Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030870 | Mre11 complex | 3 | 10 |
GO:0032991 | protein-containing complex | 1 | 10 |
GO:0140513 | nuclear protein-containing complex | 2 | 10 |
GO:0000228 | nuclear chromosome | 6 | 1 |
GO:0000793 | condensed chromosome | 6 | 1 |
GO:0000794 | condensed nuclear chromosome | 7 | 1 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005694 | chromosome | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000723 | telomere maintenance | 5 | 10 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006259 | DNA metabolic process | 4 | 10 |
GO:0006281 | DNA repair | 5 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0006950 | response to stress | 2 | 10 |
GO:0006974 | DNA damage response | 4 | 10 |
GO:0006996 | organelle organization | 4 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016043 | cellular component organization | 3 | 10 |
GO:0032200 | telomere organization | 6 | 10 |
GO:0033554 | cellular response to stress | 3 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0050896 | response to stimulus | 1 | 10 |
GO:0051276 | chromosome organization | 5 | 10 |
GO:0051716 | cellular response to stimulus | 2 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0071840 | cellular component organization or biogenesis | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
GO:0000722 | telomere maintenance via recombination | 6 | 1 |
GO:0006278 | RNA-templated DNA biosynthetic process | 6 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0006312 | mitotic recombination | 6 | 1 |
GO:0007004 | telomere maintenance via telomerase | 7 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0010833 | telomere maintenance via telomere lengthening | 6 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022414 | reproductive process | 1 | 1 |
GO:0032392 | DNA geometric change | 7 | 1 |
GO:0032508 | DNA duplex unwinding | 8 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0070192 | chromosome organization involved in meiotic cell cycle | 3 | 1 |
GO:0071103 | DNA conformation change | 6 | 1 |
GO:0071897 | DNA biosynthetic process | 5 | 1 |
GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
GO:1903046 | meiotic cell cycle process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 10 |
GO:0016462 | pyrophosphatase activity | 5 | 10 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 10 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 10 |
GO:0016887 | ATP hydrolysis activity | 7 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 10 |
GO:0140299 | small molecule sensor activity | 1 | 10 |
GO:0140612 | DNA damage sensor activity | 2 | 10 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 10 |
GO:0140657 | ATP-dependent activity | 1 | 10 |
GO:0140664 | ATP-dependent DNA damage sensor activity | 3 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003690 | double-stranded DNA binding | 5 | 1 |
GO:0003691 | double-stranded telomeric DNA binding | 6 | 1 |
GO:0003697 | single-stranded DNA binding | 5 | 1 |
GO:0042162 | telomeric DNA binding | 6 | 1 |
GO:0043047 | single-stranded telomeric DNA binding | 7 | 1 |
GO:0043565 | sequence-specific DNA binding | 5 | 1 |
GO:0051880 | G-quadruplex DNA binding | 5 | 1 |
GO:0098847 | sequence-specific single stranded DNA binding | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 114 | 118 | PF00656 | 0.471 |
CLV_C14_Caspase3-7 | 1295 | 1299 | PF00656 | 0.501 |
CLV_NRD_NRD_1 | 1049 | 1051 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 1230 | 1232 | PF00675 | 0.215 |
