| 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:0005737 | cytoplasm | 2 | 11 |
| GO:0110165 | cellular anatomical entity | 1 | 11 |
| GO:0005657 | replication fork | 2 | 1 |
Related structures:
AlphaFold database: E9B075
| 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: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:0009987 | cellular process | 1 | 11 |
| 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: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:1901360 | organic cyclic compound metabolic process | 3 | 11 |
| GO:0006260 | DNA replication | 5 | 1 |
| GO:0032392 | DNA geometric change | 7 | 1 |
| GO:0032508 | DNA duplex unwinding | 8 | 1 |
| GO:0071103 | DNA conformation change | 6 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000166 | nucleotide binding | 3 | 11 |
| GO:0003678 | DNA helicase activity | 3 | 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:0008094 | ATP-dependent activity, acting on DNA | 2 | 11 |
| GO:0016462 | pyrophosphatase activity | 5 | 11 |
| GO:0016787 | hydrolase activity | 2 | 11 |
| GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
| GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
| GO:0016887 | ATP hydrolysis activity | 7 | 11 |
| GO:0017076 | purine nucleotide binding | 4 | 11 |
| GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 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:0043167 | ion binding | 2 | 11 |
| GO:0043168 | anion binding | 3 | 11 |
| GO:0097159 | organic cyclic compound binding | 2 | 11 |
| GO:0097367 | carbohydrate derivative binding | 2 | 11 |
| GO:0140097 | catalytic activity, acting on DNA | 3 | 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 |
| GO:0000287 | magnesium ion binding | 5 | 1 |
| GO:0043169 | cation binding | 3 | 1 |
| GO:0046872 | metal ion binding | 4 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 377 | 381 | PF00656 | 0.335 |
| CLV_C14_Caspase3-7 | 610 | 614 | PF00656 | 0.750 |
| CLV_C14_Caspase3-7 | 620 | 624 | PF00656 | 0.786 |
| CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.668 |
| CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.564 |
| CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.448 |
| CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.451 |
| CLV_NRD_NRD_1 | 562 | 564 | PF00675 | 0.759 |
| CLV_NRD_NRD_1 | 659 | 661 | PF00675 | 0.719 |
| CLV_NRD_NRD_1 | 672 | 674 | PF00675 | 0.611 |
| CLV_NRD_NRD_1 | 772 | 774 | PF00675 | 0.496 |
| CLV_NRD_NRD_1 | 873 | 875 | PF00675 | 0.532 |
| CLV_NRD_NRD_1 | 892 | 894 | PF00675 | 0.361 |
| CLV_PCSK_FUR_1 | 670 | 674 | PF00082 | 0.713 |
| CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.695 |
| CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.607 |
| CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.509 |
| CLV_PCSK_KEX2_1 | 486 | 488 | PF00082 | 0.474 |
| CLV_PCSK_KEX2_1 | 669 | 671 | PF00082 | 0.714 |
