Sequence of OLEA_XANCP
EC Number:2.3.3.20
EC Number
Recommended Name
Accession Code
Organism
No of amino acids
Molecular Weight [Da]
Source
acyl-CoA:acyl-CoA alkyltransferase
Q8PDX2
Xanthomonas campestris pv. campestris (strain ATCC 33913 / DSM 3586 / NCPPB 528 / LMG 568 / P 25)
338
36629
Reaction
2 an acyl-CoA + H2O = a (2R)-2-alkyl-3-oxoalkanoate + 2 CoA
Other sequences found for EC No. 2.3.3.20
General information:
Sequence
0 MLFQNVSIAG LAHIDAPHTL TSKEINERLQ PTYDRLGIKT DVLGDVAGIH ARRLWDQDVQ
60 ASDAATQAAR KALIDANIGI EKIGLLINTS VSRDYLEPST ASIVSGNLGV SDHCMTFDVA
120 NACLAFINGM DIAARMLERG EIDYALVVDG ETANLVYEKT LERMTSPDVT EEEFRNELAA
180 LTLGCGAAAM VMARSELVPD APRYKGGVTR SATEWNKLCR GNLDRMVTDT RLLLIEGIKL
240 AQKTFVAAKQ VLGWAVEELD QFVIHQVSRP HTAAFVKSFG IDPAKVMTIF GEHGNIGPAS
300 VPIVLSKLKE LGRLKKGDRI ALLGIGSGLN CSMAEVVW
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Sequence Reference
Authors
Title
Journal
Volume
Pages
Year
PubMed ID
580426
da Silva A.C.R.,Ferro J.A.,Reinach F.C.,Farah C.S.,Furlan L.R.,Quaggio R.B.,Monteiro-Vitorello C.B.,Van Sluys M.A.,Almeida N.F. Jr.,Alves L.M.C.,do Amaral A.M.,Bertolini M.C.,Camargo L.E.A.,Camarotte G.,Cannavan F.,Cardozo J.,Chambergo F.,Ciapina L.P.,Cicarelli R.M.B.,Coutinho L.L.,Cursino-Santos J.R.,El-Dorry H.,Faria J.B.,Ferreira A.J.S.,Ferreira R.C.C.,Ferro M.I.T.,Formighieri E.F.,Franco M.C.,Greggio C.C.,Gruber A.,Katsuyama A.M.,Kishi L.T.,Leite R.P.,Lemos E.G.M.,Lemos M.V.F.,Locali E.C.,Machado M.A.,Madeira A.M.B.N.,Martinez-Rossi N.M.,Martins E.C.,Meidanis J.,Menck C.F.M.,Miyaki C.Y.,Moon D.H.,Moreira L.M.,Novo M.T.M.,Okura V.K.,Oliveira M.C.,Oliveira V.R.,Pereira H.A.,Rossi A.,Sena J.A.D.,Silva C.,de Souza R.F.,Spinola L.A.F.,Takita M.A.,Tamura R.E.,Teixeira E.C.,Tezza R.I.D.,Trindade dos Santos M.,Truffi D.,Tsai S.M.,White F.F.,Setubal J.C.,Kitajima J.P.
Comparison of the genomes of two Xanthomonas pathogens with differing host specificities.
Nature
417
459-463
2002
580427
Frias J.A.,Richman J.E.,Erickson J.S.,Wackett L.P.
Purification and characterization of OleA from Xanthomonas campestris and demonstration of a non-decarboxylative Claisen condensation reaction.
J. Biol. Chem.
286
10930-10938
2011
580428
Christenson J.K.,Jensen M.R.,Goblirsch B.R.,Mohamed F.,Zhang W.,Wilmot C.M.,Wackett L.P.
Active multienzyme assemblies for long-chain olefinic hydrocarbon biosynthesis.
J. Bacteriol.
199
0-0
2017
580429
Goblirsch B.R.,Frias J.A.,Wackett L.P.,Wilmot C.M.
Crystal structures of Xanthomonas campestris OleA reveal features that promote head-to-head condensation of two long-chain fatty acids.
Biochemistry
51
4138-4146
2012
580430
Goblirsch B.R.,Jensen M.R.,Mohamed F.A.,Wackett L.P.,Wilmot C.M.
Substrate trapping in crystals of the thiolase OleA identifies three channels that enable long chain olefin biosynthesis.
J. Biol. Chem.
291
26698-26706
2016
580431
Jensen M.R.,Goblirsch B.R.,Christenson J.K.,Esler M.A.,Mohamed F.A.,Wackett L.P.,Wilmot C.M.
OleA Glu117 is key to condensation of two fatty-acyl coenzyme A substrates in long-chain olefin biosynthesis.
Biochem. J.
474
3871-3886
2017
580433
Jensen M.R.,Goblirsch B.R.,Esler M.A.,Christenson J.K.,Mohamed F.A.,Wackett L.P.,Wilmot C.M.
The role of OleA His285 in orchestration of long-chain acyl-coenzyme A substrates.
FEBS Lett.
592
987-998
2018
