Actin, alpha skeletal muscle (ACTA1)

Homo sapiens — UniProt P68133

Gene: ACTA1Homo sapiensSwissProt reviewed

About Actin, alpha skeletal muscle

Actin, alpha skeletal muscle (ACTA1) is a protein from Homo sapiens identified by UniProt accession P68133, 377 residues long. MolForge cross-references it against 0 known binders and 880 disease associations.

Target properties

Protein nameActin, alpha skeletal muscle
UniProt accessionP68133
GeneACTA1
OrganismHomo sapiens
Length377 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 (880)

Diseases linked to this target (Open Targets).

  • nemaline myopathy 3 · score 0.86
  • severe congenital nemaline myopathy · score 0.67
  • progressive scapulohumeroperoneal distal myopathy · score 0.65
  • congenital myopathy 2b, severe infantile, autosomal recessive · score 0.62
  • congenital fiber-type disproportion myopathy · score 0.60
  • alpha-actinopathy · score 0.54
  • nemaline myopathy · score 0.49
  • neuromuscular disease · score 0.46
  • dilated cardiomyopathy · score 0.45
  • myopathy · score 0.44

3D Structure (1)

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

StructureSourceMethodMean pLDDTResolution (Å)
AF-P68133-F1alphafoldPREDICTED95.10—

Amino-acid sequence (377 residues)

MCDEDETTAL VCDNGSGLVK AGFAGDDAPR AVFPSIVGRP RHQGVMVGMG QKDSYVGDEA QSKRGILTLK YPIEHGIITN WDDMEKIWHH TFYNELRVAP EEHPTLLTEA PLNPKANREK MTQIMFETFN VPAMYVAIQA VLSLYASGRT TGIVLDSGDG VTHNVPIYEG YALPHAIMRL DLAGRDLTDY LMKILTERGY SFVTTAEREI VRDIKEKLCY VALDFENEMA TAASSSSLEK SYELPDGQVI TIGNERFRCP ETLFQPSFIG MESAGIHETT YNSIMKCDID IRKDLYANNV MSGGTTMYPG IADRMQKEIT ALAPSTMKIK IIAPPERKYS VWIGGSILAS LSTFQQMWIT KQEYDEAGPS IVHRKCF

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Quick facts

UniProtP68133
GeneACTA1
OrganismHomo sapiens
Length377
Binders0
Diseases880
View on UniProt