5.3.1.1: triose-phosphate isomerase
This is an abbreviated version!
For detailed information about triose-phosphate isomerase, go to the full flat file.
Word Map on EC 5.3.1.1
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5.3.1.1
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giardia
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assemblage
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aldolase
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duodenalis
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dihydroxyacetone
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enolase
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phosphoglycerate
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zoonotic
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barrel
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fecal
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trypanosoma
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multilocus
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fructose
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giardiasis
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dhap
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cryptosporidium
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brucei
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protozoan
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isomerases
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gapdh
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province
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cysts
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malate
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stool
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lamblia
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methylglyoxal
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phosphofructokinase
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cruzi
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schistosoma
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enediolate
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2-phosphoglycolate
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parvum
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hemolytic
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intestinalis
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fructose-1,6-bisphosphate
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deamidation
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alpha-enolase
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1,6-bisphosphate
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glucosephosphate
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tim-barrel
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hungarian
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hominis
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phosphite
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dianion
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phosphoglucose
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glycosomes
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enzymopathy
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fructose-bisphosphate
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ige-binding
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subgenotype
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diagnostics
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synthesis
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analysis
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biofuel production
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medicine
- 5.3.1.1
- giardia
-
assemblage
- aldolase
- duodenalis
- dihydroxyacetone
- enolase
- phosphoglycerate
-
zoonotic
-
barrel
-
fecal
- trypanosoma
-
multilocus
- fructose
- giardiasis
- dhap
- cryptosporidium
- brucei
-
protozoan
- isomerases
- gapdh
-
province
- cysts
- malate
-
stool
- lamblia
- methylglyoxal
-
phosphofructokinase
- cruzi
- schistosoma
-
enediolate
- 2-phosphoglycolate
- parvum
-
hemolytic
- intestinalis
- fructose-1,6-bisphosphate
-
deamidation
- alpha-enolase
- 1,6-bisphosphate
-
glucosephosphate
-
tim-barrel
-
hungarian
- hominis
- phosphite
-
dianion
-
phosphoglucose
- glycosomes
-
enzymopathy
-
fructose-bisphosphate
-
ige-binding
-
subgenotype
- diagnostics
- synthesis
- analysis
- biofuel production
- medicine
Reaction
Synonyms
CP 25, CTIMC, cTPI, cytoplasmic TPI, cytoplasmic triosephosphate isomerase, cytoTPI, D-glyceraldehyde-3-phosphate ketol-isomerase, GlTIM, Isomerase, triose phosphate, Lactacin B inducer protein, monoTIM, PfTIM, PfuTIM, Phosphotriose isomerase, plastidic TPI, plastidic triosephosphate isomerase, pTPI, SSO2592, TcTIM, TIM, TIM1, TIM2, TonTIM, TpI, TPI1, TpiA, Triose phosphate isomerase, Triose phosphate mutase, Triose phosphoisomerase, Triosephosphate isomerase, Triosephosphate mutase, vTIM
ECTree
5.3.1.1 triose-phosphate isomeraseAdvanced search results
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results (Application
Application on EC 5.3.1.1 - triose-phosphate isomerase
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APPLICATION 
ORGANISM
UNIPROT
COMMENTARY 
LITERATURE
analysis
biofuel production
proteome analysis as well as enzyme assays performed in cell-free extracts demonstrates that glycerol is degraded via glyceraldehyde-3-phosphate, which is further metabolized through the lower part of glycolysis leading to formation of mainly ethanol and hydrogen. Fermentation of glycerol to ethanol and hydrogen by this bacterium represents a remarkable option to add value to the biodiesel industries by utilization of surplus glycerol
diagnostics
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triosephosphate isomerase is a serum marker for human lung squamous cell carcinoma
medicine
synthesis
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enzymatic synthesis of D-xylulose 5-phosphate using triosephosphate isomerase and transketolase. Comparison of use of glyceraldehyde 3-phosphate or dihydroxyacetone phosphate as starting substrate by process modeling via the use of windows of operation
additional information
analysis
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specific polymerase chain reaction protocols used to determine the prevalence of toxigenic Clostridium difficile in Vhembe, South Africa. The study confirms the usefulness of PCR methodologies in the detection of toxigenic Clostridium difficile and suggests that Clostridium difficile is responsible for a small, but underappreciated, proportion of diarrheal cases in the region
analysis
systematic mutagenesis method to find critical residues for certain physico-chemical properties of a protein. The method is a shorter alternative to random mutagenesis, saturation mutagenesis or directed evolution to find multiple amino acids critical for certain properties of proteins
analysis
systematic mutagenesis method to find critical residues for certain physico-chemical properties of a protein. The method is a shorter alternative to random mutagenesis, saturation mutagenesis or directed evolution to find multiple amino acids critical for certain properties of proteins
medicine
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triosephosphate isomerase is a promising antischistosome vaccine antigen
medicine
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67% of 39 patients suffering from adverse reactions to lychee show allergic reactions resp. IgE binding of their sera to enzyme protein
medicine
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analysis of key aspects of triosephosphate isomerase deficiency glycolytic enzymopathy pathogenesis identified using the TPIsugarkill mutation M80T, a Drosophila model of the human disease deficiency. Mutant protein is expressed, capable of forming a homodimer, and is functional. However, the mutant protein is degraded by the 20S proteasome core leading to loss-of-function pathogenesis
medicine
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evaluation of the ability of naive monocyte-derived dendritic cells to sensitize peripheral blood mononuclear cells to the Schistosoma vaccine candidate MAP4 using a priming in vitro assay. MAP4 is a multiple antigen peptide containing B- and T-cell epitopes derived from the enzyme triose phosphate isomerase. Cytokine production from activated MAP4 priming in vitro cells is predominantly Th1-like, consisting mainly of IFN-gamma. Naive donor dendritic cells, sensitized with MAP4, thus are able to prime and clonally expand MAP4-specific T cells towards a Th1-type response
medicine
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in drug-resistant SGC7901 cells induced by vincristine sulfate, triosephosphate isomerase is downregulated.The sensitivity of TPI-SGC7901/VCR cells to adriamycin, vincristine, 5-fluorouracil and cis-dichlorodiamine platinum, as well as the accumulation and retention to adriamycin, are significantly increased when compared to their control cell lines
medicine
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specific polymerase chain reaction protocols used to determine the prevalence of toxigenic Clostridium difficile in Vhembe, South Africa. The study confirms the usefulness of PCR methodologies in the detection of toxigenic Clostridium difficile and suggests that Clostridium difficile is responsible for a small, but underappreciated, proportion of diarrheal cases in the region
medicine
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TPI1 expression is greatly decreased in clinical hepatocellular carcinoma samples, positively correlated with overall survival, and negatively associated with histological differentiation, tumor size and organ metastasis. Forced expression of TPI1 in hepatocellular carcinoma cells inhibits cell growth, migration, and invasion in vitro. Knockdown of TPI1 by shRNA promotes cell growth, migration and invasion. Overexpression of TPI1 leads to slowed tumor growth and decreased tumor weight in vivo. Cell cycle arrest is induced by TPI1 overexpression
additional information
the glycolytic enzyme triosephosphate isomerase occupies a central position in the development of structural and mechanistic enzymology
additional information
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the glycolytic enzyme triosephosphate isomerase occupies a central position in the development of structural and mechanistic enzymology
