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: A0A3Q8IVN0
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_NRD_NRD_1 | 237 | 239 | PF00675 | 0.311 |
CLV_NRD_NRD_1 | 599 | 601 | PF00675 | 0.283 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.259 |
CLV_PCSK_KEX2_1 | 474 | 476 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 624 | 626 | PF00082 | 0.512 |
CLV_PCSK_PC1ET2_1 | 116 | 118 | PF00082 | 0.300 |
CLV_PCSK_PC1ET2_1 | 474 | 476 | PF00082 | 0.529 |
CLV_PCSK_PC1ET2_1 | 624 | 626 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.256 |
DEG_APCC_DBOX_1 | 329 | 337 | PF00400 | 0.399 |
DEG_ODPH_VHL_1 | 514 | 526 | PF01847 | 0.528 |
DOC_CDC14_PxL_1 | 24 | 32 | PF14671 | 0.545 |
DOC_CDC14_PxL_1 | 560 | 568 | PF14671 | 0.338 |
DOC_CYCLIN_RxL_1 | 405 | 414 | PF00134 | 0.180 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 392 | 401 | PF00134 | 0.273 |
DOC_CYCLIN_yCln2_LP_2 | 461 | 467 | PF00134 | 0.208 |
DOC_CYCLIN_yCln2_LP_2 | 503 | 509 | PF00134 | 0.407 |
DOC_MAPK_gen_1 | 474 | 482 | PF00069 | 0.330 |
DOC_MAPK_MEF2A_6 | 354 | 362 | PF00069 | 0.184 |
DOC_MAPK_MEF2A_6 | 41 | 49 | PF00069 | 0.558 |
DOC_MAPK_MEF2A_6 | 474 | 482 | PF00069 | 0.363 |
DOC_PP1_RVXF_1 | 380 | 387 | PF00149 | 0.485 |
DOC_PP2B_LxvP_1 | 395 | 398 | PF13499 | 0.385 |
DOC_PP2B_LxvP_1 | 410 | 413 | PF13499 | 0.325 |
DOC_PP2B_LxvP_1 | 503 | 506 | PF13499 | 0.348 |
DOC_PP4_FxxP_1 | 305 | 308 | PF00568 | 0.464 |
DOC_PP4_FxxP_1 | 374 | 377 | PF00568 | 0.326 |
DOC_PP4_FxxP_1 | 577 | 580 | PF00568 | 0.266 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.272 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.333 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 447 | 451 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 463 | 467 | PF00917 | 0.333 |
DOC_USP7_MATH_1 | 516 | 520 | PF00917 | 0.493 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.752 |
LIG_14-3-3_CanoR_1 | 67 | 71 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 87 | 92 | PF00244 | 0.498 |
LIG_Actin_WH2_2 | 9 | 27 | PF00022 | 0.496 |
LIG_APCC_ABBA_1 | 166 | 171 | PF00400 | 0.528 |
LIG_APCC_ABBA_1 | 231 | 236 | PF00400 | 0.415 |
LIG_BIR_III_4 | 301 | 305 | PF00653 | 0.551 |
LIG_BRCT_BRCA1_1 | 370 | 374 | PF00533 | 0.266 |
LIG_BRCT_BRCA1_1 | 418 | 422 | PF00533 | 0.325 |
LIG_BRCT_BRCA1_1 | 449 | 453 | PF00533 | 0.467 |
LIG_BRCT_BRCA1_1 | 520 | 524 | PF00533 | 0.500 |
LIG_EH1_1 | 495 | 503 | PF00400 | 0.379 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.536 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.345 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.436 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.360 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.365 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.388 |
LIG_FHA_1 | 567 | 573 | PF00498 | 0.425 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.210 |
LIG_FHA_2 | 608 | 614 | PF00498 | 0.696 |
LIG_GBD_Chelix_1 | 343 | 351 | PF00786 | 0.325 |
LIG_LIR_Apic_2 | 371 | 377 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 107 | 114 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 353 | 363 | PF02991 | 0.302 |
LIG_LIR_Gen_1 | 421 | 430 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 439 | 447 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 466 | 473 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 521 | 531 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 107 | 112 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 115 | 121 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 356 | 362 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 371 | 376 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 419 | 425 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 439 | 445 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 450 | 454 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 466 | 471 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 521 | 527 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 547 | 553 | PF02991 | 0.299 |
LIG_MLH1_MIPbox_1 | 370 | 374 | PF16413 | 0.408 |
LIG_NRBOX | 223 | 229 | PF00104 | 0.343 |
LIG_PCNA_TLS_4 | 307 | 314 | PF02747 | 0.393 |
LIG_Pex14_1 | 355 | 359 | PF04695 | 0.293 |
LIG_Pex14_2 | 418 | 422 | PF04695 | 0.313 |
LIG_Pex14_2 | 442 | 446 | PF04695 | 0.375 |
LIG_PTB_Apo_2 | 399 | 406 | PF02174 | 0.401 |
LIG_PTB_Phospho_1 | 399 | 405 | PF10480 | 0.411 |
LIG_SH2_CRK | 119 | 123 | PF00017 | 0.378 |
LIG_SH2_CRK | 134 | 138 | PF00017 | 0.332 |
LIG_SH2_CRK | 451 | 455 | PF00017 | 0.503 |