| CLV_PCSK_KEX2_1 | 672 | 674 | PF00082 | 0.657 |
| CLV_PCSK_KEX2_1 | 772 | 774 | PF00082 | 0.496 |
| CLV_PCSK_KEX2_1 | 892 | 894 | PF00082 | 0.490 |
| CLV_PCSK_PC1ET2_1 | 669 | 671 | PF00082 | 0.751 |
| CLV_PCSK_PC7_1 | 152 | 158 | PF00082 | 0.631 |
| CLV_PCSK_PC7_1 | 222 | 228 | PF00082 | 0.608 |
| CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.445 |
| CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.679 |
| CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.626 |
| CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.311 |
| CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.563 |
| CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.354 |
| CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.317 |
| CLV_PCSK_SKI1_1 | 594 | 598 | PF00082 | 0.473 |
| CLV_PCSK_SKI1_1 | 672 | 676 | PF00082 | 0.638 |
| CLV_PCSK_SKI1_1 | 779 | 783 | PF00082 | 0.564 |
| CLV_PCSK_SKI1_1 | 893 | 897 | PF00082 | 0.481 |
| DEG_APCC_DBOX_1 | 542 | 550 | PF00400 | 0.522 |
| DEG_COP1_1 | 565 | 575 | PF00400 | 0.442 |
| DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.680 |
| DEG_ODPH_VHL_1 | 730 | 743 | PF01847 | 0.431 |
| DEG_SCF_FBW7_2 | 78 | 85 | PF00400 | 0.479 |
| DEG_SPOP_SBC_1 | 107 | 111 | PF00917 | 0.558 |
| DOC_CKS1_1 | 269 | 274 | PF01111 | 0.649 |
| DOC_CKS1_1 | 437 | 442 | PF01111 | 0.408 |
| DOC_CYCLIN_RxL_1 | 542 | 553 | PF00134 | 0.328 |
| DOC_CYCLIN_yCln2_LP_2 | 269 | 275 | PF00134 | 0.646 |
| DOC_CYCLIN_yCln2_LP_2 | 28 | 34 | PF00134 | 0.476 |
| DOC_CYCLIN_yCln2_LP_2 | 437 | 443 | PF00134 | 0.408 |
| DOC_CYCLIN_yCln2_LP_2 | 469 | 475 | PF00134 | 0.628 |
| DOC_CYCLIN_yCln2_LP_2 | 828 | 834 | PF00134 | 0.517 |
| DOC_MAPK_DCC_7 | 789 | 799 | PF00069 | 0.508 |
| DOC_MAPK_gen_1 | 25 | 34 | PF00069 | 0.622 |
| DOC_MAPK_gen_1 | 660 | 666 | PF00069 | 0.666 |
| DOC_MAPK_gen_1 | 734 | 743 | PF00069 | 0.379 |
| DOC_MAPK_gen_1 | 772 | 782 | PF00069 | 0.559 |
| DOC_MAPK_gen_1 | 872 | 881 | PF00069 | 0.395 |
| DOC_MAPK_gen_1 | 892 | 898 | PF00069 | 0.222 |
| DOC_MAPK_MEF2A_6 | 25 | 32 | PF00069 | 0.471 |
| DOC_MAPK_MEF2A_6 | 287 | 294 | PF00069 | 0.252 |
| DOC_MAPK_MEF2A_6 | 399 | 408 | PF00069 | 0.314 |
| DOC_MAPK_MEF2A_6 | 430 | 437 | PF00069 | 0.336 |
| DOC_MAPK_MEF2A_6 | 773 | 782 | PF00069 | 0.594 |
| DOC_MAPK_RevD_3 | 879 | 893 | PF00069 | 0.445 |
| DOC_PP1_RVXF_1 | 777 | 783 | PF00149 | 0.541 |
| DOC_PP2B_LxvP_1 | 28 | 31 | PF13499 | 0.601 |
| DOC_PP2B_LxvP_1 | 828 | 831 | PF13499 | 0.519 |
| DOC_PP4_FxxP_1 | 21 | 24 | PF00568 | 0.632 |
| DOC_PP4_FxxP_1 | 34 | 37 | PF00568 | 0.592 |
| DOC_PP4_FxxP_1 | 349 | 352 | PF00568 | 0.335 |
| DOC_PP4_FxxP_1 | 68 | 71 | PF00568 | 0.487 |
| DOC_PP4_FxxP_1 | 762 | 765 | PF00568 | 0.415 |
| DOC_PP4_FxxP_1 | 98 | 101 | PF00568 | 0.448 |
| DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.519 |
| DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.793 |
| DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.762 |
| DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.406 |
| DOC_USP7_MATH_1 | 571 | 575 | PF00917 | 0.667 |
| DOC_USP7_MATH_1 | 765 | 769 | PF00917 | 0.556 |
| DOC_USP7_MATH_1 | 905 | 909 | PF00917 | 0.629 |
| DOC_USP7_MATH_1 | 917 | 921 | PF00917 | 0.536 |
| DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.582 |
| DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.586 |
| DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.268 |
| DOC_WW_Pin1_4 | 436 | 441 | PF00397 | 0.408 |
| DOC_WW_Pin1_4 | 506 | 511 | PF00397 | 0.477 |
| DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.723 |
| DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.692 |
| DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.687 |
| DOC_WW_Pin1_4 | 910 | 915 | PF00397 | 0.601 |
| LIG_14-3-3_CanoR_1 | 108 | 113 | PF00244 | 0.549 |
| LIG_14-3-3_CanoR_1 | 192 | 201 | PF00244 | 0.766 |
| LIG_14-3-3_CanoR_1 | 326 | 335 | PF00244 | 0.368 |
| LIG_14-3-3_CanoR_1 | 672 | 677 | PF00244 | 0.604 |
| LIG_14-3-3_CanoR_1 | 772 | 780 | PF00244 | 0.570 |
| LIG_14-3-3_CanoR_1 | 892 | 898 | PF00244 | 0.519 |
| LIG_14-3-3_CanoR_1 | 906 | 914 | PF00244 | 0.530 |
| LIG_14-3-3_CanoR_1 | 919 | 923 | PF00244 | 0.454 |
| LIG_Actin_WH2_2 | 246 | 263 | PF00022 | 0.594 |
| LIG_Actin_WH2_2 | 313 | 328 | PF00022 | 0.335 |
| LIG_Actin_WH2_2 | 723 | 738 | PF00022 | 0.547 |
| LIG_BRCT_BRCA1_1 | 425 | 429 | PF00533 | 0.335 |
| LIG_BRCT_BRCA1_1 | 90 | 94 | PF00533 | 0.645 |
| LIG_CtBP_PxDLS_1 | 706 | 710 | PF00389 | 0.498 |
| LIG_EH_1 | 99 | 103 | PF12763 | 0.473 |
| LIG_FHA_1 | 231 | 237 | PF00498 | 0.607 |
| LIG_FHA_1 | 308 | 314 | PF00498 | 0.335 |
| LIG_FHA_1 | 330 | 336 | PF00498 | 0.335 |
| LIG_FHA_1 | 475 | 481 | PF00498 | 0.588 |
| LIG_FHA_1 | 591 | 597 | PF00498 | 0.524 |
| LIG_FHA_1 | 636 | 642 | PF00498 | 0.571 |
| LIG_FHA_1 | 669 | 675 | PF00498 | 0.700 |
| LIG_FHA_1 | 67 | 73 | PF00498 | 0.511 |
| LIG_FHA_1 | 713 | 719 | PF00498 | 0.638 |
| LIG_FHA_1 | 827 | 833 | PF00498 | 0.521 |
| LIG_FHA_1 | 84 | 90 | PF00498 | 0.675 |
| LIG_FHA_1 | 849 | 855 | PF00498 | 0.384 |
| LIG_FHA_2 | 265 | 271 | PF00498 | 0.532 |
| LIG_FHA_2 | 715 | 721 | PF00498 | 0.523 |
| LIG_Integrin_isoDGR_2 | 103 | 105 | PF01839 | 0.642 |
| LIG_LIR_Apic_2 | 33 | 37 | PF02991 | 0.577 |
| LIG_LIR_Apic_2 | 481 | 485 | PF02991 | 0.419 |
| LIG_LIR_Apic_2 | 760 | 765 | PF02991 | 0.414 |
| LIG_LIR_Apic_2 | 96 | 101 | PF02991 | 0.454 |
| LIG_LIR_Gen_1 | 244 | 253 | PF02991 | 0.603 |
| LIG_LIR_Gen_1 | 255 | 265 | PF02991 | 0.638 |
| LIG_LIR_Gen_1 | 411 | 419 | PF02991 | 0.335 |
| LIG_LIR_Gen_1 | 464 | 474 | PF02991 | 0.578 |
| LIG_LIR_LC3C_4 | 877 | 881 | PF02991 | 0.497 |
| LIG_LIR_Nem_3 | 244 | 249 | PF02991 | 0.553 |
| LIG_LIR_Nem_3 | 255 | 260 | PF02991 | 0.580 |
| LIG_LIR_Nem_3 | 411 | 415 | PF02991 | 0.328 |
