Up, down, and around: identifying recurrent interactions within and between super-secondary structures in β-propellers
- PMID: 22987345
- DOI: 10.1007/978-1-62703-065-6_3
Up, down, and around: identifying recurrent interactions within and between super-secondary structures in β-propellers
Abstract
The examination and analysis of super-secondary structures or other specific structural patterns associated with particular functions, sequence motifs, or structural contexts require that the set of structures examined shares the same feature. This seems obvious but in practice this may often present problems such as identifying complete sets of data avoiding false positives. In the case of the β-propeller structures the symmetry of the propeller creates problems for many structure similarity search programs. Here we present a procedure that will identify propeller structures in PDB and assign them to the different N-propeller types. In addition we outline methods to examine similarities and differences within and between the four stranded up-and-down blades of the β-propeller.
Similar articles
-
The automatic detection of known beta-propeller structural motifs from protein tertiary structure.Int J Biol Macromol. 2005 Aug;36(3):176-83. doi: 10.1016/j.ijbiomac.2005.05.007. Int J Biol Macromol. 2005. PMID: 16039708
-
Functional structural motifs for protein-ligand, protein-protein, and protein-nucleic acid interactions and their connection to supersecondary structures.Methods Mol Biol. 2013;932:295-315. doi: 10.1007/978-1-62703-065-6_18. Methods Mol Biol. 2013. PMID: 22987360
-
Structural plasticity associated with the beta-propeller architecture.Int J Biol Macromol. 2004 Apr;34(1-2):55-61. doi: 10.1016/j.ijbiomac.2004.03.003. Int J Biol Macromol. 2004. PMID: 15178010
-
The many blades of the β-propeller proteins: conserved but versatile.Trends Biochem Sci. 2011 Oct;36(10):553-61. doi: 10.1016/j.tibs.2011.07.004. Epub 2011 Sep 15. Trends Biochem Sci. 2011. PMID: 21924917 Review.
-
Computational prediction of protein-protein interactions.Methods Mol Biol. 2004;261:445-68. doi: 10.1385/1-59259-762-9:445. Methods Mol Biol. 2004. PMID: 15064475 Review.
Cited by
-
Bacterial death and TRADD-N domains help define novel apoptosis and immunity mechanisms shared by prokaryotes and metazoans.Elife. 2021 Jun 1;10:e70394. doi: 10.7554/eLife.70394. Elife. 2021. PMID: 34061031 Free PMC article.
-
Highly regulated, diversifying NTP-dependent biological conflict systems with implications for the emergence of multicellularity.Elife. 2020 Feb 26;9:e52696. doi: 10.7554/eLife.52696. Elife. 2020. PMID: 32101166 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
