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 | 0.498 |
CLV_C14_Caspase3-7 | 1296 | 1300 | PF00656 | 0.528 |
CLV_NRD_NRD_1 | 1050 | 1052 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 1231 | 1233 | PF00675 | 0.242 |
CLV_NRD_NRD_1 | 1308 | 1310 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.242 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 635 | 637 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 672 | 674 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 755 | 757 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 782 | 784 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 824 | 826 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 844 | 846 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 906 | 908 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 961 | 963 | PF00675 | 0.402 |
CLV_PCSK_KEX2_1 | 1050 | 1052 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 1155 | 1157 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 1231 | 1233 | PF00082 | 0.231 |
CLV_PCSK_KEX2_1 | 1241 | 1243 | PF00082 | 0.231 |
CLV_PCSK_KEX2_1 | 1308 | 1310 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.233 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.273 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 502 | 504 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 635 | 637 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 672 | 674 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 755 | 757 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 824 | 826 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 844 | 846 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 961 | 963 | PF00082 | 0.449 |
CLV_PCSK_PC1ET2_1 | 1155 | 1157 | PF00082 | 0.396 |
CLV_PCSK_PC1ET2_1 | 1241 | 1243 | PF00082 | 0.236 |
CLV_PCSK_PC1ET2_1 | 177 | 179 | PF00082 | 0.335 |
CLV_PCSK_PC1ET2_1 | 328 | 330 | PF00082 | 0.521 |
CLV_PCSK_PC1ET2_1 | 502 | 504 | PF00082 | 0.449 |
CLV_PCSK_PC7_1 | 1237 | 1243 | PF00082 | 0.231 |
CLV_PCSK_PC7_1 | 282 | 288 | PF00082 | 0.561 |
CLV_PCSK_PC7_1 | 820 | 826 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 1266 | 1270 | PF00082 | 0.231 |
CLV_PCSK_SKI1_1 | 1309 | 1313 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.233 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.227 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.198 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 558 | 562 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 673 | 677 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 711 | 715 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 908 | 912 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 961 | 965 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 978 | 982 | PF00082 | 0.490 |
CLV_Separin_Metazoa | 492 | 496 | PF03568 | 0.338 |
DEG_APCC_DBOX_1 | 258 | 266 | PF00400 | 0.542 |
DEG_APCC_DBOX_1 | 470 | 478 | PF00400 | 0.496 |
DEG_APCC_DBOX_1 | 557 | 565 | PF00400 | 0.428 |
DEG_APCC_DBOX_1 | 672 | 680 | PF00400 | 0.537 |
DEG_APCC_DBOX_1 | 754 | 762 | PF00400 | 0.404 |
DEG_APCC_DBOX_1 | 938 | 946 | PF00400 | 0.437 |
DEG_APCC_KENBOX_2 | 455 | 459 | PF00400 | 0.362 |
DEG_COP1_1 | 137 | 147 | PF00400 | 0.480 |
DEG_SPOP_SBC_1 | 130 | 134 | PF00917 | 0.474 |
DEG_SPOP_SBC_1 | 295 | 299 | PF00917 | 0.364 |
DOC_CDC14_PxL_1 | 758 | 766 | PF14671 | 0.390 |
DOC_CYCLIN_RxL_1 | 604 | 614 | PF00134 | 0.422 |
DOC_CYCLIN_RxL_1 | 959 | 969 | PF00134 | 0.585 |
DOC_CYCLIN_RxL_1 | 986 | 994 | PF00134 | 0.538 |
DOC_CYCLIN_yCln2_LP_2 | 993 | 999 | PF00134 | 0.287 |
DOC_MAPK_gen_1 | 1155 | 1164 | PF00069 | 0.390 |
DOC_MAPK_gen_1 | 1308 | 1319 | PF00069 | 0.297 |