| LIG_LIR_Nem_3 | 426 | 432 | PF02991 | 0.335 |
| LIG_LIR_Nem_3 | 464 | 469 | PF02991 | 0.581 |
| LIG_LIR_Nem_3 | 682 | 686 | PF02991 | 0.419 |
| LIG_LIR_Nem_3 | 88 | 93 | PF02991 | 0.716 |
| LIG_PCNA_yPIPBox_3 | 250 | 261 | PF02747 | 0.629 |
| LIG_PCNA_yPIPBox_3 | 789 | 800 | PF02747 | 0.541 |
| LIG_PDZ_Class_2 | 930 | 935 | PF00595 | 0.653 |
| LIG_Pex14_2 | 118 | 122 | PF04695 | 0.539 |
| LIG_Pex14_2 | 345 | 349 | PF04695 | 0.321 |
| LIG_Pex14_2 | 94 | 98 | PF04695 | 0.496 |
| LIG_SH2_CRK | 123 | 127 | PF00017 | 0.595 |
| LIG_SH2_CRK | 257 | 261 | PF00017 | 0.633 |
| LIG_SH2_CRK | 90 | 94 | PF00017 | 0.678 |
| LIG_SH2_GRB2like | 248 | 251 | PF00017 | 0.620 |
| LIG_SH2_SRC | 315 | 318 | PF00017 | 0.190 |
| LIG_SH2_STAP1 | 424 | 428 | PF00017 | 0.447 |
| LIG_SH2_STAP1 | 836 | 840 | PF00017 | 0.473 |
| LIG_SH2_STAT3 | 882 | 885 | PF00017 | 0.570 |
| LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.557 |
| LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.252 |
| LIG_SH2_STAT5 | 482 | 485 | PF00017 | 0.418 |
| LIG_SH2_STAT5 | 821 | 824 | PF00017 | 0.483 |
| LIG_SH2_STAT5 | 867 | 870 | PF00017 | 0.357 |
| LIG_SH3_3 | 123 | 129 | PF00018 | 0.539 |
| LIG_SH3_3 | 16 | 22 | PF00018 | 0.729 |
| LIG_SH3_3 | 269 | 275 | PF00018 | 0.688 |
| LIG_SH3_3 | 469 | 475 | PF00018 | 0.566 |
| LIG_SH3_3 | 578 | 584 | PF00018 | 0.459 |
| LIG_SH3_3 | 671 | 677 | PF00018 | 0.495 |
| LIG_SH3_3 | 802 | 808 | PF00018 | 0.411 |
| LIG_SH3_CIN85_PxpxPR_1 | 22 | 27 | PF14604 | 0.695 |
| LIG_SUMO_SIM_anti_2 | 369 | 375 | PF11976 | 0.331 |
| LIG_SUMO_SIM_anti_2 | 579 | 584 | PF11976 | 0.565 |
| LIG_SUMO_SIM_par_1 | 369 | 375 | PF11976 | 0.294 |
| LIG_SUMO_SIM_par_1 | 638 | 644 | PF11976 | 0.597 |
| LIG_SUMO_SIM_par_1 | 662 | 668 | PF11976 | 0.686 |
| LIG_SUMO_SIM_par_1 | 710 | 715 | PF11976 | 0.501 |
| LIG_SUMO_SIM_par_1 | 850 | 855 | PF11976 | 0.375 |
| LIG_SUMO_SIM_par_1 | 929 | 934 | PF11976 | 0.474 |
| LIG_TRAF2_1 | 162 | 165 | PF00917 | 0.447 |
| MOD_CDK_SPxK_1 | 436 | 442 | PF00069 | 0.408 |
| MOD_CDK_SPxK_1 | 506 | 512 | PF00069 | 0.533 |
| MOD_CDK_SPxxK_3 | 280 | 287 | PF00069 | 0.190 |
| MOD_CK1_1 | 178 | 184 | PF00069 | 0.713 |
| MOD_CK1_1 | 304 | 310 | PF00069 | 0.378 |
| MOD_CK1_1 | 627 | 633 | PF00069 | 0.737 |
| MOD_CK1_1 | 70 | 76 | PF00069 | 0.750 |
| MOD_CK1_1 | 752 | 758 | PF00069 | 0.423 |
| MOD_CK2_1 | 132 | 138 | PF00069 | 0.586 |
| MOD_CK2_1 | 197 | 203 | PF00069 | 0.584 |
| MOD_CK2_1 | 676 | 682 | PF00069 | 0.537 |
| MOD_CK2_1 | 891 | 897 | PF00069 | 0.412 |
| MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.708 |
| MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.708 |
| MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.778 |
| MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.371 |
| MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.534 |
| MOD_GlcNHglycan | 620 | 623 | PF01048 | 0.776 |