CLV_NRD_NRD_1 | 1307 | 1309 | PF00675 | 0.354 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.215 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 407 | 409 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 635 | 637 | PF00675 | 0.395 |
CLV_NRD_NRD_1 | 714 | 716 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 824 | 826 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 843 | 845 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 905 | 907 | PF00675 | 0.554 |
CLV_PCSK_KEX2_1 | 1049 | 1051 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 1154 | 1156 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 1230 | 1232 | PF00082 | 0.204 |
CLV_PCSK_KEX2_1 | 1240 | 1242 | PF00082 | 0.204 |
CLV_PCSK_KEX2_1 | 1307 | 1309 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.205 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 452 | 454 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 635 | 637 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 672 | 674 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 945 | 947 | PF00082 | 0.605 |
CLV_PCSK_PC1ET2_1 | 1154 | 1156 | PF00082 | 0.371 |
CLV_PCSK_PC1ET2_1 | 1240 | 1242 | PF00082 | 0.209 |
CLV_PCSK_PC1ET2_1 | 177 | 179 | PF00082 | 0.308 |
CLV_PCSK_PC1ET2_1 | 328 | 330 | PF00082 | 0.560 |
CLV_PCSK_PC1ET2_1 | 672 | 674 | PF00082 | 0.371 |
CLV_PCSK_PC1ET2_1 | 945 | 947 | PF00082 | 0.600 |
CLV_PCSK_PC7_1 | 1236 | 1242 | PF00082 | 0.204 |
CLV_PCSK_PC7_1 | 282 | 288 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 1265 | 1269 | PF00082 | 0.204 |
CLV_PCSK_SKI1_1 | 1308 | 1312 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.205 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.200 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.171 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 558 | 562 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 596 | 600 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 673 | 677 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.231 |
CLV_PCSK_SKI1_1 | 882 | 886 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 977 | 981 | PF00082 | 0.488 |
DEG_APCC_DBOX_1 | 258 | 266 | PF00400 | 0.543 |
DEG_APCC_DBOX_1 | 470 | 478 | PF00400 | 0.483 |
DEG_APCC_DBOX_1 | 557 | 565 | PF00400 | 0.387 |
DEG_APCC_DBOX_1 | 672 | 680 | PF00400 | 0.465 |
DEG_APCC_KENBOX_2 | 455 | 459 | PF00400 | 0.408 |
DEG_COP1_1 | 138 | 147 | PF00400 | 0.445 |
DEG_SPOP_SBC_1 | 130 | 134 | PF00917 | 0.446 |
DEG_SPOP_SBC_1 | 409 | 413 | PF00917 | 0.336 |
DOC_CYCLIN_RxL_1 | 606 | 614 | PF00134 | 0.375 |
DOC_CYCLIN_RxL_1 | 958 | 968 | PF00134 | 0.580 |
DOC_CYCLIN_RxL_1 | 985 | 993 | PF00134 | 0.546 |
DOC_MAPK_DCC_7 | 758 | 766 | PF00069 | 0.358 |
DOC_MAPK_gen_1 | 1154 | 1163 | PF00069 | 0.363 |
DOC_MAPK_gen_1 | 1307 | 1318 | PF00069 | 0.272 |
DOC_MAPK_gen_1 | 346 | 353 | PF00069 | 0.509 |
DOC_MAPK_gen_1 | 755 | 763 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 1007 | 1016 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 1257 | 1266 | PF00069 | 0.404 |
DOC_MAPK_MEF2A_6 | 746 | 754 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 758 | 766 | PF00069 | 0.503 |
DOC_MAPK_MEF2A_6 | 81 | 88 | PF00069 | 0.404 |
DOC_MAPK_NFAT4_5 | 81 | 89 | PF00069 | 0.415 |
DOC_PP1_RVXF_1 | 108 | 114 | PF00149 | 0.508 |
DOC_PP1_RVXF_1 | 83 | 89 | PF00149 | 0.404 |
DOC_PP2B_LxvP_1 | 170 | 173 | PF13499 | 0.411 |
DOC_PP2B_LxvP_1 | 992 | 995 | PF13499 | 0.513 |
DOC_PP4_FxxP_1 | 27 | 30 | PF00568 | 0.404 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 1183 | 1187 | PF00917 | 0.338 |
