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. | yes | 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: 70 |
NetGPI | no | yes: 0, no: 70 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 7 |
GO:0016020 | membrane | 2 | 71 |
GO:0110165 | cellular anatomical entity | 1 | 71 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: Q4QHH9
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 | 669 | 673 | PF00656 | 0.803 |
CLV_MEL_PAP_1 | 442 | 448 | PF00089 | 0.285 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.454 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 523 | 525 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.455 |
CLV_PCSK_PC1ET2_1 | 137 | 139 | PF00082 | 0.331 |
CLV_PCSK_PC1ET2_1 | 523 | 525 | PF00082 | 0.556 |
CLV_PCSK_PC1ET2_1 | 9 | 11 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 120 | 124 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.383 |
DEG_APCC_DBOX_1 | 280 | 288 | PF00400 | 0.460 |
DEG_SPOP_SBC_1 | 667 | 671 | PF00917 | 0.636 |
DOC_CDC14_PxL_1 | 613 | 621 | PF14671 | 0.366 |
DOC_CKS1_1 | 625 | 630 | PF01111 | 0.467 |
DOC_CYCLIN_yCln2_LP_2 | 630 | 636 | PF00134 | 0.412 |
DOC_MAPK_gen_1 | 137 | 143 | PF00069 | 0.540 |
DOC_MAPK_gen_1 | 261 | 271 | PF00069 | 0.583 |
DOC_MAPK_gen_1 | 276 | 284 | PF00069 | 0.575 |
DOC_MAPK_gen_1 | 523 | 531 | PF00069 | 0.357 |
DOC_MAPK_gen_1 | 641 | 650 | PF00069 | 0.622 |
DOC_MAPK_MEF2A_6 | 231 | 238 | PF00069 | 0.363 |
DOC_MAPK_MEF2A_6 | 523 | 531 | PF00069 | 0.391 |
DOC_PP1_RVXF_1 | 499 | 505 | PF00149 | 0.554 |
DOC_PP2B_LxvP_1 | 630 | 633 | PF13499 | 0.399 |
DOC_PP2B_PxIxI_1 | 231 | 237 | PF00149 | 0.322 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 565 | 569 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 667 | 671 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 703 | 707 | PF00917 | 0.810 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 624 | 629 | PF00397 | 0.449 |
LIG_14-3-3_CanoR_1 | 108 | 113 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 261 | 271 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 501 | 505 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 581 | 590 | PF00244 | 0.533 |
LIG_Actin_WH2_2 | 54 | 69 | PF00022 | 0.655 |
LIG_APCC_ABBA_1 | 54 | 59 | PF00400 | 0.670 |
LIG_APCC_ABBAyCdc20_2 | 53 | 59 | PF00400 | 0.542 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.801 |
LIG_BIR_III_4 | 17 | 21 | PF00653 | 0.852 |
LIG_Clathr_ClatBox_1 | 269 | 273 | PF01394 | 0.482 |
LIG_EH1_1 | 503 | 511 | PF00400 | 0.375 |
LIG_eIF4E_1 | 613 | 619 | PF01652 | 0.265 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.604 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.372 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.625 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.391 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.293 |
LIG_FHA_1 | 485 | 491 | PF00498 | 0.429 |
LIG_FHA_1 | 501 | 507 | PF00498 | 0.526 |
LIG_FHA_1 | 625 | 631 | PF00498 | 0.452 |
LIG_FHA_2 | 273 | 279 | PF00498 | 0.605 |
LIG_FHA_2 | 602 | 608 | PF00498 | 0.262 |
LIG_GBD_Chelix_1 | 482 | 490 | PF00786 | 0.267 |
LIG_GBD_Chelix_1 | 505 | 513 | PF00786 | 0.509 |
LIG_GBD_Chelix_1 | 543 | 551 | PF00786 | 0.538 |
LIG_LIR_Apic_2 | 33 | 39 | PF02991 | 0.656 |
LIG_LIR_Apic_2 | 352 | 358 | PF02991 | 0.564 |
LIG_LIR_Apic_2 | 420 | 426 | PF02991 | 0.452 |
LIG_LIR_Apic_2 | 457 | 461 | PF02991 | 0.366 |
LIG_LIR_Apic_2 | 596 | 600 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 128 | 135 | PF02991 | 0.554 |
LIG_LIR_Gen_1 | 206 | 217 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 470 | 479 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 489 | 496 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 570 | 580 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 91 | 99 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 128 | 133 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 136 | 142 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.620 |
LIG_LIR_Nem_3 | 206 | 212 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 246 | 252 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 375 | 381 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 419 | 425 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 468 | 472 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 489 | 494 | PF02991 | 0.376 |
LIG_Pex14_2 | 173 | 177 | PF04695 | 0.400 |
