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Sequence of ICS1_CAMIR

EC Number:2.1.1.159

EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
theobromine synthase
Q2HXL9
Camellia irrawadiensis
365
40937
Reaction
S-adenosyl-L-methionine + 7-methylxanthine = S-adenosyl-L-homocysteine + 3,7-dimethylxanthine

General information:

Sequence
show sequence in fasta format
  0 MGKVNEVLFM NRGEGEISYA QNSAFTQKVA SMAMPALENA VETLFSKDFH LLQALTAADL
 60 GCAAGPNTFA VISTIKRMME KKCRELYCQT LELQVYLNDL FGNDFNTLFK GLSSEVVGNK
120 CEEVSCYVMG VPGSFHGRLF PRNSLHLVHS SYSVHWLTQA PKGLTSREGL ALNKGKIYIS
180 KTSPPVVKEA YLSQFHEDFT MFLNARSQEV VPNGCMVLIL HGRQSSDPSE MESCFTWELL
240 AIAIAELVSQ GLIDEDKLDT FNVPSYWPSL EEVKDIVERD GSFTIDHLEG FELDSLEMQE
300 NDKWVRGDKF AKMVRAFTEP IISNQFGHEI MDKLYDKFTH ILVSDLEAEL PKTTSIILVL
360 SKIVG
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Sequence related references
Sequence Reference
Authors
Title
Journal
Volume
Pages
Year
PubMed ID
788310
Yoneyama N.,Morimoto H.,Ye C.-X.,Ashihara H.,Mizuno K.,Kato M.
Substrate specificity of N-methyltransferase involved in purine alkaloids synthesis is dependent upon one amino acid residue of the enzyme.
Mol. Genet. Genomics
275
125-135
2006
788311
Jin J.-Q.,Yao M.-Z.,Ma C.-L.,Ma J.-Q.,Chen L.
Natural allelic variations of TCS1 play a crucial role in caffeine biosynthesis of tea plant and its related species.
Plant Physiol. Biochem.
100
18-26
2016