DOC_USP7_MATH_1 | 1229 | 1233 | PF00917 | 0.259 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 576 | 580 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 678 | 682 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 702 | 706 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 740 | 744 | PF00917 | 0.360 |
DOC_USP7_MATH_1 | 859 | 863 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 951 | 955 | PF00917 | 0.504 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 720 | 725 | PF00397 | 0.414 |
LIG_14-3-3_CanoR_1 | 1079 | 1085 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 110 | 120 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 1101 | 1106 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 1155 | 1161 | PF00244 | 0.351 |
LIG_14-3-3_CanoR_1 | 1204 | 1208 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 1230 | 1234 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 1249 | 1259 | PF00244 | 0.346 |
LIG_14-3-3_CanoR_1 | 136 | 144 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 309 | 319 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 407 | 416 | PF00244 | 0.657 |
LIG_14-3-3_CanoR_1 | 719 | 724 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 882 | 890 | PF00244 | 0.616 |
LIG_Actin_WH2_2 | 248 | 265 | PF00022 | 0.531 |
LIG_Actin_WH2_2 | 805 | 822 | PF00022 | 0.505 |
LIG_Actin_WH2_2 | 983 | 1001 | PF00022 | 0.288 |
LIG_AP2alpha_1 | 180 | 184 | PF02296 | 0.446 |
LIG_BRCT_BRCA1_1 | 1268 | 1272 | PF00533 | 0.404 |
LIG_BRCT_BRCA1_1 | 199 | 203 | PF00533 | 0.428 |
LIG_DLG_GKlike_1 | 1101 | 1108 | PF00625 | 0.381 |
LIG_FHA_1 | 1111 | 1117 | PF00498 | 0.489 |
LIG_FHA_1 | 1163 | 1169 | PF00498 | 0.322 |
LIG_FHA_1 | 1212 | 1218 | PF00498 | 0.416 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.415 |
LIG_FHA_1 | 1283 | 1289 | PF00498 | 0.404 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.408 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.404 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.404 |
LIG_FHA_1 | 489 | 495 | PF00498 | 0.347 |
LIG_FHA_1 | 606 | 612 | PF00498 | 0.472 |
LIG_FHA_1 | 693 | 699 | PF00498 | 0.460 |
LIG_FHA_1 | 814 | 820 | PF00498 | 0.510 |
LIG_FHA_1 | 872 | 878 | PF00498 | 0.524 |
LIG_FHA_2 | 1041 | 1047 | PF00498 | 0.686 |
LIG_FHA_2 | 1105 | 1111 | PF00498 | 0.449 |
LIG_FHA_2 | 1115 | 1121 | PF00498 | 0.471 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.471 |
LIG_FHA_2 | 1284 | 1290 | PF00498 | 0.404 |
LIG_FHA_2 | 1317 | 1323 | PF00498 | 0.252 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.520 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.519 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.395 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.404 |
LIG_FHA_2 | 515 | 521 | PF00498 | 0.318 |
LIG_FHA_2 | 720 | 726 | PF00498 | 0.457 |
LIG_FHA_2 | 809 | 815 | PF00498 | 0.444 |
LIG_FHA_2 | 937 | 943 | PF00498 | 0.644 |
LIG_Integrin_isoDGR_2 | 280 | 282 | PF01839 | 0.422 |
LIG_Integrin_RGD_1 | 1145 | 1147 | PF01839 | 0.445 |
LIG_LIR_Gen_1 | 112 | 121 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 1147 | 1156 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 1158 | 1168 | PF02991 | 0.297 |
LIG_LIR_Gen_1 | 1174 | 1184 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 1344 | 1355 | PF02991 | 0.259 |
