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PDBsum entry 4oir
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Transcription, transferase/antibiotic
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PDB id
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4oir
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Contents |
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231 a.a.
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1112 a.a.
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1485 a.a.
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94 a.a.
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346 a.a.
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PDB id:
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| Name: |
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Transcription, transferase/antibiotic
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Title:
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Crystal structure of thermus thermophilus RNA polymerase transcription initiation complex soaked with ge23077 and rifamycin sv
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Structure:
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DNA-directed RNA polymerase subunit alpha. Chain: a, b. Synonym: rnap subunit alpha, RNA polymerase subunit alpha, transcriptase subunit alpha. DNA-directed RNA polymerase subunit beta. Chain: c. Synonym: rnap subunit beta, RNA polymerase subunit beta, transcriptase subunit beta. DNA-directed RNA polymerase subunit beta'.
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Source:
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Thermus thermophilus. Organism_taxid: 300852. Strain: hb8 / atcc 27634 / dsm 579. Gene: rpod, ttha0532. Expressed in: escherichia coli. Expression_system_taxid: 469008. Synthetic: yes. Actinomadura sp.. Organism_taxid: 1989
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Resolution:
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3.11Å
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R-factor:
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0.209
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R-free:
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0.253
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Authors:
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Y.Zhang,R.H.Ebright,E.Arnold
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Key ref:
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Y.Zhang
et al.
(2014).
GE23077 binds to the RNA polymerase 'i' and 'i+1' sites and prevents the binding of initiating nucleotides.
Elife,
3,
e02450.
PubMed id:
DOI:
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Date:
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20-Jan-14
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Release date:
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07-May-14
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PROCHECK
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Headers
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References
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Q5SHR6
(RPOA_THET8) -
DNA-directed RNA polymerase subunit alpha from Thermus thermophilus (strain ATCC 27634 / DSM 579 / HB8)
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Seq: Struc:
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315 a.a.
231 a.a.
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Q8RQE9
(RPOB_THET8) -
DNA-directed RNA polymerase subunit beta from Thermus thermophilus (strain ATCC 27634 / DSM 579 / HB8)
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Seq: Struc:
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1119 a.a.
1112 a.a.
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Q8RQE8
(RPOC_THET8) -
DNA-directed RNA polymerase subunit beta' from Thermus thermophilus (strain ATCC 27634 / DSM 579 / HB8)
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Seq: Struc:
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1524 a.a.
1485 a.a.
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Enzyme class:
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Chains A, B, C, D, E:
E.C.2.7.7.6
- DNA-directed Rna polymerase.
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Reaction:
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RNA(n) + a ribonucleoside 5'-triphosphate = RNA(n+1) + diphosphate
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RNA(n)
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+
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ribonucleoside 5'-triphosphate
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=
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RNA(n+1)
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+
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diphosphate
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Molecule diagrams generated from .mol files obtained from the
KEGG ftp site
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DOI no:
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Elife
3:e02450
(2014)
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PubMed id:
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GE23077 binds to the RNA polymerase 'i' and 'i+1' sites and prevents the binding of initiating nucleotides.
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Y.Zhang,
D.Degen,
M.X.Ho,
E.Sineva,
K.Y.Ebright,
Y.W.Ebright,
V.Mekler,
H.Vahedian-Movahed,
Y.Feng,
R.Yin,
S.Tuske,
H.Irschik,
R.Jansen,
S.Maffioli,
S.Donadio,
E.Arnold,
R.H.Ebright.
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ABSTRACT
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Using a combination of genetic, biochemical, and structural approaches, we show
that the cyclic-peptide antibiotic GE23077 (GE) binds directly to the bacterial
RNA polymerase (RNAP) active-center 'i' and 'i+1' nucleotide binding sites,
preventing the binding of initiating nucleotides, and thereby preventing
transcription initiation. The target-based resistance spectrum for GE is
unusually small, reflecting the fact that the GE binding site on RNAP includes
residues of the RNAP active center that cannot be substituted without loss of
RNAP activity. The GE binding site on RNAP is different from the rifamycin
binding site. Accordingly, GE and rifamycins do not exhibit cross-resistance,
and GE and a rifamycin can bind simultaneously to RNAP. The GE binding site on
RNAP is immediately adjacent to the rifamycin binding site. Accordingly,
covalent linkage of GE to a rifamycin provides a bipartite inhibitor having very
high potency and very low susceptibility to target-based resistance. DOI:
http://dx.doi.org/10.7554/eLife.02450.001.
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');
}
}
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