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: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000151 | ubiquitin ligase complex | 3 | 2 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1990234 | transferase complex | 3 | 2 |
Related structures:
AlphaFold database: A0A3Q8II83
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 17 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 17 |
GO:0006807 | nitrogen compound metabolic process | 2 | 17 |
GO:0008152 | metabolic process | 1 | 17 |
GO:0009056 | catabolic process | 2 | 17 |
GO:0009057 | macromolecule catabolic process | 4 | 17 |
GO:0009987 | cellular process | 1 | 17 |
GO:0019538 | protein metabolic process | 3 | 17 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 17 |
GO:0043170 | macromolecule metabolic process | 3 | 17 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 17 |
GO:0044237 | cellular metabolic process | 2 | 17 |
GO:0044238 | primary metabolic process | 2 | 17 |
GO:0044248 | cellular catabolic process | 3 | 17 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 17 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 17 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 17 |
GO:0071704 | organic substance metabolic process | 2 | 17 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 17 |
GO:1901575 | organic substance catabolic process | 3 | 17 |
GO:0016567 | protein ubiquitination | 7 | 2 |
GO:0032446 | protein modification by small protein conjugation | 6 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 17 |
GO:0005515 | protein binding | 2 | 17 |
GO:0019899 | enzyme binding | 3 | 17 |
GO:0031625 | ubiquitin protein ligase binding | 5 | 17 |
GO:0044389 | ubiquitin-like protein ligase binding | 4 | 17 |
GO:0030674 | protein-macromolecule adaptor activity | 2 | 2 |
GO:0060090 | molecular adaptor activity | 1 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 4 | 8 | PF00656 | 0.483 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.318 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 512 | 514 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 710 | 712 | PF00675 | 0.568 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.276 |
CLV_PCSK_KEX2_1 | 417 | 419 | PF00082 | 0.318 |
CLV_PCSK_KEX2_1 | 512 | 514 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 692 | 694 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 216 | 218 | PF00082 | 0.260 |
CLV_PCSK_PC1ET2_1 | 417 | 419 | PF00082 | 0.318 |
CLV_PCSK_PC1ET2_1 | 692 | 694 | PF00082 | 0.442 |
CLV_PCSK_PC7_1 | 688 | 694 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 675 | 679 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 692 | 696 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 701 | 705 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.255 |
DEG_APCC_DBOX_1 | 133 | 141 | PF00400 | 0.518 |
DEG_APCC_DBOX_1 | 687 | 695 | PF00400 | 0.374 |
DEG_APCC_DBOX_1 | 78 | 86 | PF00400 | 0.518 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.458 |
DOC_ANK_TNKS_1 | 303 | 310 | PF00023 | 0.415 |
DOC_CKS1_1 | 124 | 129 | PF01111 | 0.518 |
DOC_CYCLIN_RxL_1 | 413 | 425 | PF00134 | 0.518 |
DOC_CYCLIN_RxL_1 | 697 | 708 | PF00134 | 0.384 |
DOC_MAPK_gen_1 | 118 | 125 | PF00069 | 0.518 |
DOC_MAPK_gen_1 | 325 | 334 | PF00069 | 0.432 |
DOC_MAPK_gen_1 | 383 | 392 | PF00069 | 0.558 |
DOC_MAPK_gen_1 | 512 | 520 | PF00069 | 0.439 |
DOC_MAPK_gen_1 | 76 | 85 | PF00069 | 0.454 |
DOC_PP1_RVXF_1 | 515 | 521 | PF00149 | 0.466 |
DOC_PP1_RVXF_1 | 545 | 551 | PF00149 | 0.529 |
DOC_PP4_FxxP_1 | 520 | 523 | PF00568 | 0.415 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 534 | 538 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 540 | 544 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 587 | 591 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 610 | 614 | PF00917 | 0.535 |
DOC_USP7_MATH_2 | 623 | 629 | PF00917 | 0.389 |
DOC_USP7_UBL2_3 | 27 | 31 | PF12436 | 0.594 |
DOC_USP7_UBL2_3 | 413 | 417 | PF12436 | 0.432 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.518 |
LIG_14-3-3_CanoR_1 | 118 | 124 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 128 | 137 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 220 | 229 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 246 | 256 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 350 | 359 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 641 | 651 | PF00244 | 0.727 |
LIG_14-3-3_CanoR_1 | 76 | 82 | PF00244 | 0.469 |
LIG_BRCT_BRCA1_1 | 197 | 201 | PF00533 | 0.518 |
LIG_Clathr_ClatBox_1 | 101 | 105 | PF01394 | 0.511 |
