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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 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:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HLM1
Term | Name | Level | Count |
---|---|---|---|
GO:0001522 | pseudouridine synthesis | 6 | 11 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009451 | RNA modification | 5 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0009982 | pseudouridine synthase activity | 4 | 11 |
GO:0016853 | isomerase activity | 2 | 11 |
GO:0016866 | intramolecular transferase activity | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 655 | 659 | PF00656 | 0.674 |
CLV_C14_Caspase3-7 | 894 | 898 | PF00656 | 0.587 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 547 | 549 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 606 | 608 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 635 | 637 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 730 | 732 | PF00675 | 0.748 |
CLV_PCSK_FUR_1 | 275 | 279 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.722 |
CLV_PCSK_KEX2_1 | 546 | 548 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 605 | 607 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 635 | 637 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 730 | 732 | PF00082 | 0.746 |
CLV_PCSK_KEX2_1 | 831 | 833 | PF00082 | 0.755 |
CLV_PCSK_PC1ET2_1 | 103 | 105 | PF00082 | 0.542 |
CLV_PCSK_PC1ET2_1 | 546 | 548 | PF00082 | 0.566 |
CLV_PCSK_PC1ET2_1 | 831 | 833 | PF00082 | 0.781 |
CLV_PCSK_PC7_1 | 271 | 277 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 445 | 449 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 458 | 462 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 636 | 640 | PF00082 | 0.621 |
CLV_PCSK_SKI1_1 | 662 | 666 | PF00082 | 0.761 |
CLV_PCSK_SKI1_1 | 754 | 758 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 787 | 791 | PF00082 | 0.686 |
CLV_PCSK_SKI1_1 | 834 | 838 | PF00082 | 0.708 |
CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.601 |
DEG_APCC_DBOX_1 | 457 | 465 | PF00400 | 0.525 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.715 |
DEG_SIAH_1 | 821 | 829 | PF03145 | 0.713 |
DOC_ANK_TNKS_1 | 31 | 38 | PF00023 | 0.509 |
DOC_ANK_TNKS_1 | 325 | 332 | PF00023 | 0.507 |
DOC_CKS1_1 | 81 | 86 | PF01111 | 0.707 |
DOC_CYCLIN_RxL_1 | 751 | 761 | PF00134 | 0.545 |
DOC_MAPK_MEF2A_6 | 445 | 452 | PF00069 | 0.410 |
DOC_MAPK_NFAT4_5 | 445 | 453 | PF00069 | 0.281 |
DOC_PP4_FxxP_1 | 774 | 777 | PF00568 | 0.593 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 816 | 820 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 846 | 850 | PF00917 | 0.604 |
DOC_USP7_UBL2_3 | 99 | 103 | PF12436 | 0.639 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 481 | 486 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 520 | 525 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 662 | 667 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 724 | 729 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 738 | 743 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.759 |
LIG_14-3-3_CanoR_1 | 104 | 110 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 286 | 293 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 375 | 381 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 671 | 676 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 734 | 742 | PF00244 | 0.765 |
LIG_14-3-3_CanoR_1 | 834 | 841 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 879 | 883 | PF00244 | 0.536 |
LIG_Actin_WH2_2 | 163 | 179 | PF00022 | 0.454 |
LIG_Actin_WH2_2 | 882 | 898 | PF00022 | 0.549 |
LIG_BRCT_BRCA1_1 | 348 | 352 | PF00533 | 0.364 |
LIG_BRCT_BRCA1_1 | 530 | 534 | PF00533 | 0.423 |
LIG_CSL_BTD_1 | 129 | 132 | PF09270 | 0.493 |
LIG_deltaCOP1_diTrp_1 | 589 | 596 | PF00928 | 0.486 |
LIG_deltaCOP1_diTrp_1 | 614 | 623 | PF00928 | 0.233 |
LIG_EVH1_1 | 774 | 778 | PF00568 | 0.375 |
LIG_EVH1_2 | 280 | 284 | PF00568 | 0.331 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.494 |
LIG_FHA_1 | 415 | 421 | PF00498 | 0.304 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.273 |
LIG_FHA_1 | 535 | 541 | PF00498 | 0.478 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.668 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.475 |
LIG_FHA_1 | 835 | 841 | PF00498 | 0.656 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.506 |
