SNTB2: Difference between revisions

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<!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. -->
{{Infobox_gene}}
{{PBB_Controls
'''Beta-2-syntrophin''' is a [[protein]] that in humans is encoded by the ''SNTB2'' [[gene]].<ref name="pmid8576247">{{cite journal | vauthors = Ahn AH, Freener CA, Gussoni E, Yoshida M, Ozawa E, Kunkel LM | title = The three human syntrophin genes are expressed in diverse tissues, have distinct chromosomal locations, and each bind to dystrophin and its relatives | journal = J Biol Chem | volume = 271 | issue = 5 | pages = 2724–30 | date = March 1996 | pmid = 8576247 | pmc =  | doi = 10.1074/jbc.271.5.2724 }}</ref><ref name="pmid8183929">{{cite journal | vauthors = Ahn AH, Yoshida M, Anderson MS, Feener CA, Selig S, Hagiwara Y, Ozawa E, Kunkel LM | title = Cloning of human basic A1, a distinct 59-kDa dystrophin-associated protein encoded on chromosome 8q23-24 | journal = Proc Natl Acad Sci U S A | volume = 91 | issue = 10 | pages = 4446–50 | date = June 1994 | pmid = 8183929 | pmc = 43802 | doi = 10.1073/pnas.91.10.4446 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: SNTB2 syntrophin, beta 2 (dystrophin-associated protein A1, 59kDa, basic component 2)| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=6645| accessdate = }}</ref>
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| require_manual_inspection = no
| update_protein_box = yes
| update_summary = yes
| update_citations = yes
}}


<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot.  See Template:PBB_Controls to Stop updates. -->
== Function ==
{{GNF_Protein_box
| image =
| image_source =
| PDB =
| Name = Syntrophin, beta 2 (dystrophin-associated protein A1, 59kDa, basic component 2)
| HGNCid = 11169
| Symbol = SNTB2
| AltSymbols =; D16S2531E; EST25263; SNT2B2; SNT3; SNTL
| OMIM = 600027
| ECnumber = 
| Homologene = 4911
| MGIid = 101771
| Function = {{GNF_GO|id=GO:0003779 |text = actin binding}} {{GNF_GO|id=GO:0005509 |text = calcium ion binding}} {{GNF_GO|id=GO:0005516 |text = calmodulin binding}}
| Component = {{GNF_GO|id=GO:0005624 |text = membrane fraction}} {{GNF_GO|id=GO:0005856 |text = cytoskeleton}} {{GNF_GO|id=GO:0005874 |text = microtubule}} {{GNF_GO|id=GO:0016010 |text = dystrophin-associated glycoprotein complex}} {{GNF_GO|id=GO:0016020 |text = membrane}} {{GNF_GO|id=GO:0045202 |text = synapse}}
| Process =
| Orthologs = {{GNF_Ortholog_box
    | Hs_EntrezGene = 6645
    | Hs_Ensembl = ENSG00000168807
    | Hs_RefseqProtein = NP_006741
    | Hs_RefseqmRNA = NM_006750
    | Hs_GenLoc_db = 
    | Hs_GenLoc_chr = 16
    | Hs_GenLoc_start = 67778533
    | Hs_GenLoc_end = 67892379
    | Hs_Uniprot = Q13425
    | Mm_EntrezGene = 20650
    | Mm_Ensembl = ENSMUSG00000041308
    | Mm_RefseqmRNA = XM_994799
    | Mm_RefseqProtein = XP_999893
    | Mm_GenLoc_db = 
    | Mm_GenLoc_chr = 8
    | Mm_GenLoc_start = 109824879
    | Mm_GenLoc_end = 109903321
    | Mm_Uniprot = Q3V2N5
  }}
}}
'''Syntrophin, beta 2 (dystrophin-associated protein A1, 59kDa, basic component 2)''', also known as '''SNTB2''', is a human [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: SNTB2 syntrophin, beta 2 (dystrophin-associated protein A1, 59kDa, basic component 2)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=6645| accessdate = }}</ref>


