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ACTC1

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Protein-coding gene in the species Homo sapiens
ACTC1
Identifiers
AliasesACTC1, ACTC, ASD5, CMD1R, CMH11, LVNC4, actin, alpha, cardiac muscle 1, actin alpha cardiac muscle 1
External IDsOMIM: 102540; MGI: 87905; HomoloGene: 68446; GeneCards: ACTC1; OMA:ACTC1 - orthologs
Gene location (Human)
Chromosome 15 (human)
Chr.Chromosome 15 (human)
Chromosome 15 (human)Genomic location for ACTC1Genomic location for ACTC1
Band15q14Start34,790,230 bp
End34,795,549 bp
Gene location (Mouse)
Chromosome 2 (mouse)
Chr.Chromosome 2 (mouse)
Chromosome 2 (mouse)Genomic location for ACTC1Genomic location for ACTC1
Band2 E4|2 57.55 cMStart113,877,763 bp
End113,884,029 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • myocardium of left ventricle

  • right ventricle

  • cardiac muscle tissue of right atrium

  • right auricle

  • apex of heart

  • vena cava

  • glutes

  • seminal vesicula

  • tibialis anterior muscle

  • popliteal artery
Top expressed in
  • atrioventricular valve

  • endocardial cushion

  • cardiac muscle tissue of left ventricle

  • atrium

  • interventricular septum

  • vastus lateralis muscle

  • triceps brachii muscle

  • human fetus

  • extraocular muscle

  • digastric muscle
More reference expression data
BioGPS
More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

70

11464

Ensembl

ENSG00000159251

ENSMUSG00000068614

UniProt

P68032

P68033

RefSeq (mRNA)

NM_005159

NM_009608

RefSeq (protein)

NP_005150

NP_033738

Location (UCSC)Chr 15: 34.79 – 34.8 MbChr 2: 113.88 – 113.88 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

ACTC1 encodes cardiac muscle alpha actin. This isoform differs from the alpha actin that is expressed in skeletal muscle, ACTA1. Alpha cardiac actin is the major protein of the thin filament in cardiac sarcomeres, which are responsible for muscle contraction and generation of force to support the pump function of the heart.

Structure

Cardiac alpha actin is a 42.0 kDa protein composed of 377 amino acids. Cardiac alpha actin is a filamentous protein extending from a complex mesh with cardiac alpha-actinin (ACTN2) at Z-lines towards the center of the sarcomere. Polymerization of globular actin (G-actin) leads to a structural filament (F-actin) in the form of a two-stranded helix. Each actin can bind to four others. The atomic structure of monomeric actin was solved by Kabsch et al., and closely thereafter this same group published the structure of the actin filament. Actins are highly conserved proteins; the alpha actins are found in muscle tissues and are a major constituent of the contractile apparatus. Cardiac (ACTC1) and skeletal (ACTA1) alpha actins differ by only four amino acids (Asp4Glu, Glu5Asp, Leu301Met, Ser360Thr; cardiac/skeletal). The actin monomer has two asymmetric domains; the larger inner domain comprised by sub-domains 3 and 4, and the smaller outer domain by sub-domains 1 and 2. Both the amino and carboxy-termini lie in sub-domain 1 of the outer domain.

Function

Actin is a dynamic structure that can adapt two states of flexibility, with the greatest difference between the states occurring as a result of movement within sub-domain 2. Myosin binding increases the flexibility of actin, and cross-linking studies have shown that myosin subfragment-1 binds to actin amino acid residues 48-67 within actin sub-domain 2, which may account for this effect.

It has been suggested that the ACTC1 gene has a role during development. Experiments in chick embryos found an association between ACTC1 knockdown and a reduction in the atrial septa.

Clinical significance

Polymorphisms in ACTC1 have been linked to dilated cardiomyopathy in a small number of Japanese patients. Further studies in patients from South Africa found no association. The E101K missense mutation has been associated with hypertrophic cardiomyopathy and left ventricular noncompaction. Another mutation has in the ACTC1 gene has been associated with atrial septal defects.

