Transporters, pteridine transporter
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) | yes | 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: 72 |
NetGPI | no | yes: 0, no: 72 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 73 |
GO:0110165 | cellular anatomical entity | 1 | 73 |
GO:0005737 | cytoplasm | 2 | 6 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: E9AG72
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 | 289 | 293 | PF00656 | 0.554 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.357 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 623 | 625 | PF00675 | 0.489 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 485 | 487 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 623 | 625 | PF00082 | 0.495 |
CLV_PCSK_PC1ET2_1 | 132 | 134 | PF00082 | 0.320 |
CLV_PCSK_PC1ET2_1 | 271 | 273 | PF00082 | 0.385 |
CLV_PCSK_PC1ET2_1 | 485 | 487 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 461 | 465 | PF00082 | 0.255 |
DOC_CDC14_PxL_1 | 40 | 48 | PF14671 | 0.553 |
DOC_CDC14_PxL_1 | 571 | 579 | PF14671 | 0.357 |
DOC_CKS1_1 | 583 | 588 | PF01111 | 0.468 |
DOC_CYCLIN_yCln2_LP_2 | 385 | 391 | PF00134 | 0.477 |
DOC_CYCLIN_yCln2_LP_2 | 583 | 589 | PF00134 | 0.418 |
DOC_MAPK_gen_1 | 132 | 138 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 259 | 267 | PF00069 | 0.586 |
DOC_MAPK_gen_1 | 459 | 467 | PF00069 | 0.475 |
DOC_MAPK_gen_1 | 485 | 493 | PF00069 | 0.351 |
DOC_MAPK_gen_1 | 599 | 608 | PF00069 | 0.618 |
DOC_MAPK_MEF2A_6 | 225 | 233 | PF00069 | 0.359 |
DOC_MAPK_MEF2A_6 | 393 | 400 | PF00069 | 0.507 |
DOC_MAPK_MEF2A_6 | 485 | 493 | PF00069 | 0.390 |
DOC_MAPK_MEF2A_6 | 572 | 579 | PF00069 | 0.277 |
DOC_MAPK_MEF2A_6 | 62 | 69 | PF00069 | 0.563 |
DOC_MAPK_NFAT4_5 | 62 | 70 | PF00069 | 0.633 |
DOC_PP2B_LxvP_1 | 385 | 388 | PF13499 | 0.477 |
DOC_PP2B_LxvP_1 | 406 | 409 | PF13499 | 0.414 |
DOC_PP2B_LxvP_1 | 588 | 591 | PF13499 | 0.395 |
DOC_PP2B_LxvP_1 | 595 | 598 | PF13499 | 0.358 |
DOC_PP4_FxxP_1 | 316 | 319 | PF00568 | 0.492 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.295 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 474 | 478 | PF00917 | 0.362 |
DOC_USP7_MATH_1 | 544 | 548 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 551 | 555 | PF00917 | 0.428 |
DOC_USP7_UBL2_3 | 271 | 275 | PF12436 | 0.559 |
DOC_WW_Pin1_4 | 582 | 587 | PF00397 | 0.451 |
LIG_14-3-3_CanoR_1 | 103 | 108 | PF00244 | 0.526 |
LIG_APCC_ABBA_1 | 247 | 252 | PF00400 | 0.443 |
LIG_APCC_ABBA_1 | 49 | 54 | PF00400 | 0.663 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.792 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.628 |
LIG_BIR_III_4 | 443 | 447 | PF00653 | 0.222 |
LIG_BRCT_BRCA1_1 | 429 | 433 | PF00533 | 0.352 |
LIG_EH1_1 | 284 | 292 | PF00400 | 0.407 |
LIG_EVH1_2 | 567 | 571 | PF00568 | 0.372 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.386 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.425 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.357 |
LIG_FHA_1 | 528 | 534 | PF00498 | 0.508 |
LIG_FHA_1 | 583 | 589 | PF00498 | 0.455 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.725 |
LIG_FHA_2 | 617 | 623 | PF00498 | 0.687 |
LIG_GBD_Chelix_1 | 467 | 475 | PF00786 | 0.506 |
LIG_GBD_Chelix_1 | 505 | 513 | PF00786 | 0.532 |
LIG_LIR_Apic_2 | 30 | 34 | PF02991 | 0.645 |
LIG_LIR_Apic_2 | 313 | 319 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 402 | 412 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 432 | 441 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 477 | 484 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 532 | 541 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 227 | 231 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 241 | 247 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 402 | 408 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 430 | 434 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 477 | 482 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 532 | 538 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 558 | 563 | PF02991 | 0.324 |
LIG_NRBOX | 399 | 405 | PF00104 | 0.447 |
LIG_Pex14_1 | 204 | 208 | PF04695 | 0.420 |
LIG_Pex14_2 | 168 | 172 | PF04695 | 0.405 |
LIG_Pex14_2 | 243 | 247 | PF04695 | 0.330 |
LIG_Pex14_2 | 429 | 433 | PF04695 | 0.341 |
LIG_Pex14_2 | 453 | 457 | PF04695 | 0.397 |
LIG_Pex14_2 | 59 | 63 | PF04695 | 0.508 |
LIG_PTB_Apo_2 | 570 | 577 | PF02174 | 0.355 |
