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: A4H619
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 | 287 | 291 | PF00656 | 0.479 |
CLV_C14_Caspase3-7 | 308 | 312 | PF00656 | 0.531 |
CLV_MEL_PAP_1 | 431 | 437 | PF00089 | 0.250 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.419 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.298 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 512 | 514 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 675 | 677 | PF00082 | 0.520 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.296 |
CLV_PCSK_PC1ET2_1 | 300 | 302 | PF00082 | 0.383 |
CLV_PCSK_PC1ET2_1 | 512 | 514 | PF00082 | 0.525 |
CLV_PCSK_PC1ET2_1 | 675 | 677 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.274 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.598 |
DEG_SCF_FBW7_2 | 14 | 19 | PF00400 | 0.606 |
DOC_CDC14_PxL_1 | 602 | 610 | PF14671 | 0.335 |
DOC_CKS1_1 | 614 | 619 | PF01111 | 0.436 |
DOC_CKS1_1 | 692 | 697 | PF01111 | 0.614 |
DOC_CYCLIN_yCln2_LP_2 | 619 | 625 | PF00134 | 0.375 |
DOC_MAPK_gen_1 | 138 | 144 | PF00069 | 0.504 |
DOC_MAPK_gen_1 | 262 | 272 | PF00069 | 0.552 |
DOC_MAPK_gen_1 | 277 | 285 | PF00069 | 0.544 |
DOC_MAPK_gen_1 | 512 | 520 | PF00069 | 0.327 |
DOC_MAPK_gen_1 | 630 | 639 | PF00069 | 0.589 |
DOC_MAPK_MEF2A_6 | 232 | 239 | PF00069 | 0.332 |
DOC_MAPK_MEF2A_6 | 512 | 520 | PF00069 | 0.360 |
DOC_PP1_RVXF_1 | 488 | 494 | PF00149 | 0.509 |
DOC_PP2B_LxvP_1 | 619 | 622 | PF13499 | 0.361 |
DOC_PP2B_PxIxI_1 | 232 | 238 | PF00149 | 0.288 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.268 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.328 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 485 | 489 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 667 | 671 | PF00917 | 0.796 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.337 |
DOC_WW_Pin1_4 | 613 | 618 | PF00397 | 0.419 |
DOC_WW_Pin1_4 | 691 | 696 | PF00397 | 0.788 |
LIG_14-3-3_CanoR_1 | 10 | 16 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 109 | 116 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 262 | 272 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 434 | 438 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 490 | 494 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 570 | 579 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 645 | 649 | PF00244 | 0.449 |
LIG_APCC_ABBA_1 | 55 | 60 | PF00400 | 0.637 |
LIG_APCC_ABBAyCdc20_2 | 54 | 60 | PF00400 | 0.505 |
LIG_BRCT_BRCA1_1 | 456 | 460 | PF00533 | 0.321 |
LIG_CtBP_PxDLS_1 | 622 | 626 | PF00389 | 0.189 |
LIG_EH1_1 | 492 | 500 | PF00400 | 0.346 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.572 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.592 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.355 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.258 |
LIG_FHA_1 | 430 | 436 | PF00498 | 0.417 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.406 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.400 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.490 |
LIG_FHA_1 | 614 | 620 | PF00498 | 0.422 |
LIG_FHA_2 | 274 | 280 | PF00498 | 0.559 |
LIG_FHA_2 | 682 | 688 | PF00498 | 0.620 |
LIG_GBD_Chelix_1 | 389 | 397 | PF00786 | 0.469 |
LIG_GBD_Chelix_1 | 471 | 479 | PF00786 | 0.233 |
LIG_GBD_Chelix_1 | 494 | 502 | PF00786 | 0.477 |
LIG_GBD_Chelix_1 | 532 | 540 | PF00786 | 0.505 |
LIG_Integrin_RGD_1 | 676 | 678 | PF01839 | 0.418 |
LIG_LIR_Apic_2 | 34 | 40 | PF02991 | 0.621 |
LIG_LIR_Apic_2 | 341 | 347 | PF02991 | 0.533 |
LIG_LIR_Apic_2 | 409 | 415 | PF02991 | 0.406 |
LIG_LIR_Apic_2 | 446 | 450 | PF02991 | 0.336 |
LIG_LIR_Apic_2 | 585 | 589 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 129 | 136 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 207 | 215 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 459 | 468 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 559 | 569 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 90 | 100 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 129 | 134 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 137 | 143 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 207 | 213 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 247 | 253 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 364 | 370 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 409 | 414 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 457 | 461 | PF02991 | 0.300 |
LIG_Pex14_2 | 174 | 178 | PF04695 | 0.371 |
LIG_Pex14_2 | 456 | 460 | PF04695 | 0.310 |
