| 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: 5 | 
| NetGPI | no | yes: 0, no: 5 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0005886 | plasma membrane | 3 | 2 | 
| GO:0016020 | membrane | 2 | 6 | 
| GO:0110165 | cellular anatomical entity | 1 | 6 | 
Related structures:
AlphaFold database: Q4QHX6
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0006810 | transport | 3 | 2 | 
| GO:0006811 | monoatomic ion transport | 4 | 2 | 
| GO:0006812 | monoatomic cation transport | 5 | 2 | 
| GO:0006813 | potassium ion transport | 7 | 2 | 
| GO:0009987 | cellular process | 1 | 2 | 
| GO:0030001 | metal ion transport | 6 | 2 | 
| GO:0032879 | regulation of localization | 3 | 6 | 
| GO:0034220 | monoatomic ion transmembrane transport | 3 | 2 | 
| GO:0034762 | regulation of transmembrane transport | 4 | 6 | 
| GO:0034765 | regulation of monoatomic ion transmembrane transport | 5 | 6 | 
| GO:0043269 | regulation of monoatomic ion transport | 5 | 6 | 
| GO:0050789 | regulation of biological process | 2 | 6 | 
| GO:0050794 | regulation of cellular process | 3 | 6 | 
| GO:0051049 | regulation of transport | 4 | 6 | 
| GO:0051179 | localization | 1 | 2 | 
| GO:0051234 | establishment of localization | 2 | 2 | 
| GO:0055085 | transmembrane transport | 2 | 2 | 
| GO:0065007 | biological regulation | 1 | 6 | 
| GO:0071805 | potassium ion transmembrane transport | 6 | 2 | 
| GO:0098655 | monoatomic cation transmembrane transport | 4 | 2 | 
| GO:0098657 | import into cell | 4 | 2 | 
| GO:0098659 | inorganic cation import across plasma membrane | 5 | 2 | 
| GO:0098660 | inorganic ion transmembrane transport | 4 | 2 | 
| GO:0098662 | inorganic cation transmembrane transport | 5 | 2 | 
| GO:0098739 | import across plasma membrane | 3 | 2 | 
| GO:0099587 | inorganic ion import across plasma membrane | 4 | 2 | 
| GO:1990573 | potassium ion import across plasma membrane | 6 | 2 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0005215 | transporter activity | 1 | 6 | 
| GO:0005216 | monoatomic ion channel activity | 4 | 6 | 
| GO:0005242 | inward rectifier potassium channel activity | 7 | 6 | 
| GO:0005244 | voltage-gated monoatomic ion channel activity | 4 | 6 | 
| GO:0005249 | voltage-gated potassium channel activity | 6 | 6 | 
| GO:0005261 | monoatomic cation channel activity | 5 | 6 | 
| GO:0005267 | potassium channel activity | 6 | 6 | 
| GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 6 | 
| GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 6 | 
| GO:0015079 | potassium ion transmembrane transporter activity | 6 | 6 | 
| GO:0015267 | channel activity | 4 | 6 | 
| GO:0015276 | ligand-gated monoatomic ion channel activity | 5 | 6 | 
| GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 6 | 
