Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 12 |
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: 6 |
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 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HJU8
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0019538 | protein metabolic process | 3 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004175 | endopeptidase activity | 4 | 10 |
GO:0004222 | metalloendopeptidase activity | 5 | 10 |
GO:0008233 | peptidase activity | 3 | 10 |
GO:0008237 | metallopeptidase activity | 4 | 10 |
GO:0016740 | transferase activity | 2 | 5 |
GO:0016757 | glycosyltransferase activity | 3 | 5 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 13 | 17 | PF00656 | 0.492 |
CLV_C14_Caspase3-7 | 629 | 633 | PF00656 | 0.375 |
CLV_C14_Caspase3-7 | 677 | 681 | PF00656 | 0.416 |
CLV_C14_Caspase3-7 | 737 | 741 | PF00656 | 0.633 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.370 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.326 |
CLV_NRD_NRD_1 | 705 | 707 | PF00675 | 0.523 |
CLV_PCSK_KEX2_1 | 270 | 272 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 617 | 619 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 705 | 707 | PF00082 | 0.523 |
CLV_PCSK_PC1ET2_1 | 617 | 619 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 651 | 655 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 671 | 675 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 706 | 710 | PF00082 | 0.514 |
DEG_APCC_DBOX_1 | 26 | 34 | PF00400 | 0.531 |
DEG_APCC_DBOX_1 | 552 | 560 | PF00400 | 0.451 |
DEG_APCC_DBOX_1 | 705 | 713 | PF00400 | 0.575 |
DOC_CKS1_1 | 112 | 117 | PF01111 | 0.473 |
DOC_CYCLIN_yCln2_LP_2 | 187 | 193 | PF00134 | 0.579 |
DOC_MAPK_gen_1 | 356 | 363 | PF00069 | 0.519 |
DOC_MAPK_MEF2A_6 | 356 | 363 | PF00069 | 0.304 |
DOC_PP1_RVXF_1 | 59 | 65 | PF00149 | 0.525 |
DOC_PP1_RVXF_1 | 590 | 597 | PF00149 | 0.380 |
DOC_PP2B_LxvP_1 | 187 | 190 | PF13499 | 0.595 |
DOC_PP2B_LxvP_1 | 233 | 236 | PF13499 | 0.368 |
DOC_PP2B_LxvP_1 | 733 | 736 | PF13499 | 0.501 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.514 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.368 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.368 |
DOC_WW_Pin1_4 | 482 | 487 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 525 | 530 | PF00397 | 0.446 |
LIG_14-3-3_CanoR_1 | 220 | 225 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 403 | 409 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 447 | 455 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 692 | 701 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 758 | 763 | PF00244 | 0.549 |
LIG_Actin_WH2_2 | 16 | 33 | PF00022 | 0.532 |
LIG_Actin_WH2_2 | 460 | 476 | PF00022 | 0.600 |
LIG_BRCT_BRCA1_1 | 542 | 546 | PF00533 | 0.412 |
LIG_CtBP_PxDLS_1 | 230 | 234 | PF00389 | 0.479 |
LIG_EH_1 | 238 | 242 | PF12763 | 0.368 |
LIG_EH1_1 | 500 | 508 | PF00400 | 0.280 |
LIG_eIF4E_1 | 431 | 437 | PF01652 | 0.517 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.619 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.449 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.514 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.559 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.432 |
LIG_FHA_1 | 694 | 700 | PF00498 | 0.543 |
LIG_FHA_1 | 728 | 734 | PF00498 | 0.638 |
LIG_FHA_2 | 162 | 168 | PF00498 | 0.787 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.462 |
LIG_FHA_2 | 607 | 613 | PF00498 | 0.358 |
LIG_FHA_2 | 658 | 664 | PF00498 | 0.561 |
LIG_FHA_2 | 735 | 741 | PF00498 | 0.573 |
LIG_GBD_Chelix_1 | 32 | 40 | PF00786 | 0.332 |
LIG_LIR_Gen_1 | 183 | 193 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 349 | 359 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 422 | 432 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 499 | 508 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 51 | 58 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 544 | 555 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 639 | 648 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 24 | 29 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 244 | 249 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 349 | 355 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 369 | 374 | PF02991 | 0.182 |
