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Complex I assembly factor ACAD9, mitochondrial (ACAD9)

Homo sapiens — UniProt Q9H845

Gene: ACAD9Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Complex I assembly factor ACAD9, mitochondrial (ACAD9) is a protein from Homo sapiens identified by UniProt accession Q9H845, 621 residues long. MolForge cross-references it against 0 known binders and 58 disease associations.

  • UniProt accession: Q9H845; gene symbol ACAD9.
  • Organism: Homo sapiens.
  • Length: 621 amino acids.
  • Top disease associations (Open Targets): acyl-CoA dehydrogenase 9 deficiency, mitochondrial complex I deficiency and neurodegenerative disease.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameComplex I assembly factor ACAD9, mitochondrial
UniProt accessionQ9H845
GeneACAD9
OrganismHomo sapiens
Length621 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 (58)

Diseases linked to this target (Open Targets).

  • acyl-CoA dehydrogenase 9 deficiency · score 0.85
  • mitochondrial complex I deficiency · score 0.65
  • neurodegenerative disease · score 0.52
  • hypophosphatasia · score 0.27
  • lysosomal storage disease · score 0.22
  • genetic disorder · score 0.19
  • myeloid white cell count · score 0.19
  • leukocyte count · score 0.12
  • BMI-adjusted hip circumference · score 0.08
  • self reported educational attainment · score 0.07

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9H845-F1alphafoldPREDICTED91.85—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9H845.

Amino-acid sequence (621 residues)

MSGCGLFLRT TAAARACRGL VVSTANRRLL RTSPPVRAFA KELFLGKIKK KEVFPFPEVS QDELNEINQF LGPVEKFFTE EVDSRKIDQE GKIPDETLEK LKSLGLFGLQ VPEEYGGLGF SNTMYSRLGE IISMDGSITV TLAAHQAIGL KGIILAGTEE QKAKYLPKLA SGEHIAAFCL TEPASGSDAA SIRSRATLSE DKKHYILNGS KVWITNGGLA NIFTVFAKTE VVDSDGSVKD KITAFIVERD FGGVTNGKPE DKLGIRGSNT CEVHFENTKI PVENILGEVG DGFKVAMNIL NSGRFSMGSV VAGLLKRLIE MTAEYACTRK QFNKRLSEFG LIQEKFALMA QKAYVMESMT YLTAGMLDQP GFPDCSIEAA MVKVFSSEAA WQCVSEALQI LGGLGYTRDY PYERILRDTR ILLIFEGTNE ILRMYIALTG LQHAGRILTT RIHELKQAKV STVMDTVGRR LRDSLGRTVD LGLTGNHGVV HPSLADSANK FEENTYCFGR TVETLLLRFG KTIMEEQLVL KRVANILINL YGMTAVLSRA SRSIRIGLRN HDHEVLLANT FCVEAYLQNL FSLSQLDKYA PENLDEQIKK VSQQILEKRA YICAHPLDRT C

Frequently asked questions

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

Which diseases are associated with ACAD9?

The strongest Open Targets associations for ACAD9 are acyl-CoA dehydrogenase 9 deficiency, mitochondrial complex I deficiency, neurodegenerative disease, hypophosphatasia and lysosomal storage disease.

How long is the ACAD9 protein?

The Homo sapiens ACAD9 protein (UniProt Q9H845) is 621 amino acids long.

Browse: Targets: A · 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

UniProtQ9H845
GeneACAD9
OrganismHomo sapiens
Length621
Binders0
Diseases58
View on UniProt