Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 1 |
Forrest at al. (metacyclic) | no | yes: 3 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 36 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 94 |
NetGPI | no | yes: 0, no: 95 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
GO:0005737 | cytoplasm | 2 | 3 |
GO:0005930 | axoneme | 2 | 1 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0005856 | cytoskeleton | 5 | 1 |
GO:0020016 | ciliary pocket | 2 | 1 |
GO:0020038 | subpellicular network | 2 | 1 |
GO:0030863 | cortical cytoskeleton | 6 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4HJ24
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 96 |
GO:0006807 | nitrogen compound metabolic process | 2 | 96 |
GO:0008152 | metabolic process | 1 | 96 |
GO:0019538 | protein metabolic process | 3 | 96 |
GO:0043170 | macromolecule metabolic process | 3 | 96 |
GO:0044238 | primary metabolic process | 2 | 96 |
GO:0071704 | organic substance metabolic process | 2 | 96 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 96 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 96 |
GO:0004175 | endopeptidase activity | 4 | 96 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 96 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 96 |
GO:0008233 | peptidase activity | 3 | 96 |
GO:0008234 | cysteine-type peptidase activity | 4 | 96 |
GO:0016787 | hydrolase activity | 2 | 96 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 96 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 494 | 498 | PF00656 | 0.506 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.284 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 478 | 480 | PF00675 | 0.273 |
CLV_NRD_NRD_1 | 551 | 553 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.229 |
CLV_PCSK_FUR_1 | 2 | 6 | PF00082 | 0.411 |
CLV_PCSK_FUR_1 | 273 | 277 | PF00082 | 0.137 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.239 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 538 | 540 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 551 | 553 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.220 |
CLV_PCSK_KEX2_1 | 687 | 689 | PF00082 | 0.538 |
CLV_PCSK_PC1ET2_1 | 21 | 23 | PF00082 | 0.557 |
CLV_PCSK_PC1ET2_1 | 275 | 277 | PF00082 | 0.248 |
CLV_PCSK_PC1ET2_1 | 538 | 540 | PF00082 | 0.269 |
CLV_PCSK_PC1ET2_1 | 58 | 60 | PF00082 | 0.220 |
CLV_PCSK_PC1ET2_1 | 687 | 689 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.255 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.212 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 473 | 477 | PF00082 | 0.141 |
CLV_PCSK_SKI1_1 | 541 | 545 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 564 | 568 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 634 | 638 | PF00082 | 0.433 |
DEG_APCC_DBOX_1 | 443 | 451 | PF00400 | 0.520 |
DEG_MDM2_SWIB_1 | 491 | 499 | PF02201 | 0.441 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.408 |
DEG_SCF_FBW7_1 | 640 | 646 | PF00400 | 0.512 |
DOC_CKS1_1 | 395 | 400 | PF01111 | 0.452 |
DOC_CKS1_1 | 640 | 645 | PF01111 | 0.387 |
DOC_CYCLIN_RxL_1 | 561 | 571 | PF00134 | 0.468 |
DOC_MAPK_DCC_7 | 177 | 186 | PF00069 | 0.539 |
DOC_MAPK_DCC_7 | 438 | 447 | PF00069 | 0.571 |
DOC_MAPK_gen_1 | 385 | 395 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 537 | 544 | PF00069 | 0.392 |
DOC_MAPK_gen_1 | 693 | 700 | PF00069 | 0.534 |
DOC_MAPK_HePTP_8 | 435 | 447 | PF00069 | 0.478 |
DOC_MAPK_MEF2A_6 | 177 | 186 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 438 | 447 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 604 | 612 | PF00069 | 0.456 |
DOC_MAPK_RevD_3 | 524 | 538 | PF00069 | 0.481 |
DOC_PP1_RVXF_1 | 539 | 545 | PF00149 | 0.400 |
DOC_PP1_RVXF_1 | 650 | 656 | PF00149 | 0.373 |
DOC_PP2B_PxIxI_1 | 622 | 628 | PF00149 | 0.352 |
DOC_PP4_FxxP_1 | 267 | 270 | PF00568 | 0.457 |
DOC_PP4_FxxP_1 | 3 | 6 | PF00568 | 0.408 |
