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: Q4QJ48
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 | 0.680 |
CLV_C14_Caspase3-7 | 311 | 315 | PF00656 | 0.577 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.226 |
CLV_NRD_NRD_1 | 664 | 666 | PF00675 | 0.456 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.251 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 524 | 526 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 664 | 666 | PF00082 | 0.468 |
CLV_PCSK_PC1ET2_1 | 150 | 152 | PF00082 | 0.293 |
CLV_PCSK_PC1ET2_1 | 285 | 287 | PF00082 | 0.354 |
CLV_PCSK_PC1ET2_1 | 524 | 526 | PF00082 | 0.521 |
CLV_PCSK_PC7_1 | 205 | 211 | PF00082 | 0.210 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.305 |
DEG_APCC_DBOX_1 | 19 | 27 | PF00400 | 0.660 |
DOC_CDC14_PxL_1 | 423 | 431 | PF14671 | 0.200 |
DOC_CDC14_PxL_1 | 610 | 618 | PF14671 | 0.331 |
DOC_CYCLIN_yCln2_LP_2 | 317 | 323 | PF00134 | 0.394 |
DOC_CYCLIN_yCln2_LP_2 | 627 | 633 | PF00134 | 0.371 |
DOC_CYCLIN_yCln2_LP_2 | 635 | 641 | PF00134 | 0.490 |
DOC_MAPK_gen_1 | 242 | 249 | PF00069 | 0.211 |
DOC_MAPK_gen_1 | 524 | 532 | PF00069 | 0.323 |
DOC_MAPK_HePTP_8 | 239 | 251 | PF00069 | 0.220 |
DOC_MAPK_MEF2A_6 | 242 | 251 | PF00069 | 0.320 |
DOC_MAPK_MEF2A_6 | 524 | 532 | PF00069 | 0.357 |
DOC_MAPK_MEF2A_6 | 80 | 87 | PF00069 | 0.524 |
DOC_MAPK_NFAT4_5 | 80 | 88 | PF00069 | 0.604 |
DOC_PP1_RVXF_1 | 125 | 131 | PF00149 | 0.606 |
DOC_PP2B_LxvP_1 | 445 | 448 | PF13499 | 0.374 |
DOC_PP2B_LxvP_1 | 627 | 630 | PF13499 | 0.358 |
DOC_PP4_FxxP_1 | 598 | 601 | PF00568 | 0.271 |
DOC_SPAK_OSR1_1 | 111 | 115 | PF12202 | 0.413 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.325 |
DOC_USP7_MATH_1 | 566 | 570 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 585 | 589 | PF00917 | 0.490 |
DOC_USP7_UBL2_3 | 308 | 312 | PF12436 | 0.410 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.483 |
LIG_14-3-3_CanoR_1 | 20 | 29 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 502 | 506 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 80 | 86 | PF00244 | 0.519 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.733 |
LIG_BRCT_BRCA1_1 | 258 | 262 | PF00533 | 0.273 |
LIG_BRCT_BRCA1_1 | 335 | 339 | PF00533 | 0.384 |
LIG_BRCT_BRCA1_1 | 433 | 437 | PF00533 | 0.491 |
LIG_BRCT_BRCA1_1 | 438 | 442 | PF00533 | 0.432 |
LIG_BRCT_BRCA1_1 | 468 | 472 | PF00533 | 0.317 |
LIG_BRCT_BRCA1_1 | 499 | 503 | PF00533 | 0.460 |
LIG_CaM_NSCaTE_8 | 222 | 229 | PF13499 | 0.241 |
LIG_CSL_BTD_1 | 553 | 556 | PF09270 | 0.397 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.424 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.325 |
LIG_FHA_1 | 555 | 561 | PF00498 | 0.239 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.570 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.573 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.607 |
LIG_FHA_2 | 341 | 347 | PF00498 | 0.461 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.498 |
LIG_GBD_Chelix_1 | 87 | 95 | PF00786 | 0.230 |
LIG_LIR_Apic_2 | 46 | 52 | PF02991 | 0.624 |
LIG_LIR_Apic_2 | 597 | 601 | PF02991 | 0.302 |
LIG_LIR_Gen_1 | 200 | 211 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 403 | 413 | PF02991 | 0.295 |
LIG_LIR_Gen_1 | 439 | 450 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 500 | 511 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 516 | 523 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 571 | 580 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 607 | 618 | PF02991 | 0.271 |
