Alanine--glyoxylate aminotransferase (AGXT)

Homo sapiens — UniProt P21549

Gene: AGXTHomo sapiensSwissProt reviewed

About Alanine--glyoxylate aminotransferase

Alanine--glyoxylate aminotransferase (AGXT) is a protein from Homo sapiens identified by UniProt accession P21549, 392 residues long. MolForge cross-references it against 0 known binders and 365 disease associations.

Target properties

Protein nameAlanine--glyoxylate aminotransferase
UniProt accessionP21549
GeneAGXT
OrganismHomo sapiens
Length392 residues
Molecular weight—
EC numbers—
Target classUNCLASSIFIED
Subcellular location—
Keywords—

Druggability

Target tractability assessment (Open Targets + pocket analysis). No approved drug

Druggability tierMEDIUM
Druggability score—
Pocket score—
Max clinical phase—

Disease associations (365)

Diseases linked to this target (Open Targets).

  • primary hyperoxaluria type 1 · score 0.87
  • primary hyperoxaluria · score 0.68
  • alanine glyoxylate aminotransferase deficiency · score 0.45
  • nephrolithiasis · score 0.39
  • nephrocalcinosis · score 0.37
  • nephrotic syndrome · score 0.34
  • cardiac arrhythmia · score 0.27
  • Abnormality of metabolism/homeostasis · score 0.27
  • genetic disorder · score 0.19
  • body height · score 0.15

3D Structure (1)

Experimental (PDB) and predicted (AlphaFold) structures for this protein.

StructureSourceMethodMean pLDDTResolution (Å)
AF-P21549-F1alphafoldPREDICTED98.28—

Amino-acid sequence (392 residues)

MASHKLLVTP PKALLKPLSI PNQLLLGPGP SNLPPRIMAA GGLQMIGSMS KDMYQIMDEI KEGIQYVFQT RNPLTLVISG SGHCALEAAL VNVLEPGDSF LVGANGIWGQ RAVDIGERIG ARVHPMTKDP GGHYTLQEVE EGLAQHKPVL LFLTHGESST GVLQPLDGFG ELCHRYKCLL LVDSVASLGG TPLYMDRQGI DILYSGSQKA LNAPPGTSLI SFSDKAKKKM YSRKTKPFSF YLDIKWLANF WGCDDQPRMY HHTIPVISLY SLRESLALIA EQGLENSWRQ HREAAAYLHG RLQALGLQLF VKDPALRLPT VTTVAVPAGY DWRDIVSYVI DHFDIEIMGG LGPSTGKVLR IGLLGCNATR ENVDRVTEAL RAALQHCPKK KL

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Quick facts

UniProtP21549
GeneAGXT
OrganismHomo sapiens
Length392
Binders0
Diseases365
View on UniProt