Essential cell-intrinsic requirement for GMDS in T cell development. [PDF]
Yabas M +5 more
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Acod1/itaconate activates Nrf2 in pulmonary microvascular endothelial cells to protect against the obesity-induced pulmonary microvascular endotheliopathy. [PDF]
Zhu L +6 more
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Elucidation of interface interactions between a dehydratase domain and an acyl carrier protein in cremimycin polyketide synthase. [PDF]
Kotagiri K +8 more
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Phytoplankton dynamics shape bacterioplankton community structure and metabolism during the austral summer-autumn transition in the Western Antarctic Peninsula. [PDF]
Pavlovska M +9 more
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Itaconate suppresses house dust mite-induced allergic airways disease and Th2 cell differentiation. [PDF]
Li Y +13 more
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iNOS modulates inflammatory responses in an NO-independent manner through direct interaction with IRG1 in mitochondria. [PDF]
Diotallevi M +16 more
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Suppression of ATP-dependent (S)-NAD(P)H-hydrate dehydratase expression inhibits adipocyte differentiation of 3T3-L1 preadipocytes by increasing excessive accumulation of NADHX. [PDF]
Nakajima K +7 more
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Identification of dehydrogenase, hydratase, and aldolase responsible for the propionyl residue removal in degradation of cholic acid C-17 side chain in <i>Comamonas testosteroni</i> TA441. [PDF]
Horinouchi M.
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Pork liver has been shown to contain a soluble enzyme, L-fuconate hydro-lyase (L-fuconate dehydratase), capable of dehydrating L-fuconate to 2-keto-3-deoxy-L-fuconate. The enzyme has been partially purified. The Km for L-fuconate is 1.0 mM; D-arabonate is also an excellent substrate (Km 1.3 mM) but the enzyme is inactive with D-fuconate, L-arabonate ...
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d‐Altronate hydratase and d‐mannonate hydratase belong to a class of Fe2+‐requiring enzymes, but the function of iron in these enzymes is largely unknown. Methods are described for the convenient preparation of both these hydratases from Escherichia coli and studies related to metal activation are presented.
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