| 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:0005634 | nucleus | 5 | 12 | 
| GO:0032991 | protein-containing complex | 1 | 12 | 
| GO:0042555 | MCM complex | 2 | 12 | 
| GO:0043226 | organelle | 2 | 12 | 
| GO:0043227 | membrane-bounded organelle | 3 | 12 | 
| GO:0043229 | intracellular organelle | 3 | 12 | 
| GO:0043231 | intracellular membrane-bounded organelle | 4 | 12 | 
| GO:0110165 | cellular anatomical entity | 1 | 12 | 
Related structures:
AlphaFold database: E9AWT2
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 | 
| GO:0006259 | DNA metabolic process | 4 | 12 | 
| GO:0006270 | DNA replication initiation | 5 | 12 | 
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 | 
| GO:0006807 | nitrogen compound metabolic process | 2 | 12 | 
| GO:0007049 | cell cycle | 2 | 12 | 
| GO:0008152 | metabolic process | 1 | 12 | 
| GO:0009987 | cellular process | 1 | 12 | 
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 | 
| GO:0043170 | macromolecule metabolic process | 3 | 12 | 
| GO:0044237 | cellular metabolic process | 2 | 12 | 
| GO:0044238 | primary metabolic process | 2 | 12 | 
| GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 | 
| GO:0046483 | heterocycle metabolic process | 3 | 12 | 
| GO:0071704 | organic substance metabolic process | 2 | 12 | 
| GO:0090304 | nucleic acid metabolic process | 4 | 12 | 
| GO:1901360 | organic cyclic compound metabolic process | 3 | 12 | 
| GO:0000724 | double-strand break repair via homologous recombination | 7 | 1 | 
| GO:0000725 | recombinational repair | 6 | 1 | 
| GO:0000727 | double-strand break repair via break-induced replication | 8 | 1 | 
| GO:0006281 | DNA repair | 5 | 1 | 
| GO:0006302 | double-strand break repair | 6 | 1 | 
| GO:0006310 | DNA recombination | 5 | 1 | 
| GO:0006950 | response to stress | 2 | 1 | 
| GO:0006974 | DNA damage response | 4 | 1 | 
| GO:0033554 | cellular response to stress | 3 | 1 | 
| GO:0050896 | response to stimulus | 1 | 1 | 
| GO:0051716 | cellular response to stimulus | 2 | 1 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0000166 | nucleotide binding | 3 | 12 | 
| GO:0003676 | nucleic acid binding | 3 | 12 | 
| GO:0003677 | DNA binding | 4 | 12 | 
| GO:0003678 | DNA helicase activity | 3 | 12 | 
| GO:0003688 | DNA replication origin binding | 7 | 12 | 
| GO:0003690 | double-stranded DNA binding | 5 | 12 | 
| GO:0003824 | catalytic activity | 1 | 12 | 
| GO:0004386 | helicase activity | 2 | 12 | 
| GO:0005488 | binding | 1 | 12 | 
| GO:0005524 | ATP binding | 5 | 12 | 
| GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 12 | 
| GO:0016462 | pyrophosphatase activity | 5 | 11 | 
| GO:0016787 | hydrolase activity | 2 | 12 | 
| 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 | 12 | 
| GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 | 
| 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:0043565 | sequence-specific DNA binding | 5 | 12 | 
| GO:0097159 | organic cyclic compound binding | 2 | 12 | 
| GO:0097367 | carbohydrate derivative binding | 2 | 12 | 
