Abstract:We have cloned two cDNAs that encode N66-like proteins in Pinctada maxima and are named N36 and N45, respectively. The open reading frame (ORF) of N36 was 987 bp long, encoding 329 amino acids with molecular mass estimated to be 35.7 kD while the ORF of N45 was 1 164 bp, encoding 387 amino acids with estimated molecular mass of 44.6 kD. Both proteins were rich in Gly, Asn and Asp residues. There was no signal peptide in N36 protein while the amino acid residues 1-22 in N45 showed a typical signal peptide. N36 and N45 contained 2 and 1 putative glycosylation sequences, 9 and 16 putative phosphorylation sites, respectively. Their secondary structure consisted of α-helix,β-sheet and coil. Phylogenetic analysis indicated that N36 and N45 were more closely related to N66 than other nacrein-like proteins. Similar to nacrein in P. fucata and N66 in P. maxima, N36 and N45 proteins contained two functional domains: α-carbonic anhydrase domain and Gly-Xaa-Asn (Xaa = Asp, Asn or Glu) repeat domain, suggesting that both N36 and N45 are likely to participate in calcium carbonate crystal formation in nacreous layer.