LIG_LIR_Nem_3 | 388 | 394 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 420 | 424 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 499 | 504 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 544 | 550 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 639 | 645 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 668 | 673 | PF02991 | 0.415 |
LIG_MLH1_MIPbox_1 | 543 | 547 | PF16413 | 0.423 |
LIG_Pex14_2 | 670 | 674 | PF04695 | 0.476 |
LIG_PTB_Apo_2 | 223 | 230 | PF02174 | 0.287 |
LIG_PTB_Phospho_1 | 223 | 229 | PF10480 | 0.287 |
LIG_REV1ctd_RIR_1 | 672 | 682 | PF16727 | 0.495 |
LIG_RPA_C_Fungi | 673 | 685 | PF08784 | 0.573 |
LIG_RPA_C_Fungi | 687 | 699 | PF08784 | 0.358 |
LIG_SH2_CRK | 208 | 212 | PF00017 | 0.514 |
LIG_SH2_CRK | 293 | 297 | PF00017 | 0.331 |
LIG_SH2_CRK | 301 | 305 | PF00017 | 0.372 |
LIG_SH2_CRK | 319 | 323 | PF00017 | 0.368 |
LIG_SH2_CRK | 37 | 41 | PF00017 | 0.406 |
LIG_SH2_CRK | 391 | 395 | PF00017 | 0.479 |
LIG_SH2_NCK_1 | 249 | 253 | PF00017 | 0.269 |
LIG_SH2_NCK_1 | 750 | 754 | PF00017 | 0.355 |
LIG_SH2_SRC | 374 | 377 | PF00017 | 0.406 |
LIG_SH2_SRC | 431 | 434 | PF00017 | 0.528 |
LIG_SH2_STAP1 | 301 | 305 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 319 | 323 | PF00017 | 0.288 |
LIG_SH2_STAP1 | 348 | 352 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 371 | 375 | PF00017 | 0.394 |
LIG_SH2_STAP1 | 750 | 754 | PF00017 | 0.583 |
LIG_SH2_STAT3 | 109 | 112 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 558 | 561 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 588 | 591 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 642 | 645 | PF00017 | 0.491 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.466 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.254 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.479 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.374 |
LIG_SH3_3 | 466 | 472 | PF00018 | 0.490 |
LIG_SH3_3 | 505 | 511 | PF00018 | 0.531 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.428 |
LIG_Sin3_3 | 351 | 358 | PF02671 | 0.406 |
LIG_SUMO_SIM_anti_2 | 360 | 365 | PF11976 | 0.406 |
LIG_SUMO_SIM_anti_2 | 9 | 16 | PF11976 | 0.335 |
LIG_SUMO_SIM_par_1 | 18 | 24 | PF11976 | 0.563 |
LIG_SUMO_SIM_par_1 | 696 | 702 | PF11976 | 0.340 |
LIG_SUMO_SIM_par_1 | 727 | 737 | PF11976 | 0.675 |
LIG_TRAF2_1 | 138 | 141 | PF00917 | 0.654 |
LIG_TRAF2_1 | 181 | 184 | PF00917 | 0.649 |
LIG_TRAF2_1 | 367 | 370 | PF00917 | 0.514 |
LIG_TRAF2_1 | 609 | 612 | PF00917 | 0.578 |
LIG_TRAF2_1 | 714 | 717 | PF00917 | 0.702 |
LIG_TYR_ITIM | 35 | 40 | PF00017 | 0.437 |
LIG_UBA3_1 | 394 | 400 | PF00899 | 0.287 |
LIG_UBA3_1 | 620 | 626 | PF00899 | 0.580 |
LIG_WRC_WIRS_1 | 424 | 429 | PF05994 | 0.553 |
LIG_WRC_WIRS_1 | 498 | 503 | PF05994 | 0.573 |
LIG_WRC_WIRS_1 | 735 | 740 | PF05994 | 0.609 |
MOD_CDK_SPK_2 | 482 | 487 | PF00069 | 0.388 |
MOD_CDK_SPK_2 | 525 | 530 | PF00069 | 0.574 |
MOD_CDK_SPxxK_3 | 292 | 299 | PF00069 | 0.411 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.505 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.485 |
MOD_CK1_1 | 659 | 665 | PF00069 | 0.557 |
MOD_CK1_1 | 690 | 696 | PF00069 | 0.460 |
MOD_CK1_1 | 724 | 730 | PF00069 | 0.701 |
MOD_CK1_1 | 749 | 755 | PF00069 | 0.577 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.715 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.710 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.438 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.479 |
MOD_CK2_1 | 595 | 601 | PF00069 | 0.548 |
MOD_CK2_1 | 606 | 612 | PF00069 | 0.396 |
MOD_CK2_1 | 643 | 649 | PF00069 | 0.569 |
MOD_CK2_1 | 657 | 663 | PF00069 | 0.525 |
MOD_CK2_1 | 711 | 717 | PF00069 | 0.707 |
MOD_CK2_1 | 740 | 746 | PF00069 | 0.508 |
MOD_CK2_1 | 749 | 755 | PF00069 | 0.410 |
MOD_GlcNHglycan | 165 | 170 | PF01048 | 0.775 |
MOD_GlcNHglycan | 176 | 181 | PF01048 | 0.603 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.399 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.346 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.427 |
MOD_GlcNHglycan | 597 | 600 | PF01048 | 0.389 |
MOD_GlcNHglycan | 689 | 692 | PF01048 | 0.433 |
MOD_GlcNHglycan | 701 | 704 | PF01048 | 0.459 |