LIG_FHA_2 | 565 | 571 | PF00498 | 0.574 |
LIG_FHA_2 | 698 | 704 | PF00498 | 0.580 |
LIG_FHA_2 | 786 | 792 | PF00498 | 0.632 |
LIG_FHA_2 | 799 | 805 | PF00498 | 0.420 |
LIG_HCF-1_HBM_1 | 722 | 725 | PF13415 | 0.464 |
LIG_HP1_1 | 457 | 461 | PF01393 | 0.535 |
LIG_LIR_Apic_2 | 722 | 728 | PF02991 | 0.471 |
LIG_LIR_Apic_2 | 773 | 777 | PF02991 | 0.588 |
LIG_LIR_Gen_1 | 157 | 168 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 614 | 625 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 157 | 163 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 614 | 620 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 750 | 756 | PF02991 | 0.512 |
LIG_PCNA_yPIPBox_3 | 474 | 487 | PF02747 | 0.427 |
LIG_PDZ_Class_1 | 895 | 900 | PF00595 | 0.644 |
LIG_PDZ_Wminus1_1 | 898 | 900 | PF00595 | 0.430 |
LIG_Pex14_1 | 770 | 774 | PF04695 | 0.561 |
LIG_REV1ctd_RIR_1 | 532 | 540 | PF16727 | 0.489 |
LIG_SH2_CRK | 490 | 494 | PF00017 | 0.390 |
LIG_SH2_CRK | 725 | 729 | PF00017 | 0.487 |
LIG_SH2_NCK_1 | 264 | 268 | PF00017 | 0.414 |
LIG_SH2_NCK_1 | 549 | 553 | PF00017 | 0.480 |
LIG_SH2_SRC | 202 | 205 | PF00017 | 0.457 |
LIG_SH2_SRC | 47 | 50 | PF00017 | 0.710 |
LIG_SH2_SRC | 549 | 552 | PF00017 | 0.466 |
LIG_SH2_STAP1 | 287 | 291 | PF00017 | 0.495 |
LIG_SH2_STAP1 | 490 | 494 | PF00017 | 0.390 |
LIG_SH2_STAP1 | 549 | 553 | PF00017 | 0.463 |
LIG_SH2_STAT3 | 93 | 96 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.666 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.700 |
LIG_SH2_STAT5 | 521 | 524 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.406 |
LIG_SH3_1 | 772 | 778 | PF00018 | 0.362 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.728 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.611 |
LIG_SH3_3 | 647 | 653 | PF00018 | 0.565 |
LIG_SH3_3 | 772 | 778 | PF00018 | 0.362 |
LIG_SH3_3 | 780 | 786 | PF00018 | 0.459 |
LIG_Sin3_3 | 212 | 219 | PF02671 | 0.443 |
LIG_SUMO_SIM_anti_2 | 674 | 679 | PF11976 | 0.323 |
LIG_SUMO_SIM_anti_2 | 887 | 894 | PF11976 | 0.270 |
LIG_SUMO_SIM_par_1 | 429 | 435 | PF11976 | 0.369 |
LIG_SUMO_SIM_par_1 | 694 | 704 | PF11976 | 0.640 |
LIG_TRFH_1 | 649 | 653 | PF08558 | 0.339 |
LIG_TYR_ITIM | 488 | 493 | PF00017 | 0.501 |
LIG_WRC_WIRS_1 | 106 | 111 | PF05994 | 0.642 |
LIG_WRC_WIRS_1 | 302 | 307 | PF05994 | 0.468 |
LIG_WRC_WIRS_1 | 620 | 625 | PF05994 | 0.236 |
LIG_WW_3 | 279 | 283 | PF00397 | 0.355 |
MOD_CDC14_SPxK_1 | 484 | 487 | PF00782 | 0.617 |
MOD_CDC14_SPxK_1 | 727 | 730 | PF00782 | 0.489 |
MOD_CDK_SPxK_1 | 481 | 487 | PF00069 | 0.651 |
MOD_CDK_SPxK_1 | 724 | 730 | PF00069 | 0.487 |
MOD_CDK_SPxxK_3 | 664 | 671 | PF00069 | 0.500 |
MOD_CDK_SPxxK_3 | 724 | 731 | PF00069 | 0.490 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.651 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.736 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.685 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.529 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.548 |
MOD_CK1_1 | 701 | 707 | PF00069 | 0.460 |
MOD_CK1_1 | 732 | 738 | PF00069 | 0.792 |
MOD_CK1_1 | 743 | 749 | PF00069 | 0.662 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.689 |
MOD_CK1_1 | 854 | 860 | PF00069 | 0.522 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.602 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.597 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.613 |
MOD_CK2_1 | 564 | 570 | PF00069 | 0.578 |
MOD_CK2_1 | 697 | 703 | PF00069 | 0.605 |
MOD_CK2_1 | 770 | 776 | PF00069 | 0.535 |
MOD_CK2_1 | 785 | 791 | PF00069 | 0.591 |
MOD_CMANNOS | 592 | 595 | PF00535 | 0.505 |
MOD_Cter_Amidation | 633 | 636 | PF01082 | 0.401 |
MOD_DYRK1A_RPxSP_1 | 239 | 243 | PF00069 | 0.680 |
MOD_DYRK1A_RPxSP_1 | 662 | 666 | PF00069 | 0.520 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.761 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.582 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.663 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.275 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.496 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.613 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.519 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.515 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.655 |
MOD_GlcNHglycan | 662 | 665 | PF01048 | 0.764 |
MOD_GlcNHglycan | 671 | 674 | PF01048 | 0.700 |
MOD_GlcNHglycan | 742 | 745 | PF01048 | 0.635 |
