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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0043564 | Ku70:Ku80 complex | 3 | 11 |
GO:0140513 | nuclear protein-containing complex | 2 | 11 |
Related structures:
AlphaFold database: E9ADW3
Term | Name | Level | Count |
---|---|---|---|
GO:0000723 | telomere maintenance | 5 | 11 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006259 | DNA metabolic process | 4 | 11 |
GO:0006281 | DNA repair | 5 | 11 |
GO:0006302 | double-strand break repair | 6 | 11 |
GO:0006303 | double-strand break repair via nonhomologous end joining | 7 | 11 |
GO:0006310 | DNA recombination | 5 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0006950 | response to stress | 2 | 11 |
GO:0006974 | DNA damage response | 4 | 11 |
GO:0006996 | organelle organization | 4 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009314 | response to radiation | 3 | 2 |
GO:0009628 | response to abiotic stimulus | 2 | 2 |
GO:0009987 | cellular process | 1 | 11 |
GO:0010165 | response to X-ray | 5 | 2 |
GO:0010212 | response to ionizing radiation | 4 | 2 |
GO:0010332 | response to gamma radiation | 5 | 2 |
GO:0016043 | cellular component organization | 3 | 11 |
GO:0032200 | telomere organization | 6 | 11 |
GO:0033554 | cellular response to stress | 3 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0050896 | response to stimulus | 1 | 11 |
GO:0051276 | chromosome organization | 5 | 11 |
GO:0051716 | cellular response to stimulus | 2 | 11 |
GO:0071214 | cellular response to abiotic stimulus | 3 | 2 |
GO:0071478 | cellular response to radiation | 4 | 2 |
GO:0071479 | cellular response to ionizing radiation | 5 | 2 |
GO:0071480 | cellular response to gamma radiation | 6 | 2 |
GO:0071481 | cellular response to X-ray | 6 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:0104004 | cellular response to environmental stimulus | 3 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003677 | DNA binding | 4 | 11 |
GO:0003684 | damaged DNA binding | 5 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004386 | helicase activity | 2 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0042162 | telomeric DNA binding | 6 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0043565 | sequence-specific DNA binding | 5 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 20 | 24 | PF00656 | 0.558 |
CLV_C14_Caspase3-7 | 270 | 274 | PF00656 | 0.454 |
CLV_C14_Caspase3-7 | 484 | 488 | PF00656 | 0.519 |
CLV_C14_Caspase3-7 | 595 | 599 | PF00656 | 0.579 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.251 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 495 | 497 | PF00675 | 0.261 |
CLV_NRD_NRD_1 | 572 | 574 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 607 | 609 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 632 | 634 | PF00675 | 0.299 |
CLV_NRD_NRD_1 | 758 | 760 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 843 | 845 | PF00675 | 0.713 |
CLV_NRD_NRD_1 | 908 | 910 | PF00675 | 0.442 |
CLV_PCSK_FUR_1 | 256 | 260 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.251 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.421 |
CLV_PCSK_KEX2_1 | 495 | 497 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 574 | 576 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 601 | 603 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 607 | 609 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 632 | 634 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 670 | 672 | PF00082 | 0.326 |
CLV_PCSK_KEX2_1 | 758 | 760 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 843 | 845 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 908 | 910 | PF00082 | 0.447 |
CLV_PCSK_PC1ET2_1 | 574 | 576 | PF00082 | 0.287 |
CLV_PCSK_PC1ET2_1 | 601 | 603 | PF00082 | 0.287 |
CLV_PCSK_PC1ET2_1 | 670 | 672 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.197 |
CLV_PCSK_SKI1_1 | 706 | 710 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 758 | 762 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 819 | 823 | PF00082 | 0.476 |
DEG_APCC_DBOX_1 | 426 | 434 | PF00400 | 0.498 |
DEG_COP1_1 | 690 | 698 | PF00400 | 0.470 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.670 |
DEG_SCF_TRCP1_1 | 522 | 527 | PF00400 | 0.454 |
