Sequence of ADH1A_MAIZE
EC Number:1.2.1.8
EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
Reaction
betaine aldehyde + NAD+ + H2O = betaine + NADH + 2 H+
Other sequences found for EC No. 1.2.1.8
EC Number:1.2.1.19
EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
Reaction
4-aminobutanal + NAD+ + H2O = 4-aminobutanoate + NADH + H+
Other sequences found for EC No. 1.2.1.19
EC Number:1.2.1.47
EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
Reaction
4-trimethylammoniobutanal + NAD+ + H2O = 4-trimethylammoniobutanoate + NADH + 2 H+
Other sequences found for EC No. 1.2.1.47
EC Number:1.2.1.54
EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
Reaction
4-guanidinobutanal + NAD+ + H2O = 4-guanidinobutanoate + NADH + H+
Other sequences found for EC No. 1.2.1.54
General information:
Sequence
0 MASPAMVPLR QLFVDGEWRP PAQGRRLPVV NPTTEAHIGE IPAGTAEDVD AAVAAARAAL
60 KRNRGRDWAR APGAVRAKYL RAIAAKVIER KPELAKLEAL DCGKPYDEAA WDMDDVAGCF
120 EYFADQAEAL DKRQNSPVSL PMETFKCHLR REPIGVVGLI TPWNYPLLMA TWKIAPALAA
180 GCTAVLKPSE LASVTCLELA DICKEVGLPS GVLNIVTGLG PDAGAPLSAH PDVDKVAFTG
240 SFETGKKIMA SAAPMVKPVT LELGGKSPIV VFDDVDIDKA VEWTLFGCFW TNGQICSATS
300 RLLIHTKIAK KFNERMVAWA KNIKVSDPLE EGCRLGPVVS EGQYEKIKKF ISNAKSQGAT
360 ILTGGVRPAH LEKGFFIEPT IITDITTSME IWREEVFGPV LCVKEFSTED EAIELANDTQ
420 YGLAGAVISG DRERCQRLSE EIDAGCIWVN CSQPCFCQAP WGGNKRSGFG RELGEGGIDN
480 YLSVKQVTEY ISDEPWGWYQ SPSKL
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Sequence Reference
Authors
Title
Journal
Volume
Pages
Year
PubMed ID
1154361
Kopecny D.,Tylichova M.,Snegaroff J.,Popelkova H.,Sebela M.
Carboxylate and aromatic active-site residues are determinants of high-affinity binding of omega-aminoaldehydes to plant aminoaldehyde dehydrogenases.
FEBS J.
278
3130-3139
2011
1154362
Schnable P.S.,Ware D.,Fulton R.S.,Stein J.C.,Wei F.,Pasternak S.,Liang C.,Zhang J.,Fulton L.,Graves T.A.,Minx P.,Reily A.D.,Courtney L.,Kruchowski S.S.,Tomlinson C.,Strong C.,Delehaunty K.,Fronick C.,Courtney B.,Rock S.M.,Belter E.,Du F.,Kim K.,Abbott R.M.,Cotton M.,Levy A.,Marchetto P.,Ochoa K.,Jackson S.M.,Gillam B.,Chen W.,Yan L.,Higginbotham J.,Cardenas M.,Waligorski J.,Applebaum E.,Phelps L.,Falcone J.,Kanchi K.,Thane T.,Scimone A.,Thane N.,Henke J.,Wang T.,Ruppert J.,Shah N.,Rotter K.,Hodges J.,Ingenthron E.,Cordes M.,Kohlberg S.,Sgro J.,Delgado B.,Mead K.,Chinwalla A.,Leonard S.,Crouse K.,Collura K.,Kudrna D.,Currie J.,He R.,Angelova A.,Rajasekar S.,Mueller T.,Lomeli R.,Scara G.,Ko A.,Delaney K.,Wissotski M.,Lopez G.,Campos D.,Braidotti M.,Ashley E.,Golser W.,Kim H.,Lee S.,Lin J.,Dujmic Z.,Kim W.,Talag J.,Zuccolo A.,Fan C.,Sebastian A.,Kramer M.,Spiegel L.,Nascimento L.,Zutavern T.,Miller B.,Ambroise C.,Muller S.,Spooner W.,Narechania A.,Ren L.,Wei S.,Kumari S.,Faga B.,Levy M.J.,McMahan L.,Van Buren P.,Vaughn M.W.,Ying K.,Yeh C.-T.,Emrich S.J.,Jia Y.,Kalyanaraman A.,Hsia A.-P.,Barbazuk W.B.,Baucom R.S.,Brutnell T.P.,Carpita N.C.,Chaparro C.,Chia J.-M.,Deragon J.-M.,Estill J.C.,Fu Y.,Jeddeloh J.A.,Han Y.,Lee H.,Li P.,Lisch D.R.,Liu S.,Liu Z.,Nagel D.H.,McCann M.C.,SanMiguel P.,Myers A.M.,Nettleton D.,Nguyen J.,Penning B.W.,Ponnala L.,Schneider K.L.,Schwartz D.C.,Sharma A.,Soderlund C.,Springer N.M.,Sun Q.,Wang H.,Waterman M.,Westerman R.,Wolfgruber T.K.,Yang L.,Yu Y.,Zhang L.,Zhou S.,Zhu Q.,Bennetzen J.L.,Dawe R.K.,Jiang J.,Jiang N.,Presting G.G.,Wessler S.R.,Aluru S.,Martienssen R.A.,Clifton S.W.,McCombie W.R.,Wing R.A.,Wilson R.K.
The B73 maize genome: complexity, diversity, and dynamics.
Science
326
1112-1115
2009
1154363
Soderlund C.,Descour A.,Kudrna D.,Bomhoff M.,Boyd L.,Currie J.,Angelova A.,Collura K.,Wissotski M.,Ashley E.,Morrow D.,Fernandes J.,Walbot V.,Yu Y.
Sequencing, mapping, and analysis of 27,455 maize full-length cDNAs.
PLoS Genet.
5
0-0
2009
1154364
Kopecny D.,Koncitikova R.,Tylichova M.,Vigouroux A.,Moskalikova H.,Soural M.,Sebela M.,Morera S.
Plant ALDH10 family: identifying critical residues for substrate specificity and trapping a thiohemiacetal intermediate.
J. Biol. Chem.
288
9491-9507
2013
