rec. | Subject | Hit Length | Description | Align.Len | E value | Bit score | % ident. | % pos. | GO associations |
1 | P35362 | 376 | OPSD_SPHSP Rhodopsin OS=Sphodromantis sp. (Ma... | 40 | 1.2 | 30.4 | 30 | 60 | GO:0016021; C:integral to membrane; IEA:UniProtKB-KW. | | | | | | | | | | GO:0004930; F:G-protein coupled receptor activity; IEA:UniProtKB-KW.::GO:0009881; F:photoreceptor activity; IEA:UniProtKB-KW. | | | | | | | | | | GO:0007602; P:phototransduction; IEA:UniProtKB-KW.::GO:0018298; P:protein-chromophore linkage; IEA:UniProtKB-KW.::GO:0007601; P:visual perception; IEA:UniProtKB-KW. | 2 | O14254 | 439 | IDHP_SCHPO Probable isocitrate dehydrogenase ... | 31 | 2.7 | 29.3 | 45 | 61 | GO:0005739; C:mitochondrion; IDA:PomBase. | | | | | | | | | | GO:0004450; F:isocitrate dehydrogenase (NADP+) activity; ISS:PomBase.::GO:0000287; F:magnesium ion binding; IEA:InterPro.::GO:0051287; F:NAD binding; IEA:InterPro. | | | | | | | | | | GO:0006537; P:glutamate biosynthetic process; ISS:PomBase.::GO:0006102; P:isocitrate metabolic process; ISS:PomBase.::GO:0006740; P:NADPH regeneration; ISS:PomBase.::GO:0006099; P:tricarboxylic acid cycle; IC:PomBase. | 3 | Q4PGL2 | 1910 | INO80_USTMA Putative DNA helicase INO80 OS=Us... | 44 | 3.4 | 29.3 | 34 | 52 | GO:0005634; C:nucleus; IEA:UniProtKB-SubCell. | | | | | | | | | | GO:0005524; F:ATP binding; IEA:UniProtKB-KW.::GO:0003677; F:DNA binding; IEA:UniProtKB-KW.::GO:0004386; F:helicase activity; IEA:UniProtKB-KW. | | | | | | | | | | GO:0016568; P:chromatin modification; IEA:UniProtKB-KW.::GO:0006281; P:DNA repair; IEA:UniProtKB-KW.::GO:0006355; P:regulation of transcription, DNA-dependent; IEA:UniProtKB-KW.::GO:0006351; P:transcription, DNA-dependent; IEA:UniProtKB-KW. | 4 | B3P2S2 | 782 | UFL1_DROER E3 UFM1-protein ligase 1 homolog O... | 15 | 3.5 | 28.9 | 73 | 80 | | | | | | | | | | | GO:0016874; F:ligase activity; IEA:UniProtKB-KW. | | | | | | | | | | | 5 | P20196 | 154 | A154_SSV1 Uncharacterized protein A-154 OS=Su... | 37 | 8.1 | 27.7 | 38 | 59 | | | | | | | | | | | | | | | | | | | | | |