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: A0A3Q8I8X7
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 | 651 | 655 | PF00656 | 0.643 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.321 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.251 |
CLV_PCSK_PC1ET2_1 | 134 | 136 | PF00082 | 0.296 |
CLV_PCSK_PC1ET2_1 | 192 | 194 | PF00082 | 0.208 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.208 |
CLV_PCSK_SKI1_1 | 588 | 592 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.358 |
DEG_SCF_TRCP1_1 | 225 | 230 | PF00400 | 0.202 |
DEG_SPOP_SBC_1 | 559 | 563 | PF00917 | 0.460 |
DEG_SPOP_SBC_1 | 575 | 579 | PF00917 | 0.246 |
DOC_ANK_TNKS_1 | 104 | 111 | PF00023 | 0.501 |
DOC_CKS1_1 | 596 | 601 | PF01111 | 0.432 |
DOC_CYCLIN_RxL_1 | 77 | 87 | PF00134 | 0.602 |
DOC_CYCLIN_yCln2_LP_2 | 398 | 404 | PF00134 | 0.442 |
DOC_MAPK_gen_1 | 134 | 140 | PF00069 | 0.500 |
DOC_MAPK_gen_1 | 261 | 268 | PF00069 | 0.553 |
DOC_MAPK_MEF2A_6 | 228 | 235 | PF00069 | 0.329 |
DOC_MAPK_MEF2A_6 | 499 | 506 | PF00069 | 0.357 |
DOC_MAPK_MEF2A_6 | 64 | 71 | PF00069 | 0.530 |
DOC_MAPK_NFAT4_5 | 64 | 72 | PF00069 | 0.601 |
DOC_PP2B_LxvP_1 | 398 | 401 | PF13499 | 0.442 |
DOC_PP2B_PxIxI_1 | 228 | 234 | PF00149 | 0.281 |
DOC_PP4_FxxP_1 | 596 | 599 | PF00568 | 0.254 |
DOC_USP7_MATH_1 | 559 | 563 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 575 | 579 | PF00917 | 0.270 |
DOC_USP7_UBL2_3 | 296 | 300 | PF12436 | 0.408 |
DOC_USP7_UBL2_3 | 632 | 636 | PF12436 | 0.555 |
DOC_USP7_UBL2_3 | 646 | 650 | PF12436 | 0.610 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.786 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 576 | 581 | PF00397 | 0.349 |
DOC_WW_Pin1_4 | 595 | 600 | PF00397 | 0.414 |
LIG_14-3-3_CanoR_1 | 351 | 356 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 476 | 480 | PF00244 | 0.491 |
LIG_APCC_ABBAyCdc20_2 | 31 | 37 | PF00400 | 0.528 |
LIG_BIR_III_2 | 43 | 47 | PF00653 | 0.608 |
LIG_BRCT_BRCA1_1 | 110 | 114 | PF00533 | 0.480 |
LIG_BRCT_BRCA1_1 | 123 | 127 | PF00533 | 0.397 |
LIG_BRCT_BRCA1_1 | 442 | 446 | PF00533 | 0.317 |
LIG_BRCT_BRCA1_1 | 544 | 548 | PF00533 | 0.492 |
LIG_BRCT_BRCA1_1 | 592 | 596 | PF00533 | 0.204 |
LIG_EVH1_2 | 580 | 584 | PF00568 | 0.360 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.569 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.350 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.486 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.570 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.349 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.260 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.411 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.325 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.721 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.523 |
LIG_FHA_1 | 596 | 602 | PF00498 | 0.417 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.418 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.562 |
LIG_GBD_Chelix_1 | 71 | 79 | PF00786 | 0.229 |
LIG_IRF3_LxIS_1 | 587 | 593 | PF10401 | 0.400 |
LIG_LIR_Apic_2 | 15 | 21 | PF02991 | 0.750 |
LIG_LIR_Apic_2 | 302 | 308 | PF02991 | 0.385 |
LIG_LIR_Apic_2 | 593 | 599 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 100 | 109 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 124 | 132 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 184 | 195 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 203 | 214 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 263 | 273 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 329 | 338 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 377 | 386 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 395 | 405 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 445 | 454 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 490 | 497 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 545 | 554 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 583 | 592 | PF02991 | 0.264 |
