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: 9 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 52 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 71 |
NetGPI | no | yes: 0, no: 71 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 72 |
GO:0110165 | cellular anatomical entity | 1 | 72 |
GO:0005737 | cytoplasm | 2 | 6 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: E9AI40
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0015877 | biopterin transport | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 1 |
GO:0015224 | biopterin transmembrane transporter activity | 3 | 1 |
GO:0022857 | transmembrane transporter activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 282 | 286 | PF00656 | 0.482 |
CLV_C14_Caspase3-7 | 303 | 307 | PF00656 | 0.535 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 638 | 640 | PF00675 | 0.281 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 481 | 483 | PF00082 | 0.214 |
CLV_PCSK_KEX2_1 | 507 | 509 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 676 | 678 | PF00082 | 0.472 |
CLV_PCSK_PC1ET2_1 | 133 | 135 | PF00082 | 0.300 |
CLV_PCSK_PC1ET2_1 | 295 | 297 | PF00082 | 0.385 |
CLV_PCSK_PC1ET2_1 | 481 | 483 | PF00082 | 0.214 |
CLV_PCSK_PC1ET2_1 | 507 | 509 | PF00082 | 0.529 |
CLV_PCSK_PC1ET2_1 | 676 | 678 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.371 |
DEG_COP1_1 | 301 | 313 | PF00400 | 0.388 |
DOC_CDC14_PxL_1 | 597 | 605 | PF14671 | 0.338 |
DOC_CYCLIN_yCln2_LP_2 | 614 | 620 | PF00134 | 0.380 |
DOC_CYCLIN_yCln2_LP_2 | 654 | 660 | PF00134 | 0.577 |
DOC_MAPK_gen_1 | 133 | 139 | PF00069 | 0.507 |
DOC_MAPK_gen_1 | 257 | 267 | PF00069 | 0.555 |
DOC_MAPK_gen_1 | 272 | 280 | PF00069 | 0.547 |
DOC_MAPK_gen_1 | 481 | 488 | PF00069 | 0.448 |
DOC_MAPK_gen_1 | 507 | 515 | PF00069 | 0.330 |
DOC_MAPK_gen_1 | 624 | 633 | PF00069 | 0.591 |
DOC_MAPK_MEF2A_6 | 227 | 234 | PF00069 | 0.336 |
DOC_MAPK_MEF2A_6 | 507 | 515 | PF00069 | 0.363 |
DOC_MAPK_RevD_3 | 467 | 482 | PF00069 | 0.353 |
DOC_PP1_RVXF_1 | 483 | 489 | PF00149 | 0.513 |
DOC_PP2B_LxvP_1 | 614 | 617 | PF13499 | 0.366 |
DOC_PP2B_LxvP_1 | 620 | 623 | PF13499 | 0.335 |
DOC_PP2B_PxIxI_1 | 227 | 233 | PF00149 | 0.288 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.272 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.333 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 526 | 530 | PF00917 | 0.325 |
DOC_USP7_MATH_1 | 549 | 553 | PF00917 | 0.493 |
DOC_USP7_UBL2_3 | 636 | 640 | PF12436 | 0.449 |
DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 429 | 434 | PF00397 | 0.342 |
DOC_WW_Pin1_4 | 653 | 658 | PF00397 | 0.630 |
LIG_14-3-3_CanoR_1 | 257 | 267 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 485 | 489 | PF00244 | 0.498 |
LIG_APCC_ABBA_1 | 50 | 55 | PF00400 | 0.641 |
LIG_APCC_ABBAyCdc20_2 | 30 | 36 | PF00400 | 0.535 |
LIG_APCC_ABBAyCdc20_2 | 49 | 55 | PF00400 | 0.507 |
LIG_BRCT_BRCA1_1 | 451 | 455 | PF00533 | 0.325 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.575 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.347 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.404 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.594 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.360 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.261 |
LIG_FHA_1 | 485 | 491 | PF00498 | 0.494 |
LIG_FHA_1 | 498 | 504 | PF00498 | 0.359 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.562 |
LIG_GBD_Chelix_1 | 384 | 392 | PF00786 | 0.473 |
LIG_HP1_1 | 539 | 543 | PF01393 | 0.409 |
LIG_LIR_Apic_2 | 336 | 342 | PF02991 | 0.537 |
LIG_LIR_Apic_2 | 404 | 410 | PF02991 | 0.411 |
LIG_LIR_Apic_2 | 580 | 584 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 124 | 131 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 183 | 194 | PF02991 | 0.526 |
LIG_LIR_Gen_1 | 202 | 209 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 454 | 463 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 473 | 479 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 491 | 497 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 554 | 564 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 87 | 95 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 124 | 129 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 359 | 365 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 404 | 409 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 452 | 456 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 473 | 478 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 491 | 496 | PF02991 | 0.330 |
