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Mitochondrial import inner membrane translocase subunit TIM16 (PAM16)

Homo sapiens — UniProt Q9Y3D7

Gene: PAM16Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Mitochondrial import inner membrane translocase subunit TIM16 (PAM16) is a protein from Homo sapiens identified by UniProt accession Q9Y3D7, 125 residues long. MolForge cross-references it against 0 known binders and 51 disease associations.

  • UniProt accession: Q9Y3D7; gene symbol PAM16.
  • Organism: Homo sapiens.
  • Length: 125 amino acids.
  • Top disease associations (Open Targets): Autosomal recessive spondylometaphyseal dysplasia, Mégarbané type, autosomal recessive spondylometaphyseal dysplasia, Megarbane type and nephronophthisis.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameMitochondrial import inner membrane translocase subunit TIM16
UniProt accessionQ9Y3D7
GenePAM16
OrganismHomo sapiens
Length125 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 (51)

Diseases linked to this target (Open Targets).

  • Autosomal recessive spondylometaphyseal dysplasia, Mégarbané type · score 0.55
  • autosomal recessive spondylometaphyseal dysplasia, Megarbane type · score 0.53
  • nephronophthisis · score 0.49
  • neurodegenerative disease · score 0.32
  • lysosomal storage disease · score 0.32
  • multiple sclerosis · score 0.32
  • Alzheimer disease · score 0.32
  • Parkinson disease · score 0.32
  • acute megakaryoblastic leukaemia · score 0.11
  • mediastinal germ cell tumor · score 0.11

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9Y3D7-F1alphafoldPREDICTED89.27—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9Y3D7.

Amino-acid sequence (125 residues)

MAKYLAQIIV MGVQVVGRAF ARALRQEFAA SRAAADARGR AGHRSAAASN LSGLSLQEAQ QILNVSKLSP EEVQKNYEHL FKVNDKSVGG SFYLQSKVVR AKERLDEELK IQAQEDREKG QMPHT

Frequently asked questions

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

Which diseases are associated with PAM16?

The strongest Open Targets associations for PAM16 are Autosomal recessive spondylometaphyseal dysplasia, Mégarbané type, autosomal recessive spondylometaphyseal dysplasia, Megarbane type, nephronophthisis, neurodegenerative disease and lysosomal storage disease.

How long is the PAM16 protein?

The Homo sapiens PAM16 protein (UniProt Q9Y3D7) is 125 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

UniProtQ9Y3D7
GenePAM16
OrganismHomo sapiens
Length125
Binders0
Diseases51
View on UniProt