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: Q4QHH8
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 | 703 | 707 | PF00656 | 0.796 |
CLV_MEL_PAP_1 | 476 | 482 | PF00089 | 0.285 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.452 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 557 | 559 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.486 |
CLV_PCSK_PC1ET2_1 | 171 | 173 | PF00082 | 0.331 |
CLV_PCSK_PC1ET2_1 | 43 | 45 | PF00082 | 0.485 |
CLV_PCSK_PC1ET2_1 | 557 | 559 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.383 |
DEG_APCC_DBOX_1 | 314 | 322 | PF00400 | 0.460 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.689 |
DEG_SPOP_SBC_1 | 701 | 705 | PF00917 | 0.631 |
DOC_CDC14_PxL_1 | 647 | 655 | PF14671 | 0.366 |
DOC_CKS1_1 | 659 | 664 | PF01111 | 0.467 |
DOC_CYCLIN_yCln2_LP_2 | 664 | 670 | PF00134 | 0.412 |
DOC_MAPK_DCC_7 | 139 | 148 | PF00069 | 0.417 |
DOC_MAPK_gen_1 | 139 | 148 | PF00069 | 0.417 |
DOC_MAPK_gen_1 | 171 | 177 | PF00069 | 0.540 |
DOC_MAPK_gen_1 | 295 | 305 | PF00069 | 0.583 |
DOC_MAPK_gen_1 | 310 | 318 | PF00069 | 0.575 |
DOC_MAPK_gen_1 | 557 | 565 | PF00069 | 0.357 |
DOC_MAPK_gen_1 | 675 | 684 | PF00069 | 0.622 |
DOC_MAPK_MEF2A_6 | 142 | 149 | PF00069 | 0.499 |
DOC_MAPK_MEF2A_6 | 265 | 272 | PF00069 | 0.363 |
DOC_MAPK_MEF2A_6 | 557 | 565 | PF00069 | 0.391 |
DOC_PP2B_LxvP_1 | 2 | 5 | PF13499 | 0.866 |
DOC_PP2B_LxvP_1 | 664 | 667 | PF13499 | 0.399 |
DOC_PP2B_PxIxI_1 | 265 | 271 | PF00149 | 0.322 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 599 | 603 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 701 | 705 | PF00917 | 0.670 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 658 | 663 | PF00397 | 0.449 |
LIG_14-3-3_CanoR_1 | 295 | 305 | PF00244 | 0.620 |
LIG_Actin_WH2_2 | 88 | 103 | PF00022 | 0.660 |
LIG_APCC_ABBA_1 | 88 | 93 | PF00400 | 0.672 |
LIG_APCC_ABBAyCdc20_2 | 87 | 93 | PF00400 | 0.543 |
LIG_BIR_III_4 | 51 | 55 | PF00653 | 0.870 |
LIG_Clathr_ClatBox_1 | 303 | 307 | PF01394 | 0.482 |
LIG_EH1_1 | 537 | 545 | PF00400 | 0.375 |
LIG_eIF4E_1 | 647 | 653 | PF01652 | 0.265 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.596 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.604 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.372 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.625 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.391 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.293 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.429 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.712 |
LIG_FHA_1 | 535 | 541 | PF00498 | 0.372 |
LIG_FHA_1 | 659 | 665 | PF00498 | 0.452 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.605 |
LIG_FHA_2 | 636 | 642 | PF00498 | 0.262 |
LIG_GBD_Chelix_1 | 539 | 547 | PF00786 | 0.509 |
LIG_GBD_Chelix_1 | 577 | 585 | PF00786 | 0.538 |
LIG_LIR_Apic_2 | 386 | 392 | PF02991 | 0.564 |
LIG_LIR_Apic_2 | 454 | 460 | PF02991 | 0.452 |
LIG_LIR_Apic_2 | 491 | 495 | PF02991 | 0.366 |
LIG_LIR_Apic_2 | 630 | 634 | PF02991 | 0.336 |
LIG_LIR_Apic_2 | 67 | 73 | PF02991 | 0.669 |
LIG_LIR_Gen_1 | 123 | 133 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 162 | 169 | PF02991 | 0.554 |
LIG_LIR_Gen_1 | 240 | 251 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 504 | 513 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 523 | 530 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 604 | 614 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 162 | 167 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 240 | 246 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 280 | 286 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 409 | 415 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 453 | 459 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 502 | 506 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 523 | 528 | PF02991 | 0.376 |
LIG_PDZ_Class_3 | 727 | 732 | PF00595 | 0.647 |
LIG_Pex14_2 | 207 | 211 | PF04695 | 0.400 |
LIG_Pex14_2 | 501 | 505 | PF04695 | 0.345 |
LIG_Pex14_2 | 525 | 529 | PF04695 | 0.406 |
LIG_PTB_Apo_2 | 497 | 504 | PF02174 | 0.407 |
LIG_PTB_Apo_2 | 523 | 530 | PF02174 | 0.474 |
LIG_PTB_Phospho_1 | 497 | 503 | PF10480 | 0.440 |
LIG_SH2_CRK | 140 | 144 | PF00017 | 0.546 |
LIG_SH2_CRK | 174 | 178 | PF00017 | 0.410 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.361 |
