Aprataxin (APTX)

Homo sapiens — UniProt Q7Z2E3

Gene: APTXHomo sapiensSwissProt reviewed

About Aprataxin

Aprataxin (APTX) is a protein from Homo sapiens identified by UniProt accession Q7Z2E3, 356 residues long. MolForge cross-references it against 0 known binders and 103 disease associations.

Target properties

Protein nameAprataxin
UniProt accessionQ7Z2E3
GeneAPTX
OrganismHomo sapiens
Length356 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 (103)

Diseases linked to this target (Open Targets).

  • ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia · score 0.82
  • Ataxia - oculomotor apraxia type 1 · score 0.79
  • genetic disorder · score 0.47
  • Dystonia · score 0.46
  • epilepsy · score 0.34
  • reticulocyte count · score 0.22
  • PHF-tau measurement · score 0.20
  • spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2 · score 0.18
  • reticulocyte measurement · score 0.17
  • age at menopause · score 0.14

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q7Z2E3-F1alphafoldPREDICTED80.76—

Amino-acid sequence (356 residues)

MSNVNLSVSD FWRVMMRVCW LVRQDSRHQR IRLPHLEAVV IGRGPETKIT DKKCSRQQVQ LKAECNKGYV KVKQVGVNPT SIDSVVIGKD QEVKLQPGQV LHMVNELYPY IVEFEEEAKN PGLETHRKRK RSGNSDSIER DAAQEAEAGT GLEPGSNSGQ CSVPLKKGKD APIKKESLGH WSQGLKISMQ DPKMQVYKDE QVVVIKDKYP KARYHWLVLP WTSISSLKAV AREHLELLKH MHTVGEKVIV DFAGSSKLRF RLGYHAIPSM SHVHLHVISQ DFDSPCLKNK KHWNSFNTEY FLESQAVIEM VQEAGRVTVR DGMPELLKLP LRCHECQQLL PSIPQLKEHL RKHWTQ

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Quick facts

UniProtQ7Z2E3
GeneAPTX
OrganismHomo sapiens
Length356
Binders0
Diseases103
View on UniProt