ahi0369120.00.51.01.5Time(h)OD600induced, +NAMuninduced, +NAMuninduced,−NAMinduced,−NAMSfSTING WT NAM supplementation0 369120.00.51.01.5Time(h)OD600induced, +NAMuninduced, +NAMuninduced,−NAMinduced,−NAMSfSTING D259A NAM supplementation10 −3 10 −2 10 −1 100 101 10202×10^54×10^56×10^58×10^5[c-di-GMP] (μM)ε-NADCleavage(RFU)WT
N163A K167A S262AF165A R168A T263ASfSTING mutant ε-NADturnover after 1 hbResidue mutated in SfSTING
(FsSTING equivalent)Observed 3 ', 3 '-cGAMP
contact in FsSTING
N163 (N91)
F165 (F92)
K167 (F94)
R168 (P95)D259 (D169)
S262 (N172)
T263 (T173)R234 (R153)Phosphodiester bond
Base stacking (outer face)
None/predicted only for SfSTING
None/predicted only for SfSTINGN2 of guanosine base
Phosphodiester bond
Potential clash with free 3 '-OH
of 2 '–5' linked CDNsBase stacking (inner face)Amino acids targeted for mutagenesisf1.52.0 2.53.0 3.50.00.51.0Retention time (min)Normalized absorbance 254 nmWT Apo
WT + c-di-GMP
E84A + c-di-GMP
R234A + c-di-GMP
D259A + c-di-GMPgWT E84A R234A D259A02×10^54×10^56×10^5ε-NAD Cleavage (RFU)—+ —+ —+ —+cdc-di-AMPc-di-GMP
3',3'-cGAMP2',3'-cGAMPc-di-AMPc-di-GMP3',3'-cGAMP2',3'-cGAMPSfSTING Mutant:R234A D259AFree
CDN[α^32 P] CDN:
Well
STING–CDN
ComplexSTING:—SfSTING D259A (TIR)Free
c-di-GMPWellSTING–CDN
Complex100 nm[SfSTING D259A] (μM)10 −3 10 −2 10 −1 100 101 102 1030.00.40.81.2Fractionboundc-di-GMP
WT fitKd= 28.78 μM (2 orders of magnitude shift)eExtended Data Fig. 6 | See next page for caption.