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000159251Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000068614Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Kramer PL, Luty JA, Litt M (Jul 1992). "Regional localization of the gene for cardiac muscle actin (ACTC) on chromosome 15q". Genomics. 13 (3): 904–5. doi:10.1016/0888-7543(92)90185-U. PMID 1639426.
  6. "Entrez Gene: ACTC1 actin, alpha, cardiac muscle 1".
  7. "Protein Information – Basic Information: Protein COPaKB ID: P68032". Cardiac Organellar Protein Atlas Knowledgebase. Archived from the original on 2015-09-24. Retrieved 2015-03-15.
  8. Zong NC, Li H, Li H, Lam MP, Jimenez RC, Kim CS, Deng N, Kim AK, Choi JH, Zelaya I, Liem D, Meyer D, Odeberg J, Fang C, Lu HJ, Xu T, Weiss J, Duan H, Uhlen M, Yates JR, Apweiler R, Ge J, Hermjakob H, Ping P (Oct 2013). "Integration of cardiac proteome biology and medicine by a specialized knowledgebase". Circulation Research. 113 (9): 1043–53. doi:10.1161/CIRCRESAHA.113.301151. PMC 4076475. PMID 23965338.
  9. Kabsch W, Mannherz HG, Suck D, Pai EF, Holmes KC (Sep 1990). "Atomic structure of the actin:DNase I complex". Nature. 347 (6288): 37–44. Bibcode:1990Natur.347...37K. doi:10.1038/347037a0. PMID 2395459. S2CID 925337.
  10. Holmes KC, Popp D, Gebhard W, Kabsch W (Sep 1990). "Atomic model of the actin filament". Nature. 347 (6288): 44–9. Bibcode:1990Natur.347...44H. doi:10.1038/347044a0. PMID 2395461. S2CID 4317981.
  11. Egelman EH, Orlova A (Apr 1995). "New insights into actin filament dynamics". Current Opinion in Structural Biology. 5 (2): 172–80. doi:10.1016/0959-440x(95)80072-7. PMID 7648318.
  12. Orlova A, Egelman EH (Jul 1993). "A conformational change in the actin subunit can change the flexibility of the actin filament". Journal of Molecular Biology. 232 (2): 334–41. doi:10.1006/jmbi.1993.1393. PMID 8345515.
  13. Bertrand R, Derancourt J, Kassab R (May 1994). "The covalent maleimidobenzoyl-actin-myosin head complex. Cross-linking of the 50 kDa heavy chain region to actin subdomain-2". FEBS Letters. 345 (2–3): 113–9. Bibcode:1994FEBSL.345..113B. doi:10.1016/0014-5793(94)00398-x. PMID 8200441.
