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: 10 |
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:0005874 | microtubule | 6 | 12 |
GO:0099080 | supramolecular complex | 2 | 12 |
GO:0099081 | supramolecular polymer | 3 | 12 |
GO:0099512 | supramolecular fiber | 4 | 12 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005929 | cilium | 4 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0097542 | ciliary tip | 2 | 1 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
Related structures:
AlphaFold database: A4H720
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 12 |
GO:0007018 | microtubule-based movement | 3 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007019 | microtubule depolymerization | 5 | 1 |
GO:0010938 | cytoplasmic microtubule depolymerization | 5 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022411 | cellular component disassembly | 4 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0030030 | cell projection organization | 4 | 1 |
GO:0030031 | cell projection assembly | 5 | 1 |
GO:0031109 | microtubule polymerization or depolymerization | 4 | 1 |
GO:0031122 | cytoplasmic microtubule organization | 4 | 1 |
GO:0032984 | protein-containing complex disassembly | 5 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0044782 | cilium organization | 5 | 1 |
GO:0051261 | protein depolymerization | 6 | 1 |
GO:0060271 | cilium assembly | 6 | 1 |
GO:0060404 | axonemal microtubule depolymerization | 6 | 1 |
GO:0061523 | cilium disassembly | 6 | 1 |
GO:0070925 | organelle assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0097435 | supramolecular fiber organization | 4 | 1 |
GO:0120031 | plasma membrane bounded cell projection assembly | 6 | 1 |
GO:0120036 | plasma membrane bounded cell projection organization | 5 | 1 |
GO:1903008 | organelle disassembly | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003774 | cytoskeletal motor activity | 1 | 12 |
GO:0003777 | microtubule motor activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005515 | protein binding | 2 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008017 | microtubule binding | 5 | 12 |
GO:0008092 | cytoskeletal protein binding | 3 | 12 |
GO:0008270 | zinc ion binding | 6 | 11 |
GO:0015631 | tubulin binding | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
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:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0046914 | transition metal ion binding | 5 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 40 | 44 | PF00656 | 0.295 |
CLV_C14_Caspase3-7 | 578 | 582 | PF00656 | 0.481 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.310 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.233 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 557 | 559 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 564 | 566 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 635 | 637 | PF00675 | 0.486 |
CLV_PCSK_FUR_1 | 433 | 437 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 557 | 559 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 564 | 566 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 635 | 637 | PF00082 | 0.500 |
CLV_PCSK_PC1ET2_1 | 230 | 232 | PF00082 | 0.325 |
CLV_PCSK_PC1ET2_1 | 314 | 316 | PF00082 | 0.564 |
CLV_PCSK_PC1ET2_1 | 434 | 436 | PF00082 | 0.477 |
CLV_PCSK_PC7_1 | 310 | 316 | PF00082 | 0.554 |
CLV_PCSK_PC7_1 | 553 | 559 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.278 |
DEG_APCC_DBOX_1 | 68 | 76 | PF00400 | 0.331 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.373 |
DEG_SCF_FBW7_1 | 452 | 458 | PF00400 | 0.679 |
DEG_SCF_FBW7_2 | 3 | 10 | PF00400 | 0.453 |
DEG_SPOP_SBC_1 | 463 | 467 | PF00917 | 0.539 |
DOC_CKS1_1 | 452 | 457 | PF01111 | 0.680 |
DOC_CYCLIN_RxL_1 | 211 | 221 | PF00134 | 0.281 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 600 | 609 | PF00134 | 0.421 |
DOC_MAPK_gen_1 | 158 | 168 | PF00069 | 0.300 |
DOC_MAPK_gen_1 | 229 | 235 | PF00069 | 0.276 |
DOC_MAPK_MEF2A_6 | 161 | 170 | PF00069 | 0.281 |
DOC_PP1_RVXF_1 | 181 | 187 | PF00149 | 0.411 |
DOC_PP1_SILK_1 | 485 | 490 | PF00149 | 0.533 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.314 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.189 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 495 | 499 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 534 | 538 | PF00917 | 0.768 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.266 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 537 | 542 | PF00397 | 0.644 |
LIG_14-3-3_CanoR_1 | 158 | 168 | PF00244 | 0.352 |
LIG_14-3-3_CanoR_1 | 183 | 187 | PF00244 | 0.281 |
