001     16636
005     20200402210044.0
024 7 _ |2 pmid
|a pmid:21347827
024 7 _ |2 DOI
|a 10.1007/s12104-011-9299-0
024 7 _ |2 WOS
|a WOS:000294559700017
037 _ _ |a PreJuSER-16636
041 _ _ |a eng
082 _ _ |a 570
084 _ _ |2 WoS
|a Biophysics
084 _ _ |2 WoS
|a Spectroscopy
100 1 _ |a Lecher, J.
|b 0
|u FZJ
|0 P:(DE-Juel1)VDB94799
245 _ _ |a 1H, 15N and 13³C resonance assignment of the N-terminal C39 peptidase-like domain of the ABC transporter Haemolysin B (HlyB)
260 _ _ |a Dordrecht [u.a.]
|b Springer Netherlands
|c 2011
300 _ _ |a 199 - 201
336 7 _ |a Journal Article
|0 PUB:(DE-HGF)16
|2 PUB:(DE-HGF)
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|0 0
|2 EndNote
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a article
|2 DRIVER
440 _ 0 |a Biomolecular NMR Assignments
|x 1874-2718
|0 18205
|y 2
|v 5
500 _ _ |a We would like to thank Melanie Schwarten for helpful discussions. The research has been funded by a fellowship from the International Helmholtz Research School on Biophysics and Soft Matter ("Biosoft") to Justin Lecher. We thank the Ministry of Innovation, Science, and Research of the German Federal State North Rhine-Westphalia (NRW) and the Heinrich-Heine-Universitaet Duesseldorf (scholarship from the CLIB-Graduate Cluster Industrial Biotechnology for Christian Schwarz).
520 _ _ |a ATP-binding cassette (ABC) transporters are ubiquitous integral membrane proteins, which catalyze the translocation of molecules across biological membranes in an ATP-dependent manner. Despite the diversity in the transported substrates, they all share the same architecture, comprised of two transmembrane (TMD) and two nucleotide-binding domains (NBD). Members of the bacteriocin ABC transporter subfamily feature a special domain, belonging to the C39 (cystein protease family 39) peptidase protein family. These domains are assumed to cleave a C-terminal signal sequence from the protein or peptide substrate before or during the transport process. Although the C39 peptidase-like domain of the ABC transporter haemolysin B from E. coli shows no proteolytic activity, it is essential for the function of this transporter. In order to elucidate the contribution of the isolated C39 peptidase-like domain in the whole transport process, the backbone and side chain (1)H, (15)N and (13)C-NMR chemical shifts have been assigned.
536 _ _ |a Funktion und Dysfunktion des Nervensystems
|c P33
|2 G:(DE-HGF)
|0 G:(DE-Juel1)FUEK409
|x 0
536 _ _ |a BioSoft: Makromolekulare Systeme und biologische Informationsverarbeitung
|c P45
|0 G:(DE-Juel1)FUEK505
|x 1
588 _ _ |a Dataset connected to Web of Science, Pubmed
650 _ 2 |2 MeSH
|a ATP-Binding Cassette Transporters: chemistry
650 _ 2 |2 MeSH
|a Catalytic Domain
650 _ 2 |2 MeSH
|a Escherichia coli: enzymology
650 _ 2 |2 MeSH
|a Escherichia coli Proteins: chemistry
650 _ 2 |2 MeSH
|a Hemolysin Proteins: chemistry
650 _ 2 |2 MeSH
|a Isotopes: chemistry
650 _ 2 |2 MeSH
|a Nuclear Magnetic Resonance, Biomolecular
650 _ 7 |0 0
|2 NLM Chemicals
|a ATP-Binding Cassette Transporters
650 _ 7 |0 0
|2 NLM Chemicals
|a Escherichia coli Proteins
650 _ 7 |0 0
|2 NLM Chemicals
|a Hemolysin Proteins
650 _ 7 |0 0
|2 NLM Chemicals
|a Isotopes
650 _ 7 |0 EC 3.6.1.3
|2 NLM Chemicals
|a hemolysin B
650 _ 7 |a J
|2 WoSType
653 2 0 |2 Author
|a ABC transporter
653 2 0 |2 Author
|a C39 peptidase-like
653 2 0 |2 Author
|a Heteronuclear NMR
653 2 0 |2 Author
|a Resonance assignment
700 1 _ |a Stoldt, M.
|b 1
|u FZJ
|0 P:(DE-Juel1)VDB21601
700 1 _ |a Schwarz, C.K.W.
|b 2
|0 P:(DE-HGF)0
700 1 _ |a Smits, S.H.J.
|b 3
|0 P:(DE-HGF)0
700 1 _ |a Schmitt, L.
|b 4
|0 P:(DE-HGF)0
700 1 _ |a Willbold, D.
|b 5
|u FZJ
|0 P:(DE-Juel1)132029
773 _ _ |a 10.1007/s12104-011-9299-0
|g Vol. 5, p. 199 - 201
|p 199 - 201
|q 5<199 - 201
|0 PERI:(DE-600)2388861-1
|t Biomolecular NMR assignments
|v 5
|y 2011
|x 1874-2718
856 7 _ |u http://dx.doi.org/10.1007/s12104-011-9299-0
909 C O |o oai:juser.fz-juelich.de:16636
|p VDB
913 1 _ |k P33
|v Funktion und Dysfunktion des Nervensystems
|l Funktion und Dysfunktion des Nervensystems
|b Gesundheit
|0 G:(DE-Juel1)FUEK409
|x 0
913 1 _ |k P45
|v BioSoft: Makromolekulare Systeme und biologische Informationsverarbeitung
|l Biologische Informationsverarbeitung
|b Schlüsseltechnologien
|0 G:(DE-Juel1)FUEK505
|x 1
913 2 _ |a DE-HGF
|b Key Technologies
|l BioSoft Fundamentals for future Technologies in the fields of Soft Matter and Life Sciences
|1 G:(DE-HGF)POF3-550
|0 G:(DE-HGF)POF3-551
|2 G:(DE-HGF)POF3-500
|v Functional Macromolecules and Complexes
|x 0
914 1 _ |y 2011
915 _ _ |0 StatID:(DE-HGF)0030
|2 StatID
|a Peer review
920 1 _ |k ICS-6
|l Strukturbiochemie
|g ICS
|0 I:(DE-Juel1)ICS-6-20110106
|x 0
970 _ _ |a VDB:(DE-Juel1)130807
980 _ _ |a VDB
980 _ _ |a ConvertedRecord
980 _ _ |a journal
980 _ _ |a I:(DE-Juel1)ICS-6-20110106
980 _ _ |a UNRESTRICTED
981 _ _ |a I:(DE-Juel1)IBI-7-20200312


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21