| GO:0140097 | catalytic activity, acting on DNA | 3 | 12 | 
| GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 | 
| GO:0140657 | ATP-dependent activity | 1 | 12 | 
| GO:1901265 | nucleoside phosphate binding | 3 | 12 | 
| GO:1901363 | heterocyclic compound binding | 2 | 12 | 
| GO:1990837 | sequence-specific double-stranded DNA binding | 6 | 12 | 
| GO:0003697 | single-stranded DNA binding | 5 | 1 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 315 | 319 | PF00656 | 0.517 | 
| CLV_C14_Caspase3-7 | 703 | 707 | PF00656 | 0.493 | 
| CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.252 | 
| CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.253 | 
| CLV_NRD_NRD_1 | 576 | 578 | PF00675 | 0.718 | 
| CLV_NRD_NRD_1 | 641 | 643 | PF00675 | 0.253 | 
| CLV_NRD_NRD_1 | 748 | 750 | PF00675 | 0.424 | 
| CLV_NRD_NRD_1 | 790 | 792 | PF00675 | 0.437 | 
| CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.522 | 
| CLV_PCSK_KEX2_1 | 391 | 393 | PF00082 | 0.287 | 
| CLV_PCSK_KEX2_1 | 576 | 578 | PF00082 | 0.730 | 
| CLV_PCSK_KEX2_1 | 641 | 643 | PF00082 | 0.253 | 
| CLV_PCSK_KEX2_1 | 747 | 749 | PF00082 | 0.438 | 
| CLV_PCSK_KEX2_1 | 784 | 786 | PF00082 | 0.446 | 
| CLV_PCSK_PC1ET2_1 | 282 | 284 | PF00082 | 0.538 | 
| CLV_PCSK_PC1ET2_1 | 391 | 393 | PF00082 | 0.287 | 
| CLV_PCSK_PC1ET2_1 | 784 | 786 | PF00082 | 0.461 | 
| CLV_PCSK_SKI1_1 | 114 | 118 | PF00082 | 0.463 | 
| CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.253 | 
| CLV_PCSK_SKI1_1 | 631 | 635 | PF00082 | 0.339 | 
| CLV_PCSK_SKI1_1 | 712 | 716 | PF00082 | 0.264 | 
| CLV_PCSK_SKI1_1 | 749 | 753 | PF00082 | 0.462 | 
| CLV_PCSK_SKI1_1 | 794 | 798 | PF00082 | 0.525 | 
| CLV_Separin_Metazoa | 248 | 252 | PF03568 | 0.453 | 
| DEG_APCC_DBOX_1 | 694 | 702 | PF00400 | 0.477 | 
| DEG_APCC_DBOX_1 | 793 | 801 | PF00400 | 0.545 | 
| DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.650 | 
| DEG_SPOP_SBC_1 | 158 | 162 | PF00917 | 0.539 | 
| DOC_CYCLIN_RxL_1 | 111 | 121 | PF00134 | 0.613 | 
| DOC_CYCLIN_RxL_1 | 628 | 635 | PF00134 | 0.539 | 
| DOC_CYCLIN_RxL_1 | 94 | 104 | PF00134 | 0.466 | 
| DOC_CYCLIN_yClb5_NLxxxL_5 | 62 | 71 | PF00134 | 0.453 | 
| DOC_MAPK_DCC_7 | 419 | 429 | PF00069 | 0.464 | 
| DOC_MAPK_gen_1 | 214 | 223 | PF00069 | 0.513 | 
| DOC_MAPK_gen_1 | 378 | 386 | PF00069 | 0.450 | 
| DOC_MAPK_gen_1 | 475 | 484 | PF00069 | 0.453 | 
| DOC_MAPK_MEF2A_6 | 122 | 130 | PF00069 | 0.402 | 
| DOC_MAPK_MEF2A_6 | 214 | 223 | PF00069 | 0.513 | 
| DOC_MAPK_MEF2A_6 | 378 | 386 | PF00069 | 0.453 | 
| DOC_MAPK_MEF2A_6 | 399 | 406 | PF00069 | 0.464 | 
| DOC_PP2B_PxIxI_1 | 673 | 679 | PF00149 | 0.453 | 
| DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.657 | 
| DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.553 | 
| DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.464 | 
| DOC_USP7_MATH_1 | 570 | 574 | PF00917 | 0.589 | 
| DOC_USP7_MATH_1 | 582 | 586 | PF00917 | 0.620 | 
| DOC_USP7_MATH_1 | 592 | 596 | PF00917 | 0.670 | 
| DOC_USP7_MATH_1 | 702 | 706 | PF00917 | 0.532 | 
| DOC_USP7_MATH_1 | 721 | 725 | PF00917 | 0.272 | 
