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1 rmediates or undergoes hyperoxidation to the sulfinic acid.
2 on and protect against hyperoxidation to the sulfinic acid.
3 ate Cys levels through converting Cys to Cys sulfinic acid.
4 enation of cysteine by O(2) to give cysteine sulfinic acid.
5 yzes the oxidation of l-cysteine to cysteine sulfinic acid.
6  the thiol residue of the cysteine switch to sulfinic acid.
7 cysteine switch domain had been converted to sulfinic acid.
8 earing substrates to yield the corresponding sulfinic acid.
9 tions based on the unique nucleophilicity of sulfinic acids.
10 e substituted sulfinamides that hydrolyze to sulfinic acids.
11 cts; other minor products including cysteine sulfinic acid (+32 Da mass shift) and serine (-16 Da mas
12 plet-sensitized photodegradation of cysteine sulfinic acid, a (photo)degradation product of cysteine,
13  is subsequently hydrolyzed back to cysteine sulfinic acid and AMP in a futile cycle.
14  a comeback: The inefficient condensation of sulfinic acid and aryl nitroso compounds has been transf
15 cs of two alternative substrates: L-cysteine sulfinic acid and d-aspartate.
16  competitive C-S bond cleavage giving phenyl sulfinic acid and ionization to diphenyl sulfide radical
17 rsion of amino-terminal cysteine to cysteine sulfinic acid and is related to the plant cysteine oxida
18 , C-S bond cleavage, finally leading to aryl sulfinic acid and sensitized oxidation leading to S-oxid
19 oxy nitroso compounds to AhpC C165S yields a sulfinic acid and sulfinamide modification.
20                     Here we demonstrate that sulfinic acids and nitrosothiols react to form a stable
21 alyze decarboxylation of aspartate, cysteine sulfinic acid, and cysteic acid to beta-alanine, hypotau
22 enic acid oxoform from the thiol, disulfide, sulfinic acid, and S-nitrosated forms of cysteine while
23          In addition, the MS data identified sulfinic acid as the irreversibly inactivated enzyme spe
24 dize further to the irreversibly inactivated sulfinic acid, as determined by using kinetic partitioni
25 herited parkinsonism, readily forms cysteine-sulfinic acid at a conserved cysteine residue (Cys106 in
26                       We observed a cysteine-sulfinic acid at C106 in crystalline DJ-1 but no modific
27 e that PCO dioxygenase activity produces Cys-sulfinic acid at the N terminus of an ERF-VII peptide, w
28                                   L-cysteine sulfinic acid bound with higher affinity than L-aspartat
29 the conversion of cysteine (Cys) to cysteine sulfinic acid by an unclarified mechanism.
30 ne begins with its sulfoxidation to cysteine sulfinic acid by the enzyme cysteine dioxygenase (CDO).
31 ulfinated proteins, confirming that a single sulfinic acid can react with a nitrosothiol to form a th
32            Prior work showed that L-cysteine sulfinic acid competitively inhibits this enzyme by inte
33 that results in the accumulation of cysteine sulfinic acid (CSA) in glioblastoma.
34  such as homocysteic acid (HCA) and cysteine sulfinic acid (CSA), which may cause seizures and excito
35 eversible metabolism of cysteine to cysteine sulfinic acid (CSA).
36                                     Cysteine sulfinic acid (Cys-SO 2 H), a modification of reactive c
37 oxins (Prxs) undergo reversible oxidation to sulfinic acid (Cys-SO2H) and the reduction reaction is c
38 rx enzymes undergoes reversible oxidation to sulfinic acid (Cys-SO2H) during catalysis, and sulfiredo
39            Among many proteins with cysteine sulfinic acid (Cys-SO2H) residues, the sulfinic forms of
40 duced Cys(34), whereas the levels of Cys(34) sulfinic acid (Cys-SO2H), Cys(34)-sulfonic acid (Cys-SO3
41 s-SOH moiety can react with H2O2 to form Cys sulfinic acid (Cys-SO2H), resulting in inactivation.
42  reaction, the reduction of protein cysteine sulfinic acid, Cys-SO(2)(-).
43 onally relevant reversible and irreversible (sulfinic acid; Cys to dehydroalanine) oxidations of GAPD
44 esizing enzyme in the brain, namely cysteine sulfinic acid decarboxylase (CSAD), is activated when ph
45 omics interaction revealed that the cysteine sulfinic acid decarboxylase (CSAD)-regulated taurine pat
46 enosylhomocysteine (SAH) hydrolase, cysteine sulfinic acid decarboxylase, and oxidation-reduction pat
47 ase B, sarcosine dehydrogenase, and cysteine sulfinic acid decarboxylase, are involved in carbohydrat
48 n enzyme that catalyzes the reduction of Cys-sulfinic acid derivatives of 2-Cys peroxiredoxins (2-Cys
49 d lays the groundwork for the development of sulfinic acid detection methods in biological systems.
50                               While cysteine sulfinic acid did not itself constitute a clinically use
51                    In physiological buffers, sulfinic acids do not react with iodoacetamide or disulf
52 ine in typical 2-Cys peroxiredoxins (Prx) to sulfinic acid during oxidative stress plays an important
53 e hydroxide (LDH) nanosheets and formamidine sulfinic acid (FAS), followed by spray-coating with a po
54 sidue can be permanently overoxidized to the sulfinic acid form, and (ii) Sec protects the body of th
55 ntioxidant enzyme peroxiredoxin (Prx) to the sulfinic acid form, Prx-SO(2)(-).
