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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0016020 | membrane | 2 | 3 |
Related structures:
AlphaFold database: E9AKI1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006396 | RNA processing | 6 | 10 |
GO:0006399 | tRNA metabolic process | 7 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008033 | tRNA processing | 8 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016070 | RNA metabolic process | 5 | 10 |
GO:0034470 | ncRNA processing | 7 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0034660 | ncRNA metabolic process | 6 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
GO:0006400 | tRNA modification | 6 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0031590 | wybutosine metabolic process | 4 | 1 |
GO:0031591 | wybutosine biosynthetic process | 5 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 1 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
GO:1901657 | glycosyl compound metabolic process | 4 | 1 |
GO:1901659 | glycosyl compound biosynthetic process | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0010181 | FMN binding | 4 | 10 |
GO:0016829 | lyase activity | 2 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0043169 | cation binding | 3 | 10 |
GO:0046872 | metal ion binding | 4 | 10 |
GO:0051536 | iron-sulfur cluster binding | 3 | 10 |
GO:0051539 | 4 iron, 4 sulfur cluster binding | 4 | 10 |
GO:0051540 | metal cluster binding | 2 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 160 | 164 | PF00656 | 0.432 |
CLV_C14_Caspase3-7 | 338 | 342 | PF00656 | 0.761 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.261 |
CLV_NRD_NRD_1 | 601 | 603 | PF00675 | 0.181 |
CLV_NRD_NRD_1 | 785 | 787 | PF00675 | 0.377 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.224 |
CLV_PCSK_PC1ET2_1 | 579 | 581 | PF00082 | 0.224 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.232 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.191 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.244 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.206 |
CLV_PCSK_SKI1_1 | 507 | 511 | PF00082 | 0.230 |
CLV_PCSK_SKI1_1 | 558 | 562 | PF00082 | 0.209 |
CLV_PCSK_SKI1_1 | 583 | 587 | PF00082 | 0.206 |
CLV_PCSK_SKI1_1 | 606 | 610 | PF00082 | 0.206 |
CLV_PCSK_SKI1_1 | 640 | 644 | PF00082 | 0.206 |
CLV_PCSK_SKI1_1 | 728 | 732 | PF00082 | 0.245 |
DEG_APCC_DBOX_1 | 53 | 61 | PF00400 | 0.589 |
DEG_MDM2_SWIB_1 | 586 | 594 | PF02201 | 0.406 |
DEG_MDM2_SWIB_1 | 731 | 739 | PF02201 | 0.515 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.321 |
DOC_CKS1_1 | 683 | 688 | PF01111 | 0.474 |
DOC_CYCLIN_yCln2_LP_2 | 12 | 18 | PF00134 | 0.271 |
DOC_MAPK_DCC_7 | 473 | 483 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 558 | 568 | PF00069 | 0.403 |
DOC_MAPK_gen_1 | 602 | 613 | PF00069 | 0.409 |
DOC_MAPK_MEF2A_6 | 475 | 483 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 558 | 566 | PF00069 | 0.413 |
DOC_PIKK_1 | 362 | 370 | PF02985 | 0.632 |
DOC_PP2B_LxvP_1 | 12 | 15 | PF13499 | 0.271 |
DOC_PP2B_LxvP_1 | 225 | 228 | PF13499 | 0.489 |
DOC_PP4_FxxP_1 | 230 | 233 | PF00568 | 0.488 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 693 | 697 | PF00917 | 0.331 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.478 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 501 | 506 | PF00397 | 0.406 |
DOC_WW_Pin1_4 | 571 | 576 | PF00397 | 0.394 |
DOC_WW_Pin1_4 | 682 | 687 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 761 | 766 | PF00397 | 0.458 |
LIG_14-3-3_CanoR_1 | 188 | 192 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 247 | 257 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 312 | 317 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 419 | 425 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 507 | 514 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 542 | 547 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 592 | 600 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 610 | 614 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 790 | 795 | PF00244 | 0.664 |
LIG_Actin_WH2_2 | 563 | 581 | PF00022 | 0.424 |
LIG_BRCT_BRCA1_1 | 169 | 173 | PF00533 | 0.414 |
LIG_BRCT_BRCA1_1 | 257 | 261 | PF00533 | 0.381 |
LIG_BRCT_BRCA1_1 | 468 | 472 | PF00533 | 0.424 |
LIG_Clathr_ClatBox_1 | 723 | 727 | PF01394 | 0.489 |
