Structural investigation of ribosomally synthesized natural products by hypothetical structure enumeration and evaluation using tandem MS.

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Structural investigation of ribosomally synthesized natural products by hypothetical structure enumeration and evaluation using tandem MS. is …
instance of (P31):
scholarly articleQ13442814

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P819ADS bibcode2014PNAS..11112031Z
P356DOI10.1073/PNAS.1406418111
P932PMC publication ID4143002
P698PubMed publication ID25092299
P5875ResearchGate publication ID264501417

P50authorWilfred van der DonkQ42054552
Yanxiang ShiQ60143800
P2093author name stringManuel Ortega
Qi Zhang
Huan Wang
Douglas A Mitchell
Joel O Melby
Weixin Tang
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Ribosomally synthesized and post-translationally modified peptide natural products: overview and recommendations for a universal nomenclatureQ34312732
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Identification of a novel two-peptide lantibiotic, lichenicidin, following rational genome mining for LanM proteins.Q37333234
Distributive and directional behavior of lantibiotic synthetases revealed by high-resolution tandem mass spectrometry.Q37335058
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Determining the structure and mode of action of microbisporicin, a potent lantibiotic active against multiresistant pathogens.Q43570394
Structural characterization of lacticin 3147, a two-peptide lantibiotic with synergistic activity.Q44800747
Structure revision of the lantibiotic 97518.Q46080850
Posttranslational heterocyclization of cysteine and serine residues in the antibiotic microcin B17: distributivity and directionalityQ73201411
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P433issue33
P407language of work or nameEnglishQ1860
P921main subjectnatural productQ901227
P304page(s)12031-12036
P577publication date2014-08-04
P1433published inProceedings of the National Academy of Sciences of the United States of AmericaQ1146531
P1476titleStructural investigation of ribosomally synthesized natural products by hypothetical structure enumeration and evaluation using tandem MS
P478volume111

Reverse relations

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