  14. ^ Matsson H, Eason J, Bookwalter CS, Klar J, Gustavsson P, Sunnegårdh J, Enell H, Jonzon A, Vikkula M, Gutierrez I, Granados-Riveron J, Pope M, Bu'Lock F, Cox J, Robinson TE, Song F, Brook DJ, Marston S, Trybus KM, Dahl N (Jan 2008). "Alpha-cardiac actin mutations produce atrial septal defects". Human Molecular Genetics. 17 (2): 256–65. doi:10.1093/hmg/ddm302. PMID 17947298.
  15. Takai E; et al. (Oct 1999). "Mutational analysis of the cardiac actin gene in familial and sporadic dilated cardiomyopathy". Am J Med Genet. 86 (4): 325–7. doi:10.1002/(sici)1096-8628(19991008)86:4<325::aid-ajmg5>3.0.co;2-u. PMID 10494087.
  16. Mayosi BM; et al. (Oct 1999). "Cardiac and skeletal actin gene mutations are not a common cause of dilated cardiomyopathy". J Med Genet. 36 (10): 796–7. doi:10.1136/jmg.36.10.796. PMC 1734242. PMID 10528865.
  17. Olson TM, Doan TP, Kishimoto NY, Whitby FG, Ackerman MJ, Fananapazir L (Sep 2000). "Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy". Journal of Molecular and Cellular Cardiology. 32 (9): 1687–94. doi:10.1006/jmcc.2000.1204. PMID 10966831.
  18. Arad M, Penas-Lado M, Monserrat L, Maron BJ, Sherrid M, Ho CY, Barr S, Karim A, Olson TM, Kamisago M, Seidman JG, Seidman CE (Nov 2005). "Gene mutations in apical hypertrophic cardiomyopathy". Circulation. 112 (18): 2805–11. doi:10.1161/CIRCULATIONAHA.105.547448. PMID 16267253.
  19. Monserrat L, Hermida-Prieto M, Fernandez X, Rodríguez I, Dumont C, Cazón L, Cuesta MG, Gonzalez-Juanatey C, Peteiro J, Alvarez N, Penas-Lado M, Castro-Beiras A (Aug 2007). "Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects". European Heart Journal. 28 (16): 1953–61. doi:10.1093/eurheartj/ehm239. PMID 17611253.
  20. Morita H, Rehm HL, Menesses A, McDonough B, Roberts AE, Kucherlapati R, Towbin JA, Seidman JG, Seidman CE (May 2008). "Shared genetic causes of cardiac hypertrophy in children and adults". The New England Journal of Medicine. 358 (18): 1899–908. doi:10.1056/NEJMoa075463. PMC 2752150. PMID 18403758.
  21. Klaassen S, Probst S, Oechslin E, Gerull B, Krings G, Schuler P, Greutmann M, Hürlimann D, Yegitbasi M, Pons L, Gramlich M, Drenckhahn JD, Heuser A, Berger F, Jenni R, Thierfelder L (Jun 2008). "Mutations in sarcomere protein genes in left ventricular noncompaction". Circulation. 117 (22): 2893–901. doi:10.1161/CIRCULATIONAHA.107.746164. PMID 18506004.

