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: E9AKQ9
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 | 27 | 31 | PF00656 | 0.668 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.225 |
CLV_NRD_NRD_1 | 661 | 663 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 665 | 667 | PF00675 | 0.450 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.291 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.250 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.272 |
CLV_PCSK_KEX2_1 | 525 | 527 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 665 | 667 | PF00082 | 0.462 |
CLV_PCSK_PC1ET2_1 | 150 | 152 | PF00082 | 0.291 |
CLV_PCSK_PC1ET2_1 | 285 | 287 | PF00082 | 0.354 |
CLV_PCSK_PC1ET2_1 | 289 | 291 | PF00082 | 0.357 |
CLV_PCSK_PC1ET2_1 | 525 | 527 | PF00082 | 0.520 |
CLV_PCSK_PC7_1 | 205 | 211 | PF00082 | 0.210 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.295 |
DEG_APCC_DBOX_1 | 19 | 27 | PF00400 | 0.647 |
DOC_CDC14_PxL_1 | 424 | 432 | PF14671 | 0.200 |
DOC_CDC14_PxL_1 | 611 | 619 | PF14671 | 0.330 |
DOC_CYCLIN_yCln2_LP_2 | 318 | 324 | PF00134 | 0.393 |
DOC_CYCLIN_yCln2_LP_2 | 628 | 634 | PF00134 | 0.368 |
DOC_CYCLIN_yCln2_LP_2 | 636 | 642 | PF00134 | 0.492 |
DOC_MAPK_gen_1 | 242 | 249 | PF00069 | 0.210 |
DOC_MAPK_gen_1 | 525 | 533 | PF00069 | 0.322 |
DOC_MAPK_HePTP_8 | 239 | 251 | PF00069 | 0.219 |
DOC_MAPK_MEF2A_6 | 242 | 251 | PF00069 | 0.319 |
DOC_MAPK_MEF2A_6 | 525 | 533 | PF00069 | 0.356 |
DOC_MAPK_MEF2A_6 | 80 | 87 | PF00069 | 0.533 |
DOC_MAPK_NFAT4_5 | 80 | 88 | PF00069 | 0.604 |
DOC_PP1_RVXF_1 | 125 | 131 | PF00149 | 0.605 |
DOC_PP1_RVXF_1 | 91 | 98 | PF00149 | 0.409 |
DOC_PP2B_LxvP_1 | 446 | 449 | PF13499 | 0.373 |
DOC_PP2B_LxvP_1 | 628 | 631 | PF13499 | 0.354 |
DOC_PP4_FxxP_1 | 599 | 602 | PF00568 | 0.263 |
DOC_SPAK_OSR1_1 | 111 | 115 | PF12202 | 0.412 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.324 |
DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 586 | 590 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.645 |
DOC_USP7_UBL2_3 | 285 | 289 | PF12436 | 0.488 |
LIG_14-3-3_CanoR_1 | 151 | 160 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 20 | 29 | PF00244 | 0.546 |
LIG_14-3-3_CanoR_1 | 503 | 507 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 80 | 86 | PF00244 | 0.513 |
LIG_Actin_WH2_2 | 275 | 291 | PF00022 | 0.398 |
LIG_APCC_ABBA_1 | 538 | 543 | PF00400 | 0.245 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.750 |
LIG_BRCT_BRCA1_1 | 258 | 262 | PF00533 | 0.272 |
LIG_BRCT_BRCA1_1 | 434 | 438 | PF00533 | 0.490 |
LIG_BRCT_BRCA1_1 | 439 | 443 | PF00533 | 0.431 |
LIG_BRCT_BRCA1_1 | 469 | 473 | PF00533 | 0.316 |
LIG_BRCT_BRCA1_1 | 500 | 504 | PF00533 | 0.459 |
LIG_BRCT_BRCA1_1 | 83 | 87 | PF00533 | 0.460 |
LIG_CSL_BTD_1 | 554 | 557 | PF09270 | 0.396 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.423 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.453 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.324 |
LIG_FHA_1 | 556 | 562 | PF00498 | 0.242 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.604 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.606 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.441 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.447 |
LIG_LIR_Apic_2 | 46 | 52 | PF02991 | 0.621 |
LIG_LIR_Apic_2 | 598 | 602 | PF02991 | 0.301 |
LIG_LIR_Gen_1 | 200 | 211 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 404 | 414 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 440 | 451 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 501 | 512 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 517 | 524 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 572 | 581 | PF02991 | 0.510 |
