ProGP551 (Pls (Plasmin sensitive surface protein))

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ProGP ID ProGP551 (Pls (Plasmin sensitive surface protein))
Validation Status Uncharacterized
Organism Information
Organism NameStaphylococcus aureus strain 1061
Domain Bacteria
Classification Phylum : Firmicutes
Class : Bacilli
Orders : Bacillales
Family : Staphylococcaeae
Genus : Staphylococcus
Species : aureus
Strain : COL
Taxonomic ID (NCBI) 93062
Genome Information
GenBank CP000255
EMBL CP000255
Organism Additional Information S. aureus is a human pathogen responsible for life-threatening infections as it is able to attach to surfaces, form biofilms, and persist inside the host. It causes mild skin infections and even serious and life-threatening infections, such as endocarditis, osteomyelitis, pneumonia, meningitis, and sepsis.
Gene Information
Gene Namepls
Protein Information
Protein NamePls (Plasmin sensitive surface protein)
UniProtKB/SwissProt ID P80544
EMBL-CDSAAD09131.2
UniProtKB Sequence >sp|P80544|PLS_STAAU Surface protein OS=Staphylococcus aureus GN=pls PE=1 SV=2 MNKNSKKKLDFLPNKLNKYSIRRFTVGTASILVGATLIFGVANDQAEAAENNTTQKQDDS SDASKVKGNVQTIEQSSANSNESDIPEQVDVTKDTTEQASTEEKANTTEQASTEEKADTT EQATTEEAPKAEGTDKVETEEAPKAEETDKATTEEAPKAEETDKATEEAPKTEETDKATT EEAPAAEETSKAATEEAPKAEETSKAATEEAPKAEETEKTATEEAPKTEETDKVETEEAP KAEETSKAATEKAPKAEETNKVETEEAPAAEETNKAATEETPAVEDTNAKSNSNAQPSET ERTQVVDTVAKDLYKKSEVTEAEKAEIEKVLPKDISNLSNEEIKKIALSEVLKETANKEN AQPRATFRSVSSNARTTNVNYSATALRAAAQDTVTKKGTGNFTAHGDIIHKTYKEEFPNE GTLTAFNTNFNPNTGTKGALEYNDKIDFNKDFTITVPVANNNQGNTTGADGWGFMFTQGN GQDFLNQGGILRDKGMANASGFKIDTAYNNVNGKVDKLDADKTNNLSQIGAAKVGYGTFV KNGADGVTNQVGQNALNTKDKPVNKIIYADNTTNHLDGQFHGQRLNDVVLNYDAATSTIT ATYAGKTWKATTDDLGIDKSQKYNFLITSSHMQNRYSNGIMRTNLEGVTITTPQADLIDD VEVTKQPIPHKTIREFDPTLEPGSPDVIVQKGEDGEKTTTTPTKVDPDTGDVVERGEPTT EVTKNPVDEIVHFTPEEVPQGHKDEFDPNLPIDGTEEVPGKPGIKNPETGEVVTPPVDDV TKHGPKAGEPEVTKEEIPFEKKREFNPDLKPGEEKVTQEGQTGEKTTTTPTTINPLTGEK VGEGEPTTEVTKEPVDEITQFGGEEVPQGHKDEFDPNLPIDGTEEVPGKPGIKNPETGEV VTPPVDDVTKHGPKAGEPEVTKEEIPFEKKREFNPDLKPGEEKVTQEGQTGEKTTTTPTT INPLTGEKVGEGEPTTEVTKEPVDEITQFGGEEVPQGHKDEFDPNLPIDGTEEVPGKPGI KNPETGEVVTPPVDDVTKHGPKAGEPEVTKEEIPFEKKREFNPDLKPGEEKVTQEGQTGE KTTTTPTTINPLTGEKVGEGEPTTEVTKEPVDEITQFGGEEVPQGHKDEFDPNLPIDGTE EVPGKPGIKNPETGEVVTPPVDDVTKHGPKAGEPEVTKEEIPYETKRVLDPTMEPGSPDK VAQKGENGEKTTTTPTTINPLTGEKVGEGEPTTEVTKEPIDEIVNYAPEIIPHGTREEID PNLPEGETKVIPGKDGLKDPETGEIIEEPQDEVIIHGAKDDSDADSDSDADSDSDADSDS DADSDSDADSDSDSDSDSDSDSDSDADSDSDSDSDSDADSDSDADSDSDADSDSDSDADS DSDSDADSDSDSDSDSDADSDSDSDSDSDADSDSDADSDSDSDSDSDADSDSDSDSDSDA DSDSDADSDSDADSDSDADSDSDSDSDSDADSDSDADSDSDADSDSDADSDSDSDSDSDA DSDSDSDSDSDSDADSDSDADSDSDSDADSDSDADSDSDADGDSDADSDSDADSDSDSDS DSDSDSDSDADSDSDSDSDSDADRDHNDKTDKPNNKELPDTGNDAQNNGTLFGSLFAALG GLFLVGRRRKNKNNEEK
Sequence length 1637 AA
Subcellular LocationSurface
Function Pls is a virulence factor that reduces the adherence of S. aureus to Fg, Fn, or endothelial cells, internalization by human host cells and phagocytosis by polymorphonuclear neutrophils (PMNs) independently of its glycosylation status.
Glycosylation Status
Glycosylation Type O- (Ser) linked
Technique(s) used for Glycosylation DetectionPeriodic acid-Schiff staining
Protein Glycosylation- Implication Biofilm formation (in S. aureus Newman) is enhanced upon expression of GtfC/GtfD-glycosylated Pls that may contribute to MRSA (methicillin-resistant S. aureus) pathogenicity. The glycoprotein may serve as a future antibacterial target to combat or prevent infections.
Glycan Information
Glycan Annotation N-acetylhexosaminyl residues
Protein Glycosylation linked (PGL) gene(s)
OST ProGT IDProGT66 ProGT67
Characterized Accessory Gene(s)gtfC, gtfD, sdgA and sdgB
Literature
Year of Identification2017
Year of Identification Month Wise2017.01.12
ReferenceBleiziffer, I., Eikmeier, J., Pohlentz, G., McAulay, K., Xia, G., Hussain, M., Peschel, A., Foster, S., Peters, G. and Heilmann, C., 2017. The plasmin-sensitive protein Pls in methicillin-resistant Staphylococcus aureus (MRSA) is a glycoprotein. PLoS pathogens, 13(1), p.e1006110.
Corresponding Author Christine Heilmann
ContactInstitute of Medical Microbiology, University of Münster, Münster, Germany, Interdisciplinary Center for Clinical Research (IZKF), University of Münster, Münster, Germany