DOC_MAPK_gen_1 | 346 | 353 | PF00069 | 0.482 |
DOC_MAPK_gen_1 | 502 | 509 | PF00069 | 0.579 |
DOC_MAPK_gen_1 | 939 | 947 | PF00069 | 0.370 |
DOC_MAPK_MEF2A_6 | 1258 | 1267 | PF00069 | 0.431 |
DOC_MAPK_MEF2A_6 | 502 | 511 | PF00069 | 0.550 |
DOC_MAPK_MEF2A_6 | 81 | 88 | PF00069 | 0.431 |
DOC_MAPK_NFAT4_5 | 81 | 89 | PF00069 | 0.442 |
DOC_PP1_RVXF_1 | 108 | 114 | PF00149 | 0.535 |
DOC_PP1_RVXF_1 | 83 | 89 | PF00149 | 0.431 |
DOC_PP2B_LxvP_1 | 170 | 173 | PF13499 | 0.438 |
DOC_PP2B_LxvP_1 | 993 | 996 | PF13499 | 0.511 |
DOC_PP4_FxxP_1 | 27 | 30 | PF00568 | 0.431 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 1184 | 1188 | PF00917 | 0.374 |
DOC_USP7_MATH_1 | 1230 | 1234 | PF00917 | 0.286 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.376 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 860 | 864 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 952 | 956 | PF00917 | 0.484 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 720 | 725 | PF00397 | 0.450 |
LIG_14-3-3_CanoR_1 | 1042 | 1046 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 1074 | 1082 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 110 | 120 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 1156 | 1162 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 1205 | 1209 | PF00244 | 0.350 |
LIG_14-3-3_CanoR_1 | 1231 | 1235 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 1250 | 1260 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 136 | 144 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 589 | 598 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 635 | 639 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 808 | 813 | PF00244 | 0.551 |
LIG_Actin_WH2_2 | 248 | 265 | PF00022 | 0.535 |
LIG_Actin_WH2_2 | 805 | 822 | PF00022 | 0.526 |
LIG_AP2alpha_1 | 180 | 184 | PF02296 | 0.474 |
LIG_BRCT_BRCA1_1 | 1269 | 1273 | PF00533 | 0.431 |
LIG_BRCT_BRCA1_1 | 199 | 203 | PF00533 | 0.456 |
LIG_Clathr_ClatBox_1 | 508 | 512 | PF01394 | 0.456 |
LIG_EH1_1 | 1090 | 1098 | PF00400 | 0.517 |
LIG_FHA_1 | 1112 | 1118 | PF00498 | 0.507 |
LIG_FHA_1 | 1164 | 1170 | PF00498 | 0.350 |
LIG_FHA_1 | 1213 | 1219 | PF00498 | 0.437 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.442 |
LIG_FHA_1 | 1284 | 1290 | PF00498 | 0.431 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.421 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.436 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.431 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.431 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.437 |
LIG_FHA_1 | 470 | 476 | PF00498 | 0.296 |
LIG_FHA_1 | 577 | 583 | PF00498 | 0.414 |
LIG_FHA_1 | 590 | 596 | PF00498 | 0.343 |
LIG_FHA_1 | 606 | 612 | PF00498 | 0.503 |
LIG_FHA_1 | 626 | 632 | PF00498 | 0.476 |
LIG_FHA_1 | 814 | 820 | PF00498 | 0.550 |
LIG_FHA_1 | 873 | 879 | PF00498 | 0.571 |
LIG_FHA_2 | 1026 | 1032 | PF00498 | 0.477 |
LIG_FHA_2 | 1042 | 1048 | PF00498 | 0.687 |
LIG_FHA_2 | 1074 | 1080 | PF00498 | 0.389 |
LIG_FHA_2 | 1116 | 1122 | PF00498 | 0.492 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.498 |
LIG_FHA_2 | 1285 | 1291 | PF00498 | 0.431 |
LIG_FHA_2 | 1301 | 1307 | PF00498 | 0.465 |
LIG_FHA_2 | 1318 | 1324 | PF00498 | 0.281 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.501 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.431 |
LIG_FHA_2 | 477 | 483 | PF00498 | 0.304 |
LIG_FHA_2 | 720 | 726 | PF00498 | 0.493 |
LIG_FHA_2 | 809 | 815 | PF00498 | 0.458 |
LIG_FHA_2 | 938 | 944 | PF00498 | 0.619 |
LIG_Integrin_RGD_1 | 1146 | 1148 | PF01839 | 0.464 |
