Predicted to enable rRNA (uridine-N3-)-methyltransferase activity. Predicted to be involved in rRNA base methylation. Is an ortholog of C. elegans eef-1B.2.
Predicted to enable protein tyrosine phosphatase activity and uracil DNA N-glycosylase activity. Predicted to be involved in base-excision repair. Predicted to be located in cytoplasm.
Predicted to enable DNA binding activity and zinc ion binding activity. Predicted to be involved in DNA repair. Is an ortholog of C. elegans apn-1. In C. elegans, apn-1 is involved in base-excision repair.
Predicted to enable DNA binding activity and zinc ion binding activity. Predicted to be involved in DNA repair. Is an ortholog of C. elegans apn-1. In C. elegans, apn-1 is involved in base-excision repair.
Predicted to enable calcium ion binding activity; damaged DNA binding activity; and oxidized purine nucleobase lesion DNA N-glycosylase activity. Predicted to be involved in base-excision repair and nucleotide-excision repair. Is an ortholog of B. malayi Bm4972.
Predicted to enable rRNA (pseudouridine) methyltransferase activity. Predicted to be a structural constituent of ribosome. Predicted to be involved in rRNA base methylation and translation. Predicted to be located in ribosome. Is an ortholog of C. elegans Y39A1A.14.
Predicted to enable DNA binding activity and catalytic activity. Predicted to be involved in base-excision repair. Is an ortholog of C. elegans nth-1. In C. elegans, nth-1 is involved in cellular response to hydrogen peroxide and depyrimidination.
Predicted to enable damaged DNA binding activity. Predicted to be involved in DNA repair. Predicted to be located in nucleus. Is an ortholog of C. elegans ercc-1. In C. elegans, ercc-1 is involved in UV-damage excision repair and base-excision repair.