| DOC_USP7_MATH_2 | 344 | 350 | PF00917 | 0.425 | 
| DOC_USP7_UBL2_3 | 351 | 355 | PF12436 | 0.513 | 
| DOC_USP7_UBL2_3 | 419 | 423 | PF12436 | 0.464 | 
| DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.453 | 
| DOC_WW_Pin1_4 | 670 | 675 | PF00397 | 0.464 | 
| LIG_14-3-3_CanoR_1 | 251 | 256 | PF00244 | 0.453 | 
| LIG_14-3-3_CanoR_1 | 335 | 341 | PF00244 | 0.581 | 
| LIG_14-3-3_CanoR_1 | 507 | 511 | PF00244 | 0.453 | 
| LIG_14-3-3_CanoR_1 | 618 | 625 | PF00244 | 0.466 | 
| LIG_14-3-3_CanoR_1 | 64 | 74 | PF00244 | 0.518 | 
| LIG_14-3-3_CanoR_1 | 688 | 696 | PF00244 | 0.443 | 
| LIG_14-3-3_CanoR_1 | 760 | 768 | PF00244 | 0.430 | 
| LIG_14-3-3_CanoR_1 | 791 | 797 | PF00244 | 0.461 | 
| LIG_APCC_ABBA_1 | 51 | 56 | PF00400 | 0.481 | 
| LIG_Clathr_ClatBox_1 | 222 | 226 | PF01394 | 0.464 | 
| LIG_FHA_1 | 123 | 129 | PF00498 | 0.428 | 
| LIG_FHA_1 | 244 | 250 | PF00498 | 0.450 | 
| LIG_FHA_1 | 252 | 258 | PF00498 | 0.436 | 
| LIG_FHA_1 | 440 | 446 | PF00498 | 0.453 | 
| LIG_FHA_1 | 490 | 496 | PF00498 | 0.453 | 
| LIG_FHA_1 | 499 | 505 | PF00498 | 0.453 | 
| LIG_FHA_1 | 5 | 11 | PF00498 | 0.701 | 
| LIG_FHA_1 | 506 | 512 | PF00498 | 0.453 | 
| LIG_FHA_1 | 609 | 615 | PF00498 | 0.305 | 
| LIG_FHA_1 | 671 | 677 | PF00498 | 0.464 | 
| LIG_FHA_1 | 95 | 101 | PF00498 | 0.459 | 
| LIG_FHA_2 | 313 | 319 | PF00498 | 0.518 | 
| LIG_HP1_1 | 219 | 223 | PF01393 | 0.513 | 
| LIG_IBAR_NPY_1 | 218 | 220 | PF08397 | 0.453 | 
| LIG_Integrin_RGD_1 | 399 | 401 | PF01839 | 0.264 | 
| LIG_LIR_Gen_1 | 358 | 367 | PF02991 | 0.496 | 
| LIG_LIR_Gen_1 | 471 | 480 | PF02991 | 0.453 | 
| LIG_LIR_Gen_1 | 539 | 548 | PF02991 | 0.452 | 
| LIG_LIR_Gen_1 | 56 | 67 | PF02991 | 0.460 | 
| LIG_LIR_Gen_1 | 635 | 644 | PF02991 | 0.453 | 
| LIG_LIR_Gen_1 | 75 | 84 | PF02991 | 0.386 | 
| LIG_LIR_Nem_3 | 347 | 353 | PF02991 | 0.453 | 
| LIG_LIR_Nem_3 | 358 | 363 | PF02991 | 0.453 | 
| LIG_LIR_Nem_3 | 520 | 524 | PF02991 | 0.463 | 
| LIG_LIR_Nem_3 | 539 | 544 | PF02991 | 0.356 | 
| LIG_LIR_Nem_3 | 611 | 616 | PF02991 | 0.459 | 
| LIG_LIR_Nem_3 | 635 | 640 | PF02991 | 0.453 | 
| LIG_LIR_Nem_3 | 75 | 79 | PF02991 | 0.490 | 
| LIG_NRP_CendR_1 | 799 | 801 | PF00754 | 0.448 | 
| LIG_PCNA_PIPBox_1 | 630 | 639 | PF02747 | 0.453 | 
| LIG_PCNA_yPIPBox_3 | 140 | 151 | PF02747 | 0.453 | 
| LIG_Pex14_2 | 47 | 51 | PF04695 | 0.453 | 
| LIG_Pex14_2 | 541 | 545 | PF04695 | 0.453 | 
| LIG_RPA_C_Fungi | 502 | 514 | PF08784 | 0.305 | 
| LIG_RPA_C_Fungi | 699 | 711 | PF08784 | 0.321 | 
| LIG_RPA_C_Fungi | 755 | 767 | PF08784 | 0.446 | 
| LIG_SH2_CRK | 521 | 525 | PF00017 | 0.321 | 
| LIG_SH2_CRK | 780 | 784 | PF00017 | 0.441 | 
| LIG_SH2_GRB2like | 182 | 185 | PF00017 | 0.340 | 
| LIG_SH2_NCK_1 | 616 | 620 | PF00017 | 0.297 | 
| LIG_SH2_PTP2 | 220 | 223 | PF00017 | 0.390 | 
| LIG_SH2_PTP2 | 637 | 640 | PF00017 | 0.321 | 
| LIG_SH2_SRC | 182 | 185 | PF00017 | 0.340 | 
| LIG_SH2_STAT3 | 229 | 232 | PF00017 | 0.305 | 
| LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.321 | 
| LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.305 | 
| LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.305 | 
| LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.364 | 
| LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.305 | 
| LIG_SH2_STAT5 | 613 | 616 | PF00017 | 0.305 | 
| LIG_SH2_STAT5 | 637 | 640 | PF00017 | 0.321 | 
| LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.425 | 
| LIG_SH3_3 | 218 | 224 | PF00018 | 0.390 | 
| LIG_SH3_3 | 544 | 550 | PF00018 | 0.305 | 
| LIG_SUMO_SIM_par_1 | 149 | 154 | PF11976 | 0.374 | 
| LIG_SUMO_SIM_par_1 | 253 | 258 | PF11976 | 0.305 | 
| LIG_SUMO_SIM_par_1 | 275 | 281 | PF11976 | 0.305 | 
| LIG_TRAF2_1 | 278 | 281 | PF00917 | 0.432 | 
| LIG_TRAF2_1 | 344 | 347 | PF00917 | 0.544 | 
| LIG_TRFH_1 | 220 | 224 | PF08558 | 0.321 | 
| LIG_UBA3_1 | 371 | 379 | PF00899 | 0.305 | 
| MOD_CDK_SPxxK_3 | 263 | 270 | PF00069 | 0.305 | 
| MOD_CK1_1 | 121 | 127 | PF00069 | 0.476 | 
| MOD_CK1_1 | 160 | 166 | PF00069 | 0.373 | 
| MOD_CK1_1 | 176 | 182 | PF00069 | 0.187 | 
| MOD_CK1_1 | 266 | 272 | PF00069 | 0.305 | 
| MOD_CK1_1 | 336 | 342 | PF00069 | 0.600 | 
| MOD_CK1_1 | 444 | 450 | PF00069 | 0.306 | 
| MOD_CK1_1 | 506 | 512 | PF00069 | 0.305 | 
| MOD_CK1_1 | 536 | 542 | PF00069 | 0.305 | 
| MOD_CK1_1 | 587 | 593 | PF00069 | 0.721 | 
| MOD_CK1_1 | 65 | 71 | PF00069 | 0.452 | 
| MOD_CK1_1 | 670 | 676 | PF00069 | 0.380 | 
| MOD_CK2_1 | 275 | 281 | PF00069 | 0.305 | 
| MOD_CK2_1 | 702 | 708 | PF00069 | 0.425 | 
| MOD_Cter_Amidation | 574 | 577 | PF01082 | 0.746 | 
| MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.686 | 
| MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.308 | 
| MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.699 | 
| MOD_GlcNHglycan | 197 | 201 | PF01048 | 0.452 | 
| MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.335 | 
| MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.719 | 
| MOD_GlcNHglycan | 363 | 366 | PF01048 | 0.403 | 
| MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.305 | 
| MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.305 | 
| MOD_GlcNHglycan | 568 | 571 | PF01048 | 0.535 | 
| MOD_GlcNHglycan | 572 | 575 | PF01048 | 0.589 | 
| MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.565 | 
| MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.614 | 
| MOD_GlcNHglycan | 594 | 597 | PF01048 | 0.679 | 
| MOD_GlcNHglycan | 656 | 659 | PF01048 | 0.314 | 
| MOD_GlcNHglycan | 660 | 663 | PF01048 | 0.295 | 
| MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.384 | 
| MOD_GlcNHglycan | 723 | 726 | PF01048 | 0.468 | 
| MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.227 | 
| MOD_GSK3_1 | 118 | 125 | PF00069 | 0.529 | 
| MOD_GSK3_1 | 13 | 20 | PF00069 | 0.716 | 
| MOD_GSK3_1 | 172 | 179 | PF00069 | 0.305 | 
| MOD_GSK3_1 | 31 | 38 | PF00069 | 0.596 | 
| MOD_GSK3_1 | 313 | 320 | PF00069 | 0.481 | 
| MOD_GSK3_1 | 329 | 336 | PF00069 | 0.534 | 
| MOD_GSK3_1 | 4 | 11 | PF00069 | 0.704 | 
| MOD_GSK3_1 | 408 | 415 | PF00069 | 0.305 | 
| MOD_GSK3_1 | 429 | 436 | PF00069 | 0.300 | 
| MOD_GSK3_1 | 499 | 506 | PF00069 | 0.305 | 
