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: E9AL06
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 | 10 | 12 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.330 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.399 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 132 | 134 | PF00082 | 0.300 |
CLV_PCSK_PC1ET2_1 | 482 | 484 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 458 | 462 | PF00082 | 0.269 |
DOC_CDC14_PxL_1 | 40 | 48 | PF14671 | 0.524 |
DOC_CDC14_PxL_1 | 568 | 576 | PF14671 | 0.329 |
DOC_CKS1_1 | 580 | 585 | PF01111 | 0.441 |
DOC_CYCLIN_yCln2_LP_2 | 382 | 388 | PF00134 | 0.450 |
DOC_CYCLIN_yCln2_LP_2 | 580 | 586 | PF00134 | 0.402 |
DOC_MAPK_gen_1 | 132 | 138 | PF00069 | 0.514 |
DOC_MAPK_gen_1 | 259 | 267 | PF00069 | 0.560 |
DOC_MAPK_gen_1 | 456 | 464 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 482 | 490 | PF00069 | 0.323 |
DOC_MAPK_gen_1 | 596 | 605 | PF00069 | 0.592 |
DOC_MAPK_MEF2A_6 | 225 | 233 | PF00069 | 0.331 |
DOC_MAPK_MEF2A_6 | 390 | 397 | PF00069 | 0.473 |
DOC_MAPK_MEF2A_6 | 62 | 69 | PF00069 | 0.547 |
DOC_MAPK_NFAT4_5 | 62 | 70 | PF00069 | 0.608 |
DOC_PP2B_LxvP_1 | 382 | 385 | PF13499 | 0.450 |
DOC_PP2B_LxvP_1 | 403 | 406 | PF13499 | 0.385 |
DOC_PP2B_LxvP_1 | 585 | 588 | PF13499 | 0.375 |
DOC_PP2B_LxvP_1 | 592 | 595 | PF13499 | 0.335 |
DOC_PP4_FxxP_1 | 313 | 316 | PF00568 | 0.464 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.272 |
DOC_USP7_MATH_1 | 541 | 545 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 548 | 552 | PF00917 | 0.400 |
DOC_WW_Pin1_4 | 579 | 584 | PF00397 | 0.424 |
LIG_14-3-3_CanoR_1 | 103 | 108 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 483 | 491 | PF00244 | 0.182 |
LIG_APCC_ABBA_1 | 247 | 252 | PF00400 | 0.415 |
LIG_APCC_ABBA_1 | 49 | 54 | PF00400 | 0.634 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.769 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.608 |
LIG_BRCT_BRCA1_1 | 426 | 430 | PF00533 | 0.325 |
LIG_DLG_GKlike_1 | 103 | 110 | PF00625 | 0.427 |
LIG_EVH1_2 | 564 | 568 | PF00568 | 0.345 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.562 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.365 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.416 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.358 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.481 |
LIG_FHA_1 | 575 | 581 | PF00498 | 0.425 |
LIG_GBD_Chelix_1 | 464 | 472 | PF00786 | 0.481 |
LIG_GBD_Chelix_1 | 502 | 510 | PF00786 | 0.507 |
LIG_LIR_Apic_2 | 310 | 316 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 399 | 409 | PF02991 | 0.358 |
LIG_LIR_Gen_1 | 429 | 438 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 474 | 481 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 529 | 538 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 567 | 576 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 131 | 137 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 227 | 231 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 241 | 247 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 399 | 405 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 427 | 431 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 474 | 479 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 529 | 535 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 555 | 560 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 567 | 571 | PF02991 | 0.266 |
LIG_NRBOX | 396 | 402 | PF00104 | 0.419 |
LIG_Pex14_1 | 204 | 208 | PF04695 | 0.392 |
LIG_Pex14_2 | 168 | 172 | PF04695 | 0.376 |
LIG_Pex14_2 | 243 | 247 | PF04695 | 0.302 |
LIG_Pex14_2 | 426 | 430 | PF04695 | 0.318 |
LIG_Pex14_2 | 450 | 454 | PF04695 | 0.375 |
LIG_Pex14_2 | 59 | 63 | PF04695 | 0.494 |
LIG_PTB_Apo_2 | 567 | 574 | PF02174 | 0.328 |
LIG_PTB_Phospho_1 | 567 | 573 | PF10480 | 0.328 |
LIG_REV1ctd_RIR_1 | 451 | 460 | PF16727 | 0.388 |
LIG_SH2_CRK | 101 | 105 | PF00017 | 0.514 |
LIG_SH2_CRK | 135 | 139 | PF00017 | 0.386 |
LIG_SH2_CRK | 150 | 154 | PF00017 | 0.337 |
LIG_SH2_CRK | 342 | 346 | PF00017 | 0.357 |
LIG_SH2_CRK | 367 | 371 | PF00017 | 0.368 |
LIG_SH2_CRK | 431 | 435 | PF00017 | 0.311 |
LIG_SH2_CRK | 459 | 463 | PF00017 | 0.503 |
LIG_SH2_GRB2like | 396 | 399 | PF00017 | 0.389 |
LIG_SH2_NCK_1 | 367 | 371 | PF00017 | 0.422 |
LIG_SH2_PTP2 | 228 | 231 | PF00017 | 0.208 |
LIG_SH2_PTP2 | 48 | 51 | PF00017 | 0.640 |
