Nebulin

NEB
Available structures
PDB	Human UniProt search: PDBe RCSB
List of PDB id codes
	1NEB, 1ARK
Identifiers
Aliases	NEB, nebulin, NEB177D, NEM2, AMC6
External IDs	OMIM: 161650; MGI: 97292; HomoloGene: 136285; GeneCards: NEB; OMA:NEB - orthologs
Gene location (Human)
Chr.	Chromosome 2 (human)
End	151,734,487 bp
Gene location (Mouse)
Chr.	Chromosome 2 (mouse)
End	52,378,474 bp
RNA expression pattern
	Top expressed in
	glutes; ; biceps brachii; ; Skeletal muscle tissue of biceps brachii; ; tibialis anterior muscle; ; Skeletal muscle tissue of rectus abdominis; ; gastrocnemius muscle; ; deltoid muscle; ; triceps brachii muscle; ; quadriceps femoris muscle; ; vastus lateralis muscle;
	Top expressed in
	muscle of thigh; ; knee joint; ; quadriceps femoris muscle; ; soleus muscle; ; triceps brachii muscle; ; medial head of gastrocnemius muscle; ; tibialis anterior muscle; ; vastus lateralis muscle; ; skeletal muscle tissue; ; temporal muscle;
	More reference expression data
	n/a
Gene ontology
Molecular function	actin binding; structural constituent of muscle; protein binding; actin filament binding;
Cellular component	cytoplasm; cytosol; sarcomere; Z discdkac; extracellular exosome; cytoskeleton; actin cytoskeleton;
Biological process	muscle filament sliding; muscle organ development; somatic muscle development; regulation of actin filament length; cardiac muscle thin filament assembly;
	Sources:Amigo / QuickGO
Orthologs
	4703
	17996
	ENSG00000183091
	ENSMUSG00000026950
	P20929; Q05C45
	n/a
	NM_001164507; NM_001164508; NM_001271208; NM_004543
	NM_010889
	NP_001157979; NP_001157980; NP_001258137; NP_004534; NP_004534.2
	n/a
	Wikidata
View/Edit Human	View/Edit Mouse

Nebulin^[5] is an actin-binding protein which is localized to the thin filament of the sarcomeres in skeletal muscle. Nebulin in humans is coded for by the gene NEB. It is a very large protein (600–900 kDa) and binds as many as 200 actin monomers. Because its length is proportional to thin filament length, it is believed that nebulin acts as a thin filament "ruler" and regulates thin filament length during sarcomere assembly.^[6] Other functions of nebulin, such as a role in cell signaling, remain uncertain.

Nebulin has also been shown to regulate actin-myosin interactions by inhibiting ATPase activity in a calcium-calmodulin sensitive manner.^[7]

Mutations in nebulin cause some cases of the autosomal recessive disorder nemaline myopathy.^[8]

A smaller member of the nebulin protein family, termed nebulette, is expressed in cardiac muscle.

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000183091 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000026950 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ Wang, K.; Williamson, C. L. (June 1980). "Identification of an N2 line protein of striated muscle". Proceedings of the National Academy of Sciences of the United States of America. 77 (6): 3254–3258. Bibcode:1980PNAS...77.3254W. doi:10.1073/pnas.77.6.3254. ISSN 0027-8424. PMC 349593. PMID 6997874.
^ McElhinny AS, Kazmierski ST, Labeit S, Gregorio CC (July 2003). "Nebulin: the nebulous, multifunctional giant of striated muscle". Trends in Cardiovascular Medicine. 13 (5): 195–201. doi:10.1016/S1050-1738(03)00076-8. PMID 12837582.
^ Root DD, Wang K (October 1994). "Calmodulin-sensitive interaction of human nebulin fragments with actin and myosin". Biochemistry. 33 (42): 12581–91. doi:10.1021/bi00208a008. PMID 7918483.
^ Pelin K, Hilpelä P, Donner K, Sewry C, Akkari PA, Wilton SD, Wattanasirichaigoon D, Bang ML, Centner T, Hanefeld F, Odent S, Fardeau M, Urtizberea JA, Muntoni F, Dubowitz V, Beggs AH, Laing NG, Labeit S, de la Chapelle A, Wallgren-Pettersson C (March 1999). "Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy". Proceedings of the National Academy of Sciences of the United States of America. 96 (5): 2305–10. Bibcode:1999PNAS...96.2305P. doi:10.1073/pnas.96.5.2305. PMC 26779. PMID 10051637.

[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000183091 – Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000026950 – Ensembl, 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] Wang, K.; Williamson, C. L. (June 1980). "Identification of an N2 line protein of striated muscle". Proceedings of the National Academy of Sciences of the United States of America. 77 (6): 3254–3258. Bibcode:1980PNAS...77.3254W. doi:10.1073/pnas.77.6.3254. ISSN 0027-8424. PMC 349593. PMID 6997874.

[mcelhinny-6] McElhinny AS, Kazmierski ST, Labeit S, Gregorio CC (July 2003). "Nebulin: the nebulous, multifunctional giant of striated muscle". Trends in Cardiovascular Medicine. 13 (5): 195–201. doi:10.1016/S1050-1738(03)00076-8. PMID 12837582.

[rootwang-7] Root DD, Wang K (October 1994). "Calmodulin-sensitive interaction of human nebulin fragments with actin and myosin". Biochemistry. 33 (42): 12581–91. doi:10.1021/bi00208a008. PMID 7918483.

[pelin-8] Pelin K, Hilpelä P, Donner K, Sewry C, Akkari PA, Wilton SD, Wattanasirichaigoon D, Bang ML, Centner T, Hanefeld F, Odent S, Fardeau M, Urtizberea JA, Muntoni F, Dubowitz V, Beggs AH, Laing NG, Labeit S, de la Chapelle A, Wallgren-Pettersson C (March 1999). "Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy". Proceedings of the National Academy of Sciences of the United States of America. 96 (5): 2305–10. Bibcode:1999PNAS...96.2305P. doi:10.1073/pnas.96.5.2305. PMC 26779. PMID 10051637.

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Nebulin

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