<!-- The PBB_Summary template is automatically maintained by Protein Box Bot.  See Template:PBB_Controls to Stop updates. -->
Dystrophin is a large, rod-like cytoskeletal protein found at the inner surface of muscle fibers. Dystrophin is missing in Duchenne Muscular Dystrophy patients and is present in reduced amounts in Becker Muscular Dystrophy patients. The protein encoded by this gene is a peripheral membrane protein found associated with dystrophin and dystrophin-related proteins. This gene is a member of the syntrophin gene family, which contains at least two other structurally related genes.<ref name="entrez" />
{{PBB_Summary
| section_title =
| summary_text = Dystrophin is a large, rod-like cytoskeletal protein found at the inner surface of muscle fibers. Dystrophin is missing in Duchenne Muscular Dystrophy patients and is present in reduced amounts in Becker Muscular Dystrophy patients. The protein encoded by this gene is a peripheral membrane protein found associated with dystrophin and dystrophin-related proteins. This gene is a member of the syntrophin gene family, which contains at least two other structurally-related genes.<ref name="entrez">{{cite web | title = Entrez Gene: SNTB2 syntrophin, beta 2 (dystrophin-associated protein A1, 59kDa, basic component 2)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=6645| accessdate = }}</ref>
}}


==References==
== Interactions ==
{{reflist|2}}
 
==Further reading==
SNTB2 has been shown to [[Protein-protein interaction|interact]] with [[ABCA1]].<ref name=pmid12054535>{{cite journal | vauthors = Buechler C, Boettcher A, Bared SM, Probst MC, Schmitz G | title = The carboxyterminus of the ATP-binding cassette transporter A1 interacts with a beta2-syntrophin/utrophin complex | journal = Biochem. Biophys. Res. Commun. | volume = 293 | issue = 2 | pages = 759–65 | date = May 2002 | pmid = 12054535 | doi = 10.1016/S0006-291X(02)00303-0 }}</ref>
 
