2mb9

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'''Unreleased structure'''
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{{STRUCTURE_2mb9| PDB=2mb9 | SCENE= }}
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===Human Bcl10 CARD===
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{{ABSTRACT_PUBMED_24074955}}
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The entry 2mb9 is ON HOLD
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==Disease==
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[[http://www.uniprot.org/uniprot/BCL10_HUMAN BCL10_HUMAN]] A chromosomal aberration involving BCL10 is recurrent in low-grade mucosa-associated lymphoid tissue (MALT lymphoma). Translocation t(1;14)(p22;q32). Although the BCL10/IgH translocation leaves the coding region of BCL10 intact, frequent BCL10 mutations could be attributed to the Ig somatic hypermutation mechanism resulting in nucleotide transitions. Defects in BCL10 are involved in various types of cancer. The gene represented in this entry may be involved in disease pathogenesis.
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Authors: Zheng, C., Bracken, C., Wu, H.
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==Function==
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[[http://www.uniprot.org/uniprot/BCL10_HUMAN BCL10_HUMAN]] Promotes apoptosis, pro-caspase-9 maturation and activation of NF-kappa-B via NIK and IKK. May be an adapter protein between upstream TNFR1-TRADD-RIP complex and the downstream NIK-IKK-IKAP complex. Is a substrate for MALT1.<ref>PMID:18264101</ref>
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Description: Human Bcl10 CARD
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==About this Structure==
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[[2mb9]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2MB9 OCA].
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==Reference==
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<ref group="xtra">PMID:024074955</ref><references group="xtra"/><references/>
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[[Category: Homo sapiens]]
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[[Category: Bracken, C.]]
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[[Category: Wu, H.]]
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[[Category: Zheng, C.]]
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[[Category: Apoptosis]]
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[[Category: Death domain]]
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[[Category: Signaling protein]]

Revision as of 07:58, 16 October 2013

Template:STRUCTURE 2mb9

Contents

Human Bcl10 CARD

Template:ABSTRACT PUBMED 24074955

Disease

[BCL10_HUMAN] A chromosomal aberration involving BCL10 is recurrent in low-grade mucosa-associated lymphoid tissue (MALT lymphoma). Translocation t(1;14)(p22;q32). Although the BCL10/IgH translocation leaves the coding region of BCL10 intact, frequent BCL10 mutations could be attributed to the Ig somatic hypermutation mechanism resulting in nucleotide transitions. Defects in BCL10 are involved in various types of cancer. The gene represented in this entry may be involved in disease pathogenesis.

Function

[BCL10_HUMAN] Promotes apoptosis, pro-caspase-9 maturation and activation of NF-kappa-B via NIK and IKK. May be an adapter protein between upstream TNFR1-TRADD-RIP complex and the downstream NIK-IKK-IKAP complex. Is a substrate for MALT1.[1]

About this Structure

2mb9 is a 1 chain structure with sequence from Homo sapiens. Full experimental information is available from OCA.

Reference

  • Qiao Q, Yang C, Zheng C, Fontan L, David L, Yu X, Bracken C, Rosen M, Melnick A, Egelman EH, Wu H. Structural Architecture of the CARMA1/Bcl10/MALT1 Signalosome: Nucleation-Induced Filamentous Assembly. Mol Cell. 2013 Sep 26;51(6):766-79. doi: 10.1016/j.molcel.2013.08.032. PMID:24074955 doi:http://dx.doi.org/10.1016/j.molcel.2013.08.032
  1. ↑ Rebeaud F, Hailfinger S, Posevitz-Fejfar A, Tapernoux M, Moser R, Rueda D, Gaide O, Guzzardi M, Iancu EM, Rufer N, Fasel N, Thome M. The proteolytic activity of the paracaspase MALT1 is key in T cell activation. Nat Immunol. 2008 Mar;9(3):272-81. doi: 10.1038/ni1568. Epub 2008 Feb 10. PMID:18264101 doi:10.1038/ni1568

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