| MOD_GlcNHglycan | 630 | 633 | PF01048 | 0.707 |
| MOD_GlcNHglycan | 647 | 650 | PF01048 | 0.681 |
| MOD_GlcNHglycan | 678 | 681 | PF01048 | 0.568 |
| MOD_GlcNHglycan | 893 | 896 | PF01048 | 0.407 |
| MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.609 |
| MOD_GSK3_1 | 106 | 113 | PF00069 | 0.423 |
| MOD_GSK3_1 | 176 | 183 | PF00069 | 0.773 |
| MOD_GSK3_1 | 188 | 195 | PF00069 | 0.671 |
| MOD_GSK3_1 | 260 | 267 | PF00069 | 0.522 |
| MOD_GSK3_1 | 274 | 281 | PF00069 | 0.593 |
| MOD_GSK3_1 | 39 | 46 | PF00069 | 0.698 |
| MOD_GSK3_1 | 413 | 420 | PF00069 | 0.382 |
| MOD_GSK3_1 | 474 | 481 | PF00069 | 0.567 |
| MOD_GSK3_1 | 500 | 507 | PF00069 | 0.431 |
| MOD_GSK3_1 | 517 | 524 | PF00069 | 0.600 |
| MOD_GSK3_1 | 624 | 631 | PF00069 | 0.732 |
| MOD_GSK3_1 | 643 | 650 | PF00069 | 0.529 |
| MOD_GSK3_1 | 66 | 73 | PF00069 | 0.712 |
| MOD_GSK3_1 | 668 | 675 | PF00069 | 0.683 |
| MOD_GSK3_1 | 685 | 692 | PF00069 | 0.488 |
| MOD_GSK3_1 | 710 | 717 | PF00069 | 0.615 |
| MOD_GSK3_1 | 74 | 81 | PF00069 | 0.661 |
| MOD_GSK3_1 | 745 | 752 | PF00069 | 0.448 |
| MOD_GSK3_1 | 844 | 851 | PF00069 | 0.403 |
| MOD_N-GLC_1 | 475 | 480 | PF02516 | 0.551 |
| MOD_N-GLC_1 | 745 | 750 | PF02516 | 0.472 |
| MOD_N-GLC_1 | 752 | 757 | PF02516 | 0.425 |
| MOD_N-GLC_1 | 923 | 928 | PF02516 | 0.577 |
| MOD_NEK2_1 | 106 | 111 | PF00069 | 0.517 |
| MOD_NEK2_1 | 260 | 265 | PF00069 | 0.418 |
| MOD_NEK2_1 | 329 | 334 | PF00069 | 0.335 |
| MOD_NEK2_1 | 43 | 48 | PF00069 | 0.683 |
| MOD_NEK2_1 | 517 | 522 | PF00069 | 0.505 |
| MOD_NEK2_1 | 712 | 717 | PF00069 | 0.569 |
| MOD_NEK2_1 | 814 | 819 | PF00069 | 0.597 |
| MOD_NEK2_1 | 848 | 853 | PF00069 | 0.389 |
| MOD_NEK2_1 | 94 | 99 | PF00069 | 0.588 |
| MOD_NEK2_2 | 341 | 346 | PF00069 | 0.354 |
| MOD_NEK2_2 | 655 | 660 | PF00069 | 0.670 |
| MOD_NEK2_2 | 765 | 770 | PF00069 | 0.496 |
| MOD_NEK2_2 | 836 | 841 | PF00069 | 0.376 |
| MOD_PIKK_1 | 146 | 152 | PF00454 | 0.614 |
| MOD_PIKK_1 | 215 | 221 | PF00454 | 0.615 |
| MOD_PKA_1 | 672 | 678 | PF00069 | 0.594 |
| MOD_PKA_2 | 107 | 113 | PF00069 | 0.499 |
| MOD_PKA_2 | 193 | 199 | PF00069 | 0.744 |
| MOD_PKA_2 | 260 | 266 | PF00069 | 0.649 |
| MOD_PKA_2 | 628 | 634 | PF00069 | 0.750 |
| MOD_PKA_2 | 672 | 678 | PF00069 | 0.630 |
| MOD_PKA_2 | 771 | 777 | PF00069 | 0.628 |
| MOD_PKA_2 | 891 | 897 | PF00069 | 0.480 |
| MOD_PKA_2 | 905 | 911 | PF00069 | 0.503 |
| MOD_PKA_2 | 918 | 924 | PF00069 | 0.410 |
| MOD_PKA_2 | 94 | 100 | PF00069 | 0.577 |
| MOD_PKB_1 | 670 | 678 | PF00069 | 0.613 |
| MOD_Plk_1 | 374 | 380 | PF00069 | 0.335 |
| MOD_Plk_1 | 39 | 45 | PF00069 | 0.560 |
| MOD_Plk_1 | 417 | 423 | PF00069 | 0.381 |
| MOD_Plk_1 | 475 | 481 | PF00069 | 0.503 |
| MOD_Plk_1 | 504 | 510 | PF00069 | 0.400 |
| MOD_Plk_1 | 765 | 771 | PF00069 | 0.541 |
| MOD_Plk_2-3 | 374 | 380 | PF00069 | 0.335 |
| MOD_Plk_4 | 260 | 266 | PF00069 | 0.386 |