LIG_Pex14_2 | 169 | 173 | PF04695 | 0.376 |
LIG_Pex14_2 | 451 | 455 | PF04695 | 0.313 |
LIG_Pex14_2 | 475 | 479 | PF04695 | 0.375 |
LIG_PTB_Apo_2 | 447 | 454 | PF02174 | 0.377 |
LIG_PTB_Phospho_1 | 447 | 453 | PF10480 | 0.408 |
LIG_SH2_CRK | 102 | 106 | PF00017 | 0.520 |
LIG_SH2_CRK | 136 | 140 | PF00017 | 0.378 |
LIG_SH2_CRK | 151 | 155 | PF00017 | 0.332 |
LIG_SH2_CRK | 186 | 190 | PF00017 | 0.522 |
LIG_SH2_CRK | 339 | 343 | PF00017 | 0.620 |
LIG_SH2_CRK | 367 | 371 | PF00017 | 0.357 |
LIG_SH2_CRK | 456 | 460 | PF00017 | 0.306 |
LIG_SH2_CRK | 581 | 585 | PF00017 | 0.332 |
LIG_SH2_GRB2like | 427 | 430 | PF00017 | 0.415 |
LIG_SH2_GRB2like | 438 | 441 | PF00017 | 0.363 |
LIG_SH2_NCK_1 | 456 | 460 | PF00017 | 0.308 |
LIG_SH2_PTP2 | 427 | 430 | PF00017 | 0.360 |
LIG_SH2_PTP2 | 512 | 515 | PF00017 | 0.402 |
LIG_SH2_SRC | 427 | 430 | PF00017 | 0.486 |
LIG_SH2_SRC | 438 | 441 | PF00017 | 0.352 |
LIG_SH2_STAP1 | 131 | 135 | PF00017 | 0.508 |
LIG_SH2_STAP1 | 186 | 190 | PF00017 | 0.494 |
LIG_SH2_STAP1 | 367 | 371 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 557 | 561 | PF00017 | 0.350 |
LIG_SH2_STAP1 | 88 | 92 | PF00017 | 0.544 |
LIG_SH2_STAT3 | 421 | 424 | PF00017 | 0.208 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 427 | 430 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 477 | 480 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 521 | 524 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.530 |
LIG_SH3_1 | 339 | 345 | PF00018 | 0.589 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.599 |
LIG_SH3_3 | 606 | 612 | PF00018 | 0.351 |
LIG_SUMO_SIM_par_1 | 539 | 545 | PF11976 | 0.340 |
LIG_TRFH_1 | 151 | 155 | PF08558 | 0.372 |
LIG_TYR_ITIM | 149 | 154 | PF00017 | 0.388 |
LIG_UBA3_1 | 149 | 157 | PF00899 | 0.359 |
LIG_UBA3_1 | 167 | 175 | PF00899 | 0.195 |
LIG_Vh1_VBS_1 | 365 | 383 | PF01044 | 0.418 |
LIG_Vh1_VBS_1 | 455 | 473 | PF01044 | 0.397 |
LIG_WRC_WIRS_1 | 490 | 495 | PF05994 | 0.316 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.364 |
MOD_CK1_1 | 480 | 486 | PF00069 | 0.363 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.423 |
MOD_Cter_Amidation | 293 | 296 | PF01082 | 0.476 |
MOD_GlcNHglycan | 158 | 162 | PF01048 | 0.362 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.382 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.347 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.204 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.402 |
MOD_GlcNHglycan | 660 | 663 | PF01048 | 0.680 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.417 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.450 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.430 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.478 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.408 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.371 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.380 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.374 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.386 |
MOD_N-GLC_1 | 449 | 454 | PF02516 | 0.366 |
MOD_N-GLC_2 | 442 | 444 | PF02516 | 0.200 |
MOD_N-GLC_2 | 608 | 610 | PF02516 | 0.492 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.387 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.292 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.349 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.356 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.337 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.420 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.375 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.376 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.307 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.405 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.366 |
MOD_NEK2_1 | 488 | 493 | PF00069 | 0.374 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.364 |
MOD_NEK2_2 | 228 | 233 | PF00069 | 0.474 |
MOD_NEK2_2 | 29 | 34 | PF00069 | 0.381 |
MOD_PKA_2 | 484 | 490 | PF00069 | 0.360 |
MOD_PKA_2 | 549 | 555 | PF00069 | 0.346 |
MOD_Plk_1 | 13 | 19 | PF00069 | 0.476 |
MOD_Plk_1 | 449 | 455 | PF00069 | 0.384 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.349 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.336 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.526 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.402 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.445 |
