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tRNA dimethylallyltransferase (TRIT1)

Homo sapiens — UniProt Q9H3H1

Gene: TRIT1Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

tRNA dimethylallyltransferase (TRIT1) is a protein from Homo sapiens identified by UniProt accession Q9H3H1, 467 residues long. MolForge cross-references it against 0 known binders and 73 disease associations.

  • UniProt accession: Q9H3H1; gene symbol TRIT1.
  • Organism: Homo sapiens.
  • Length: 467 amino acids.
  • Top disease associations (Open Targets): combined oxidative phosphorylation deficiency 35, neurodegenerative disease and genetic disorder.
  • 3D structure: AlphaFold model available.

Target properties

Protein nametRNA dimethylallyltransferase
UniProt accessionQ9H3H1
GeneTRIT1
OrganismHomo sapiens
Length467 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 (73)

Diseases linked to this target (Open Targets).

  • combined oxidative phosphorylation deficiency 35 · score 0.80
  • neurodegenerative disease · score 0.51
  • genetic disorder · score 0.50
  • mitochondrial disease · score 0.37
  • Epileptic encephalopathy · score 0.27
  • Macrocephaly · score 0.27
  • IGF-1 measurement · score 0.23
  • FEV/FVC ratio · score 0.22
  • balding measurement · score 0.19
  • leukocyte count · score 0.17

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9H3H1-F1alphafoldPREDICTED84.53—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9H3H1.

Amino-acid sequence (467 residues)

MASVAAARAV PVGSGLRGLQ RTLPLVVILG ATGTGKSTLA LQLGQRLGGE IVSADSMQVY EGLDIITNKV SAQEQRICRH HMISFVDPLV TNYTVVDFRN RATALIEDIF ARDKIPIVVG GTNYYIESLL WKVLVNTKPQ EMGTEKVIDR KVELEKEDGL VLHKRLSQVD PEMAAKLHPH DKRKVARSLQ VFEETGISHS EFLHRQHTEE GGGPLGGPLK FSNPCILWLH ADQAVLDERL DKRVDDMLAA GLLEELRDFH RRYNQKNVSE NSQDYQHGIF QSIGFKEFHE YLITEGKCTL ETSNQLLKKG IEALKQVTKR YARKQNRWVK NRFLSRPGPI VPPVYGLEVS DVSKWEESVL EPALEIVQSF IQGHKPTATP IKMPYNEAEN KRSYHLCDLC DRIIIGDREW AAHIKSKSHL NQLKKRRRLD SDAVNTIESQ SVSPDHNKEP KEKGSPGQND QELKCSV

Frequently asked questions

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

Which diseases are associated with TRIT1?

The strongest Open Targets associations for TRIT1 are combined oxidative phosphorylation deficiency 35, neurodegenerative disease, genetic disorder, mitochondrial disease and Epileptic encephalopathy.

How long is the TRIT1 protein?

The Homo sapiens TRIT1 protein (UniProt Q9H3H1) is 467 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

UniProtQ9H3H1
GeneTRIT1
OrganismHomo sapiens
Length467
Binders0
Diseases73
View on UniProt