An expanded family of eukaryotic equlibrative nuceloside transporters.
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 45 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | yes | yes: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 45 |
NetGPI | no | yes: 0, no: 45 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 5 |
GO:0016020 | membrane | 2 | 46 |
GO:0110165 | cellular anatomical entity | 1 | 46 |
Related structures:
AlphaFold database: Q4QF59
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0015851 | nucleobase 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 | 46 |
GO:0005337 | nucleoside transmembrane transporter activity | 4 | 46 |
GO:0015932 | nucleobase-containing compound transmembrane transporter activity | 3 | 46 |
GO:0022857 | transmembrane transporter activity | 2 | 46 |
GO:1901505 | carbohydrate derivative transmembrane transporter activity | 3 | 46 |
GO:0015205 | nucleobase transmembrane transporter activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 412 | 416 | PF00656 | 0.593 |
CLV_MEL_PAP_1 | 540 | 546 | PF00089 | 0.280 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.342 |
CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.232 |
CLV_PCSK_FUR_1 | 129 | 133 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 493 | 495 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 623 | 625 | PF00082 | 0.246 |
CLV_PCSK_PC1ET2_1 | 623 | 625 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 493 | 497 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 569 | 573 | PF00082 | 0.332 |
DEG_ODPH_VHL_1 | 91 | 102 | PF01847 | 0.544 |
DOC_CYCLIN_RxL_1 | 138 | 147 | PF00134 | 0.522 |
DOC_MAPK_DCC_7 | 569 | 578 | PF00069 | 0.314 |
DOC_MAPK_FxFP_2 | 511 | 514 | PF00069 | 0.422 |
DOC_MAPK_gen_1 | 268 | 276 | PF00069 | 0.554 |
DOC_MAPK_gen_1 | 370 | 381 | PF00069 | 0.327 |
DOC_MAPK_gen_1 | 493 | 500 | PF00069 | 0.499 |
DOC_MAPK_gen_1 | 554 | 563 | PF00069 | 0.539 |
DOC_MAPK_MEF2A_6 | 268 | 276 | PF00069 | 0.552 |
DOC_MAPK_MEF2A_6 | 374 | 383 | PF00069 | 0.385 |
DOC_MAPK_MEF2A_6 | 525 | 534 | PF00069 | 0.384 |
DOC_MAPK_MEF2A_6 | 543 | 550 | PF00069 | 0.298 |
DOC_MAPK_MEF2A_6 | 569 | 578 | PF00069 | 0.345 |
DOC_PP1_RVXF_1 | 491 | 498 | PF00149 | 0.582 |
DOC_PP1_RVXF_1 | 567 | 573 | PF00149 | 0.407 |
DOC_PP2B_LxvP_1 | 91 | 94 | PF13499 | 0.527 |
DOC_PP2B_PxIxI_1 | 513 | 519 | PF00149 | 0.481 |
DOC_PP4_FxxP_1 | 213 | 216 | PF00568 | 0.385 |
DOC_PP4_FxxP_1 | 511 | 514 | PF00568 | 0.426 |
DOC_PP4_FxxP_1 | 550 | 553 | PF00568 | 0.577 |
DOC_SPAK_OSR1_1 | 132 | 136 | PF12202 | 0.521 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.533 |
DOC_USP7_UBL2_3 | 370 | 374 | PF12436 | 0.255 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 542 | 547 | PF00397 | 0.394 |
LIG_14-3-3_CanoR_1 | 12 | 21 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 146 | 151 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 24 | 30 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 395 | 400 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 47 | 56 | PF00244 | 0.550 |
LIG_APCC_ABBA_1 | 518 | 523 | PF00400 | 0.246 |
LIG_BRCT_BRCA1_1 | 523 | 527 | PF00533 | 0.382 |
LIG_BRCT_BRCA1_1 | 546 | 550 | PF00533 | 0.525 |
LIG_BRCT_BRCA1_1 | 58 | 62 | PF00533 | 0.542 |
LIG_BRCT_BRCA1_1 | 9 | 13 | PF00533 | 0.537 |
LIG_deltaCOP1_diTrp_1 | 523 | 533 | PF00928 | 0.246 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.551 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.528 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.564 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.324 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.333 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.361 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.326 |
LIG_FHA_1 | 527 | 533 | PF00498 | 0.360 |
LIG_FHA_1 | 647 | 653 | PF00498 | 0.486 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.563 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.656 |
LIG_FHA_2 | 186 | 192 | PF00498 | 0.539 |
LIG_FHA_2 | 476 | 482 | PF00498 | 0.522 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.545 |
LIG_FHA_2 | 649 | 655 | PF00498 | 0.288 |
LIG_GBD_Chelix_1 | 484 | 492 | PF00786 | 0.391 |
LIG_LIR_Apic_2 | 509 | 514 | PF02991 | 0.388 |
LIG_LIR_Apic_2 | 547 | 553 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 190 | 200 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 245 | 253 | PF02991 | 0.268 |