| MOD_GSK3_1 | 532 | 539 | PF00069 | 0.321 | 
| MOD_GSK3_1 | 562 | 569 | PF00069 | 0.365 | 
| MOD_GSK3_1 | 592 | 599 | PF00069 | 0.639 | 
| MOD_GSK3_1 | 608 | 615 | PF00069 | 0.308 | 
| MOD_GSK3_1 | 654 | 661 | PF00069 | 0.340 | 
| MOD_GSK3_1 | 666 | 673 | PF00069 | 0.265 | 
| MOD_GSK3_1 | 729 | 736 | PF00069 | 0.497 | 
| MOD_LATS_1 | 758 | 764 | PF00433 | 0.493 | 
| MOD_N-GLC_1 | 24 | 29 | PF02516 | 0.661 | 
| MOD_N-GLC_1 | 328 | 333 | PF02516 | 0.518 | 
| MOD_N-GLC_1 | 498 | 503 | PF02516 | 0.305 | 
| MOD_N-GLC_1 | 570 | 575 | PF02516 | 0.675 | 
| MOD_N-GLC_1 | 65 | 70 | PF02516 | 0.423 | 
| MOD_N-GLC_1 | 658 | 663 | PF02516 | 0.451 | 
| MOD_N-GLC_1 | 670 | 675 | PF02516 | 0.375 | 
| MOD_NEK2_1 | 13 | 18 | PF00069 | 0.641 | 
| MOD_NEK2_1 | 196 | 201 | PF00069 | 0.438 | 
| MOD_NEK2_1 | 312 | 317 | PF00069 | 0.414 | 
| MOD_NEK2_1 | 386 | 391 | PF00069 | 0.321 | 
| MOD_NEK2_1 | 441 | 446 | PF00069 | 0.305 | 
| MOD_NEK2_1 | 503 | 508 | PF00069 | 0.305 | 
| MOD_NEK2_1 | 533 | 538 | PF00069 | 0.293 | 
| MOD_NEK2_1 | 566 | 571 | PF00069 | 0.607 | 
| MOD_NEK2_1 | 62 | 67 | PF00069 | 0.361 | 
| MOD_NEK2_2 | 617 | 622 | PF00069 | 0.390 | 
| MOD_PIKK_1 | 313 | 319 | PF00454 | 0.581 | 
| MOD_PIKK_1 | 412 | 418 | PF00454 | 0.321 | 
| MOD_PIKK_1 | 46 | 52 | PF00454 | 0.413 | 
| MOD_PKA_2 | 121 | 127 | PF00069 | 0.444 | 
| MOD_PKA_2 | 313 | 319 | PF00069 | 0.581 | 
| MOD_PKA_2 | 336 | 342 | PF00069 | 0.658 | 
| MOD_PKA_2 | 506 | 512 | PF00069 | 0.305 | 
| MOD_PKA_2 | 617 | 623 | PF00069 | 0.305 | 
| MOD_PKA_2 | 687 | 693 | PF00069 | 0.305 | 
| MOD_PKB_1 | 333 | 341 | PF00069 | 0.561 | 
| MOD_PKB_1 | 390 | 398 | PF00069 | 0.362 | 
| MOD_Plk_1 | 346 | 352 | PF00069 | 0.390 | 
| MOD_Plk_1 | 498 | 504 | PF00069 | 0.305 | 
| MOD_Plk_4 | 251 | 257 | PF00069 | 0.317 | 
| MOD_Plk_4 | 441 | 447 | PF00069 | 0.305 | 
| MOD_Plk_4 | 456 | 462 | PF00069 | 0.305 | 
| MOD_Plk_4 | 499 | 505 | PF00069 | 0.305 | 
| MOD_Plk_4 | 506 | 512 | PF00069 | 0.305 | 
| MOD_Plk_4 | 533 | 539 | PF00069 | 0.295 | 
| MOD_Plk_4 | 682 | 688 | PF00069 | 0.301 | 
| MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.305 | 
| MOD_ProDKin_1 | 670 | 676 | PF00069 | 0.321 | 
| MOD_SUMO_for_1 | 783 | 786 | PF00179 | 0.448 | 
| MOD_SUMO_rev_2 | 109 | 117 | PF00179 | 0.321 | 
| MOD_SUMO_rev_2 | 375 | 380 | PF00179 | 0.340 | 
| TRG_DiLeu_BaEn_1 | 757 | 762 | PF01217 | 0.407 | 
| TRG_DiLeu_BaLyEn_6 | 38 | 43 | PF01217 | 0.544 | 
| TRG_DiLeu_LyEn_5 | 757 | 762 | PF01217 | 0.423 | 
| TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.305 | 
| TRG_ENDOCYTIC_2 | 521 | 524 | PF00928 | 0.305 | 
| TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.305 | 
| TRG_ENDOCYTIC_2 | 637 | 640 | PF00928 | 0.321 | 
| TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.296 | 
| TRG_ENDOCYTIC_2 | 780 | 783 | PF00928 | 0.411 | 
| TRG_ER_diArg_1 | 334 | 337 | PF00400 | 0.669 | 
| TRG_ER_diArg_1 | 390 | 393 | PF00400 | 0.374 | 
| TRG_ER_diArg_1 | 640 | 642 | PF00400 | 0.305 | 
| TRG_ER_diArg_1 | 695 | 698 | PF00400 | 0.321 | 
| TRG_ER_diArg_1 | 746 | 749 | PF00400 | 0.418 | 
