Protein Info for Psyr_1963 in Pseudomonas syringae pv. syringae B728a ΔmexB
Annotation: Cyclic peptide transporter
These analyses and tools can help you predict a protein's function, but be skeptical. For enzymes, over 10% of annotations from KEGG or SEED are probably incorrect. For other types of proteins, the error rates may be much higher. MetaCyc and Swiss-Prot have low error rates, but the best hits in these databases are often quite distant, so this protein's function may not be the same. TIGRFam has low error rates. Finally, many experimentally-characterized proteins are not in any of these databases. To find relevant papers, use PaperBLAST.
Protein Families and Features
Best Hits
KEGG orthology group: K06160, putative ATP-binding cassette transporter (inferred from 100% identity to psb:Psyr_1963)MetaCyc: 61% identical to ABC-type myristoylated ferribactin transporter (Pseudomonas aeruginosa PAO1)
7.4.2.-
Predicted SEED Role
"PvdE, pyoverdine ABC export system, fused ATPase and permease components" in subsystem Siderophore Pyoverdine
MetaCyc Pathways
- pyoverdine I biosynthesis (5/11 steps found)
Sequence Analysis Tools
PaperBLAST (search for papers about homologs of this protein)
Search CDD (the Conserved Domains Database, which includes COG and superfam)
Predict protein localization: PSORTb (Gram-negative bacteria)
Predict transmembrane helices and signal peptides: Phobius
Check the current SEED with FIGfam search
Find homologs in fast.genomics or the ENIGMA genome browser
See Q4ZV16 at UniProt or InterPro
Protein Sequence (558 amino acids)
>Psyr_1963 Cyclic peptide transporter (Pseudomonas syringae pv. syringae B728a ΔmexB) MTRTTESLARETLRILKPFWWLVALSTLLGIVSGLSVTGLLATINNAMNRPGGPDTQTAL LFAGLCVLTLACSTLSNLSTNYVGQRVVANLRRELAAKVLVAPIEQLERYRAHRLIPVLL NDVNTISTFALSVAPMVISFTVTLGCLAYLAVLSWQILALTVLTVVLGTGAQYLAHAFGM RSILAARNSEDELQKHYQALSAGAKELRIQRKRRQHMLDEKIHGATEHICRSNIRAANIF VSAETFGSMLFFAVIGMAIAFQAMWPTTEKTVLGGFVLVMLYMKGPLERLMTALPGISRA QIAMRRIAELSWKFSSPEPHLLVSDRPTSLASMHTLELHNLRYDYPPVEGSDAFHLGPVD LSIKQGDIVFIVGENGCGKTTLIKLLLGLYTPQQGEIRLNGQAVTAENLDDYRQLFTTIF ADYYLFDEPLQGQAALPQDAGKYLERLDIAHKVSIENGVFTTTDLSTGQRKRLALINAWL DERQVLVFDEWAADQDPAFRRVFYAELLPELKQQGKTIIVISHDDRYFYVADQLVRMQTG QIQVEQVRNETRDKTITA