LIG_LIR_Gen_1 | 334 | 344 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 387 | 396 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 486 | 495 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 524 | 535 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 566 | 575 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 580 | 589 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 16 | 21 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 190 | 196 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 221 | 225 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 237 | 243 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 245 | 250 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 265 | 270 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 323 | 329 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 334 | 339 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 364 | 369 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 373 | 379 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 387 | 391 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 486 | 492 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 524 | 530 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 566 | 570 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 580 | 584 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 587 | 592 | PF02991 | 0.331 |
LIG_NRBOX | 349 | 355 | PF00104 | 0.280 |
LIG_Pex14_1 | 552 | 556 | PF04695 | 0.582 |
LIG_Pex14_2 | 312 | 316 | PF04695 | 0.471 |
LIG_Pex14_2 | 332 | 336 | PF04695 | 0.448 |
LIG_PTB_Apo_2 | 12 | 19 | PF02174 | 0.540 |
LIG_SH2_CRK | 247 | 251 | PF00017 | 0.360 |
LIG_SH2_CRK | 581 | 585 | PF00017 | 0.330 |
LIG_SH2_CRK | 589 | 593 | PF00017 | 0.324 |
LIG_SH2_GRB2like | 236 | 239 | PF00017 | 0.381 |
LIG_SH2_GRB2like | 246 | 249 | PF00017 | 0.298 |
LIG_SH2_NCK_1 | 247 | 251 | PF00017 | 0.419 |
LIG_SH2_PTP2 | 193 | 196 | PF00017 | 0.466 |
LIG_SH2_SRC | 193 | 196 | PF00017 | 0.424 |
LIG_SH2_SRC | 583 | 586 | PF00017 | 0.338 |
LIG_SH2_STAP1 | 185 | 189 | PF00017 | 0.620 |
LIG_SH2_STAP1 | 236 | 240 | PF00017 | 0.424 |
LIG_SH2_STAT3 | 225 | 228 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 583 | 586 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 591 | 594 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 603 | 606 | PF00017 | 0.285 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.549 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.567 |
LIG_SH3_3 | 471 | 477 | PF00018 | 0.553 |
LIG_SH3_3 | 607 | 613 | PF00018 | 0.431 |
LIG_SH3_3 | 97 | 103 | PF00018 | 0.554 |
LIG_SUMO_SIM_anti_2 | 259 | 265 | PF11976 | 0.478 |
LIG_SUMO_SIM_anti_2 | 286 | 292 | PF11976 | 0.321 |
LIG_SUMO_SIM_anti_2 | 387 | 393 | PF11976 | 0.343 |
LIG_SUMO_SIM_anti_2 | 643 | 649 | PF11976 | 0.364 |
LIG_SUMO_SIM_par_1 | 105 | 111 | PF11976 | 0.554 |
LIG_SUMO_SIM_par_1 | 259 | 265 | PF11976 | 0.445 |
LIG_SUMO_SIM_par_1 | 280 | 286 | PF11976 | 0.318 |
LIG_SUMO_SIM_par_1 | 574 | 580 | PF11976 | 0.435 |
LIG_SUMO_SIM_par_1 | 643 | 649 | PF11976 | 0.280 |
LIG_TYR_ITSM | 243 | 250 | PF00017 | 0.306 |
LIG_UBA3_1 | 353 | 359 | PF00899 | 0.377 |
LIG_UBA3_1 | 488 | 496 | PF00899 | 0.566 |
LIG_ULM_U2AF65_1 | 493 | 498 | PF00076 | 0.432 |
LIG_WRC_WIRS_1 | 396 | 401 | PF05994 | 0.520 |
MOD_CDK_SPK_2 | 117 | 122 | PF00069 | 0.568 |
MOD_CDK_SPxxK_3 | 117 | 124 | PF00069 | 0.568 |
MOD_CDK_SPxxK_3 | 542 | 549 | PF00069 | 0.280 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.528 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.566 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.571 |
MOD_CK1_1 | 646 | 652 | PF00069 | 0.452 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.553 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.551 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.427 |
MOD_CK2_1 | 439 | 445 | PF00069 | 0.578 |
MOD_CK2_1 | 475 | 481 | PF00069 | 0.528 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.543 |
MOD_CK2_1 | 648 | 654 | PF00069 | 0.437 |
MOD_Cter_Amidation | 621 | 624 | PF01082 | 0.246 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.358 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.332 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.378 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.552 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.328 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.300 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.364 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.347 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.564 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.330 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.358 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.239 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.447 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.312 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.548 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.324 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.541 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.529 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.333 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.561 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.353 |