LIG_LIR_Gen_1 | 681 | 690 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 739 | 747 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 800 | 809 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 862 | 871 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 112 | 116 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 1147 | 1152 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 1158 | 1163 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 1174 | 1180 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 119 | 125 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 1232 | 1238 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 1334 | 1340 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 1344 | 1350 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 1352 | 1358 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 653 | 658 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 681 | 686 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 739 | 744 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 800 | 806 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 862 | 866 | PF02991 | 0.434 |
LIG_LYPXL_SIV_4 | 869 | 877 | PF13949 | 0.507 |
LIG_NRBOX | 301 | 307 | PF00104 | 0.565 |
LIG_NRBOX | 390 | 396 | PF00104 | 0.517 |
LIG_PCNA_yPIPBox_3 | 1191 | 1203 | PF02747 | 0.306 |
LIG_PDZ_Class_2 | 1355 | 1360 | PF00595 | 0.266 |
LIG_Pex14_1 | 1203 | 1207 | PF04695 | 0.310 |
LIG_Pex14_2 | 1355 | 1359 | PF04695 | 0.248 |
LIG_Pex14_2 | 180 | 184 | PF04695 | 0.404 |
LIG_RPA_C_Fungi | 658 | 670 | PF08784 | 0.324 |
LIG_RPA_C_Plants | 966 | 977 | PF08784 | 0.444 |
LIG_SH2_CRK | 1235 | 1239 | PF00017 | 0.239 |
LIG_SH2_GRB2like | 1149 | 1152 | PF00017 | 0.436 |
LIG_SH2_NCK_1 | 870 | 874 | PF00017 | 0.380 |
LIG_SH2_SRC | 1149 | 1152 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 1000 | 1003 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 1338 | 1341 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.604 |
LIG_SH3_2 | 169 | 174 | PF14604 | 0.254 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.254 |
LIG_SH3_3 | 566 | 572 | PF00018 | 0.487 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.239 |
LIG_SUMO_SIM_anti_2 | 537 | 542 | PF11976 | 0.416 |
LIG_SUMO_SIM_par_1 | 1213 | 1222 | PF11976 | 0.428 |
LIG_SUMO_SIM_par_1 | 1277 | 1283 | PF11976 | 0.239 |
LIG_SUMO_SIM_par_1 | 1314 | 1319 | PF11976 | 0.271 |
LIG_SUMO_SIM_par_1 | 189 | 194 | PF11976 | 0.254 |
LIG_SUMO_SIM_par_1 | 762 | 767 | PF11976 | 0.293 |
LIG_SUMO_SIM_par_1 | 814 | 822 | PF11976 | 0.443 |
LIG_TRAF2_1 | 1026 | 1029 | PF00917 | 0.510 |
LIG_TRAF2_1 | 264 | 267 | PF00917 | 0.415 |
LIG_TRAF2_1 | 339 | 342 | PF00917 | 0.569 |
LIG_TRAF2_1 | 490 | 493 | PF00917 | 0.531 |
LIG_TRAF2_1 | 618 | 621 | PF00917 | 0.478 |
LIG_TRAF2_1 | 690 | 693 | PF00917 | 0.245 |
LIG_TRAF2_1 | 736 | 739 | PF00917 | 0.434 |
LIG_TRAF2_1 | 862 | 865 | PF00917 | 0.463 |
LIG_WRC_WIRS_1 | 12 | 17 | PF05994 | 0.239 |
LIG_WRC_WIRS_1 | 709 | 714 | PF05994 | 0.489 |
LIG_WRC_WIRS_1 | 99 | 104 | PF05994 | 0.254 |
MOD_CK1_1 | 1083 | 1089 | PF00069 | 0.533 |
MOD_CK1_1 | 1104 | 1110 | PF00069 | 0.454 |
MOD_CK1_1 | 581 | 587 | PF00069 | 0.414 |
MOD_CK1_1 | 705 | 711 | PF00069 | 0.499 |
MOD_CK2_1 | 1104 | 1110 | PF00069 | 0.416 |
MOD_CK2_1 | 1114 | 1120 | PF00069 | 0.367 |
MOD_CK2_1 | 1175 | 1181 | PF00069 | 0.484 |
MOD_CK2_1 | 1216 | 1222 | PF00069 | 0.529 |
MOD_CK2_1 | 1316 | 1322 | PF00069 | 0.252 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.424 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.492 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.239 |
MOD_CK2_1 | 514 | 520 | PF00069 | 0.442 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.239 |