| MOD_Plk_4 | 307 | 313 | PF00069 | 0.373 |
| MOD_Plk_4 | 374 | 380 | PF00069 | 0.335 |
| MOD_Plk_4 | 423 | 429 | PF00069 | 0.346 |
| MOD_Plk_4 | 636 | 642 | PF00069 | 0.526 |
| MOD_Plk_4 | 705 | 711 | PF00069 | 0.472 |
| MOD_Plk_4 | 765 | 771 | PF00069 | 0.522 |
| MOD_Plk_4 | 817 | 823 | PF00069 | 0.438 |
| MOD_Plk_4 | 848 | 854 | PF00069 | 0.384 |
| MOD_Plk_4 | 94 | 100 | PF00069 | 0.550 |
| MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.586 |
| MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.588 |
| MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.268 |
| MOD_ProDKin_1 | 436 | 442 | PF00069 | 0.408 |
| MOD_ProDKin_1 | 506 | 512 | PF00069 | 0.487 |
| MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.725 |
| MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.693 |
| MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.689 |
| MOD_ProDKin_1 | 910 | 916 | PF00069 | 0.606 |
| MOD_SUMO_rev_2 | 165 | 172 | PF00179 | 0.405 |
| MOD_SUMO_rev_2 | 489 | 498 | PF00179 | 0.427 |
| TRG_DiLeu_BaEn_3 | 704 | 710 | PF01217 | 0.553 |
| TRG_DiLeu_BaLyEn_6 | 542 | 547 | PF01217 | 0.639 |
| TRG_DiLeu_BaLyEn_6 | 795 | 800 | PF01217 | 0.439 |
| TRG_ENDOCYTIC_2 | 123 | 126 | PF00928 | 0.615 |
| TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.523 |
| TRG_ENDOCYTIC_2 | 317 | 320 | PF00928 | 0.479 |
| TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.293 |
| TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.653 |
| TRG_ER_diArg_1 | 156 | 158 | PF00400 | 0.672 |
| TRG_ER_diArg_1 | 225 | 227 | PF00400 | 0.592 |
| TRG_ER_diArg_1 | 24 | 27 | PF00400 | 0.526 |
| TRG_ER_diArg_1 | 456 | 458 | PF00400 | 0.493 |
| TRG_ER_diArg_1 | 485 | 488 | PF00400 | 0.458 |
| TRG_ER_diArg_1 | 597 | 600 | PF00400 | 0.417 |
| TRG_ER_diArg_1 | 670 | 673 | PF00400 | 0.690 |
| TRG_ER_diArg_1 | 771 | 773 | PF00400 | 0.494 |
| TRG_ER_diArg_1 | 891 | 893 | PF00400 | 0.575 |
| TRG_NLS_MonoExtC_3 | 183 | 189 | PF00514 | 0.628 |
| TRG_NLS_MonoExtC_3 | 668 | 673 | PF00514 | 0.733 |
| TRG_Pf-PMV_PEXEL_1 | 251 | 255 | PF00026 | 0.597 |
| TRG_Pf-PMV_PEXEL_1 | 604 | 609 | PF00026 | 0.475 |
| TRG_Pf-PMV_PEXEL_1 | 700 | 704 | PF00026 | 0.583 |
| TRG_Pf-PMV_PEXEL_1 | 779 | 783 | PF00026 | 0.433 |
| TRG_Pf-PMV_PEXEL_1 | 798 | 803 | PF00026 | 0.417 |
| TRG_Pf-PMV_PEXEL_1 | 874 | 878 | PF00026 | 0.472 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PCJ6 | Leptomonas seymouri | 58% | 84% |
| A0A1X0NSB2 | Trypanosomatidae | 50% | 100% |
| A0A3Q8IGY7 | Leishmania donovani | 90% | 100% |
| A0A422NKI2 | Trypanosoma rangeli | 49% | 100% |
| A4HGV5 | Leishmania braziliensis | 79% | 100% |
| A4I3Y5 | Leishmania infantum | 90% | 100% |
| D0A956 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
| Q383A1 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 47% | 100% |
| Q4Q810 | Leishmania major | 89% | 100% |
| V5BL79 | Trypanosoma cruzi | 50% | 100% |