| TRG_NES_CRM1_1 | 628 | 643 | PF08389 | 0.321 | 
| TRG_NLS_Bipartite_1 | 378 | 394 | PF00514 | 0.321 | 
| TRG_Pf-PMV_PEXEL_1 | 140 | 144 | PF00026 | 0.305 | 
| TRG_Pf-PMV_PEXEL_1 | 259 | 263 | PF00026 | 0.305 | 
| TRG_Pf-PMV_PEXEL_1 | 41 | 46 | PF00026 | 0.513 | 
| TRG_Pf-PMV_PEXEL_1 | 760 | 764 | PF00026 | 0.420 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N0P686 | Leptomonas seymouri | 34% | 93% | 
| A0A0N0P860 | Leptomonas seymouri | 30% | 81% | 
| A0A0N0P9H0 | Leptomonas seymouri | 28% | 87% | 
| A0A0N1I2J6 | Leptomonas seymouri | 28% | 90% | 
| A0A0N1I371 | Leptomonas seymouri | 31% | 100% | 
| A0A0N1I383 | Leptomonas seymouri | 31% | 78% | 
| A0A0N1PC47 | Leptomonas seymouri | 88% | 100% | 
| A0A0S4IVB8 | Bodo saltans | 30% | 92% | 
| A0A0S4IW18 | Bodo saltans | 31% | 99% | 
| A0A0S4IYQ3 | Bodo saltans | 60% | 100% | 
| A0A0S4J5X8 | Bodo saltans | 29% | 100% | 
| A0A1X0NNF6 | Trypanosomatidae | 31% | 88% | 
| A0A1X0NQM5 | Trypanosomatidae | 30% | 90% | 
| A0A1X0NT66 | Trypanosomatidae | 30% | 100% | 
| A0A1X0NVE7 | Trypanosomatidae | 72% | 100% | 
| A0A1X0NZT6 | Trypanosomatidae | 31% | 85% | 
| A0A1X0P1Q1 | Trypanosomatidae | 27% | 100% | 
| A0A1X0P4W1 | Trypanosomatidae | 27% | 100% | 
| A0A3Q8IAX4 | Leishmania donovani | 30% | 82% | 
| A0A3R7MUG3 | Trypanosoma rangeli | 28% | 100% | 
| A0A3R7NBN0 | Trypanosoma rangeli | 31% | 84% | 
| A0A3S5H7J9 | Leishmania donovani | 30% | 91% | 
| A0A3S5H7S8 | Leishmania donovani | 31% | 100% | 
| A0A3S7WQI8 | Leishmania donovani | 30% | 89% | 
| A0A3S7WY81 | Leishmania donovani | 98% | 100% | 
| A0A3S7X726 | Leishmania donovani | 33% | 91% | 
| A0A422N694 | Trypanosoma rangeli | 30% | 100% | 
| A0A422NDD9 | Trypanosoma rangeli | 31% | 92% | 
| A0A422NDR0 | Trypanosoma rangeli | 26% | 100% | 
| A0A422NHH5 | Trypanosoma rangeli | 70% | 100% | 
| A0A422NZW3 | Trypanosoma rangeli | 30% | 100% | 
| A4FUD9 | Bos taurus | 33% | 99% | 
| A4H5K0 | Leishmania braziliensis | 30% | 87% | 
| A4HDE7 | Leishmania braziliensis | 93% | 100% | 
| A4HGC9 | Leishmania braziliensis | 30% | 82% | 
| A4HGU2 | Leishmania braziliensis | 29% | 100% | 
| A4HKT9 | Leishmania braziliensis | 30% | 100% | 
| A4HNF5 | Leishmania braziliensis | 26% | 87% | 
| A4HTX2 | Leishmania infantum | 30% | 89% | 
| A4I0T0 | Leishmania infantum | 98% | 100% | 
| A4I3G2 | Leishmania infantum | 30% | 82% | 
| A4I3W9 | Leishmania infantum | 30% | 91% | 
| A4I8B8 | Leishmania infantum | 31% | 100% | 
| A4I9B0 | Leishmania infantum | 33% | 91% | 
| B8AEH3 | Oryza sativa subsp. indica | 40% | 100% | 
| B8AZ14 | Oryza sativa subsp. indica | 31% | 100% | 
| B8AZ99 | Oryza sativa subsp. indica | 33% | 100% | 
| B8AZX3 | Oryza sativa subsp. indica | 31% | 97% | 
| B8B406 | Oryza sativa subsp. indica | 29% | 100% | 
| B8BKI8 | Oryza sativa subsp. indica | 32% | 83% | 
| B8BMI1 | Oryza sativa subsp. indica | 31% | 100% | 
| B9FKM7 | Oryza sativa subsp. japonica | 32% | 100% | 
| C9ZYH2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% | 
| D0A4I0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% | 