MOD_CK2_1 | 624 | 630 | PF00069 | 0.430 |
MOD_CK2_1 | 719 | 725 | PF00069 | 0.417 |
MOD_CK2_1 | 775 | 781 | PF00069 | 0.339 |
MOD_CK2_1 | 808 | 814 | PF00069 | 0.498 |
MOD_CK2_1 | 859 | 865 | PF00069 | 0.472 |
MOD_CK2_1 | 936 | 942 | PF00069 | 0.665 |
MOD_GlcNHglycan | 1020 | 1023 | PF01048 | 0.557 |
MOD_GlcNHglycan | 1050 | 1053 | PF01048 | 0.608 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.384 |
MOD_GlcNHglycan | 1177 | 1180 | PF01048 | 0.379 |
MOD_GlcNHglycan | 1252 | 1255 | PF01048 | 0.239 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.432 |
MOD_GlcNHglycan | 546 | 551 | PF01048 | 0.417 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.236 |
MOD_GlcNHglycan | 601 | 606 | PF01048 | 0.246 |
MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.244 |
MOD_GlcNHglycan | 847 | 850 | PF01048 | 0.673 |
MOD_GSK3_1 | 1110 | 1117 | PF00069 | 0.472 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.181 |
MOD_GSK3_1 | 1162 | 1169 | PF00069 | 0.465 |
MOD_GSK3_1 | 1203 | 1210 | PF00069 | 0.321 |
MOD_GSK3_1 | 1218 | 1225 | PF00069 | 0.421 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.441 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.443 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.231 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.251 |
MOD_GSK3_1 | 746 | 753 | PF00069 | 0.557 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.245 |
MOD_N-GLC_1 | 514 | 519 | PF02516 | 0.538 |
MOD_N-GLC_2 | 1003 | 1005 | PF02516 | 0.415 |
MOD_N-GLC_2 | 51 | 53 | PF02516 | 0.254 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.239 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.230 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.283 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.541 |
MOD_NEK2_1 | 580 | 585 | PF00069 | 0.468 |
MOD_NEK2_1 | 775 | 780 | PF00069 | 0.311 |
MOD_NEK2_1 | 808 | 813 | PF00069 | 0.429 |
MOD_NEK2_1 | 819 | 824 | PF00069 | 0.493 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.239 |
MOD_NEK2_1 | 990 | 995 | PF00069 | 0.503 |
MOD_NEK2_2 | 678 | 683 | PF00069 | 0.328 |
MOD_PIKK_1 | 296 | 302 | PF00454 | 0.562 |
MOD_PIKK_1 | 501 | 507 | PF00454 | 0.592 |
MOD_PIKK_1 | 587 | 593 | PF00454 | 0.433 |
MOD_PIKK_1 | 839 | 845 | PF00454 | 0.546 |
MOD_PIKK_1 | 982 | 988 | PF00454 | 0.398 |
MOD_PK_1 | 746 | 752 | PF00069 | 0.550 |
MOD_PKA_1 | 496 | 502 | PF00069 | 0.345 |
MOD_PKA_2 | 1040 | 1046 | PF00069 | 0.636 |
MOD_PKA_2 | 1048 | 1054 | PF00069 | 0.570 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.397 |
MOD_PKA_2 | 1156 | 1162 | PF00069 | 0.350 |
MOD_PKA_2 | 1203 | 1209 | PF00069 | 0.317 |
MOD_PKA_2 | 1229 | 1235 | PF00069 | 0.254 |
MOD_PKA_2 | 1250 | 1256 | PF00069 | 0.272 |
MOD_PKA_2 | 135 | 141 | PF00069 | 0.373 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.612 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.391 |
MOD_PKA_2 | 819 | 825 | PF00069 | 0.575 |
MOD_PKB_1 | 195 | 203 | PF00069 | 0.272 |
MOD_PKB_1 | 406 | 414 | PF00069 | 0.453 |
MOD_Plk_1 | 1063 | 1069 | PF00069 | 0.515 |
MOD_Plk_1 | 1077 | 1083 | PF00069 | 0.419 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.268 |
MOD_Plk_1 | 1166 | 1172 | PF00069 | 0.454 |
MOD_Plk_1 | 1351 | 1357 | PF00069 | 0.255 |
MOD_Plk_1 | 210 | 216 | PF00069 | 0.298 |
MOD_Plk_1 | 242 | 248 | PF00069 | 0.347 |
MOD_Plk_1 | 387 | 393 | PF00069 | 0.513 |
MOD_Plk_1 | 514 | 520 | PF00069 | 0.512 |
MOD_Plk_1 | 601 | 607 | PF00069 | 0.432 |
MOD_Plk_1 | 705 | 711 | PF00069 | 0.408 |