LIG_SH2_CRK | 224 | 228 | PF00017 | 0.549 |
LIG_SH2_CRK | 389 | 393 | PF00017 | 0.653 |
LIG_SH2_CRK | 417 | 421 | PF00017 | 0.380 |
LIG_SH2_CRK | 492 | 496 | PF00017 | 0.362 |
LIG_SH2_CRK | 506 | 510 | PF00017 | 0.337 |
LIG_SH2_CRK | 631 | 635 | PF00017 | 0.359 |
LIG_SH2_CRK | 647 | 651 | PF00017 | 0.392 |
LIG_SH2_GRB2like | 488 | 491 | PF00017 | 0.392 |
LIG_SH2_GRB2like | 647 | 650 | PF00017 | 0.385 |
LIG_SH2_NCK_1 | 372 | 376 | PF00017 | 0.471 |
LIG_SH2_NCK_1 | 506 | 510 | PF00017 | 0.335 |
LIG_SH2_PTP2 | 562 | 565 | PF00017 | 0.434 |
LIG_SH2_PTP2 | 70 | 73 | PF00017 | 0.661 |
LIG_SH2_SRC | 372 | 375 | PF00017 | 0.474 |
LIG_SH2_SRC | 376 | 379 | PF00017 | 0.462 |
LIG_SH2_SRC | 70 | 73 | PF00017 | 0.667 |
LIG_SH2_STAP1 | 122 | 126 | PF00017 | 0.565 |
LIG_SH2_STAP1 | 169 | 173 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 224 | 228 | PF00017 | 0.524 |
LIG_SH2_STAP1 | 372 | 376 | PF00017 | 0.466 |
LIG_SH2_STAP1 | 417 | 421 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 607 | 611 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 488 | 491 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 534 | 537 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 562 | 565 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 571 | 574 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.656 |
LIG_SH3_1 | 389 | 395 | PF00018 | 0.620 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.795 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.782 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.631 |
LIG_SH3_3 | 477 | 483 | PF00018 | 0.394 |
LIG_SUMO_SIM_anti_2 | 552 | 557 | PF11976 | 0.355 |
LIG_SUMO_SIM_anti_2 | 661 | 667 | PF11976 | 0.489 |
LIG_SUMO_SIM_par_1 | 102 | 109 | PF11976 | 0.444 |
LIG_SUMO_SIM_par_1 | 518 | 523 | PF11976 | 0.270 |
LIG_SUMO_SIM_par_1 | 590 | 595 | PF11976 | 0.363 |
LIG_TRFH_1 | 189 | 193 | PF08558 | 0.396 |
LIG_TYR_ITIM | 187 | 192 | PF00017 | 0.416 |
LIG_TYR_ITSM | 502 | 509 | PF00017 | 0.439 |
LIG_UBA3_1 | 146 | 154 | PF00899 | 0.320 |
LIG_UBA3_1 | 187 | 195 | PF00899 | 0.393 |
LIG_UBA3_1 | 303 | 311 | PF00899 | 0.556 |
LIG_UBA3_1 | 524 | 531 | PF00899 | 0.450 |
LIG_UBA3_1 | 670 | 675 | PF00899 | 0.270 |
LIG_Vh1_VBS_1 | 415 | 433 | PF01044 | 0.442 |
MOD_CK1_1 | 658 | 664 | PF00069 | 0.280 |
MOD_CK1_1 | 704 | 710 | PF00069 | 0.647 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.467 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.697 |
MOD_Cter_Amidation | 335 | 338 | PF01082 | 0.505 |
MOD_GlcNHglycan | 196 | 200 | PF01048 | 0.394 |
MOD_GlcNHglycan | 22 | 26 | PF01048 | 0.730 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.406 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.398 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.338 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.354 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.476 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.702 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.456 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.515 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.409 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.309 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.414 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.399 |
MOD_GSK3_1 | 612 | 619 | PF00069 | 0.410 |
MOD_GSK3_1 | 700 | 707 | PF00069 | 0.662 |
MOD_N-GLC_1 | 499 | 504 | PF02516 | 0.390 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.492 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.411 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.317 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.372 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.361 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.445 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.407 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.333 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.397 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.401 |
MOD_NEK2_1 | 616 | 621 | PF00069 | 0.390 |
MOD_NEK2_1 | 655 | 660 | PF00069 | 0.483 |
MOD_NEK2_2 | 266 | 271 | PF00069 | 0.503 |
MOD_OFUCOSY | 203 | 210 | PF10250 | 0.247 |
MOD_PIKK_1 | 13 | 19 | PF00454 | 0.568 |
MOD_PIKK_1 | 217 | 223 | PF00454 | 0.361 |
MOD_PIKK_1 | 635 | 641 | PF00454 | 0.542 |
MOD_PK_1 | 474 | 480 | PF00069 | 0.423 |