LIG_LIR_Gen_1 | 112 | 121 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 1148 | 1157 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 1159 | 1169 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 1175 | 1185 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 1345 | 1356 | PF02991 | 0.296 |
LIG_LIR_Gen_1 | 653 | 662 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 681 | 690 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 742 | 752 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 800 | 809 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 863 | 872 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 112 | 116 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 1148 | 1153 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 1159 | 1164 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 1175 | 1181 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 1233 | 1239 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 1335 | 1340 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 1345 | 1351 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 1353 | 1359 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 681 | 686 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 740 | 744 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 800 | 806 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 863 | 867 | PF02991 | 0.431 |
LIG_NRBOX | 301 | 307 | PF00104 | 0.535 |
LIG_PCNA_yPIPBox_3 | 1192 | 1204 | PF02747 | 0.342 |
LIG_PDZ_Class_2 | 1356 | 1361 | PF00595 | 0.294 |
LIG_Pex14_1 | 1204 | 1208 | PF04695 | 0.334 |
LIG_Pex14_2 | 1356 | 1360 | PF04695 | 0.276 |
LIG_Pex14_2 | 180 | 184 | PF04695 | 0.431 |
LIG_SH2_CRK | 1236 | 1240 | PF00017 | 0.431 |
LIG_SH2_GRB2like | 1150 | 1153 | PF00017 | 0.460 |
LIG_SH2_NCK_1 | 1024 | 1028 | PF00017 | 0.423 |
LIG_SH2_SRC | 1150 | 1153 | PF00017 | 0.460 |
LIG_SH2_STAP1 | 655 | 659 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 1001 | 1004 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 1339 | 1342 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.582 |
LIG_SH3_1 | 756 | 762 | PF00018 | 0.332 |
LIG_SH3_2 | 169 | 174 | PF14604 | 0.442 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.442 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.431 |
LIG_SH3_3 | 756 | 762 | PF00018 | 0.438 |
LIG_SH3_3 | 854 | 860 | PF00018 | 0.392 |
LIG_SUMO_SIM_anti_2 | 537 | 542 | PF11976 | 0.463 |
LIG_SUMO_SIM_par_1 | 1134 | 1139 | PF11976 | 0.340 |
LIG_SUMO_SIM_par_1 | 1214 | 1223 | PF11976 | 0.448 |
LIG_SUMO_SIM_par_1 | 1278 | 1284 | PF11976 | 0.431 |
LIG_SUMO_SIM_par_1 | 1315 | 1320 | PF11976 | 0.298 |
LIG_SUMO_SIM_par_1 | 189 | 194 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 507 | 513 | PF11976 | 0.347 |
LIG_SUMO_SIM_par_1 | 608 | 614 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 814 | 822 | PF11976 | 0.486 |
LIG_TRAF2_1 | 1027 | 1030 | PF00917 | 0.536 |
LIG_TRAF2_1 | 258 | 261 | PF00917 | 0.461 |
LIG_TRAF2_1 | 264 | 267 | PF00917 | 0.454 |
LIG_TRAF2_1 | 618 | 621 | PF00917 | 0.531 |
LIG_TRAF2_1 | 770 | 773 | PF00917 | 0.364 |
LIG_TRAF2_1 | 863 | 866 | PF00917 | 0.457 |
LIG_WRC_WIRS_1 | 12 | 17 | PF05994 | 0.266 |
LIG_WRC_WIRS_1 | 99 | 104 | PF05994 | 0.281 |
MOD_CK1_1 | 1084 | 1090 | PF00069 | 0.566 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.371 |
MOD_CK1_1 | 581 | 587 | PF00069 | 0.451 |
MOD_CK1_1 | 625 | 631 | PF00069 | 0.462 |
MOD_CK1_1 | 702 | 708 | PF00069 | 0.497 |
MOD_CK2_1 | 1019 | 1025 | PF00069 | 0.502 |
MOD_CK2_1 | 1073 | 1079 | PF00069 | 0.380 |
MOD_CK2_1 | 1115 | 1121 | PF00069 | 0.388 |
MOD_CK2_1 | 1176 | 1182 | PF00069 | 0.511 |
MOD_CK2_1 | 1217 | 1223 | PF00069 | 0.550 |
MOD_CK2_1 | 1300 | 1306 | PF00069 | 0.286 |
