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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0016281 | eukaryotic translation initiation factor 4F complex | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QHA6
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006412 | translation | 4 | 2 |
GO:0006518 | peptide metabolic process | 4 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009059 | macromolecule biosynthetic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 2 |
GO:0043043 | peptide biosynthetic process | 5 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043603 | amide metabolic process | 3 | 2 |
GO:0043604 | amide biosynthetic process | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 12 |
GO:0003729 | mRNA binding | 5 | 2 |
GO:0003743 | translation initiation factor activity | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008135 | translation factor activity, RNA binding | 3 | 12 |
GO:0045182 | translation regulator activity | 1 | 12 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 145 | 149 | PF00656 | 0.549 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.227 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 706 | 708 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 740 | 742 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 780 | 782 | PF00675 | 0.603 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.315 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.221 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.220 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.679 |
CLV_PCSK_PC1ET2_1 | 272 | 274 | PF00082 | 0.251 |
CLV_PCSK_PC1ET2_1 | 377 | 379 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.256 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.145 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 604 | 608 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 703 | 707 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 708 | 712 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 734 | 738 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 741 | 745 | PF00082 | 0.383 |
CLV_Separin_Metazoa | 251 | 255 | PF03568 | 0.524 |
CLV_Separin_Metazoa | 704 | 708 | PF03568 | 0.457 |
DEG_APCC_DBOX_1 | 505 | 513 | PF00400 | 0.349 |
DEG_APCC_DBOX_1 | 740 | 748 | PF00400 | 0.444 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.612 |
DOC_CKS1_1 | 67 | 72 | PF01111 | 0.539 |
DOC_CYCLIN_yCln2_LP_2 | 67 | 73 | PF00134 | 0.592 |
DOC_MAPK_gen_1 | 186 | 196 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 292 | 299 | PF00069 | 0.420 |
DOC_MAPK_MEF2A_6 | 713 | 722 | PF00069 | 0.439 |
DOC_PP1_RVXF_1 | 207 | 213 | PF00149 | 0.485 |
DOC_PP1_RVXF_1 | 284 | 290 | PF00149 | 0.444 |
DOC_PP1_RVXF_1 | 375 | 382 | PF00149 | 0.460 |
DOC_SPAK_OSR1_1 | 611 | 615 | PF12202 | 0.307 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.429 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.696 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 619 | 624 | PF00397 | 0.384 |
DOC_WW_Pin1_4 | 66 | 71 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 666 | 671 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 676 | 681 | PF00397 | 0.362 |
LIG_14-3-3_CanoR_1 | 19 | 24 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 197 | 204 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 257 | 261 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 273 | 278 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 495 | 501 | PF00244 | 0.346 |
LIG_14-3-3_CanoR_1 | 762 | 766 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 8 | 13 | PF00244 | 0.643 |
LIG_Actin_WH2_2 | 691 | 709 | PF00022 | 0.458 |
LIG_Actin_WH2_2 | 747 | 764 | PF00022 | 0.457 |
LIG_APCC_ABBAyCdc20_2 | 147 | 153 | PF00400 | 0.606 |
LIG_BRCT_BRCA1_1 | 684 | 688 | PF00533 | 0.281 |
LIG_BRCT_BRCA1_1 | 731 | 735 | PF00533 | 0.363 |
LIG_CaM_IQ_9 | 284 | 300 | PF13499 | 0.451 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.445 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.465 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.603 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.323 |
LIG_FHA_1 | 569 | 575 | PF00498 | 0.303 |
LIG_FHA_1 | 715 | 721 | PF00498 | 0.393 |
LIG_FHA_2 | 198 | 204 | PF00498 | 0.442 |
LIG_FHA_2 | 214 | 220 | PF00498 | 0.442 |
LIG_FHA_2 | 364 | 370 | PF00498 | 0.485 |
LIG_FHA_2 | 596 | 602 | PF00498 | 0.619 |
LIG_FHA_2 | 637 | 643 | PF00498 | 0.552 |
LIG_FHA_2 | 657 | 663 | PF00498 | 0.532 |
LIG_FHA_2 | 762 | 768 | PF00498 | 0.433 |
LIG_HCF-1_HBM_1 | 101 | 104 | PF13415 | 0.587 |