| GO:0022803 | passive transmembrane transporter activity | 3 | 6 | 
| GO:0022832 | voltage-gated channel activity | 6 | 6 | 
| GO:0022834 | ligand-gated channel activity | 6 | 6 | 
| GO:0022836 | gated channel activity | 5 | 6 | 
| GO:0022843 | voltage-gated monoatomic cation channel activity | 5 | 6 | 
| GO:0022857 | transmembrane transporter activity | 2 | 6 | 
| GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 6 | 
| GO:0046873 | metal ion transmembrane transporter activity | 5 | 6 | 
| GO:0099094 | ligand-gated monoatomic cation channel activity | 6 | 6 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 192 | 196 | PF00656 | 0.582 | 
| CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.710 | 
| CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.740 | 
| CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.799 | 
| CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.739 | 
| CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.686 | 
| CLV_PCSK_KEX2_1 | 553 | 555 | PF00082 | 0.730 | 
| CLV_PCSK_KEX2_1 | 686 | 688 | PF00082 | 0.624 | 
| CLV_PCSK_PC1ET2_1 | 360 | 362 | PF00082 | 0.799 | 
| CLV_PCSK_PC1ET2_1 | 433 | 435 | PF00082 | 0.679 | 
| CLV_PCSK_PC1ET2_1 | 553 | 555 | PF00082 | 0.730 | 
| CLV_PCSK_PC1ET2_1 | 686 | 688 | PF00082 | 0.624 | 
| CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.556 | 
| CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.610 | 
| CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.539 | 
| CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.701 | 
| CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.760 | 
| CLV_PCSK_SKI1_1 | 554 | 558 | PF00082 | 0.675 | 
| CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.443 | 
| CLV_PCSK_SKI1_1 | 630 | 634 | PF00082 | 0.575 | 
| CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.491 | 
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.745 | 
| DEG_SPOP_SBC_1 | 382 | 386 | PF00917 | 0.478 | 
| DEG_SPOP_SBC_1 | 486 | 490 | PF00917 | 0.573 | 
| DOC_CYCLIN_yCln2_LP_2 | 373 | 379 | PF00134 | 0.473 | 
| DOC_CYCLIN_yCln2_LP_2 | 613 | 619 | PF00134 | 0.356 | 
| DOC_MAPK_gen_1 | 202 | 210 | PF00069 | 0.603 | 
| DOC_MAPK_gen_1 | 254 | 262 | PF00069 | 0.308 | 
| DOC_MAPK_gen_1 | 605 | 613 | PF00069 | 0.403 | 
| DOC_MAPK_HePTP_8 | 623 | 635 | PF00069 | 0.392 | 
| DOC_MAPK_MEF2A_6 | 581 | 590 | PF00069 | 0.459 | 
| DOC_MAPK_MEF2A_6 | 626 | 635 | PF00069 | 0.394 | 
| DOC_PP1_RVXF_1 | 237 | 243 | PF00149 | 0.386 | 
| DOC_PP1_RVXF_1 | 257 | 263 | PF00149 | 0.245 | 
| DOC_PP2B_LxvP_1 | 29 | 32 | PF13499 | 0.727 | 
| DOC_PP2B_LxvP_1 | 373 | 376 | PF13499 | 0.476 | 
| DOC_PP2B_LxvP_1 | 633 | 636 | PF13499 | 0.417 | 
| DOC_PP4_FxxP_1 | 34 | 37 | PF00568 | 0.733 | 
| DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.599 | 
| DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.557 | 
| DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.516 | 
| DOC_USP7_MATH_1 | 564 | 568 | PF00917 | 0.541 | 
| DOC_USP7_MATH_1 | 709 | 713 | PF00917 | 0.403 | 
| DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.697 | 
| DOC_USP7_UBL2_3 | 360 | 364 | PF12436 | 0.655 | 
| DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.496 | 
| DOC_WW_Pin1_4 | 501 | 506 | PF00397 | 0.528 | 
| DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.721 | 
| DOC_WW_Pin1_4 | 534 | 539 | PF00397 | 0.493 | 
| DOC_WW_Pin1_4 | 624 | 629 | PF00397 | 0.408 | 
| DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.587 | 
| LIG_14-3-3_CanoR_1 | 118 | 123 | PF00244 | 0.613 | 
| LIG_14-3-3_CanoR_1 | 202 | 210 | PF00244 | 0.501 | 
| LIG_14-3-3_CanoR_1 | 239 | 248 | PF00244 | 0.382 | 
| LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.760 | 
| LIG_14-3-3_CanoR_1 | 367 | 376 | PF00244 | 0.519 | 
| LIG_14-3-3_CanoR_1 | 421 | 431 | PF00244 | 0.559 | 
| LIG_14-3-3_CanoR_1 | 434 | 438 | PF00244 | 0.497 | 
| LIG_14-3-3_CanoR_1 | 594 | 602 | PF00244 | 0.439 | 
| LIG_14-3-3_CanoR_1 | 608 | 614 | PF00244 | 0.276 | 
| LIG_14-3-3_CanoR_1 | 81 | 90 | PF00244 | 0.708 | 
| LIG_APCC_ABBA_1 | 629 | 634 | PF00400 | 0.410 | 
| LIG_APCC_ABBA_1 | 705 | 710 | PF00400 | 0.399 | 
| LIG_BRCT_BRCA1_1 | 473 | 477 | PF00533 | 0.526 | 
| LIG_BRCT_BRCA1_1 | 546 | 550 | PF00533 | 0.489 | 
| LIG_BRCT_BRCA1_1 | 79 | 83 | PF00533 | 0.679 | 
| LIG_CtBP_PxDLS_1 | 726 | 730 | PF00389 | 0.436 | 
| LIG_deltaCOP1_diTrp_1 | 256 | 262 | PF00928 | 0.359 | 
| LIG_EH1_1 | 143 | 151 | PF00400 | 0.385 | 
| LIG_eIF4E_1 | 144 | 150 | PF01652 | 0.385 | 
| LIG_FHA_1 | 107 | 113 | PF00498 | 0.562 | 
| LIG_FHA_1 | 132 | 138 | PF00498 | 0.529 | 
| LIG_FHA_1 | 203 | 209 | PF00498 | 0.532 | 
| LIG_FHA_1 | 231 | 237 | PF00498 | 0.431 | 
| LIG_FHA_1 | 93 | 99 | PF00498 | 0.763 | 
| LIG_FHA_2 | 190 | 196 | PF00498 | 0.593 | 
| LIG_FHA_2 | 599 | 605 | PF00498 | 0.445 | 
| LIG_FHA_2 | 673 | 679 | PF00498 | 0.426 | 
| LIG_FHA_2 | 733 | 739 | PF00498 | 0.541 | 
| LIG_KLC1_Yacidic_2 | 600 | 604 | PF13176 | 0.443 | 
| LIG_LIR_Gen_1 | 130 | 141 | PF02991 | 0.532 | 
| LIG_LIR_Gen_1 | 212 | 221 | PF02991 | 0.385 | 
| LIG_LIR_Gen_1 | 243 | 252 | PF02991 | 0.382 | 
| LIG_LIR_Gen_1 | 717 | 726 | PF02991 | 0.390 | 
| LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.656 | 
| LIG_LIR_Nem_3 | 123 | 128 | PF02991 | 0.552 | 
| LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.439 | 
| LIG_LIR_Nem_3 | 138 | 142 | PF02991 | 0.246 | 
| LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.385 | 
| LIG_LIR_Nem_3 | 212 | 216 | PF02991 | 0.385 | 
| LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.370 | 
| LIG_LIR_Nem_3 | 256 | 261 | PF02991 | 0.309 | 
| LIG_LIR_Nem_3 | 315 | 321 | PF02991 | 0.444 | 
| LIG_LIR_Nem_3 | 38 | 43 | PF02991 | 0.655 | 
| LIG_LIR_Nem_3 | 572 | 577 | PF02991 | 0.431 | 
| LIG_LIR_Nem_3 | 717 | 721 | PF02991 | 0.392 | 
| LIG_Pex14_1 | 258 | 262 | PF04695 | 0.374 | 
| LIG_PTB_Apo_2 | 212 | 219 | PF02174 | 0.385 | 
| LIG_SH2_CRK | 139 | 143 | PF00017 | 0.342 | 
| LIG_SH2_CRK | 40 | 44 | PF00017 | 0.675 | 
| LIG_SH2_GRB2like | 213 | 216 | PF00017 | 0.385 | 
| LIG_SH2_GRB2like | 689 | 692 | PF00017 | 0.368 | 
| LIG_SH2_GRB2like | 720 | 723 | PF00017 | 0.378 | 
| LIG_SH2_PTP2 | 213 | 216 | PF00017 | 0.385 | 
| LIG_SH2_SRC | 144 | 147 | PF00017 | 0.385 | 
| LIG_SH2_SRC | 213 | 216 | PF00017 | 0.385 | 
| LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.385 | 
| LIG_SH2_STAT3 | 291 | 294 | PF00017 | 0.409 | 
| LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.588 | 
| LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.275 | 
| LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.407 | 
| LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.506 | 
| LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.316 | 
| LIG_SH2_STAT5 | 602 | 605 | PF00017 | 0.530 | 
| LIG_SH2_STAT5 | 720 | 723 | PF00017 | 0.378 | 
| LIG_SH3_3 | 11 | 17 | PF00018 | 0.707 | 
| LIG_SH3_3 | 29 | 35 | PF00018 | 0.654 | 
| LIG_SH3_3 | 320 | 326 | PF00018 | 0.444 | 
| LIG_SH3_3 | 372 | 378 | PF00018 | 0.548 | 
| LIG_SH3_3 | 50 | 56 | PF00018 | 0.695 | 
| LIG_SH3_3 | 563 | 569 | PF00018 | 0.482 | 
| LIG_SH3_3 | 625 | 631 | PF00018 | 0.411 | 
| LIG_SH3_5 | 99 | 103 | PF00018 | 0.596 | 
| LIG_Sin3_3 | 223 | 230 | PF02671 | 0.455 | 
| LIG_SUMO_SIM_par_1 | 133 | 138 | PF11976 | 0.369 | 
| LIG_SUMO_SIM_par_1 | 146 | 152 | PF11976 | 0.276 | 
| LIG_SUMO_SIM_par_1 | 205 | 212 | PF11976 | 0.385 | 
| LIG_SUMO_SIM_par_1 | 667 | 673 | PF11976 | 0.373 | 
| LIG_TRAF2_1 | 526 | 529 | PF00917 | 0.490 | 
| LIG_TYR_ITIM | 137 | 142 | PF00017 | 0.342 | 
| LIG_TYR_ITSM | 36 | 43 | PF00017 | 0.549 | 
| LIG_WRC_WIRS_1 | 114 | 119 | PF05994 | 0.565 | 
| MOD_CDC14_SPxK_1 | 430 | 433 | PF00782 | 0.580 | 
| MOD_CDC14_SPxK_1 | 627 | 630 | PF00782 | 0.399 | 
| MOD_CDK_SPK_2 | 501 | 506 | PF00069 | 0.659 | 
| MOD_CDK_SPxK_1 | 427 | 433 | PF00069 | 0.614 | 
| MOD_CDK_SPxK_1 | 624 | 630 | PF00069 | 0.424 | 
| MOD_CDK_SPxxK_3 | 427 | 434 | PF00069 | 0.589 | 
| MOD_CDK_SPxxK_3 | 501 | 508 | PF00069 | 0.596 | 
| MOD_CK1_1 | 316 | 322 | PF00069 | 0.640 | 
| MOD_CK1_1 | 381 | 387 | PF00069 | 0.780 | 
| MOD_CK1_1 | 391 | 397 | PF00069 | 0.628 | 
| MOD_CK1_1 | 425 | 431 | PF00069 | 0.754 | 
| MOD_CK1_1 | 436 | 442 | PF00069 | 0.698 | 
| MOD_CK1_1 | 450 | 456 | PF00069 | 0.717 | 
