Dysbindin (DTNBP1)

Homo sapiens — UniProt Q96EV8

Gene: DTNBP1Homo sapiensSwissProt reviewed

About Dysbindin

Dysbindin (DTNBP1) is a protein from Homo sapiens identified by UniProt accession Q96EV8, 351 residues long. MolForge cross-references it against 0 known binders and 199 disease associations.

Target properties

Protein nameDysbindin
UniProt accessionQ96EV8
GeneDTNBP1
OrganismHomo sapiens
Length351 residues
Molecular weight—
EC numbers—
Target classUNCLASSIFIED
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 (199)

Diseases linked to this target (Open Targets).

  • Hermansky-Pudlak syndrome 7 · score 0.68
  • Hermansky-Pudlak syndrome · score 0.57
  • Hermansky-Pudlak syndrome type 7 · score 0.48
  • alkaline phosphatase measurement · score 0.42
  • body height · score 0.24
  • appendicular lean mass · score 0.21
  • squamous cell carcinoma · score 0.19
  • genetic disorder · score 0.19
  • blood protein measurement · score 0.18
  • refractive error measurement · score 0.16

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-Q96EV8-F1alphafoldPREDICTED74.85—

Amino-acid sequence (351 residues)

MLETLRERLL SVQQDFTSGL KTLSDKSREA KVKSKPRTVP FLPKYSAGLE LLSRYEDTWA ALHRRAKDCA SAGELVDSEV VMLSAHWEKK KTSLVELQEQ LQQLPALIAD LESMTANLTH LEASFEEVEN NLLHLEDLCG QCELERCKHM QSQQLENYKK NKRKELETFK AELDAEHAQK VLEMEHTQQM KLKERQKFFE EAFQQDMEQY LSTGYLQIAE RREPIGSMSS MEVNVDMLEQ MDLMDISDQE ALDVFLNSGG EENTVLSPAL GPESSTCQNE ITLQVPNPSE LRAKPPSSSS TCTDSATRDI SEGGESPVVQ SDEEEVQVDT ALATSHTDRE ATPDGGEDSD S

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Quick facts

UniProtQ96EV8
GeneDTNBP1
OrganismHomo sapiens
Length351
Binders0
Diseases199
View on UniProt