Sequence of MPPJ_STRHY
EC Number:2.1.1.281
EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
Reaction
S-adenosyl-L-methionine + 3-phenylpyruvate = S-adenosyl-L-homocysteine + (3S)-2-oxo-3-phenylbutanoate
Other sequences found for EC No. 2.1.1.281
General information:
Sequence
0 MSTEVSEAQA RRAVADIFNS TLASSAIGAA WELGALDELR ENGKLDVSDF AVRHDLHEPA
60 VVGMFTALAS VGIVRREGAT VVVGPYFDEA NHHRSLFHWL NQGSGELFRR MPQVLPNENR
120 TGKFYQRDAG AISYACREIS ERYFDPAFWA AVDGLGYTPT TVADLGSGSG ERLIQIARRF
180 PGVRGLGVDI ADGAIAMAEK EVAAKGFGDQ ISFVRGDART IDQVSARGEF AEVDLLTCFM
240 MGHDFWPREN CVQTLRKLRA AFPNVRRFLL GDATRTVGIP DRELPVFTLG FEFGHDMMGV
300 YLPTLDEWDG VFEEGGWRCV KKHAIDSLSV SVVFELE
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Sequence Reference
Authors
Title
Journal
Volume
Pages
Year
PubMed ID
1086047
Magarvey N.A.,Haltli B.,He M.,Greenstein M.,Hucul J.A.
Biosynthetic pathway for mannopeptimycins, lipoglycopeptide antibiotics active against drug-resistant gram-positive pathogens.
Antimicrob. Agents Chemother.
50
2167-2177
2006
1086048
Huang Y.T.,Lyu S.Y.,Chuang P.H.,Hsu N.S.,Li Y.S.,Chan H.C.,Huang C.J.,Liu Y.C.,Wu C.J.,Yang W.B.,Li T.L.
In vitro characterization of enzymes involved in the synthesis of nonproteinogenic residue (2S,3S)-beta-methylphenylalanine in glycopeptide antibiotic mannopeptimycin.
ChemBioChem
10
2480-2487
2009