| MOD_CK1_1 | 457 | 463 | PF00069 | 0.683 | 
| MOD_CK1_1 | 466 | 472 | PF00069 | 0.552 | 
| MOD_CK1_1 | 479 | 485 | PF00069 | 0.670 | 
| MOD_CK1_1 | 504 | 510 | PF00069 | 0.603 | 
| MOD_CK1_1 | 523 | 529 | PF00069 | 0.639 | 
| MOD_CK1_1 | 537 | 543 | PF00069 | 0.595 | 
| MOD_CK1_1 | 641 | 647 | PF00069 | 0.594 | 
| MOD_CK1_1 | 681 | 687 | PF00069 | 0.498 | 
| MOD_CK1_1 | 74 | 80 | PF00069 | 0.616 | 
| MOD_CK2_1 | 225 | 231 | PF00069 | 0.418 | 
| MOD_CK2_1 | 382 | 388 | PF00069 | 0.656 | 
| MOD_CK2_1 | 523 | 529 | PF00069 | 0.632 | 
| MOD_CK2_1 | 672 | 678 | PF00069 | 0.481 | 
| MOD_CK2_1 | 730 | 736 | PF00069 | 0.650 | 
| MOD_Cter_Amidation | 492 | 495 | PF01082 | 0.607 | 
| MOD_Cter_Amidation | 551 | 554 | PF01082 | 0.619 | 
| MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.385 | 
| MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.654 | 
| MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.769 | 
| MOD_GlcNHglycan | 388 | 393 | PF01048 | 0.671 | 
| MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.818 | 
| MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.689 | 
| MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.707 | 
| MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.642 | 
| MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.677 | 
| MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.550 | 
| MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.594 | 
| MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.663 | 
| MOD_GlcNHglycan | 643 | 646 | PF01048 | 0.715 | 
| MOD_GlcNHglycan | 652 | 655 | PF01048 | 0.673 | 
| MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.596 | 
| MOD_GSK3_1 | 127 | 134 | PF00069 | 0.443 | 
| MOD_GSK3_1 | 240 | 247 | PF00069 | 0.467 | 
| MOD_GSK3_1 | 35 | 42 | PF00069 | 0.638 | 
| MOD_GSK3_1 | 352 | 359 | PF00069 | 0.585 | 
| MOD_GSK3_1 | 378 | 385 | PF00069 | 0.757 | 
| MOD_GSK3_1 | 404 | 411 | PF00069 | 0.763 | 
| MOD_GSK3_1 | 43 | 50 | PF00069 | 0.614 | 
| MOD_GSK3_1 | 446 | 453 | PF00069 | 0.755 | 
| MOD_GSK3_1 | 454 | 461 | PF00069 | 0.729 | 
| MOD_GSK3_1 | 463 | 470 | PF00069 | 0.630 | 
| MOD_GSK3_1 | 472 | 479 | PF00069 | 0.561 | 
| MOD_GSK3_1 | 52 | 59 | PF00069 | 0.485 | 
| MOD_GSK3_1 | 520 | 527 | PF00069 | 0.711 | 
| MOD_GSK3_1 | 552 | 559 | PF00069 | 0.750 | 
| MOD_GSK3_1 | 650 | 657 | PF00069 | 0.621 | 
| MOD_GSK3_1 | 67 | 74 | PF00069 | 0.627 | 
| MOD_GSK3_1 | 672 | 679 | PF00069 | 0.549 | 
| MOD_GSK3_1 | 681 | 688 | PF00069 | 0.391 | 
| MOD_GSK3_1 | 730 | 737 | PF00069 | 0.652 | 
| MOD_GSK3_1 | 88 | 95 | PF00069 | 0.644 | 
| MOD_LATS_1 | 366 | 372 | PF00433 | 0.660 | 
| MOD_N-GLC_1 | 105 | 110 | PF02516 | 0.414 | 
| MOD_N-GLC_1 | 521 | 526 | PF02516 | 0.639 | 
