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: A4HNH7
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 | 264 | 268 | PF00656 | 0.489 |
CLV_C14_Caspase3-7 | 9 | 13 | PF00656 | 0.627 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 600 | 602 | PF00675 | 0.279 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 475 | 477 | PF00082 | 0.521 |
CLV_PCSK_PC1ET2_1 | 122 | 124 | PF00082 | 0.292 |
CLV_PCSK_PC1ET2_1 | 278 | 280 | PF00082 | 0.406 |
CLV_PCSK_PC1ET2_1 | 475 | 477 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 331 | 335 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.251 |
DEG_APCC_DBOX_1 | 330 | 338 | PF00400 | 0.398 |
DEG_ODPH_VHL_1 | 515 | 527 | PF01847 | 0.520 |
DOC_CDC14_PxL_1 | 30 | 38 | PF14671 | 0.531 |
DOC_CDC14_PxL_1 | 561 | 569 | PF14671 | 0.331 |
DOC_CKS1_1 | 573 | 578 | PF01111 | 0.432 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 393 | 402 | PF00134 | 0.264 |
DOC_CYCLIN_yCln2_LP_2 | 462 | 468 | PF00134 | 0.206 |
DOC_CYCLIN_yCln2_LP_2 | 504 | 510 | PF00134 | 0.397 |
DOC_CYCLIN_yCln2_LP_2 | 578 | 584 | PF00134 | 0.369 |
DOC_MAPK_gen_1 | 475 | 483 | PF00069 | 0.323 |
DOC_MAPK_gen_1 | 601 | 608 | PF00069 | 0.563 |
DOC_MAPK_MEF2A_6 | 475 | 483 | PF00069 | 0.357 |
DOC_MAPK_MEF2A_6 | 52 | 59 | PF00069 | 0.535 |
DOC_PP1_RVXF_1 | 252 | 258 | PF00149 | 0.381 |
DOC_PP1_RVXF_1 | 381 | 388 | PF00149 | 0.477 |
DOC_PP2B_LxvP_1 | 504 | 507 | PF13499 | 0.337 |
DOC_PP4_FxxP_1 | 306 | 309 | PF00568 | 0.458 |
DOC_PP4_FxxP_1 | 375 | 378 | PF00568 | 0.316 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.264 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.323 |
DOC_USP7_MATH_1 | 448 | 452 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.322 |
DOC_USP7_UBL2_3 | 278 | 282 | PF12436 | 0.585 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 572 | 577 | PF00397 | 0.414 |
LIG_14-3-3_CanoR_1 | 453 | 459 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 93 | 98 | PF00244 | 0.491 |
LIG_14-3-3_CterR_2 | 625 | 628 | PF00244 | 0.604 |
LIG_APCC_ABBA_1 | 172 | 177 | PF00400 | 0.520 |
LIG_APCC_ABBA_1 | 237 | 242 | PF00400 | 0.406 |
LIG_APCC_ABBA_1 | 307 | 312 | PF00400 | 0.381 |
LIG_APCC_ABBA_1 | 488 | 493 | PF00400 | 0.246 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.700 |
LIG_BIR_III_4 | 302 | 306 | PF00653 | 0.545 |
LIG_BRCT_BRCA1_1 | 371 | 375 | PF00533 | 0.257 |
LIG_BRCT_BRCA1_1 | 419 | 423 | PF00533 | 0.317 |
LIG_BRCT_BRCA1_1 | 450 | 454 | PF00533 | 0.460 |
LIG_BRCT_BRCA1_1 | 521 | 525 | PF00533 | 0.492 |
LIG_eIF4E_1 | 329 | 335 | PF01652 | 0.381 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.548 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.327 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.433 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.425 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.349 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.332 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.354 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.378 |
LIG_FHA_1 | 568 | 574 | PF00498 | 0.416 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.412 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.563 |
LIG_FHA_2 | 352 | 358 | PF00498 | 0.208 |
LIG_LIR_Apic_2 | 372 | 378 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 113 | 120 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 354 | 363 | PF02991 | 0.295 |
LIG_LIR_Gen_1 | 422 | 431 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 440 | 448 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 467 | 474 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 522 | 532 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 113 | 118 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 121 | 127 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 357 | 363 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 372 | 377 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 420 | 424 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 440 | 446 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 451 | 455 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 467 | 472 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 522 | 528 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 548 | 554 | PF02991 | 0.291 |
