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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005802 | trans-Golgi network | 4 | 3 |
GO:0005829 | cytosol | 2 | 16 |
GO:0031984 | organelle subcompartment | 2 | 3 |
GO:0098791 | Golgi apparatus subcompartment | 3 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
GO:0005794 | Golgi apparatus | 5 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
Related structures:
AlphaFold database: Q4Q3V2
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 16 |
GO:0009987 | cellular process | 1 | 16 |
GO:0016043 | cellular component organization | 3 | 3 |
GO:0016192 | vesicle-mediated transport | 4 | 16 |
GO:0016197 | endosomal transport | 4 | 16 |
GO:0016482 | cytosolic transport | 4 | 16 |
GO:0042147 | retrograde transport, endosome to Golgi | 5 | 16 |
GO:0046907 | intracellular transport | 3 | 16 |
GO:0051179 | localization | 1 | 16 |
GO:0051234 | establishment of localization | 2 | 16 |
GO:0051641 | cellular localization | 2 | 16 |
GO:0051649 | establishment of localization in cell | 3 | 16 |
GO:0071840 | cellular component organization or biogenesis | 2 | 3 |
GO:0099022 | vesicle tethering | 4 | 3 |
GO:0099041 | vesicle tethering to Golgi | 5 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 356 | 360 | PF00656 | 0.604 |
CLV_C14_Caspase3-7 | 81 | 85 | PF00656 | 0.492 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.342 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 489 | 491 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 768 | 770 | PF00675 | 0.696 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.582 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 489 | 491 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 568 | 570 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 633 | 635 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 768 | 770 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.582 |
CLV_PCSK_PC1ET2_1 | 434 | 436 | PF00082 | 0.626 |
CLV_PCSK_PC1ET2_1 | 568 | 570 | PF00082 | 0.583 |
CLV_PCSK_PC1ET2_1 | 633 | 635 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 331 | 335 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 525 | 529 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 769 | 773 | PF00082 | 0.655 |
DEG_APCC_DBOX_1 | 117 | 125 | PF00400 | 0.495 |
DEG_APCC_DBOX_1 | 321 | 329 | PF00400 | 0.399 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.653 |
DEG_SCF_FBW7_1 | 384 | 389 | PF00400 | 0.435 |
DEG_SPOP_SBC_1 | 245 | 249 | PF00917 | 0.485 |
DEG_SPOP_SBC_1 | 792 | 796 | PF00917 | 0.752 |
DOC_CYCLIN_RxL_1 | 320 | 330 | PF00134 | 0.366 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 509 | 518 | PF00134 | 0.408 |
DOC_CYCLIN_yCln2_LP_2 | 304 | 310 | PF00134 | 0.443 |
DOC_MAPK_gen_1 | 322 | 328 | PF00069 | 0.424 |
DOC_MAPK_gen_1 | 732 | 740 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 525 | 533 | PF00069 | 0.487 |
DOC_MAPK_RevD_3 | 308 | 323 | PF00069 | 0.361 |
DOC_PP1_RVXF_1 | 294 | 301 | PF00149 | 0.443 |
DOC_PP1_RVXF_1 | 389 | 396 | PF00149 | 0.504 |
DOC_PP2B_LxvP_1 | 771 | 774 | PF13499 | 0.703 |
DOC_PP4_FxxP_1 | 257 | 260 | PF00568 | 0.443 |
DOC_PP4_FxxP_1 | 343 | 346 | PF00568 | 0.393 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 623 | 627 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 649 | 653 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 681 | 685 | PF00917 | 0.789 |
DOC_USP7_MATH_1 | 755 | 759 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 761 | 765 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 783 | 787 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 793 | 797 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 833 | 837 | PF00917 | 0.657 |
DOC_USP7_UBL2_3 | 582 | 586 | PF12436 | 0.458 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.290 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 552 | 557 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.769 |
DOC_WW_Pin1_4 | 739 | 744 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 774 | 779 | PF00397 | 0.765 |
DOC_WW_Pin1_4 | 788 | 793 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 828 | 833 | PF00397 | 0.626 |
LIG_14-3-3_CanoR_1 | 212 | 220 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 322 | 326 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 361 | 365 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 569 | 576 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 768 | 774 | PF00244 | 0.654 |
LIG_14-3-3_CanoR_1 | 806 | 811 | PF00244 | 0.714 |
LIG_14-3-3_CanoR_1 | 91 | 97 | PF00244 | 0.531 |
LIG_Actin_WH2_2 | 390 | 407 | PF00022 | 0.458 |
LIG_Actin_WH2_2 | 719 | 737 | PF00022 | 0.617 |
LIG_APCC_ABBA_1 | 395 | 400 | PF00400 | 0.493 |
LIG_BIR_III_2 | 444 | 448 | PF00653 | 0.548 |
