2.7.1.16: ribulokinase

This is an abbreviated version!
For detailed information about ribulokinase, go to the full flat file.

Reaction

Synonyms

AraB, AraK, L-ribulokinase, ribulokinase (phosphorylating)

ECTree

     2 Transferases

         2.7 Transferring phosphorus-containing groups

             2.7.1 Phosphotransferases with an alcohol group as acceptor

                2.7.1.16 ribulokinase

Advanced search results

Do not include text mining results

Include results (more...)

Include results (more...)

Results	in table
1	Activating Compound
6842	AA Sequence
1	Application
1	CAS Registry Number
5	Cloned(Commentary)
2	Crystallization (Commentary)
1	General Information
2	General Stability
5	Inhibitors
15	KM Value [mM]
2	Localization
4	Metals/Ions
2	Molecular Weight [Da]
14	Natural Substrates/ Products (Substrates)
15	Organism
5	Pathway
4	PDB ID
2	pH Optimum
2	pH Range
3	pH Stability
5	Purification (Commentary)
1	Reaction
1	Reaction Type
13	Reference
2	Specific Activity [micromol/min/mg]
1	Storage Stability
38	Substrates and Products (Substrate)
2	Subunits
8	Synonyms
1	Systematic Name
4	Temperature Optimum [°C]
1	Temperature Range [°C]
2	Temperature Stability [°C]
8	Turnover Number [1/s]

Cloned

print visible entries

print all entries

Go back to the abbreviated version
of the Enzyme Summary Page.

Cloned on EC 2.7.1.16 - ribulokinase

Please wait a moment until all data is loaded. This message will disappear when all data is loaded.

top print hide Go to Cloned (commentary) Search

Please wait a moment until the data is sorted. This message will disappear when the data is sorted.

CLONED (Commentary)

ORGANISM

UNIPROT

LITERATURE

expressed in Escherichia coli

Clostridium acetobutylicum

-

722536

expressed in Escherichia coli BL21(DE3)-codon+RIL cells

Halalkalibacterium halodurans

Q9KBQ3

723743

expression in Corynebacterium glutamicum. Corynebacterium glutamicum is metabolically engineered to broaden its substrate utilization range to include L-arabinose. The resultant CRA1 recombinant strain expressed the Escherichia coli genes araA, araB, and araD encoding L-arabinose isomerase, L-ribulokinase, and L-ribulose-5-phosphate 4-epimerase, respectively, under the control of a constitutive promoter. Unlike the wild-type strain, CRA1 is able to grow on mineral salts medium containing L-arabinose as the sole carbon and energy source. The three cloned genes are expressed to the same levels whether cells are cultured in the presence of D-glucose or L-arabinose. Strain CRA1 is able to utilize L-arabinose as a substrate for organic acid production even in the presence of D-glucose

Escherichia coli

-

671568

expression in Escherichia coli

Anoxybacillus kestanbolensis

U5JE22

739743

expression in Saccharomyces cerevisiae. Improvement of a bacterial L-arabinose utilization pathway consisting of L-arabinose isomerase from Bacillus subtilis and L-ribulokinase and L-ribulose-5-phosphate 4-epimerase from Escherichia coli after expression of the corresponding genes in Saccharomyces cerevisiae. These improvements make up a new starting point for the construction of more-efficient industrial L-arabinose-fermenting yeast strains by evolutionary engineering

Escherichia coli

-

684574