
Alanine--glyoxylate aminotransferase 2, mitochondrial
Also known as: AGT2, AGT2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BYV1
- Gene
- AGXT2
- Ensembl
- ENSG00000113492
- Chromosome
- 5
- Canonical length
- 514 aa
- Protein class
- Enzymes, Metabolic proteins, Predicted intracellular proteins
- Quaternary structure
- Homotetramer
OverviewNCBI Gene
The protein encoded by this gene is a class III pyridoxal-phosphate-dependent mitochondrial aminotransferase. It catalyzes the conversion of glyoxylate to glycine using L-alanine as the amino donor. It is an important regulator of methylarginines and is involved in the control of blood pressure in kidney. Polymorphisms in this gene affect methylarginine and beta-aminoisobutyrate metabolism, and are associated with carotid atherosclerosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2015]
Canonical amino-acid sequenceUniProt
514 residues, UniProt reviewed canonical sequence.
>Q9BYV1|AGXT2
1 MTLIWRHLLR PLCLVTSAPR ILEMHPFLSL GTSRTSVTKL SLHTKPRMPP CDFMPERYQS
61 LGYNRVLEIH KEHLSPVVTA YFQKPLLLHQ GHMEWLFDAE GSRYLDFFSG IVTVSVGHCH
121 PKVNAVAQKQ LGRLWHTSTV FFHPPMHEYA EKLAALLPEP LKVIFLVNSG SEANELAMLM
181 ARAHSNNIDI ISFRGAYHGC SPYTLGLTNV GTYKMELPGG TGCQPTMCPD VFRGPWGGSH
241 CRDSPVQTIR KCSCAPDCCQ AKDQYIEQFK DTLSTSVAKS IAGFFAEPIQ GVNGVVQYPK
301 GFLKEAFELV RARGGVCIAD EVQTGFGRLG SHFWGFQTHD VLPDIVTMAK GIGNGFPMAA
361 VITTPEIAKS LAKCLQHFNT FGGNPMACAI GSAVLEVIKE ENLQENSQEV GTYMLLKFAK
421 LRDEFEIVGD VRGKGLMIGI EMVQDKISCR PLPREEVNQI HEDCKHMGLL VGRGSIFSQT
481 FRIAPSMCIT KPEVDFAVEV FRSALTQHME RRAKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against AGXT2 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.26
- Highest tissue expression
- 194 nTPM
Expression across tissuesHPA
Tissue
- kidney: 194 nTPM
- liver: 115 nTPM
- small intestine: 3.5 nTPM
- gallbladder: 0.7 nTPM
- duodenum: 0.3 nTPM
- parathyroid gland: 0.3 nTPM
Single-cell type
- proximal tubule cells: 417 nCPM
- hepatocytes: 133 nCPM
- epididymal efferent duct absorptive cells: 23 nCPM
- enterocytes: 16 nCPM
- breast hormone-responsive cells: 8.6 nCPM
- podocytes: 7 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- midbrain: 0.4 nTPM
- choroid plexus: 0.2 nTPM
- hypothalamus: 0.2 nTPM
- amygdala: 0.1 nTPM
- cerebral cortex: 0.1 nTPM
- thalamus: 0.1 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.69
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.66
- DepMap mean gene effect
- 0.09
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- glycine biosynthetic process, by transamination of glyoxylate
- glyoxylate catabolic process
- positive regulation of nitric oxide biosynthetic process
- L-alanine catabolic process, by transamination
- N(omega),N(omega)-dimethyl-L-arginine catabolic process
Molecular functions
- alanine-glyoxylate transaminase activity
- pyridoxal phosphate binding
- (R)-3-amino-2-methylpropionate-pyruvate transaminase activity
- beta-alanine:pyruvate transaminase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads AGXT2 as an antibody target. Whether an autoantibody or antibody against AGXT2 could matter depends on whether native AGXT2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
AGXT2 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label AGXT2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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