LIG_deltaCOP1_diTrp_1 | 732 | 738 | PF00928 | 0.515 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.512 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.457 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.505 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.491 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.438 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.504 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.620 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.406 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.406 |
LIG_FHA_1 | 617 | 623 | PF00498 | 0.406 |
LIG_FHA_1 | 780 | 786 | PF00498 | 0.614 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.584 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.501 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.372 |
LIG_FHA_2 | 336 | 342 | PF00498 | 0.634 |
LIG_FHA_2 | 572 | 578 | PF00498 | 0.406 |
LIG_FHA_2 | 735 | 741 | PF00498 | 0.440 |
LIG_FHA_2 | 754 | 760 | PF00498 | 0.389 |
LIG_GBD_Chelix_1 | 17 | 25 | PF00786 | 0.359 |
LIG_LIR_Gen_1 | 170 | 181 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 208 | 218 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 635 | 644 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 740 | 748 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 753 | 763 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 208 | 214 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 244 | 249 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 391 | 397 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 435 | 439 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 635 | 639 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 737 | 741 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 742 | 748 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 753 | 758 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 759 | 763 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 764 | 770 | PF02991 | 0.420 |
LIG_LYPXL_S_1 | 393 | 397 | PF13949 | 0.292 |
LIG_LYPXL_S_1 | 527 | 531 | PF13949 | 0.206 |
LIG_LYPXL_yS_3 | 394 | 397 | PF13949 | 0.499 |
LIG_LYPXL_yS_3 | 528 | 531 | PF13949 | 0.406 |
LIG_MAD2 | 783 | 791 | PF02301 | 0.593 |
LIG_Pex14_2 | 586 | 590 | PF04695 | 0.406 |
LIG_Pex14_2 | 731 | 735 | PF04695 | 0.526 |
LIG_PTB_Apo_2 | 547 | 554 | PF02174 | 0.406 |
LIG_SH2_CRK | 406 | 410 | PF00017 | 0.456 |
LIG_SH2_CRK | 491 | 495 | PF00017 | 0.489 |
LIG_SH2_CRK | 683 | 687 | PF00017 | 0.489 |
LIG_SH2_CRK | 760 | 764 | PF00017 | 0.450 |
LIG_SH2_NCK_1 | 745 | 749 | PF00017 | 0.495 |
LIG_SH2_NCK_1 | 760 | 764 | PF00017 | 0.416 |
LIG_SH2_STAP1 | 151 | 155 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 22 | 26 | PF00017 | 0.583 |
LIG_SH2_STAP1 | 236 | 240 | PF00017 | 0.519 |
LIG_SH2_STAP1 | 625 | 629 | PF00017 | 0.406 |
LIG_SH2_STAP1 | 741 | 745 | PF00017 | 0.523 |
LIG_SH2_STAT3 | 86 | 89 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 567 | 570 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 644 | 647 | PF00017 | 0.406 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.527 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.461 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.476 |
LIG_SH3_3 | 519 | 525 | PF00018 | 0.406 |
LIG_SH3_3 | 68 | 74 | PF00018 | 0.553 |
LIG_SH3_3 | 760 | 766 | PF00018 | 0.416 |
LIG_SH3_4 | 561 | 568 | PF00018 | 0.387 |
LIG_SUMO_SIM_anti_2 | 696 | 702 | PF11976 | 0.478 |
LIG_SUMO_SIM_par_1 | 722 | 727 | PF11976 | 0.489 |
LIG_TRAF2_1 | 574 | 577 | PF00917 | 0.424 |
LIG_TRAF2_1 | 702 | 705 | PF00917 | 0.510 |
LIG_TRAF2_2 | 554 | 559 | PF00917 | 0.422 |
LIG_TYR_ITIM | 20 | 25 | PF00017 | 0.511 |
LIG_TYR_ITIM | 392 | 397 | PF00017 | 0.487 |
LIG_TYR_ITIM | 526 | 531 | PF00017 | 0.406 |
LIG_TYR_ITIM | 758 | 763 | PF00017 | 0.543 |
LIG_UBA3_1 | 723 | 728 | PF00899 | 0.504 |
LIG_WRC_WIRS_1 | 543 | 548 | PF05994 | 0.428 |
LIG_WW_1 | 233 | 236 | PF00397 | 0.473 |
LIG_WW_3 | 166 | 170 | PF00397 | 0.489 |
MOD_CDK_SPxK_1 | 501 | 507 | PF00069 | 0.406 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.497 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.433 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.594 |
MOD_CK1_1 | 648 | 654 | PF00069 | 0.406 |
MOD_CK1_1 | 750 | 756 | PF00069 | 0.497 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.507 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.509 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.703 |
MOD_CK2_1 | 571 | 577 | PF00069 | 0.406 |
MOD_CMANNOS | 735 | 738 | PF00535 | 0.219 |
MOD_Cter_Amidation | 191 | 194 | PF01082 | 0.226 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.480 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.392 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.557 |
