Publication identifier(s): 31356625
GPI-anchored cell surface protease. Broad-spectrum ectoenzyme involved in pathogenesis. Heavily expanded family in all parazitic species.. Localization: Cell surface (experimental)
                
                    by homology
Contact email: albert.descoteaux@iaf.inrs.ca
Publication title: The host cell secretory pathway mediates the export of Leishmania virulence factors out of the parasitophorous vacuole
Publication 1st author(s): Amandine Isnard
Publication Identifier(s): 25826301
Host organism: -1
Interaction detection method(s): protease assay
Interaction type: physical association
Identification method participant A: monoclonal antibody western blot
Identification method participant B: monoclonal antibody western blot
ID(s) interactor A: P05627
ID(s) interactor B: P08148
Taxid interactor A: Mus musculus
Taxid interactor B: Leishmania major
Biological role(s) interactor A: enzyme
Biological role(s) interactor B: enzyme target
Experimental role(s) interactor A: neutral component
                
| Source | Evidence on protein | Close homologs | 
|---|---|---|
| Cuervo et al. | no | yes: 0 | 
| Hassani et al. | no | yes: 0 | 
| Forrest at al. (metacyclic) | no | yes: 2 | 
| Forrest at al. (procyclic) | no | yes: 4 | 
| Silverman et al. | no | yes: 0 | 
| Pissara et al. | no | yes: 51 | 
| Source | Evidence on protein | Close homologs | 
|---|---|---|
| Pires et al. | no | yes: 0 | 
| Source | Evidence on protein | Close homologs | 
|---|---|---|
| Silverman et al. | no | yes: 5 | 
| Source | Evidence on protein | Close homologs | 
|---|---|---|
| Jamdhade et al. | no | yes: 0 | 
| Source | Evidence on protein | Close homologs | 
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 41, no: 8 | 
| NetGPI | no | yes: 0, no: 49 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0016020 | membrane | 2 | 50 | 
| GO:0110165 | cellular anatomical entity | 1 | 50 | 
| GO:0005737 | cytoplasm | 2 | 4 | 
| GO:0018995 | host cellular component | 2 | 4 | 
| GO:0033643 | host cell part | 3 | 4 | 
| GO:0033646 | host intracellular part | 4 | 4 | 
| GO:0033647 | host intracellular organelle | 5 | 4 | 
| GO:0033648 | host intracellular membrane-bounded organelle | 6 | 4 | 
| GO:0042025 | host cell nucleus | 7 | 4 | 
Related structures:
AlphaFold database: A4H6E0
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0006508 | proteolysis | 4 | 50 | 
| GO:0006807 | nitrogen compound metabolic process | 2 | 50 | 
| GO:0007155 | cell adhesion | 2 | 50 | 
| GO:0008152 | metabolic process | 1 | 50 | 
| GO:0009987 | cellular process | 1 | 50 | 
| GO:0019538 | protein metabolic process | 3 | 50 | 
| GO:0043170 | macromolecule metabolic process | 3 | 50 | 
| GO:0044238 | primary metabolic process | 2 | 50 | 
| GO:0071704 | organic substance metabolic process | 2 | 50 | 
| GO:1901564 | organonitrogen compound metabolic process | 3 | 50 | 
| GO:0009966 | regulation of signal transduction | 4 | 4 | 
| GO:0010646 | regulation of cell communication | 4 | 4 | 
| GO:0010749 | regulation of nitric oxide mediated signal transduction | 6 | 4 | 
