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. 2023 Jan 10;24(2):1341. doi: 10.3390/ijms24021341

Table 1.

Intracellular and extracellular S100A6 ligands.

Ligand Target Region Direct Effect Proposed Function Reference
Actin and tropomyosin ND ND Regulation of actin filament dynamics [48,57]
Caldesmon C-terminus Decrease in caldesmon affinity to actin and
heavy meromyosin (HMM)
Regulation of caldesmon function in smooth muscle contraction [49,50,51,52,53]
Calponin ND Stabilization of calponin Regulation of calponin function in smooth muscle contraction [54,55]
Coffilin ND Decrease in actin depolymerization Regulation of actin polymerization [58]
Non-muscle myosin IIA ND ND Modulation of cell motility [56]
Tubulin α
and β
ND ND Regulation of microtubule organization [59]
Kinesin light chain (KLC) TPR domain dissociation of the KLC-JIP1 complex Modulation of KLC–cargo interaction [60]
FOR20, FOP and OFD1 N-terminus (aa 1–30) ND Modulation of cilia formation [61]
TPPP (tubulin polymerization-promoting protein) C-terminal region (aa 110–160) Inhibition of TPPP dimerization Modulation of microtubule organization [62]
Lamin B1 and A/C ND ND Regulation of chromatin organization [40,63]
Importin α Armadillo motif; NLS-cargo-binding domain Inhibition of importin–NPM1 binding Inhibition of nuclear transport [66]
HMG20A C-terminus (aa 311–347) ND Regulation of neuronal differentiation [65]
RSK1 ND ND Regulation of cell survival and proliferation [56]
Annexins: Anx1, Anx2, Anx6 and Anx11 N-terminus ND Modulation of membrane dynamics [70,71,72,96]
Sgt1 SGS domain Inhibition of Sgt1-Hsp90 binding Modulation of chaperone complexes [74]
CacyBP/SIP SGS domain Inhibition of CacyBP/SIP phosphorylation by CKII Regulation of CacyBP/SIP phosphatase activity and ERK1/2-Elk-1 signaling pathway [81,82,100]
Hop and TOM70 TPR domain Dissociation of Hop and TOM70 complexes with Hsp90 or Hsp70 Modulation of chaperone complexes [60]
Melusin C-terminus ND Regulation of cardioprotective pathway [76]
CHIP TPR and U-box domains Moderate inhibition of CHIP interaction with Hsp90 and Hsp70; suppression of mutant p53 degradation Modulation of chaperone complexes and p53 degradation [77]
Cyp-40 and FKBP52 TPR domain Inhibition of Cyp-40 and FKBP52 binding with Hsp90 Modulation of chaperone complexes [79]
FKBP38 TPR domain Dissociation of the FKBP38-Hsp90 and FKBP38-Bcl2 complexes; suppression of Bcl2 stability Modulation of chaperone complexes [78]
PP5 TPR domain Dissociation of the PP5-Hsp90 complex; stimulation of PP5 activity Modulation of chaperone complexes [80]
P53, p63 and p73 P53: C-terminal tetramerization domain (aa 293–393); N-terminal transactivation domain (aa 1–57) Inhibition of p53 tetramerization Regulation of p53, p63 and p73 oligomerization and activity [83,84,87]
Mdm2 N-terminus (aa 2–125) ND Moderate inhibition of p53 ubiquitination [86]
RAGE V, C1 and C2 domains Induction of RAGE dimerization/clustering Modulation of signal transduction through RAGE [89,90,120]
Integrin β1 Extracellular domain Increase in FAK and PAK phosphorylation Modulation of integrin- dependent signaling [59]
NCX1 and TRPM4 ND ND Modulation of ion transport [56]
Erythropoietin N- and C- terminus ND Regulation of erythropoietin secretion and/or activity [92]
Cytokines, e.g., IFN-β, IL-11 and CNTF ND No effect on IFN-β-induced cytotoxicity Modulation of cytokine activity/signaling [91,93]
Lysozyme N-terminus Inhibition of S100A6-RAGE interaction Modulation of RAGE-dependent signaling [55,95]
Lumican, PRELP and IGFBP-1 ND Competition of the IGF-1–IGFBP-1 interaction Remodeling of extracellular matrix [94]
GAPDH ND ND Regulation of metabolic processes [96]

TPR—tetratricopeptide; SGS—SGT1 specific, ND—not determined.