MOD_GlcNHglycan | 848 | 851 | PF01048 | 0.598 |
MOD_GlcNHglycan | 857 | 860 | PF01048 | 0.649 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.437 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.739 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.644 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.639 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.663 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.568 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.674 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.515 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.423 |
MOD_GSK3_1 | 660 | 667 | PF00069 | 0.775 |
MOD_GSK3_1 | 669 | 676 | PF00069 | 0.681 |
MOD_GSK3_1 | 697 | 704 | PF00069 | 0.548 |
MOD_GSK3_1 | 846 | 853 | PF00069 | 0.539 |
MOD_N-GLC_1 | 197 | 202 | PF02516 | 0.460 |
MOD_N-GLC_1 | 748 | 753 | PF02516 | 0.649 |
MOD_N-GLC_1 | 792 | 797 | PF02516 | 0.650 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.746 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.597 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.579 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.620 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.589 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.413 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.393 |
MOD_NEK2_1 | 669 | 674 | PF00069 | 0.571 |
MOD_NEK2_1 | 729 | 734 | PF00069 | 0.638 |
MOD_NEK2_1 | 855 | 860 | PF00069 | 0.534 |
MOD_NEK2_1 | 895 | 900 | PF00069 | 0.567 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.629 |
MOD_NEK2_2 | 348 | 353 | PF00069 | 0.470 |
MOD_NEK2_2 | 685 | 690 | PF00069 | 0.496 |
MOD_NEK2_2 | 792 | 797 | PF00069 | 0.377 |
MOD_PIKK_1 | 113 | 119 | PF00454 | 0.749 |
MOD_PIKK_1 | 729 | 735 | PF00454 | 0.743 |
MOD_PIKK_1 | 743 | 749 | PF00454 | 0.729 |
MOD_PIKK_1 | 804 | 810 | PF00454 | 0.515 |
MOD_PK_1 | 671 | 677 | PF00069 | 0.379 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.471 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.516 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.522 |
MOD_PKA_2 | 729 | 735 | PF00069 | 0.673 |
MOD_PKA_2 | 878 | 884 | PF00069 | 0.536 |
MOD_PKB_1 | 832 | 840 | PF00069 | 0.683 |
MOD_Plk_1 | 748 | 754 | PF00069 | 0.637 |
MOD_Plk_1 | 792 | 798 | PF00069 | 0.642 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.496 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.605 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.607 |
MOD_Plk_4 | 673 | 679 | PF00069 | 0.337 |
MOD_Plk_4 | 792 | 798 | PF00069 | 0.604 |
MOD_Plk_4 | 851 | 857 | PF00069 | 0.636 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.701 |
MOD_ProDKin_1 | 481 | 487 | PF00069 | 0.656 |
MOD_ProDKin_1 | 520 | 526 | PF00069 | 0.432 |
MOD_ProDKin_1 | 662 | 668 | PF00069 | 0.735 |
MOD_ProDKin_1 | 724 | 730 | PF00069 | 0.624 |
MOD_ProDKin_1 | 738 | 744 | PF00069 | 0.718 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.757 |
MOD_SUMO_rev_2 | 189 | 199 | PF00179 | 0.383 |
TRG_DiLeu_BaLyEn_6 | 752 | 757 | PF01217 | 0.532 |
TRG_ENDOCYTIC_2 | 490 | 493 | PF00928 | 0.391 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 224 | 227 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 275 | 278 | PF00400 | 0.678 |
TRG_ER_diArg_1 | 547 | 549 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 604 | 607 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 623 | 626 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 729 | 731 | PF00400 | 0.736 |
TRG_ER_diArg_1 | 822 | 825 | PF00400 | 0.612 |
TRG_NES_CRM1_1 | 614 | 627 | PF08389 | 0.407 |
TRG_NLS_MonoExtC_3 | 545 | 551 | PF00514 | 0.508 |
TRG_NLS_MonoExtN_4 | 828 | 835 | PF00514 | 0.715 |
TRG_Pf-PMV_PEXEL_1 | 184 | 188 | PF00026 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 445 | 449 | PF00026 | 0.535 |
TRG_Pf-PMV_PEXEL_1 | 479 | 483 | PF00026 | 0.439 |
TRG_Pf-PMV_PEXEL_1 | 834 | 838 | PF00026 | 0.676 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0E0 | Leptomonas seymouri | 45% | 99% |
A0A1X0P134 | Trypanosomatidae | 25% | 100% |
A0A3Q8IEW6 | Leishmania donovani | 78% | 100% |
A0A3R7KAP3 | Trypanosoma rangeli | 29% | 100% |
A4I932 | Leishmania infantum | 78% | 100% |
D0A535 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9B3Z7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q4Q427 | Leishmania major | 78% | 100% |
V5BLS1 | Trypanosoma cruzi | 29% | 100% |