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1 se produced by Escherichia coli (ASNase) and Erwinia chrysanthemi.
2 the GH 5 endoxylanase secreted by strains of Erwinia chrysanthemi.
3 rticular the cbr locus of the plant pathogen Erwinia chrysanthemi.
4 carried on cosmid pCPP2156, was cloned from Erwinia chrysanthemi, a pathogen that differs from P. sy
5 trates in the enzymatic activity of PME from Erwinia chrysanthemi, a processive enzyme that catalyzes
6 ously reported homologous enzyme, XynA, from Erwinia chrysanthemi and analyzes the ligand binding sit
8 pe II systems from Klebsiella oxytoca (pul), Erwinia chrysanthemi and carotovora (out), Xanthomonas c
13 sequence showed 40% identity with PelE from Erwinia chrysanthemi and the pectate lyase from Glomerel
14 om Nectria haematococca, Erwinia carotovora, Erwinia chrysanthemi, and Bacillus subtilis, and a purif
15 ally homologous to the C terminus of PelB of Erwinia chrysanthemi belonging to family 1 of pectate ly
17 We report that the type III machinery of Erwinia chrysanthemi cloned in Escherichia coli recogniz
18 1,4-xylan hydrolase (xylanase A) produced by Erwinia chrysanthemi D1 isolated from corn was analyzed
20 ations were introduced into the pelC gene of Erwinia chrysanthemi EC16 that directed single or double
23 n of exoenzymes), is a close relative of the Erwinia chrysanthemi (Echr) gene pecT and encodes a memb
24 rystal structure of a bacterial homolog from Erwinia chrysanthemi (ELIC) agrees with previous structu
26 annels from Gloeobacter violaceus (GLIC) and Erwinia chrysanthemi (ELIC), whose crystal structures ar
30 C 3.2.1.8) from the bacterial plant pathogen Erwinia chrysanthemi expressed in Escherichia coli, a 45
31 Genes homologous to Escherichia coli and Erwinia chrysanthemi glucuronate and galacturonate metab
32 mensional structure of shikimate kinase from Erwinia chrysanthemi has been determined by multiple iso
33 the pentameric ligand-gated ion channel from Erwinia chrysanthemi, is a prototype for Cys-loop recept
34 ted our recently described structures of the Erwinia chrysanthemi l-asparaginase (ErA) to inform the
35 ution crystal structures of the complexes of Erwinia chrysanthemi L-asparaginase (ErA) with the produ
36 we report the x-ray crystal structure of the Erwinia chrysanthemi ligand-gated ion channel (ELIC) in
37 ptors, ion channels from prokaryote homologs-Erwinia chrysanthemi ligand-gated ion channel (ELIC), Gl
38 m, and negatively regulated by HexA (PecT in Erwinia chrysanthemi; LrhA [LysR homolog A] in Escherich
43 w that l-ases from both Escherichia coli and Erwinia chrysanthemi profoundly inhibit mTORC1 and prote
44 (typified by Escherichia coli HlyBD/TolC or Erwinia chrysanthemi PrtDEF) that utilize C-terminal sec
45 al structure of MtSK (this work) and that of Erwinia chrysanthemi SK suggest a concerted conformation
47 elicitor harpin (HrpN) of soft rot pathogen Erwinia chrysanthemi strains 3937 and EC16 is secreted v
48 When modeled based on pectate lyase C of Erwinia chrysanthemi, the RHbetaH of AlgG has a long sha
50 resembles that of pehX, an exo-PG gene from Erwinia chrysanthemi, with 47.2% identity at the amino a
51 mophilus influenzae, Pseudomonas aeruginosa, Erwinia chrysanthemi, Yersinia pseudotuberculosis, Vibri
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