LIG_LIR_Gen_1 | 632 | 641 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 165 | 171 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 200 | 206 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 229 | 234 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 403 | 408 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 420 | 426 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 434 | 440 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 469 | 473 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 504 | 510 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 516 | 521 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 571 | 577 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 607 | 613 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 632 | 636 | PF02991 | 0.282 |
LIG_LRP6_Inhibitor_1 | 647 | 653 | PF00058 | 0.188 |
LIG_MLH1_MIPbox_1 | 433 | 437 | PF16413 | 0.571 |
LIG_PDZ_Class_2 | 671 | 676 | PF00595 | 0.587 |
LIG_Pex14_1 | 220 | 224 | PF04695 | 0.375 |
LIG_Pex14_1 | 405 | 409 | PF04695 | 0.285 |
LIG_Pex14_1 | 424 | 428 | PF04695 | 0.329 |
LIG_Pex14_2 | 108 | 112 | PF04695 | 0.406 |
LIG_Pex14_2 | 186 | 190 | PF04695 | 0.365 |
LIG_Pex14_2 | 263 | 267 | PF04695 | 0.285 |
LIG_Pex14_2 | 438 | 442 | PF04695 | 0.366 |
LIG_Pex14_2 | 468 | 472 | PF04695 | 0.306 |
LIG_Pex14_2 | 492 | 496 | PF04695 | 0.365 |
LIG_Pex14_2 | 503 | 507 | PF04695 | 0.365 |
LIG_SH2_CRK | 119 | 123 | PF00017 | 0.512 |
LIG_SH2_CRK | 168 | 172 | PF00017 | 0.321 |
LIG_SH2_CRK | 203 | 207 | PF00017 | 0.515 |
LIG_SH2_CRK | 384 | 388 | PF00017 | 0.346 |
LIG_SH2_CRK | 409 | 413 | PF00017 | 0.355 |
LIG_SH2_CRK | 440 | 444 | PF00017 | 0.338 |
LIG_SH2_CRK | 473 | 477 | PF00017 | 0.298 |
LIG_SH2_CRK | 574 | 578 | PF00017 | 0.218 |
LIG_SH2_CRK | 97 | 101 | PF00017 | 0.527 |
LIG_SH2_GRB2like | 328 | 331 | PF00017 | 0.391 |
LIG_SH2_NCK_1 | 409 | 413 | PF00017 | 0.416 |
LIG_SH2_NCK_1 | 473 | 477 | PF00017 | 0.300 |
LIG_SH2_NCK_1 | 574 | 578 | PF00017 | 0.299 |
LIG_SH2_NCK_1 | 97 | 101 | PF00017 | 0.391 |
LIG_SH2_PTP2 | 49 | 52 | PF00017 | 0.614 |
LIG_SH2_PTP2 | 529 | 532 | PF00017 | 0.400 |
LIG_SH2_SRC | 49 | 52 | PF00017 | 0.620 |
LIG_SH2_STAP1 | 102 | 106 | PF00017 | 0.530 |
LIG_SH2_STAP1 | 148 | 152 | PF00017 | 0.501 |
LIG_SH2_STAP1 | 203 | 207 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 384 | 388 | PF00017 | 0.394 |
LIG_SH2_STAP1 | 409 | 413 | PF00017 | 0.284 |
LIG_SH2_STAP1 | 440 | 444 | PF00017 | 0.328 |
LIG_SH2_STAP1 | 546 | 550 | PF00017 | 0.406 |
LIG_SH2_STAP1 | 574 | 578 | PF00017 | 0.339 |
LIG_SH2_STAT3 | 509 | 512 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 444 | 447 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.261 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.609 |
LIG_SH2_STAT5 | 494 | 497 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 529 | 532 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 538 | 541 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 551 | 554 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.517 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.280 |
LIG_SH3_3 | 631 | 637 | PF00018 | 0.396 |
LIG_SUMO_SIM_anti_2 | 410 | 416 | PF11976 | 0.399 |
LIG_SUMO_SIM_anti_2 | 519 | 524 | PF11976 | 0.315 |
LIG_SUMO_SIM_anti_2 | 557 | 562 | PF11976 | 0.251 |
LIG_SUMO_SIM_par_1 | 385 | 391 | PF11976 | 0.300 |
LIG_SUMO_SIM_par_1 | 556 | 562 | PF11976 | 0.329 |
LIG_TRFH_1 | 633 | 637 | PF08558 | 0.291 |
LIG_TYR_ITIM | 117 | 122 | PF00017 | 0.299 |
LIG_TYR_ITIM | 166 | 171 | PF00017 | 0.377 |
LIG_TYR_ITIM | 407 | 412 | PF00017 | 0.374 |
LIG_TYR_ITIM | 471 | 476 | PF00017 | 0.338 |
LIG_TYR_ITIM | 95 | 100 | PF00017 | 0.451 |
LIG_WRC_WIRS_1 | 187 | 192 | PF05994 | 0.251 |
LIG_WRC_WIRS_1 | 451 | 456 | PF05994 | 0.335 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.350 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.410 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.347 |
MOD_CK1_1 | 497 | 503 | PF00069 | 0.352 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.499 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.435 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.382 |
