※ Search Results for Serine Phosphorylation Proteins in Actinobacteria
dbPSP proteins : 175
dbPSP proteins : 175
UniProt Accession | Organism | Name / Alias | ||||||
---|---|---|---|---|---|---|---|---|
Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) |
Putative integral membrane protein; SCO3288 | |||||||
Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) |
Putative integral membrane protein; SCO3302 | |||||||
Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) |
ATP-dependent zinc metalloprotease FtsH; ftsH; SCO3404 | |||||||
Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) |
Putative membrane protein; SCO3362 | |||||||
Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) |
Integral membrane protein with kinase activity; SCO3542 | |||||||
Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) |
Putative membrane protein; SCO3862 | |||||||
Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) |
Putative DNA-binding protein; SCO3859 | |||||||
Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) |
Putative molybdopterin-guanine dinucleotide biosynthesis protein; SCO3828 | |||||||
Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) |
Uncharacterized protein; SCO3822 | |||||||
Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) |
Transketolase; SCO1935 | |||||||
Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) |
NADH-quinone oxidoreductase subunit C; nuoC; SCO4564; ORFNames=SCD16A.19c | |||||||
Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) |
NADH-quinone oxidoreductase subunit I 1; nuoI1; SCO4570; ORFNames=SCD16A.13c | |||||||
Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) |
Uncharacterized protein; SCO5507 | |||||||
Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) |
Thiamine-monophosphate kinase; TMP kinase;Thiamine-phosphate kinase; thiL; SCO5562 | |||||||
Streptomyces coelicolor (strain ATCC BAA-471 / A3(2) / M145) |
Putative two-component system response regulator; SCO6162 | |||||||
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