LIG_LIR_Gen_1 | 608 | 619 | PF02991 | 0.265 |
LIG_LIR_Gen_1 | 633 | 642 | PF02991 | 0.280 |
LIG_LIR_Gen_1 | 84 | 95 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 165 | 171 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 200 | 206 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 404 | 409 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 435 | 441 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 470 | 474 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 505 | 511 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 517 | 522 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 572 | 578 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 608 | 614 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 633 | 637 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 84 | 90 | PF02991 | 0.426 |
LIG_MLH1_MIPbox_1 | 434 | 438 | PF16413 | 0.570 |
LIG_PALB2_WD40_1 | 219 | 227 | PF16756 | 0.205 |
LIG_Pex14_1 | 220 | 224 | PF04695 | 0.373 |
LIG_Pex14_1 | 406 | 410 | PF04695 | 0.284 |
LIG_Pex14_1 | 425 | 429 | PF04695 | 0.327 |
LIG_Pex14_2 | 108 | 112 | PF04695 | 0.406 |
LIG_Pex14_2 | 186 | 190 | PF04695 | 0.373 |
LIG_Pex14_2 | 263 | 267 | PF04695 | 0.284 |
LIG_Pex14_2 | 439 | 443 | PF04695 | 0.364 |
LIG_Pex14_2 | 469 | 473 | PF04695 | 0.305 |
LIG_Pex14_2 | 493 | 497 | PF04695 | 0.363 |
LIG_Pex14_2 | 504 | 508 | PF04695 | 0.364 |
LIG_SH2_CRK | 119 | 123 | PF00017 | 0.511 |
LIG_SH2_CRK | 168 | 172 | PF00017 | 0.320 |
LIG_SH2_CRK | 203 | 207 | PF00017 | 0.514 |
LIG_SH2_CRK | 385 | 389 | PF00017 | 0.344 |
LIG_SH2_CRK | 410 | 414 | PF00017 | 0.354 |
LIG_SH2_CRK | 441 | 445 | PF00017 | 0.337 |
LIG_SH2_CRK | 474 | 478 | PF00017 | 0.297 |
LIG_SH2_CRK | 575 | 579 | PF00017 | 0.218 |
LIG_SH2_NCK_1 | 410 | 414 | PF00017 | 0.415 |
LIG_SH2_NCK_1 | 474 | 478 | PF00017 | 0.299 |
LIG_SH2_NCK_1 | 575 | 579 | PF00017 | 0.298 |
LIG_SH2_PTP2 | 49 | 52 | PF00017 | 0.611 |
LIG_SH2_PTP2 | 530 | 533 | PF00017 | 0.399 |
LIG_SH2_SRC | 331 | 334 | PF00017 | 0.380 |
LIG_SH2_SRC | 49 | 52 | PF00017 | 0.617 |
LIG_SH2_STAP1 | 148 | 152 | PF00017 | 0.500 |
LIG_SH2_STAP1 | 203 | 207 | PF00017 | 0.485 |
LIG_SH2_STAP1 | 385 | 389 | PF00017 | 0.392 |
LIG_SH2_STAP1 | 410 | 414 | PF00017 | 0.282 |
LIG_SH2_STAP1 | 441 | 445 | PF00017 | 0.326 |
LIG_SH2_STAP1 | 547 | 551 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 575 | 579 | PF00017 | 0.338 |
LIG_SH2_STAT3 | 510 | 513 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 445 | 448 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 495 | 498 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 510 | 513 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 530 | 533 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 539 | 542 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 552 | 555 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.516 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.279 |
LIG_SH3_3 | 620 | 626 | PF00018 | 0.338 |
LIG_SH3_3 | 632 | 638 | PF00018 | 0.389 |
LIG_SUMO_SIM_anti_2 | 411 | 417 | PF11976 | 0.397 |
LIG_SUMO_SIM_anti_2 | 558 | 563 | PF11976 | 0.250 |
LIG_SUMO_SIM_par_1 | 557 | 563 | PF11976 | 0.327 |
LIG_TRFH_1 | 634 | 638 | PF08558 | 0.290 |
LIG_TYR_ITIM | 117 | 122 | PF00017 | 0.298 |
LIG_TYR_ITIM | 166 | 171 | PF00017 | 0.376 |
LIG_TYR_ITIM | 408 | 413 | PF00017 | 0.373 |
LIG_TYR_ITIM | 472 | 477 | PF00017 | 0.337 |
LIG_WRC_WIRS_1 | 187 | 192 | PF05994 | 0.242 |
LIG_WRC_WIRS_1 | 452 | 457 | PF05994 | 0.334 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.336 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.355 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.345 |