| GO:0023051 | regulation of signaling | 3 | 4 | 
| GO:0035821 | modulation of process of another organism | 2 | 4 | 
| GO:0044003 | modulation by symbiont of host process | 3 | 4 | 
| GO:0044068 | modulation by symbiont of host cellular process | 4 | 4 | 
| GO:0044081 | modulation by symbiont of host nitric oxide-mediated signal transduction | 5 | 4 | 
| GO:0044403 | biological process involved in symbiotic interaction | 2 | 4 | 
| GO:0044419 | biological process involved in interspecies interaction between organisms | 1 | 4 | 
| GO:0044501 | modulation of signal transduction in another organism | 3 | 4 | 
| GO:0048583 | regulation of response to stimulus | 3 | 4 | 
| GO:0050789 | regulation of biological process | 2 | 4 | 
| GO:0050794 | regulation of cellular process | 3 | 4 | 
| GO:0051701 | biological process involved in interaction with host | 3 | 4 | 
| GO:0052027 | modulation by symbiont of host signal transduction pathway | 4 | 4 | 
| GO:0065007 | biological regulation | 1 | 4 | 
| GO:0075130 | modulation by symbiont of host protein kinase-mediated signal transduction | 5 | 4 | 
| GO:1902531 | regulation of intracellular signal transduction | 5 | 4 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 50 | 
| GO:0004175 | endopeptidase activity | 4 | 50 | 
| GO:0004222 | metalloendopeptidase activity | 5 | 50 | 
| GO:0005488 | binding | 1 | 50 | 
| GO:0008233 | peptidase activity | 3 | 50 | 
| GO:0008237 | metallopeptidase activity | 4 | 50 | 
| GO:0016787 | hydrolase activity | 2 | 50 | 
| GO:0043167 | ion binding | 2 | 50 | 
| GO:0043169 | cation binding | 3 | 50 | 
| GO:0046872 | metal ion binding | 4 | 50 | 
| GO:0140096 | catalytic activity, acting on a protein | 2 | 50 | 
| GO:0008047 | enzyme activator activity | 3 | 4 | 
| GO:0008160 | protein tyrosine phosphatase activator activity | 6 | 4 | 
| GO:0019208 | phosphatase regulator activity | 3 | 4 | 
| GO:0019211 | phosphatase activator activity | 4 | 4 | 
| GO:0019888 | protein phosphatase regulator activity | 4 | 4 | 
| GO:0030234 | enzyme regulator activity | 2 | 4 | 
| GO:0072542 | protein phosphatase activator activity | 5 | 4 | 
| GO:0098772 | molecular function regulator activity | 1 | 4 | 
| GO:0140677 | molecular function activator activity | 2 | 4 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 671 | 675 | PF00656 | 0.221 | 
| CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.410 | 
| CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.487 | 
| CLV_NRD_NRD_1 | 536 | 538 | PF00675 | 0.422 | 
| CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.419 | 
| CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.409 | 
| CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.500 | 
| CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.573 | 
| CLV_PCSK_KEX2_1 | 536 | 538 | PF00082 | 0.421 | 
| CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.419 | 
| CLV_PCSK_PC1ET2_1 | 277 | 279 | PF00082 | 0.565 | 
| CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.548 | 
| CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.489 | 
