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. 2020 Sep 25;9(10):787. doi: 10.3390/pathogens9100787

Table 1.

Commonly-enriched candidate LPS-interacting PM-associated proteins from the three affinity chromatography systems with LPS chemotype Xcc 8004 as ligand (compiled from Tables S1, S4 and S7).

Protein a Accession Number b
Common proteins bound to LPS Xcc 8004 -functionalized Polymyxin B and MagReSynTM
Putative GTP-binding protein ara-3 Q9FJF1
Putative permeability-increasing protein (BPI)/LPS-binding protein (LBP) family protein At1g04970 Q9MAU5
MLP-like protein 423 Q93VR4
Heat shock protein 70 (Hsp 70) family protein F4K007
Ras-related protein RABE1c P28186
Ras-related protein RABA1f Q9FJH0
Ras-related protein RABG3a Q948K8
V-type proton ATPase subunit G1 O82628
V-type proton ATPase subunit d2 Q9LHA4
Tubulin alpha-5 chain B9DHQ0
Annexin D2 Q9XEE2
Tubulin beta-2 chain Q56YW9
Nitrilase 1 P32961
Adenine phosphoribosyl transferase 1 F4HSX1
Common proteins bound to LPS Xcc 8004-functionalized MagReSynTM and EndoTrap®
Mannose-binding lectin superfamily protein A0A1I9LQM9
ATPase 2 P19456
Plasma membrane ATPase F4JPJ7
Aldolase-type TIM barrel family protein A8MS37

a the protein identified by LC/MS/MS. b the accession number of the proteins. The perception and signaling proteins are highlighted in red, the defense and response proteins are highlighted in blue, and the membrane trafficking and transport are highlighted in green. The proteins highlighted in black pertain to structure and metabolic process.