| Hauptseite > Publikationsdatenbank > Preliminary X-ray characterization of the ribonuclease P (C5 protein) from Escherichia coli : expression, crystallization and cryoconditions > print |
| 001 | 26893 | ||
| 005 | 20200402210434.0 | ||
| 024 | 7 | _ | |2 pmid |a pmid:12554950 |
| 024 | 7 | _ | |2 DOI |a 10.1107/S0907444902020784 |
| 024 | 7 | _ | |2 WOS |a WOS:000180641900020 |
| 037 | _ | _ | |a PreJuSER-26893 |
| 041 | _ | _ | |a eng |
| 082 | _ | _ | |a 570 |
| 084 | _ | _ | |2 WoS |a Biochemical Research Methods |
| 084 | _ | _ | |2 WoS |a Biochemistry & Molecular Biology |
| 084 | _ | _ | |2 WoS |a Biophysics |
| 084 | _ | _ | |2 WoS |a Crystallography |
| 100 | 1 | _ | |a Choe, B. J. |b 0 |0 P:(DE-HGF)0 |
| 245 | _ | _ | |a Preliminary X-ray characterization of the ribonuclease P (C5 protein) from Escherichia coli : expression, crystallization and cryoconditions |
| 260 | _ | _ | |a Copenhagen |b Munksgaard |c 2003 |
| 300 | _ | _ | |a 350 - 352 |
| 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 Acta Crystallographica D |x 0907-4449 |0 56 |y 2 |v 59 |
| 500 | _ | _ | |a Record converted from VDB: 12.11.2012 |
| 520 | _ | _ | |a The gene for Escherichia coli ribonuclease P (RNase P) protein (also known as C5 protein) and its mutant C5-C113A have been expressed as GST fusion proteins in E. coli at a high level. After cleavage of the fusion protein, highly purified functional C5 protein is obtained that can be crystallized with 2.5-2.6 M (NH(4))(2)HPO(4)/(NH(4))H(2)PO(4) pH 7.0 at room temperature. These crystals are suitable for X-ray analysis, belong to the space group P3(1)21 or P3(2)21 (unit-cell parameters a = b = 66.67, c = 142.09 A) and diffract to 2.9 A at 100 K using sorbitol and glycerol as cryoprotectants. For three molecules in the asymmetric unit a V(M) of 2.17 A(3) Da(-1) was calculated. |
| 536 | _ | _ | |a Neurowissenschaften |c L01 |2 G:(DE-HGF) |0 G:(DE-Juel1)FUEK255 |x 0 |
| 588 | _ | _ | |a Dataset connected to Web of Science, Pubmed |
| 650 | _ | 2 | |2 MeSH |a Amino Acid Substitution |
| 650 | _ | 2 | |2 MeSH |a Cryoprotective Agents: chemistry |
| 650 | _ | 2 | |2 MeSH |a Crystallization |
| 650 | _ | 2 | |2 MeSH |a Crystallography, X-Ray |
| 650 | _ | 2 | |2 MeSH |a Endoribonucleases: chemistry |
| 650 | _ | 2 | |2 MeSH |a Endoribonucleases: genetics |
| 650 | _ | 2 | |2 MeSH |a Endoribonucleases: metabolism |
| 650 | _ | 2 | |2 MeSH |a Escherichia coli: enzymology |
| 650 | _ | 2 | |2 MeSH |a Escherichia coli Proteins |
| 650 | _ | 2 | |2 MeSH |a Glutathione Transferase: genetics |
| 650 | _ | 2 | |2 MeSH |a Glycerol: chemistry |
| 650 | _ | 2 | |2 MeSH |a RNA, Catalytic: chemistry |
| 650 | _ | 2 | |2 MeSH |a RNA, Catalytic: genetics |