LIG_LIR_Gen_1 | 86 | 96 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 100 | 106 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 124 | 130 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 184 | 190 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 263 | 268 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 329 | 333 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 377 | 382 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 395 | 400 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 417 | 421 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 445 | 450 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 45 | 50 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 490 | 495 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 498 | 503 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 545 | 551 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 583 | 587 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 86 | 92 | PF02991 | 0.438 |
LIG_NRBOX | 586 | 592 | PF00104 | 0.223 |
LIG_Pex14_1 | 633 | 637 | PF04695 | 0.479 |
LIG_Pex14_2 | 170 | 174 | PF04695 | 0.365 |
LIG_Pex14_2 | 242 | 246 | PF04695 | 0.300 |
LIG_Pex14_2 | 247 | 251 | PF04695 | 0.285 |
LIG_Pex14_2 | 409 | 413 | PF04695 | 0.386 |
LIG_Pex14_2 | 442 | 446 | PF04695 | 0.306 |
LIG_Pex14_2 | 466 | 470 | PF04695 | 0.365 |
LIG_SH2_CRK | 103 | 107 | PF00017 | 0.512 |
LIG_SH2_CRK | 137 | 141 | PF00017 | 0.367 |
LIG_SH2_CRK | 152 | 156 | PF00017 | 0.321 |
LIG_SH2_CRK | 18 | 22 | PF00017 | 0.609 |
LIG_SH2_CRK | 187 | 191 | PF00017 | 0.515 |
LIG_SH2_CRK | 358 | 362 | PF00017 | 0.346 |
LIG_SH2_CRK | 379 | 383 | PF00017 | 0.310 |
LIG_SH2_CRK | 447 | 451 | PF00017 | 0.301 |
LIG_SH2_NCK_1 | 18 | 22 | PF00017 | 0.605 |
LIG_SH2_NCK_1 | 447 | 451 | PF00017 | 0.300 |
LIG_SH2_PTP2 | 265 | 268 | PF00017 | 0.396 |
LIG_SH2_PTP2 | 33 | 36 | PF00017 | 0.622 |
LIG_SH2_PTP2 | 418 | 421 | PF00017 | 0.350 |
LIG_SH2_PTP2 | 50 | 53 | PF00017 | 0.622 |
LIG_SH2_PTP2 | 503 | 506 | PF00017 | 0.400 |
LIG_SH2_SRC | 33 | 36 | PF00017 | 0.628 |
LIG_SH2_SRC | 50 | 53 | PF00017 | 0.545 |
LIG_SH2_STAP1 | 132 | 136 | PF00017 | 0.501 |
LIG_SH2_STAP1 | 187 | 191 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 520 | 524 | PF00017 | 0.406 |
LIG_SH2_STAP1 | 543 | 547 | PF00017 | 0.495 |
LIG_SH2_STAP1 | 89 | 93 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.619 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 464 | 467 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.517 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.299 |
LIG_SH3_3 | 434 | 440 | PF00018 | 0.280 |
LIG_SH3_3 | 57 | 63 | PF00018 | 0.514 |
LIG_SH3_3 | 605 | 611 | PF00018 | 0.390 |
LIG_SH3_3 | 615 | 621 | PF00018 | 0.493 |
LIG_SH3_4 | 646 | 653 | PF00018 | 0.629 |
LIG_SUMO_SIM_anti_2 | 493 | 498 | PF11976 | 0.315 |
LIG_SUMO_SIM_par_1 | 365 | 370 | PF11976 | 0.297 |
LIG_SUMO_SIM_par_1 | 493 | 498 | PF11976 | 0.348 |
LIG_TRAF2_1 | 21 | 24 | PF00917 | 0.648 |
LIG_TYR_ITIM | 150 | 155 | PF00017 | 0.377 |
LIG_TYR_ITIM | 381 | 386 | PF00017 | 0.374 |
LIG_TYR_ITIM | 416 | 421 | PF00017 | 0.333 |
LIG_TYR_ITSM | 443 | 450 | PF00017 | 0.404 |
LIG_UBA3_1 | 266 | 270 | PF00899 | 0.524 |
LIG_UBA3_1 | 534 | 541 | PF00899 | 0.222 |
LIG_Vh1_VBS_1 | 367 | 385 | PF01044 | 0.448 |
LIG_WRC_WIRS_1 | 551 | 556 | PF05994 | 0.225 |
MOD_CDK_SPxxK_3 | 42 | 49 | PF00069 | 0.299 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.380 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.406 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.352 |