MOD_GlcNHglycan | 328 | 333 | PF01048 | 0.492 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.229 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.447 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.419 |
MOD_GlcNHglycan | 749 | 752 | PF01048 | 0.284 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.489 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.698 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.755 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.673 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.424 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.406 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.657 |
MOD_GSK3_1 | 640 | 647 | PF00069 | 0.406 |
MOD_GSK3_1 | 750 | 757 | PF00069 | 0.557 |
MOD_GSK3_1 | 790 | 797 | PF00069 | 0.606 |
MOD_N-GLC_1 | 439 | 444 | PF02516 | 0.317 |
MOD_N-GLC_2 | 138 | 140 | PF02516 | 0.374 |
MOD_N-GLC_2 | 455 | 457 | PF02516 | 0.206 |
MOD_N-GLC_2 | 667 | 669 | PF02516 | 0.131 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.444 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.406 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.724 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.441 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.406 |
MOD_NEK2_1 | 609 | 614 | PF00069 | 0.406 |
MOD_NEK2_1 | 747 | 752 | PF00069 | 0.472 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.359 |
MOD_NEK2_2 | 151 | 156 | PF00069 | 0.437 |
MOD_NEK2_2 | 266 | 271 | PF00069 | 0.575 |
MOD_NEK2_2 | 432 | 437 | PF00069 | 0.428 |
MOD_OFUCOSY | 714 | 720 | PF10250 | 0.206 |
MOD_PIKK_1 | 167 | 173 | PF00454 | 0.424 |
MOD_PIKK_1 | 239 | 245 | PF00454 | 0.536 |
MOD_PIKK_1 | 312 | 318 | PF00454 | 0.689 |
MOD_PIKK_1 | 439 | 445 | PF00454 | 0.516 |
MOD_PIKK_1 | 85 | 91 | PF00454 | 0.466 |
MOD_PKA_1 | 271 | 277 | PF00069 | 0.610 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.449 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.531 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.466 |
MOD_PKA_2 | 541 | 547 | PF00069 | 0.426 |
MOD_PKA_2 | 609 | 615 | PF00069 | 0.406 |
MOD_PKA_2 | 789 | 795 | PF00069 | 0.603 |
MOD_Plk_1 | 753 | 759 | PF00069 | 0.552 |
MOD_Plk_1 | 779 | 785 | PF00069 | 0.561 |
MOD_Plk_2-3 | 754 | 760 | PF00069 | 0.542 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.464 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.435 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.498 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.505 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.365 |
MOD_Plk_4 | 517 | 523 | PF00069 | 0.406 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.428 |
MOD_Plk_4 | 609 | 615 | PF00069 | 0.406 |
MOD_Plk_4 | 734 | 740 | PF00069 | 0.427 |
MOD_Plk_4 | 790 | 796 | PF00069 | 0.618 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.680 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.669 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.406 |
MOD_ProDKin_1 | 501 | 507 | PF00069 | 0.406 |
MOD_ProDKin_1 | 571 | 577 | PF00069 | 0.394 |
MOD_ProDKin_1 | 682 | 688 | PF00069 | 0.474 |
MOD_ProDKin_1 | 761 | 767 | PF00069 | 0.457 |
MOD_SUMO_rev_2 | 203 | 211 | PF00179 | 0.331 |
MOD_SUMO_rev_2 | 555 | 563 | PF00179 | 0.394 |
MOD_SUMO_rev_2 | 571 | 581 | PF00179 | 0.417 |
MOD_SUMO_rev_2 | 635 | 642 | PF00179 | 0.406 |
TRG_DiLeu_BaEn_1 | 388 | 393 | PF01217 | 0.509 |
TRG_ENDOCYTIC_2 | 22 | 25 | PF00928 | 0.653 |
TRG_ENDOCYTIC_2 | 394 | 397 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 406 | 409 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 491 | 494 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 567 | 570 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 625 | 628 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 741 | 744 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 745 | 748 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 760 | 763 | PF00928 | 0.455 |
TRG_ER_diArg_1 | 425 | 428 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 706 | 709 | PF00400 | 0.461 |
TRG_NES_CRM1_1 | 559 | 571 | PF08389 | 0.422 |
TRG_Pf-PMV_PEXEL_1 | 216 | 220 | PF00026 | 0.289 |
TRG_Pf-PMV_PEXEL_1 | 583 | 587 | PF00026 | 0.206 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I710 | Leptomonas seymouri | 67% | 90% |
A0A3S5H5J8 | Leishmania donovani | 89% | 97% |
A0A3S5IRA8 | Trypanosoma rangeli | 56% | 100% |
A4H4B8 | Leishmania braziliensis | 79% | 99% |
A4HSJ7 | Leishmania infantum | 89% | 97% |
C9ZU99 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 96% |
Q2KHP8 | Xenopus laevis | 41% | 100% |
Q4QJC7 | Leishmania major | 89% | 100% |
Q8BJM7 | Mus musculus | 42% | 100% |
V5AVD9 | Trypanosoma cruzi | 54% | 97% |