DEG_SPOP_SBC_1 | 442 | 446 | PF00917 | 0.490 |
DOC_CDC14_PxL_1 | 649 | 657 | PF14671 | 0.390 |
DOC_CDC14_PxL_1 | 692 | 700 | PF14671 | 0.469 |
DOC_CYCLIN_RxL_1 | 241 | 251 | PF00134 | 0.526 |
DOC_CYCLIN_RxL_1 | 255 | 264 | PF00134 | 0.558 |
DOC_CYCLIN_RxL_1 | 755 | 765 | PF00134 | 0.427 |
DOC_MAPK_gen_1 | 37 | 46 | PF00069 | 0.424 |
DOC_MAPK_gen_1 | 424 | 433 | PF00069 | 0.493 |
DOC_MAPK_gen_1 | 492 | 500 | PF00069 | 0.462 |
DOC_MAPK_gen_1 | 573 | 579 | PF00069 | 0.487 |
DOC_MAPK_gen_1 | 632 | 642 | PF00069 | 0.512 |
DOC_MAPK_gen_1 | 670 | 676 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 908 | 916 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 135 | 142 | PF00069 | 0.451 |
DOC_MAPK_MEF2A_6 | 289 | 296 | PF00069 | 0.543 |
DOC_MAPK_RevD_3 | 245 | 259 | PF00069 | 0.494 |
DOC_PP1_RVXF_1 | 563 | 569 | PF00149 | 0.497 |
DOC_PP2B_LxvP_1 | 471 | 474 | PF13499 | 0.454 |
DOC_PP2B_LxvP_1 | 888 | 891 | PF13499 | 0.513 |
DOC_PP4_FxxP_1 | 357 | 360 | PF00568 | 0.481 |
DOC_PP4_FxxP_1 | 921 | 924 | PF00568 | 0.524 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 713 | 717 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 767 | 771 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 845 | 849 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 900 | 904 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.720 |
DOC_USP7_MATH_2 | 794 | 800 | PF00917 | 0.400 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.735 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 522 | 527 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 658 | 663 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 706 | 711 | PF00397 | 0.554 |
LIG_14-3-3_CanoR_1 | 146 | 150 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 244 | 250 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 319 | 324 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 466 | 472 | PF00244 | 0.350 |
LIG_14-3-3_CanoR_1 | 607 | 612 | PF00244 | 0.555 |
LIG_Actin_WH2_2 | 677 | 695 | PF00022 | 0.494 |
LIG_APCC_ABBA_1 | 590 | 595 | PF00400 | 0.519 |
LIG_BRCT_BRCA1_1 | 110 | 114 | PF00533 | 0.528 |
LIG_BRCT_BRCA1_1 | 150 | 154 | PF00533 | 0.487 |
LIG_BRCT_BRCA1_1 | 226 | 230 | PF00533 | 0.495 |
LIG_BRCT_BRCA1_1 | 309 | 313 | PF00533 | 0.670 |
LIG_CaM_IQ_9 | 811 | 826 | PF13499 | 0.419 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.390 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.590 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.517 |
LIG_FHA_1 | 587 | 593 | PF00498 | 0.495 |
LIG_FHA_1 | 707 | 713 | PF00498 | 0.553 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.630 |
LIG_FHA_1 | 897 | 903 | PF00498 | 0.621 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.627 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.584 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.484 |
LIG_FHA_2 | 449 | 455 | PF00498 | 0.575 |
LIG_FHA_2 | 567 | 573 | PF00498 | 0.512 |
LIG_FHA_2 | 580 | 586 | PF00498 | 0.474 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.717 |
LIG_GBD_Chelix_1 | 724 | 732 | PF00786 | 0.377 |
LIG_LIR_Apic_2 | 355 | 360 | PF02991 | 0.521 |
LIG_LIR_Apic_2 | 554 | 560 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 185 | 195 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 585 | 596 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 809 | 817 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 825 | 833 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 185 | 191 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 227 | 233 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 355 | 361 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 470 | 475 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 585 | 591 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 809 | 813 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 825 | 829 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 882 | 888 | PF02991 | 0.587 |
LIG_NBox_RRM_1 | 235 | 245 | PF00076 | 0.487 |
LIG_NRBOX | 408 | 414 | PF00104 | 0.527 |
LIG_PCNA_yPIPBox_3 | 410 | 424 | PF02747 | 0.445 |
LIG_PCNA_yPIPBox_3 | 489 | 498 | PF02747 | 0.578 |
LIG_PCNA_yPIPBox_3 | 50 | 64 | PF02747 | 0.487 |
LIG_Pex14_2 | 352 | 356 | PF04695 | 0.571 |
LIG_Pex14_2 | 810 | 814 | PF04695 | 0.445 |