LIG_Clathr_ClatBox_1 | 124 | 128 | PF01394 | 0.524 |
LIG_deltaCOP1_diTrp_1 | 299 | 302 | PF00928 | 0.420 |
LIG_EH1_1 | 547 | 555 | PF00400 | 0.397 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.469 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.435 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.531 |
LIG_FHA_1 | 245 | 251 | PF00498 | 0.395 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.378 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.559 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.617 |
LIG_FHA_1 | 539 | 545 | PF00498 | 0.436 |
LIG_FHA_1 | 662 | 668 | PF00498 | 0.782 |
LIG_FHA_1 | 735 | 741 | PF00498 | 0.662 |
LIG_FHA_2 | 172 | 178 | PF00498 | 0.508 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.443 |
LIG_FHA_2 | 405 | 411 | PF00498 | 0.558 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.702 |
LIG_LIR_Apic_2 | 190 | 195 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 299 | 308 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 461 | 471 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 818 | 828 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 143 | 148 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 222 | 227 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 299 | 303 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 461 | 467 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 818 | 824 | PF02991 | 0.559 |
LIG_NRBOX | 120 | 126 | PF00104 | 0.490 |
LIG_PCNA_PIPBox_1 | 270 | 279 | PF02747 | 0.443 |
LIG_PCNA_yPIPBox_3 | 212 | 224 | PF02747 | 0.497 |
LIG_PCNA_yPIPBox_3 | 270 | 283 | PF02747 | 0.443 |
LIG_PCNA_yPIPBox_3 | 71 | 80 | PF02747 | 0.564 |
LIG_Pex14_2 | 821 | 825 | PF04695 | 0.558 |
LIG_PTAP_UEV_1 | 750 | 755 | PF05743 | 0.542 |
LIG_SH2_CRK | 122 | 126 | PF00017 | 0.380 |
LIG_SH2_CRK | 224 | 228 | PF00017 | 0.427 |
LIG_SH2_CRK | 464 | 468 | PF00017 | 0.424 |
LIG_SH2_GRB2like | 192 | 195 | PF00017 | 0.524 |
LIG_SH2_NCK_1 | 243 | 247 | PF00017 | 0.484 |
LIG_SH2_SRC | 243 | 246 | PF00017 | 0.491 |
LIG_SH2_SRC | 451 | 454 | PF00017 | 0.492 |
LIG_SH2_STAP1 | 148 | 152 | PF00017 | 0.568 |
LIG_SH2_STAP1 | 291 | 295 | PF00017 | 0.438 |
LIG_SH2_STAT3 | 148 | 151 | PF00017 | 0.371 |
LIG_SH2_STAT3 | 258 | 261 | PF00017 | 0.434 |
LIG_SH2_STAT3 | 597 | 600 | PF00017 | 0.688 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 521 | 524 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 597 | 600 | PF00017 | 0.688 |
LIG_SH3_2 | 730 | 735 | PF14604 | 0.625 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.570 |
LIG_SH3_3 | 416 | 422 | PF00018 | 0.520 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.691 |
LIG_SH3_3 | 727 | 733 | PF00018 | 0.675 |
LIG_SH3_3 | 748 | 754 | PF00018 | 0.759 |
LIG_SH3_3 | 786 | 792 | PF00018 | 0.756 |
LIG_SUMO_SIM_anti_2 | 324 | 330 | PF11976 | 0.442 |
LIG_SUMO_SIM_anti_2 | 720 | 728 | PF11976 | 0.612 |
LIG_SUMO_SIM_par_1 | 123 | 129 | PF11976 | 0.552 |
LIG_SUMO_SIM_par_1 | 283 | 290 | PF11976 | 0.385 |
LIG_SUMO_SIM_par_1 | 736 | 742 | PF11976 | 0.567 |
LIG_SxIP_EBH_1 | 535 | 546 | PF03271 | 0.460 |
LIG_TRAF2_1 | 140 | 143 | PF00917 | 0.677 |
LIG_TRFH_1 | 395 | 399 | PF08558 | 0.476 |
LIG_UBA3_1 | 226 | 232 | PF00899 | 0.415 |
LIG_UBA3_1 | 325 | 331 | PF00899 | 0.462 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.515 |
MOD_CK1_1 | 458 | 464 | PF00069 | 0.465 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.794 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.728 |
MOD_CK1_1 | 640 | 646 | PF00069 | 0.604 |
MOD_CK1_1 | 651 | 657 | PF00069 | 0.652 |
MOD_CK1_1 | 670 | 676 | PF00069 | 0.704 |
MOD_CK1_1 | 679 | 685 | PF00069 | 0.682 |
MOD_CK1_1 | 791 | 797 | PF00069 | 0.802 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.559 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.485 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.564 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.709 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.704 |
MOD_CK2_1 | 635 | 641 | PF00069 | 0.736 |
MOD_CK2_1 | 710 | 716 | PF00069 | 0.707 |
MOD_CK2_1 | 761 | 767 | PF00069 | 0.813 |
MOD_CK2_1 | 839 | 845 | PF00069 | 0.693 |
MOD_Cter_Amidation | 566 | 569 | PF01082 | 0.489 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.604 |
MOD_GlcNHglycan | 587 | 590 | PF01048 | 0.713 |
MOD_GlcNHglycan | 593 | 597 | PF01048 | 0.705 |
MOD_GlcNHglycan | 653 | 656 | PF01048 | 0.718 |
MOD_GlcNHglycan | 667 | 670 | PF01048 | 0.630 |
MOD_GlcNHglycan | 673 | 676 | PF01048 | 0.619 |
MOD_GlcNHglycan | 678 | 681 | PF01048 | 0.765 |
MOD_GlcNHglycan | 751 | 754 | PF01048 | 0.735 |
MOD_GlcNHglycan | 758 | 761 | PF01048 | 0.652 |
MOD_GlcNHglycan | 763 | 766 | PF01048 | 0.547 |
MOD_GlcNHglycan | 795 | 798 | PF01048 | 0.726 |
