rec. | Subject | Hit Length | Description | Align.Len | E value | Bit score | % ident. | % pos. | GO associations |
1 | P33301 | 854 | XRS2_YEAST DNA repair protein XRS2 OS=Sacchar... | 854 | 0 | 1748 | 100 | 100 | GO:0030870; C:Mre11 complex; IPI:SGD.::GO:0005654; C:nucleoplasm; TAS:Reactome. | | | | | | | | | | GO:0003691; F:double-stranded telomeric DNA binding; IDA:SGD.::GO:0051880; F:G-quadruplex DNA binding; IDA:SGD.::GO:0030674; F:protein binding, bridging; IDA:SGD.::GO:0043047; F:single-stranded telomeric DNA binding; IDA:SGD. | | | | | | | | | | GO:0006284; P:base-excision repair; IMP:SGD.::GO:0000727; P:double-strand break repair via break-induced replication; TAS:SGD.::GO:0006303; P:double-strand break repair via nonhomologous end joining; IMP:SGD.::GO:0042138; P:meiotic DNA double-strand break formation; IMP:SGD.::GO:0030435; P:sporulation resulting in formation of a cellular spore; IMP:SGD.::GO:0000723; P:telomere maintenance; IMP:SGD. | 2 | Q8CMN4 | 115 | RNPA_STAES Ribonuclease P protein component O... | 88 | 0.84 | 34.7 | 30 | 51 | | | | | | | | | | | GO:0004526; F:ribonuclease P activity; IEA:EC.::GO:0000049; F:tRNA binding; IEA:InterPro. | | | | | | | | | | GO:0008033; P:tRNA processing; IEA:UniProtKB-KW. | 3 | Q5HS37 | 115 | RNPA_STAEQ Ribonuclease P protein component O... | 88 | 0.84 | 34.7 | 30 | 51 | | | | | | | | | | | GO:0004526; F:ribonuclease P activity; IEA:EC.::GO:0000049; F:tRNA binding; IEA:InterPro. | | | | | | | | | | GO:0008033; P:tRNA processing; IEA:UniProtKB-KW. | 4 | O64692 | 335 | G2OX3_ARATH Gibberellin 2-beta-dioxygenase 3 ... | 64 | 2.6 | 35 | 36 | 58 | | | | | | | | | | | GO:0045543; F:gibberellin 2-beta-dioxygenase activity; IEA:EC.::GO:0046872; F:metal ion binding; IEA:UniProtKB-KW.::GO:0016702; F:oxidoreductase activity, acting on single donors with incorporation of molecular oxygen, incorporation of two atoms of oxygen; IEA:UniProtKB-KW. | | | | | | | | | | | 5 | Q8PNG1 | 106 | Y1110_XANAC UPF0133 protein XAC1110 OS=Xantho... | 84 | 8 | 31.6 | 27 | 52 | | | | | | | | | | | | | | | | | | | | | |