DOC_PP4_FxxP_1 | 440 | 443 | PF00568 | 0.495 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 643 | 647 | PF00917 | 0.534 |
DOC_USP7_UBL2_3 | 118 | 122 | PF12436 | 0.472 |
DOC_USP7_UBL2_3 | 260 | 264 | PF12436 | 0.564 |
DOC_USP7_UBL2_3 | 330 | 334 | PF12436 | 0.453 |
DOC_USP7_UBL2_3 | 466 | 470 | PF12436 | 0.484 |
DOC_USP7_UBL2_3 | 537 | 541 | PF12436 | 0.460 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 552 | 557 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 614 | 619 | PF00397 | 0.314 |
DOC_WW_Pin1_4 | 639 | 644 | PF00397 | 0.331 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.422 |
LIG_14-3-3_CanoR_1 | 478 | 486 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 652 | 656 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 666 | 672 | PF00244 | 0.446 |
LIG_APCC_ABBAyCdc20_2 | 60 | 66 | PF00400 | 0.347 |
LIG_BRCT_BRCA1_1 | 376 | 380 | PF00533 | 0.509 |
LIG_deltaCOP1_diTrp_1 | 458 | 464 | PF00928 | 0.442 |
LIG_deltaCOP1_diTrp_1 | 494 | 502 | PF00928 | 0.464 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.324 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.441 |
LIG_FHA_1 | 577 | 583 | PF00498 | 0.412 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.391 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.452 |
LIG_FHA_2 | 454 | 460 | PF00498 | 0.411 |
LIG_FHA_2 | 697 | 703 | PF00498 | 0.481 |
LIG_LIR_Apic_2 | 209 | 215 | PF02991 | 0.441 |
LIG_LIR_Apic_2 | 265 | 270 | PF02991 | 0.457 |
LIG_LIR_Apic_2 | 617 | 623 | PF02991 | 0.297 |
LIG_LIR_Apic_2 | 708 | 713 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 113 | 120 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 322 | 332 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 338 | 347 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 431 | 440 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 596 | 606 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 654 | 663 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 113 | 119 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 306 | 310 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 322 | 327 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 329 | 335 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 338 | 342 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 355 | 360 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 377 | 383 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 41 | 46 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 431 | 435 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 513 | 517 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 522 | 526 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 560 | 566 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 596 | 601 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 654 | 658 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 664 | 668 | PF02991 | 0.433 |
LIG_MLH1_MIPbox_1 | 376 | 380 | PF16413 | 0.514 |
LIG_PCNA_yPIPBox_3 | 291 | 304 | PF02747 | 0.406 |
LIG_PDZ_Class_2 | 709 | 714 | PF00595 | 0.601 |
LIG_Pex14_2 | 362 | 366 | PF04695 | 0.442 |
LIG_Pex14_2 | 491 | 495 | PF04695 | 0.450 |
LIG_Pex14_2 | 515 | 519 | PF04695 | 0.389 |
LIG_REV1ctd_RIR_1 | 377 | 385 | PF16727 | 0.467 |
LIG_SH2_CRK | 307 | 311 | PF00017 | 0.566 |
LIG_SH2_CRK | 33 | 37 | PF00017 | 0.325 |
LIG_SH2_CRK | 332 | 336 | PF00017 | 0.450 |
LIG_SH2_CRK | 339 | 343 | PF00017 | 0.451 |
LIG_SH2_CRK | 432 | 436 | PF00017 | 0.467 |
LIG_SH2_CRK | 517 | 521 | PF00017 | 0.337 |
LIG_SH2_CRK | 563 | 567 | PF00017 | 0.390 |
LIG_SH2_GRB2like | 288 | 291 | PF00017 | 0.491 |
LIG_SH2_PTP2 | 620 | 623 | PF00017 | 0.395 |
LIG_SH2_SRC | 218 | 221 | PF00017 | 0.476 |
LIG_SH2_SRC | 391 | 394 | PF00017 | 0.441 |
LIG_SH2_SRC | 598 | 601 | PF00017 | 0.479 |
LIG_SH2_SRC | 620 | 623 | PF00017 | 0.371 |
LIG_SH2_STAP1 | 321 | 325 | PF00017 | 0.491 |