MOD_GlcNHglycan | 808 | 811 | PF01048 | 0.564 |
MOD_GlcNHglycan | 841 | 844 | PF01048 | 0.723 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.389 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.511 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.709 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.434 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.463 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.815 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.356 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.495 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.791 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.846 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.589 |
MOD_GSK3_1 | 645 | 652 | PF00069 | 0.584 |
MOD_GSK3_1 | 661 | 668 | PF00069 | 0.646 |
MOD_GSK3_1 | 679 | 686 | PF00069 | 0.834 |
MOD_GSK3_1 | 769 | 776 | PF00069 | 0.742 |
MOD_GSK3_1 | 788 | 795 | PF00069 | 0.685 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.528 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.555 |
MOD_N-GLC_1 | 404 | 409 | PF02516 | 0.564 |
MOD_N-GLC_1 | 563 | 568 | PF02516 | 0.503 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.464 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.473 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.443 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.558 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.377 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.368 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.489 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.493 |
MOD_NEK2_1 | 662 | 667 | PF00069 | 0.719 |
MOD_NEK2_1 | 725 | 730 | PF00069 | 0.558 |
MOD_NEK2_1 | 734 | 739 | PF00069 | 0.610 |
MOD_NEK2_2 | 187 | 192 | PF00069 | 0.421 |
MOD_NEK2_2 | 92 | 97 | PF00069 | 0.661 |
MOD_PIKK_1 | 332 | 338 | PF00454 | 0.490 |
MOD_PIKK_1 | 386 | 392 | PF00454 | 0.443 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.560 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.443 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.474 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.595 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.410 |
MOD_PKA_2 | 635 | 641 | PF00069 | 0.593 |
MOD_PKA_2 | 702 | 708 | PF00069 | 0.693 |
MOD_PKA_2 | 734 | 740 | PF00069 | 0.726 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.559 |
MOD_Plk_1 | 187 | 193 | PF00069 | 0.540 |
MOD_Plk_1 | 826 | 832 | PF00069 | 0.770 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.538 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.308 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.392 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.433 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.447 |
MOD_Plk_4 | 734 | 740 | PF00069 | 0.696 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.396 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.660 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.612 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.288 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.425 |
MOD_ProDKin_1 | 552 | 558 | PF00069 | 0.534 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.766 |
MOD_ProDKin_1 | 739 | 745 | PF00069 | 0.665 |
MOD_ProDKin_1 | 774 | 780 | PF00069 | 0.767 |
MOD_ProDKin_1 | 788 | 794 | PF00069 | 0.675 |
MOD_ProDKin_1 | 828 | 834 | PF00069 | 0.626 |
MOD_SUMO_rev_2 | 63 | 72 | PF00179 | 0.650 |
TRG_DiLeu_BaEn_1 | 510 | 515 | PF01217 | 0.403 |
TRG_DiLeu_BaEn_1 | 721 | 726 | PF01217 | 0.682 |
TRG_DiLeu_BaEn_4 | 510 | 516 | PF01217 | 0.403 |
TRG_DiLeu_BaLyEn_6 | 280 | 285 | PF01217 | 0.443 |
TRG_DiLeu_BaLyEn_6 | 540 | 545 | PF01217 | 0.394 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 464 | 467 | PF00928 | 0.456 |
TRG_ER_diArg_1 | 282 | 284 | PF00400 | 0.343 |
TRG_ER_diArg_1 | 488 | 490 | PF00400 | 0.529 |
TRG_Pf-PMV_PEXEL_1 | 283 | 288 | PF00026 | 0.507 |
TRG_Pf-PMV_PEXEL_1 | 409 | 413 | PF00026 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 506 | 510 | PF00026 | 0.449 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P357 | Leptomonas seymouri | 57% | 99% |
A0A1X0P274 | Trypanosomatidae | 30% | 100% |
A0A3Q8IGR4 | Leishmania donovani | 92% | 99% |
A0A3R7MQU5 | Trypanosoma rangeli | 35% | 100% |
A0A3S7X2Z8 | Leishmania donovani | 92% | 96% |
A4HHY0 | Leishmania braziliensis | 76% | 100% |
A4HLU8 | Leishmania braziliensis | 76% | 100% |
A4I560 | Leishmania infantum | 92% | 77% |
C9ZQI6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AHQ3 | Leishmania infantum | 92% | 99% |
E9B0F7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 99% |
E9B474 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 99% |
Q4Q7S6 | Leishmania major | 100% | 100% |
V5DD41 | Trypanosoma cruzi | 38% | 100% |