Actin, cytoplasmic 1 (ACTB)

Homo sapiens — UniProt P60709

Gene: ACTBHomo sapiensSwissProt reviewed

About Actin, cytoplasmic 1

Actin, cytoplasmic 1 (ACTB) is a protein from Homo sapiens identified by UniProt accession P60709, 375 residues long. MolForge cross-references it against 0 known binders and 1,301 disease associations.

Target properties

Protein nameActin, cytoplasmic 1
UniProt accessionP60709
GeneACTB
OrganismHomo sapiens
Length375 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 (1301)

Diseases linked to this target (Open Targets).

  • Baraitser-Winter syndrome 1 · score 0.82
  • Baraitser-Winter syndrome · score 0.78
  • developmental malformations-deafness-dystonia syndrome · score 0.74
  • Developmental malformations - deafness - dystonia · score 0.68
  • cancer · score 0.62
  • genetic disorder · score 0.53
  • Noonan syndrome · score 0.53
  • hypertrophic cardiomyopathy · score 0.51
  • Costello syndrome · score 0.50
  • Intellectual disability · score 0.47

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-P60709-F1alphafoldPREDICTED95.20—

Amino-acid sequence (375 residues)

MDDDIAALVV DNGSGMCKAG FAGDDAPRAV FPSIVGRPRH QGVMVGMGQK DSYVGDEAQS KRGILTLKYP IEHGIVTNWD DMEKIWHHTF YNELRVAPEE HPVLLTEAPL NPKANREKMT QIMFETFNTP AMYVAIQAVL SLYASGRTTG IVMDSGDGVT HTVPIYEGYA LPHAILRLDL AGRDLTDYLM KILTERGYSF TTTAEREIVR DIKEKLCYVA LDFEQEMATA ASSSSLEKSY ELPDGQVITI GNERFRCPEA LFQPSFLGME SCGIHETTFN SIMKCDVDIR KDLYANTVLS GGTTMYPGIA DRMQKEITAL APSTMKIKII APPERKYSVW IGGSILASLS TFQQMWISKQ EYDESGPSIV HRKCF

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Quick facts

UniProtP60709
GeneACTB
OrganismHomo sapiens
Length375
Binders0
Diseases1,301
View on UniProt