MOD_Plk_1 | 813 | 819 | PF00069 | 0.552 |
MOD_Plk_2-3 | 1211 | 1217 | PF00069 | 0.404 |
MOD_Plk_2-3 | 1351 | 1357 | PF00069 | 0.255 |
MOD_Plk_4 | 1156 | 1162 | PF00069 | 0.349 |
MOD_Plk_4 | 1258 | 1264 | PF00069 | 0.243 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.332 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.439 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.264 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.239 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.239 |
MOD_Plk_4 | 708 | 714 | PF00069 | 0.527 |
MOD_Plk_4 | 746 | 752 | PF00069 | 0.375 |
MOD_Plk_4 | 798 | 804 | PF00069 | 0.368 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.282 |
MOD_ProDKin_1 | 720 | 726 | PF00069 | 0.416 |
MOD_SUMO_for_1 | 598 | 601 | PF00179 | 0.420 |
MOD_SUMO_for_1 | 690 | 693 | PF00179 | 0.300 |
MOD_SUMO_for_1 | 918 | 921 | PF00179 | 0.451 |
MOD_SUMO_rev_2 | 67 | 75 | PF00179 | 0.241 |
MOD_SUMO_rev_2 | 767 | 775 | PF00179 | 0.461 |
MOD_SUMO_rev_2 | 77 | 82 | PF00179 | 0.244 |
MOD_SUMO_rev_2 | 900 | 909 | PF00179 | 0.488 |
TRG_DiLeu_BaEn_1 | 1091 | 1096 | PF01217 | 0.285 |
TRG_DiLeu_BaEn_2 | 63 | 69 | PF01217 | 0.254 |
TRG_DiLeu_BaEn_4 | 601 | 607 | PF01217 | 0.364 |
TRG_DiLeu_BaLyEn_6 | 390 | 395 | PF01217 | 0.517 |
TRG_DiLeu_BaLyEn_6 | 82 | 87 | PF01217 | 0.254 |
TRG_ENDOCYTIC_2 | 1149 | 1152 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 1177 | 1180 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 1235 | 1238 | PF00928 | 0.239 |
TRG_ENDOCYTIC_2 | 1337 | 1340 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 655 | 658 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 683 | 686 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 741 | 744 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 803 | 806 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 863 | 866 | PF00928 | 0.426 |
TRG_ER_diArg_1 | 1248 | 1251 | PF00400 | 0.254 |
TRG_ER_diArg_1 | 203 | 205 | PF00400 | 0.254 |
TRG_ER_diArg_1 | 290 | 292 | PF00400 | 0.601 |
TRG_ER_diArg_1 | 336 | 338 | PF00400 | 0.578 |
TRG_ER_diArg_1 | 406 | 408 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 451 | 454 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 758 | 761 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 938 | 941 | PF00400 | 0.588 |
TRG_NES_CRM1_1 | 559 | 573 | PF08389 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 1007 | 1011 | PF00026 | 0.597 |
TRG_Pf-PMV_PEXEL_1 | 1294 | 1298 | PF00026 | 0.239 |
TRG_Pf-PMV_PEXEL_1 | 1301 | 1305 | PF00026 | 0.292 |
TRG_Pf-PMV_PEXEL_1 | 1326 | 1331 | PF00026 | 0.279 |
TRG_Pf-PMV_PEXEL_1 | 205 | 209 | PF00026 | 0.332 |
TRG_Pf-PMV_PEXEL_1 | 253 | 257 | PF00026 | 0.561 |
TRG_Pf-PMV_PEXEL_1 | 369 | 373 | PF00026 | 0.511 |
TRG_Pf-PMV_PEXEL_1 | 506 | 510 | PF00026 | 0.588 |
TRG_Pf-PMV_PEXEL_1 | 596 | 601 | PF00026 | 0.394 |
TRG_Pf-PMV_PEXEL_1 | 609 | 614 | PF00026 | 0.298 |
TRG_Pf-PMV_PEXEL_1 | 901 | 905 | PF00026 | 0.625 |
TRG_Pf-PMV_PEXEL_1 | 928 | 932 | PF00026 | 0.510 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3D5 | Leptomonas seymouri | 70% | 100% |
A0A0S4JAY7 | Bodo saltans | 38% | 100% |
A0A1X0NYH4 | Trypanosomatidae | 47% | 100% |
A0A3R7N260 | Trypanosoma rangeli | 47% | 100% |
A0A3S7X1A7 | Leishmania donovani | 93% | 100% |
A4HG93 | Leishmania braziliensis | 84% | 100% |
A4I3C7 | Leishmania infantum | 93% | 100% |
D0A818 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
P70388 | Mus musculus | 28% | 100% |
Q4Q8L7 | Leishmania major | 93% | 100% |
V5BQC9 | Trypanosoma cruzi | 46% | 100% |