LIG_SH2_CRK | 85 | 89 | PF00017 | 0.515 |
LIG_SH2_GRB2like | 388 | 391 | PF00017 | 0.392 |
LIG_SH2_GRB2like | 394 | 397 | PF00017 | 0.415 |
LIG_SH2_GRB2like | 560 | 563 | PF00017 | 0.357 |
LIG_SH2_NCK_1 | 560 | 564 | PF00017 | 0.303 |
LIG_SH2_PTP2 | 15 | 18 | PF00017 | 0.638 |
LIG_SH2_PTP2 | 359 | 362 | PF00017 | 0.198 |
LIG_SH2_PTP2 | 583 | 586 | PF00017 | 0.208 |
LIG_SH2_SRC | 15 | 18 | PF00017 | 0.644 |
LIG_SH2_STAP1 | 114 | 118 | PF00017 | 0.508 |
LIG_SH2_STAP1 | 169 | 173 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.633 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.229 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 394 | 397 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 488 | 491 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 543 | 546 | PF00017 | 0.264 |
LIG_SH2_STAT5 | 583 | 586 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.399 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.695 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.548 |
LIG_SH3_3 | 403 | 409 | PF00018 | 0.339 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.287 |
LIG_SH3_3 | 457 | 463 | PF00018 | 0.208 |
LIG_SH3_3 | 581 | 587 | PF00018 | 0.401 |
LIG_SUMO_SIM_anti_2 | 469 | 474 | PF11976 | 0.326 |
LIG_SUMO_SIM_par_1 | 220 | 225 | PF11976 | 0.208 |
LIG_TRAF2_1 | 614 | 617 | PF00917 | 0.627 |
LIG_TRFH_1 | 134 | 138 | PF08558 | 0.372 |
LIG_TRFH_1 | 583 | 587 | PF08558 | 0.301 |
LIG_TYR_ITIM | 132 | 137 | PF00017 | 0.388 |
LIG_TYR_ITIM | 357 | 362 | PF00017 | 0.385 |
LIG_TYR_ITIM | 392 | 397 | PF00017 | 0.344 |
LIG_TYR_ITIM | 581 | 586 | PF00017 | 0.507 |
LIG_UBA3_1 | 132 | 140 | PF00899 | 0.359 |
LIG_UBA3_1 | 248 | 256 | PF00899 | 0.624 |
LIG_UBA3_1 | 467 | 474 | PF00899 | 0.334 |
LIG_WRC_WIRS_1 | 370 | 375 | PF05994 | 0.296 |
LIG_WRC_WIRS_1 | 40 | 45 | PF05994 | 0.566 |
LIG_WRC_WIRS_1 | 401 | 406 | PF05994 | 0.346 |
MOD_CDC14_SPxK_1 | 269 | 272 | PF00782 | 0.399 |
MOD_CDK_SPxK_1 | 266 | 272 | PF00069 | 0.399 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.393 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.562 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.208 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.368 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.517 |
MOD_CK2_1 | 607 | 613 | PF00069 | 0.723 |
MOD_Cter_Amidation | 598 | 601 | PF01082 | 0.328 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.387 |
MOD_GlcNHglycan | 141 | 145 | PF01048 | 0.506 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.290 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.397 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.325 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.389 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.401 |
MOD_GlcNHglycan | 587 | 590 | PF01048 | 0.402 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.496 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.303 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.322 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.385 |
MOD_GSK3_1 | 554 | 561 | PF00069 | 0.403 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.521 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.550 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.493 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.432 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.361 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.334 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.337 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.296 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.546 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.364 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.312 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.387 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.374 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.357 |
MOD_NEK2_1 | 533 | 538 | PF00069 | 0.364 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.309 |
MOD_NEK2_1 | 566 | 571 | PF00069 | 0.464 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.486 |
MOD_NEK2_2 | 369 | 374 | PF00069 | 0.468 |
MOD_NEK2_2 | 39 | 44 | PF00069 | 0.424 |
MOD_NEK2_2 | 463 | 468 | PF00069 | 0.379 |
MOD_PIKK_1 | 551 | 557 | PF00454 | 0.411 |
MOD_PKA_2 | 436 | 442 | PF00069 | 0.355 |
MOD_PKA_2 | 516 | 522 | PF00069 | 0.497 |
MOD_PKA_2 | 589 | 595 | PF00069 | 0.401 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.411 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.490 |
MOD_PKB_1 | 307 | 315 | PF00069 | 0.395 |