| CLV_PCSK_SKI1_1 | 564 | 568 | PF00082 | 0.407 | 
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.610 | 
| DEG_SCF_FBW7_1 | 659 | 666 | PF00400 | 0.230 | 
| DEG_SCF_FBW7_1 | 96 | 102 | PF00400 | 0.589 | 
| DEG_SPOP_SBC_1 | 218 | 222 | PF00917 | 0.266 | 
| DOC_CKS1_1 | 424 | 429 | PF01111 | 0.203 | 
| DOC_CKS1_1 | 78 | 83 | PF01111 | 0.612 | 
| DOC_CKS1_1 | 96 | 101 | PF01111 | 0.582 | 
| DOC_CYCLIN_yCln2_LP_2 | 72 | 78 | PF00134 | 0.608 | 
| DOC_MAPK_gen_1 | 415 | 423 | PF00069 | 0.337 | 
| DOC_MAPK_gen_1 | 44 | 54 | PF00069 | 0.609 | 
| DOC_MAPK_MEF2A_6 | 44 | 52 | PF00069 | 0.610 | 
| DOC_PP2B_LxvP_1 | 197 | 200 | PF13499 | 0.266 | 
| DOC_PP2B_LxvP_1 | 469 | 472 | PF13499 | 0.381 | 
| DOC_PP2B_LxvP_1 | 52 | 55 | PF13499 | 0.607 | 
| DOC_PP2B_LxvP_1 | 97 | 100 | PF13499 | 0.594 | 
| DOC_PP4_FxxP_1 | 319 | 322 | PF00568 | 0.398 | 
| DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.662 | 
| DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.270 | 
| DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.248 | 
| DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.602 | 
| DOC_USP7_MATH_1 | 599 | 603 | PF00917 | 0.249 | 
| DOC_USP7_MATH_1 | 622 | 626 | PF00917 | 0.291 | 
| DOC_USP7_MATH_1 | 663 | 667 | PF00917 | 0.243 | 
| DOC_USP7_MATH_1 | 670 | 674 | PF00917 | 0.231 | 
| DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.285 | 
| DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.608 | 
| DOC_WW_Pin1_4 | 423 | 428 | PF00397 | 0.253 | 
| DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.600 | 
| DOC_WW_Pin1_4 | 597 | 602 | PF00397 | 0.249 | 
| DOC_WW_Pin1_4 | 618 | 623 | PF00397 | 0.234 | 
| DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.594 | 
| DOC_WW_Pin1_4 | 659 | 664 | PF00397 | 0.398 | 
| DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.607 | 
| DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.591 | 
| LIG_14-3-3_CanoR_1 | 118 | 128 | PF00244 | 0.637 | 
| LIG_14-3-3_CanoR_1 | 132 | 141 | PF00244 | 0.708 | 
| LIG_14-3-3_CanoR_1 | 179 | 185 | PF00244 | 0.377 | 
| LIG_14-3-3_CanoR_1 | 235 | 243 | PF00244 | 0.387 | 
| LIG_14-3-3_CanoR_1 | 574 | 578 | PF00244 | 0.207 | 
| LIG_14-3-3_CanoR_1 | 643 | 649 | PF00244 | 0.363 | 
| LIG_14-3-3_CanoR_1 | 90 | 97 | PF00244 | 0.617 | 
| LIG_APCC_ABBA_1 | 290 | 295 | PF00400 | 0.402 | 
| LIG_APCC_ABBA_1 | 484 | 489 | PF00400 | 0.371 | 
| LIG_APCC_ABBA_1 | 606 | 611 | PF00400 | 0.398 | 
| LIG_BRCT_BRCA1_1 | 509 | 513 | PF00533 | 0.261 | 
| LIG_BRCT_BRCA1_1 | 672 | 676 | PF00533 | 0.398 | 
| LIG_FHA_1 | 111 | 117 | PF00498 | 0.599 | 
| LIG_FHA_1 | 231 | 237 | PF00498 | 0.322 | 
| LIG_FHA_1 | 238 | 244 | PF00498 | 0.324 | 
| LIG_FHA_1 | 281 | 287 | PF00498 | 0.262 | 
| LIG_FHA_1 | 303 | 309 | PF00498 | 0.303 | 
| LIG_FHA_1 | 316 | 322 | PF00498 | 0.299 | 
| LIG_FHA_1 | 370 | 376 | PF00498 | 0.219 | 
| LIG_FHA_1 | 424 | 430 | PF00498 | 0.205 | 
| LIG_FHA_1 | 481 | 487 | PF00498 | 0.389 | 
| LIG_FHA_1 | 547 | 553 | PF00498 | 0.309 | 
| LIG_FHA_1 | 645 | 651 | PF00498 | 0.383 | 
| LIG_FHA_2 | 242 | 248 | PF00498 | 0.233 | 
| LIG_FHA_2 | 307 | 313 | PF00498 | 0.232 | 