LIG_Pex14_2 | 480 | 484 | PF04695 | 0.370 |
LIG_PTB_Apo_2 | 452 | 459 | PF02174 | 0.375 |
LIG_PTB_Apo_2 | 478 | 485 | PF02174 | 0.444 |
LIG_PTB_Phospho_1 | 452 | 458 | PF10480 | 0.407 |
LIG_SH2_CRK | 107 | 111 | PF00017 | 0.516 |
LIG_SH2_CRK | 141 | 145 | PF00017 | 0.373 |
LIG_SH2_CRK | 156 | 160 | PF00017 | 0.327 |
LIG_SH2_CRK | 191 | 195 | PF00017 | 0.518 |
LIG_SH2_CRK | 344 | 348 | PF00017 | 0.619 |
LIG_SH2_CRK | 372 | 376 | PF00017 | 0.351 |
LIG_SH2_CRK | 447 | 451 | PF00017 | 0.329 |
LIG_SH2_CRK | 461 | 465 | PF00017 | 0.302 |
LIG_SH2_CRK | 586 | 590 | PF00017 | 0.329 |
LIG_SH2_GRB2like | 443 | 446 | PF00017 | 0.360 |
LIG_SH2_NCK_1 | 447 | 451 | PF00017 | 0.320 |
LIG_SH2_NCK_1 | 461 | 465 | PF00017 | 0.304 |
LIG_SH2_PTP2 | 37 | 40 | PF00017 | 0.616 |
LIG_SH2_PTP2 | 517 | 520 | PF00017 | 0.401 |
LIG_SH2_SRC | 37 | 40 | PF00017 | 0.622 |
LIG_SH2_SRC | 443 | 446 | PF00017 | 0.348 |
LIG_SH2_STAP1 | 136 | 140 | PF00017 | 0.505 |
LIG_SH2_STAP1 | 191 | 195 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 372 | 376 | PF00017 | 0.399 |
LIG_SH2_STAP1 | 562 | 566 | PF00017 | 0.345 |
LIG_SH2_STAP1 | 89 | 93 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 443 | 446 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 517 | 520 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 526 | 529 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.524 |
LIG_SH3_1 | 344 | 350 | PF00018 | 0.587 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.598 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.362 |
LIG_SH3_3 | 689 | 695 | PF00018 | 0.832 |
LIG_SUMO_SIM_par_1 | 545 | 550 | PF11976 | 0.334 |
LIG_TRAF2_1 | 684 | 687 | PF00917 | 0.617 |
LIG_TRFH_1 | 156 | 160 | PF08558 | 0.367 |
LIG_TYR_ITIM | 154 | 159 | PF00017 | 0.383 |
LIG_UBA3_1 | 154 | 162 | PF00899 | 0.359 |
LIG_UBA3_1 | 479 | 486 | PF00899 | 0.396 |
LIG_Vh1_VBS_1 | 370 | 388 | PF01044 | 0.413 |
LIG_Vh1_VBS_1 | 460 | 478 | PF01044 | 0.392 |
MOD_CDK_SPxK_1 | 691 | 697 | PF00069 | 0.754 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.358 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.671 |
MOD_CK2_1 | 273 | 279 | PF00069 | 0.418 |
MOD_CK2_1 | 657 | 663 | PF00069 | 0.597 |
MOD_CK2_1 | 667 | 673 | PF00069 | 0.699 |
MOD_CK2_1 | 681 | 687 | PF00069 | 0.837 |
MOD_Cter_Amidation | 298 | 301 | PF01082 | 0.473 |
MOD_Cter_Amidation | 673 | 676 | PF01082 | 0.493 |
MOD_DYRK1A_RPxSP_1 | 434 | 438 | PF00069 | 0.421 |
MOD_GlcNHglycan | 163 | 167 | PF01048 | 0.357 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.377 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.342 |
MOD_GlcNHglycan | 32 | 36 | PF01048 | 0.502 |
MOD_GlcNHglycan | 575 | 578 | PF01048 | 0.397 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.322 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.446 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.426 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.476 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.365 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.397 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.249 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.375 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.369 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.380 |
MOD_N-GLC_1 | 454 | 459 | PF02516 | 0.360 |
MOD_N-GLC_2 | 613 | 615 | PF02516 | 0.490 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.382 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.288 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.344 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.350 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.330 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.415 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.370 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.371 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.302 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.393 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.361 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.368 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.359 |
MOD_NEK2_2 | 233 | 238 | PF00069 | 0.472 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.332 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.306 |
MOD_PK_1 | 109 | 115 | PF00069 | 0.456 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.382 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.463 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.355 |
MOD_PKA_2 | 554 | 560 | PF00069 | 0.340 |
MOD_PKA_2 | 572 | 578 | PF00069 | 0.340 |
