Actin, cytoplasmic 2 (ACTG1)

Homo sapiens — UniProt P63261

Gene: ACTG1Homo sapiensSwissProt reviewed

About Actin, cytoplasmic 2

Actin, cytoplasmic 2 (ACTG1) is a protein from Homo sapiens identified by UniProt accession P63261, 375 residues long. MolForge cross-references it against 0 known binders and 290 disease associations.

Target properties

Protein nameActin, cytoplasmic 2
UniProt accessionP63261
GeneACTG1
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 (290)

Diseases linked to this target (Open Targets).

  • Baraitser-Winter syndrome · score 0.82
  • autosomal dominant nonsyndromic hearing loss · score 0.65
  • cancer · score 0.60
  • Noonan syndrome · score 0.53
  • hypertrophic cardiomyopathy · score 0.50
  • Costello syndrome · score 0.50
  • neurodegenerative disease · score 0.50
  • genetic disorder · score 0.48
  • nonsyndromic genetic hearing loss · score 0.45
  • external ear disease · score 0.43

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-P63261-F1alphafoldPREDICTED95.37—

Amino-acid sequence (375 residues)

MEEEIAALVI 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

UniProtP63261
GeneACTG1
OrganismHomo sapiens
Length375
Binders0
Diseases290
View on UniProt