LIG_PTB_Phospho_1 | 570 | 576 | PF10480 | 0.355 |
LIG_REV1ctd_RIR_1 | 454 | 463 | PF16727 | 0.366 |
LIG_SH2_CRK | 101 | 105 | PF00017 | 0.542 |
LIG_SH2_CRK | 135 | 139 | PF00017 | 0.407 |
LIG_SH2_CRK | 150 | 154 | PF00017 | 0.361 |
LIG_SH2_CRK | 345 | 349 | PF00017 | 0.385 |
LIG_SH2_CRK | 370 | 374 | PF00017 | 0.395 |
LIG_SH2_CRK | 434 | 438 | PF00017 | 0.333 |
LIG_SH2_CRK | 462 | 466 | PF00017 | 0.530 |
LIG_SH2_GRB2like | 399 | 402 | PF00017 | 0.421 |
LIG_SH2_NCK_1 | 31 | 35 | PF00017 | 0.699 |
LIG_SH2_NCK_1 | 370 | 374 | PF00017 | 0.453 |
LIG_SH2_PTP2 | 228 | 231 | PF00017 | 0.232 |
LIG_SH2_PTP2 | 48 | 51 | PF00017 | 0.645 |
LIG_SH2_SRC | 31 | 34 | PF00017 | 0.661 |
LIG_SH2_SRC | 399 | 402 | PF00017 | 0.536 |
LIG_SH2_SRC | 576 | 579 | PF00017 | 0.232 |
LIG_SH2_STAP1 | 130 | 134 | PF00017 | 0.536 |
LIG_SH2_STAP1 | 345 | 349 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 462 | 466 | PF00017 | 0.537 |
LIG_SH2_STAP1 | 507 | 511 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 399 | 402 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 416 | 419 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 499 | 502 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 576 | 579 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.545 |
LIG_SH3_1 | 421 | 427 | PF00018 | 0.288 |
LIG_SH3_3 | 421 | 427 | PF00018 | 0.310 |
LIG_SH3_3 | 624 | 630 | PF00018 | 0.749 |
LIG_Sin3_3 | 593 | 600 | PF02671 | 0.232 |
LIG_SUMO_SIM_anti_2 | 175 | 181 | PF11976 | 0.401 |
LIG_SUMO_SIM_anti_2 | 480 | 485 | PF11976 | 0.349 |
LIG_SUMO_SIM_anti_2 | 585 | 591 | PF11976 | 0.461 |
LIG_TRAF2_1 | 6 | 9 | PF00917 | 0.797 |
LIG_TRAF2_1 | 619 | 622 | PF00917 | 0.810 |
LIG_TRFH_1 | 150 | 154 | PF08558 | 0.401 |
LIG_TRFH_1 | 594 | 598 | PF08558 | 0.329 |
LIG_TYR_ITIM | 148 | 153 | PF00017 | 0.416 |
LIG_TYR_ITIM | 226 | 231 | PF00017 | 0.496 |
LIG_TYR_ITIM | 343 | 348 | PF00017 | 0.281 |
LIG_TYR_ITIM | 368 | 373 | PF00017 | 0.414 |
LIG_TYR_ITIM | 403 | 408 | PF00017 | 0.363 |
LIG_TYR_ITIM | 46 | 51 | PF00017 | 0.505 |
LIG_TYR_ITIM | 574 | 579 | PF00017 | 0.425 |
LIG_TYR_ITSM | 430 | 437 | PF00017 | 0.442 |
LIG_UBA3_1 | 217 | 225 | PF00899 | 0.232 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.373 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.226 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.585 |
MOD_CK2_1 | 616 | 622 | PF00069 | 0.631 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.385 |
MOD_GlcNHglycan | 157 | 161 | PF01048 | 0.391 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.715 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.411 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.460 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.436 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.417 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.434 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.344 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.428 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.360 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.409 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.393 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.415 |
MOD_N-GLC_1 | 254 | 259 | PF02516 | 0.359 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.416 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.398 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.385 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.373 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.378 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.379 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.385 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.364 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.393 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.395 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.397 |
MOD_NEK2_1 | 511 | 516 | PF00069 | 0.404 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.444 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.467 |
MOD_NEK2_2 | 374 | 379 | PF00069 | 0.390 |
MOD_NEK2_2 | 474 | 479 | PF00069 | 0.408 |
MOD_PIKK_1 | 178 | 184 | PF00454 | 0.366 |
MOD_PIKK_1 | 352 | 358 | PF00454 | 0.228 |
MOD_PKA_2 | 527 | 533 | PF00069 | 0.374 |