LIG_SH2_STAP1 | 339 | 343 | PF00017 | 0.450 |
LIG_SH2_STAP1 | 598 | 602 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 600 | 603 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 620 | 623 | PF00017 | 0.334 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.297 |
LIG_SH3_3 | 553 | 559 | PF00018 | 0.537 |
LIG_SH3_3 | 589 | 595 | PF00018 | 0.451 |
LIG_SH3_3 | 653 | 659 | PF00018 | 0.397 |
LIG_SUMO_SIM_anti_2 | 252 | 259 | PF11976 | 0.469 |
LIG_SUMO_SIM_par_1 | 391 | 397 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 581 | 588 | PF11976 | 0.521 |
LIG_TRAF2_1 | 370 | 373 | PF00917 | 0.490 |
LIG_UBA3_1 | 392 | 400 | PF00899 | 0.499 |
LIG_ULM_U2AF65_1 | 4 | 9 | PF00076 | 0.416 |
LIG_WRC_WIRS_1 | 668 | 673 | PF05994 | 0.441 |
LIG_WRC_WIRS_1 | 75 | 80 | PF05994 | 0.392 |
MOD_CDK_SPxK_1 | 394 | 400 | PF00069 | 0.467 |
MOD_CDK_SPxK_1 | 639 | 645 | PF00069 | 0.444 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.650 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.437 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.434 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.431 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.491 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.499 |
MOD_CK1_1 | 639 | 645 | PF00069 | 0.492 |
MOD_CK1_1 | 646 | 652 | PF00069 | 0.503 |
MOD_CK1_1 | 696 | 702 | PF00069 | 0.382 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.455 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.445 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.445 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.456 |
MOD_CK2_1 | 696 | 702 | PF00069 | 0.418 |
MOD_CMANNOS | 492 | 495 | PF00535 | 0.252 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.491 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.285 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.242 |
MOD_GlcNHglycan | 401 | 405 | PF01048 | 0.262 |
MOD_GlcNHglycan | 648 | 651 | PF01048 | 0.455 |
MOD_GlcNHglycan | 695 | 698 | PF01048 | 0.417 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.660 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.390 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.445 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.493 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.477 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.492 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.480 |
MOD_GSK3_1 | 639 | 646 | PF00069 | 0.453 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.318 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.315 |
MOD_N-GLC_1 | 205 | 210 | PF02516 | 0.336 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.295 |
MOD_N-GLC_1 | 643 | 648 | PF02516 | 0.594 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.453 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.463 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.465 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.456 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.518 |
MOD_NEK2_1 | 544 | 549 | PF00069 | 0.341 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.407 |
MOD_NEK2_1 | 651 | 656 | PF00069 | 0.363 |
MOD_NEK2_1 | 701 | 706 | PF00069 | 0.434 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.277 |
MOD_PIKK_1 | 120 | 126 | PF00454 | 0.581 |
MOD_PIKK_1 | 153 | 159 | PF00454 | 0.444 |
MOD_PIKK_1 | 188 | 194 | PF00454 | 0.517 |
MOD_PIKK_1 | 374 | 380 | PF00454 | 0.515 |
MOD_PIKK_1 | 544 | 550 | PF00454 | 0.351 |
MOD_PIKK_1 | 576 | 582 | PF00454 | 0.522 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.464 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.517 |
MOD_PKA_2 | 386 | 392 | PF00069 | 0.431 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.497 |
MOD_PKA_2 | 477 | 483 | PF00069 | 0.501 |
MOD_PKA_2 | 651 | 657 | PF00069 | 0.400 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.357 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.430 |