MOD_CK1_1 | 498 | 504 | PF00069 | 0.350 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.232 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.498 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.453 |
MOD_CK2_1 | 313 | 319 | PF00069 | 0.395 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.332 |
MOD_CMANNOS | 220 | 223 | PF00535 | 0.250 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.276 |
MOD_GlcNHglycan | 175 | 179 | PF01048 | 0.350 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.356 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.541 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.385 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.312 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.308 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.268 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.429 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.436 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.459 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.450 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.446 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.293 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.362 |
MOD_GSK3_1 | 584 | 591 | PF00069 | 0.373 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.318 |
MOD_N-GLC_1 | 21 | 26 | PF02516 | 0.393 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.300 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.375 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.341 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.282 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.351 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.450 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.279 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.364 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.348 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.327 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.319 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.348 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.360 |
MOD_NEK2_1 | 584 | 589 | PF00069 | 0.352 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.421 |
MOD_NEK2_2 | 103 | 108 | PF00069 | 0.190 |
MOD_NEK2_2 | 341 | 346 | PF00069 | 0.319 |
MOD_NEK2_2 | 432 | 437 | PF00069 | 0.422 |
MOD_NEK2_2 | 451 | 456 | PF00069 | 0.336 |
MOD_PIKK_1 | 252 | 258 | PF00454 | 0.200 |
MOD_PK_1 | 121 | 127 | PF00069 | 0.451 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.200 |
MOD_PKA_2 | 502 | 508 | PF00069 | 0.348 |
MOD_PKA_2 | 567 | 573 | PF00069 | 0.333 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.401 |
MOD_PKB_1 | 208 | 216 | PF00069 | 0.200 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.400 |
MOD_Plk_1 | 547 | 553 | PF00069 | 0.328 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.339 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.350 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.302 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.437 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.337 |
MOD_Plk_4 | 547 | 553 | PF00069 | 0.307 |
MOD_Plk_4 | 555 | 561 | PF00069 | 0.306 |
MOD_Plk_4 | 569 | 575 | PF00069 | 0.369 |
MOD_Plk_4 | 591 | 597 | PF00069 | 0.338 |
MOD_Plk_4 | 630 | 636 | PF00069 | 0.367 |
MOD_SUMO_for_1 | 284 | 287 | PF00179 | 0.391 |
MOD_SUMO_rev_2 | 240 | 245 | PF00179 | 0.408 |
MOD_SUMO_rev_2 | 305 | 314 | PF00179 | 0.418 |
MOD_SUMO_rev_2 | 594 | 602 | PF00179 | 0.200 |
TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 168 | 171 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 203 | 206 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 385 | 388 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 410 | 413 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 445 | 448 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 474 | 477 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 530 | 533 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 575 | 578 | PF00928 | 0.339 |
TRG_ER_diArg_1 | 18 | 21 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 207 | 210 | PF00400 | 0.261 |
TRG_NES_CRM1_1 | 447 | 461 | PF08389 | 0.300 |
TRG_NLS_MonoExtC_3 | 661 | 666 | PF00514 | 0.657 |
TRG_Pf-PMV_PEXEL_1 | 290 | 294 | PF00026 | 0.294 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 48% | 96% |
A0A0N1HY49 | Leptomonas seymouri | 65% | 100% |
A0A0N1HZ06 | Leptomonas seymouri | 43% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 43% | 95% |
A0A0N1PAY4 | Leptomonas seymouri | 42% | 77% |
A0A0N1PB77 | Leptomonas seymouri | 38% | 100% |
A0A0N1PBZ2 | Leptomonas seymouri | 46% | 100% |
A0A0N1PCC1 | Leptomonas seymouri | 50% | 100% |
A0A0S4INN8 | Bodo saltans | 29% | 100% |
A0A381MBI0 | Leishmania infantum | 44% | 100% |
A0A3Q8I8X7 | Leishmania donovani | 44% | 100% |
A0A3Q8IAZ0 | Leishmania donovani | 42% | 97% |
A0A3Q8IH50 | Leishmania donovani | 49% | 94% |
A0A3Q8IVN0 | Leishmania donovani | 39% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 46% | 100% |
A0A3S5H5P4 | Leishmania donovani | 91% | 100% |
A0A3S5H5V2 | Leishmania donovani | 43% | 100% |
A0A3S5H6F6 | Leishmania donovani | 43% | 97% |
A0A3S5H763 | Leishmania donovani | 48% | 100% |
A0A3S7WR10 | Leishmania donovani | 47% | 91% |
A0A3S7WR14 | Leishmania donovani | 45% | 99% |
A0A3S7WR15 | Leishmania donovani | 42% | 80% |
A0A3S7WR24 | Leishmania donovani | 43% | 96% |
A4H4T8 | Leishmania braziliensis | 43% | 100% |
A4H5Y4 | Leishmania braziliensis | 45% | 100% |
A4H617 | Leishmania braziliensis | 44% | 100% |
A4H618 | Leishmania braziliensis | 44% | 100% |
A4H619 | Leishmania braziliensis | 44% | 100% |
A4H620 | Leishmania braziliensis | 50% | 100% |
A4H6C3 | Leishmania braziliensis | 44% | 100% |
A4HNH7 | Leishmania braziliensis | 37% | 98% |
A4HSS2 | Leishmania infantum | 91% | 100% |
A4HUE4 | Leishmania infantum | 47% | 91% |
A4HUE5 | Leishmania infantum | 42% | 98% |
A4HUE6 | Leishmania infantum | 45% | 99% |
A4HUE7 | Leishmania infantum | 42% | 97% |
A4HUE8 | Leishmania infantum | 42% | 96% |
A4HUF4 | Leishmania infantum | 43% | 97% |
A4HUF5 | Leishmania infantum | 48% | 100% |
A4HYA9 | Leishmania infantum | 48% | 100% |
A4IC33 | Leishmania infantum | 38% | 100% |
C9ZIK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
C9ZIK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
C9ZVE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
C9ZVE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
C9ZVF1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
D0A423 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
E9AG72 | Leishmania infantum | 43% | 100% |
E9AI40 | Leishmania braziliensis | 43% | 100% |
E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 91% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 41% | 100% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
E9AN47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 95% |
E9ANE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
Q4QDC4 | Leishmania major | 52% | 100% |
Q4QH81 | Leishmania major | 44% | 100% |
Q4QHH7 | Leishmania major | 50% | 100% |
Q4QHH8 | Leishmania major | 42% | 100% |
Q4QHH9 | Leishmania major | 42% | 100% |
Q4QHI0 | Leishmania major | 41% | 100% |
Q4QHI1 | Leishmania major | 44% | 100% |
Q4QHI2 | Leishmania major | 43% | 100% |
Q4QIU9 | Leishmania major | 44% | 100% |
Q4QJ48 | Leishmania major | 91% | 100% |
Q7KIP2 | Leishmania major | 38% | 99% |