LIG_14-3-3_CanoR_1 | 224 | 229 | PF00244 | 0.325 |
LIG_14-3-3_CanoR_1 | 251 | 260 | PF00244 | 0.325 |
LIG_14-3-3_CanoR_1 | 456 | 463 | PF00244 | 0.745 |
LIG_14-3-3_CanoR_1 | 543 | 551 | PF00244 | 0.737 |
LIG_14-3-3_CterR_2 | 653 | 656 | PF00244 | 0.421 |
LIG_Actin_WH2_2 | 133 | 150 | PF00022 | 0.348 |
LIG_APCC_ABBA_1 | 620 | 625 | PF00400 | 0.458 |
LIG_BRCT_BRCA1_1 | 546 | 550 | PF00533 | 0.677 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.331 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.266 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.266 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.446 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.630 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.386 |
LIG_FHA_2 | 183 | 189 | PF00498 | 0.274 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.360 |
LIG_FHA_2 | 23 | 29 | PF00498 | 0.360 |
LIG_FHA_2 | 386 | 392 | PF00498 | 0.460 |
LIG_FHA_2 | 464 | 470 | PF00498 | 0.691 |
LIG_FHA_2 | 576 | 582 | PF00498 | 0.586 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.432 |
LIG_GBD_Chelix_1 | 605 | 613 | PF00786 | 0.547 |
LIG_LIR_Apic_2 | 592 | 597 | PF02991 | 0.585 |
LIG_LIR_Gen_1 | 116 | 126 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 13 | 20 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 185 | 190 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 476 | 483 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 116 | 121 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 13 | 19 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 185 | 189 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 476 | 481 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 92 | 97 | PF02991 | 0.272 |
LIG_NRBOX | 100 | 106 | PF00104 | 0.266 |
LIG_PCNA_yPIPBox_3 | 626 | 638 | PF02747 | 0.490 |
LIG_SH2_CRK | 102 | 106 | PF00017 | 0.411 |
LIG_SH2_CRK | 118 | 122 | PF00017 | 0.366 |
LIG_SH2_CRK | 478 | 482 | PF00017 | 0.472 |
LIG_SH2_CRK | 594 | 598 | PF00017 | 0.528 |
LIG_SH2_GRB2like | 118 | 121 | PF00017 | 0.435 |
LIG_SH2_NCK_1 | 16 | 20 | PF00017 | 0.411 |
LIG_SH2_NCK_1 | 478 | 482 | PF00017 | 0.472 |
LIG_SH2_SRC | 118 | 121 | PF00017 | 0.411 |
LIG_SH2_SRC | 16 | 19 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 16 | 20 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 276 | 280 | PF00017 | 0.266 |
LIG_SH2_STAP1 | 623 | 627 | PF00017 | 0.434 |
LIG_SH2_STAP1 | 73 | 77 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.442 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.607 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.434 |
LIG_SH3_3 | 488 | 494 | PF00018 | 0.616 |
LIG_SH3_3 | 584 | 590 | PF00018 | 0.544 |
LIG_SUMO_SIM_anti_2 | 457 | 467 | PF11976 | 0.675 |
LIG_SUMO_SIM_par_1 | 215 | 221 | PF11976 | 0.281 |
LIG_TRAF2_1 | 25 | 28 | PF00917 | 0.331 |
LIG_TRAF2_1 | 388 | 391 | PF00917 | 0.478 |
LIG_TRAF2_2 | 380 | 385 | PF00917 | 0.478 |
LIG_UBA3_1 | 216 | 220 | PF00899 | 0.281 |
MOD_CDC14_SPxK_1 | 342 | 345 | PF00782 | 0.440 |
MOD_CDC14_SPxK_1 | 540 | 543 | PF00782 | 0.490 |
MOD_CDK_SPK_2 | 451 | 456 | PF00069 | 0.675 |
MOD_CDK_SPxK_1 | 339 | 345 | PF00069 | 0.437 |
MOD_CDK_SPxK_1 | 537 | 543 | PF00069 | 0.491 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.360 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.291 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.266 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.634 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.617 |
MOD_CK1_1 | 499 | 505 | PF00069 | 0.704 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.691 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.648 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.281 |
MOD_CK1_1 | 647 | 653 | PF00069 | 0.607 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.331 |
MOD_CK2_1 | 172 | 178 | PF00069 | 0.364 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.360 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.331 |
MOD_CK2_1 | 262 | 268 | PF00069 | 0.314 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.489 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.388 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.266 |
MOD_Cter_Amidation | 562 | 565 | PF01082 | 0.535 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.743 |
MOD_GlcNHglycan | 546 | 549 | PF01048 | 0.651 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.281 |
MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.590 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.322 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.308 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.282 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.491 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.591 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.586 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.609 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.689 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.210 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.459 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.707 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.669 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.604 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.456 |
MOD_GSK3_1 | 643 | 650 | PF00069 | 0.541 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.235 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.265 |
MOD_N-GLC_1 | 212 | 217 | PF02516 | 0.266 |
MOD_N-GLC_1 | 448 | 453 | PF02516 | 0.515 |
MOD_N-GLC_1 | 581 | 586 | PF02516 | 0.501 |
MOD_N-GLC_1 | 609 | 614 | PF02516 | 0.326 |
MOD_N-GLC_2 | 567 | 569 | PF02516 | 0.478 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.389 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.272 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.256 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.260 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.612 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.564 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.295 |
MOD_NEK2_1 | 544 | 549 | PF00069 | 0.640 |
MOD_NEK2_1 | 609 | 614 | PF00069 | 0.582 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.279 |
MOD_NEK2_2 | 525 | 530 | PF00069 | 0.493 |
MOD_PIKK_1 | 238 | 244 | PF00454 | 0.274 |
MOD_PIKK_1 | 385 | 391 | PF00454 | 0.579 |
MOD_PIKK_1 | 468 | 474 | PF00454 | 0.741 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.340 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.274 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.252 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.266 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.266 |
MOD_PKA_2 | 385 | 391 | PF00069 | 0.439 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.675 |
MOD_PKA_2 | 499 | 505 | PF00069 | 0.732 |
MOD_PKA_2 | 506 | 512 | PF00069 | 0.711 |
MOD_PKA_2 | 542 | 548 | PF00069 | 0.592 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.339 |
MOD_Plk_1 | 212 | 218 | PF00069 | 0.266 |
MOD_Plk_1 | 267 | 273 | PF00069 | 0.266 |
MOD_Plk_1 | 448 | 454 | PF00069 | 0.591 |
MOD_Plk_1 | 609 | 615 | PF00069 | 0.479 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.331 |
MOD_Plk_2-3 | 575 | 581 | PF00069 | 0.482 |
MOD_Plk_2-3 | 79 | 85 | PF00069 | 0.331 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.266 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.287 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.482 |
MOD_Plk_4 | 515 | 521 | PF00069 | 0.490 |
MOD_Plk_4 | 546 | 552 | PF00069 | 0.634 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.266 |
MOD_Plk_4 | 609 | 615 | PF00069 | 0.487 |
MOD_Plk_4 | 618 | 624 | PF00069 | 0.414 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.270 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.266 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.453 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.567 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.572 |
MOD_ProDKin_1 | 537 | 543 | PF00069 | 0.647 |
MOD_SUMO_rev_2 | 107 | 114 | PF00179 | 0.360 |
MOD_SUMO_rev_2 | 162 | 170 | PF00179 | 0.325 |
MOD_SUMO_rev_2 | 196 | 205 | PF00179 | 0.364 |
MOD_SUMO_rev_2 | 278 | 286 | PF00179 | 0.331 |
MOD_SUMO_rev_2 | 391 | 397 | PF00179 | 0.478 |
TRG_DiLeu_BaLyEn_6 | 33 | 38 | PF01217 | 0.281 |
TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.475 |
TRG_ER_diArg_1 | 228 | 231 | PF00400 | 0.325 |
TRG_ER_diArg_1 | 432 | 435 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 564 | 566 | PF00400 | 0.604 |
TRG_ER_diArg_1 | 634 | 636 | PF00400 | 0.500 |
TRG_NES_CRM1_1 | 180 | 193 | PF08389 | 0.331 |
TRG_NES_CRM1_1 | 611 | 625 | PF08389 | 0.345 |
TRG_NLS_MonoCore_2 | 432 | 437 | PF00514 | 0.516 |
TRG_NLS_MonoExtC_3 | 432 | 438 | PF00514 | 0.446 |
TRG_Pf-PMV_PEXEL_1 | 381 | 385 | PF00026 | 0.315 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P647 | Leptomonas seymouri | 70% | 89% |
A0A0S4IJP8 | Bodo saltans | 50% | 88% |
A0A1X0NNY0 | Trypanosomatidae | 63% | 100% |
A0A1X0NQ03 | Trypanosomatidae | 25% | 79% |
A0A3S7WS99 | Leishmania donovani | 86% | 90% |
A0A422NBP2 | Trypanosoma rangeli | 53% | 100% |
A4HVE9 | Leishmania infantum | 86% | 90% |
D0A6W1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 95% |
E9AP47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 90% |
Q4QGE1 | Leishmania major | 85% | 100% |