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PR domain zinc finger protein 5 (PRDM5)

Homo sapiens — UniProt Q9NQX1

Gene: PRDM5Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

PR domain zinc finger protein 5 (PRDM5) is a protein from Homo sapiens identified by UniProt accession Q9NQX1, 630 residues long. MolForge cross-references it against 0 known binders and 115 disease associations.

  • UniProt accession: Q9NQX1; gene symbol PRDM5.
  • Organism: Homo sapiens.
  • Length: 630 amino acids.
  • Top disease associations (Open Targets): brittle cornea syndrome, Abnormality of the cardiovascular system and Ehlers-Danlos syndrome.
  • 3D structure: AlphaFold model available.

Target properties

Protein namePR domain zinc finger protein 5
UniProt accessionQ9NQX1
GenePRDM5
OrganismHomo sapiens
Length630 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 (115)

Diseases linked to this target (Open Targets).

  • brittle cornea syndrome · score 0.74
  • Abnormality of the cardiovascular system · score 0.47
  • Ehlers-Danlos syndrome · score 0.41
  • Connective tissue disease with eye involvement · score 0.37
  • cortical thickness · score 0.35
  • cortical surface area measurement · score 0.35
  • IGF-1 measurement · score 0.33
  • type 2 diabetes mellitus · score 0.31
  • insulin like growth factor measurement · score 0.29
  • osteoarthritis · score 0.28

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9NQX1-F1alphafoldPREDICTED72.24—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9NQX1.

Amino-acid sequence (630 residues)

MLGMYVPDRF SLKSSRVQDG MGLYTARRVR KGEKFGPFAG EKRMPEDLDE NMDYRLMWEV RGSKGEVLYI LDATNPRHSN WLRFVHEAPS QEQKNLAAIQ EGENIFYLAV EDIETDTELL IGYLDSDMEA EEEEQQIMTV IKEGEVENSR RQSTAGRKDR LGCKEDYACP QCESSFTSED ILAEHLQTLH QKPTEEKEFK CKNCGKKFPV KQALQRHVLQ CTAKSSLKES SRSFQCSVCN SSFSSASSFE QHQETCRGDA RFVCKADSCG KRLKSKDALK RHQENVHTGD PKKKLICSVC NKKCSSASSL QEHRKIHEIF DCQECMKKFI SANQLKRHMI THSEKRPYNC EICNKSFKRL DQVGAHKVIH SEDKPYKCKL CGKGFAHRNV YKNHKKTHSE ERPFQCEECK ALFRTPFSLQ RHLLIHNSER TFKCHHCDAT FKRKDTLNVH VQVVHERHKK YRCELCNKAF VTPSVLRSHK KTHTGEKEKI CPYCGQKFAS SGTLRVHIRS HTGERPYQCP YCEKGFSKND GLKMHIRTHT REKPYKCSEC SKAFSQKRGL DEHKRTHTGE KPFQCDVCDL AFSLKKMLIR HKMTHNPNRP LAECQFCHKK FTRNDYLKVH MDNIHGVADS

Frequently asked questions

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

Which diseases are associated with PRDM5?

The strongest Open Targets associations for PRDM5 are brittle cornea syndrome, Abnormality of the cardiovascular system, Ehlers-Danlos syndrome, Connective tissue disease with eye involvement and cortical thickness.

How long is the PRDM5 protein?

The Homo sapiens PRDM5 protein (UniProt Q9NQX1) is 630 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

UniProtQ9NQX1
GenePRDM5
OrganismHomo sapiens
Length630
Binders0
Diseases115
View on UniProt