LIG_Pex14_2 | 467 | 471 | PF04695 | 0.345 |
LIG_Pex14_2 | 491 | 495 | PF04695 | 0.406 |
LIG_PTB_Apo_2 | 463 | 470 | PF02174 | 0.407 |
LIG_PTB_Apo_2 | 489 | 496 | PF02174 | 0.474 |
LIG_PTB_Phospho_1 | 463 | 469 | PF10480 | 0.440 |
LIG_SH2_CRK | 106 | 110 | PF00017 | 0.546 |
LIG_SH2_CRK | 140 | 144 | PF00017 | 0.410 |
LIG_SH2_CRK | 155 | 159 | PF00017 | 0.361 |
LIG_SH2_CRK | 190 | 194 | PF00017 | 0.549 |
LIG_SH2_CRK | 355 | 359 | PF00017 | 0.653 |
LIG_SH2_CRK | 383 | 387 | PF00017 | 0.380 |
LIG_SH2_CRK | 458 | 462 | PF00017 | 0.362 |
LIG_SH2_CRK | 472 | 476 | PF00017 | 0.337 |
LIG_SH2_CRK | 597 | 601 | PF00017 | 0.359 |
LIG_SH2_CRK | 613 | 617 | PF00017 | 0.392 |
LIG_SH2_GRB2like | 454 | 457 | PF00017 | 0.392 |
LIG_SH2_GRB2like | 613 | 616 | PF00017 | 0.385 |
LIG_SH2_NCK_1 | 338 | 342 | PF00017 | 0.471 |
LIG_SH2_NCK_1 | 472 | 476 | PF00017 | 0.335 |
LIG_SH2_PTP2 | 36 | 39 | PF00017 | 0.650 |
LIG_SH2_PTP2 | 528 | 531 | PF00017 | 0.434 |
LIG_SH2_SRC | 338 | 341 | PF00017 | 0.474 |
LIG_SH2_SRC | 342 | 345 | PF00017 | 0.462 |
LIG_SH2_SRC | 36 | 39 | PF00017 | 0.656 |
LIG_SH2_STAP1 | 135 | 139 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 190 | 194 | PF00017 | 0.524 |
LIG_SH2_STAP1 | 338 | 342 | PF00017 | 0.466 |
LIG_SH2_STAP1 | 383 | 387 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 573 | 577 | PF00017 | 0.374 |
LIG_SH2_STAP1 | 92 | 96 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.645 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 454 | 457 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 528 | 531 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 537 | 540 | PF00017 | 0.328 |
LIG_SH3_1 | 355 | 361 | PF00018 | 0.620 |
LIG_SH3_3 | 355 | 361 | PF00018 | 0.631 |
LIG_SH3_3 | 443 | 449 | PF00018 | 0.394 |
LIG_SUMO_SIM_anti_2 | 518 | 523 | PF11976 | 0.355 |
LIG_SUMO_SIM_par_1 | 484 | 489 | PF11976 | 0.270 |
LIG_SUMO_SIM_par_1 | 556 | 561 | PF11976 | 0.363 |
LIG_TRFH_1 | 155 | 159 | PF08558 | 0.396 |
LIG_TYR_ITIM | 153 | 158 | PF00017 | 0.416 |
LIG_TYR_ITSM | 468 | 475 | PF00017 | 0.439 |
LIG_UBA3_1 | 153 | 161 | PF00899 | 0.393 |
LIG_UBA3_1 | 269 | 277 | PF00899 | 0.556 |
LIG_UBA3_1 | 490 | 497 | PF00899 | 0.450 |
LIG_UBA3_1 | 636 | 641 | PF00899 | 0.270 |
LIG_Vh1_VBS_1 | 381 | 399 | PF01044 | 0.442 |
LIG_Vh1_VBS_1 | 471 | 489 | PF01044 | 0.421 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.397 |
MOD_CK1_1 | 624 | 630 | PF00069 | 0.280 |
MOD_CK1_1 | 670 | 676 | PF00069 | 0.657 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.467 |
MOD_Cter_Amidation | 301 | 304 | PF01082 | 0.505 |
MOD_GlcNHglycan | 162 | 166 | PF01048 | 0.394 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.406 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.442 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.354 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.476 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.456 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.515 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.409 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.309 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.414 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.399 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.409 |
MOD_GSK3_1 | 620 | 627 | PF00069 | 0.419 |
MOD_GSK3_1 | 666 | 673 | PF00069 | 0.669 |
MOD_N-GLC_1 | 465 | 470 | PF02516 | 0.390 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.411 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.317 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.372 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.361 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.445 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.407 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.333 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.397 |
MOD_NEK2_1 | 504 | 509 | PF00069 | 0.401 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.390 |
MOD_NEK2_1 | 620 | 625 | PF00069 | 0.488 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.488 |
MOD_NEK2_2 | 232 | 237 | PF00069 | 0.503 |
MOD_OFUCOSY | 169 | 176 | PF10250 | 0.247 |
MOD_PIKK_1 | 183 | 189 | PF00454 | 0.361 |
MOD_PIKK_1 | 601 | 607 | PF00454 | 0.542 |
MOD_PK_1 | 440 | 446 | PF00069 | 0.423 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.411 |
MOD_PKA_2 | 500 | 506 | PF00069 | 0.384 |
MOD_PKA_2 | 565 | 571 | PF00069 | 0.369 |