MOD_NEK2_1 | 483 | 488 | PF00069 | 0.515 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.361 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.544 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.367 |
MOD_NEK2_1 | 597 | 602 | PF00069 | 0.431 |
MOD_NEK2_1 | 631 | 636 | PF00069 | 0.359 |
MOD_NEK2_1 | 648 | 653 | PF00069 | 0.355 |
MOD_NEK2_2 | 112 | 117 | PF00069 | 0.569 |
MOD_PIKK_1 | 57 | 63 | PF00454 | 0.543 |
MOD_PIKK_1 | 646 | 652 | PF00454 | 0.565 |
MOD_PKA_1 | 370 | 376 | PF00069 | 0.246 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.565 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.545 |
MOD_PKB_1 | 45 | 53 | PF00069 | 0.555 |
MOD_Plk_1 | 321 | 327 | PF00069 | 0.522 |
MOD_Plk_1 | 465 | 471 | PF00069 | 0.445 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.552 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.351 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.286 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.292 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.343 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.327 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.396 |
MOD_Plk_4 | 335 | 341 | PF00069 | 0.452 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.308 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.345 |
MOD_Plk_4 | 626 | 632 | PF00069 | 0.510 |
MOD_Plk_4 | 640 | 646 | PF00069 | 0.297 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.567 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.528 |
MOD_ProDKin_1 | 542 | 548 | PF00069 | 0.394 |
MOD_SUMO_for_1 | 457 | 460 | PF00179 | 0.591 |
MOD_SUMO_rev_2 | 615 | 625 | PF00179 | 0.446 |
TRG_DiLeu_BaEn_1 | 259 | 264 | PF01217 | 0.280 |
TRG_DiLeu_BaEn_1 | 286 | 291 | PF01217 | 0.346 |
TRG_DiLeu_BaLyEn_6 | 272 | 277 | PF01217 | 0.482 |
TRG_DiLeu_BaLyEn_6 | 571 | 576 | PF01217 | 0.370 |
TRG_ENDOCYTIC_2 | 136 | 139 | PF00928 | 0.518 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 366 | 369 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 376 | 379 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 581 | 584 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 589 | 592 | PF00928 | 0.324 |
TRG_ER_diArg_1 | 121 | 124 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 129 | 132 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 267 | 269 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 492 | 494 | PF00400 | 0.440 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P486 | Leptomonas seymouri | 33% | 100% |
A0A0N0P6Z5 | Leptomonas seymouri | 30% | 100% |
A0A0N1I1J0 | Leptomonas seymouri | 27% | 100% |
A0A0N1I8E8 | Leptomonas seymouri | 23% | 100% |
A0A0N1PBQ1 | Leptomonas seymouri | 33% | 100% |
A0A0S4JBS4 | Bodo saltans | 30% | 100% |
A0A1X0NN91 | Trypanosomatidae | 35% | 100% |
A0A1X0NPL0 | Trypanosomatidae | 34% | 100% |
A0A1X0NV38 | Trypanosomatidae | 30% | 100% |
A0A1X0NWJ5 | Trypanosomatidae | 31% | 100% |
A0A3Q8ICX7 | Leishmania donovani | 33% | 100% |
A0A3R7NQR3 | Trypanosoma rangeli | 34% | 100% |
A0A3S7WTL0 | Leishmania donovani | 96% | 100% |
A0A3S7XAS5 | Leishmania donovani | 32% | 100% |
A0A422MQ08 | Trypanosoma rangeli | 30% | 100% |
A0A422N8M2 | Trypanosoma rangeli | 31% | 100% |
A0A422NHH9 | Trypanosoma rangeli | 30% | 100% |
A0A422NR81 | Trypanosoma rangeli | 50% | 100% |
A1A4N1 | Bos taurus | 21% | 100% |
A4H7A5 | Leishmania braziliensis | 34% | 100% |
A4HG96 | Leishmania braziliensis | 23% | 100% |
A4HP60 | Leishmania braziliensis | 31% | 100% |
A4HUW2 | Leishmania infantum | 27% | 100% |
A4HVP9 | Leishmania infantum | 33% | 100% |
A4HWK9 | Leishmania infantum | 95% | 100% |
A4IDG6 | Leishmania infantum | 32% | 100% |
C9ZJU3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZJU5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZJU7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZKT6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZN88 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZY31 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AGM5 | Leishmania infantum | 96% | 100% |
E9AGM6 | Leishmania infantum | 95% | 100% |
E9AGM7 | Leishmania infantum | 95% | 100% |
E9ANK1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9APE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9AQB5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9AQB6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
E9ASW8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
O76343 | Leishmania donovani | 95% | 100% |
Q4Q1M9 | Leishmania major | 32% | 100% |
Q4QF58 | Leishmania major | 99% | 100% |
Q4QG33 | Leishmania major | 33% | 100% |
Q9JIM1 | Mus musculus | 25% | 100% |
V5BGB1 | Trypanosoma cruzi | 33% | 100% |
V5BRM5 | Trypanosoma cruzi | 30% | 100% |
V5DSF4 | Trypanosoma cruzi | 32% | 100% |