MOD_CK1_1 | 560 | 566 | PF00069 | 0.358 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.395 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.298 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.319 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.614 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.348 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.386 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.382 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.373 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.437 |
MOD_GlcNHglycan | 592 | 595 | PF01048 | 0.320 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.410 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.347 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.399 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.438 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.394 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.444 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.373 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.364 |
MOD_GSK3_1 | 557 | 564 | PF00069 | 0.375 |
MOD_GSK3_1 | 648 | 655 | PF00069 | 0.770 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.389 |
MOD_N-GLC_1 | 351 | 356 | PF02516 | 0.519 |
MOD_N-GLC_1 | 84 | 89 | PF02516 | 0.377 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.376 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.343 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.283 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.338 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.362 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.331 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.388 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.511 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.299 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.349 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.355 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.363 |
MOD_NEK2_1 | 533 | 538 | PF00069 | 0.319 |
MOD_NEK2_1 | 557 | 562 | PF00069 | 0.353 |
MOD_NEK2_1 | 569 | 574 | PF00069 | 0.351 |
MOD_NEK2_1 | 590 | 595 | PF00069 | 0.457 |
MOD_NEK2_1 | 637 | 642 | PF00069 | 0.367 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.357 |
MOD_NEK2_2 | 543 | 548 | PF00069 | 0.222 |
MOD_PIKK_1 | 440 | 446 | PF00454 | 0.222 |
MOD_PK_1 | 351 | 357 | PF00069 | 0.222 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.376 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.229 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.350 |
MOD_Plk_1 | 290 | 296 | PF00069 | 0.192 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.215 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.389 |
MOD_Plk_1 | 543 | 549 | PF00069 | 0.296 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.402 |
MOD_Plk_2-3 | 24 | 30 | PF00069 | 0.561 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.440 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.319 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.458 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.380 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.441 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.338 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.320 |
MOD_Plk_4 | 543 | 549 | PF00069 | 0.358 |
MOD_Plk_4 | 569 | 575 | PF00069 | 0.348 |
MOD_Plk_4 | 625 | 631 | PF00069 | 0.565 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.750 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.307 |
MOD_ProDKin_1 | 576 | 582 | PF00069 | 0.417 |
MOD_ProDKin_1 | 595 | 601 | PF00069 | 0.414 |