MOD_Plk_1 | 184 | 190 | PF00069 | 0.453 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.504 |
MOD_Plk_1 | 400 | 406 | PF00069 | 0.435 |
MOD_Plk_1 | 413 | 419 | PF00069 | 0.525 |
MOD_Plk_1 | 634 | 640 | PF00069 | 0.443 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.303 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.313 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.482 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.493 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.426 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.447 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.472 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.458 |
MOD_Plk_4 | 510 | 516 | PF00069 | 0.354 |
MOD_Plk_4 | 519 | 525 | PF00069 | 0.389 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.342 |
MOD_Plk_4 | 636 | 642 | PF00069 | 0.404 |
MOD_Plk_4 | 651 | 657 | PF00069 | 0.460 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.466 |
MOD_ProDKin_1 | 552 | 558 | PF00069 | 0.469 |
MOD_ProDKin_1 | 614 | 620 | PF00069 | 0.310 |
MOD_ProDKin_1 | 639 | 645 | PF00069 | 0.341 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.422 |
MOD_SUMO_for_1 | 277 | 280 | PF00179 | 0.434 |
MOD_SUMO_rev_2 | 142 | 150 | PF00179 | 0.438 |
MOD_SUMO_rev_2 | 252 | 262 | PF00179 | 0.527 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 307 | 310 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 332 | 335 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 339 | 342 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 43 | 46 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 432 | 435 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 563 | 566 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 598 | 601 | PF00928 | 0.429 |
TRG_ER_diArg_1 | 174 | 177 | PF00400 | 0.278 |
TRG_ER_diArg_1 | 20 | 23 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 212 | 214 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 3 | 5 | PF00400 | 0.701 |
TRG_ER_diArg_1 | 477 | 479 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 551 | 554 | PF00400 | 0.480 |
TRG_NLS_Bipartite_1 | 4 | 24 | PF00514 | 0.405 |
TRG_NLS_MonoExtC_3 | 536 | 541 | PF00514 | 0.430 |
TRG_NLS_MonoExtN_4 | 18 | 24 | PF00514 | 0.499 |
TRG_NLS_MonoExtN_4 | 537 | 542 | PF00514 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 151 | 155 | PF00026 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 275 | 279 | PF00026 | 0.244 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 69% | 100% |
A0A0N1I8N2 | Leptomonas seymouri | 28% | 72% |
A0A0N1IGQ2 | Leptomonas seymouri | 36% | 100% |
A0A0N1ILF1 | Leptomonas seymouri | 34% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 35% | 91% |
A0A0N1P9P1 | Leptomonas seymouri | 34% | 84% |
A0A0N1PCA9 | Leptomonas seymouri | 30% | 97% |
A0A0N1PE91 | Leptomonas seymouri | 25% | 80% |
A0A0N1PFI4 | Leptomonas seymouri | 33% | 92% |
A0A0S4JLK6 | Bodo saltans | 31% | 88% |
A0A0S4JS70 | Bodo saltans | 27% | 93% |
A0A0S4KGT2 | Bodo saltans | 40% | 95% |
A0A0S4KKP7 | Bodo saltans | 21% | 96% |
A0A1X0NJ61 | Trypanosomatidae | 40% | 100% |
A0A1X0NJK2 | Trypanosomatidae | 44% | 94% |
A0A1X0NJX8 | Trypanosomatidae | 35% | 92% |
A0A1X0NKT7 | Trypanosomatidae | 30% | 90% |
A0A1X0NKX8 | Trypanosomatidae | 32% | 87% |
A0A1X0NMT3 | Trypanosomatidae | 33% | 84% |
A0A1X0NW84 | Trypanosomatidae | 35% | 100% |
A0A1X0NW85 | Trypanosomatidae | 34% | 100% |
A0A1X0NW89 | Trypanosomatidae | 36% | 83% |
A0A1X0NWA6 | Trypanosomatidae | 26% | 82% |
A0A1X0NWW1 | Trypanosomatidae | 35% | 99% |
A0A1X0P1P4 | Trypanosomatidae | 21% | 69% |
A0A3Q8IBS3 | Leishmania donovani | 34% | 78% |
A0A3Q8IDD4 | Leishmania donovani | 36% | 100% |
A0A3Q8IJT4 | Leishmania donovani | 24% | 95% |
A0A3S5H5A5 | Leishmania donovani | 31% | 84% |
