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Threonine aspartase 1 (TASP1)

Homo sapiens — UniProt Q9H6P5

Gene: TASP1Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Threonine aspartase 1 (TASP1) is a protein from Homo sapiens identified by UniProt accession Q9H6P5, 420 residues long. MolForge cross-references it against 0 known binders and 207 disease associations.

  • UniProt accession: Q9H6P5; gene symbol TASP1.
  • Organism: Homo sapiens.
  • Length: 420 amino acids.
  • Top disease associations (Open Targets): Suleiman-El-Hattab syndrome, Global developmental delay and protein measurement.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameThreonine aspartase 1
UniProt accessionQ9H6P5
GeneTASP1
OrganismHomo sapiens
Length420 residues
Molecular weight—
EC numbers—
Target class—
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 (207)

Diseases linked to this target (Open Targets).

  • Suleiman-El-Hattab syndrome · score 0.62
  • Global developmental delay · score 0.43
  • protein measurement · score 0.41
  • Neurodevelopmental disorder · score 0.37
  • FEV/FVC ratio · score 0.36
  • Abnormal facial shape · score 0.33
  • Happy demeanor · score 0.33
  • peak expiratory flow · score 0.31
  • developmental disability · score 0.27
  • multiple congenital anomalies/dysmorphic syndrome-intellectual disability · score 0.27

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9H6P5-F1alphafoldPREDICTED86.79—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9H6P5.

Amino-acid sequence (420 residues)

MTMEKGMSSG EGLPSRSSQV SAGKITAKEL ETKQSYKEKR GGFVLVHAGA GYHSESKAKE YKHVCKRACQ KAIEKLQAGA LATDAVTAAL VELEDSPFTN AGMGSNLNLL GEIECDASIM DGKSLNFGAV GALSGIKNPV SVANRLLCEG QKGKLSAGRI PPCFLVGEGA YRWAVDHGIP SCPPNIMTTR FSLAAFKRNK RKLELAERVD TDFMQLKKRR QSSEKENDSG TLDTVGAVVV DHEGNVAAAV SSGGLALKHP GRVGQAALYG CGCWAENTGA HNPYSTAVST SGCGEHLVRT ILARECSHAL QAEDAHQALL ETMQNKFISS PFLASEDGVL GGVIVLRSCR CSAEPDSSQN KQTLLVEFLW SHTTESMCVG YMSAQDGKAK THISRLPPGA VAGQSVAIEG GVCRLESPVN

Frequently asked questions

Answers are generated from the structured data on this page, not written by hand.

Which diseases are associated with TASP1?

The strongest Open Targets associations for TASP1 are Suleiman-El-Hattab syndrome, Global developmental delay, protein measurement, Neurodevelopmental disorder and FEV/FVC ratio.

How long is the TASP1 protein?

The Homo sapiens TASP1 protein (UniProt Q9H6P5) is 420 amino acids long.

Browse: Targets: T · all protein targets A–Z · drugs A–Z.

Sources

How this page is built: methodology · editorial policy & corrections.

For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.

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Quick facts

UniProtQ9H6P5
GeneTASP1
OrganismHomo sapiens
Length420
Binders0
Diseases207
View on UniProt