| MOD_NEK2_1 | 127 | 132 | PF00069 | 0.463 | 
| MOD_NEK2_1 | 149 | 154 | PF00069 | 0.359 | 
| MOD_NEK2_1 | 209 | 214 | PF00069 | 0.463 | 
| MOD_NEK2_1 | 225 | 230 | PF00069 | 0.305 | 
| MOD_NEK2_1 | 24 | 29 | PF00069 | 0.695 | 
| MOD_NEK2_1 | 304 | 309 | PF00069 | 0.597 | 
| MOD_NEK2_1 | 313 | 318 | PF00069 | 0.556 | 
| MOD_NEK2_1 | 369 | 374 | PF00069 | 0.594 | 
| MOD_NEK2_1 | 402 | 407 | PF00069 | 0.717 | 
| MOD_NEK2_1 | 468 | 473 | PF00069 | 0.704 | 
| MOD_NEK2_1 | 478 | 483 | PF00069 | 0.594 | 
| MOD_NEK2_1 | 593 | 598 | PF00069 | 0.498 | 
| MOD_NEK2_2 | 113 | 118 | PF00069 | 0.565 | 
| MOD_PIKK_1 | 127 | 133 | PF00454 | 0.463 | 
| MOD_PIKK_1 | 524 | 530 | PF00454 | 0.544 | 
| MOD_PK_1 | 544 | 550 | PF00069 | 0.542 | 
| MOD_PKA_1 | 433 | 439 | PF00069 | 0.582 | 
| MOD_PKA_2 | 304 | 310 | PF00069 | 0.679 | 
| MOD_PKA_2 | 433 | 439 | PF00069 | 0.592 | 
| MOD_PKA_2 | 593 | 599 | PF00069 | 0.505 | 
| MOD_PKA_2 | 88 | 94 | PF00069 | 0.577 | 
| MOD_PKB_1 | 118 | 126 | PF00069 | 0.528 | 
| MOD_Plk_1 | 194 | 200 | PF00069 | 0.457 | 
| MOD_Plk_1 | 314 | 320 | PF00069 | 0.542 | 
| MOD_Plk_1 | 463 | 469 | PF00069 | 0.649 | 
| MOD_Plk_1 | 521 | 527 | PF00069 | 0.638 | 
| MOD_Plk_2-3 | 189 | 195 | PF00069 | 0.465 | 
| MOD_Plk_4 | 120 | 126 | PF00069 | 0.516 | 
| MOD_Plk_4 | 137 | 143 | PF00069 | 0.227 | 
| MOD_Plk_4 | 209 | 215 | PF00069 | 0.385 | 
| MOD_Plk_4 | 24 | 30 | PF00069 | 0.658 | 
| MOD_Plk_4 | 598 | 604 | PF00069 | 0.538 | 
| MOD_Plk_4 | 609 | 615 | PF00069 | 0.362 | 
| MOD_Plk_4 | 74 | 80 | PF00069 | 0.622 | 
| MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.614 | 
| MOD_ProDKin_1 | 501 | 507 | PF00069 | 0.659 | 
| MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.649 | 
| MOD_ProDKin_1 | 534 | 540 | PF00069 | 0.609 | 
| MOD_ProDKin_1 | 624 | 630 | PF00069 | 0.490 | 
| MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.454 | 
| MOD_SUMO_rev_2 | 19 | 27 | PF00179 | 0.662 | 
| TRG_DiLeu_BaLyEn_6 | 320 | 325 | PF01217 | 0.533 | 
| TRG_DiLeu_BaLyEn_6 | 53 | 58 | PF01217 | 0.609 | 
| TRG_ENDOCYTIC_2 | 139 | 142 | PF00928 | 0.375 | 
| TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.350 | 
| TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.385 | 
| TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.392 | 
| TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.595 | 
| TRG_ER_diArg_1 | 201 | 204 | PF00400 | 0.437 | 
| TRG_ER_diArg_1 | 367 | 369 | PF00400 | 0.593 | 
| TRG_Pf-PMV_PEXEL_1 | 311 | 315 | PF00026 | 0.532 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A3S7WQM3 | Leishmania donovani | 89% | 99% | 
| A4H5M5 | Leishmania braziliensis | 60% | 90% | 
| A4HTW2 | Leishmania infantum | 88% | 99% | 
| E9AMP9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |