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KICSTOR complex protein kaptin (KPTN)

Homo sapiens — UniProt Q9Y664

Gene: KPTNHomo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

KICSTOR complex protein kaptin (KPTN) is a protein from Homo sapiens identified by UniProt accession Q9Y664, 436 residues long. MolForge cross-references it against 0 known binders and 58 disease associations.

  • UniProt accession: Q9Y664; gene symbol KPTN.
  • Organism: Homo sapiens.
  • Length: 436 amino acids.
  • Top disease associations (Open Targets): macrocephaly-developmental delay syndrome, genetic disorder and Intellectual disability.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameKICSTOR complex protein kaptin
UniProt accessionQ9Y664
GeneKPTN
OrganismHomo sapiens
Length436 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).

  • macrocephaly-developmental delay syndrome · score 0.77
  • genetic disorder · score 0.47
  • Intellectual disability · score 0.27
  • craniosynostosis · score 0.18
  • Immunodeficiency due to a late component of complements deficiency · score 0.07
  • mannose-binding lectin deficiency · score 0.06
  • sex hormone-binding globulin measurement · score 0.05
  • recurrent Neisseria infections due to factor D deficiency · score 0.05
  • immunodeficiency 28 · score 0.05
  • immunodeficiency 31B · score 0.05

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9Y664-F1alphafoldPREDICTED88.85—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9Y664.

Amino-acid sequence (436 residues)

MMGEAAVAAG PCPLREDSFT RFSSQSNVYG LAGGAGGRGE LLAATLKGKV LGFRYQDLRQ KIRPVAKELQ FNYIPVDAEI VSIDTFNKSP PKRGLVVGIT FIKDSGDKGS PFLNIYCDYE PGSEYNLDSI AQSCLNLELQ FTPFQLCHAE VQVGDQLETV FLLSGNDPAI HLYKENEGLH QFEEQPVENL FPELTNLTSS VLWLDVHNFP GTSRRLSALG CQSGYVRVAH VDQRSREVLQ MWSVLQDGPI SRVIVFSLSA AKETKDRPLQ DEYSVLVASM LEPAVVYRDL LNRGLEDQLL LPGSDQFDSV LCSLVTDVDL DGRPEVLVAT YGQELLCYKY RGPESGLPEA QHGFHLLWQR SFSSPLLAMA HVDLTGDGLQ ELAVVSLKGV HILQHSLIQA SELVLTRLRH QVEQRRRRLQ GLEDGAGAGP AENAAS

Frequently asked questions

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

Which diseases are associated with KPTN?

The strongest Open Targets associations for KPTN are macrocephaly-developmental delay syndrome, genetic disorder, Intellectual disability, craniosynostosis and Immunodeficiency due to a late component of complements deficiency.

How long is the KPTN protein?

The Homo sapiens KPTN protein (UniProt Q9Y664) is 436 amino acids long.

Browse: Targets: K · 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

UniProtQ9Y664
GeneKPTN
OrganismHomo sapiens
Length436
Binders0
Diseases58
View on UniProt