The modular nature of protein evolution: domain rearrangement rates across eukaryotic life
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2148
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
The modular nature of protein evolution: domain rearrangement rates across eukaryotic life ; volume:20 ; number:1 ; day:14 ; month:2 ; year:2020 ; pages:1-13 ; date:12.2020
BMC evolutionary biology ; 20, Heft 1 (14.2.2020), 1-13, 12.2020
- Creator
-
Dohmen, Elias
Klasberg, Steffen
Bornberg-Bauer, Erich
Perrey, Sören
Kemena, Carsten
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s12862-020-1591-0
- URN
-
urn:nbn:de:101:1-2020051223465441929188
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:57 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Dohmen, Elias
- Klasberg, Steffen
- Bornberg-Bauer, Erich
- Perrey, Sören
- Kemena, Carsten
- SpringerLink (Online service)
Other Objects (12)
Conserved phosphorylation hotspots in eukaryotic protein domain families
The eukaryotic chaperonin TRiC : domain-wise folding of multi-domain proteins
The eukaryotic chaperonin TRiC domain-wise folding of multi-domain proteins
Kinase domain activation through gene rearrangement in multiple myeloma
Modular, rule-based modeling for the design of eukaryotic synthetic gene circuits
Structures and nucleic acid-binding preferences of the eukaryotic ARID domain
High-resolution structure of eukaryotic Fibrillarin interacting with Nop56 amino-terminal domain
The OXR domain defines a conserved family of eukaryotic oxidation resistance proteins
The crystal structure of the catalytic domain of a eukaryotic guanylate cyclase
Comparative genomics reveals selective distribution and domain organization of FYVE and PX domain proteins across eukaryotic lineages
In Silico Prediction of Modular Domain-Peptide Interactions
L11 domain rearrangement upon binding to RNA and thiostrepton studied by NMR spectroscopy
Conserved phosphorylation hotspots in eukaryotic protein domain families
The eukaryotic chaperonin TRiC : domain-wise folding of multi-domain proteins
The eukaryotic chaperonin TRiC domain-wise folding of multi-domain proteins
Kinase domain activation through gene rearrangement in multiple myeloma
Modular, rule-based modeling for the design of eukaryotic synthetic gene circuits
Structures and nucleic acid-binding preferences of the eukaryotic ARID domain
High-resolution structure of eukaryotic Fibrillarin interacting with Nop56 amino-terminal domain
The OXR domain defines a conserved family of eukaryotic oxidation resistance proteins
The crystal structure of the catalytic domain of a eukaryotic guanylate cyclase
Comparative genomics reveals selective distribution and domain organization of FYVE and PX domain proteins across eukaryotic lineages
In Silico Prediction of Modular Domain-Peptide Interactions
L11 domain rearrangement upon binding to RNA and thiostrepton studied by NMR spectroscopy
Conserved phosphorylation hotspots in eukaryotic protein domain families
The eukaryotic chaperonin TRiC : domain-wise folding of multi-domain proteins
The eukaryotic chaperonin TRiC domain-wise folding of multi-domain proteins
Kinase domain activation through gene rearrangement in multiple myeloma
Modular, rule-based modeling for the design of eukaryotic synthetic gene circuits
Structures and nucleic acid-binding preferences of the eukaryotic ARID domain
High-resolution structure of eukaryotic Fibrillarin interacting with Nop56 amino-terminal domain
The OXR domain defines a conserved family of eukaryotic oxidation resistance proteins
The crystal structure of the catalytic domain of a eukaryotic guanylate cyclase
Comparative genomics reveals selective distribution and domain organization of FYVE and PX domain proteins across eukaryotic lineages
In Silico Prediction of Modular Domain-Peptide Interactions