MOD_PKA_2 | 599 | 605 | PF00069 | 0.369 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.428 |
MOD_Plk_1 | 499 | 505 | PF00069 | 0.408 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.334 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.655 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.380 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.371 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.390 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.429 |
MOD_Plk_4 | 501 | 507 | PF00069 | 0.498 |
MOD_Plk_4 | 520 | 526 | PF00069 | 0.241 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.380 |
MOD_Plk_4 | 601 | 607 | PF00069 | 0.416 |
MOD_Plk_4 | 666 | 672 | PF00069 | 0.416 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.553 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.261 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.509 |
MOD_ProDKin_1 | 658 | 664 | PF00069 | 0.449 |
MOD_SUMO_for_1 | 42 | 45 | PF00179 | 0.587 |
MOD_SUMO_rev_2 | 680 | 689 | PF00179 | 0.442 |
TRG_DiLeu_BaEn_2 | 299 | 305 | PF01217 | 0.350 |
TRG_DiLeu_BaLyEn_6 | 648 | 653 | PF01217 | 0.415 |
TRG_DiLeu_BaLyEn_6 | 659 | 664 | PF01217 | 0.355 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 417 | 420 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 506 | 509 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 562 | 565 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 607 | 610 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 647 | 650 | PF00928 | 0.459 |
TRG_ER_diArg_1 | 86 | 88 | PF00400 | 0.623 |
TRG_Pf-PMV_PEXEL_1 | 295 | 300 | PF00026 | 0.523 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 47% | 100% |
A0A0N1HY49 | Leptomonas seymouri | 44% | 100% |
A0A0N1HZ06 | Leptomonas seymouri | 36% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 37% | 100% |
A0A0N1PAY4 | Leptomonas seymouri | 46% | 83% |
A0A0N1PB77 | Leptomonas seymouri | 34% | 100% |
A0A0N1PBZ2 | Leptomonas seymouri | 66% | 100% |
A0A0N1PCC1 | Leptomonas seymouri | 41% | 100% |
A0A381MBI0 | Leishmania infantum | 43% | 100% |
A0A3Q8I8X7 | Leishmania donovani | 44% | 100% |
A0A3Q8IAZ0 | Leishmania donovani | 91% | 100% |
A0A3Q8IH50 | Leishmania donovani | 58% | 100% |
A0A3Q8IVN0 | Leishmania donovani | 37% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 40% | 100% |
A0A3S5H5P4 | Leishmania donovani | 43% | 100% |
A0A3S5H5V2 | Leishmania donovani | 44% | 100% |
A0A3S5H6F6 | Leishmania donovani | 92% | 100% |
A0A3S5H763 | Leishmania donovani | 51% | 100% |
A0A3S7WR10 | Leishmania donovani | 42% | 98% |
A0A3S7WR14 | Leishmania donovani | 79% | 100% |
A0A3S7WR15 | Leishmania donovani | 68% | 86% |
A0A3S7WR24 | Leishmania donovani | 91% | 100% |
A4H4T8 | Leishmania braziliensis | 43% | 100% |
A4H5Y4 | Leishmania braziliensis | 44% | 100% |
A4H617 | Leishmania braziliensis | 78% | 100% |
A4H618 | Leishmania braziliensis | 79% | 100% |
A4H619 | Leishmania braziliensis | 81% | 100% |
A4H620 | Leishmania braziliensis | 55% | 100% |
A4H6C3 | Leishmania braziliensis | 43% | 100% |
A4HNH7 | Leishmania braziliensis | 36% | 100% |
A4HSS2 | Leishmania infantum | 43% | 100% |
A4HUE4 | Leishmania infantum | 42% | 98% |
A4HUE5 | Leishmania infantum | 71% | 100% |
A4HUE6 | Leishmania infantum | 79% | 100% |
A4HUE7 | Leishmania infantum | 90% | 100% |
A4HUE8 | Leishmania infantum | 91% | 100% |
A4HUF4 | Leishmania infantum | 91% | 100% |
A4HUF5 | Leishmania infantum | 57% | 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) | 38% | 100% |
C9ZVE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
C9ZVF1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
D0A423 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9AG72 | Leishmania infantum | 44% | 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% | 98% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
E9AN47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 100% |
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) | 37% | 100% |
Q4QDC4 | Leishmania major | 51% | 100% |
Q4QH81 | Leishmania major | 44% | 100% |
Q4QHH7 | Leishmania major | 60% | 100% |
Q4QHH9 | Leishmania major | 96% | 100% |
Q4QHI0 | Leishmania major | 91% | 100% |
Q4QHI1 | Leishmania major | 87% | 100% |
Q4QHI2 | Leishmania major | 78% | 100% |
Q4QIU9 | Leishmania major | 44% | 100% |
Q4QJ48 | Leishmania major | 43% | 100% |
Q7KIP2 | Leishmania major | 36% | 100% |