Further reading

External links

PDB gallery
  • 1atn: Atomic structure of the actin:DNASE I complex 1atn: Atomic structure of the actin:DNASE I complex
  • 1c0g: CRYSTAL STRUCTURE OF 1:1 COMPLEX BETWEEN GELSOLIN SEGMENT 1 AND A DICTYOSTELIUM/TETRAHYMENA CHIMERA ACTIN (MUTANT 228: Q228K/T229A/A230Y/E360H) 1c0g: CRYSTAL STRUCTURE OF 1:1 COMPLEX BETWEEN GELSOLIN SEGMENT 1 AND A DICTYOSTELIUM/TETRAHYMENA CHIMERA ACTIN (MUTANT 228: Q228K/T229A/A230Y/E360H)
  • 1d4x: Crystal Structure of Caenorhabditis Elegans Mg-ATP Actin Complexed with Human Gelsolin Segment 1 at 1.75 A resolution. 1d4x: Crystal Structure of Caenorhabditis Elegans Mg-ATP Actin Complexed with Human Gelsolin Segment 1 at 1.75 A resolution.
  • 1dej: CRYSTAL STRUCTURE OF A DICTYOSTELIUM/TETRAHYMENA CHIMERA ACTIN (MUTANT 646: Q228K/T229A/A230Y/A231K/S232E/E360H) IN COMPLEX WITH HUMAN GELSOLIN SEGMENT 1 1dej: CRYSTAL STRUCTURE OF A DICTYOSTELIUM/TETRAHYMENA CHIMERA ACTIN (MUTANT 646: Q228K/T229A/A230Y/A231K/S232E/E360H) IN COMPLEX WITH HUMAN GELSOLIN SEGMENT 1
  • 1eqy: COMPLEX BETWEEN RABBIT MUSCLE ALPHA-ACTIN: HUMAN GELSOLIN DOMAIN 1 1eqy: COMPLEX BETWEEN RABBIT MUSCLE ALPHA-ACTIN: HUMAN GELSOLIN DOMAIN 1
  • 1esv: COMPLEX BETWEEN LATRUNCULIN A:RABBIT MUSCLE ALPHA ACTIN:HUMAN GELSOLIN DOMAIN 1 1esv: COMPLEX BETWEEN LATRUNCULIN A:RABBIT MUSCLE ALPHA ACTIN:HUMAN GELSOLIN DOMAIN 1
  • 1h1v: GELSOLIN G4-G6/ACTIN COMPLEX 1h1v: GELSOLIN G4-G6/ACTIN COMPLEX
  • 1hlu: STRUCTURE OF BOVINE BETA-ACTIN-PROFILIN COMPLEX WITH ACTIN BOUND ATP PHOSPHATES SOLVENT ACCESSIBLE 1hlu: STRUCTURE OF BOVINE BETA-ACTIN-PROFILIN COMPLEX WITH ACTIN BOUND ATP PHOSPHATES SOLVENT ACCESSIBLE
  • 1ijj: THE X-RAY CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN RABBIT SKELETAL MUSCLE ACTIN AND LATRUNCULIN A AT 2.85 A RESOLUTION 1ijj: THE X-RAY CRYSTAL STRUCTURE OF THE COMPLEX BETWEEN RABBIT SKELETAL MUSCLE ACTIN AND LATRUNCULIN A AT 2.85 A RESOLUTION
  • 1j6z: UNCOMPLEXED ACTIN 1j6z: UNCOMPLEXED ACTIN
  • 1kxp: CRYSTAL STRUCTURE OF HUMAN VITAMIN D-BINDING PROTEIN IN COMPLEX WITH SKELETAL ACTIN 1kxp: CRYSTAL STRUCTURE OF HUMAN VITAMIN D-BINDING PROTEIN IN COMPLEX WITH SKELETAL ACTIN
  • 1lcu: Polylysine Induces an Antiparallel Actin Dimer that Nucleates Filament Assembly: Crystal Structure at 3.5 A Resolution 1lcu: Polylysine Induces an Antiparallel Actin Dimer that Nucleates Filament Assembly: Crystal Structure at 3.5 A Resolution
  • 1lot: CRYSTAL STRUCTURE OF THE COMPLEX OF ACTIN WITH VITAMIN D-BINDING PROTEIN 1lot: CRYSTAL STRUCTURE OF THE COMPLEX OF ACTIN WITH VITAMIN D-BINDING PROTEIN
  • 1m8q: Molecular Models of Averaged Rigor Crossbridges from Tomograms of Insect Flight Muscle 1m8q: Molecular Models of Averaged Rigor Crossbridges from Tomograms of Insect Flight Muscle
  • 1ma9: Crystal structure of the complex of human vitamin D binding protein and rabbit muscle actin 1ma9: Crystal structure of the complex of human vitamin D binding protein and rabbit muscle actin
  • 1mdu: Crystal structure of the chicken actin trimer complexed with human gelsolin segment 1 (GS-1) 1mdu: Crystal structure of the chicken actin trimer complexed with human gelsolin segment 1 (GS-1)
  • 1mvw: MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE 1mvw: MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE
  • 1nlv: Crystal Structure Of Dictyostelium Discoideum Actin Complexed With Ca ATP And Human Gelsolin Segment 1 1nlv: Crystal Structure Of Dictyostelium Discoideum Actin Complexed With Ca ATP And Human Gelsolin Segment 1
