The tip influence on the energy level alignment at the SnPc/Ag(111) interface has been addressed via scanning tunneling spectroscopy (STS). A collective effect characteristic for both molecular conformations up and down is reported to shift the corresponding first filled and empty levels toward the Fermi energy via a tip鈭抯ample distance decrease. The importance of the tin ion coupling to the metal electrodes is emphasized for the newly reported 鈥渃ross-bending鈥?effect as well as for a controllable tip-induced single-molecule switching and 鈥渘ano-writing鈥?within densely packed molecular arrays.