| D0A759 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 72% | 100% | 
| D0A7X6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 84% | 
| D0A936 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 92% | 
| D0A999 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 96% | 
| D0AAI9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% | 
| D3ZVK1 | Rattus norvegicus | 31% | 97% | 
| E1BPX4 | Bos taurus | 31% | 98% | 
| E9AFW6 | Leishmania major | 27% | 88% | 
| E9AMM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 89% | 
| E9AZQ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 82% | 
| E9B059 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 91% | 
| E9B377 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% | 
| E9B4B0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 92% | 
| E9B719 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 88% | 
| F1M5F3 | Rattus norvegicus | 29% | 71% | 
| F1N2W9 | Bos taurus | 28% | 70% | 
| F1QDI9 | Danio rerio | 29% | 71% | 
| F4IFF3 | Arabidopsis thaliana | 28% | 100% | 
| F4KAB8 | Arabidopsis thaliana | 32% | 96% | 
| F6RIX4 | Xenopus tropicalis | 29% | 72% | 
| I0IUP3 | Gallus gallus | 31% | 97% | 
| I0IUP4 | Gallus gallus | 27% | 69% | 
| O75001 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% | 
| O80786 | Arabidopsis thaliana | 40% | 100% | 
| P24279 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 82% | 
| P25205 | Homo sapiens | 33% | 99% | 
| P25206 | Mus musculus | 33% | 99% | 
| P29458 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 86% | 
| P29469 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 92% | 
| P29496 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 38% | 100% | 
| P30664 | Xenopus laevis | 31% | 93% | 
| P30665 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 86% | 
| P30666 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 91% | 
| P33991 | Homo sapiens | 31% | 93% | 
| P33992 | Homo sapiens | 39% | 100% | 
| P33993 | Homo sapiens | 32% | 100% | 
| P34647 | Caenorhabditis elegans | 30% | 99% | 
| P38132 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 33% | 95% | 
| P40377 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 97% | 
| P41389 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 38% | 100% | 
| P43299 | Arabidopsis thaliana | 32% | 100% | 
| P49717 | Mus musculus | 31% | 93% | 
| P49718 | Mus musculus | 39% | 100% | 
| P49731 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 90% | 
| P49735 | Drosophila melanogaster | 30% | 90% | 
| P49736 | Homo sapiens | 30% | 89% | 
| P49739 | Xenopus laevis | 34% | 99% | 
| P53091 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 79% | 
| P55861 | Xenopus laevis | 31% | 90% | 
| P55862 | Xenopus laevis | 38% | 100% | 
| P97310 | Mus musculus | 30% | 89% | 
| P97311 | Mus musculus | 31% | 98% | 
| Q0DHC4 | Oryza sativa subsp. japonica | 33% | 100% | 
| Q0V8B7 | Bos taurus | 39% | 100% | 
| Q0V9Q6 | Xenopus tropicalis | 31% | 95% | 
| Q0WVF5 | Arabidopsis thaliana | 31% | 95% | 