MOD_PKA_2 | 583 | 589 | PF00069 | 0.369 |
MOD_Plk_1 | 465 | 471 | PF00069 | 0.408 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.380 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.371 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.390 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.544 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.429 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.498 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.361 |
MOD_Plk_4 | 486 | 492 | PF00069 | 0.241 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.380 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.416 |
MOD_Plk_4 | 632 | 638 | PF00069 | 0.416 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.509 |
MOD_ProDKin_1 | 624 | 630 | PF00069 | 0.449 |
MOD_SUMO_for_1 | 8 | 11 | PF00179 | 0.549 |
MOD_SUMO_rev_2 | 646 | 655 | PF00179 | 0.442 |
TRG_DiLeu_BaEn_2 | 265 | 271 | PF01217 | 0.350 |
TRG_DiLeu_BaLyEn_6 | 614 | 619 | PF01217 | 0.415 |
TRG_DiLeu_BaLyEn_6 | 625 | 630 | PF01217 | 0.355 |
TRG_ENDOCYTIC_2 | 106 | 109 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 3 | 6 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 472 | 475 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 573 | 576 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 613 | 616 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.387 |
TRG_ER_diArg_1 | 52 | 54 | PF00400 | 0.627 |
TRG_Pf-PMV_PEXEL_1 | 261 | 266 | PF00026 | 0.523 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 48% | 100% |
A0A0N1HY49 | Leptomonas seymouri | 45% | 100% |
A0A0N1HZ06 | Leptomonas seymouri | 37% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 37% | 99% |
A0A0N1PAY4 | Leptomonas seymouri | 46% | 80% |
A0A0N1PB77 | Leptomonas seymouri | 35% | 100% |
A0A0N1PBZ2 | Leptomonas seymouri | 67% | 100% |
A0A0N1PCC1 | Leptomonas seymouri | 41% | 100% |
A0A381MBI0 | Leishmania infantum | 43% | 100% |
A0A3Q8I8X7 | Leishmania donovani | 44% | 100% |
A0A3Q8IAZ0 | Leishmania donovani | 88% | 100% |
A0A3Q8IH50 | Leishmania donovani | 58% | 98% |
A0A3Q8IVN0 | Leishmania donovani | 37% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 41% | 100% |
A0A3S5H5P4 | Leishmania donovani | 43% | 100% |
A0A3S5H5V2 | Leishmania donovani | 43% | 100% |
A0A3S5H6F6 | Leishmania donovani | 91% | 100% |
A0A3S5H763 | Leishmania donovani | 51% | 100% |
A0A3S7WR10 | Leishmania donovani | 42% | 95% |
A0A3S7WR14 | Leishmania donovani | 79% | 100% |
A0A3S7WR15 | Leishmania donovani | 68% | 83% |
A0A3S7WR24 | Leishmania donovani | 92% | 100% |
A4H4T8 | Leishmania braziliensis | 43% | 100% |
A4H5Y4 | Leishmania braziliensis | 44% | 100% |
A4H617 | Leishmania braziliensis | 78% | 100% |
A4H618 | Leishmania braziliensis | 78% | 100% |
A4H619 | Leishmania braziliensis | 80% | 100% |
A4H620 | Leishmania braziliensis | 56% | 100% |
A4H6C3 | Leishmania braziliensis | 42% | 100% |
A4HNH7 | Leishmania braziliensis | 36% | 100% |
A4HSS2 | Leishmania infantum | 43% | 100% |
A4HUE4 | Leishmania infantum | 41% | 95% |
A4HUE5 | Leishmania infantum | 71% | 100% |
A4HUE6 | Leishmania infantum | 79% | 100% |
A4HUE7 | Leishmania infantum | 89% | 100% |
A4HUE8 | Leishmania infantum | 93% | 100% |
A4HUF4 | Leishmania infantum | 91% | 100% |
A4HUF5 | Leishmania infantum | 56% | 100% |
A4HYA9 | Leishmania infantum | 51% | 100% |
A4IC33 | Leishmania infantum | 36% | 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) | 39% | 100% |
C9ZVF1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
D0A423 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
E9AG72 | Leishmania infantum | 43% | 100% |
E9AI40 | Leishmania braziliensis | 72% | 100% |
E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 95% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9AN47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 99% |
E9ANE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 100% |
E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
Q4QDC4 | Leishmania major | 51% | 100% |
Q4QH81 | Leishmania major | 44% | 100% |
Q4QHH7 | Leishmania major | 59% | 100% |
Q4QHH8 | Leishmania major | 96% | 100% |
Q4QHI0 | Leishmania major | 90% | 100% |
Q4QHI1 | Leishmania major | 87% | 100% |
Q4QHI2 | Leishmania major | 78% | 100% |
Q4QIU9 | Leishmania major | 44% | 100% |
Q4QJ48 | Leishmania major | 43% | 100% |
Q7KIP2 | Leishmania major | 37% | 100% |