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Nuclear lamins are nucleus-specific intermediate filaments (IF) found at the inner nuclear membrane (INM) of the nuclear envelope (NE). Together with nuclear envelope transmembrane proteins, they form the nuclear lamina and are crucial for gene regulation and mechanical robustness of the nucleus and the whole cell. Recently, we characterized <i>Dictyostelium</i> NE81 as an evolutionarily conserved lamin-like protein, both on the sequence and functional level. Here, we show on the structural level that the <i>Dictyostelium</i> NE81 is also capable of assembling into filaments, just as metazoan lamin filament assemblies. Using field-emission scanning electron microscopy, we show that NE81 expressed in <i>Xenopous</i> oocytes forms filamentous structures with an overall appearance highly reminiscent of <i>Xenopus</i> lamin B2. The in vitro assembly properties of recombinant His-tagged NE81 purified from <i>Dictyostelium</i> extracts are very similar to those of metazoan lamins. Super-resolution stimulated emission depletion (STED) and expansion microscopy (ExM), as well as transmission electron microscopy of negatively stained purified NE81, demonstrated its capability of forming filamentous structures under low-ionic-strength conditions. These results recommend <i>Dictyostelium</i> as a non-mammalian model organism with a well-characterized nuclear envelope involving all relevant protein components known in animal cells.