56 rovides molecular evidence of N-terminal Cys-sulfinic acid formation and arginylation by N-end rule p
57 Several stimuli, including peroxide-mediated sulfinic acid formation at the active site cysteine, hav
58 homologues are likely stabilized by cysteine-sulfinic acid formation but destabilized by further oxid
59       For proteins such as Prx VI and GAPDH, sulfinic acid formation might be an irreversible process
60 eroxiredoxin, whose oxidative stress-induced sulfinic acid formation turns the peroxidase into a mole
61 on oxygenases that catalyze the formation of sulfinic acids from sulfhydryl-containing substrates and
62               The oxidation of Cys106 to the sulfinic acid had minimal effect on the structural prope
63                    The formation of cysteine-sulfinic acid has recently become appreciated as a modif
64 and generation of cysteine sulfonic acid and sulfinic acid; however, the rate of oxidation is signifi
65  in DJ-1 is oxidized readily to the cysteine-sulfinic acid in both flies and humans, and this may reg
66 " is oxidized to either cysteine sulfenic or sulfinic acid in the two molecules in the asymmetric uni
67 ible-light-driven generation of a weak acid (sulfinic acid, in nitrogen-purged solutions) or a strong
68                   Unlike either the cysteine sulfinic acid interaction with AS-B or the sulfoximine i
69  presumably via the unstable doubly oxidized sulfinic acid intermediate.
70  into a chemoselective process that converts sulfinic acid into stable cyclic sulfonamide analogues (
71  therefore conclude that formation of Cys106-sulfinic acid is a key modification that regulates the p
72           Here, we demonstrate that cysteine sulfinic acid is also a partial substrate for E. coli as
73              Thiol oxidation to dioxygenated sulfinic acid is catalyzed by an enzyme family character
74 on of two cysteine thiolates to sulfenic and sulfinic acids is essential for enzyme activity.
75 olism, the oxidation of cysteine to cysteine sulfinic acid, is catalyzed by cysteine dioxygenase (CDO
76 increased oxidant stress confirmed cysteinyl sulfinic acid (m/z 435), sulfonic acid (m/z 443), and di
77            Conversely, substitution with the sulfinic acid mimic aspartic acid resulted in constituti
78 e, the scope and biological role of sulfenic/sulfinic acid modifications have been recently expanded
79                                  The Cys(52) sulfinic acid moiety was substituted by mutating this re
80                The reduction of the cysteine sulfinic acid moiety within the active site of the Prx b
81 direct quantitative determination of methane sulfinic acid (MSA) produced by hydroxyl radical oxidati
82 the addition of two oxygen atoms to form the sulfinic acid of Cys106 (2O DJ-1) (no 1O oxidized state
83  as well as cysteine oxidation determined as sulfinic acid on alpha-Cys-104 and sulfonic acid on alph
84  by intraseptal injection of L-AP4, cysteine sulfinic acid or DHPG.
85  site disulfide and a reduction irreversible sulfinic acid or sulfinamide modification at Cys244.
86   The latter was converted to closo-1,12-bis(sulfinic acid)-p-carborane (13) via H(+)-exchange.
87  obtained directly in 88% yield by heating 1-sulfinic acid-p-carborane (17) in H(2)O(2) (30%).
88 to the sulfinic moiety of PrxI to generate a sulfinic acid phosphoryl ester (Prx-Cys-S(=O)OPO3(2-)).
89 n (18)O exchange study revealed that the Prx sulfinic acid phosphoryl ester is rapidly formed and hyd
90 s, procedures for the diversification of the sulfinic acid products into a range of medicinally relev
91 ormation between simple terminal alkynes and sulfinic acids provides access to various alpha-substitu
92                          Sodium salt of aryl sulfinic acid reacts with enynone in a different manner,
93 resh muscle or kidney extracts with cysteine sulfinic acid resulted in the detection of hypotaurine o
94                        In addition, although sulfinic acid [RS(O)OH] formation is observed upon prolo
95                         One-pot reactions of sulfinic acid salts (produced from organometallic reagen
96 alization of enamides and enecarbamates with sulfinic acid salts and alcohols is described.
97                                          The sulfinic acid salts were prepared from the reaction of t
98  various other proteins are also oxidized to sulfinic acid, suggesting that formation of Cys-SO2H mig
99 rometric analysis identified the products as sulfinic acid, sulfonic acid, and a dimer containing a d
100 function of Srx is the reduction of cysteine sulfinic acid to sulfenic acid in proteins subject to ox
101 rminal cysteine of ERF-VIIs to form cysteine sulfinic acid, triggering degradation via the Cys/Arg br
102  E18Q, allow Cys106 to be oxidized to Cys106-sulfinic acid under mild conditions.
103 e-containing proteins to their corresponding sulfinic acids using O(2) as a cosubstrate.
104 (sp(3))-H bonds into the corresponding alkyl sulfinic acids via decatungstate photocatalysis.
105 cells, the initial formation rate of methane sulfinic acid was significantly lower in cells containin
106 ese proteins to oxidize cysteine to cysteine sulfinic acid was then compared against recombinant rat
107 duct analysis indicated cystine and cysteine sulfinic acid were the major photooxidation products.
108 alyzes the oxidation of cysteine to cysteine sulfinic acid, which is the first major step in cysteine
109  of cysteine with dioxygen to yield cysteine sulfinic acid, which lies at the branching point of cyst
110 roduct from nucleophilic addition eliminates sulfinic acid, yielding a propargylic diazene that perfo

 
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