Cloned (Comment) | Organism |
---|---|
recombinant YbiN carrying a N-terminal His6 tag is expressed in Escherichia coli and purified | Escherichia coli |
Molecular Weight [Da] | Molecular Weight Maximum [Da] | Comment | Organism |
---|---|---|---|
34000 | - |
x * 34000, SDS-PAGE | Escherichia coli |
Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|
S-adenosyl-L-methionine + adenine1618 in 23S rRNA | Escherichia coli | - |
S-adenosyl-L-homocysteine + 6-methyladenine1618 in 23S rRNA | - |
? |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Escherichia coli | P75782 | - |
- |
Purification (Comment) | Organism |
---|---|
recombinant YbiN carrying a N-terminal His6 tag is expressed in Escherichia coli and purified | Escherichia coli |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
S-adenosyl-L-methionine + adenine1618 in 23S rRNA | - |
Escherichia coli | S-adenosyl-L-homocysteine + 6-methyladenine1618 in 23S rRNA | - |
? | |
S-adenosyl-L-methionine + adenine1618 in 23S rRNA | the recombinant YbiN protein is able to methylate partially deproteinized 50 S ribosomal subunit, but neither the completely assembled 50 S subunit nor completely deproteinized 23 S rRNA | Escherichia coli | S-adenosyl-L-homocysteine + 6-methyladenine1618 in 23S rRNA | - |
? |
Subunits | Comment | Organism |
---|---|---|
? | x * 34000, SDS-PAGE | Escherichia coli |
Synonyms | Comment | Organism |
---|---|---|
m6A1618 methyltransferase | - |
Escherichia coli |
rlmF | - |
Escherichia coli |
rRNA large subunit methyltransferase F | - |
Escherichia coli |
ybiN | - |
Escherichia coli |
YbiN protein | - |
Escherichia coli |
Temperature Optimum [°C] | Temperature Optimum Maximum [°C] | Comment | Organism |
---|---|---|---|
37 | - |
assay at | Escherichia coli |
pH Optimum Minimum | pH Optimum Maximum | Comment | Organism |
---|---|---|---|
7.6 | - |
assay at | Escherichia coli |
General Information | Comment | Organism |
---|---|---|
malfunction | knockout of the ybiN gene leads to loss of modification at adenine1618. The modification is restored if ybiN knock-out strain has been co-transformed with a plasmid expressing the ybiN gene. Both lack of the ybiN gene and it's overexpression leads to growth retardation and loss of cell fitness comparative to the parental strain | Escherichia coli |
physiological function | A1618 modification could be necessary for the exit tunnel interaction with some unknown regulatory peptides | Escherichia coli |