LIG_SH2_SRC | 31 | 34 | PF00017 | 0.630 |
LIG_SH2_SRC | 396 | 399 | PF00017 | 0.501 |
LIG_SH2_SRC | 573 | 576 | PF00017 | 0.208 |
LIG_SH2_STAP1 | 130 | 134 | PF00017 | 0.508 |
LIG_SH2_STAP1 | 342 | 346 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 459 | 463 | PF00017 | 0.509 |
LIG_SH2_STAP1 | 504 | 508 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.267 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.592 |
LIG_SH2_STAT5 | 496 | 499 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 573 | 576 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.528 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.548 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.436 |
LIG_SH3_3 | 418 | 424 | PF00018 | 0.287 |
LIG_SH3_3 | 621 | 627 | PF00018 | 0.737 |
LIG_Sin3_3 | 590 | 597 | PF02671 | 0.208 |
LIG_SUMO_SIM_anti_2 | 175 | 181 | PF11976 | 0.373 |
LIG_SUMO_SIM_anti_2 | 477 | 482 | PF11976 | 0.325 |
LIG_SUMO_SIM_anti_2 | 582 | 588 | PF11976 | 0.462 |
LIG_SUMO_SIM_par_1 | 294 | 300 | PF11976 | 0.380 |
LIG_TRAF2_1 | 6 | 9 | PF00917 | 0.768 |
LIG_TRAF2_1 | 616 | 619 | PF00917 | 0.808 |
LIG_TRFH_1 | 150 | 154 | PF08558 | 0.372 |
LIG_TRFH_1 | 591 | 595 | PF08558 | 0.301 |
LIG_TYR_ITIM | 148 | 153 | PF00017 | 0.392 |
LIG_TYR_ITIM | 226 | 231 | PF00017 | 0.208 |
LIG_TYR_ITIM | 340 | 345 | PF00017 | 0.253 |
LIG_TYR_ITIM | 365 | 370 | PF00017 | 0.385 |
LIG_TYR_ITIM | 400 | 405 | PF00017 | 0.326 |
LIG_TYR_ITIM | 46 | 51 | PF00017 | 0.471 |
LIG_TYR_ITIM | 571 | 576 | PF00017 | 0.396 |
LIG_TYR_ITSM | 427 | 434 | PF00017 | 0.414 |
LIG_UBA3_1 | 217 | 225 | PF00899 | 0.208 |
LIG_UBA3_1 | 246 | 254 | PF00899 | 0.402 |
LIG_UBA3_1 | 475 | 482 | PF00899 | 0.334 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.361 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.344 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.228 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.202 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.289 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.373 |
MOD_GlcNHglycan | 157 | 161 | PF01048 | 0.368 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.692 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.382 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.432 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.408 |
MOD_GlcNHglycan | 560 | 563 | PF01048 | 0.388 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.402 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.322 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.390 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.325 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.386 |
MOD_N-GLC_1 | 254 | 259 | PF02516 | 0.390 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.403 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.378 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.358 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.291 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.338 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.360 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.379 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.337 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.364 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.374 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.375 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.377 |
MOD_NEK2_1 | 574 | 579 | PF00069 | 0.464 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.443 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.462 |
MOD_PIKK_1 | 178 | 184 | PF00454 | 0.337 |
MOD_PIKK_1 | 349 | 355 | PF00454 | 0.204 |
MOD_PK_1 | 294 | 300 | PF00069 | 0.181 |
MOD_PKA_2 | 524 | 530 | PF00069 | 0.346 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.281 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.350 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.348 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.327 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.200 |
MOD_Plk_4 | 294 | 300 | PF00069 | 0.421 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.365 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.470 |
MOD_Plk_4 | 464 | 470 | PF00069 | 0.335 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.328 |
MOD_Plk_4 | 508 | 514 | PF00069 | 0.326 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.350 |
MOD_Plk_4 | 620 | 626 | PF00069 | 0.665 |
MOD_ProDKin_1 | 579 | 585 | PF00069 | 0.424 |
MOD_SUMO_for_1 | 29 | 32 | PF00179 | 0.363 |
MOD_SUMO_rev_2 | 222 | 227 | PF00179 | 0.419 |
MOD_SUMO_rev_2 | 289 | 296 | PF00179 | 0.207 |
MOD_SUMO_rev_2 | 644 | 651 | PF00179 | 0.532 |
TRG_DiLeu_BaLyEn_6 | 335 | 340 | PF01217 | 0.388 |
TRG_DiLeu_BaLyEn_6 | 382 | 387 | PF01217 | 0.369 |
TRG_DiLeu_BaLyEn_6 | 580 | 585 | PF01217 | 0.331 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 228 | 231 | PF00928 | 0.208 |
TRG_ENDOCYTIC_2 | 342 | 345 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 402 | 405 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 459 | 462 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 573 | 576 | PF00928 | 0.428 |
TRG_ER_diArg_1 | 271 | 273 | PF00400 | 0.349 |
TRG_NES_CRM1_1 | 238 | 252 | PF08389 | 0.382 |
TRG_NES_CRM1_1 | 317 | 331 | PF08389 | 0.227 |
TRG_NES_CRM1_1 | 500 | 516 | PF08389 | 0.208 |
TRG_Pf-PMV_PEXEL_1 | 187 | 191 | PF00026 | 0.181 |
TRG_Pf-PMV_PEXEL_1 | 271 | 275 | PF00026 | 0.368 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 47% | 92% |
A0A0N1HY49 | Leptomonas seymouri | 45% | 97% |
A0A0N1HZ06 | Leptomonas seymouri | 47% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 41% | 91% |
A0A0N1PAY4 | Leptomonas seymouri | 40% | 74% |
A0A0N1PB77 | Leptomonas seymouri | 43% | 100% |
A0A0N1PBZ2 | Leptomonas seymouri | 42% | 97% |
A0A0N1PCC1 | Leptomonas seymouri | 44% | 97% |
A0A0S4IKN0 | Bodo saltans | 33% | 100% |
A0A381MBI0 | Leishmania infantum | 43% | 99% |
A0A3Q8I8X7 | Leishmania donovani | 43% | 99% |
A0A3Q8IAZ0 | Leishmania donovani | 43% | 93% |
A0A3Q8IH50 | Leishmania donovani | 44% | 90% |
A0A3Q8IVN0 | Leishmania donovani | 46% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 45% | 100% |
A0A3S5H5P4 | Leishmania donovani | 46% | 96% |
A0A3S5H5V2 | Leishmania donovani | 90% | 100% |
A0A3S5H6F6 | Leishmania donovani | 43% | 93% |
A0A3S5H763 | Leishmania donovani | 44% | 97% |
A0A3S7WR10 | Leishmania donovani | 46% | 100% |
A0A3S7WR14 | Leishmania donovani | 43% | 95% |
A0A3S7WR15 | Leishmania donovani | 41% | 77% |
A0A3S7WR24 | Leishmania donovani | 43% | 92% |
A4H4T8 | Leishmania braziliensis | 82% | 100% |
A4H5Y4 | Leishmania braziliensis | 44% | 100% |
A4H617 | Leishmania braziliensis | 43% | 100% |
A4H618 | Leishmania braziliensis | 44% | 100% |
A4H619 | Leishmania braziliensis | 44% | 100% |
A4H620 | Leishmania braziliensis | 46% | 100% |
A4H6C3 | Leishmania braziliensis | 44% | 100% |
A4HNH7 | Leishmania braziliensis | 45% | 100% |
A4HSS2 | Leishmania infantum | 46% | 96% |
A4HUE4 | Leishmania infantum | 46% | 100% |
A4HUE5 | Leishmania infantum | 40% | 94% |
A4HUE6 | Leishmania infantum | 43% | 95% |
A4HUE7 | Leishmania infantum | 43% | 93% |
A4HUE8 | Leishmania infantum | 43% | 92% |
A4HUF4 | Leishmania infantum | 43% | 93% |
A4HUF5 | Leishmania infantum | 43% | 99% |
A4HYA9 | Leishmania infantum | 44% | 97% |
A4IC33 | Leishmania infantum | 46% | 100% |
C9ZIK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
C9ZIK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
C9ZVE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
C9ZVE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
C9ZVF1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
D0A423 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9AG72 | Leishmania infantum | 89% | 100% |
E9AI40 | Leishmania braziliensis | 43% | 100% |
E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 87% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 99% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
E9AN47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 91% |
E9ANE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 99% |
E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 97% |
E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
Q4QDC4 | Leishmania major | 45% | 100% |
Q4QH81 | Leishmania major | 45% | 100% |
Q4QHH7 | Leishmania major | 44% | 100% |
Q4QHH8 | Leishmania major | 43% | 100% |
Q4QHH9 | Leishmania major | 43% | 100% |
Q4QHI0 | Leishmania major | 43% | 100% |
Q4QHI1 | Leishmania major | 45% | 100% |
Q4QHI2 | Leishmania major | 41% | 100% |
Q4QIU9 | Leishmania major | 90% | 100% |
Q4QJ48 | Leishmania major | 47% | 100% |
Q7KIP2 | Leishmania major | 45% | 100% |