LIG_Integrin_isoDGR_2 | 428 | 430 | PF01839 | 0.602 |
LIG_LIR_Apic_2 | 353 | 359 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 107 | 117 | PF02991 | 0.585 |
LIG_LIR_Gen_1 | 220 | 231 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 333 | 343 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 453 | 461 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 511 | 521 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 541 | 552 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 652 | 661 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 685 | 695 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 107 | 112 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 333 | 338 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 391 | 397 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 453 | 457 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 511 | 516 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 541 | 547 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 610 | 615 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 652 | 657 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 685 | 691 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 700 | 705 | PF02991 | 0.351 |
LIG_MLH1_MIPbox_1 | 684 | 688 | PF16413 | 0.358 |
LIG_NRBOX | 317 | 323 | PF00104 | 0.429 |
LIG_NRBOX | 614 | 620 | PF00104 | 0.361 |
LIG_PCNA_PIPBox_1 | 380 | 389 | PF02747 | 0.451 |
LIG_PCNA_yPIPBox_3 | 307 | 318 | PF02747 | 0.581 |
LIG_PCNA_yPIPBox_3 | 377 | 387 | PF02747 | 0.524 |
LIG_Pex14_1 | 492 | 496 | PF04695 | 0.441 |
LIG_Pex14_2 | 735 | 739 | PF04695 | 0.318 |
LIG_REV1ctd_RIR_1 | 209 | 217 | PF16727 | 0.485 |
LIG_RPA_C_Fungi | 745 | 757 | PF08784 | 0.469 |
LIG_SH2_CRK | 335 | 339 | PF00017 | 0.427 |
LIG_SH2_CRK | 621 | 625 | PF00017 | 0.412 |
LIG_SH2_GRB2like | 496 | 499 | PF00017 | 0.362 |
LIG_SH2_GRB2like | 653 | 656 | PF00017 | 0.345 |
LIG_SH2_PTP2 | 227 | 230 | PF00017 | 0.249 |
LIG_SH2_SRC | 356 | 359 | PF00017 | 0.294 |
LIG_SH2_STAP1 | 126 | 130 | PF00017 | 0.571 |
LIG_SH2_STAP1 | 223 | 227 | PF00017 | 0.396 |
LIG_SH2_STAP1 | 693 | 697 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 488 | 491 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 496 | 499 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 550 | 553 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 621 | 624 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 653 | 656 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 723 | 726 | PF00017 | 0.308 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.635 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.396 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.565 |
LIG_SH3_3 | 446 | 452 | PF00018 | 0.456 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.656 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.669 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.578 |
LIG_SH3_4 | 62 | 69 | PF00018 | 0.539 |
LIG_SUMO_SIM_anti_2 | 471 | 479 | PF11976 | 0.372 |
LIG_SUMO_SIM_anti_2 | 483 | 488 | PF11976 | 0.351 |
LIG_SUMO_SIM_anti_2 | 639 | 646 | PF11976 | 0.386 |
LIG_SUMO_SIM_anti_2 | 767 | 776 | PF11976 | 0.508 |
LIG_SUMO_SIM_par_1 | 471 | 479 | PF11976 | 0.514 |
LIG_SUMO_SIM_par_1 | 716 | 721 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 767 | 776 | PF11976 | 0.359 |
LIG_TRAF2_1 | 200 | 203 | PF00917 | 0.396 |
LIG_TRAF2_1 | 443 | 446 | PF00917 | 0.566 |
LIG_TRAF2_1 | 538 | 541 | PF00917 | 0.501 |
LIG_TRAF2_1 | 77 | 80 | PF00917 | 0.721 |
LIG_TRAF2_1 | 81 | 84 | PF00917 | 0.733 |
LIG_TRAF2_2 | 600 | 605 | PF00917 | 0.619 |
LIG_TYR_ITSM | 331 | 338 | PF00017 | 0.396 |
LIG_UBA3_1 | 512 | 519 | PF00899 | 0.386 |
LIG_UBA3_1 | 543 | 549 | PF00899 | 0.418 |
LIG_WRC_WIRS_1 | 687 | 692 | PF05994 | 0.288 |
LIG_WW_2 | 74 | 77 | PF00397 | 0.496 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.511 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.415 |
MOD_CK1_1 | 475 | 481 | PF00069 | 0.393 |
MOD_CK1_1 | 568 | 574 | PF00069 | 0.314 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.594 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.365 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.175 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.249 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.396 |
MOD_CK2_1 | 260 | 266 | PF00069 | 0.438 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.396 |
MOD_CK2_1 | 466 | 472 | PF00069 | 0.380 |
MOD_CK2_1 | 535 | 541 | PF00069 | 0.488 |
MOD_CK2_1 | 595 | 601 | PF00069 | 0.529 |
MOD_CK2_1 | 761 | 767 | PF00069 | 0.422 |