| LIG_FHA_2 | 398 | 404 | PF00498 | 0.247 | 
| LIG_FHA_2 | 441 | 447 | PF00498 | 0.217 | 
| LIG_FHA_2 | 496 | 502 | PF00498 | 0.232 | 
| LIG_FHA_2 | 669 | 675 | PF00498 | 0.246 | 
| LIG_GBD_Chelix_1 | 391 | 399 | PF00786 | 0.426 | 
| LIG_LIR_Apic_2 | 283 | 287 | PF02991 | 0.226 | 
| LIG_LIR_Apic_2 | 318 | 322 | PF02991 | 0.384 | 
| LIG_LIR_Apic_2 | 416 | 422 | PF02991 | 0.284 | 
| LIG_LIR_Apic_2 | 535 | 541 | PF02991 | 0.230 | 
| LIG_LIR_Apic_2 | 554 | 558 | PF02991 | 0.199 | 
| LIG_LIR_Gen_1 | 327 | 338 | PF02991 | 0.211 | 
| LIG_LIR_Gen_1 | 377 | 387 | PF02991 | 0.350 | 
| LIG_LIR_Gen_1 | 400 | 408 | PF02991 | 0.256 | 
| LIG_LIR_Gen_1 | 441 | 449 | PF02991 | 0.397 | 
| LIG_LIR_Gen_1 | 49 | 59 | PF02991 | 0.605 | 
| LIG_LIR_Gen_1 | 605 | 612 | PF02991 | 0.271 | 
| LIG_LIR_Nem_3 | 228 | 234 | PF02991 | 0.292 | 
| LIG_LIR_Nem_3 | 247 | 252 | PF02991 | 0.210 | 
| LIG_LIR_Nem_3 | 327 | 333 | PF02991 | 0.340 | 
| LIG_LIR_Nem_3 | 334 | 338 | PF02991 | 0.370 | 
| LIG_LIR_Nem_3 | 377 | 382 | PF02991 | 0.350 | 
| LIG_LIR_Nem_3 | 400 | 405 | PF02991 | 0.254 | 
| LIG_LIR_Nem_3 | 441 | 447 | PF02991 | 0.360 | 
| LIG_LIR_Nem_3 | 489 | 493 | PF02991 | 0.219 | 
| LIG_LIR_Nem_3 | 49 | 54 | PF02991 | 0.608 | 
| LIG_LIR_Nem_3 | 561 | 566 | PF02991 | 0.317 | 
| LIG_LIR_Nem_3 | 575 | 580 | PF02991 | 0.286 | 
| LIG_LIR_Nem_3 | 605 | 609 | PF02991 | 0.279 | 
| LIG_MYND_1 | 101 | 105 | PF01753 | 0.575 | 
| LIG_Pex14_1 | 526 | 530 | PF04695 | 0.387 | 
| LIG_PTB_Apo_2 | 329 | 336 | PF02174 | 0.387 | 
| LIG_SH2_CRK | 379 | 383 | PF00017 | 0.347 | 
| LIG_SH2_CRK | 479 | 483 | PF00017 | 0.402 | 
| LIG_SH2_CRK | 538 | 542 | PF00017 | 0.235 | 
| LIG_SH2_CRK | 555 | 559 | PF00017 | 0.232 | 
| LIG_SH2_CRK | 580 | 584 | PF00017 | 0.275 | 
| LIG_SH2_CRK | 632 | 636 | PF00017 | 0.359 | 
| LIG_SH2_GRB2like | 479 | 482 | PF00017 | 0.209 | 
| LIG_SH2_GRB2like | 555 | 558 | PF00017 | 0.202 | 
| LIG_SH2_PTP2 | 687 | 690 | PF00017 | 0.394 | 
| LIG_SH2_SRC | 555 | 558 | PF00017 | 0.217 | 
| LIG_SH2_SRC | 687 | 690 | PF00017 | 0.394 | 
| LIG_SH2_STAP1 | 379 | 383 | PF00017 | 0.354 | 
| LIG_SH2_STAP1 | 648 | 652 | PF00017 | 0.398 | 
| LIG_SH2_STAT3 | 252 | 255 | PF00017 | 0.259 | 
| LIG_SH2_STAT3 | 648 | 651 | PF00017 | 0.383 | 
| LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.375 | 
| LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.242 | 
| LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.269 | 
| LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.379 | 
| LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.213 | 
| LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.324 | 
| LIG_SH2_STAT5 | 507 | 510 | PF00017 | 0.200 | 
| LIG_SH2_STAT5 | 562 | 565 | PF00017 | 0.382 | 
| LIG_SH2_STAT5 | 580 | 583 | PF00017 | 0.215 | 
| LIG_SH2_STAT5 | 658 | 661 | PF00017 | 0.329 | 
| LIG_SH2_STAT5 | 681 | 684 | PF00017 | 0.394 | 
| LIG_SH2_STAT5 | 687 | 690 | PF00017 | 0.329 | 
| LIG_SH3_1 | 53 | 59 | PF00018 | 0.603 | 
| LIG_SH3_2 | 39 | 44 | PF14604 | 0.597 | 
| LIG_SH3_3 | 109 | 115 | PF00018 | 0.601 | 
| LIG_SH3_3 | 340 | 346 | PF00018 | 0.253 | 
