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Pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial (PDPR)

Homo sapiens — UniProt Q8NCN5

Gene: PDPRHomo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

Pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial (PDPR) is a protein from Homo sapiens identified by UniProt accession Q8NCN5, 879 residues long. MolForge cross-references it against 0 known binders and 34 disease associations.

  • UniProt accession: Q8NCN5; gene symbol PDPR.
  • Organism: Homo sapiens.
  • Length: 879 amino acids.
  • Top disease associations (Open Targets): Parkinson disease, lysosomal storage disease and Alzheimer disease.
  • 3D structure: AlphaFold model available.

Target properties

Protein namePyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial
UniProt accessionQ8NCN5
GenePDPR
OrganismHomo sapiens
Length879 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 (34)

Diseases linked to this target (Open Targets).

  • Parkinson disease · score 0.22
  • lysosomal storage disease · score 0.22
  • Alzheimer disease · score 0.22
  • multiple sclerosis · score 0.22
  • neurodegenerative disease · score 0.22
  • haptoglobin measurement · score 0.21
  • lymphocyte count · score 0.14
  • protein measurement · score 0.08
  • amino acid measurement · score 0.08
  • blood metabolite measurement · score 0.08

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q8NCN5-F1alphafoldPREDICTED90.79—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q8NCN5.

Amino-acid sequence (879 residues)

MMFYRLLSIV GRQRASPGWQ NWSSARNSTS AAEARSMALP TQAQVVICGG GITGTSVAYH LSKMGWKDIV LLEQGRLAAG STRFCAGILS TARHLTIEQK MADYSNKLYY QLEQETGIQT GYTRTGSIFL AQTQDRLISL KRINAGLNVI GIPSEIISPK KVAELHHLLN VHDLVGAMHV PEDAVVSSAD VALALASAAS QNGVQIYDRT SVLHVMVKKG QVTGVETDKG QIECQYFVNC AGQWAYELGL SNEEPVSIPL HACEHFYLLT RPLETPLQSS TPTIVDADGR IYIRNWQGGI LSGGFEKNPK PIFTEGKNQL EIQNLQEDWD HFEPLLSSLL RRMPELETLE IMKLVNCPET FTPDMRCIMG ESPAVQGYFV LAGMNSAGLS FGGGAGKYLA EWMVHGYPSE NVWELDLKRF GALQSSRTFL RHRVMEVMPL MYDLKVPRWD FQTGRQLRTS PLYDRLDAQG ARWMEKHGFE RPKYFVPPDK DLLALEQSKT FYKPDWFDIV ESEVKCCKEA VCVIDMSSFT KFEITSTGDQ ALEVLQYLFS NDLDVPVGHI VHTGMLNEGG GYENDCSIAR LNKRSFFMIS PTDQQVHCWA WLKKHMPKDS NLLLEDVTWK YTALNLIGPR AVDVLSELSY APMTPDHFPS LFCKEMSVGY ANGIRVMSMT HTGEPGFMLY IPIEYALHVY NEVMSVGQKY GIRNAGYYAL RSLRIEKFFA FWGQDINNLT TPLECGRESR VKLEKGMDFI GRDALLQQKQ NGVYKRLTMF ILDDHDSDLD LWPWWGEPIY RNGQYVGKTT SSAYSYSLER HVCLGFVHNF SEDTGEEQVV TADFINRGEY EIDIAGYRFQ AKAKLYPVAS LFTQKRRKDD MELSDLHGK

Frequently asked questions

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

Which diseases are associated with PDPR?

The strongest Open Targets associations for PDPR are Parkinson disease, lysosomal storage disease, Alzheimer disease, multiple sclerosis and neurodegenerative disease.

How long is the PDPR protein?

The Homo sapiens PDPR protein (UniProt Q8NCN5) is 879 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

UniProtQ8NCN5
GenePDPR
OrganismHomo sapiens
Length879
Binders0
Diseases34
View on UniProt