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: Q4QHI2
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 | 22 | 24 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 625 | 627 | PF00675 | 0.314 |
CLV_PCSK_FUR_1 | 2 | 6 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 493 | 495 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 625 | 627 | PF00082 | 0.325 |
CLV_PCSK_PC1ET2_1 | 107 | 109 | PF00082 | 0.331 |
CLV_PCSK_PC1ET2_1 | 493 | 495 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.388 |
DEG_APCC_DBOX_1 | 250 | 258 | PF00400 | 0.460 |
DOC_AGCK_PIF_1 | 434 | 439 | PF00069 | 0.226 |
DOC_CYCLIN_yCln2_LP_2 | 600 | 606 | PF00134 | 0.412 |
DOC_MAPK_gen_1 | 107 | 113 | PF00069 | 0.540 |
DOC_MAPK_gen_1 | 231 | 241 | PF00069 | 0.583 |
DOC_MAPK_gen_1 | 246 | 254 | PF00069 | 0.575 |
DOC_MAPK_gen_1 | 493 | 501 | PF00069 | 0.357 |
DOC_MAPK_gen_1 | 610 | 619 | PF00069 | 0.622 |
DOC_MAPK_MEF2A_6 | 201 | 208 | PF00069 | 0.363 |
DOC_MAPK_MEF2A_6 | 493 | 501 | PF00069 | 0.391 |
DOC_PP1_RVXF_1 | 469 | 475 | PF00149 | 0.554 |
DOC_PP2B_LxvP_1 | 600 | 603 | PF13499 | 0.399 |
DOC_PP2B_LxvP_1 | 606 | 609 | PF13499 | 0.365 |
DOC_PP2B_PxIxI_1 | 201 | 207 | PF00149 | 0.322 |
DOC_PP4_FxxP_1 | 6 | 9 | PF00568 | 0.593 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 512 | 516 | PF00917 | 0.349 |
DOC_USP7_MATH_1 | 535 | 539 | PF00917 | 0.520 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.365 |
DOC_WW_Pin1_4 | 639 | 644 | PF00397 | 0.671 |
LIG_14-3-3_CanoR_1 | 231 | 241 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 471 | 475 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 554 | 563 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 68 | 74 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 78 | 85 | PF00244 | 0.525 |
LIG_APCC_ABBA_1 | 24 | 29 | PF00400 | 0.668 |
LIG_APCC_ABBAyCdc20_2 | 23 | 29 | PF00400 | 0.539 |
LIG_APCC_ABBAyCdc20_2 | 4 | 10 | PF00400 | 0.545 |
LIG_BRCT_BRCA1_1 | 437 | 441 | PF00533 | 0.352 |
LIG_Clathr_ClatBox_1 | 239 | 243 | PF01394 | 0.482 |
LIG_Clathr_ClatBox_1 | 632 | 636 | PF01394 | 0.573 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.625 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.391 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.293 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.412 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.594 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.526 |
LIG_FHA_1 | 485 | 491 | PF00498 | 0.393 |
LIG_FHA_1 | 603 | 609 | PF00498 | 0.451 |
LIG_FHA_1 | 635 | 641 | PF00498 | 0.687 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.604 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.605 |
LIG_FHA_2 | 572 | 578 | PF00498 | 0.262 |
LIG_HP1_1 | 525 | 529 | PF01393 | 0.434 |
LIG_LIR_Apic_2 | 322 | 328 | PF02991 | 0.564 |
LIG_LIR_Apic_2 | 390 | 396 | PF02991 | 0.452 |
LIG_LIR_Apic_2 | 566 | 570 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 106 | 116 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 157 | 168 | PF02991 | 0.563 |
LIG_LIR_Gen_1 | 176 | 184 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 440 | 449 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 459 | 465 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 477 | 486 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 540 | 550 | PF02991 | 0.551 |
LIG_LIR_Gen_1 | 61 | 69 | PF02991 | 0.573 |
LIG_LIR_Gen_1 | 98 | 105 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 140 | 144 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 157 | 163 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 16 | 21 | PF02991 | 0.632 |
LIG_LIR_Nem_3 | 176 | 182 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 216 | 222 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 345 | 351 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 390 | 395 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 431 | 437 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 438 | 442 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 459 | 464 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 477 | 482 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 98 | 103 | PF02991 | 0.529 |
LIG_NRBOX | 585 | 591 | PF00104 | 0.261 |
LIG_PDZ_Class_3 | 660 | 665 | PF00595 | 0.640 |
LIG_Pex14_2 | 143 | 147 | PF04695 | 0.400 |
LIG_Pex14_2 | 437 | 441 | PF04695 | 0.345 |
