Literature summary for 2.7.7.7 extracted from

Choi, J.J.; Nam, K.H.; Min, B.; Kim, S.J.; Soell, D.; Kwon, S.T.
Protein trans-splicing and characterization of a split family B-type DNA polymerase from the hyperthermophilic archaeal parasite Nanoarchaeum equitans (2006), J. Mol. Biol., 356, 1093-1106.

Search for more literature for 2.7.7.7

Cloned(Commentary)

Cloned (Comment)	Organism
the two Neq DNA polymerase genes are cloned and expressed in Escherichia coli individually, together (for the Neq C), and as a genetically protein splicing-processed form (Neq P)	Nanoarchaeum equitans

Natural Substrates/ Products (Substrates)

Natural Substrates	Organism	Comment (Nat. Sub.)	Natural Products	Comment (Nat. Pro.)	Rev.	Reac.
additional information	Nanoarchaeum equitans	Neq L and Neq S are needed to form the active DNA polymerase that possesses higher proofreading activity. The genetically protein splicing-processed Neq P shows the same properties as the protein trans-spliced Neq C	?	-	?

Organism

Organism	UniProt	Comment	Textmining
Nanoarchaeum equitans	-	-	-

Substrates and Products (Substrate)

Substrates	Comment Substrates	Organism	Products	Comment (Products)	Rev.	Reac.
additional information	Neq L and Neq S are needed to form the active DNA polymerase that possesses higher proofreading activity. The genetically protein splicing-processed Neq P shows the same properties as the protein trans-spliced Neq C	Nanoarchaeum equitans	?	-	?

Synonyms

Synonyms	Comment	Organism
family B-type DNA polymerase	-	Nanoarchaeum equitans
Neq DNA polymerase	-	Nanoarchaeum equitans

Use of this online version of BRENDA is free under the CC BY 4.0 license. See terms of use for full details.

Release 2023.1 (January 2023)