  • 1nm1: Crystal Structure of D. Dicsoideum Actin Complexed With Gelsolin Segment 1 and Mg ATP at 1.8 A Resolution 1nm1: Crystal Structure of D. Dicsoideum Actin Complexed With Gelsolin Segment 1 and Mg ATP at 1.8 A Resolution
  • 1nmd: Crystal Structure of D. Discoideum Actin-Gelsolin Segment 1 Complex Crystallized In Presence Of Lithium ATP 1nmd: Crystal Structure of D. Discoideum Actin-Gelsolin Segment 1 Complex Crystallized In Presence Of Lithium ATP
  • 1nwk: CRYSTAL STRUCTURE OF MONOMERIC ACTIN IN THE ATP STATE 1nwk: CRYSTAL STRUCTURE OF MONOMERIC ACTIN IN THE ATP STATE
  • 1o18: MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE 1o18: MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE
  • 1o19: MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE 1o19: MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE
  • 1o1a: MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE 1o1a: MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE
  • 1o1b: MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE 1o1b: MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE
  • 1o1c: MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE 1o1c: MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE
  • 1o1d: MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE 1o1d: MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE
  • 1o1e: MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE 1o1e: MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE
  • 1o1f: MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE 1o1f: MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE
  • 1o1g: MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE 1o1g: MOLECULAR MODELS OF AVERAGED RIGOR CROSSBRIDGES FROM TOMOGRAMS OF INSECT FLIGHT MUSCLE
  • 1p8z: Complex Between Rabbit Muscle alpha-Actin: Human Gelsolin Residues Val26-Glu156 1p8z: Complex Between Rabbit Muscle alpha-Actin: Human Gelsolin Residues Val26-Glu156
  • 1qz5: Structure of rabbit actin in complex with kabiramide C 1qz5: Structure of rabbit actin in complex with kabiramide C
  • 1qz6: Structure of rabbit actin in complex with jaspisamide A 1qz6: Structure of rabbit actin in complex with jaspisamide A
  • 1rdw: Actin Crystal Dynamics: Structural Implications for F-actin Nucleation, Polymerization and Branching Mediated by the Anti-parallel Dimer 1rdw: Actin Crystal Dynamics: Structural Implications for F-actin Nucleation, Polymerization and Branching Mediated by the Anti-parallel Dimer
  • 1rfq: Actin Crystal Dynamics: Structural Implications for F-actin Nucleation, Polymerization and Branching Mediated by the Anti-parallel Dimer 1rfq: Actin Crystal Dynamics: Structural Implications for F-actin Nucleation, Polymerization and Branching Mediated by the Anti-parallel Dimer
  • 1rgi: Crystal structure of gelsolin domains G1-G3 bound to actin 1rgi: Crystal structure of gelsolin domains G1-G3 bound to actin
  • 1s22: Absolute Stereochemistry of Ulapualide A 1s22: Absolute Stereochemistry of Ulapualide A
  • 1sqk: CRYSTAL STRUCTURE OF CIBOULOT IN COMPLEX WITH SKELETAL ACTIN 1sqk: CRYSTAL STRUCTURE OF CIBOULOT IN COMPLEX WITH SKELETAL ACTIN
  • 1t44: Structural basis of actin sequestration by thymosin-B4: Implications for arp2/3 activation 1t44: Structural basis of actin sequestration by thymosin-B4: Implications for arp2/3 activation
  • 1wua: The structure of Aplyronine A-actin complex 1wua: The structure of Aplyronine A-actin complex
  • 1y64: Bni1p Formin Homology 2 Domain complexed with ATP-actin 1y64: Bni1p Formin Homology 2 Domain complexed with ATP-actin
  • 1yxq: Crystal structure of actin in complex with swinholide A 1yxq: Crystal structure of actin in complex with swinholide A
