Complement regulator-acquiring surface protein: Difference between revisions
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**[[1w33]], [[1w3z]], [[4bl4]] – BbCRASP-1 extracellular domain- ''Borrelia burgdorferi''<br /> | **[[1w33]], [[1w3z]], [[4bl4]], [[5a2u]] – BbCRASP-1 extracellular domain- ''Borrelia burgdorferi''<br /> | ||
*CRASP-2 | *CRASP-2 |
Revision as of 12:07, 4 April 2017
FunctionComplement regulator-acquiring surface protein (CRASP) are proteins of the Lyme-disease causing bacteria Borrelia burgdorferi which bind to several human extracellular matrix proteins. For details on CRASP-1 see Borrelia burgdorferi Complement Regulator-Acquiring Surface Protein 1.[1][2] DiseaseLyme-disease adhesion factors.
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3D structures of Complement regulator-acquiring surface protein3D structures of Complement regulator-acquiring surface protein
Updated on 04-April-2017
ReferencesReferences
- ↑ Hallstrom T, Haupt K, Kraiczy P, Hortschansky P, Wallich R, Skerka C, Zipfel PF. Complement regulator-acquiring surface protein 1 of Borrelia burgdorferi binds to human bone morphogenic protein 2, several extracellular matrix proteins, and plasminogen. J Infect Dis. 2010 Aug 15;202(3):490-8. doi: 10.1086/653825. PMID:20565259 doi:10.1086/653825
- ↑ Brangulis K, Petrovskis I, Kazaks A, Bogans J, Otikovs M, Jaudzems K, Ranka R, Tars K. Structural characterization of CspZ, a complement regulator factor H and FHL-1 binding protein from Borrelia burgdorferi. FEBS J. 2014 Apr 7. doi: 10.1111/febs.12808. PMID:24702793 doi:http://dx.doi.org/10.1111/febs.12808