Difference between revisions of "PnpA"
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* '''Expression browser:''' [http://genome.jouy.inra.fr/cgi-bin/seb/viewdetail.py?id=pnpA_1739383_1741500_1 pnpA] {{PubMed|22383849}} | * '''Expression browser:''' [http://genome.jouy.inra.fr/cgi-bin/seb/viewdetail.py?id=pnpA_1739383_1741500_1 pnpA] {{PubMed|22383849}} | ||
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* '''Regulation:''' | * '''Regulation:''' | ||
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** GP1021 (spc, based on [[pGP1331]]), available in [[Jörg Stülke]]'s lab | ** GP1021 (spc, based on [[pGP1331]]), available in [[Jörg Stülke]]'s lab | ||
** GP1076 (ermC), available in [[Jörg Stülke]]'s lab | ** GP1076 (ermC), available in [[Jörg Stülke]]'s lab | ||
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* '''Antibody:''' | * '''Antibody:''' |
Revision as of 15:16, 26 November 2012
- Description: polynucleotide phosphorylase, RNase, involved in double-strand break repair
Gene name | pnpA |
Synonyms | comR |
Essential | no |
Product | polynucleotide phosphorylase (PNPase) (EC 2.7.7.8) |
Function | DNA repair, competence development, RNA degradation |
Gene expression levels in SubtiExpress: pnpA | |
Interactions involving this protein in SubtInteract: PnpA | |
MW, pI | 77 kDa, 4.89 |
Gene length, protein length | 2115 bp, 705 aa |
Immediate neighbours | rpsO, ylxY |
Get the DNA and protein sequences (Barbe et al., 2009) | |
Genetic context This image was kindly provided by SubtiList
| |
Expression at a glance PubMed |
Contents
Categories containing this gene/protein
genetic competence, DNA repair/ recombination, Rnases
This gene is a member of the following regulons
The gene
Basic information
- Locus tag: BSU16690
Phenotypes of a mutant
- The pnpA mutant is cold sensitive and sensitive to tetracyclin, it shows multiseptate filamentous growth. PubMed
- The mutant is deficient in genetic competence (no expression of the late competence genes) PubMed
- The mutant overexpresses the trp and putB-putC-putP operons.
Database entries
- DBTBS entry: no entry
- SubtiList entry: [1]
Additional information
The protein
Basic information/ Evolution
- Catalyzed reaction/ biological activity:
- 3'-5' exoribonuclease, RNase
- PNPase degrades the trp mRNA from the RNA-TRAP complex
- involved in double-strand break (DSB) repair via homologous recombination (HR) or non-homologous end-joining (NHEJ) PubMed
- degrades ssDNA (3' --> 5') (stimulated by RecA, inhibited by SsbA) PubMed
- can polymerize ssDNA at a free 3' OH end, stimulated by RecN PubMed
- Protein family:
- Paralogous protein(s):
Extended information on the protein
- Kinetic information:
- Domains:
- Modification:
- Cofactor(s):
- Effectors of protein activity:
Database entries
- Structure: 3CDI (protein from E. coli), 3GCM (protein from E. coli, PNPase/RNase E micro-domain/RNA tetragonal crystal form )
- UniProt: P50849
- KEGG entry: [2]
- E.C. number:
Additional information
required for the expression of late competence genes comGA and comK, requirement bypassed by a mecA disruption; may be necessary for modification of the srfAA transcript (stabilization or translation activation)
Expression and regulation
- Operon:
- Regulatory mechanism:
- Additional information:
Biological materials
- Mutant: GP584 (aphA3), available in Stülke lab
- Expression vector:
- for expression, purification in E. coli with N-terminal His-tag, in pWH844: pGP838, available in Jörg Stülke's lab
- for expression/ purification from B. subtilis with N-terminal Strep-tag, for SPINE, in pGP380: pGP1342, available in Jörg Stülke's lab
- for chromosomal expression of PnpA-Strep (cat): GP1002, available in Jörg Stülke's lab
- for chromosomal expression of PnpA-Strep (spc): GP1038, available in Jörg Stülke's lab
- lacZ fusion:
- GFP fusion:
- two-hybrid system: B. pertussis adenylate cyclase-based bacterial two hybrid system (BACTH), available in Jörg Stülke's lab
- FLAG-tag construct:
- GP1021 (spc, based on pGP1331), available in Jörg Stülke's lab
- GP1076 (ermC), available in Jörg Stülke's lab
- Antibody:
Labs working on this gene/protein
David Bechhofer, Mount Sinai School, New York, USA Homepage
Your additional remarks
References
Reviews
Lehnik-Habrink M, Lewis RJ, Mäder U, Stülke J RNA degradation in Bacillus subtilis: an interplay of essential endo- and exoribonucleases. Mol Microbiol.: 2012, 84(6) 1005-1017. PubMed:22568516
Original publications
Additional publications: PubMed
PNPase in E. coli