MOD_Plk_2-3 | 616 | 622 | PF00069 | 0.461 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.304 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.373 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.371 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.357 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.225 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.412 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.444 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.409 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.473 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.345 |
MOD_Plk_4 | 474 | 480 | PF00069 | 0.351 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.346 |
MOD_Plk_4 | 551 | 557 | PF00069 | 0.379 |
MOD_ProDKin_1 | 582 | 588 | PF00069 | 0.451 |
MOD_SUMO_rev_2 | 222 | 227 | PF00179 | 0.447 |
MOD_SUMO_rev_2 | 289 | 299 | PF00179 | 0.232 |
MOD_SUMO_rev_2 | 615 | 620 | PF00179 | 0.706 |
MOD_SUMO_rev_2 | 647 | 653 | PF00179 | 0.747 |
TRG_DiLeu_BaLyEn_6 | 338 | 343 | PF01217 | 0.417 |
TRG_DiLeu_BaLyEn_6 | 385 | 390 | PF01217 | 0.398 |
TRG_DiLeu_BaLyEn_6 | 583 | 588 | PF01217 | 0.360 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 228 | 231 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 434 | 437 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 462 | 465 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 576 | 579 | PF00928 | 0.423 |
TRG_NES_CRM1_1 | 238 | 252 | PF08389 | 0.411 |
TRG_NES_CRM1_1 | 320 | 334 | PF08389 | 0.251 |
TRG_NES_CRM1_1 | 503 | 519 | PF08389 | 0.232 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 46% | 93% |
A0A0N1HY49 | Leptomonas seymouri | 42% | 97% |
A0A0N1HZ06 | Leptomonas seymouri | 46% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 40% | 91% |
A0A0N1PAY4 | Leptomonas seymouri | 40% | 74% |
A0A0N1PB77 | Leptomonas seymouri | 42% | 100% |
A0A0N1PBZ2 | Leptomonas seymouri | 43% | 97% |
A0A0N1PCC1 | Leptomonas seymouri | 43% | 98% |
A0A0S4IKN0 | Bodo saltans | 32% | 100% |
A0A0S4INN8 | Bodo saltans | 31% | 100% |
A0A381MBI0 | Leishmania infantum | 46% | 100% |
A0A3Q8I8X7 | Leishmania donovani | 46% | 99% |
A0A3Q8IAZ0 | Leishmania donovani | 43% | 93% |
A0A3Q8IH50 | Leishmania donovani | 45% | 90% |
A0A3Q8IVN0 | Leishmania donovani | 45% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 46% | 100% |
A0A3S5H5P4 | Leishmania donovani | 44% | 96% |
A0A3S5H5V2 | Leishmania donovani | 100% | 100% |
A0A3S5H6F6 | Leishmania donovani | 43% | 94% |
A0A3S5H763 | Leishmania donovani | 45% | 97% |
A0A3S7WR10 | Leishmania donovani | 45% | 88% |
A0A3S7WR14 | Leishmania donovani | 43% | 95% |
A0A3S7WR15 | Leishmania donovani | 42% | 77% |
A0A3S7WR24 | Leishmania donovani | 42% | 93% |
A4H4T8 | Leishmania braziliensis | 84% | 100% |
A4H5Y4 | Leishmania braziliensis | 44% | 100% |
A4H617 | Leishmania braziliensis | 45% | 100% |
A4H618 | Leishmania braziliensis | 45% | 100% |
A4H619 | Leishmania braziliensis | 44% | 100% |
A4H620 | Leishmania braziliensis | 47% | 100% |
A4H6C3 | Leishmania braziliensis | 44% | 100% |
A4HNH7 | Leishmania braziliensis | 44% | 100% |
A4HSS2 | Leishmania infantum | 45% | 100% |
A4HUE4 | Leishmania infantum | 45% | 100% |
A4HUE5 | Leishmania infantum | 43% | 100% |
A4HUE6 | Leishmania infantum | 43% | 100% |
A4HUE7 | Leishmania infantum | 43% | 100% |
A4HUE8 | Leishmania infantum | 42% | 100% |
A4HUF4 | Leishmania infantum | 41% | 100% |
A4HUF5 | Leishmania infantum | 45% | 100% |
A4HYA9 | Leishmania infantum | 46% | 100% |
A4IC33 | Leishmania infantum | 45% | 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) | 42% | 100% |
C9ZVE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
C9ZVF1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
D0A423 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
E9AI40 | Leishmania braziliensis | 44% | 100% |
E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 100% |
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) | 43% | 100% |
E9ANE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 100% |
E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 97% |
Q4QDC4 | Leishmania major | 46% | 100% |
Q4QH81 | Leishmania major | 45% | 100% |
Q4QHH7 | Leishmania major | 46% | 100% |
Q4QHH8 | Leishmania major | 44% | 100% |
Q4QHH9 | Leishmania major | 43% | 100% |
Q4QHI0 | Leishmania major | 44% | 100% |
Q4QHI1 | Leishmania major | 46% | 100% |
Q4QHI2 | Leishmania major | 42% | 100% |
Q4QIU9 | Leishmania major | 93% | 100% |
Q4QJ48 | Leishmania major | 46% | 100% |
Q7KIP2 | Leishmania major | 43% | 99% |