MOD_GlcNHglycan | 751 | 754 | PF01048 | 0.589 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.544 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.767 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.481 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.611 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.582 |
MOD_GSK3_1 | 643 | 650 | PF00069 | 0.594 |
MOD_GSK3_1 | 674 | 681 | PF00069 | 0.491 |
MOD_GSK3_1 | 724 | 731 | PF00069 | 0.728 |
MOD_GSK3_1 | 736 | 743 | PF00069 | 0.521 |
MOD_GSK3_1 | 745 | 752 | PF00069 | 0.393 |
MOD_N-GLC_1 | 493 | 498 | PF02516 | 0.651 |
MOD_N-GLC_1 | 83 | 88 | PF02516 | 0.514 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.526 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.566 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.553 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.509 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.428 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.374 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.352 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.428 |
MOD_NEK2_1 | 541 | 546 | PF00069 | 0.385 |
MOD_NEK2_1 | 561 | 566 | PF00069 | 0.231 |
MOD_NEK2_1 | 643 | 648 | PF00069 | 0.490 |
MOD_NEK2_1 | 674 | 679 | PF00069 | 0.430 |
MOD_NEK2_1 | 699 | 704 | PF00069 | 0.393 |
MOD_NEK2_2 | 275 | 280 | PF00069 | 0.287 |
MOD_PIKK_1 | 341 | 347 | PF00454 | 0.479 |
MOD_PK_1 | 357 | 363 | PF00069 | 0.304 |
MOD_PK_1 | 758 | 764 | PF00069 | 0.385 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.479 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.506 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.578 |
MOD_PKA_2 | 480 | 486 | PF00069 | 0.503 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.526 |
MOD_Plk_1 | 15 | 21 | PF00069 | 0.474 |
MOD_Plk_1 | 244 | 250 | PF00069 | 0.368 |
MOD_Plk_1 | 493 | 499 | PF00069 | 0.659 |
MOD_Plk_1 | 727 | 733 | PF00069 | 0.587 |
MOD_Plk_1 | 745 | 751 | PF00069 | 0.502 |
MOD_Plk_2-3 | 126 | 132 | PF00069 | 0.456 |
MOD_Plk_2-3 | 161 | 167 | PF00069 | 0.738 |
MOD_Plk_2-3 | 370 | 376 | PF00069 | 0.497 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.497 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.457 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.514 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.631 |
MOD_Plk_4 | 502 | 508 | PF00069 | 0.532 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.423 |
MOD_Plk_4 | 728 | 734 | PF00069 | 0.602 |
MOD_Plk_4 | 758 | 764 | PF00069 | 0.420 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.479 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.488 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.422 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.368 |
MOD_ProDKin_1 | 482 | 488 | PF00069 | 0.460 |
MOD_ProDKin_1 | 525 | 531 | PF00069 | 0.446 |
MOD_SUMO_for_1 | 56 | 59 | PF00179 | 0.488 |
MOD_SUMO_rev_2 | 485 | 493 | PF00179 | 0.532 |
MOD_SUMO_rev_2 | 659 | 668 | PF00179 | 0.497 |
TRG_DiLeu_BaEn_1 | 433 | 438 | PF01217 | 0.520 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.246 |
TRG_ENDOCYTIC_2 | 348 | 351 | PF00928 | 0.477 |
TRG_ENDOCYTIC_2 | 37 | 40 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 391 | 394 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 53 | 56 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 558 | 561 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 642 | 645 | PF00928 | 0.535 |
TRG_ER_diArg_1 | 269 | 271 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 379 | 381 | PF00400 | 0.287 |
TRG_ER_diArg_1 | 478 | 481 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 550 | 553 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 705 | 707 | PF00400 | 0.522 |
TRG_Pf-PMV_PEXEL_1 | 111 | 116 | PF00026 | 0.601 |
TRG_Pf-PMV_PEXEL_1 | 618 | 622 | PF00026 | 0.502 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P423 | Leptomonas seymouri | 62% | 71% |
A0A1X0NIF3 | Trypanosomatidae | 39% | 71% |
A0A3R7LVD3 | Trypanosoma rangeli | 41% | 72% |
A0A3S7X521 | Leishmania donovani | 80% | 68% |
A4HJV3 | Leishmania braziliensis | 99% | 71% |
A4I7B5 | Leishmania infantum | 80% | 68% |
C9ZWJ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 72% |
E9B2A8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 71% |
O22941 | Arabidopsis thaliana | 23% | 79% |
Q4Q5U8 | Leishmania major | 78% | 100% |
V5BDV9 | Trypanosoma cruzi | 41% | 84% |