Biological replicators are locked in deeply intertwined genetic conflicts with each other. Using comparative genomics, protein sequence and structure analysis and evolutionary investigations, my lab has uncovered a staggering diversity of molecular armaments and mechanisms regulating their deployment, collectively termed biological conflict systems. These include toxins used in interorganismal interactions and a host of mechanisms involved in self/nonself discrimination, especially in the context of host-selfish element conflicts. Our studies have helped identify shared syntactical features in the organizational logic of biological conflict systems. These principles can be exploited to discover new conflict systems through computational analyses. Further, we find that across the range of biological organization, from intragenomic conflicts to interorganismal conflicts, a circumscribed set of effector protein domain families is deployed, targeting genetic information flow through the Central Dogma, certain membranes, and key molecules like NAD+ and NTPs. This has led to significant advances in discovering new biochemistry of these systems and furnished new biotechnological reagents for genome editing, sequencing and beyond. I’ll discuss this using specific examples of toxins in interorganismal conflict and effectors in antiviral immunity.