MOD_SUMO_for_1 | 269 | 272 | PF00179 | 0.419 |
MOD_SUMO_rev_2 | 617 | 624 | PF00179 | 0.408 |
TRG_DiLeu_BaEn_1 | 254 | 259 | PF01217 | 0.459 |
TRG_DiLeu_BaEn_2 | 262 | 268 | PF01217 | 0.306 |
TRG_DiLeu_BaLyEn_6 | 186 | 191 | PF01217 | 0.276 |
TRG_DiLeu_BaLyEn_6 | 596 | 601 | PF01217 | 0.320 |
TRG_ENDOCYTIC_2 | 103 | 106 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 379 | 382 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 418 | 421 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 447 | 450 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 503 | 506 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.351 |
TRG_Pf-PMV_PEXEL_1 | 256 | 260 | PF00026 | 0.505 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 44% | 94% |
A0A0N1HY49 | Leptomonas seymouri | 46% | 98% |
A0A0N1HZ06 | Leptomonas seymouri | 38% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 38% | 92% |
A0A0N1PAY4 | Leptomonas seymouri | 42% | 75% |
A0A0N1PB77 | Leptomonas seymouri | 40% | 100% |
A0A0N1PBZ2 | Leptomonas seymouri | 45% | 98% |
A0A0N1PCC1 | Leptomonas seymouri | 43% | 99% |
A0A0S4INN8 | Bodo saltans | 30% | 100% |
A0A381MBI0 | Leishmania infantum | 100% | 100% |
A0A3Q8IAZ0 | Leishmania donovani | 44% | 94% |
A0A3Q8IH50 | Leishmania donovani | 48% | 91% |
A0A3Q8IVN0 | Leishmania donovani | 40% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 41% | 100% |
A0A3S5H5P4 | Leishmania donovani | 45% | 97% |
A0A3S5H5V2 | Leishmania donovani | 46% | 100% |
A0A3S5H6F6 | Leishmania donovani | 42% | 94% |
A0A3S5H763 | Leishmania donovani | 48% | 98% |
A0A3S7WR10 | Leishmania donovani | 40% | 88% |
A0A3S7WR14 | Leishmania donovani | 45% | 96% |
A0A3S7WR15 | Leishmania donovani | 43% | 78% |
A0A3S7WR24 | Leishmania donovani | 42% | 94% |
A4H4T8 | Leishmania braziliensis | 45% | 100% |
A4H5Y4 | Leishmania braziliensis | 84% | 100% |
A4H617 | Leishmania braziliensis | 45% | 100% |
A4H618 | Leishmania braziliensis | 44% | 100% |
A4H619 | Leishmania braziliensis | 45% | 100% |
A4H620 | Leishmania braziliensis | 48% | 100% |
A4H6C3 | Leishmania braziliensis | 84% | 100% |
A4HNH7 | Leishmania braziliensis | 39% | 97% |
A4HSS2 | Leishmania infantum | 45% | 100% |
A4HUE4 | Leishmania infantum | 40% | 100% |
A4HUE5 | Leishmania infantum | 43% | 100% |
A4HUE6 | Leishmania infantum | 45% | 100% |
A4HUE7 | Leishmania infantum | 43% | 100% |
A4HUE8 | Leishmania infantum | 42% | 100% |
A4HUF4 | Leishmania infantum | 41% | 100% |
A4HUF5 | Leishmania infantum | 49% | 100% |
A4HYA9 | Leishmania infantum | 47% | 100% |
A4IC33 | Leishmania infantum | 39% | 100% |
C9ZIK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
C9ZIK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
C9ZVE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
C9ZVE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
C9ZVF1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
D0A423 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9AG72 | Leishmania infantum | 46% | 100% |
E9AI40 | Leishmania braziliensis | 46% | 100% |
E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 98% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
E9AN47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 100% |
E9ANE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
Q4QDC4 | Leishmania major | 47% | 100% |
Q4QH81 | Leishmania major | 94% | 100% |
Q4QHH7 | Leishmania major | 46% | 100% |
Q4QHH8 | Leishmania major | 44% | 100% |
Q4QHH9 | Leishmania major | 44% | 100% |
Q4QHI0 | Leishmania major | 44% | 100% |
Q4QHI1 | Leishmania major | 46% | 100% |
Q4QHI2 | Leishmania major | 43% | 100% |
Q4QIU9 | Leishmania major | 44% | 100% |
Q4QJ48 | Leishmania major | 44% | 100% |
Q7KIP2 | Leishmania major | 39% | 100% |