Transmembrane activator and CAML interactor: Difference between revisions

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Template:PBB Tumor necrosis factor receptor superfamily member 13B, also known as TNFRSF13B or more commonly as TACI, is a transmembrane receptor protein found predominantly on the surface of B cells, which are an important part of the immune system.^[1]

Template:PBB Summary

Functions of TACI

TACI controls T cell-independent B cell antibody responses, isotype switching, and B cell homeostasis.

Medical significance

TACI mutations are associated with immunodeficiency in humans, as a significant proportion of CVID patients have TACI mutations. People with this condition produce abnormally low amounts of antibodies, which are needed for protection against infections.

In humans, the gene encoding this protein is located within the Smith-Magenis syndrome region on chromosome 17.^[1]

Interactions

TNFRSF13B has been shown to interact with B-cell activating factor,^[2]^[3] TRAF6,^[3] TRAF5,^[3] TNFSF13,^[2] TRAF2^[3] and CAMLG.^[3]^[4]

References

^ ^a ^b "Entrez Gene: TNFRSF13B tumor necrosis factor receptor superfamily, member 13B".
^ ^a ^b Wu, Y (2000). "Tumor necrosis factor (TNF) receptor superfamily member TACI is a high affinity receptor for TNF family members APRIL and BLyS". J. Biol. Chem. 275 (45). UNITED STATES: 35478–85. doi:10.1074/jbc.M005224200. ISSN 0021-9258. PMID 10956646. {{cite journal}}: Cite has empty unknown parameters: |laydate=, |laysummary=, and |laysource= (help); Unknown parameter |coauthors= ignored (|author= suggested) (help); Unknown parameter |month= ignored (help)CS1 maint: unflagged free DOI (link)
^ ^a ^b ^c ^d ^e Xia, X Z (2000). "TACI is a TRAF-interacting receptor for TALL-1, a tumor necrosis factor family member involved in B cell regulation". J. Exp. Med. 192 (1). UNITED STATES: 137–43. doi:10.1084/jem.192.1.137. ISSN 0022-1007. PMC 1887716. PMID 10880535. {{cite journal}}: Cite has empty unknown parameters: |laydate=, |laysummary=, and |laysource= (help); Unknown parameter |coauthors= ignored (|author= suggested) (help); Unknown parameter |month= ignored (help)
^ von Bülow, G U (1997). "NF-AT activation induced by a CAML-interacting member of the tumor necrosis factor receptor superfamily". Science. 278 (5335). UNITED STATES: 138–41. doi:10.1126/science.278.5335.138. ISSN 0036-8075. PMID 9311921. {{cite journal}}: Cite has empty unknown parameters: |laydate=, |laysummary=, and |laysource= (help); Unknown parameter |coauthors= ignored (|author= suggested) (help); Unknown parameter |month= ignored (help)

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 ==Interactions==
-TNFRSF13B has been shown to [[Protein-protein interaction|interact]] with [[B-cell activating factor]],<ref name=pmid10956646>{{cite journal |last=Wu |first=Y |authorlink= |coauthors=Bressette D, Carrell J A, Kaufman T, Feng P, Taylor K, Gan Y, Cho Y H, Garcia A D, Gollatz E, Dimke D, LaFleur D, Migone T S, Nardelli B, Wei P, Ruben S M, Ullrich S J, Olsen H S, Kanakaraj P, Moore P A, Baker K P |year=2000|month=Nov. |title=Tumor necrosis factor (TNF) receptor superfamily member TACI is a high affinity receptor for TNF family members APRIL and BLyS |journal=J. Biol. Chem. |volume=275 |issue=45 |pages=35478–85 |publisher= |location = UNITED STATES| issn = 0021-9258| pmid = 10956646 |doi = 10.1074/jbc.M005224200 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = }}</ref><ref name=pmid10880535>{{cite journal |last=Xia |first=X Z |authorlink= |coauthors=Treanor J, Senaldi G, Khare S D, Boone T, Kelley M, Theill L E, Colombero A, Solovyev I, Lee F, McCabe S, Elliott R, Miner K, Hawkins N, Guo J, Stolina M, Yu G, Wang J, Delaney J, Meng S Y, Boyle W J, Hsu H |year=2000|month=Jul. |title=TACI is a TRAF-interacting receptor for TALL-1, a tumor necrosis factor family member involved in B cell regulation |journal=J. Exp. Med. |volume=192 |issue=1 |pages=137–43 |publisher= |location = UNITED STATES| issn = 0022-1007| pmid = 10880535 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = |doi=10.1084/jem.192.1.137 |pmc=1887716 }}</ref> [[TRAF6]],<ref name=pmid10880535/> [[TRAF5]],<ref name=pmid10880535/> [[TNFSF13]],<ref name=pmid10956646/> [[TRAF2]]<ref name=pmid10880535/> and [[CAMLG]].<ref name=pmid10880535/><ref name=pmid9311921>{{cite journal |last=von Bülow |first=G U |authorlink= |coauthors=Bram R J |year=1997|month=Oct. |title=NF-AT activation induced by a CAML-interacting member of the tumor necrosis factor receptor superfamily |journal=[[Science (journal)|Science]] |volume=278 |issue=5335 |pages=138–41 |publisher= |location = UNITED STATES| issn = 0036-8075| pmid = 9311921 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = |doi=10.1126/science.278.5335.138 }}</ref>
+TNFRSF13B has been shown to [[Protein-protein interaction|interact]] with [[B-cell activating factor]],<ref name=pmid10956646>{{cite journal |last=Wu |first=Y |authorlink= |coauthors=Bressette D, Carrell J A, Kaufman T, Feng P, Taylor K, Gan Y, Cho Y H, Garcia A D, Gollatz E, Dimke D, LaFleur D, Migone T S, Nardelli B, Wei P, Ruben S M, Ullrich S J, Olsen H S, Kanakaraj P, Moore P A, Baker K P |year=2000|month=November  |title=Tumor necrosis factor (TNF) receptor superfamily member TACI is a high affinity receptor for TNF family members APRIL and BLyS |journal=J. Biol. Chem. |volume=275 |issue=45 |pages=35478–85 |publisher= |location = UNITED STATES| issn = 0021-9258| pmid = 10956646 |doi = 10.1074/jbc.M005224200 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = }}</ref><ref name=pmid10880535>{{cite journal |last=Xia |first=X Z |authorlink= |coauthors=Treanor J, Senaldi G, Khare S D, Boone T, Kelley M, Theill L E, Colombero A, Solovyev I, Lee F, McCabe S, Elliott R, Miner K, Hawkins N, Guo J, Stolina M, Yu G, Wang J, Delaney J, Meng S Y, Boyle W J, Hsu H |year=2000|month=July  |title=TACI is a TRAF-interacting receptor for TALL-1, a tumor necrosis factor family member involved in B cell regulation |journal=J. Exp. Med. |volume=192 |issue=1 |pages=137–43 |publisher= |location = UNITED STATES| issn = 0022-1007| pmid = 10880535 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = |doi=10.1084/jem.192.1.137 |pmc=1887716 }}</ref> [[TRAF6]],<ref name=pmid10880535/> [[TRAF5]],<ref name=pmid10880535/> [[TNFSF13]],<ref name=pmid10956646/> [[TRAF2]]<ref name=pmid10880535/> and [[CAMLG]].<ref name=pmid10880535/><ref name=pmid9311921>{{cite journal |last=von Bülow |first=G U |authorlink= |coauthors=Bram R J |year=1997|month=October  |title=NF-AT activation induced by a CAML-interacting member of the tumor necrosis factor receptor superfamily |journal=[[Science (journal)|Science]] |volume=278 |issue=5335 |pages=138–41 |publisher= |location = UNITED STATES| issn = 0036-8075| pmid = 9311921 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = |doi=10.1126/science.278.5335.138 }}</ref>
 ==References==