MOD_Plk_4 | 551 | 557 | PF00069 | 0.382 |
MOD_Plk_4 | 616 | 622 | PF00069 | 0.379 |
MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.227 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.480 |
MOD_ProDKin_1 | 429 | 435 | PF00069 | 0.342 |
MOD_ProDKin_1 | 653 | 659 | PF00069 | 0.528 |
MOD_SUMO_rev_2 | 629 | 638 | PF00179 | 0.418 |
TRG_DiLeu_BaLyEn_6 | 598 | 603 | PF01217 | 0.392 |
TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 136 | 139 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 186 | 189 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 427 | 430 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 456 | 459 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 512 | 515 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 537 | 540 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 557 | 560 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.361 |
TRG_ER_diArg_1 | 275 | 278 | PF00400 | 0.329 |
TRG_ER_diArg_1 | 47 | 49 | PF00400 | 0.582 |
TRG_NLS_MonoExtC_3 | 638 | 644 | PF00514 | 0.330 |
TRG_NLS_MonoExtN_4 | 636 | 643 | PF00514 | 0.183 |
TRG_Pf-PMV_PEXEL_1 | 257 | 262 | PF00026 | 0.493 |
TRG_Pf-PMV_PEXEL_1 | 317 | 321 | PF00026 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 81 | 86 | PF00026 | 0.205 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 48% | 97% |
A0A0N1HY49 | Leptomonas seymouri | 45% | 100% |
A0A0N1HZ06 | Leptomonas seymouri | 38% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 40% | 95% |
A0A0N1PAY4 | Leptomonas seymouri | 47% | 77% |
A0A0N1PB77 | Leptomonas seymouri | 35% | 100% |
A0A0N1PBZ2 | Leptomonas seymouri | 65% | 100% |
A0A0N1PCC1 | Leptomonas seymouri | 43% | 100% |
A0A0S4INN8 | Bodo saltans | 29% | 100% |
A0A381MBI0 | Leishmania infantum | 46% | 100% |
A0A3Q8I8X7 | Leishmania donovani | 46% | 100% |
A0A3Q8IAZ0 | Leishmania donovani | 77% | 97% |
A0A3Q8IH50 | Leishmania donovani | 60% | 94% |
A0A3Q8IVN0 | Leishmania donovani | 38% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 42% | 100% |
A0A3S5H5P4 | Leishmania donovani | 43% | 100% |
A0A3S5H5V2 | Leishmania donovani | 45% | 100% |
A0A3S5H6F6 | Leishmania donovani | 77% | 97% |
A0A3S5H763 | Leishmania donovani | 52% | 100% |
A0A3S7WR10 | Leishmania donovani | 44% | 91% |
A0A3S7WR14 | Leishmania donovani | 74% | 99% |
A0A3S7WR15 | Leishmania donovani | 77% | 80% |
A0A3S7WR24 | Leishmania donovani | 76% | 97% |
A4H4T8 | Leishmania braziliensis | 42% | 96% |
A4H5Y4 | Leishmania braziliensis | 46% | 100% |
A4H617 | Leishmania braziliensis | 84% | 100% |
A4H618 | Leishmania braziliensis | 83% | 100% |
A4H619 | Leishmania braziliensis | 83% | 100% |
A4H620 | Leishmania braziliensis | 62% | 100% |
A4H6C3 | Leishmania braziliensis | 47% | 100% |
A4HNH7 | Leishmania braziliensis | 35% | 97% |
A4HSS2 | Leishmania infantum | 43% | 100% |
A4HUE4 | Leishmania infantum | 44% | 91% |
A4HUE5 | Leishmania infantum | 77% | 98% |
A4HUE6 | Leishmania infantum | 74% | 99% |
A4HUE7 | Leishmania infantum | 77% | 97% |
A4HUE8 | Leishmania infantum | 76% | 97% |
A4HUF4 | Leishmania infantum | 76% | 97% |
A4HUF5 | Leishmania infantum | 60% | 100% |
A4HYA9 | Leishmania infantum | 52% | 100% |
A4IC33 | Leishmania infantum | 38% | 100% |
C9ZIK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
C9ZIK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
C9ZVE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
C9ZVE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
C9ZVF1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
D0A423 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 98% |
E9AG72 | Leishmania infantum | 44% | 100% |
E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 91% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
E9AN47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 96% |
E9ANE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 100% |
E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
Q4QDC4 | Leishmania major | 53% | 100% |
Q4QH81 | Leishmania major | 46% | 100% |
Q4QHH7 | Leishmania major | 58% | 100% |
Q4QHH8 | Leishmania major | 72% | 100% |
Q4QHH9 | Leishmania major | 72% | 100% |
Q4QHI0 | Leishmania major | 74% | 100% |
Q4QHI1 | Leishmania major | 74% | 100% |
Q4QHI2 | Leishmania major | 79% | 100% |
Q4QIU9 | Leishmania major | 43% | 100% |
Q4QJ48 | Leishmania major | 44% | 100% |
Q7KIP2 | Leishmania major | 36% | 100% |