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Peptidyl-tRNA hydrolase 2, mitochondrial (PTRH2)

Homo sapiens — UniProt Q9Y3E5

Gene: PTRH2Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Peptidyl-tRNA hydrolase 2, mitochondrial (PTRH2) is a protein from Homo sapiens identified by UniProt accession Q9Y3E5, 179 residues long. MolForge cross-references it against 0 known binders and 97 disease associations.

  • UniProt accession: Q9Y3E5; gene symbol PTRH2.
  • Organism: Homo sapiens.
  • Length: 179 amino acids.
  • Top disease associations (Open Targets): neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 1, neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset and intellectual disability, autosomal dominant 56.
  • 3D structure: AlphaFold model available.

Target properties

Protein namePeptidyl-tRNA hydrolase 2, mitochondrial
UniProt accessionQ9Y3E5
GenePTRH2
OrganismHomo sapiens
Length179 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 (97)

Diseases linked to this target (Open Targets).

  • neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 1 · score 0.69
  • neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset · score 0.54
  • intellectual disability, autosomal dominant 56 · score 0.27
  • Global developmental delay · score 0.26
  • Hearing impairment · score 0.26
  • cerebellar ataxia · score 0.26
  • breast adenocarcinoma · score 0.23
  • genetic disorder · score 0.18
  • leukocyte count · score 0.11
  • neoplasm · score 0.10

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9Y3E5-F1alphafoldPREDICTED83.85—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9Y3E5.

Amino-acid sequence (179 residues)

MPSKSLVMEY LAHPSTLGLA VGVACGMCLG WSLRVCFGML PKSKTSKTHT DTESEASILG DSGEYKMILV VRNDLKMGKG KVAAQCSHAA VSAYKQIQRR NPEMLKQWEY CGQPKVVVKA PDEETLIALL AHAKMLGLTV SLIQDAGRTQ IAPGSQTVLG IGPGPADLID KVTGHLKLY

Frequently asked questions

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

Which diseases are associated with PTRH2?

The strongest Open Targets associations for PTRH2 are neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 1, neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset, intellectual disability, autosomal dominant 56, Global developmental delay and Hearing impairment.

How long is the PTRH2 protein?

The Homo sapiens PTRH2 protein (UniProt Q9Y3E5) is 179 amino acids long.

Browse: Targets: P · 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

UniProtQ9Y3E5
GenePTRH2
OrganismHomo sapiens
Length179
Binders0
Diseases97
View on UniProt