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

 
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