== References ==
{{reflist}}
 
== Further reading ==
{{refbegin | 2}}
{{refbegin | 2}}
{{PBB_Further_reading
* {{cite journal | vauthors = Blake DJ | title = Dystrobrevin dynamics in muscle-cell signalling: a possible target for therapeutic intervention in Duchenne muscular dystrophy? | journal = Neuromuscul. Disord. | volume = 12 Suppl 1 | issue =  | pages = S110–7 | year = 2002 | pmid = 12206805 | doi = 10.1016/S0960-8966(02)00091-3 }}
| citations =
* {{cite journal | vauthors = Gee SH, Madhavan R, Levinson SR, Caldwell JH, Sealock R, Froehner SC | title = Interaction of muscle and brain sodium channels with multiple members of the syntrophin family of dystrophin-associated proteins | journal = J. Neurosci. | volume = 18 | issue = 1 | pages = 128–37 | year = 1998 | pmid = 9412493 | doi =  }}
*{{cite journal | author=Blake DJ |title=Dystrobrevin dynamics in muscle-cell signalling: a possible target for therapeutic intervention in Duchenne muscular dystrophy? |journal=Neuromuscul. Disord. |volume=12 Suppl 1 |issue=  |pages= S110-7 |year= 2002 |pmid= 12206805 |doi= }}
* {{cite journal | vauthors = Lumeng C, Phelps S, Crawford GE, Walden PD, Barald K, Chamberlain JS | title = Interactions between beta 2-syntrophin and a family of microtubule-associated serine/threonine kinases | journal = Nat. Neurosci. | volume = 2 | issue = 7 | pages = 611–7 | year = 1999 | pmid = 10404183 | doi = 10.1038/10165 }}
*{{cite journal  | author=Ahn AH, Yoshida M, Anderson MS, ''et al.'' |title=Cloning of human basic A1, a distinct 59-kDa dystrophin-associated protein encoded on chromosome 8q23-24. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=91 |issue= 10 |pages= 4446-50 |year= 1994 |pmid= 8183929 |doi=  }}
* {{cite journal | vauthors = Garcia RA, Vasudevan K, Buonanno A | title = The neuregulin receptor ErbB-4 interacts with PDZ-containing proteins at neuronal synapses | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 97 | issue = 7 | pages = 3596–601 | year = 2000 | pmid = 10725395 | pmc = 16285 | doi = 10.1073/pnas.070042497 }}
*{{cite journal | author=Ahn AH, Freener CA, Gussoni E, ''et al.'' |title=The three human syntrophin genes are expressed in diverse tissues, have distinct chromosomal locations, and each bind to dystrophin and its relatives. |journal=J. Biol. Chem. |volume=271 |issue= 5 |pages= 2724-30 |year= 1996 |pmid= 8576247 |doi=  }}
* {{cite journal | vauthors = Adams ME, Kramarcy N, Krall SP, Rossi SG, Rotundo RL, Sealock R, Froehner SC | title = Absence of α-Syntrophin Leads to Structurally Aberrant Neuromuscular Synapses Deficient in Utrophin | journal = J. Cell Biol. | volume = 150 | issue = 6 | pages = 1385–98 | year = 2000 | pmid = 10995443 | pmc = 2150701 | doi = 10.1083/jcb.150.6.1385 }}
*{{cite journal  | author=Gee SH, Madhavan R, Levinson SR, ''et al.'' |title=Interaction of muscle and brain sodium channels with multiple members of the syntrophin family of dystrophin-associated proteins. |journal=J. Neurosci. |volume=18 |issue= 1 |pages= 128-37 |year= 1998 |pmid= 9412493 |doi=  }}
* {{cite journal | vauthors = Ort T, Maksimova E, Dirkx R, Kachinsky AM, Berghs S, Froehner SC, Solimena M | title = The receptor tyrosine phosphatase-like protein ICA512 binds the PDZ domains of beta2-syntrophin and nNOS in pancreatic beta-cells | journal = Eur. J. Cell Biol. | volume = 79 | issue = 9 | pages = 621–30 | year = 2001 | pmid = 11043403 | doi = 10.1078/0171-9335-00095 }}
*{{cite journal | author=Lumeng C, Phelps S, Crawford GE, ''et al.'' |title=Interactions between beta 2-syntrophin and a family of microtubule-associated serine/threonine kinases. |journal=Nat. Neurosci. |volume=2 |issue= 7 |pages= 611-7 |year= 1999 |pmid= 10404183 |doi= 10.1038/10165 }}
* {{cite journal | vauthors = Marchand S, Stetzkowski-Marden F, Cartaud J | title = Differential targeting of components of the dystrophin complex to the postsynaptic membrane | journal = Eur. J. Neurosci. | volume = 13 | issue = 2 | pages = 221–9 | year = 2001 | pmid = 11168526 | doi = 10.1046/j.1460-9568.2001.01373.x }}
*{{cite journal | author=Garcia RA, Vasudevan K, Buonanno A |title=The neuregulin receptor ErbB-4 interacts with PDZ-containing proteins at neuronal synapses. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=97 |issue= 7 |pages= 3596-601 |year= 2000 |pmid= 10725395 |doi= 10.1073/pnas.070042497 }}
* {{cite journal | vauthors = Hogan A, Shepherd L, Chabot J, Quenneville S, Prescott SM, Topham MK, Gee SH | title = Interaction of gamma 1-syntrophin with diacylglycerol kinase-zeta. Regulation of nuclear localization by PDZ interactions | journal = J. Biol. Chem. | volume = 276 | issue = 28 | pages = 26526–33 | year = 2001 | pmid = 11352924 | doi = 10.1074/jbc.M104156200 }}
*{{cite journal | author=Adams ME, Kramarcy N, Krall SP, ''et al.'' |title=Absence of alpha-syntrophin leads to structurally aberrant neuromuscular synapses deficient in utrophin. |journal=J. Cell Biol. |volume=150 |issue= 6 |pages= 1385-98 |year= 2000 |pmid= 10995443 |doi= }}
* {{cite journal | vauthors = Ort T, Voronov S, Guo J, Zawalich K, Froehner SC, Zawalich W, Solimena M | title = Dephosphorylation of β2-syntrophin and Ca2+/µ-calpain-mediated cleavage of ICA512 upon stimulation of insulin secretion | journal = EMBO J. | volume = 20 | issue = 15 | pages = 4013–23 | year = 2001 | pmid = 11483505 | pmc = 149140 | doi = 10.1093/emboj/20.15.4013 }}
