Skip to content

AP-4 complex subunit beta-1 (AP4B1)

Homo sapiens — UniProt Q9Y6B7

Gene: AP4B1Homo sapiensSwissProt reviewed

Data last refreshed: (UniProt release unknown)

Key facts

AP-4 complex subunit beta-1 (AP4B1) is a protein from Homo sapiens identified by UniProt accession Q9Y6B7, 739 residues long. MolForge cross-references it against 0 known binders and 47 disease associations.

  • UniProt accession: Q9Y6B7; gene symbol AP4B1.
  • Organism: Homo sapiens.
  • Length: 739 amino acids.
  • Top disease associations (Open Targets): Severe intellectual disability and progressive spastic paraplegia, Spastic paraplegia and genetic disorder.
  • 3D structure: AlphaFold model available.

Target properties

Protein nameAP-4 complex subunit beta-1
UniProt accessionQ9Y6B7
GeneAP4B1
OrganismHomo sapiens
Length739 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 (47)

Diseases linked to this target (Open Targets).

  • Severe intellectual disability and progressive spastic paraplegia · score 0.79
  • Spastic paraplegia · score 0.71
  • genetic disorder · score 0.52
  • AP-4 deficiency syndrome · score 0.37
  • hereditary spastic paraplegia · score 0.34
  • Abnormality of the nervous system · score 0.34
  • Abnormal brain morphology · score 0.33
  • breast carcinoma · score 0.21
  • Hoyeraal-Hreidarsson syndrome · score 0.17
  • systemic lupus erythematosus · score 0.15

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q9Y6B7-F1alphafoldPREDICTED86.27—

Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9Y6B7.

Amino-acid sequence (739 residues)

MPYLGSEDVV KELKKALCNP HIQADRLRYR NVIQRVIRYM TQGLDMSGVF MEMVKASATV DIVQKKLVYL YMCTYAPLKP DLALLAINTL CKDCSDPNPM VRGLALRSMC SLRMPGVQEY IQQPILNGLR DKASYVRRVA VLGCAKMHNL HGDSEVDGAL VNELYSLLRD QDPIVVVNCL RSLEEILKQE GGVVINKPIA HHLLNRMSKL DQWGQAEVLN FLLRYQPRSE EELFDILNLL DSFLKSSSPG VVMGATKLFL ILAKMFPHVQ TDVLVRVKGP LLAACSSESR ELCFVALCHV RQILHSLPGH FSSHYKKFFC SYSEPHYIKL QKVEVLCELV NDENVQQVLE ELRGYCTDVS ADFAQAAIFA IGGIARTYTD QCVQILTELL GLRQEHITTV VVQTFRDLVW LCPQCTEAVC QALPGCEENI QDSEGKQALI WLLGVHGERI PNAPYVLEDF VENVKSETFP AVKMELLTAL LRLFLSRPAE CQDMLGRLLY YCIEEEKDMA VRDRGLFYYR LLLVGIDEVK RILCSPKSDP TLGLLEDPAE RPVNSWASDF NTLVPVYGKA HWATISKCQG AERCDPELPK TSSFAASGPL IPEENKERVQ ELPDSGALML VPNRQLTADY FEKTWLSLKV AHQQVLPWRG EFHPDTLQMA LQVVNIQTIA MSRAGSRPWK AYLSAQDDTG CLFLTELLLE PGNSEMQISV KQNEARTETL NSFISVLETV IGTIEEIKS

Frequently asked questions

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

Which diseases are associated with AP4B1?

The strongest Open Targets associations for AP4B1 are Severe intellectual disability and progressive spastic paraplegia, Spastic paraplegia, genetic disorder, AP-4 deficiency syndrome and hereditary spastic paraplegia.

How long is the AP4B1 protein?

The Homo sapiens AP4B1 protein (UniProt Q9Y6B7) is 739 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.

Explore AP-4 complex subunit beta-1 with MolForge

Find binders, run structure-based screening, and map this target across diseases and approved drugs with our AI-powered platform.

Browse all targets

Quick facts

UniProtQ9Y6B7
GeneAP4B1
OrganismHomo sapiens
Length739
Binders0
Diseases47
View on UniProt