| LIG_SH3_3 | 36 | 42 | PF00018 | 0.604 | 
| LIG_SH3_3 | 365 | 371 | PF00018 | 0.203 | 
| LIG_SH3_3 | 52 | 58 | PF00018 | 0.607 | 
| LIG_SH3_3 | 625 | 631 | PF00018 | 0.235 | 
| LIG_SH3_3 | 73 | 79 | PF00018 | 0.610 | 
| LIG_SH3_3 | 98 | 104 | PF00018 | 0.582 | 
| LIG_SUMO_SIM_anti_2 | 403 | 410 | PF11976 | 0.226 | 
| LIG_SUMO_SIM_par_1 | 581 | 589 | PF11976 | 0.196 | 
| LIG_SUMO_SIM_par_1 | 74 | 80 | PF11976 | 0.609 | 
| LIG_TRFH_1 | 95 | 99 | PF08558 | 0.494 | 
| LIG_TYR_ITIM | 578 | 583 | PF00017 | 0.204 | 
| LIG_WW_2 | 39 | 42 | PF00397 | 0.476 | 
| MOD_CDK_SPK_2 | 618 | 623 | PF00069 | 0.256 | 
| MOD_CDK_SPxxK_3 | 597 | 604 | PF00069 | 0.217 | 
| MOD_CK1_1 | 209 | 215 | PF00069 | 0.317 | 
| MOD_CK1_1 | 26 | 32 | PF00069 | 0.510 | 
| MOD_CK1_1 | 341 | 347 | PF00069 | 0.479 | 
| MOD_CK1_1 | 551 | 557 | PF00069 | 0.270 | 
| MOD_CK1_1 | 597 | 603 | PF00069 | 0.348 | 
| MOD_CK1_1 | 610 | 616 | PF00069 | 0.248 | 
| MOD_CK1_1 | 68 | 74 | PF00069 | 0.509 | 
| MOD_CK1_1 | 77 | 83 | PF00069 | 0.502 | 
| MOD_CK2_1 | 306 | 312 | PF00069 | 0.249 | 
| MOD_CK2_1 | 440 | 446 | PF00069 | 0.247 | 
| MOD_CK2_1 | 495 | 501 | PF00069 | 0.492 | 
| MOD_CK2_1 | 599 | 605 | PF00069 | 0.258 | 
| MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.460 | 
| MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.343 | 
| MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.259 | 
| MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.298 | 
| MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.249 | 
| MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.409 | 
| MOD_GlcNHglycan | 655 | 658 | PF01048 | 0.418 | 
| MOD_GSK3_1 | 118 | 125 | PF00069 | 0.516 | 
| MOD_GSK3_1 | 126 | 133 | PF00069 | 0.529 | 
| MOD_GSK3_1 | 205 | 212 | PF00069 | 0.271 | 
| MOD_GSK3_1 | 217 | 224 | PF00069 | 0.256 | 
| MOD_GSK3_1 | 237 | 244 | PF00069 | 0.322 | 
| MOD_GSK3_1 | 302 | 309 | PF00069 | 0.334 | 
| MOD_GSK3_1 | 324 | 331 | PF00069 | 0.482 | 
| MOD_GSK3_1 | 54 | 61 | PF00069 | 0.490 | 
| MOD_GSK3_1 | 595 | 602 | PF00069 | 0.274 | 
| MOD_GSK3_1 | 618 | 625 | PF00069 | 0.256 | 
| MOD_GSK3_1 | 659 | 666 | PF00069 | 0.248 | 
| MOD_GSK3_1 | 85 | 92 | PF00069 | 0.507 | 
| MOD_GSK3_1 | 95 | 102 | PF00069 | 0.476 | 
| MOD_N-GLC_1 | 480 | 485 | PF02516 | 0.222 | 
| MOD_N-GLC_1 | 521 | 526 | PF02516 | 0.391 | 
| MOD_N-GLC_1 | 531 | 536 | PF02516 | 0.243 | 
| MOD_NEK2_1 | 116 | 121 | PF00069 | 0.515 | 
| MOD_NEK2_1 | 217 | 222 | PF00069 | 0.252 | 
| MOD_NEK2_1 | 383 | 388 | PF00069 | 0.365 | 
| MOD_NEK2_1 | 397 | 402 | PF00069 | 0.395 | 
| MOD_NEK2_1 | 447 | 452 | PF00069 | 0.249 | 
| MOD_NEK2_1 | 455 | 460 | PF00069 | 0.223 | 
| MOD_NEK2_1 | 566 | 571 | PF00069 | 0.299 | 
| MOD_PIKK_1 | 23 | 29 | PF00454 | 0.516 | 
| MOD_PIKK_1 | 521 | 527 | PF00454 | 0.369 | 
| MOD_PIKK_1 | 89 | 95 | PF00454 | 0.509 | 
| MOD_PK_1 | 137 | 143 | PF00069 | 0.629 | 
| MOD_PKA_1 | 137 | 143 | PF00069 | 0.561 | 
| MOD_PKA_2 | 119 | 125 | PF00069 | 0.546 | 
| MOD_PKA_2 | 131 | 137 | PF00069 | 0.587 | 
| MOD_PKA_2 | 34 | 40 | PF00069 | 0.505 | 
| MOD_PKA_2 | 46 | 52 | PF00069 | 0.503 | 
| MOD_PKA_2 | 573 | 579 | PF00069 | 0.222 | 
