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Items: 1 to 20 of 122

1.

Identification of a hotdog fold thioesterase involved in the biosynthesis of menaquinone in Escherichia coli.

Chen M, Ma X, Chen X, Jiang M, Song H, Guo Z.

J Bacteriol. 2013 Jun;195(12):2768-75. doi: 10.1128/JB.00141-13. Epub 2013 Apr 5.

2.

Divergence of substrate specificity and function in the Escherichia coli hotdog-fold thioesterase paralogs YdiI and YbdB.

Latham JA, Chen D, Allen KN, Dunaway-Mariano D.

Biochemistry. 2014 Jul 29;53(29):4775-87. doi: 10.1021/bi500333m. Epub 2014 Jul 18.

3.

Phylloquinone (vitamin K(1) ) biosynthesis in plants: two peroxisomal thioesterases of Lactobacillales origin hydrolyze 1,4-dihydroxy-2-naphthoyl-CoA.

Widhalm JR, Ducluzeau AL, Buller NE, Elowsky CG, Olsen LJ, Basset GJ.

Plant J. 2012 Jul;71(2):205-15. doi: 10.1111/j.1365-313X.2012.04972.x. Epub 2012 Jun 19.

4.

A dedicated thioesterase of the Hotdog-fold family is required for the biosynthesis of the naphthoquinone ring of vitamin K1.

Widhalm JR, van Oostende C, Furt F, Basset GJ.

Proc Natl Acad Sci U S A. 2009 Apr 7;106(14):5599-603. doi: 10.1073/pnas.0900738106. Epub 2009 Mar 25.

5.

Functional convergence of structurally distinct thioesterases from cyanobacteria and plants involved in phylloquinone biosynthesis.

Furt F, Allen WJ, Widhalm JR, Madzelan P, Rizzo RC, Basset G, Wilson MA.

Acta Crystallogr D Biol Crystallogr. 2013 Oct;69(Pt 10):1876-88. doi: 10.1107/S0907444913015771. Epub 2013 Sep 20.

6.
8.

A novel paradigm of fatty acid beta-oxidation exemplified by the thioesterase-dependent partial degradation of conjugated linoleic acid that fully supports growth of Escherichia coli.

Nie L, Ren Y, Janakiraman A, Smith S, Schulz H.

Biochemistry. 2008 Sep 9;47(36):9618-26. doi: 10.1021/bi801074e. Epub 2008 Aug 15.

PMID:
18702504
9.
10.

A bicarbonate cofactor modulates 1,4-dihydroxy-2-naphthoyl-coenzyme a synthase in menaquinone biosynthesis of Escherichia coli.

Jiang M, Chen M, Guo ZF, Guo Z.

J Biol Chem. 2010 Sep 24;285(39):30159-69. doi: 10.1074/jbc.M110.147702. Epub 2010 Jul 19.

11.
12.

Structure and catalysis in the Escherichia coli hotdog-fold thioesterase paralogs YdiI and YbdB.

Wu R, Latham JA, Chen D, Farelli J, Zhao H, Matthews K, Allen KN, Dunaway-Mariano D.

Biochemistry. 2014 Jul 29;53(29):4788-805. doi: 10.1021/bi500334v. Epub 2014 Jul 18.

13.
14.

Aerobic culture of Propionibacterium freudenreichii ET-3 can increase production ratio of 1,4-dihydroxy-2-naphthoic acid to menaquinone.

Furuichi K, Hojo K, Katakura Y, Ninomiya K, Shioya S.

J Biosci Bioeng. 2006 Jun;101(6):464-70.

PMID:
16935247
15.

Identification and characterization of Escherichia coli thioesterase III that functions in fatty acid beta-oxidation.

Nie L, Ren Y, Schulz H.

Biochemistry. 2008 Jul 22;47(29):7744-51. doi: 10.1021/bi800595f. Epub 2008 Jun 25.

PMID:
18576672
16.

Menaquinone (vitamin K2) biosynthesis: localization and characterization of the menA gene from Escherichia coli.

Suvarna K, Stevenson D, Meganathan R, Hudspeth ME.

J Bacteriol. 1998 May;180(10):2782-7.

17.

Benzoyl-coenzyme A thioesterase of Azoarcus evansii: properties and function.

Ismail W.

Arch Microbiol. 2008 Oct;190(4):451-60. doi: 10.1007/s00203-008-0393-3. Epub 2008 Jun 10.

PMID:
18542924
18.

A derivative of the menaquinone precursor 1,4-dihydroxy-2-naphthoate is involved in the reductive transformation of carbon tetrachloride by aerobically grown Shewanella oneidensis MR-1.

Ward MJ, Fu QS, Rhoads KR, Yeung CH, Spormann AM, Criddle CS.

Appl Microbiol Biotechnol. 2004 Feb;63(5):571-7. Epub 2003 Aug 8.

PMID:
12908086
19.
20.

Co-evolution of HAD phosphatase and hotdog-fold thioesterase domain function in the menaquinone-pathway fusion proteins BF1314 and PG1653.

Wang M, Song F, Wu R, Allen KN, Mariano PS, Dunaway-Mariano D.

FEBS Lett. 2013 Sep 2;587(17):2851-9. doi: 10.1016/j.febslet.2013.07.009. Epub 2013 Jul 10.

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