MOD_CK2_1 | 769 | 775 | PF00069 | 0.393 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.651 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.555 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.404 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.399 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.741 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.499 |
MOD_GlcNHglycan | 684 | 687 | PF01048 | 0.300 |
MOD_GlcNHglycan | 82 | 88 | PF01048 | 0.686 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.529 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.341 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.504 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.467 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.423 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.611 |
MOD_GSK3_1 | 666 | 673 | PF00069 | 0.449 |
MOD_GSK3_1 | 682 | 689 | PF00069 | 0.213 |
MOD_N-GLC_1 | 142 | 147 | PF02516 | 0.636 |
MOD_N-GLC_1 | 154 | 159 | PF02516 | 0.621 |
MOD_N-GLC_1 | 212 | 217 | PF02516 | 0.281 |
MOD_N-GLC_1 | 416 | 421 | PF02516 | 0.680 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.263 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.299 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.411 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.280 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.288 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.281 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.385 |
MOD_NEK2_1 | 512 | 517 | PF00069 | 0.420 |
MOD_NEK2_1 | 682 | 687 | PF00069 | 0.354 |
MOD_NEK2_1 | 697 | 702 | PF00069 | 0.334 |
MOD_NEK2_1 | 729 | 734 | PF00069 | 0.466 |
MOD_NEK2_1 | 761 | 766 | PF00069 | 0.503 |
MOD_NEK2_2 | 218 | 223 | PF00069 | 0.263 |
MOD_PIKK_1 | 62 | 68 | PF00454 | 0.734 |
MOD_PIKK_1 | 697 | 703 | PF00454 | 0.461 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.262 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.407 |
MOD_PKA_2 | 363 | 369 | PF00069 | 0.294 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.668 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.645 |
MOD_PKA_2 | 761 | 767 | PF00069 | 0.470 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.636 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.625 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.279 |
MOD_Plk_1 | 333 | 339 | PF00069 | 0.294 |
MOD_Plk_1 | 504 | 510 | PF00069 | 0.490 |
MOD_Plk_1 | 649 | 655 | PF00069 | 0.444 |
MOD_Plk_1 | 766 | 772 | PF00069 | 0.502 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.666 |
MOD_Plk_2-3 | 142 | 148 | PF00069 | 0.636 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.374 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.602 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.396 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.294 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.575 |
MOD_Plk_4 | 472 | 478 | PF00069 | 0.472 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.497 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.482 |
MOD_Plk_4 | 560 | 566 | PF00069 | 0.526 |
MOD_Plk_4 | 636 | 642 | PF00069 | 0.628 |
MOD_Plk_4 | 649 | 655 | PF00069 | 0.405 |
MOD_Plk_4 | 714 | 720 | PF00069 | 0.377 |
MOD_Plk_4 | 766 | 772 | PF00069 | 0.474 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.396 |
MOD_ProDKin_1 | 619 | 625 | PF00069 | 0.402 |
MOD_ProDKin_1 | 66 | 72 | PF00069 | 0.603 |
MOD_ProDKin_1 | 666 | 672 | PF00069 | 0.471 |
MOD_ProDKin_1 | 676 | 682 | PF00069 | 0.358 |
MOD_SUMO_for_1 | 187 | 190 | PF00179 | 0.249 |
MOD_SUMO_for_1 | 77 | 80 | PF00179 | 0.617 |
MOD_SUMO_rev_2 | 160 | 168 | PF00179 | 0.479 |
MOD_SUMO_rev_2 | 593 | 600 | PF00179 | 0.521 |
MOD_SUMO_rev_2 | 601 | 608 | PF00179 | 0.489 |
TRG_DiLeu_BaEn_3 | 242 | 248 | PF01217 | 0.294 |
TRG_ENDOCYTIC_2 | 223 | 226 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 335 | 338 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 702 | 705 | PF00928 | 0.430 |
TRG_ER_diArg_1 | 506 | 509 | PF00400 | 0.353 |
TRG_NES_CRM1_1 | 185 | 198 | PF08389 | 0.306 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEC9 | Leptomonas seymouri | 71% | 100% |
A0A0S4J374 | Bodo saltans | 30% | 90% |
A0A1X0NQC6 | Trypanosomatidae | 44% | 100% |
A0A3R7KDY4 | Trypanosoma rangeli | 40% | 100% |
A0A3S7WRD0 | Leishmania donovani | 97% | 100% |
A4H696 | Leishmania braziliensis | 90% | 100% |
A4HUL9 | Leishmania infantum | 97% | 100% |
C9ZVP6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9ANB8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
V5BTU8 | Trypanosoma cruzi | 39% | 100% |