v t e Proteins: clusters of differentiation (see also list of human clusters of differentiation)
1–50	CD1 a-c 1A 1B 1D 1E CD2 CD3 γ δ ε CD4 CD5 CD6 CD7 CD8 a CD9 CD10 CD11 a b c d CD13 CD14 CD15 CD16 A B CD18 CD19 CD20 CD21 CD22 CD23 CD24 CD25 CD26 CD27 CD28 CD29 CD30 CD31 CD32 A B CD33 CD34 CD35 CD36 CD37 CD38 CD39 CD40 CD41 CD42 a b c d CD43 CD44 CD45 CD46 CD47 CD48 CD49 a b c d e f CD50
51–100	CD51 CD52 CD53 CD54 CD55 CD56 CD57 CD58 CD59 CD61 CD62 E L P CD63 CD64 A B C CD66 a b c d e f CD68 CD69 CD70 CD71 CD72 CD73 CD74 CD78 CD79 a b CD80 CD81 CD82 CD83 CD84 CD85 a d e h j k CD86 CD87 CD88 CD89 CD90 CD91 - CD92 CD93 CD94 CD95 CD96 CD97 CD98 CD99 CD100
101–150	CD101 CD102 CD103 CD104 CD105 CD106 CD107 a b CD108 CD109 CD110 CD111 CD112 CD113 CD114 CD115 CD116 CD117 CD118 CD119 CD120 a b CD121 a b CD122 CD123 CD124 CD125 CD126 CD127 CD129 CD130 CD131 CD132 CD133 CD134 CD135 CD136 CD137 CD138 CD140b CD141 CD142 CD143 CD144 CD146 CD147 CD148 CD150
151–200	CD151 CD152 CD153 CD154 CD155 CD156 a b c CD157 CD158 (a d e i k) CD159 a c CD160 CD161 CD162 CD163 CD164 CD166 CD167 a b CD168 CD169 CD170 CD171 CD172 a b g CD174 CD177 CD178 CD179 a b CD180 CD181 CD182 CD183 CD184 CD185 CD186 CD191 CD192 CD193 CD194 CD195 CD196 CD197 CDw198 CDw199 CD200
201–250	CD201 CD202b CD204 CD205 CD206 CD207 CD208 CD209 CDw210 a b CD212 CD213a 1 2 CD217 CD218 (a b) CD220 CD221 CD222 CD223 CD224 CD225 CD226 CD227 CD228 CD229 CD230 CD233 CD234 CD235 a b CD236 CD238 CD239 CD240CE CD240D CD241 CD243 CD244 CD246 CD247 - CD248 CD249
251–300	CD252 CD253 CD254 CD256 CD257 CD258 CD261 CD262 CD263 CD264 CD265 CD266 CD267 CD268 CD269 CD271 CD272 CD273 CD274 CD275 CD276 CD278 CD279 CD280 CD281 CD282 CD283 CD284 CD286 CD288 CD289 CD290 CD292 CDw293 CD294 CD295 CD297 CD298 CD299
301–350	CD300A CD301 CD302 CD303 CD304 CD305 CD306 CD307 CD309 CD312 CD314 CD315 CD316 CD317 CD318 CD320 CD321 CD322 CD324 CD325 CD326 CD327 CD328 CD329 CD331 CD332 CD333 CD334 CD335 CD336 CD337 CD338 CD339 CD340 CD344 CD349 CD350

Revision as of 04:23, 31 May 2012

Functions of TACI

Medical significance

Interactions

References

Further reading