| MOD_PKA_2 | 89 | 95 | PF00069 | 0.515 | 
| MOD_PKB_1 | 130 | 138 | PF00069 | 0.567 | 
| MOD_PKB_1 | 537 | 545 | PF00069 | 0.256 | 
| MOD_Plk_1 | 397 | 403 | PF00069 | 0.247 | 
| MOD_Plk_1 | 480 | 486 | PF00069 | 0.235 | 
| MOD_Plk_1 | 521 | 527 | PF00069 | 0.368 | 
| MOD_Plk_4 | 248 | 254 | PF00069 | 0.273 | 
| MOD_Plk_4 | 280 | 286 | PF00069 | 0.299 | 
| MOD_Plk_4 | 425 | 431 | PF00069 | 0.311 | 
| MOD_Plk_4 | 440 | 446 | PF00069 | 0.220 | 
| MOD_Plk_4 | 46 | 52 | PF00069 | 0.503 | 
| MOD_Plk_4 | 558 | 564 | PF00069 | 0.320 | 
| MOD_Plk_4 | 573 | 579 | PF00069 | 0.217 | 
| MOD_Plk_4 | 677 | 683 | PF00069 | 0.322 | 
| MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.328 | 
| MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.500 | 
| MOD_ProDKin_1 | 423 | 429 | PF00069 | 0.284 | 
| MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.491 | 
| MOD_ProDKin_1 | 597 | 603 | PF00069 | 0.278 | 
| MOD_ProDKin_1 | 618 | 624 | PF00069 | 0.257 | 
| MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.485 | 
| MOD_ProDKin_1 | 659 | 665 | PF00069 | 0.487 | 
| MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.500 | 
| MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.471 | 
| MOD_SUMO_for_1 | 465 | 468 | PF00179 | 0.334 | 
| TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.431 | 
| TRG_ENDOCYTIC_2 | 479 | 482 | PF00928 | 0.492 | 
| TRG_ENDOCYTIC_2 | 580 | 583 | PF00928 | 0.374 | 
| TRG_ENDOCYTIC_2 | 632 | 635 | PF00928 | 0.462 | 
| TRG_ENDOCYTIC_2 | 687 | 690 | PF00928 | 0.481 | 
| TRG_ER_diArg_1 | 12 | 14 | PF00400 | 0.507 | 
| TRG_ER_diArg_1 | 137 | 139 | PF00400 | 0.628 | 
| TRG_ER_diArg_1 | 536 | 538 | PF00400 | 0.258 | 
| TRG_ER_diArg_1 | 89 | 91 | PF00400 | 0.511 | 
| TRG_NES_CRM1_1 | 398 | 410 | PF08389 | 0.262 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N1IL11 | Leptomonas seymouri | 34% | 100% | 
| A0A0S4IN60 | Bodo saltans | 31% | 79% | 
| A0A0S4ISF2 | Bodo saltans | 31% | 68% | 
| A0A0S4IYM3 | Bodo saltans | 32% | 98% | 
| A0A1X0NDG7 | Trypanosomatidae | 30% | 100% | 
| A0A1X0NDJ3 | Trypanosomatidae | 27% | 98% | 
| A0A1X0NDK7 | Trypanosomatidae | 30% | 100% | 
| A0A1X0NDM7 | Trypanosomatidae | 30% | 100% | 
| A0A1X0NET7 | Trypanosomatidae | 33% | 100% | 
| A0A1X0NEZ6 | Trypanosomatidae | 30% | 100% | 
| A0A1X0NF41 | Trypanosomatidae | 31% | 100% | 
| A0A1X0NFJ0 | Trypanosomatidae | 30% | 100% | 
| A0A1X0NFK3 | Trypanosomatidae | 30% | 100% | 
| A0A1X0NFL1 | Trypanosomatidae | 29% | 75% | 
| A0A1X0NFS0 | Trypanosomatidae | 30% | 82% | 
| A0A1X0NG20 | Trypanosomatidae | 30% | 100% | 
| A0A1X0NGP3 | Trypanosomatidae | 30% | 83% | 
| A0A1X0NGY3 | Trypanosomatidae | 29% | 93% | 
| A0A1X0NGZ3 | Trypanosomatidae | 33% | 100% | 
| A0A1X0NI38 | Trypanosomatidae | 29% | 81% | 
| A0A1X0NI74 | Trypanosomatidae | 32% | 95% | 
| A0A1X0NII4 | Trypanosomatidae | 28% | 84% | 
| A0A1X0NIZ3 | Trypanosomatidae | 33% | 100% | 
| A0A1X0NJS3 | Trypanosomatidae | 30% | 100% | 
| A0A1X0NK29 | Trypanosomatidae | 29% | 77% | 
| A0A1X0NK66 | Trypanosomatidae | 33% | 100% | 
| A0A1X0NKW9 | Trypanosomatidae | 28% | 100% | 