LIG_RPA_C_Fungi | 628 | 640 | PF08784 | 0.406 |
LIG_SH2_CRK | 472 | 476 | PF00017 | 0.208 |
LIG_SH2_CRK | 558 | 562 | PF00017 | 0.330 |
LIG_SH2_CRK | 750 | 754 | PF00017 | 0.466 |
LIG_SH2_NCK_1 | 558 | 562 | PF00017 | 0.397 |
LIG_SH2_PTP2 | 682 | 685 | PF00017 | 0.273 |
LIG_SH2_SRC | 21 | 24 | PF00017 | 0.460 |
LIG_SH2_SRC | 558 | 561 | PF00017 | 0.296 |
LIG_SH2_STAP1 | 688 | 692 | PF00017 | 0.338 |
LIG_SH2_STAT3 | 158 | 161 | PF00017 | 0.406 |
LIG_SH2_STAT3 | 831 | 834 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 567 | 570 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 645 | 648 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 682 | 685 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 831 | 834 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 896 | 899 | PF00017 | 0.378 |
LIG_SH3_1 | 419 | 425 | PF00018 | 0.386 |
LIG_SH3_2 | 422 | 427 | PF14604 | 0.486 |
LIG_SH3_3 | 419 | 425 | PF00018 | 0.421 |
LIG_SH3_3 | 523 | 529 | PF00018 | 0.206 |
LIG_SH3_3 | 656 | 662 | PF00018 | 0.297 |
LIG_SH3_3 | 681 | 687 | PF00018 | 0.284 |
LIG_SH3_3 | 738 | 744 | PF00018 | 0.416 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.620 |
LIG_SUMO_SIM_anti_2 | 136 | 142 | PF11976 | 0.335 |
LIG_SUMO_SIM_anti_2 | 912 | 918 | PF11976 | 0.464 |
LIG_SUMO_SIM_par_1 | 245 | 251 | PF11976 | 0.296 |
LIG_TRAF2_1 | 187 | 190 | PF00917 | 0.526 |
LIG_TRAF2_1 | 569 | 572 | PF00917 | 0.270 |
LIG_TRAF2_1 | 779 | 782 | PF00917 | 0.613 |
LIG_TRAF2_1 | 793 | 796 | PF00917 | 0.432 |
LIG_TRAF2_1 | 862 | 865 | PF00917 | 0.657 |
LIG_TRAF2_1 | 90 | 93 | PF00917 | 0.525 |
LIG_UBA3_1 | 122 | 129 | PF00899 | 0.341 |
LIG_UBA3_1 | 592 | 601 | PF00899 | 0.310 |
LIG_UBA3_1 | 889 | 894 | PF00899 | 0.447 |
LIG_UBA3_1 | 913 | 918 | PF00899 | 0.510 |
LIG_WRC_WIRS_1 | 807 | 812 | PF05994 | 0.435 |
LIG_WRC_WIRS_1 | 814 | 819 | PF05994 | 0.404 |
MOD_CDC14_SPxK_1 | 525 | 528 | PF00782 | 0.296 |
MOD_CDK_SPxK_1 | 522 | 528 | PF00069 | 0.296 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.476 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.462 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.602 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.326 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.602 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.728 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.713 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.643 |
MOD_CK1_1 | 647 | 653 | PF00069 | 0.438 |
MOD_CK1_1 | 730 | 736 | PF00069 | 0.429 |
MOD_CK2_1 | 391 | 397 | PF00069 | 0.511 |
MOD_CK2_1 | 566 | 572 | PF00069 | 0.292 |
MOD_CK2_1 | 579 | 585 | PF00069 | 0.292 |
MOD_CK2_1 | 859 | 865 | PF00069 | 0.749 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.718 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.476 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.537 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.610 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.436 |
MOD_GlcNHglycan | 267 | 272 | PF01048 | 0.427 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.679 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.769 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.807 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.605 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.541 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.661 |
MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.407 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.652 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.680 |
MOD_GlcNHglycan | 729 | 732 | PF01048 | 0.490 |
MOD_GlcNHglycan | 769 | 772 | PF01048 | 0.512 |
MOD_GlcNHglycan | 798 | 801 | PF01048 | 0.459 |
MOD_GlcNHglycan | 847 | 850 | PF01048 | 0.735 |
MOD_GlcNHglycan | 861 | 864 | PF01048 | 0.580 |
MOD_GlcNHglycan | 903 | 906 | PF01048 | 0.548 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.413 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.362 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.575 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.589 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.782 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.649 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.535 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.417 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.703 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.412 |
