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. | yes | yes: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0034045 | phagophore assembly site membrane | 3 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0000407 | phagophore assembly site | 2 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005773 | vacuole | 5 | 1 |
GO:0005776 | autophagosome | 6 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0000502 | proteasome complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1905368 | peptidase complex | 3 | 2 |
GO:1905369 | endopeptidase complex | 4 | 2 |
Related structures:
AlphaFold database: E9AHC0
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 12 |
GO:0006869 | lipid transport | 5 | 12 |
GO:0006914 | autophagy | 3 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009056 | catabolic process | 2 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044248 | cellular catabolic process | 3 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0061919 | process utilizing autophagic mechanism | 2 | 12 |
GO:0071702 | organic substance transport | 4 | 12 |
GO:0000422 | autophagy of mitochondrion | 4 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007005 | mitochondrion organization | 5 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022411 | cellular component disassembly | 4 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0034497 | protein localization to phagophore assembly site | 5 | 1 |
GO:0044804 | autophagy of nucleus | 4 | 1 |
GO:0044805 | late nucleophagy | 5 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0061726 | mitochondrion disassembly | 6 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1903008 | organelle disassembly | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 256 | 260 | PF00656 | 0.500 |
CLV_C14_Caspase3-7 | 504 | 508 | PF00656 | 0.500 |
CLV_C14_Caspase3-7 | 602 | 606 | PF00656 | 0.648 |
CLV_C14_Caspase3-7 | 667 | 671 | PF00656 | 0.713 |
CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 653 | 655 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 716 | 718 | PF00675 | 0.523 |
CLV_PCSK_KEX2_1 | 371 | 373 | PF00082 | 0.318 |
CLV_PCSK_KEX2_1 | 567 | 569 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 653 | 655 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 716 | 718 | PF00082 | 0.524 |
CLV_PCSK_PC1ET2_1 | 567 | 569 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 701 | 705 | PF00082 | 0.496 |
DEG_SCF_FBW7_2 | 523 | 530 | PF00400 | 0.700 |
DEG_SPOP_SBC_1 | 681 | 685 | PF00917 | 0.667 |
DOC_CKS1_1 | 151 | 156 | PF01111 | 0.479 |
DOC_CYCLIN_RxL_1 | 610 | 621 | PF00134 | 0.472 |
DOC_CYCLIN_yCln2_LP_2 | 477 | 483 | PF00134 | 0.341 |
DOC_CYCLIN_yCln2_LP_2 | 555 | 561 | PF00134 | 0.676 |
DOC_CYCLIN_yCln2_LP_2 | 94 | 100 | PF00134 | 0.316 |
DOC_MAPK_gen_1 | 11 | 19 | PF00069 | 0.663 |
DOC_MAPK_gen_1 | 463 | 470 | PF00069 | 0.296 |
DOC_MAPK_gen_1 | 567 | 576 | PF00069 | 0.621 |
DOC_MAPK_MEF2A_6 | 463 | 470 | PF00069 | 0.335 |
DOC_MAPK_MEF2A_6 | 567 | 576 | PF00069 | 0.621 |
DOC_PP2B_LxvP_1 | 10 | 13 | PF13499 | 0.680 |
DOC_PP2B_LxvP_1 | 477 | 480 | PF13499 | 0.323 |
DOC_PP2B_LxvP_1 | 94 | 97 | PF13499 | 0.341 |
DOC_PP4_FxxP_1 | 151 | 154 | PF00568 | 0.541 |
DOC_PP4_FxxP_1 | 209 | 212 | PF00568 | 0.541 |
DOC_PP4_FxxP_1 | 386 | 389 | PF00568 | 0.392 |
DOC_PP4_FxxP_1 | 655 | 658 | PF00568 | 0.791 |
DOC_SPAK_OSR1_1 | 654 | 658 | PF12202 | 0.727 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 539 | 543 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 548 | 552 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 561 | 565 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 645 | 649 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 680 | 684 | PF00917 | 0.687 |
DOC_USP7_MATH_2 | 528 | 534 | PF00917 | 0.688 |
DOC_USP7_UBL2_3 | 303 | 307 | PF12436 | 0.390 |
DOC_USP7_UBL2_3 | 567 | 571 | PF12436 | 0.652 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 523 | 528 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 596 | 601 | PF00397 | 0.750 |
LIG_14-3-3_CanoR_1 | 101 | 105 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 14 | 18 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 279 | 283 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 29 | 38 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 322 | 332 | PF00244 | 0.287 |
LIG_14-3-3_CanoR_1 | 361 | 367 | PF00244 | 0.319 |
LIG_14-3-3_CanoR_1 | 371 | 380 | PF00244 | 0.293 |
LIG_14-3-3_CanoR_1 | 6 | 10 | PF00244 | 0.700 |
LIG_14-3-3_CanoR_1 | 613 | 618 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 708 | 714 | PF00244 | 0.709 |
LIG_Actin_WH2_2 | 228 | 244 | PF00022 | 0.532 |
LIG_Actin_WH2_2 | 334 | 349 | PF00022 | 0.332 |
LIG_Actin_WH2_2 | 575 | 591 | PF00022 | 0.596 |
LIG_APCC_ABBA_1 | 332 | 337 | PF00400 | 0.255 |
LIG_APCC_ABBAyCdc20_2 | 331 | 337 | PF00400 | 0.341 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.701 |