| A0A1X0NME2 | Trypanosomatidae | 31% | 100% | 
| A0A1X0NMK3 | Trypanosomatidae | 28% | 100% | 
| A0A1X0NN43 | Trypanosomatidae | 29% | 99% | 
| A0A1X0NQW6 | Trypanosomatidae | 35% | 100% | 
| A0A1X0NVE0 | Trypanosomatidae | 29% | 91% | 
| A0A1X0NW07 | Trypanosomatidae | 29% | 100% | 
| A0A1X0NX94 | Trypanosomatidae | 30% | 100% | 
| A0A1X0NX98 | Trypanosomatidae | 30% | 89% | 
| A0A1X0NXH6 | Trypanosomatidae | 32% | 97% | 
| A0A1X0NXQ4 | Trypanosomatidae | 30% | 100% | 
| A0A1X0NXR7 | Trypanosomatidae | 34% | 95% | 
| A0A1X0NYE7 | Trypanosomatidae | 32% | 100% | 
| A0A1X0NYN2 | Trypanosomatidae | 34% | 100% | 
| A0A1X0NYS5 | Trypanosomatidae | 33% | 100% | 
| A0A1X0NZ63 | Trypanosomatidae | 31% | 100% | 
| A0A1X0NZN6 | Trypanosomatidae | 28% | 100% | 
| A0A1X0P055 | Trypanosomatidae | 34% | 100% | 
| A0A1X0P154 | Trypanosomatidae | 29% | 100% | 
| A0A1X0P331 | Trypanosomatidae | 33% | 100% | 
| A0A1X0P3K0 | Trypanosomatidae | 29% | 98% | 
| A0A1X0P544 | Trypanosomatidae | 30% | 100% | 
| A0A1X0P5J0 | Trypanosomatidae | 32% | 100% | 
| A0A1X0P7K5 | Trypanosomatidae | 32% | 80% | 
| A0A1X0PB04 | Trypanosomatidae | 32% | 100% | 
| A0A3Q8I8N3 | Leishmania donovani | 57% | 100% | 
| A0A3Q8I8P8 | Leishmania donovani | 57% | 100% | 
| A0A3Q8I8S6 | Leishmania donovani | 60% | 100% | 
| A0A3Q8I8S9 | Leishmania donovani | 57% | 100% | 
| A0A3Q8IAZ8 | Leishmania donovani | 57% | 100% | 
| A0A3Q8IC35 | Leishmania donovani | 57% | 100% | 
| A0A3Q8IC44 | Leishmania donovani | 57% | 100% | 
| A0A3Q8IH61 | Leishmania donovani | 56% | 100% | 
| A0A3Q8IIN4 | Leishmania donovani | 36% | 100% | 
| A0A3R7JTB6 | Trypanosoma rangeli | 31% | 100% | 
| A0A3R7K7T9 | Trypanosoma rangeli | 36% | 100% | 
| A0A3R7KB14 | Trypanosoma rangeli | 34% | 81% | 
| A0A3R7KLR6 | Trypanosoma rangeli | 31% | 100% | 
| A0A3R7LFZ4 | Trypanosoma rangeli | 38% | 100% | 
| A0A3R7LWG1 | Trypanosoma rangeli | 33% | 100% | 
| A0A3R7M574 | Trypanosoma rangeli | 33% | 100% | 
| A0A3R7MW36 | Trypanosoma rangeli | 31% | 100% | 
| A0A3R7N1W7 | Trypanosoma rangeli | 34% | 100% | 
| A0A3R7N289 | Trypanosoma rangeli | 33% | 98% | 
| A0A3R7R2J4 | Trypanosoma rangeli | 31% | 100% | 
| A0A3R7R5R1 | Trypanosoma rangeli | 36% | 100% | 
| A0A3R7R818 | Trypanosoma rangeli | 32% | 100% | 
| A0A3S5H6G0 | Leishmania donovani | 57% | 100% | 
| A0A3S5IQY2 | Trypanosoma rangeli | 36% | 100% | 
| A0A3S7WR43 | Leishmania donovani | 57% | 100% | 
| A0A3S7WR46 | Leishmania donovani | 57% | 100% | 
| A0A3S7WR60 | Leishmania donovani | 57% | 100% | 
| A0A3S7X192 | Leishmania donovani | 37% | 100% | 
| A0A422MVF5 | Trypanosoma rangeli | 33% | 100% | 
| A0A422MVS3 | Trypanosoma rangeli | 35% | 100% | 
| A0A422MW99 | Trypanosoma rangeli | 33% | 96% | 
| A0A422N361 | Trypanosoma rangeli | 33% | 100% | 
| A0A422NDS2 | Trypanosoma rangeli | 34% | 100% | 
| A0A422NDT3 | Trypanosoma rangeli | 31% | 100% | 
| A4H626 | Leishmania braziliensis | 81% | 99% | 
| A4H627 | Leishmania braziliensis | 79% | 100% | 
| A4H630 | Leishmania braziliensis | 73% | 100% | 
| A4H631 | Leishmania braziliensis | 79% | 98% | 