A0A3S5ISG2 | Trypanosoma rangeli | 33% | 92% |
A0A3S7WW18 | Leishmania donovani | 34% | 87% |
A0A3S7WW41 | Leishmania donovani | 31% | 96% |
A0A3S7WW71 | Leishmania donovani | 33% | 100% |
A0A3S7X430 | Leishmania donovani | 33% | 91% |
A0A3S7X438 | Leishmania donovani | 30% | 76% |
A0A3S7X460 | Leishmania donovani | 82% | 92% |
A0A3S7X463 | Leishmania donovani | 27% | 76% |
A0A3S7X470 | Leishmania donovani | 33% | 99% |
A0A422MYU1 | Trypanosoma rangeli | 36% | 78% |
A0A422MYX0 | Trypanosoma rangeli | 34% | 98% |
A4H3W4 | Leishmania braziliensis | 33% | 100% |
A4HE81 | Leishmania braziliensis | 35% | 100% |
A4HJ14 | Leishmania braziliensis | 33% | 100% |
A4HJ21 | Leishmania braziliensis | 25% | 100% |
A4HJ22 | Leishmania braziliensis | 30% | 100% |
A4HJ23 | Leishmania braziliensis | 33% | 100% |
A4HS39 | Leishmania infantum | 31% | 84% |
A4HYN0 | Leishmania infantum | 34% | 87% |
A4HYW1 | Leishmania infantum | 34% | 70% |
A4HYW2 | Leishmania infantum | 33% | 100% |
A4HYW3 | Leishmania infantum | 31% | 96% |
A4HYW4 | Leishmania infantum | 26% | 71% |
A4I1J4 | Leishmania infantum | 36% | 100% |
A4I6E4 | Leishmania infantum | 33% | 99% |
A4I6E6 | Leishmania infantum | 82% | 92% |
A4I6F0 | Leishmania infantum | 30% | 76% |
A4I6K4 | Leishmania infantum | 33% | 91% |
A4I6K5 | Leishmania infantum | 27% | 76% |
A4I6K6 | Leishmania infantum | 25% | 95% |
C9ZIE7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 66% |
C9ZIE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZIE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 98% |
C9ZN52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 90% |
C9ZN53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 84% |
C9ZWY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 89% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 83% |
E8NHF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
E8NHG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 99% |
E8NHG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 76% |
E8NHG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 91% |
E8NHM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
E8NHM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
E8NHM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
E9AIH1 | Leishmania braziliensis | 35% | 88% |
E9AIH3 | Leishmania braziliensis | 34% | 100% |
E9AIH4 | Leishmania braziliensis | 30% | 96% |
E9AIH6 | Leishmania braziliensis | 29% | 100% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 90% |
E9AUQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 76% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 96% |
E9AUR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AXM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E9B1J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 91% |
E9B1J1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 76% |
E9B1J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 95% |
E9B1J6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
O08688 | Mus musculus | 28% | 100% |
O15484 | Homo sapiens | 27% | 100% |
Q4Q6L7 | Leishmania major | 81% | 100% |
Q4Q6L9 | Leishmania major | 32% | 100% |
Q4Q6M0 | Leishmania major | 30% | 100% |
Q4Q6M2 | Leishmania major | 23% | 100% |
Q4Q6M3 | Leishmania major | 28% | 100% |
Q4Q6M4 | Leishmania major | 34% | 100% |
Q4Q9U3 | Leishmania major | 36% | 100% |
Q4QCS6 | Leishmania major | 31% | 100% |
Q4QCS7 | Leishmania major | 33% | 100% |
Q4QCS8 | Leishmania major | 34% | 100% |
Q4QCS9 | Leishmania major | 34% | 100% |
Q9U0T9 | Leishmania major | 31% | 100% |
V5AYJ1 | Trypanosoma cruzi | 43% | 100% |
V5B5I4 | Trypanosoma cruzi | 35% | 85% |
V5BA05 | Trypanosoma cruzi | 37% | 100% |
V5BEL3 | Trypanosoma cruzi | 35% | 100% |
V5BN20 | Trypanosoma cruzi | 36% | 92% |
V5D5V8 | Trypanosoma cruzi | 29% | 96% |
V5D9Y2 | Trypanosoma cruzi | 33% | 84% |
V5DES7 | Trypanosoma cruzi | 33% | 90% |