LIG_BRCT_BRCA1_1 | 205 | 209 | PF00533 | 0.541 |
LIG_Clathr_ClatBox_1 | 225 | 229 | PF01394 | 0.541 |
LIG_deltaCOP1_diTrp_1 | 327 | 332 | PF00928 | 0.279 |
LIG_deltaCOP1_diTrp_1 | 445 | 453 | PF00928 | 0.254 |
LIG_eIF4E_1 | 289 | 295 | PF01652 | 0.410 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.429 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.397 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.519 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.203 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.530 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.326 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.373 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.366 |
LIG_FHA_1 | 56 | 62 | PF00498 | 0.410 |
LIG_FHA_1 | 671 | 677 | PF00498 | 0.684 |
LIG_FHA_1 | 707 | 713 | PF00498 | 0.683 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.553 |
LIG_FHA_2 | 428 | 434 | PF00498 | 0.359 |
LIG_FHA_2 | 502 | 508 | PF00498 | 0.521 |
LIG_FHA_2 | 593 | 599 | PF00498 | 0.723 |
LIG_FHA_2 | 683 | 689 | PF00498 | 0.640 |
LIG_GBD_Chelix_1 | 379 | 387 | PF00786 | 0.344 |
LIG_GBD_Chelix_1 | 402 | 410 | PF00786 | 0.405 |
LIG_GBD_Chelix_1 | 469 | 477 | PF00786 | 0.371 |
LIG_LIR_Apic_2 | 148 | 154 | PF02991 | 0.466 |
LIG_LIR_Apic_2 | 206 | 212 | PF02991 | 0.541 |
LIG_LIR_Apic_2 | 385 | 389 | PF02991 | 0.392 |
LIG_LIR_Apic_2 | 652 | 658 | PF02991 | 0.780 |
LIG_LIR_Gen_1 | 259 | 268 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 284 | 293 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 423 | 432 | PF02991 | 0.289 |
LIG_LIR_Gen_1 | 451 | 462 | PF02991 | 0.257 |
LIG_LIR_Gen_1 | 578 | 583 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 58 | 67 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 102 | 108 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 130 | 136 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 173 | 177 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 187 | 193 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 259 | 265 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 284 | 288 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 423 | 429 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 451 | 457 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 578 | 582 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 58 | 62 | PF02991 | 0.442 |
LIG_Pex14_1 | 109 | 113 | PF04695 | 0.415 |
LIG_Pex14_2 | 100 | 104 | PF04695 | 0.359 |
LIG_Pex14_2 | 15 | 19 | PF04695 | 0.622 |
LIG_Pex14_2 | 55 | 59 | PF04695 | 0.382 |
LIG_Pex14_2 | 68 | 72 | PF04695 | 0.250 |
LIG_Rb_pABgroove_1 | 256 | 264 | PF01858 | 0.455 |
LIG_REV1ctd_RIR_1 | 459 | 469 | PF16727 | 0.341 |
LIG_SH2_CRK | 285 | 289 | PF00017 | 0.380 |
LIG_SH2_CRK | 426 | 430 | PF00017 | 0.273 |
LIG_SH2_NCK_1 | 335 | 339 | PF00017 | 0.266 |
LIG_SH2_NCK_1 | 413 | 417 | PF00017 | 0.428 |
LIG_SH2_NCK_1 | 441 | 445 | PF00017 | 0.363 |
LIG_SH2_NCK_1 | 454 | 458 | PF00017 | 0.290 |
LIG_SH2_PTP2 | 248 | 251 | PF00017 | 0.559 |
LIG_SH2_PTP2 | 299 | 302 | PF00017 | 0.428 |
LIG_SH2_SRC | 231 | 234 | PF00017 | 0.521 |
LIG_SH2_SRC | 426 | 429 | PF00017 | 0.332 |
LIG_SH2_SRC | 454 | 457 | PF00017 | 0.359 |
LIG_SH2_STAP1 | 285 | 289 | PF00017 | 0.388 |
LIG_SH2_STAT3 | 132 | 135 | PF00017 | 0.541 |
LIG_SH2_STAT3 | 160 | 163 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.341 |
LIG_SH3_2 | 215 | 220 | PF14604 | 0.541 |
LIG_SH3_3 | 209 | 215 | PF00018 | 0.541 |
LIG_SUMO_SIM_anti_2 | 407 | 412 | PF11976 | 0.364 |
LIG_SUMO_SIM_par_1 | 231 | 237 | PF11976 | 0.541 |
LIG_SUMO_SIM_par_1 | 465 | 471 | PF11976 | 0.333 |
LIG_TYR_ITIM | 283 | 288 | PF00017 | 0.459 |
LIG_TYR_ITIM | 314 | 319 | PF00017 | 0.341 |
LIG_WRC_WIRS_1 | 383 | 388 | PF05994 | 0.341 |
LIG_WRC_WIRS_1 | 56 | 61 | PF05994 | 0.453 |
LIG_WRC_WIRS_1 | 576 | 581 | PF05994 | 0.485 |
MOD_CDK_SPxxK_3 | 150 | 157 | PF00069 | 0.466 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.584 |
MOD_CK1_1 | 540 | 546 | PF00069 | 0.777 |
MOD_CK1_1 | 575 | 581 | PF00069 | 0.486 |
MOD_CK1_1 | 584 | 590 | PF00069 | 0.538 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.663 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.678 |
MOD_CK1_1 | 639 | 645 | PF00069 | 0.683 |
MOD_CK1_1 | 648 | 654 | PF00069 | 0.597 |
MOD_CK1_1 | 695 | 701 | PF00069 | 0.623 |
MOD_CK1_1 | 707 | 713 | PF00069 | 0.636 |
MOD_CK2_1 | 427 | 433 | PF00069 | 0.359 |
MOD_CK2_1 | 592 | 598 | PF00069 | 0.731 |
MOD_CK2_1 | 629 | 635 | PF00069 | 0.694 |
MOD_CK2_1 | 682 | 688 | PF00069 | 0.645 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.319 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.341 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.394 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.455 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.428 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.563 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.573 |
