KIF1A kinesins are single-headed motor proteins which move on cylindrical nano-tubes called microtubules (MT). A normal MT consists of 13 protofilaments on which the equispaced motor binding sites form a periodic array. The collective movement of the kinesins on a MT is, therefore, analogous to vehicular traffic on multi-lane highways where each protofilament is the analogue of a single lane. Does lane-changing increase or decrease the motor flux per lane? We address this fundamental question here by appropriately extending a recent model [Phys. Rev. E 75, 041905 (2007)]. By carrying out analytical calculations and computer simulations of this extended model, we predict that the flux per lane can increase or decrease with the increasing rate of lane changing, depending on the concentrations of motors and the rate of hydrolysis of ATP, the "fuel" molecules. Our predictions can be tested, in principle, by carrying out in-vitro experiments with fluorescently labelled KIF1A molecules.Members of the kinesin superfamily of motor proteins move along microtubules (MTs) which are cylindrical nano-tubes [1,2]. A normal MT consists of 13 protofilaments each of which is formed by the head-to-tail sequential lining up of basic subunits. Each subunit of a protofilament is a 8 nm heterodimer of α-β tubulins and provides a specific binding site for a single head of a kinesin motor. Often many kinesins move simultaneously along a given MT; because of close similarities with vehicular traffic [3], the collective movement of the molecular motors on a MT is sometimes referred to as molecular motor traffic [4,5,6,7,8].The effects of lane changing on the flow properties of vehicular traffic has been investigated extensively using particle-hopping models [3] which are, essentially, appropriate extensions of the totally asymmetric simple exclusion process (TASEP) [9,10,11]. Models of multi-lane TASEP, where the particles can occasionally change lane, have also been investigated analytically [12,13]. Twolane generalizations of generic models of cytoskeletal molecular motor traffic have also been reported [14,15].Recently a quantitative theoretical model has been developed [16, 17] (from now onwards, we shall refer to it as the NOSC model) for the traffic of KIF1A proteins, which are single-headed kinesins [18,19,20], by explicitly capturing the essential features of the mechano-chemical cycle of each individual KIF1A motor, in addition to their steric interactions. In this communication we extend the NOSC model by adding to the master equation all those terms which correspond to lane changing. Solving these equations analytically, we address a fundamental question: does lane changing increase or decrease flux per lane? We show that the answer to this question depends on the parameter regime of our model. We establish the * Electronic address: debch@iitk.ac.in † Electronic address: garai@iitk.ac.in ‡ Electronic address: phywjs@nus.edu.sg levels of accuracy of our analytical results by comparing with the corresponding numerical data obt...