MOD_PKA_2 | 644 | 650 | PF00069 | 0.409 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.503 |
MOD_Plk_1 | 454 | 460 | PF00069 | 0.379 |
MOD_Plk_1 | 686 | 692 | PF00069 | 0.704 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.344 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.336 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.357 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.396 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.513 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.442 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.326 |
MOD_Plk_4 | 489 | 495 | PF00069 | 0.343 |
MOD_Plk_4 | 556 | 562 | PF00069 | 0.376 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.668 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.477 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.337 |
MOD_ProDKin_1 | 613 | 619 | PF00069 | 0.419 |
MOD_ProDKin_1 | 691 | 697 | PF00069 | 0.754 |
TRG_DiLeu_BaLyEn_6 | 603 | 608 | PF01217 | 0.386 |
TRG_DiLeu_BaLyEn_6 | 614 | 619 | PF01217 | 0.326 |
TRG_ENDOCYTIC_2 | 107 | 110 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 461 | 464 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 517 | 520 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 562 | 565 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.356 |
TRG_ER_diArg_1 | 280 | 283 | PF00400 | 0.323 |
TRG_ER_diArg_1 | 52 | 54 | PF00400 | 0.576 |
TRG_ER_diArg_1 | 629 | 632 | PF00400 | 0.352 |
TRG_Pf-PMV_PEXEL_1 | 262 | 267 | PF00026 | 0.491 |
TRG_Pf-PMV_PEXEL_1 | 322 | 326 | PF00026 | 0.472 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 46% | 99% |
A0A0N1HY49 | Leptomonas seymouri | 47% | 100% |
A0A0N1HZ06 | Leptomonas seymouri | 37% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 39% | 98% |
A0A0N1PAY4 | Leptomonas seymouri | 46% | 79% |
A0A0N1PB77 | Leptomonas seymouri | 34% | 100% |
A0A0N1PBZ2 | Leptomonas seymouri | 64% | 100% |
A0A0N1PCC1 | Leptomonas seymouri | 43% | 100% |
A0A0S4INN8 | Bodo saltans | 30% | 100% |
A0A381MBI0 | Leishmania infantum | 45% | 100% |
A0A3Q8I8X7 | Leishmania donovani | 45% | 100% |
A0A3Q8IAZ0 | Leishmania donovani | 80% | 100% |
A0A3Q8IH50 | Leishmania donovani | 58% | 97% |
A0A3Q8IVN0 | Leishmania donovani | 38% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 43% | 100% |
A0A3S5H5P4 | Leishmania donovani | 45% | 100% |
A0A3S5H5V2 | Leishmania donovani | 44% | 100% |
A0A3S5H6F6 | Leishmania donovani | 81% | 100% |
A0A3S5H763 | Leishmania donovani | 53% | 100% |
A0A3S7WR10 | Leishmania donovani | 44% | 94% |
A0A3S7WR14 | Leishmania donovani | 74% | 100% |
A0A3S7WR15 | Leishmania donovani | 70% | 82% |
A0A3S7WR24 | Leishmania donovani | 81% | 99% |
A4H4T8 | Leishmania braziliensis | 43% | 100% |
A4H5Y4 | Leishmania braziliensis | 45% | 100% |
A4H617 | Leishmania braziliensis | 96% | 100% |
A4H618 | Leishmania braziliensis | 97% | 100% |
A4H620 | Leishmania braziliensis | 58% | 99% |
A4H6C3 | Leishmania braziliensis | 44% | 100% |
A4HNH7 | Leishmania braziliensis | 36% | 100% |
A4HSS2 | Leishmania infantum | 45% | 100% |
A4HUE4 | Leishmania infantum | 43% | 94% |
A4HUE5 | Leishmania infantum | 70% | 100% |
A4HUE6 | Leishmania infantum | 74% | 100% |
A4HUE7 | Leishmania infantum | 81% | 100% |
A4HUE8 | Leishmania infantum | 81% | 99% |
A4HUF4 | Leishmania infantum | 80% | 100% |
A4HUF5 | Leishmania infantum | 57% | 100% |
A4HYA9 | Leishmania infantum | 53% | 100% |
A4IC33 | Leishmania infantum | 38% | 100% |
C9ZIK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
C9ZIK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 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) | 42% | 100% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
E9AG72 | Leishmania infantum | 44% | 100% |
E9AI40 | Leishmania braziliensis | 83% | 100% |
E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 100% |
E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 94% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
E9AN47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 98% |
E9ANE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 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 | 46% | 100% |
Q4QHH7 | Leishmania major | 57% | 100% |
Q4QHH8 | Leishmania major | 81% | 100% |
Q4QHH9 | Leishmania major | 80% | 100% |
Q4QHI0 | Leishmania major | 80% | 100% |
Q4QHI1 | Leishmania major | 75% | 100% |
Q4QHI2 | Leishmania major | 72% | 100% |
Q4QIU9 | Leishmania major | 43% | 99% |
Q4QJ48 | Leishmania major | 45% | 100% |
Q7KIP2 | Leishmania major | 36% | 100% |