LIG_Pex14_2 | 461 | 465 | PF04695 | 0.406 |
LIG_PTB_Apo_2 | 433 | 440 | PF02174 | 0.407 |
LIG_PTB_Phospho_1 | 433 | 439 | PF10480 | 0.440 |
LIG_SH2_CRK | 125 | 129 | PF00017 | 0.361 |
LIG_SH2_CRK | 160 | 164 | PF00017 | 0.549 |
LIG_SH2_CRK | 325 | 329 | PF00017 | 0.653 |
LIG_SH2_CRK | 353 | 357 | PF00017 | 0.380 |
LIG_SH2_CRK | 442 | 446 | PF00017 | 0.337 |
LIG_SH2_CRK | 567 | 571 | PF00017 | 0.359 |
LIG_SH2_CRK | 76 | 80 | PF00017 | 0.546 |
LIG_SH2_GRB2like | 413 | 416 | PF00017 | 0.440 |
LIG_SH2_GRB2like | 424 | 427 | PF00017 | 0.392 |
LIG_SH2_NCK_1 | 308 | 312 | PF00017 | 0.471 |
LIG_SH2_NCK_1 | 442 | 446 | PF00017 | 0.335 |
LIG_SH2_PTP2 | 413 | 416 | PF00017 | 0.384 |
LIG_SH2_PTP2 | 498 | 501 | PF00017 | 0.434 |
LIG_SH2_SRC | 308 | 311 | PF00017 | 0.474 |
LIG_SH2_SRC | 312 | 315 | PF00017 | 0.462 |
LIG_SH2_SRC | 413 | 416 | PF00017 | 0.516 |
LIG_SH2_SRC | 424 | 427 | PF00017 | 0.379 |
LIG_SH2_STAP1 | 105 | 109 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 160 | 164 | PF00017 | 0.524 |
LIG_SH2_STAP1 | 308 | 312 | PF00017 | 0.466 |
LIG_SH2_STAP1 | 353 | 357 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 543 | 547 | PF00017 | 0.374 |
LIG_SH2_STAP1 | 62 | 66 | PF00017 | 0.571 |
LIG_SH2_STAT3 | 407 | 410 | PF00017 | 0.243 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 507 | 510 | PF00017 | 0.328 |
LIG_SH3_1 | 325 | 331 | PF00018 | 0.620 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.631 |
LIG_SH3_3 | 592 | 598 | PF00018 | 0.374 |
LIG_SUMO_SIM_anti_2 | 487 | 493 | PF11976 | 0.354 |
LIG_SUMO_SIM_par_1 | 525 | 531 | PF11976 | 0.363 |
LIG_TRFH_1 | 125 | 129 | PF08558 | 0.396 |
LIG_TYR_ITIM | 123 | 128 | PF00017 | 0.416 |
LIG_UBA3_1 | 123 | 131 | PF00899 | 0.393 |
LIG_UBA3_1 | 239 | 247 | PF00899 | 0.556 |
LIG_Vh1_VBS_1 | 351 | 369 | PF01044 | 0.442 |
LIG_WRC_WIRS_1 | 420 | 425 | PF05994 | 0.370 |
LIG_WRC_WIRS_1 | 476 | 481 | PF05994 | 0.340 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.382 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.386 |
MOD_CK1_1 | 642 | 648 | PF00069 | 0.663 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.467 |
MOD_CK2_1 | 642 | 648 | PF00069 | 0.737 |
MOD_Cter_Amidation | 271 | 274 | PF01082 | 0.505 |
MOD_GlcNHglycan | 132 | 136 | PF01048 | 0.394 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.406 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.381 |
MOD_GlcNHglycan | 556 | 559 | PF01048 | 0.426 |
MOD_GlcNHglycan | 645 | 648 | PF01048 | 0.755 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.476 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.456 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.515 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.409 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.275 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.414 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.398 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.410 |
MOD_GSK3_1 | 639 | 646 | PF00069 | 0.719 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.442 |
MOD_N-GLC_1 | 435 | 440 | PF02516 | 0.390 |
MOD_N-GLC_2 | 594 | 596 | PF02516 | 0.522 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.317 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.372 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.379 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.445 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.407 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.333 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.490 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.397 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.401 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.390 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.411 |
MOD_NEK2_2 | 202 | 207 | PF00069 | 0.503 |
MOD_NEK2_2 | 419 | 424 | PF00069 | 0.371 |
MOD_OFUCOSY | 110 | 115 | PF10250 | 0.217 |
MOD_PIKK_1 | 571 | 577 | PF00454 | 0.542 |
MOD_PKA_2 | 470 | 476 | PF00069 | 0.384 |
MOD_PKA_2 | 535 | 541 | PF00069 | 0.369 |
MOD_PKA_2 | 553 | 559 | PF00069 | 0.369 |
MOD_PKA_2 | 650 | 656 | PF00069 | 0.813 |
MOD_PKA_2 | 77 | 83 | PF00069 | 0.411 |