MOD_CK2_1 | 1317 | 1323 | PF00069 | 0.281 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.452 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.266 |
MOD_CK2_1 | 476 | 482 | PF00069 | 0.312 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.266 |
MOD_CK2_1 | 647 | 653 | PF00069 | 0.367 |
MOD_CK2_1 | 808 | 814 | PF00069 | 0.505 |
MOD_CK2_1 | 860 | 866 | PF00069 | 0.463 |
MOD_CK2_1 | 937 | 943 | PF00069 | 0.641 |
MOD_GlcNHglycan | 1021 | 1024 | PF01048 | 0.613 |
MOD_GlcNHglycan | 1051 | 1054 | PF01048 | 0.620 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.411 |
MOD_GlcNHglycan | 1178 | 1181 | PF01048 | 0.406 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.193 |
MOD_GlcNHglycan | 1253 | 1256 | PF01048 | 0.266 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.504 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.294 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.525 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.264 |
MOD_GlcNHglycan | 645 | 648 | PF01048 | 0.599 |
MOD_GlcNHglycan | 785 | 788 | PF01048 | 0.462 |
MOD_GlcNHglycan | 848 | 851 | PF01048 | 0.628 |
MOD_GSK3_1 | 1111 | 1118 | PF00069 | 0.491 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.208 |
MOD_GSK3_1 | 1163 | 1170 | PF00069 | 0.493 |
MOD_GSK3_1 | 1204 | 1211 | PF00069 | 0.343 |
MOD_GSK3_1 | 1219 | 1226 | PF00069 | 0.443 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.447 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.417 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.516 |
MOD_GSK3_1 | 639 | 646 | PF00069 | 0.585 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.338 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.273 |
MOD_N-GLC_2 | 1004 | 1006 | PF02516 | 0.443 |
MOD_N-GLC_2 | 51 | 53 | PF02516 | 0.281 |
MOD_N-GLC_2 | 615 | 617 | PF02516 | 0.295 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.266 |
MOD_NEK2_1 | 1136 | 1141 | PF00069 | 0.515 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.258 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.326 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.310 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.444 |
MOD_NEK2_1 | 819 | 824 | PF00069 | 0.543 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.266 |
MOD_NEK2_1 | 991 | 996 | PF00069 | 0.498 |
MOD_PIKK_1 | 1025 | 1031 | PF00454 | 0.477 |
MOD_PIKK_1 | 1136 | 1142 | PF00454 | 0.366 |
MOD_PIKK_1 | 1191 | 1197 | PF00454 | 0.268 |
MOD_PIKK_1 | 296 | 302 | PF00454 | 0.567 |
MOD_PIKK_1 | 469 | 475 | PF00454 | 0.397 |
MOD_PIKK_1 | 501 | 507 | PF00454 | 0.564 |
MOD_PIKK_1 | 587 | 593 | PF00454 | 0.479 |
MOD_PIKK_1 | 667 | 673 | PF00454 | 0.460 |
MOD_PIKK_1 | 789 | 795 | PF00454 | 0.374 |
MOD_PKA_1 | 783 | 789 | PF00069 | 0.530 |
MOD_PKA_2 | 1017 | 1023 | PF00069 | 0.626 |
MOD_PKA_2 | 1041 | 1047 | PF00069 | 0.636 |
MOD_PKA_2 | 1049 | 1055 | PF00069 | 0.580 |
MOD_PKA_2 | 1073 | 1079 | PF00069 | 0.417 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.425 |
MOD_PKA_2 | 1157 | 1163 | PF00069 | 0.376 |
MOD_PKA_2 | 1204 | 1210 | PF00069 | 0.340 |
MOD_PKA_2 | 1230 | 1236 | PF00069 | 0.281 |
MOD_PKA_2 | 1251 | 1257 | PF00069 | 0.300 |
MOD_PKA_2 | 135 | 141 | PF00069 | 0.400 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.581 |
MOD_PKA_2 | 634 | 640 | PF00069 | 0.621 |
MOD_PKA_2 | 819 | 825 | PF00069 | 0.626 |
MOD_PKB_1 | 195 | 203 | PF00069 | 0.300 |
MOD_Plk_1 | 1078 | 1084 | PF00069 | 0.447 |
MOD_Plk_1 | 1136 | 1142 | PF00069 | 0.327 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.296 |
MOD_Plk_1 | 1167 | 1173 | PF00069 | 0.481 |
MOD_Plk_1 | 1352 | 1358 | PF00069 | 0.285 |
MOD_Plk_1 | 210 | 216 | PF00069 | 0.325 |
