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1                              Accumulation of triosephosphates arising from high cytosolic glucose con
2 ate in the liver, one involved in generating triosephosphate from glycerol and the other involved in
3 e benfotiamine countered the accumulation of triosephosphates in experimental diabetes and inhibited
4                         We apply MPAX to the triosephosphate isomerase (beta/alpha)(8) barrel, accura
5 r the effect of the S96P mutation in chicken triosephosphate isomerase (cTIM) has been analyzed using
6 ructose-bisphosphate aldolase (EC 4.1.2.13), triosephosphate isomerase (EC 5.3.1.1), and glycerol-3-p
7                 Loop 6 in the active site of Triosephosphate Isomerase (Saccharomyces cerevisiae) mov
8 e kinetic parameters for activation of yeast triosephosphate isomerase (ScTIM), yeast orotidine monop
9 e origin for the functional specificities of triosephosphate isomerase (TIM) and methylglyoxal syntha
10                                              Triosephosphate isomerase (TIM) barrel proteins have not
11                PtmU3 adopts an unprecedented triosephosphate isomerase (TIM) barrel structural fold f
12          At one end of the HydG (betaalpha)8 triosephosphate isomerase (TIM) barrel, a canonical [4Fe
13 n of (R)-glyceraldehyde 3-phosphate (GAP) by triosephosphate isomerase (TIM) can be attributed to the
14                  D-Xylose isomerase (XI) and triosephosphate isomerase (TIM) catalyze the aldose-keto
15            Three mechanisms proposed for the triosephosphate isomerase (TIM) catalyzed reactions were
16                                              Triosephosphate isomerase (TIM) catalyzes the interconve
17                                              Triosephosphate isomerase (TIM) catalyzes the reversible
18                                              Triosephosphate isomerase (TIM) catalyzes the reversible
19  side chains of Y208 and S211 from loop 7 of triosephosphate isomerase (TIM) form hydrogen bonds to b
20 phate (DHAP) in D(2)O at pD 7.9 catalyzed by triosephosphate isomerase (TIM) from chicken and rabbit
21 te (GAP) in D(2)O at pD 7.5-7.9 catalyzed by triosephosphate isomerase (TIM) from chicken and rabbit
22  more likely to be stabilizing in our model, triosephosphate isomerase (TIM) from Saccharomyces cerev
23          We report that the K12G mutation in triosephosphate isomerase (TIM) from Saccharomyces cerev
24 GAP) to dihydroxyacetone phosphate (DHAP) by triosephosphate isomerase (TIM) from Trypanosoma brucei
25                        The L232A mutation in triosephosphate isomerase (TIM) from Trypanosoma brucei
26  simulations of the folding and unfolding of triosephosphate isomerase (TIM) from yeast were conducte
27 transfer steps in the reactions catalyzed by triosephosphate isomerase (TIM) has been studied.
28                                   The enzyme triosephosphate isomerase (TIM) has been used as a model
29 imulations are used to study the dynamics of triosephosphate isomerase (TIM) in complex with glycerol
30  carbonyl carbon ([1-(13)C]-GA) catalyzed by triosephosphate isomerase (TIM) in D(2)O at pD 7.0 in th
31 s for many enzymes, the enzymatic pathway of triosephosphate isomerase (TIM) includes the partially r
32                                   The enzyme triosephosphate isomerase (TIM) is a model of catalytic
33                                              Triosephosphate isomerase (TIM) is a proficient catalyst
34                            The Omega loop of triosephosphate isomerase (TIM) is important for prevent
35 talline uniformly (13)C,(15)N-enriched yeast triosephosphate isomerase (TIM) is sequentially assigned
36                   The K12G mutation at yeast triosephosphate isomerase (TIM) results in a 5.5 x 10(5)
37             Methylglyoxal synthase (MGS) and triosephosphate isomerase (TIM) share neither sequence n
38                         The tunnel region at triosephosphate isomerase (TIM)'s dimer interface, dista
39 e, we designed several consensus variants of triosephosphate isomerase (TIM), a large, diverse family
40     Unfolding and refolding of rabbit muscle triosephosphate isomerase (TIM), a model for (betaalpha)
41 xtent to which sites evolve codependently in triosephosphate isomerase (TIM), a ubiquitous glycolytic
42      Results are featured for three enzymes: triosephosphate isomerase (TIM), aldose reductase (AR),
43                                              Triosephosphate isomerase (TIM), an enzyme of the glycol
44 ldehyde 3-phosphate (GAP) bound to wild-type triosephosphate isomerase (TIM), as well as to the K12G,
45 nalysis of the catalytic cycle of the enzyme triosephosphate isomerase (TIM), including both the reac
46 G is a competitive inhibitor of both MGS and triosephosphate isomerase (TIM), the carboxylate groups
47 alidated (out of 12 identified), including a triosephosphate isomerase (TIM)-barrel protein that like
48                     In the case of the human triosephosphate isomerase (TPI gene), nonsense codons lo
49 in MS, we identified the glycolytic enzymes, triosephosphate isomerase (TPI) and GAPDH, using Igs fro
50        We show that the drug interferes with triosephosphate isomerase (TPI) causing release of methy
51 t causes phenotypes analogous to symptoms of triosephosphate isomerase (TPI) deficiency, a human fami
52 ilies with the inherited glycolytic disorder triosephosphate isomerase (TPI) deficiency.
