Microtubule-associated protein tau (MAPT)

Homo sapiens — UniProt P10636

Gene: MAPTHomo sapiensSwissProt reviewed

About Microtubule-associated protein tau

Microtubule-associated protein tau (MAPT) is a protein from Homo sapiens identified by UniProt accession P10636, 758 residues long. MolForge cross-references it against 0 known binders and 1,052 disease associations.

Target properties

Protein nameMicrotubule-associated protein tau
UniProt accessionP10636
GeneMAPT
OrganismHomo sapiens
Length758 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—

Approved drugs hitting this target (5)

DrugCentral-linked approved drugs that act on this protein.

Disease associations (1052)

Diseases linked to this target (Open Targets).

  • semantic dementia · score 0.77
  • Pick disease · score 0.74
  • supranuclear palsy, progressive, 1 · score 0.73
  • Classical progressive supranuclear palsy · score 0.66
  • progressive supranuclear palsy-parkinsonism syndrome · score 0.65
  • Progressive supranuclear palsy - parkinsonism · score 0.61
  • Atypical progressive supranuclear palsy · score 0.61
  • progressive supranuclear palsy · score 0.60
  • frontotemporal dementia · score 0.58
  • Parkinson disease · score 0.52

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-P10636-F1alphafoldPREDICTED49.23—

Amino-acid sequence (758 residues)

MAEPRQEFEV MEDHAGTYGL GDRKDQGGYT MHQDQEGDTD AGLKESPLQT PTEDGSEEPG SETSDAKSTP TAEDVTAPLV DEGAPGKQAA AQPHTEIPEG TTAEEAGIGD TPSLEDEAAG HVTQEPESGK VVQEGFLREP GPPGLSHQLM SGMPGAPLLP EGPREATRQP SGTGPEDTEG GRHAPELLKH QLLGDLHQEG PPLKGAGGKE RPGSKEEVDE DRDVDESSPQ DSPPSKASPA QDGRPPQTAA REATSIPGFP AEGAIPLPVD FLSKVSTEIP ASEPDGPSVG RAKGQDAPLE FTFHVEITPN VQKEQAHSEE HLGRAAFPGA PGEGPEARGP SLGEDTKEAD LPEPSEKQPA AAPRGKPVSR VPQLKARMVS KSKDGTGSDD KKAKTSTRSS AKTLKNRPCL SPKHPTPGSS DPLIQPSSPA VCPEPPSSPK YVSSVTSRTG SSGAKEMKLK GADGKTKIAT PRGAAPPGQK GQANATRIPA KTPPAPKTPP SSGEPPKSGD RSGYSSPGSP GTPGSRSRTP SLPTPPTREP KKVAVVRTPP KSPSSAKSRL QTAPVPMPDL KNVKSKIGST ENLKHQPGGG KVQIINKKLD LSNVQSKCGS KDNIKHVPGG GSVQIVYKPV DLSKVTSKCG SLGNIHHKPG GGQVEVKSEK LDFKDRVQSK IGSLDNITHV PGGGNKKIET HKLTFRENAK AKTDHGAEIV YKSPVVSGDT SPRHLSNVSS TGSIDMVDSP QLATLADEVS ASLAKQGL

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Quick facts

UniProtP10636
GeneMAPT
OrganismHomo sapiens
Length758
Binders0
Diseases1,052
View on UniProt