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β-Strand-mediated interactions of protein domains.
- Source :
-
Proteins [Proteins] 2020 Nov; Vol. 88 (11), pp. 1513-1527. Date of Electronic Publication: 2020 Jul 11. - Publication Year :
- 2020
-
Abstract
- Protein domains exist by themselves or in combination with other domains to form complex multidomain proteins. Defining domain boundaries in proteins is essential for understanding their evolution and function but is not trivial. More specifically, partitioning domains that interact by forming a single β-sheet is known to be particularly troublesome for automatic structure-based domain decomposition pipelines. Here, we study edge-to-edge β-strand interactions between domains in a protein chain, to help define the boundaries for some more difficult cases where a single β-sheet spanning over two domains gives an appearance of one. We give a number of examples where β-strands belonging to a single β-sheet do not belong to a single domain and highlight the difficulties of automatic domain parsers on these examples. This work can be used as a baseline for defining domain boundaries in homologous proteins or proteins with similar domain interactions in the future.<br /> (© 2020 Wiley Periodicals LLC.)
- Subjects :
- Amino Acid Isomerases metabolism
Amino Acid Sequence
Animals
Bacteria chemistry
Binding Sites
Databases, Protein
Datasets as Topic
Humans
Models, Molecular
Penicillin-Binding Proteins metabolism
Protein Binding
Protein Conformation, alpha-Helical
Protein Conformation, beta-Strand
Racemases and Epimerases metabolism
Thermodynamics
Amino Acid Isomerases chemistry
Penicillin-Binding Proteins chemistry
Protein Interaction Domains and Motifs
Racemases and Epimerases chemistry
Subjects
Details
- Language :
- English
- ISSN :
- 1097-0134
- Volume :
- 88
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Proteins
- Publication Type :
- Academic Journal
- Accession number :
- 32543729
- Full Text :
- https://doi.org/10.1002/prot.25970