  • 2a3z: Ternary complex of the WH2 domain of WASP with Actin-DNAse I 2a3z: Ternary complex of the WH2 domain of WASP with Actin-DNAse I
  • 2a40: Ternary complex of the WH2 domain of WAVE with Actin-DNAse I 2a40: Ternary complex of the WH2 domain of WAVE with Actin-DNAse I
  • 2a41: Ternary complex of the WH2 Domain of WIP with Actin-DNAse I 2a41: Ternary complex of the WH2 Domain of WIP with Actin-DNAse I
  • 2a42: Actin-DNAse I Complex 2a42: Actin-DNAse I Complex
  • 2a5x: Crystal Structure of a Cross-linked Actin Dimer 2a5x: Crystal Structure of a Cross-linked Actin Dimer
  • 2asm: Structure of Rabbit Actin In Complex With Reidispongiolide A 2asm: Structure of Rabbit Actin In Complex With Reidispongiolide A
  • 2aso: Structure of Rabbit Actin In Complex With Sphinxolide B 2aso: Structure of Rabbit Actin In Complex With Sphinxolide B
  • 2asp: Structure of Rabbit Actin In Complex With Reidispongiolide C 2asp: Structure of Rabbit Actin In Complex With Reidispongiolide C
  • 2btf: THE STRUCTURE OF CRYSTALLINE PROFILIN-BETA-ACTIN 2btf: THE STRUCTURE OF CRYSTALLINE PROFILIN-BETA-ACTIN
  • 2d1k: Ternary complex of the WH2 domain of mim with actin-dnase I 2d1k: Ternary complex of the WH2 domain of mim with actin-dnase I
  • 2ff3: Crystal structure of Gelsolin domain 1:N-wasp V2 motif hybrid in complex with actin 2ff3: Crystal structure of Gelsolin domain 1:N-wasp V2 motif hybrid in complex with actin
  • 2ff6: Crystal structure of Gelsolin domain 1:ciboulot domain 2 hybrid in complex with actin 2ff6: Crystal structure of Gelsolin domain 1:ciboulot domain 2 hybrid in complex with actin
  • 2fxu: X-ray Structure of Bistramide A- Actin Complex at 1.35 A resolution. 2fxu: X-ray Structure of Bistramide A- Actin Complex at 1.35 A resolution.
  • 2gwj: SpvB ADP-ribosylated actin: hexagonal crystal form 2gwj: SpvB ADP-ribosylated actin: hexagonal crystal form
  • 2gwk: SpvB ADP-ribosylated actin: orthorhombic crystal form 2gwk: SpvB ADP-ribosylated actin: orthorhombic crystal form
  • 2hf3: Crystal structure of monomeric Actin in the ADP bound state 2hf3: Crystal structure of monomeric Actin in the ADP bound state
  • 2hf4: Crystal structure of Monomeric Actin in its ATP-bound state 2hf4: Crystal structure of Monomeric Actin in its ATP-bound state
  • 2hmp: Uncomplexed actin cleaved with protease ECP32 2hmp: Uncomplexed actin cleaved with protease ECP32
  • 2oan: Structure of oxidized beta-actin 2oan: Structure of oxidized beta-actin
  • 2q1n: Actin Dimer Cross-linked Between Residues 41 and 374 2q1n: Actin Dimer Cross-linked Between Residues 41 and 374
  • 2q31: Actin Dimer Cross-linked Between Residues 41 and 374 and proteolytically cleaved by subtilisin between residues 47 and 48. 2q31: Actin Dimer Cross-linked Between Residues 41 and 374 and proteolytically cleaved by subtilisin between residues 47 and 48.
  • 2q36: Actin Dimer Cross-linked between Residues 191 and 374 and complexed with Kabiramide C 2q36: Actin Dimer Cross-linked between Residues 191 and 374 and complexed with Kabiramide C
Proteins of the cytoskeleton
Human
Microfilaments
and ABPs
Myofilament
Actins
Myosins
Other
Other
Intermediate
filaments
Type 1/2
(Keratin,
Cytokeratin)
Epithelial keratins
(soft alpha-keratins)
Hair keratins
(hard alpha-keratins)
Ungrouped alpha
Not alpha
Type 3
Type 4
Type 5
Microtubules
and MAPs
Tubulins
MAPs
Kinesins
Dyneins
Microtubule organising proteins
Microtubule severing proteins
Other
Catenins
Membrane
Other
Nonhuman
See also: cytoskeletal defects
Categories: