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: 67 |
NetGPI | no | yes: 0, no: 67 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 68 |
GO:0110165 | cellular anatomical entity | 1 | 68 |
GO:0005737 | cytoplasm | 2 | 6 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: E9AN44
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 | 285 | 289 | PF00656 | 0.458 |
CLV_C14_Caspase3-7 | 48 | 52 | PF00656 | 0.667 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.225 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.293 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.262 |
CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.317 |
CLV_PCSK_PC1ET2_1 | 115 | 117 | PF00082 | 0.211 |
CLV_PCSK_PC1ET2_1 | 155 | 157 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 413 | 417 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 648 | 652 | PF00082 | 0.417 |
CLV_Separin_Metazoa | 406 | 410 | PF03568 | 0.411 |
DOC_ANK_TNKS_1 | 46 | 53 | PF00023 | 0.551 |
DOC_CDC14_PxL_1 | 667 | 675 | PF14671 | 0.185 |
DOC_CYCLIN_yCln2_LP_2 | 661 | 667 | PF00134 | 0.380 |
DOC_MAPK_gen_1 | 299 | 309 | PF00069 | 0.555 |
DOC_MAPK_gen_1 | 672 | 681 | PF00069 | 0.581 |
DOC_MAPK_MEF2A_6 | 249 | 256 | PF00069 | 0.344 |
DOC_MAPK_MEF2A_6 | 301 | 309 | PF00069 | 0.391 |
DOC_MAPK_MEF2A_6 | 558 | 565 | PF00069 | 0.346 |
DOC_PP2B_LxvP_1 | 391 | 394 | PF13499 | 0.391 |
DOC_PP2B_LxvP_1 | 478 | 481 | PF13499 | 0.354 |
DOC_PP2B_LxvP_1 | 661 | 664 | PF13499 | 0.365 |
DOC_PP2B_LxvP_1 | 668 | 671 | PF13499 | 0.338 |
DOC_PP4_FxxP_1 | 457 | 460 | PF00568 | 0.330 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.259 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 483 | 487 | PF00917 | 0.306 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.283 |
DOC_USP7_MATH_1 | 546 | 550 | PF00917 | 0.327 |
DOC_USP7_MATH_1 | 599 | 603 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 608 | 612 | PF00917 | 0.340 |
DOC_USP7_MATH_1 | 725 | 729 | PF00917 | 0.742 |
DOC_USP7_UBL2_3 | 295 | 299 | PF12436 | 0.575 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 655 | 660 | PF00397 | 0.484 |
LIG_14-3-3_CanoR_1 | 156 | 161 | PF00244 | 0.390 |
LIG_14-3-3_CanoR_1 | 365 | 375 | PF00244 | 0.393 |
LIG_14-3-3_CanoR_1 | 703 | 711 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 726 | 733 | PF00244 | 0.793 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.747 |
LIG_BIR_III_4 | 735 | 739 | PF00653 | 0.585 |
LIG_BRCT_BRCA1_1 | 394 | 398 | PF00533 | 0.457 |
LIG_BRCT_BRCA1_1 | 501 | 505 | PF00533 | 0.304 |
LIG_BRCT_BRCA1_1 | 610 | 614 | PF00533 | 0.310 |
LIG_CaM_NSCaTE_8 | 412 | 419 | PF13499 | 0.391 |
LIG_EH1_1 | 578 | 586 | PF00400 | 0.348 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.585 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.336 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.269 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.358 |
LIG_FHA_1 | 535 | 541 | PF00498 | 0.502 |
LIG_FHA_1 | 635 | 641 | PF00498 | 0.412 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.551 |
LIG_FHA_2 | 275 | 281 | PF00498 | 0.401 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.457 |
LIG_FHA_2 | 353 | 359 | PF00498 | 0.435 |
LIG_FHA_2 | 434 | 440 | PF00498 | 0.212 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.645 |
LIG_FHA_2 | 732 | 738 | PF00498 | 0.590 |
LIG_LIR_Gen_1 | 122 | 130 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 145 | 153 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 170 | 180 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 205 | 216 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 224 | 232 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 436 | 446 | PF02991 | 0.282 |
LIG_LIR_Gen_1 | 474 | 484 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 549 | 556 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 604 | 614 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 643 | 652 | PF02991 | 0.281 |
LIG_LIR_Gen_1 | 666 | 675 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 122 | 127 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 147 | 153 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 154 | 160 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 224 | 230 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 395 | 401 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 439 | 445 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 474 | 480 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 502 | 506 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 549 | 554 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 557 | 562 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 643 | 647 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 666 | 670 | PF02991 | 0.266 |
LIG_NRBOX | 471 | 477 | PF00104 | 0.225 |
LIG_Pex14_1 | 227 | 231 | PF04695 | 0.361 |
LIG_Pex14_1 | 438 | 442 | PF04695 | 0.273 |
LIG_Pex14_2 | 268 | 272 | PF04695 | 0.289 |
LIG_Pex14_2 | 501 | 505 | PF04695 | 0.297 |
LIG_Pex14_2 | 525 | 529 | PF04695 | 0.379 |
LIG_SH2_CRK | 124 | 128 | PF00017 | 0.499 |
LIG_SH2_CRK | 158 | 162 | PF00017 | 0.363 |
LIG_SH2_CRK | 173 | 177 | PF00017 | 0.357 |
LIG_SH2_CRK | 208 | 212 | PF00017 | 0.527 |
LIG_SH2_CRK | 417 | 421 | PF00017 | 0.347 |
LIG_SH2_CRK | 442 | 446 | PF00017 | 0.335 |
LIG_SH2_CRK | 506 | 510 | PF00017 | 0.311 |
LIG_SH2_NCK_1 | 506 | 510 | PF00017 | 0.310 |
LIG_SH2_PTP2 | 562 | 565 | PF00017 | 0.396 |
LIG_SH2_STAP1 | 153 | 157 | PF00017 | 0.502 |
LIG_SH2_STAP1 | 208 | 212 | PF00017 | 0.491 |
LIG_SH2_STAP1 | 417 | 421 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 477 | 480 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 488 | 491 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 562 | 565 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 571 | 574 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.519 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.282 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.656 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.400 |
LIG_SH3_3 | 493 | 499 | PF00018 | 0.290 |
LIG_SUMO_SIM_anti_2 | 198 | 205 | PF11976 | 0.401 |
LIG_SUMO_SIM_anti_2 | 424 | 430 | PF11976 | 0.246 |
LIG_SUMO_SIM_anti_2 | 541 | 546 | PF11976 | 0.299 |
LIG_SUMO_SIM_anti_2 | 552 | 557 | PF11976 | 0.311 |
LIG_SUMO_SIM_anti_2 | 658 | 664 | PF11976 | 0.441 |
LIG_SUMO_SIM_par_1 | 552 | 557 | PF11976 | 0.421 |
LIG_TRAF2_1 | 314 | 317 | PF00917 | 0.384 |
LIG_TRAF2_1 | 386 | 389 | PF00917 | 0.408 |
LIG_TRFH_1 | 173 | 177 | PF08558 | 0.341 |
LIG_TRFH_1 | 667 | 671 | PF08558 | 0.301 |
LIG_TYR_ITIM | 171 | 176 | PF00017 | 0.396 |
LIG_TYR_ITIM | 415 | 420 | PF00017 | 0.261 |
LIG_TYR_ITIM | 440 | 445 | PF00017 | 0.354 |
LIG_TYR_ITIM | 475 | 480 | PF00017 | 0.354 |
LIG_TYR_ITIM | 504 | 509 | PF00017 | 0.318 |
LIG_Vh1_VBS_1 | 415 | 433 | PF01044 | 0.389 |
LIG_WRC_WIRS_1 | 484 | 489 | PF05994 | 0.322 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.249 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.603 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.501 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.507 |
MOD_CK2_1 | 274 | 280 | PF00069 | 0.209 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.416 |
MOD_CK2_1 | 352 | 358 | PF00069 | 0.311 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.205 |
MOD_CK2_1 | 731 | 737 | PF00069 | 0.529 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.337 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.391 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.665 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.396 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.659 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.469 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.210 |
MOD_GlcNHglycan | 5 | 9 | PF01048 | 0.740 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.413 |
MOD_GlcNHglycan | 610 | 613 | PF01048 | 0.368 |
MOD_GlcNHglycan | 704 | 707 | PF01048 | 0.608 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.269 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.354 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.434 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.405 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.372 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.315 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.263 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.343 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.372 |
MOD_GSK3_1 | 584 | 591 | PF00069 | 0.224 |
MOD_GSK3_1 | 727 | 734 | PF00069 | 0.523 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.306 |
MOD_N-GLC_1 | 490 | 495 | PF02516 | 0.402 |
MOD_N-GLC_2 | 580 | 582 | PF02516 | 0.195 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.318 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.346 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.341 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.358 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.335 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.373 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.293 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.683 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.362 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.336 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.461 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.352 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.374 |
MOD_NEK2_1 | 584 | 589 | PF00069 | 0.418 |
MOD_NEK2_1 | 616 | 621 | PF00069 | 0.362 |
MOD_NEK2_1 | 628 | 633 | PF00069 | 0.377 |
MOD_NEK2_1 | 650 | 655 | PF00069 | 0.444 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.444 |
MOD_NEK2_2 | 133 | 138 | PF00069 | 0.195 |
MOD_NEK2_2 | 483 | 488 | PF00069 | 0.317 |
MOD_NEK2_2 | 546 | 551 | PF00069 | 0.348 |
MOD_PIKK_1 | 39 | 45 | PF00454 | 0.685 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.396 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.282 |
MOD_PKA_2 | 599 | 605 | PF00069 | 0.335 |
MOD_PKA_2 | 702 | 708 | PF00069 | 0.584 |
MOD_PKA_2 | 725 | 731 | PF00069 | 0.613 |
MOD_Plk_1 | 119 | 125 | PF00069 | 0.298 |
MOD_Plk_1 | 490 | 496 | PF00069 | 0.427 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.302 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.355 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.348 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.333 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.329 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.352 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.319 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.486 |
MOD_Plk_4 | 540 | 546 | PF00069 | 0.311 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.505 |
MOD_Plk_4 | 588 | 594 | PF00069 | 0.326 |
MOD_Plk_4 | 601 | 607 | PF00069 | 0.373 |
MOD_Plk_4 | 663 | 669 | PF00069 | 0.361 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.299 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.397 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.434 |
MOD_ProDKin_1 | 655 | 661 | PF00069 | 0.484 |
MOD_SUMO_rev_2 | 285 | 292 | PF00179 | 0.236 |
MOD_SUMO_rev_2 | 304 | 312 | PF00179 | 0.433 |
MOD_SUMO_rev_2 | 34 | 40 | PF00179 | 0.696 |
MOD_SUMO_rev_2 | 354 | 362 | PF00179 | 0.193 |
TRG_DiLeu_BaLyEn_6 | 656 | 661 | PF01217 | 0.329 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 417 | 420 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 442 | 445 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 477 | 480 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 506 | 509 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 562 | 565 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 607 | 610 | PF00928 | 0.355 |
TRG_ER_diArg_1 | 212 | 214 | PF00400 | 0.265 |
TRG_ER_diArg_1 | 365 | 368 | PF00400 | 0.343 |
TRG_ER_diArg_1 | 671 | 674 | PF00400 | 0.326 |
TRG_NES_CRM1_1 | 618 | 630 | PF08389 | 0.351 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 58% | 100% |
A0A0N1HY49 | Leptomonas seymouri | 47% | 100% |
A0A0N1HZ06 | Leptomonas seymouri | 41% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 42% | 100% |
A0A0N1PAY4 | Leptomonas seymouri | 39% | 85% |
A0A0N1PB77 | Leptomonas seymouri | 39% | 100% |
A0A0N1PBZ2 | Leptomonas seymouri | 44% | 100% |
A0A0N1PCC1 | Leptomonas seymouri | 41% | 100% |
A0A381MBI0 | Leishmania infantum | 43% | 100% |
A0A3Q8I8X7 | Leishmania donovani | 43% | 100% |
A0A3Q8IAZ0 | Leishmania donovani | 42% | 100% |
A0A3Q8IH50 | Leishmania donovani | 51% | 100% |
A0A3Q8IVN0 | Leishmania donovani | 41% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 42% | 100% |
A0A3S5H5P4 | Leishmania donovani | 46% | 100% |
A0A3S5H5V2 | Leishmania donovani | 48% | 100% |
A0A3S5H6F6 | Leishmania donovani | 43% | 100% |
A0A3S5H763 | Leishmania donovani | 48% | 100% |
A0A3S7WR10 | Leishmania donovani | 85% | 100% |
A0A3S7WR14 | Leishmania donovani | 45% | 100% |
A0A3S7WR15 | Leishmania donovani | 42% | 88% |
A0A3S7WR24 | Leishmania donovani | 42% | 100% |
A4H4T8 | Leishmania braziliensis | 47% | 100% |
A4H5Y4 | Leishmania braziliensis | 42% | 100% |
A4H617 | Leishmania braziliensis | 42% | 99% |
A4H618 | Leishmania braziliensis | 43% | 100% |
A4H619 | Leishmania braziliensis | 42% | 99% |
A4H620 | Leishmania braziliensis | 48% | 96% |
A4H6C3 | Leishmania braziliensis | 41% | 100% |
A4HNH7 | Leishmania braziliensis | 39% | 95% |
A4HSS2 | Leishmania infantum | 46% | 100% |
A4HUE4 | Leishmania infantum | 85% | 100% |
A4HUE5 | Leishmania infantum | 42% | 100% |
A4HUE6 | Leishmania infantum | 45% | 100% |
A4HUE7 | Leishmania infantum | 43% | 100% |
A4HUE8 | Leishmania infantum | 43% | 100% |
A4HUF4 | Leishmania infantum | 42% | 100% |
A4HUF5 | Leishmania infantum | 50% | 100% |
A4HYA9 | Leishmania infantum | 48% | 100% |
A4IC33 | Leishmania infantum | 41% | 100% |
C9ZIK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
C9ZIK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
D0A423 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
E9AG72 | Leishmania infantum | 47% | 100% |
E9AI40 | Leishmania braziliensis | 43% | 100% |
E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 97% |
E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
E9AN47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
E9ANE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 100% |
E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
Q4QDC4 | Leishmania major | 48% | 100% |
Q4QH81 | Leishmania major | 43% | 100% |
Q4QHH7 | Leishmania major | 49% | 100% |
Q4QHH8 | Leishmania major | 42% | 100% |
Q4QHH9 | Leishmania major | 42% | 100% |
Q4QHI0 | Leishmania major | 42% | 99% |
Q4QHI1 | Leishmania major | 44% | 100% |
Q4QHI2 | Leishmania major | 43% | 98% |
Q4QIU9 | Leishmania major | 46% | 100% |
Q4QJ48 | Leishmania major | 45% | 100% |
Q7KIP2 | Leishmania major | 41% | 97% |