| A4H632 | Leishmania braziliensis | 70% | 100% | 
| A4H633 | Leishmania braziliensis | 79% | 99% | 
| A4H634 | Leishmania braziliensis | 75% | 100% | 
| A4H635 | Leishmania braziliensis | 74% | 100% | 
| A4H637 | Leishmania braziliensis | 75% | 100% | 
| A4H638 | Leishmania braziliensis | 64% | 100% | 
| A4H639 | Leishmania braziliensis | 69% | 100% | 
| A4H640 | Leishmania braziliensis | 74% | 100% | 
| A4H6D1 | Leishmania braziliensis | 82% | 100% | 
| A4H6D3 | Leishmania braziliensis | 83% | 100% | 
| A4H6D5 | Leishmania braziliensis | 87% | 99% | 
| A4H6D7 | Leishmania braziliensis | 77% | 100% | 
| A4H6D8 | Leishmania braziliensis | 93% | 100% | 
| A4H6D9 | Leishmania braziliensis | 92% | 100% | 
| A4H6E1 | Leishmania braziliensis | 81% | 100% | 
| A4H6E2 | Leishmania braziliensis | 82% | 100% | 
| A4H6E3 | Leishmania braziliensis | 83% | 100% | 
| A4H6E5 | Leishmania braziliensis | 66% | 100% | 
| A4HJI2 | Leishmania braziliensis | 36% | 100% | 
| A4HUF6 | Leishmania infantum | 57% | 100% | 
| A4HUF8 | Leishmania infantum | 57% | 100% | 
| A4HUF9 | Leishmania infantum | 60% | 100% | 
| A4HUG0 | Leishmania infantum | 57% | 93% | 
| A4I6X5 | Leishmania infantum | 37% | 100% | 
| C9ZUT5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% | 
| E9AHH5 | Leishmania infantum | 37% | 100% | 
| E9AN53 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 100% | 
| E9AN54 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 100% | 
| E9AN55 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 100% | 
| E9AN56 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 100% | 
| E9AN57 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 58% | 100% | 
| E9AZL8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% | 
| E9B1Z9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% | 
| P08148 | Leishmania major | 58% | 100% | 
| P15706 | Leishmania chagasi | 57% | 100% | 
| P23223 | Leishmania donovani | 56% | 100% | 
| P43150 | Leishmania mexicana | 60% | 100% | 
| Q00689 | Leishmania guyanensis | 73% | 100% | 
| Q06031 | Crithidia fasciculata | 51% | 100% | 
| Q27673 | Leishmania amazonensis | 56% | 100% | 
| Q29AK2 | Drosophila pseudoobscura pseudoobscura | 23% | 100% | 
| Q4Q662 | Leishmania major | 36% | 100% | 
| Q4Q8L3 | Leishmania major | 39% | 100% | 
| Q4QHG9 | Leishmania major | 59% | 100% | 
| Q4QHH0 | Leishmania major | 60% | 100% | 
| Q4QHH1 | Leishmania major | 59% | 100% | 
| Q4QHH2 | Leishmania major | 59% | 100% | 
| Q61YG1 | Caenorhabditis briggsae | 23% | 100% | 
| Q6LA77 | Leishmania infantum | 57% | 100% | 
| Q8MNZ1 | Leishmania tropica | 61% | 100% | 
| Q9VH19 | Drosophila melanogaster | 23% | 100% | 
| V5A359 | Trypanosoma cruzi | 37% | 100% | 
| V5A488 | Trypanosoma cruzi | 33% | 88% | 
| V5AII7 | Trypanosoma cruzi | 37% | 100% | 
| V5APQ4 | Trypanosoma cruzi | 33% | 90% | 
| V5AX72 | Trypanosoma cruzi | 35% | 96% | 
| V5B5M0 | Trypanosoma cruzi | 35% | 96% | 
| V5BAN1 | Trypanosoma cruzi | 33% | 90% | 
| V5BLT3 | Trypanosoma cruzi | 33% | 100% | 
| V5CI97 | Trypanosoma cruzi | 32% | 100% | 
| V5D358 | Trypanosoma cruzi | 35% | 84% |