MOD_CMANNOS | 220 | 223 | PF00535 | 0.251 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.277 |
MOD_GlcNHglycan | 175 | 179 | PF01048 | 0.355 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.358 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.397 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.555 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.387 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.258 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.303 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.498 |
MOD_GlcNHglycan | 334 | 338 | PF01048 | 0.442 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.444 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.437 |
MOD_GlcNHglycan | 646 | 650 | PF01048 | 0.516 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.278 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.456 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.376 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.294 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.364 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.375 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.320 |
MOD_N-GLC_1 | 21 | 26 | PF02516 | 0.406 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.292 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.376 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.283 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.332 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.326 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.327 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.366 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.350 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.329 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.320 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.356 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.361 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.355 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.369 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.354 |
MOD_NEK2_2 | 340 | 345 | PF00069 | 0.343 |
MOD_NEK2_2 | 431 | 436 | PF00069 | 0.423 |
MOD_NEK2_2 | 450 | 455 | PF00069 | 0.337 |
MOD_PIKK_1 | 252 | 258 | PF00454 | 0.200 |
MOD_PK_1 | 121 | 127 | PF00069 | 0.452 |
MOD_PKA_1 | 173 | 179 | PF00069 | 0.360 |
MOD_PKA_1 | 209 | 215 | PF00069 | 0.187 |
MOD_PKA_2 | 209 | 215 | PF00069 | 0.187 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.204 |
MOD_PKA_2 | 501 | 507 | PF00069 | 0.350 |
MOD_PKA_2 | 566 | 572 | PF00069 | 0.339 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.414 |
MOD_PKB_1 | 208 | 216 | PF00069 | 0.200 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.413 |
MOD_Plk_1 | 546 | 552 | PF00069 | 0.346 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.340 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.334 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.348 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.352 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.312 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.439 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.338 |
MOD_Plk_4 | 546 | 552 | PF00069 | 0.310 |
MOD_Plk_4 | 554 | 560 | PF00069 | 0.308 |
MOD_Plk_4 | 568 | 574 | PF00069 | 0.371 |
MOD_Plk_4 | 590 | 596 | PF00069 | 0.339 |
MOD_Plk_4 | 629 | 635 | PF00069 | 0.369 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.349 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.322 |
MOD_SUMO_for_1 | 172 | 175 | PF00179 | 0.197 |
MOD_SUMO_for_1 | 284 | 287 | PF00179 | 0.392 |
MOD_SUMO_rev_2 | 240 | 245 | PF00179 | 0.409 |
MOD_SUMO_rev_2 | 30 | 39 | PF00179 | 0.688 |
MOD_SUMO_rev_2 | 306 | 313 | PF00179 | 0.372 |
MOD_SUMO_rev_2 | 593 | 601 | PF00179 | 0.200 |
TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 168 | 171 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 203 | 206 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 409 | 412 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 440 | 443 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 444 | 447 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 473 | 476 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 529 | 532 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 574 | 577 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.371 |
TRG_ER_diArg_1 | 18 | 21 | PF00400 | 0.590 |
TRG_ER_diArg_1 | 207 | 210 | PF00400 | 0.271 |
TRG_NES_CRM1_1 | 446 | 460 | PF08389 | 0.301 |
TRG_Pf-PMV_PEXEL_1 | 290 | 294 | PF00026 | 0.301 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 48% | 96% |
A0A0N1HY49 | Leptomonas seymouri | 66% | 100% |
A0A0N1HZ06 | Leptomonas seymouri | 43% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 43% | 95% |
A0A0N1PAY4 | Leptomonas seymouri | 42% | 77% |
A0A0N1PB77 | Leptomonas seymouri | 39% | 100% |
A0A0N1PBZ2 | Leptomonas seymouri | 48% | 100% |
A0A0N1PCC1 | Leptomonas seymouri | 53% | 100% |
A0A0S4INN8 | Bodo saltans | 29% | 100% |
A0A381MBI0 | Leishmania infantum | 44% | 100% |
A0A3Q8I8X7 | Leishmania donovani | 44% | 100% |
A0A3Q8IAZ0 | Leishmania donovani | 43% | 97% |
A0A3Q8IH50 | Leishmania donovani | 49% | 94% |
A0A3Q8IVN0 | Leishmania donovani | 40% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 45% | 100% |
A0A3S5H5P4 | Leishmania donovani | 94% | 100% |
A0A3S5H5V2 | Leishmania donovani | 46% | 100% |
A0A3S5H6F6 | Leishmania donovani | 43% | 97% |
A0A3S5H763 | Leishmania donovani | 49% | 100% |
A0A3S7WR10 | Leishmania donovani | 45% | 91% |
A0A3S7WR14 | Leishmania donovani | 44% | 99% |
A0A3S7WR15 | Leishmania donovani | 41% | 80% |
A0A3S7WR24 | Leishmania donovani | 43% | 96% |
A4H4T8 | Leishmania braziliensis | 45% | 100% |
A4H5Y4 | Leishmania braziliensis | 46% | 100% |
A4H617 | Leishmania braziliensis | 44% | 97% |
A4H618 | Leishmania braziliensis | 45% | 99% |
A4H619 | Leishmania braziliensis | 45% | 97% |
A4H620 | Leishmania braziliensis | 50% | 96% |
A4H6C3 | Leishmania braziliensis | 46% | 100% |
A4HNH7 | Leishmania braziliensis | 39% | 100% |
A4HSS2 | Leishmania infantum | 95% | 100% |
A4HUE4 | Leishmania infantum | 45% | 91% |
A4HUE5 | Leishmania infantum | 41% | 98% |
A4HUE6 | Leishmania infantum | 44% | 99% |
A4HUE7 | Leishmania infantum | 42% | 97% |
A4HUE8 | Leishmania infantum | 43% | 96% |
A4HUF4 | Leishmania infantum | 43% | 97% |
A4HUF5 | Leishmania infantum | 48% | 100% |
A4HYA9 | Leishmania infantum | 49% | 100% |
A4IC33 | Leishmania infantum | 40% | 100% |
C9ZIK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
C9ZIK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
C9ZVE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
C9ZVE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 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% | 97% |
E9AG72 | Leishmania infantum | 46% | 100% |
E9AI40 | Leishmania braziliensis | 44% | 99% |
E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 100% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 91% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 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) | 46% | 100% |
E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 52% | 100% |
E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
Q4QDC4 | Leishmania major | 52% | 100% |
Q4QH81 | Leishmania major | 46% | 100% |
Q4QHH7 | Leishmania major | 50% | 100% |
Q4QHH8 | Leishmania major | 43% | 100% |
Q4QHH9 | Leishmania major | 43% | 100% |
Q4QHI0 | Leishmania major | 42% | 100% |
Q4QHI1 | Leishmania major | 45% | 100% |
Q4QHI2 | Leishmania major | 44% | 100% |
Q4QIU9 | Leishmania major | 47% | 100% |
Q7KIP2 | Leishmania major | 39% | 98% |