MOD_Plk_1 | 435 | 441 | PF00069 | 0.408 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.533 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.227 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.381 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.366 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.390 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.429 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.373 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.498 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.416 |
MOD_Plk_4 | 602 | 608 | PF00069 | 0.416 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.509 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.365 |
MOD_ProDKin_1 | 639 | 645 | PF00069 | 0.573 |
MOD_SUMO_rev_2 | 615 | 624 | PF00179 | 0.442 |
TRG_DiLeu_BaEn_2 | 235 | 241 | PF01217 | 0.350 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 160 | 163 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 353 | 356 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 413 | 416 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 442 | 445 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 498 | 501 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 523 | 526 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 543 | 546 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.360 |
TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 21 | 23 | PF00400 | 0.596 |
TRG_ER_diArg_1 | 624 | 626 | PF00400 | 0.334 |
TRG_Pf-PMV_PEXEL_1 | 231 | 236 | PF00026 | 0.523 |
TRG_Pf-PMV_PEXEL_1 | 50 | 54 | PF00026 | 0.235 |
TRG_Pf-PMV_PEXEL_1 | 55 | 60 | PF00026 | 0.239 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 47% | 94% |
A0A0N1HY49 | Leptomonas seymouri | 46% | 99% |
A0A0N1HZ06 | Leptomonas seymouri | 35% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 40% | 93% |
A0A0N1PAY4 | Leptomonas seymouri | 46% | 76% |
A0A0N1PB77 | Leptomonas seymouri | 34% | 100% |
A0A0N1PBZ2 | Leptomonas seymouri | 66% | 99% |
A0A0N1PCC1 | Leptomonas seymouri | 42% | 100% |
A0A381MBI0 | Leishmania infantum | 43% | 100% |
A0A3Q8I8X7 | Leishmania donovani | 43% | 100% |
A0A3Q8IAZ0 | Leishmania donovani | 79% | 95% |
A0A3Q8IH50 | Leishmania donovani | 58% | 92% |
A0A3Q8IVN0 | Leishmania donovani | 37% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 40% | 100% |
A0A3S5H5P4 | Leishmania donovani | 44% | 98% |
A0A3S5H5V2 | Leishmania donovani | 42% | 100% |
A0A3S5H6F6 | Leishmania donovani | 79% | 95% |
A0A3S5H763 | Leishmania donovani | 53% | 99% |
A0A3S7WR10 | Leishmania donovani | 43% | 89% |
A0A3S7WR14 | Leishmania donovani | 82% | 97% |
A0A3S7WR15 | Leishmania donovani | 87% | 78% |
A0A3S7WR24 | Leishmania donovani | 78% | 94% |
A4H4T8 | Leishmania braziliensis | 41% | 100% |
A4H5Y4 | Leishmania braziliensis | 44% | 100% |
A4H617 | Leishmania braziliensis | 72% | 95% |
A4H618 | Leishmania braziliensis | 70% | 97% |
A4H619 | Leishmania braziliensis | 72% | 95% |
A4H620 | Leishmania braziliensis | 62% | 94% |
A4H6C3 | Leishmania braziliensis | 44% | 100% |
A4HNH7 | Leishmania braziliensis | 35% | 100% |
A4HSS2 | Leishmania infantum | 44% | 98% |
A4HUE4 | Leishmania infantum | 43% | 89% |
A4HUE5 | Leishmania infantum | 87% | 96% |
A4HUE6 | Leishmania infantum | 82% | 97% |
A4HUE7 | Leishmania infantum | 79% | 95% |
A4HUE8 | Leishmania infantum | 78% | 94% |
A4HUF4 | Leishmania infantum | 79% | 95% |
A4HUF5 | Leishmania infantum | 57% | 100% |
A4HYA9 | Leishmania infantum | 53% | 99% |
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) | 40% | 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) | 76% | 95% |
E9AG72 | Leishmania infantum | 42% | 100% |
E9AI40 | Leishmania braziliensis | 79% | 98% |
E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 98% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 100% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 89% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
E9AN47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 93% |
E9ANE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 52% | 99% |
E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
Q4QDC4 | Leishmania major | 52% | 100% |
Q4QH81 | Leishmania major | 43% | 100% |
Q4QHH7 | Leishmania major | 59% | 100% |
Q4QHH8 | Leishmania major | 78% | 100% |
Q4QHH9 | Leishmania major | 78% | 100% |
Q4QHI0 | Leishmania major | 79% | 100% |
Q4QHI1 | Leishmania major | 82% | 99% |
Q4QIU9 | Leishmania major | 43% | 100% |
Q4QJ48 | Leishmania major | 44% | 98% |
Q7KIP2 | Leishmania major | 36% | 98% |