ProGT145 (GccA)
ProGT ID | ProGT145 (GccA) |
Organism Information | |
Organism Name | Lactobacillus plantarum KW30 |
Clinical Implication | Non-pathogenic |
Domain | Bacteria |
Classification | Phylum : Firmicutes Class : Bacilli Orders : Lactobacillales Family : Lactobacillaceae Genus : Lactobacillus Species : plantarum Strain : KW30 |
Taxonomic ID (NCBI) | 1590 |
Genome Information | |
Gene Bank | GU552553.1 |
Gene Information | |
Gene Name | gccA |
NCBI Reference Sequence | ADV57361.1 |
Protein information | |
Protein Name | GccA |
UniProtKB/ SwissProt ID | E9K9Y6 |
NCBI Ref Seq | ADV57361 |
UniProtKB Sequence | >tr|E9K9Y6|E9K9Y6_LACPN UDP-GlcNAc glycosyltransferase family 2 OS=Lactiplantibacillus plantarum OX=1590 GN=gccA PE=4 SV=1 MKNRQNEIDSYLNLHLRPVHKSFDFGNLTNIDQFRHHIYVSYIVICKNSQATIERCVNSIAQNMENGDELIVLDTGSTDETVHLVKKNMPQAKISVTNWKNDFSEVRNKALKLASKDWVFYVDSDEWLDVDDGAQLKKILFKVQAKNFKFVINPTFSDHSGQIYQTVGRIFPKKSSFHYYAKIHEEVRKEDQKLGYDVRHFACDDIILYHDGYDKEVLRDKDKIKRNIRLLQEMTCEEPQNARWPFLLARDGFDVLPQDKLKQLVKRTLDLVASDSLQEKYSPFAKKLLGRILLREGKTTQAVLSFKDVLQITGGEDSDAIYYIESFKINEIIAEAKSIEVKMLRYLNKHKGMIDVNSDISGNYYHIAQVILECDIISANYSHLFPLISEIPKNFSGDIKSSVKSAVKLYSKLQGDSKNENN |
Sequence length | 422AA |
Function in Native Organism | It is S-glycosyltransferase, catalyzes GccF, glycocin has antimicrobial activity |
Glycosyltransferase Information | |
Glycosylation Type | O- (Ser) and S- (Cys) linked |
CAZY Family | GT2 |
Mechanism of Glycan Transfer | Sequential |
Donor Type | UDP-GalNAc |
Donor Specificity | Nucleotide activated sugars |
Glycan Information | |
Glycan transferred | Monosaccharide (GlcNac) |
Experimental_strategies | in vivo |
Acceptor Subtrate Information | |
Acceptor Substrate name | Glycocin F |
ProGPdb ID | ProGP402 (Glycocin F) |
Litrature | |
Year Of Validation | 2021 |
Reference | Drummond, B.J., Loo, T.S., Patchett, M.L. and Norris, G.E., 2021. Optimized Genetic Tools Allow the Biosynthesis of Glycocin F and Analogues Designed To Test the Roles of gcc Cluster Genes in Bacteriocin Production. Journal of bacteriology, 203(7), pp.e00529-20. |
Corresponding Author | School of Fundamental Sciences, Massey University, Palmerston North, New Zealand Maurice Wilkins Centre for Molecular Biodiscovery, The University of Auckland, Auckland, New Zealand |