Sulfonation of glycopeptide antibiotics by sulfotransferase StaL depends on conformational flexibility of aglycone scaffold
about
Opportunities for synthetic biology in antibiotics: expanding glycopeptide chemical diversity.Glycopeptide antibiotic biosynthesis.Catalytic promiscuity of glycopeptide N-methyltransferases enables bio-orthogonal labelling of biosynthetic intermediates.Harnessing the synthetic capabilities of glycopeptide antibiotic tailoring enzymes: characterization of the UK-68,597 biosynthetic cluster.
P2860
Sulfonation of glycopeptide antibiotics by sulfotransferase StaL depends on conformational flexibility of aglycone scaffold
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Sulfonation of glycopeptide an ...... exibility of aglycone scaffold
@ast
Sulfonation of glycopeptide an ...... exibility of aglycone scaffold
@en
type
label
Sulfonation of glycopeptide an ...... exibility of aglycone scaffold
@ast
Sulfonation of glycopeptide an ...... exibility of aglycone scaffold
@en
prefLabel
Sulfonation of glycopeptide an ...... exibility of aglycone scaffold
@ast
Sulfonation of glycopeptide an ...... exibility of aglycone scaffold
@en
P2093
P2860
P356
P1476
Sulfonation of glycopeptide an ...... exibility of aglycone scaffold
@en
P2093
Christine Munger
Lindsay Kalan
Miroslaw Cygler
Traian Sulea
P2860
P304
11824-11829
P356
10.1073/PNAS.1205377109
P407
P577
2012-07-02T00:00:00Z