*{{cite journal | author=Ort T, Maksimova E, Dirkx R, ''et al.'' |title=The receptor tyrosine phosphatase-like protein ICA512 binds the PDZ domains of beta2-syntrophin and nNOS in pancreatic beta-cells. |journal=Eur. J. Cell Biol. |volume=79 |issue= 9 |pages= 621-30 |year= 2001 |pmid= 11043403 |doi= }}
* {{cite journal | vauthors = Buechler C, Boettcher A, Bared SM, Probst MC, Schmitz G | title = The carboxyterminus of the ATP-binding cassette transporter A1 interacts with a beta2-syntrophin/utrophin complex | journal = Biochem. Biophys. Res. Commun. | volume = 293 | issue = 2 | pages = 759–65 | year = 2002 | pmid = 12054535 | doi = 10.1016/S0006-291X(02)00303-0 }}
*{{cite journal | author=Marchand S, Stetzkowski-Marden F, Cartaud J |title=Differential targeting of components of the dystrophin complex to the postsynaptic membrane. |journal=Eur. J. Neurosci. |volume=13 |issue= 2 |pages= 221-9 |year= 2001 |pmid= 11168526 |doi= }}
* {{cite journal | vauthors = Kutsenko AS, Gizatullin RZ, Al-Amin AN, Wang F, Kvasha SM, Podowski RM, Matushkin YG, Gyanchandani A, Muravenko OV, Levitsky VG, Kolchanov NA, Protopopov AI, Kashuba VI, Kisselev LL, Wasserman W, Wahlestedt C, Zabarovsky ER | title = NotI flanking sequences: a tool for gene discovery and verification of the human genome | journal = Nucleic Acids Res. | volume = 30 | issue = 14 | pages = 3163–70 | year = 2002 | pmid = 12136098 | pmc = 135748 | doi = 10.1093/nar/gkf428 }}
*{{cite journal | author=Hogan A, Shepherd L, Chabot J, ''et al.'' |title=Interaction of gamma 1-syntrophin with diacylglycerol kinase-zeta. Regulation of nuclear localization by PDZ interactions. |journal=J. Biol. Chem. |volume=276 |issue= 28 |pages= 26526-33 |year= 2001 |pmid= 11352924 |doi= 10.1074/jbc.M104156200 }}
* {{cite journal | vauthors = Chagnon P, Michaud J, Mitchell G, Mercier J, Marion JF, Drouin E, Rasquin-Weber A, Hudson TJ, Richter A | title = A Missense Mutation (R565W) in Cirhin (FLJ14728) in North American Indian Childhood Cirrhosis | journal = Am. J. Hum. Genet. | volume = 71 | issue = 6 | pages = 1443–9 | year = 2003 | pmid = 12417987 | pmc = 378590 | doi = 10.1086/344580 }}
*{{cite journal | author=Ort T, Voronov S, Guo J, ''et al.'' |title=Dephosphorylation of beta2-syntrophin and Ca2+/mu-calpain-mediated cleavage of ICA512 upon stimulation of insulin secretion. |journal=EMBO J. |volume=20 |issue= 15 |pages= 4013-23 |year= 2001 |pmid= 11483505 |doi= 10.1093/emboj/20.15.4013 }}
* {{cite journal | vauthors = Jones KJ, Compton AG, Yang N, Mills MA, Peters MF, Mowat D, Kunkel LM, Froehner SC, North KN | title = Deficiency of the syntrophins and alpha-dystrobrevin in patients with inherited myopathy | journal = Neuromuscul. Disord. | volume = 13 | issue = 6 | pages = 456–67 | year = 2003 | pmid = 12899872 | doi = 10.1016/S0960-8966(03)00066-X }}
*{{cite journal | author=Buechler C, Boettcher A, Bared SM, ''et al.'' |title=The carboxyterminus of the ATP-binding cassette transporter A1 interacts with a beta2-syntrophin/utrophin complex. |journal=Biochem. Biophys. Res. Commun. |volume=293 |issue= 2 |pages= 759-65 |year= 2002 |pmid= 12054535 |doi= 10.1016/S0006-291X(02)00303-0 }}
* {{cite journal | vauthors = Hillman RT, Green RE, Brenner SE | title = An unappreciated role for RNA surveillance | journal = Genome Biol. | volume = 5 | issue = 2 | pages = R8 | year = 2005 | pmid = 14759258 | pmc = 395752 | doi = 10.1186/gb-2004-5-2-r8 }}
*{{cite journal | author=Kutsenko AS, Gizatullin RZ, Al-Amin AN, ''et al.'' |title=NotI flanking sequences: a tool for gene discovery and verification of the human genome. |journal=Nucleic Acids Res. |volume=30 |issue= 14 |pages= 3163-70 |year= 2002 |pmid= 12136098 |doi= }}
* {{cite journal | vauthors = Leonoudakis D, Conti LR, Anderson S, Radeke CM, McGuire LM, Adams ME, Froehner SC, Yates JR, Vandenberg CA | title = Protein trafficking and anchoring complexes revealed by proteomic analysis of inward rectifier potassium channel (Kir2.x)-associated proteins | journal = J. Biol. Chem. | volume = 279 | issue = 21 | pages = 22331–46 | year = 2004 | pmid = 15024025 | doi = 10.1074/jbc.M400285200 }}
*{{cite journal | author=Chagnon P, Michaud J, Mitchell G, ''et al.'' |title=A missense mutation (R565W) in cirhin (FLJ14728) in North American Indian childhood cirrhosis. |journal=Am. J. Hum. Genet. |volume=71 |issue= 6 |pages= 1443-9 |year= 2003 |pmid= 12417987 |doi=  }}
*{{cite journal  | author=Strausberg RL, Feingold EA, Grouse LH, ''et al.'' |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899-903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 }}
*{{cite journal | author=Jones KJ, Compton AG, Yang N, ''et al.'' |title=Deficiency of the syntrophins and alpha-dystrobrevin in patients with inherited myopathy. |journal=Neuromuscul. Disord. |volume=13 |issue= 6 |pages= 456-67 |year= 2003 |pmid= 12899872 |doi= }}
*{{cite journal | author=Hillman RT, Green RE, Brenner SE |title=An unappreciated role for RNA surveillance. |journal=Genome Biol. |volume=5 |issue= 2 |pages= R8 |year= 2005 |pmid= 14759258 |doi= 10.1186/gb-2004-5-2-r8 }}
*{{cite journal | author=Leonoudakis D, Conti LR, Anderson S, ''et al.'' |title=Protein trafficking and anchoring complexes revealed by proteomic analysis of inward rectifier potassium channel (Kir2.x)-associated proteins. |journal=J. Biol. Chem. |volume=279 |issue= 21 |pages= 22331-46 |year= 2004 |pmid= 15024025 |doi= 10.1074/jbc.M400285200 }}
*{{cite journal  | author=Gerhard DS, Wagner L, Feingold EA, ''et al.'' |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121-7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 }}
}}
{{refend}}
{{refend}}