| 650 | _ | 2 | |2 MeSH |a RNA, Catalytic: metabolism |
| 650 | _ | 2 | |2 MeSH |a Recombinant Fusion Proteins: biosynthesis |
| 650 | _ | 2 | |2 MeSH |a Recombinant Fusion Proteins: genetics |
| 650 | _ | 2 | |2 MeSH |a Ribonuclease P |
| 650 | _ | 2 | |2 MeSH |a Ribonucleoproteins: chemistry |
| 650 | _ | 2 | |2 MeSH |a Ribonucleoproteins: genetics |
| 650 | _ | 2 | |2 MeSH |a Ribonucleoproteins: metabolism |
| 650 | _ | 2 | |2 MeSH |a Sorbitol: chemistry |
| 650 | _ | 7 | |0 0 |2 NLM Chemicals |a Cryoprotective Agents |
| 650 | _ | 7 | |0 0 |2 NLM Chemicals |a Escherichia coli Proteins |
| 650 | _ | 7 | |0 0 |2 NLM Chemicals |a RNA, Catalytic |
| 650 | _ | 7 | |0 0 |2 NLM Chemicals |a Recombinant Fusion Proteins |
| 650 | _ | 7 | |0 0 |2 NLM Chemicals |a Ribonucleoproteins |
| 650 | _ | 7 | |0 50-70-4 |2 NLM Chemicals |a Sorbitol |
| 650 | _ | 7 | |0 56-81-5 |2 NLM Chemicals |a Glycerol |
| 650 | _ | 7 | |0 EC 2.5.1.18 |2 NLM Chemicals |a Glutathione Transferase |
| 650 | _ | 7 | |0 EC 3.1.- |2 NLM Chemicals |a Endoribonucleases |
| 650 | _ | 7 | |0 EC 3.1.26.5 |2 NLM Chemicals |a Ribonuclease P |
| 650 | _ | 7 | |0 EC 3.1.26.5 |2 NLM Chemicals |a ribonuclease P, E coli |
| 650 | _ | 7 | |a J |2 WoSType |
| 700 | 1 | _ | |a Jeong, D.-G. |b 1 |0 P:(DE-HGF)0 |
| 700 | 1 | _ | |a Park, K. S. |b 2 |0 P:(DE-HGF)0 |
| 700 | 1 | _ | |a Schlesinger, R. |b 3 |u FZJ |0 P:(DE-Juel1)VDB1421 |
| 700 | 1 | _ | |a Labahn, J. |b 4 |u FZJ |0 P:(DE-Juel1)VDB886 |
| 700 | 1 | _ | |a Hofmann, K. P. |b 5 |0 P:(DE-HGF)0 |
| 700 | 1 | _ | |a Büldt, G. |b 6 |u FZJ |0 P:(DE-Juel1)131957 |
| 773 | _ | _ | |a 10.1107/S0907444902020784 |g Vol. 59, p. 350 - 352 |p 350 - 352 |q 59<350 - 352 |0 PERI:(DE-600)2020492-9 |t Acta crystallographica / D |v 59 |y 2003 |x 0907-4449 |
| 856 | 7 | _ | |u http://dx.doi.org/10.1107/S0907444902020784 |
| 909 | C | O | |o oai:juser.fz-juelich.de:26893 |p VDB |
| 913 | 1 | _ | |k L01 |v Neurowissenschaften |l Funktion und Dysfunktion des Nervensystems |b Leben |0 G:(DE-Juel1)FUEK255 |x 0 |
| 914 | 1 | _ | |y 2003 |
| 915 | _ | _ | |0 StatID:(DE-HGF)0010 |a JCR/ISI refereed |
| 920 | 1 | _ | |k IBI-2 |l Biologische Strukturforschung |d 31.12.2006 |g IBI |0 I:(DE-Juel1)VDB58 |x 0 |
| 970 | _ | _ | |a VDB:(DE-Juel1)19622 |
| 980 | _ | _ | |a VDB |
| 980 | _ | _ | |a ConvertedRecord |
| 980 | _ | _ | |a journal |
| 980 | _ | _ | |a I:(DE-Juel1)ISB-2-20090406 |
| 980 | _ | _ | |a UNRESTRICTED |
| 980 | _ | _ | |a I:(DE-Juel1)ICS-6-20110106 |
| 981 | _ | _ | |a I:(DE-Juel1)IBI-7-20200312 |
| 981 | _ | _ | |a I:(DE-Juel1)ISB-2-20090406 |
| 981 | _ | _ | |a I:(DE-Juel1)ICS-6-20110106 |
| Library | Collection | CLSMajor | CLSMinor | Language | Author |
|---|