Cloned (Comment) | Organism |
---|---|
gene egt1+, DNA and amino acid sequence determination and analysis, sequence comparisons, and phylogenetic tree | Schizosaccharomyces pombe |
Protein Variants | Comment | Organism |
---|---|---|
additional information | construction of an egt1+ overexpression system by replacing its native promoter with the nmt1+ promoter, which is inducible in the absence of thiamine. Generation of a egt1+ deletion mutant, DELTAegt1, by replacing the target loci in the wild-type 972 strain with the kanamycin resistance marker (kanMX) leading to absence of all ergothioneine pathway intermediates and ergothioneine itself in DELTAegt1. Employment of three versions of the nmt1 promoter plasmid with increasing strength of expression and constructed three strains P81nmt1-egt1+, P41nmt1-egt1+, and P3nmt1-egt1+, respectively. Mutant DELTAegt1 strain shows no growth defects during cultivation in either rich (YE) or minimal (EMM2) culture media, deletion of gene egt1+ causes no significant perturbation to the intracellular metabolome of quiescent cells. No sensitivity or resistance of the mutant strains to oxidative stress compared to wild-type 972 strain | Schizosaccharomyces pombe |
Metals/Ions | Comment | Organism | Structure |
---|---|---|---|
Fe2+ | required for catalysis | Schizosaccharomyces pombe |
Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|
hercynine + L-cysteine + O2 | Schizosaccharomyces pombe | - |
S-(hercyn-2-yl)-L-cysteine S-oxide + H2O | - |
? | |
hercynine + L-cysteine + O2 | Schizosaccharomyces pombe 972 | - |
S-(hercyn-2-yl)-L-cysteine S-oxide + H2O | - |
? | |
additional information | Schizosaccharomyces pombe | the ergothioneine pathway can also synthesize selenoneine, a selenium-containing derivative of ergothioneine, when the culture medium is supplemented with selenium. Selenoneine biosynthesis, unlike ergothioneine biosynthesis, does not produce a sulfoxide as its intermediate, but produces hercynylselenocysteine instead. Enzyme Egt-1 also catalyzes the synthesis of hercynine, EC 2.1.1.44 | ? | - |
? | |
additional information | Schizosaccharomyces pombe 972 | the ergothioneine pathway can also synthesize selenoneine, a selenium-containing derivative of ergothioneine, when the culture medium is supplemented with selenium. Selenoneine biosynthesis, unlike ergothioneine biosynthesis, does not produce a sulfoxide as its intermediate, but produces hercynylselenocysteine instead. Enzyme Egt-1 also catalyzes the synthesis of hercynine, EC 2.1.1.44 | ? | - |
? |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Schizosaccharomyces pombe | O94632 | - |
- |
Schizosaccharomyces pombe 972 | O94632 | - |
- |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
hercynine + L-cysteine + O2 | - |
Schizosaccharomyces pombe | S-(hercyn-2-yl)-L-cysteine S-oxide + H2O | - |
? | |
hercynine + L-cysteine + O2 | - |
Schizosaccharomyces pombe 972 | S-(hercyn-2-yl)-L-cysteine S-oxide + H2O | - |
? | |
additional information | the ergothioneine pathway can also synthesize selenoneine, a selenium-containing derivative of ergothioneine, when the culture medium is supplemented with selenium. Selenoneine biosynthesis, unlike ergothioneine biosynthesis, does not produce a sulfoxide as its intermediate, but produces hercynylselenocysteine instead. Enzyme Egt-1 also catalyzes the synthesis of hercynine, EC 2.1.1.44 | Schizosaccharomyces pombe | ? | - |
? | |
additional information | hercynylcysteine sulfoxide can spontaneously convert into ergothioneine in the presence of pyridoxal 5'-phosphate | Schizosaccharomyces pombe | ? | - |
? | |
additional information | the ergothioneine pathway can also synthesize selenoneine, a selenium-containing derivative of ergothioneine, when the culture medium is supplemented with selenium. Selenoneine biosynthesis, unlike ergothioneine biosynthesis, does not produce a sulfoxide as its intermediate, but produces hercynylselenocysteine instead. Enzyme Egt-1 also catalyzes the synthesis of hercynine, EC 2.1.1.44 | Schizosaccharomyces pombe 972 | ? | - |
? | |
additional information | hercynylcysteine sulfoxide can spontaneously convert into ergothioneine in the presence of pyridoxal 5'-phosphate | Schizosaccharomyces pombe 972 | ? | - |
? |
Subunits | Comment | Organism |
---|---|---|
More | Egt-1 domain structure, overview | Schizosaccharomyces pombe |
Synonyms | Comment | Organism |
---|---|---|
Egt-1 | - |
Schizosaccharomyces pombe |
egt1+ | - |
Schizosaccharomyces pombe |
ergothioneine biosynthesis protein 1 | - |
Schizosaccharomyces pombe |
mug158+/SPBC1604.01 | locus name | Schizosaccharomyces pombe |
protein SPBC1604.01 | - |
Schizosaccharomyces pombe |
SPBC1604.01 | locus name | Schizosaccharomyces pombe |
General Information | Comment | Organism |
---|---|---|
evolution | mug158+/SPBC1604.01 is a distant homologue of the mycobacterial EgtD and EgtB genes, encoding a single fusion protein. The Schizosaccharomyces pombe homologue utilizes cysteine as a substrate, rather than using gamma-glutamyl-cysteine, as in the case of the bacterial EgtB enzyme, EC 1.14.99.50 | Schizosaccharomyces pombe |
metabolism | the enzyme produces hercynylcysteine sulfoxide in the ergothioneine pathway. The ergothioneine pathway can also synthesize selenoneine, a selenium-containing derivative of ergothioneine, when the culture medium is supplemented with selenium. Selenoneine biosynthesis involves an intermediate compound, hercynylselenocysteine | Schizosaccharomyces pombe |
physiological function | contribution of gene egt1+ to oxidative stress response, but gene egt1+ might not be among the primary mechanisms that protect Schizosaccharomyces pombe from exogenous peroxide | Schizosaccharomyces pombe |