{{protein-stub}}
{{Muscle tissue}}
{{WikiDoc Sources}}
 
 
{{gene-16-stub}}

Revision as of 06:47, 11 September 2017

VALUE_ERROR (nil)
Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

n/a

Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Beta-2-syntrophin is a protein that in humans is encoded by the SNTB2 gene.[1][2][3]

Function

Dystrophin is a large, rod-like cytoskeletal protein found at the inner surface of muscle fibers. Dystrophin is missing in Duchenne Muscular Dystrophy patients and is present in reduced amounts in Becker Muscular Dystrophy patients. The protein encoded by this gene is a peripheral membrane protein found associated with dystrophin and dystrophin-related proteins. This gene is a member of the syntrophin gene family, which contains at least two other structurally related genes.[3]

Interactions

SNTB2 has been shown to interact with ABCA1.[4]

References

  1. Ahn AH, Freener CA, Gussoni E, Yoshida M, Ozawa E, Kunkel LM (March 1996). "The three human syntrophin genes are expressed in diverse tissues, have distinct chromosomal locations, and each bind to dystrophin and its relatives". J Biol Chem. 271 (5): 2724–30. doi:10.1074/jbc.271.5.2724. PMID 8576247.
  2. Ahn AH, Yoshida M, Anderson MS, Feener CA, Selig S, Hagiwara Y, Ozawa E, Kunkel LM (June 1994). "Cloning of human basic A1, a distinct 59-kDa dystrophin-associated protein encoded on chromosome 8q23-24". Proc Natl Acad Sci U S A. 91 (10): 4446–50. doi:10.1073/pnas.91.10.4446. PMC 43802. PMID 8183929.
  3. 3.0 3.1 "Entrez Gene: SNTB2 syntrophin, beta 2 (dystrophin-associated protein A1, 59kDa, basic component 2)".
  4. Buechler C, Boettcher A, Bared SM, Probst MC, Schmitz G (May 2002). "The carboxyterminus of the ATP-binding cassette transporter A1 interacts with a beta2-syntrophin/utrophin complex". Biochem. Biophys. Res. Commun. 293 (2): 759–65. doi:10.1016/S0006-291X(02)00303-0. PMID 12054535.

Further reading