53             Individuals with 50% of expected triosephosphate isomerase (TPI) enzyme activity have bee
54                  Of the proteins identified, triosephosphate isomerase (TPI) exhibited a strong affin
55              We examine the evolution of the triosephosphate isomerase (TPI) gene family in fishes fo
56 >A), and -24 (TPI 573 T-->G) variants in the triosephosphate isomerase (TPI) gene occurred frequently
57 including position 192 of the human gene for triosephosphate isomerase (TPI) have been found to reduc
58 erited deficiency of the housekeeping enzyme triosephosphate isomerase (TPI) is the most severe clini
59  constructs containing a portion of the rice triosephosphate isomerase (tpi) promoter, the first tpi
60 extracts of PV4-8 had 3-fold higher level of triosephosphate isomerase (TPI) specific activities than
61 mediated inhibition of the glycolytic enzyme triosephosphate isomerase (TPI) through demalonylation o
62 etermined to be a mutated glycolytic enzyme, triosephosphate isomerase (TPI).
63 oxidase I (COIB) and the Z-chromosome-linked Triosephosphate isomerase (Tpi).
64 affected gene encodes the glycolytic enzyme, triosephosphate isomerase (Tpi).
65 essfully verified, namely cystatin B (CSTB), triosephosphate isomerase (TPI1), and deleted in maligna
66  IgE-binding capacity (10%-49%), followed by triosephosphate isomerase (TPI; 19%-34%) in raw and trop
67 ng enzymes sponsoring glycolysis (enolase 1, triosephosphate isomerase 1, and hexokinase 2), were red
68  mercury - bound proteins were identified as triosephosphate isomerase A and Protein FAM45A.
69  that observed in other gene families (e.g., triosephosphate isomerase and lactate dehydrogenase).
70 potently inhibit two key glycolytic enzymes, triosephosphate isomerase and phosphofructokinase.
71 vate kinase muscle isozyme, beta-enolase and triosephosphate isomerase and phosphoglucomutase-1.
72 r of the isomerization reaction catalyzed by triosephosphate isomerase and present the crystal struct
73 alytic efficiency of the H95N mutant chicken triosephosphate isomerase and the 60-fold regain of cata
74 driven conformational change in catalysis by triosephosphate isomerase are presented.
75                   Each monomer consists of a triosephosphate isomerase barrel and contains an active
76 to the putative active site of a neighboring triosephosphate isomerase barrel domain, while simultane
77 ypeptide chain of the Rossmann domain to the triosephosphate isomerase barrel domain.
78 rom Staphylococcus aureus, which comprises a triosephosphate isomerase barrel fold with an unusual di
79 h subunit of the MoaA dimer is an incomplete triosephosphate isomerase barrel formed by the N-termina
80        The lateral opening of the incomplete triosephosphate isomerase barrel is covered by the C-ter
81 case several systems of particular interest: triosephosphate isomerase barrel proteins, protein tyros
82 ology with aldo-keto reductases, including a triosephosphate isomerase barrel structure, conservation
83                                              Triosephosphate isomerase deficiency (TPI Df) is a rare
84 etention of the C3 deuterium at the level of triosephosphate isomerase due to a kinetic isotope effec
85 inding, paving the way for future studies of triosephosphate isomerase dynamics and mechanism.
86 hoglucose isomerase, phosphoglucomutase, and triosephosphate isomerase fail to show any decline in fl
87 ate synthase is an alpha/beta protein with a triosephosphate isomerase fold.