LIG_EH1_1 | 226 | 234 | PF00400 | 0.518 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.460 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.577 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.586 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.432 |
LIG_FHA_2 | 2 | 8 | PF00498 | 0.478 |
LIG_FHA_2 | 221 | 227 | PF00498 | 0.485 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.460 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.524 |
LIG_FHA_2 | 564 | 570 | PF00498 | 0.528 |
LIG_FHA_2 | 667 | 673 | PF00498 | 0.451 |
LIG_LIR_Apic_2 | 391 | 397 | PF02991 | 0.518 |
LIG_LIR_Apic_2 | 519 | 523 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 186 | 196 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 202 | 211 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 310 | 321 | PF02991 | 0.585 |
LIG_LIR_Gen_1 | 549 | 556 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 625 | 634 | PF02991 | 0.528 |
LIG_LIR_Gen_1 | 7 | 16 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 90 | 96 | PF02991 | 0.591 |
LIG_LIR_Gen_1 | 97 | 104 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 169 | 175 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 186 | 192 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 202 | 206 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 267 | 272 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 318 | 323 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 391 | 396 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 481 | 485 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 625 | 629 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 7 | 12 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 77 | 81 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 90 | 95 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 97 | 102 | PF02991 | 0.459 |
LIG_NRBOX | 136 | 142 | PF00104 | 0.518 |
LIG_PCNA_PIPBox_1 | 552 | 561 | PF02747 | 0.498 |
LIG_PCNA_yPIPBox_3 | 428 | 437 | PF02747 | 0.521 |
LIG_Pex14_2 | 269 | 273 | PF04695 | 0.518 |
LIG_SH2_CRK | 13 | 17 | PF00017 | 0.360 |
LIG_SH2_CRK | 172 | 176 | PF00017 | 0.482 |
LIG_SH2_CRK | 203 | 207 | PF00017 | 0.505 |
LIG_SH2_CRK | 313 | 317 | PF00017 | 0.460 |
LIG_SH2_CRK | 361 | 365 | PF00017 | 0.518 |
LIG_SH2_SRC | 424 | 427 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 313 | 317 | PF00017 | 0.574 |
LIG_SH2_STAP1 | 524 | 528 | PF00017 | 0.433 |
LIG_SH2_STAT3 | 43 | 46 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 394 | 397 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 461 | 464 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.336 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.488 |
LIG_SH3_3 | 480 | 486 | PF00018 | 0.515 |
LIG_SH3_3 | 711 | 717 | PF00018 | 0.401 |
LIG_SUMO_SIM_par_1 | 174 | 179 | PF11976 | 0.502 |
LIG_SUMO_SIM_par_1 | 682 | 687 | PF11976 | 0.428 |
LIG_TRAF2_1 | 566 | 569 | PF00917 | 0.415 |
LIG_TRAF2_1 | 669 | 672 | PF00917 | 0.524 |
LIG_TRFH_1 | 583 | 587 | PF08558 | 0.435 |
LIG_TYR_ITIM | 11 | 16 | PF00017 | 0.381 |
LIG_UBA3_1 | 282 | 288 | PF00899 | 0.574 |
LIG_WRC_WIRS_1 | 356 | 361 | PF05994 | 0.432 |
LIG_WRC_WIRS_1 | 626 | 631 | PF05994 | 0.538 |
MOD_CDK_SPK_2 | 123 | 128 | PF00069 | 0.432 |
MOD_CDK_SPxxK_3 | 20 | 27 | PF00069 | 0.572 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.415 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.488 |
MOD_CK1_1 | 492 | 498 | PF00069 | 0.449 |
MOD_CK1_1 | 563 | 569 | PF00069 | 0.548 |
MOD_CK1_1 | 604 | 610 | PF00069 | 0.465 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.510 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.460 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.474 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.510 |
MOD_CK2_1 | 563 | 569 | PF00069 | 0.541 |
MOD_CK2_1 | 574 | 580 | PF00069 | 0.507 |
MOD_CK2_1 | 666 | 672 | PF00069 | 0.426 |
MOD_CK2_1 | 684 | 690 | PF00069 | 0.303 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.281 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.313 |
MOD_GlcNHglycan | 519 | 523 | PF01048 | 0.314 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.269 |
MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.277 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.499 |
MOD_GlcNHglycan | 644 | 647 | PF01048 | 0.696 |
MOD_GlcNHglycan | 664 | 667 | PF01048 | 0.420 |
MOD_GlcNHglycan | 678 | 681 | PF01048 | 0.497 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.546 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.443 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.537 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.556 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.486 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.513 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.454 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.514 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.486 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.507 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.514 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.472 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.566 |
MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.215 |
MOD_N-GLC_2 | 338 | 340 | PF02516 | 0.318 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.538 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.473 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.459 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.495 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.487 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.497 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.468 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.499 |
MOD_NEK2_1 | 489 | 494 | PF00069 | 0.587 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.467 |
MOD_NEK2_1 | 570 | 575 | PF00069 | 0.464 |
MOD_NEK2_1 | 594 | 599 | PF00069 | 0.637 |
MOD_NEK2_1 | 662 | 667 | PF00069 | 0.470 |
MOD_NEK2_1 | 676 | 681 | PF00069 | 0.381 |
MOD_NEK2_1 | 684 | 689 | PF00069 | 0.442 |
MOD_PIKK_1 | 128 | 134 | PF00454 | 0.550 |
MOD_PIKK_1 | 247 | 253 | PF00454 | 0.509 |
MOD_PIKK_1 | 454 | 460 | PF00454 | 0.525 |
MOD_PIKK_1 | 560 | 566 | PF00454 | 0.454 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.432 |
MOD_PIKK_1 | 653 | 659 | PF00454 | 0.468 |
MOD_PIKK_1 | 706 | 712 | PF00454 | 0.407 |
MOD_PK_1 | 119 | 125 | PF00069 | 0.432 |
MOD_PKA_1 | 118 | 124 | PF00069 | 0.518 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.525 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.554 |
MOD_PKA_2 | 258 | 264 | PF00069 | 0.387 |
MOD_PKA_2 | 478 | 484 | PF00069 | 0.540 |
MOD_Plk_1 | 151 | 157 | PF00069 | 0.516 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.418 |
MOD_Plk_1 | 611 | 617 | PF00069 | 0.416 |
MOD_Plk_2-3 | 429 | 435 | PF00069 | 0.488 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.437 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.482 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.489 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.477 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.500 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.480 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.449 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.494 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.463 |
MOD_Plk_4 | 494 | 500 | PF00069 | 0.515 |
MOD_Plk_4 | 546 | 552 | PF00069 | 0.520 |
MOD_Plk_4 | 589 | 595 | PF00069 | 0.474 |
MOD_Plk_4 | 601 | 607 | PF00069 | 0.398 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.543 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.510 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.459 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.531 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.518 |
MOD_SUMO_for_1 | 159 | 162 | PF00179 | 0.518 |
MOD_SUMO_rev_2 | 212 | 218 | PF00179 | 0.602 |
MOD_SUMO_rev_2 | 260 | 265 | PF00179 | 0.554 |
MOD_SUMO_rev_2 | 687 | 694 | PF00179 | 0.554 |
TRG_DiLeu_BaEn_1 | 136 | 141 | PF01217 | 0.459 |
TRG_DiLeu_BaEn_1 | 700 | 705 | PF01217 | 0.385 |
TRG_DiLeu_BaEn_3 | 671 | 677 | PF01217 | 0.363 |
TRG_DiLeu_BaLyEn_6 | 415 | 420 | PF01217 | 0.452 |
TRG_DiLeu_BaLyEn_6 | 680 | 685 | PF01217 | 0.401 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 172 | 175 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 203 | 206 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.518 |
TRG_ENDOCYTIC_2 | 393 | 396 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.355 |
TRG_ER_diArg_1 | 246 | 249 | PF00400 | 0.387 |
TRG_NES_CRM1_1 | 545 | 557 | PF08389 | 0.462 |
TRG_Pf-PMV_PEXEL_1 | 138 | 143 | PF00026 | 0.318 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILK0 | Leptomonas seymouri | 68% | 93% |
A0A0N1PDU6 | Leptomonas seymouri | 23% | 93% |
A0A0S4J5R6 | Bodo saltans | 23% | 87% |
A0A1X0NS98 | Trypanosomatidae | 24% | 89% |
A0A3R7K7T8 | Trypanosoma rangeli | 25% | 89% |
A0A3S7X1Q2 | Leishmania donovani | 22% | 94% |
A4HGR5 | Leishmania braziliensis | 22% | 100% |
A4HGR6 | Leishmania braziliensis | 90% | 100% |
A4I3U0 | Leishmania infantum | 22% | 100% |
A4I3U1 | Leishmania infantum | 100% | 100% |
D0A911 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 89% |
E9B032 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
E9B033 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
Q4Q853 | Leishmania major | 98% | 100% |
Q4Q854 | Leishmania major | 22% | 100% |