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Literature summary for 3.5.4.B9 extracted from

  • Shlyakhtenko, L.S.; Lushnikov, A.Y.; Miyagi, A.; Li, M.; Harris, R.S.; Lyubchenko, Y.L.
    Nanoscale structure and dynamics of ABOBEC3G complexes with single-stranded DNA (2012), Biochemistry, 51, 6432-6440.
    View publication on PubMedView publication on EuropePMC

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
additional information Homo sapiens the enzyme binds with similar efficiency to the 5' and 3' single-stranded DNA substrates and binds the single-stranded region of the gap-DNA substrates with the same efficiency as tail-DNA. Enzyme monomers, dimers, and higher-order oligomers can bind single-stranded DNA substrates in a manner independent of strand polarity and availability of free single-stranded DNA ends. The efficiency of complex formation decreases about 3 times for the 18single-stranded-tail-DNA compared to that for the longer 69single-stranded-tail-DNA hybrid substrate ?
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?

Organism

Organism UniProt Comment Textmining
Homo sapiens Q9HC16
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-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
additional information the enzyme binds with similar efficiency to the 5' and 3' single-stranded DNA substrates and binds the single-stranded region of the gap-DNA substrates with the same efficiency as tail-DNA. Enzyme monomers, dimers, and higher-order oligomers can bind single-stranded DNA substrates in a manner independent of strand polarity and availability of free single-stranded DNA ends. The efficiency of complex formation decreases about 3 times for the 18single-stranded-tail-DNA compared to that for the longer 69single-stranded-tail-DNA hybrid substrate Homo sapiens ?
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?

Subunits

Subunits Comment Organism
dimer
-
Homo sapiens

Synonyms

Synonyms Comment Organism
A3G
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Homo sapiens

General Information

General Information Comment Organism
physiological function the enzyme is capable of blocking retrovirus replication by editing viral cDNA and impairing reverse transcription Homo sapiens