88 ase provides bacteria with an alternative to triosephosphate isomerase for metabolizing dihydroxyacet
89                                   Glu-167 of triosephosphate isomerase from Trypanosoma brucei brucei
90 (GAP) in D2O at pD 7.9 catalyzed by wildtype triosephosphate isomerase from Trypanosoma brucei brucei
91 opulations of the chemical entities bound to triosephosphate isomerase have been probed by using soli
92 e motion of the active site loop (loop 6) in triosephosphate isomerase is investigated in solution by
93 vent the mutant protein from complementing a triosephosphate isomerase knockout in Escherichia coli.
94    Finally, we show that backrub sampling of triosephosphate isomerase loop 6 can capture the millise
95 tabilizing reagents were used to encapsulate triosephosphate isomerase mRNA of Arabidopsis thaliana.
96                   In the glycolysis pathway, triosephosphate isomerase was up-regulated, whereas pyru
97 sis assessed inter and intra coordination of triosephosphate isomerase with other identified proteins
98  seven-letter amino acid alphabet produces a triosephosphate isomerase with wild-type activity.
99  a larger charge differential among members (triosephosphate isomerase) indicates that the smaller ch
100 se), pgk (phosphoglycerate kinase), and tpi (triosephosphate isomerase).
101            This approach has also shown that triosephosphate isomerase, aconitate hydratase, M-protei
102 bolism (alpha-enolase, malate dehydrogenase, triosephosphate isomerase, and F1 ATPase, alpha subunit)
103 esults from studies on B-phosphoglucomutase, triosephosphate isomerase, and glycerol 3-phosphate dehy
104 f typical cytosolic proteins, such as GAPDH, triosephosphate isomerase, and M2-type pyruvate kinase i
105                    A first allergenic fungal triosephosphate isomerase, Asp t 36, was discovered in A
106                    Six genes, including CD4, triosephosphate isomerase, B3 subunit of G proteins (GNB
107 n conformational changes during catalysis by triosephosphate isomerase, glycerol phosphate dehydrogen
108 ding proteins involved in energy metabolism (triosephosphate isomerase, glycerol-3-phosphate-dehydrog
109      The highly efficient glycolytic enzyme, triosephosphate isomerase, is expected to differentially
110                            A mutated form of triosephosphate isomerase, isolated by a biochemical met
111 inases, farnesyltransferase, gyrase, prions, triosephosphate isomerase, nitric oxide synthase, phosph
112 promoted the upregulation of enzymes such as triosephosphate isomerase, phosphoglycerate mutase, alph
113 lly allergenic proteins, including Hsp70 and triosephosphate isomerase, than its micellization-extrac
114 g in the isomerization reaction catalyzed by Triosephosphate Isomerase, the conversion of dihydroxyac
115 pe effects in D2O have been measured for the triosephosphate isomerase-catalyzed conversion of dihydr
116               Values of (k(cat)/K(m))GAP for triosephosphate isomerase-catalyzed reactions of (R)-gly
117  selected using in vivo complementation of a triosephosphate isomerase-deficient strain of Escherichi
118   E8 manifested very low affinity for mutant triosephosphate isomerase-HLA-DR1 despite the highly tum
119 e prototypical (beta/alpha)(8) barrel enzyme triosephosphate isomerase.
120  sequences could serve as a protein hinge in triosephosphate isomerase.
121 , including the functionally similar protein triosephosphate isomerase.
122 n of the operation of a hydrophobic clamp in triosephosphate isomerase.
123 stalled Psi site in TPI1 mRNA, which encodes triosephosphate isomerase.
124 l therapeutic targets, chorismate mutase and triosephosphate isomerase.
125  of highly optimized natural enzymes such as triosephosphate isomerase.
126  3-phosphate, a substrate analogue, to yeast triosephosphate isomerase.
127  molecule HLA-DR1 and an epitope from mutant triosephosphate isomerase.
128 s of the prototypical (beta/alpha)(8) barrel triosephosphate isomerase.
129 tial intermediates on the folding pathway of triosephosphate isomerase.
130  base-pair mutation in the glycolytic enzyme triosephosphate isomerase.
131 inal protein hinge of the active-site lid of triosephosphate isomerase.
132 ad cDNA highly homologous to plant cytosolic triosephosphate isomerases (cTPI).
133 l phosphate is in rapid equilibrium with the triosephosphate pool, resulting in rapid labeling of the
134                  Because the rate of flux of triosephosphate to glucose during fasting far exceeds th
135 mediate in the alkaline decomposition of the triosephosphates to methylglyoxal is now observed by UV
136 renal glomeruli, increased the conversion of triosephosphates to ribose-5-phosphate, and strongly inh
137 genic parasites expressing an epitope-tagged triosephosphate transporter and immunopurified on magnet

 
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