| Q14566 | Homo sapiens | 30% | 98% | 
| Q21902 | Caenorhabditis elegans | 39% | 100% | 
| Q24849 | Entamoeba histolytica | 30% | 100% | 
| Q26454 | Drosophila melanogaster | 30% | 92% | 
| Q28BS0 | Xenopus tropicalis | 34% | 99% | 
| Q28CM3 | Xenopus tropicalis | 31% | 98% | 
| Q29JI9 | Drosophila pseudoobscura pseudoobscura | 32% | 98% | 
| Q2KHI9 | Mus musculus | 27% | 71% | 
| Q2KIZ8 | Bos taurus | 30% | 98% | 
| Q2QNM1 | Oryza sativa subsp. japonica | 31% | 100% | 
| Q2R482 | Oryza sativa subsp. japonica | 31% | 83% | 
| Q3ZBH9 | Bos taurus | 31% | 100% | 
| Q43704 | Zea mays | 33% | 100% | 
| Q498J7 | Xenopus laevis | 31% | 97% | 
| Q4Q3R6 | Leishmania major | 34% | 91% | 
| Q4Q826 | Leishmania major | 29% | 100% | 
| Q4Q8I2 | Leishmania major | 30% | 83% | 
| Q4QAP2 | Leishmania major | 98% | 100% | 
| Q4QI01 | Leishmania major | 30% | 89% | 
| Q54CP4 | Dictyostelium discoideum | 40% | 100% | 
| Q561P5 | Xenopus tropicalis | 38% | 100% | 
| Q58884 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 25% | 100% | 
| Q5F310 | Xenopus laevis | 29% | 96% | 
| Q5FWY4 | Xenopus laevis | 31% | 98% | 
| Q5JKB0 | Oryza sativa subsp. japonica | 32% | 93% | 
| Q5R8G6 | Pongo abelii | 33% | 99% | 
| Q5XK83 | Xenopus laevis | 31% | 93% | 
| Q5ZMN2 | Gallus gallus | 32% | 99% | 
| Q61881 | Mus musculus | 32% | 100% | 
| Q61J08 | Caenorhabditis briggsae | 29% | 99% | 
| Q69QA6 | Oryza sativa subsp. japonica | 29% | 100% | 
| Q6DIH3 | Xenopus tropicalis | 30% | 91% | 
| Q6F353 | Oryza sativa subsp. japonica | 32% | 97% | 
| Q6GL41 | Xenopus tropicalis | 31% | 93% | 
| Q6KAJ4 | Oryza sativa subsp. japonica | 40% | 100% | 
| Q6NRM6 | Xenopus laevis | 29% | 70% | 
| Q6NX31 | Xenopus tropicalis | 29% | 100% | 
| Q6P1V8 | Xenopus tropicalis | 30% | 97% | 
| Q6PCI7 | Xenopus laevis | 38% | 100% | 
| Q7Q0Q1 | Anopheles gambiae | 30% | 98% | 
| Q7ZXB1 | Xenopus laevis | 30% | 100% | 
| Q7ZXZ0 | Xenopus laevis | 33% | 99% | 
| Q7ZY18 | Xenopus laevis | 30% | 97% | 
| Q86B14 | Dictyostelium discoideum | 31% | 92% | 
| Q91876 | Xenopus laevis | 30% | 100% | 
| Q95XQ8 | Caenorhabditis elegans | 31% | 97% | 
| Q9CWV1 | Mus musculus | 30% | 96% | 
| Q9FL33 | Arabidopsis thaliana | 31% | 100% | 
| Q9LPD9 | Arabidopsis thaliana | 31% | 86% | 
| Q9NXL9 | Homo sapiens | 28% | 70% | 
| Q9SF37 | Arabidopsis thaliana | 30% | 100% | 
| Q9SX03 | Zea mays | 33% | 100% | 
| Q9SX04 | Zea mays | 33% | 100% | 
| Q9U1E0 | Leishmania major | 30% | 100% | 
| Q9UJA3 | Homo sapiens | 31% | 95% | 
| Q9UXG1 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 30% | 100% | 
| Q9V461 | Drosophila melanogaster | 30% | 98% | 
| Q9VF30 | Drosophila melanogaster | 23% | 91% | 
| Q9VGW6 | Drosophila melanogaster | 40% | 100% | 
| Q9XYU0 | Drosophila melanogaster | 31% | 100% | 
| Q9XYU1 | Drosophila melanogaster | 34% | 98% | 
| V5B8T3 | Trypanosoma cruzi | 27% | 100% | 
| V5BGQ5 | Trypanosoma cruzi | 29% | 94% | 
| V5BQA9 | Trypanosoma cruzi | 31% | 100% | 
| V5BSG2 | Trypanosoma cruzi | 33% | 92% | 
| V5C0K6 | Trypanosoma cruzi | 71% | 100% |