Sequence of HMAS_AMYOR
EC Number:1.1.3.46
EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
Reaction
(S)-4-hydroxymandelate + O2 = 2-(4-hydroxyphenyl)-2-oxoacetate + H2O2
Other sequences found for EC No. 1.1.3.46
EC Number:1.13.11.46
EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
Reaction
4-hydroxyphenylpyruvate + O2 = (S)-4-hydroxymandelate + CO2
Other sequences found for EC No. 1.13.11.46
General information:
Sequence
0 MQNFEIDYVE MYVENLEVAA FSWVDKYAFA VAGTSRSADH RSIALRQGQV TLVLTEPTSD
60 RHPAAAYLQT HGDGVADIAM ATSDVAAAYE AAVRAGAEAV RAPGQHSEAA VTTATIGGFG
120 DVVHTLIQRD GTSAELPPGF TGSMDVTNHG KGDVDLLGID HFAICLNAGD LGPTVEYYER
180 ALGFRQIFDE HIVVGAQAMN STVVQSASGA VTLTLIEPDR NADPGQIDEF LKDHQGAGVQ
240 HIAFNSNDAV RAVKALSERG VEFLKTPGAY YDLLGERITL QTHSLDDLRA TNVLADEDHG
300 GQLFQIFTAS THPRHTIFFE VIERQGAGTF GSSNIKALYE AVELERTGQS EFGAARR
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Sequence Reference
Authors
Title
Journal
Volume
Pages
Year
PubMed ID
938370
van Wageningen A.,Kirkpatrick P.,Williams D.,Harris B.,Kershaw J.,Lennard N.,Jones M.,Jones S.,Solenberg P.
Sequencing and analysis of genes involved in the biosynthesis of a vancomycin group antibiotic.
Chem. Biol.
5
155-162
1998
938371
Hubbard B.K.,Thomas M.G.,Walsh C.T.
Biosynthesis of L-p-hydroxyphenylglycine, a non-proteinogenic amino acid constituent of peptide antibiotics.
Chem. Biol.
7
931-942
2000
938372
Brownlee J.,He P.,Moran G.R.,Harrison D.H.
Two roads diverged: the structure of hydroxymandelate synthase from Amycolatopsis orientalis in complex with 4-hydroxymandelate.
Biochemistry
47
2002-2013
2008
