Barley molybdenum cofactor sulfurase (MCSU): sequencing, modeling, and its comparison to other higher plants

Molybdenum cofactor sulfurases (MCSUs) are important enzymes for plant development and response to environmentalqueues, including processes such as nitrogen metabolism and regulation of the abscisic acid levels in plant tissues. We cloned andsequenced MCSU gene from barley and performed in silico comparison with rice, tomato, and Arabidopsis. Physico-chemical propertiesand subcellular predictions were found to be similar in different plant species. All MCSUs had three critical domains: aminotransferaseclass-V (Pfam: PF00266), MOSC N-terminal beta barrel (Pfam: PF03476), and MOSC (Pfam: PF03473). Secondary structure analysisrevealed that random coils were the most abundant, followed by α-helices and extended strands. Predicted binding sites of MCSUswere different in barley and Arabidopsis, whereas rice and tomato showed the same pattern. A conserved triple-cysteine motif wasdetected in all MCSUs with cys438-cys440-cys445, cys431-cys433-cys438, cys428-cys430-cys435, and cys425-cys427-cys432 in barley, rice, Arabidopsis, and tomato, respectively. Furthermore, a 3D structure analysis indicated that structural divergences were present in all MCSUs, even in the core domain structure. Phylogenetic analysis of MCSUs revealed that monocot–dicot divergence was clearly observed with high bootstrap values. The results of this study will contribute to the understanding of MCSU genes and proteins in plants. The data of this study will also constitute a scientific basis for wet-lab and in silico studies of MCSUs.