Melanin is the main pigment responsible for the color of human skin, hair and eye. Its biosynthesis requires three melanogenic enzymes,t yrosinase (TYR), andt he tyrosinase-relatedp roteins TYRP1 and TYRP2. Thed ifficulty of isolating pure and homogeneous proteins from endogenous sources has hampered their study,and resulted in many contradictory findings regarding their physiological functions. In this review,w es ummarize recent advances on the structure and function of TYR and TYRPs by virtue of the crystal structure of human TYRP1, which is the first available structureo f am ammalian melanogenic enzyme. This structure, combined with tyrosinase structures from other lower eukaryotes and mutagenesis studies of key actives ite residues,s heds light on the mechanism of TYR and TYRPs. Furthermore, a TYRP1-based homology model of TYR provides ah igh-quality platform to map and analyze albinism-related mutations, as wella st he design of specific antimelanogenic compounds. Finally,w ep rovide perspectives for future structure/ functionstudies of TYR and TYRPs.