MOD_Plk_1 | 319 | 325 | PF00069 | 0.409 |
MOD_Plk_1 | 382 | 388 | PF00069 | 0.515 |
MOD_Plk_1 | 699 | 705 | PF00069 | 0.418 |
MOD_Plk_1 | 813 | 819 | PF00069 | 0.589 |
MOD_Plk_2-3 | 1212 | 1218 | PF00069 | 0.425 |
MOD_Plk_2-3 | 1352 | 1358 | PF00069 | 0.285 |
MOD_Plk_4 | 1157 | 1163 | PF00069 | 0.375 |
MOD_Plk_4 | 1259 | 1265 | PF00069 | 0.271 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.360 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.331 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.292 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.344 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.266 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.266 |
MOD_Plk_4 | 997 | 1003 | PF00069 | 0.410 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.309 |
MOD_ProDKin_1 | 720 | 726 | PF00069 | 0.452 |
MOD_SUMO_for_1 | 598 | 601 | PF00179 | 0.460 |
MOD_SUMO_for_1 | 919 | 922 | PF00179 | 0.451 |
MOD_SUMO_rev_2 | 67 | 75 | PF00179 | 0.269 |
MOD_SUMO_rev_2 | 77 | 82 | PF00179 | 0.272 |
MOD_SUMO_rev_2 | 943 | 947 | PF00179 | 0.374 |
TRG_DiLeu_BaEn_1 | 355 | 360 | PF01217 | 0.274 |
TRG_DiLeu_BaEn_2 | 63 | 69 | PF01217 | 0.281 |
TRG_DiLeu_BaLyEn_6 | 82 | 87 | PF01217 | 0.281 |
TRG_ENDOCYTIC_2 | 1150 | 1153 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 1178 | 1181 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 1236 | 1239 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 655 | 658 | PF00928 | 0.588 |
TRG_ENDOCYTIC_2 | 683 | 686 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 741 | 744 | PF00928 | 0.446 |
TRG_ER_diArg_1 | 1249 | 1252 | PF00400 | 0.281 |
TRG_ER_diArg_1 | 1307 | 1309 | PF00400 | 0.209 |
TRG_ER_diArg_1 | 203 | 205 | PF00400 | 0.281 |
TRG_ER_diArg_1 | 290 | 292 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 308 | 310 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 336 | 338 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 406 | 409 | PF00400 | 0.266 |
TRG_ER_diArg_1 | 453 | 455 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 754 | 756 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 823 | 825 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 843 | 845 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 939 | 942 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 961 | 963 | PF00400 | 0.332 |
TRG_NES_CRM1_1 | 1058 | 1072 | PF08389 | 0.326 |
TRG_NLS_MonoExtC_3 | 494 | 500 | PF00514 | 0.329 |
TRG_NLS_MonoExtC_3 | 775 | 781 | PF00514 | 0.373 |
TRG_NLS_MonoExtN_4 | 774 | 780 | PF00514 | 0.369 |
TRG_Pf-PMV_PEXEL_1 | 1295 | 1299 | PF00026 | 0.266 |
TRG_Pf-PMV_PEXEL_1 | 1302 | 1306 | PF00026 | 0.314 |
TRG_Pf-PMV_PEXEL_1 | 1327 | 1332 | PF00026 | 0.313 |
TRG_Pf-PMV_PEXEL_1 | 205 | 209 | PF00026 | 0.360 |
TRG_Pf-PMV_PEXEL_1 | 253 | 257 | PF00026 | 0.439 |
TRG_Pf-PMV_PEXEL_1 | 337 | 341 | PF00026 | 0.450 |
TRG_Pf-PMV_PEXEL_1 | 369 | 373 | PF00026 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 453 | 457 | PF00026 | 0.522 |
TRG_Pf-PMV_PEXEL_1 | 609 | 614 | PF00026 | 0.330 |
TRG_Pf-PMV_PEXEL_1 | 902 | 906 | PF00026 | 0.573 |
TRG_Pf-PMV_PEXEL_1 | 929 | 933 | PF00026 | 0.508 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3D5 | Leptomonas seymouri | 68% | 100% |
A0A0S4JAY7 | Bodo saltans | 37% | 100% |
A0A1X0NYH4 | Trypanosomatidae | 46% | 100% |
A0A3R7N260 | Trypanosoma rangeli | 46% | 100% |
A0A3S7X1A7 | Leishmania donovani | 84% | 100% |
A4I3C7 | Leishmania infantum | 84% | 100% |
D0A818 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AZL4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4Q8L7 | Leishmania major | 83% | 100% |
V5BQC9 | Trypanosoma cruzi | 46% | 100% |