MOD_GSK3_1 | 644 | 651 | PF00069 | 0.365 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.393 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.601 |
MOD_GSK3_1 | 767 | 774 | PF00069 | 0.614 |
MOD_GSK3_1 | 896 | 903 | PF00069 | 0.403 |
MOD_LATS_1 | 78 | 84 | PF00433 | 0.593 |
MOD_N-GLC_1 | 537 | 542 | PF02516 | 0.296 |
MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.602 |
MOD_N-GLC_1 | 900 | 905 | PF02516 | 0.479 |
MOD_N-GLC_2 | 278 | 280 | PF02516 | 0.386 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.371 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.336 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.432 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.179 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.586 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.535 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.552 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.551 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.297 |
MOD_NEK2_1 | 611 | 616 | PF00069 | 0.373 |
MOD_NEK2_1 | 712 | 717 | PF00069 | 0.676 |
MOD_NEK2_1 | 732 | 737 | PF00069 | 0.275 |
MOD_NEK2_1 | 813 | 818 | PF00069 | 0.458 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.710 |
MOD_NEK2_2 | 330 | 335 | PF00069 | 0.525 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.614 |
MOD_PKA_1 | 607 | 613 | PF00069 | 0.373 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.296 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.614 |
MOD_PKA_2 | 372 | 378 | PF00069 | 0.607 |
MOD_PKA_2 | 502 | 508 | PF00069 | 0.375 |
MOD_PKA_2 | 606 | 612 | PF00069 | 0.437 |
MOD_PKA_2 | 845 | 851 | PF00069 | 0.586 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.386 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.602 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.766 |
MOD_Plk_1 | 456 | 462 | PF00069 | 0.627 |
MOD_Plk_1 | 713 | 719 | PF00069 | 0.533 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.453 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.568 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.292 |
MOD_Plk_4 | 540 | 546 | PF00069 | 0.318 |
MOD_Plk_4 | 607 | 613 | PF00069 | 0.281 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.438 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.739 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.645 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.673 |
MOD_ProDKin_1 | 522 | 528 | PF00069 | 0.417 |
MOD_ProDKin_1 | 658 | 664 | PF00069 | 0.316 |
MOD_ProDKin_1 | 706 | 712 | PF00069 | 0.554 |
MOD_SUMO_for_1 | 600 | 603 | PF00179 | 0.341 |
MOD_SUMO_rev_2 | 570 | 576 | PF00179 | 0.296 |
TRG_DiLeu_BaEn_3 | 571 | 577 | PF01217 | 0.296 |
TRG_DiLeu_BaLyEn_6 | 357 | 362 | PF01217 | 0.475 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 472 | 475 | PF00928 | 0.273 |
TRG_ENDOCYTIC_2 | 558 | 561 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 750 | 753 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 804 | 807 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 826 | 829 | PF00928 | 0.512 |
TRG_ER_diArg_1 | 255 | 258 | PF00400 | 0.301 |
TRG_ER_diArg_1 | 417 | 419 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 476 | 479 | PF00400 | 0.350 |
TRG_ER_diArg_1 | 494 | 496 | PF00400 | 0.295 |
TRG_ER_diArg_1 | 573 | 576 | PF00400 | 0.356 |
TRG_ER_diArg_1 | 606 | 608 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 631 | 633 | PF00400 | 0.406 |
TRG_ER_diArg_1 | 758 | 760 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 843 | 846 | PF00400 | 0.744 |
TRG_NES_CRM1_1 | 723 | 737 | PF08389 | 0.463 |
TRG_Pf-PMV_PEXEL_1 | 751 | 755 | PF00026 | 0.583 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8R7 | Leptomonas seymouri | 44% | 100% |
A0A1X0NZS3 | Trypanosomatidae | 29% | 100% |
A0A3R7KD14 | Trypanosoma rangeli | 32% | 100% |
A4HHB7 | Leishmania braziliensis | 70% | 96% |
A4I4G4 | Leishmania infantum | 87% | 96% |
C9ZLL2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E5KZN0 | Leishmania donovani | 87% | 96% |
E9ALW7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 98% |
V5BH85 | Trypanosoma cruzi | 31% | 100% |