MOD_Plk_4 | 182 | 188 | PF00069 | 0.349 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.336 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.508 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.402 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.349 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.369 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.236 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.331 |
MOD_Plk_4 | 518 | 524 | PF00069 | 0.523 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.369 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.307 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.455 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.527 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.750 |
MOD_SUMO_rev_2 | 288 | 298 | PF00179 | 0.389 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 359 | 362 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 394 | 397 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 423 | 426 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 451 | 454 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 543 | 546 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 583 | 586 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.499 |
TRG_ER_diArg_1 | 173 | 176 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 237 | 240 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 306 | 309 | PF00400 | 0.546 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 42% | 89% |
A0A0N1HY49 | Leptomonas seymouri | 40% | 93% |
A0A0N1HZ06 | Leptomonas seymouri | 59% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 39% | 88% |
A0A0N1PAY4 | Leptomonas seymouri | 39% | 71% |
A0A0N1PB77 | Leptomonas seymouri | 70% | 97% |
A0A0N1PBZ2 | Leptomonas seymouri | 38% | 93% |
A0A0N1PCC1 | Leptomonas seymouri | 38% | 94% |
A0A0S4INN8 | Bodo saltans | 28% | 97% |
A0A381MBI0 | Leishmania infantum | 40% | 100% |
A0A3Q8I8X7 | Leishmania donovani | 40% | 100% |
A0A3Q8IAZ0 | Leishmania donovani | 36% | 100% |
A0A3Q8IH50 | Leishmania donovani | 40% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 37% | 98% |
A0A3S5H5P4 | Leishmania donovani | 41% | 93% |
A0A3S5H5V2 | Leishmania donovani | 45% | 96% |
A0A3S5H6F6 | Leishmania donovani | 37% | 90% |
A0A3S5H763 | Leishmania donovani | 42% | 93% |
A0A3S7WR10 | Leishmania donovani | 40% | 84% |
A0A3S7WR14 | Leishmania donovani | 37% | 91% |
A0A3S7WR15 | Leishmania donovani | 37% | 74% |
A0A3S7WR24 | Leishmania donovani | 38% | 89% |
A4H4T8 | Leishmania braziliensis | 45% | 100% |
A4H5Y4 | Leishmania braziliensis | 39% | 100% |
A4H617 | Leishmania braziliensis | 38% | 100% |
A4H618 | Leishmania braziliensis | 37% | 100% |
A4H619 | Leishmania braziliensis | 38% | 100% |
A4H620 | Leishmania braziliensis | 41% | 100% |
A4H6C3 | Leishmania braziliensis | 40% | 100% |
A4HNH7 | Leishmania braziliensis | 85% | 100% |
A4HSS2 | Leishmania infantum | 40% | 100% |
A4HUE4 | Leishmania infantum | 40% | 100% |
A4HUE5 | Leishmania infantum | 38% | 100% |
A4HUE6 | Leishmania infantum | 37% | 100% |
A4HUE7 | Leishmania infantum | 36% | 100% |
A4HUE8 | Leishmania infantum | 38% | 100% |
A4HUF4 | Leishmania infantum | 36% | 100% |
A4HUF5 | Leishmania infantum | 40% | 100% |
A4HYA9 | Leishmania infantum | 42% | 100% |
A4IC33 | Leishmania infantum | 97% | 100% |
C9ZIK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 96% |
C9ZIK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 96% |
C9ZVE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 99% |
C9ZVE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 99% |
C9ZVF1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 99% |
D0A423 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 98% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9AG72 | Leishmania infantum | 45% | 100% |
E9AI40 | Leishmania braziliensis | 38% | 100% |
E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 100% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9AN47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9ANE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QDC4 | Leishmania major | 42% | 100% |
Q4QH81 | Leishmania major | 39% | 100% |
Q4QHH7 | Leishmania major | 39% | 100% |
Q4QHH8 | Leishmania major | 37% | 100% |
Q4QHH9 | Leishmania major | 37% | 100% |
Q4QHI0 | Leishmania major | 37% | 100% |
Q4QHI1 | Leishmania major | 37% | 100% |
Q4QHI2 | Leishmania major | 37% | 100% |
Q4QIU9 | Leishmania major | 45% | 100% |
Q4QJ48 | Leishmania major | 40% | 100% |
Q7KIP2 | Leishmania major | 91% | 100% |