MOD_GlcNHglycan | 549 | 553 | PF01048 | 0.573 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.411 |
MOD_GlcNHglycan | 631 | 634 | PF01048 | 0.457 |
MOD_GlcNHglycan | 672 | 676 | PF01048 | 0.513 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.383 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.496 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.523 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.500 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.341 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.187 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.609 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.690 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.656 |
MOD_GSK3_1 | 639 | 646 | PF00069 | 0.702 |
MOD_GSK3_1 | 692 | 699 | PF00069 | 0.565 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.322 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.296 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.233 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.463 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.519 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.530 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.417 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.452 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.359 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.489 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.300 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.365 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.648 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.524 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.330 |
MOD_NEK2_1 | 692 | 697 | PF00069 | 0.542 |
MOD_NEK2_1 | 704 | 709 | PF00069 | 0.605 |
MOD_NEK2_2 | 13 | 18 | PF00069 | 0.579 |
MOD_NEK2_2 | 645 | 650 | PF00069 | 0.776 |
MOD_PIKK_1 | 29 | 35 | PF00454 | 0.559 |
MOD_PIKK_1 | 317 | 323 | PF00454 | 0.341 |
MOD_PIKK_1 | 581 | 587 | PF00454 | 0.539 |
MOD_PIKK_1 | 692 | 698 | PF00454 | 0.576 |
MOD_PIKK_1 | 707 | 713 | PF00454 | 0.630 |
MOD_PK_1 | 203 | 209 | PF00069 | 0.541 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.338 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.654 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.500 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.541 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.325 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.701 |
MOD_PKA_2 | 639 | 645 | PF00069 | 0.717 |
MOD_PKA_2 | 707 | 713 | PF00069 | 0.714 |
MOD_PKB_1 | 345 | 353 | PF00069 | 0.300 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.298 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.509 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.510 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.483 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.489 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.533 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.333 |
MOD_Plk_4 | 398 | 404 | PF00069 | 0.341 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.306 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.699 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.323 |
MOD_Plk_4 | 550 | 556 | PF00069 | 0.748 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.455 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.559 |
MOD_ProDKin_1 | 523 | 529 | PF00069 | 0.734 |
MOD_ProDKin_1 | 596 | 602 | PF00069 | 0.745 |
TRG_DiLeu_BaEn_2 | 123 | 129 | PF01217 | 0.466 |
TRG_DiLeu_BaLyEn_6 | 462 | 467 | PF01217 | 0.351 |
TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.239 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.147 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.273 |
TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.266 |
TRG_ER_diArg_1 | 359 | 362 | PF00400 | 0.289 |
TRG_ER_diArg_1 | 370 | 372 | PF00400 | 0.275 |
TRG_ER_diArg_1 | 617 | 620 | PF00400 | 0.620 |
TRG_ER_diArg_1 | 653 | 655 | PF00400 | 0.791 |
TRG_NES_CRM1_1 | 217 | 229 | PF08389 | 0.466 |
TRG_Pf-PMV_PEXEL_1 | 255 | 259 | PF00026 | 0.307 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5S4 | Leptomonas seymouri | 69% | 100% |
A0A0S4JRE4 | Bodo saltans | 29% | 93% |
A0A1X0P5B9 | Trypanosomatidae | 36% | 100% |
A0A3S5H7H3 | Leishmania donovani | 100% | 100% |
A0A422NTE4 | Trypanosoma rangeli | 36% | 100% |
D0A5N9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9AD16 | Leishmania major | 97% | 100% |
E9AIS5 | Leishmania braziliensis | 83% | 100% |
E9AYU1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
P0CM40 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 21% | 83% |
P0CM41 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 21% | 83% |
Q8RUS5 | Arabidopsis thaliana | 22% | 84% |
V5B7I2 | Trypanosoma cruzi | 34% | 100% |