LIG_MLH1_MIPbox_1 | 371 | 375 | PF16413 | 0.399 |
LIG_NRBOX | 229 | 235 | PF00104 | 0.378 |
LIG_Pex14_1 | 356 | 360 | PF04695 | 0.285 |
LIG_Pex14_2 | 352 | 356 | PF04695 | 0.226 |
LIG_Pex14_2 | 419 | 423 | PF04695 | 0.306 |
LIG_Pex14_2 | 443 | 447 | PF04695 | 0.365 |
LIG_Pex14_2 | 49 | 53 | PF04695 | 0.492 |
LIG_PTB_Apo_2 | 400 | 407 | PF02174 | 0.391 |
LIG_PTB_Apo_2 | 446 | 453 | PF02174 | 0.553 |
LIG_PTB_Phospho_1 | 400 | 406 | PF10480 | 0.402 |
LIG_PTB_Phospho_1 | 446 | 452 | PF10480 | 0.454 |
LIG_SH2_CRK | 125 | 129 | PF00017 | 0.367 |
LIG_SH2_CRK | 140 | 144 | PF00017 | 0.321 |
LIG_SH2_CRK | 360 | 364 | PF00017 | 0.355 |
LIG_SH2_CRK | 452 | 456 | PF00017 | 0.495 |
LIG_SH2_CRK | 91 | 95 | PF00017 | 0.512 |
LIG_SH2_GRB2like | 389 | 392 | PF00017 | 0.381 |
LIG_SH2_GRB2like | 395 | 398 | PF00017 | 0.405 |
LIG_SH2_GRB2like | 561 | 564 | PF00017 | 0.351 |
LIG_SH2_NCK_1 | 360 | 364 | PF00017 | 0.416 |
LIG_SH2_NCK_1 | 561 | 565 | PF00017 | 0.295 |
LIG_SH2_PTP2 | 21 | 24 | PF00017 | 0.615 |
LIG_SH2_PTP2 | 38 | 41 | PF00017 | 0.643 |
LIG_SH2_PTP2 | 395 | 398 | PF00017 | 0.350 |
LIG_SH2_PTP2 | 584 | 587 | PF00017 | 0.206 |
LIG_SH2_SRC | 21 | 24 | PF00017 | 0.621 |
LIG_SH2_SRC | 38 | 41 | PF00017 | 0.566 |
LIG_SH2_STAP1 | 120 | 124 | PF00017 | 0.501 |
LIG_SH2_STAP1 | 175 | 179 | PF00017 | 0.487 |
LIG_SH2_STAT3 | 175 | 178 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 314 | 317 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.261 |
LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 544 | 547 | PF00017 | 0.256 |
LIG_SH2_STAT5 | 584 | 587 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.545 |
LIG_SH3_2 | 273 | 278 | PF14604 | 0.394 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.544 |
LIG_SH3_3 | 393 | 399 | PF00018 | 0.380 |
LIG_SH3_3 | 404 | 410 | PF00018 | 0.333 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.280 |
LIG_SH3_3 | 458 | 464 | PF00018 | 0.206 |
LIG_SH3_3 | 582 | 588 | PF00018 | 0.390 |
LIG_SH3_3 | 617 | 623 | PF00018 | 0.730 |
LIG_SUMO_SIM_anti_2 | 364 | 369 | PF11976 | 0.435 |
LIG_SUMO_SIM_anti_2 | 470 | 475 | PF11976 | 0.315 |
LIG_SUMO_SIM_par_1 | 226 | 231 | PF11976 | 0.206 |
LIG_SUMO_SIM_par_1 | 617 | 624 | PF11976 | 0.597 |
LIG_TRAF2_1 | 615 | 618 | PF00917 | 0.614 |
LIG_TRFH_1 | 140 | 144 | PF08558 | 0.361 |
LIG_TRFH_1 | 584 | 588 | PF08558 | 0.291 |
LIG_TYR_ITIM | 138 | 143 | PF00017 | 0.377 |
LIG_TYR_ITIM | 358 | 363 | PF00017 | 0.374 |
LIG_TYR_ITIM | 36 | 41 | PF00017 | 0.585 |
LIG_TYR_ITIM | 393 | 398 | PF00017 | 0.333 |
LIG_TYR_ITIM | 582 | 587 | PF00017 | 0.505 |
LIG_UBA3_1 | 138 | 146 | PF00899 | 0.348 |
LIG_UBA3_1 | 468 | 475 | PF00899 | 0.323 |
LIG_WRC_WIRS_1 | 371 | 376 | PF05994 | 0.287 |
LIG_WRC_WIRS_1 | 402 | 407 | PF05994 | 0.335 |
LIG_WRC_WIRS_1 | 46 | 51 | PF05994 | 0.556 |
MOD_CDC14_SPxK_1 | 275 | 278 | PF00782 | 0.398 |
MOD_CDK_SPxK_1 | 272 | 278 | PF00069 | 0.398 |
MOD_CDK_SPxxK_3 | 272 | 279 | PF00069 | 0.381 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.206 |
MOD_CK1_1 | 537 | 543 | PF00069 | 0.358 |
MOD_CK1_1 | 609 | 615 | PF00069 | 0.680 |
MOD_CK1_1 | 621 | 627 | PF00069 | 0.698 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.613 |
MOD_Cter_Amidation | 599 | 602 | PF01082 | 0.320 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.390 |
MOD_GlcNHglycan | 147 | 151 | PF01048 | 0.502 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.387 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.285 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.336 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.378 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.391 |
MOD_GlcNHglycan | 588 | 591 | PF01048 | 0.400 |
MOD_GlcNHglycan | 610 | 614 | PF01048 | 0.524 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.460 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.486 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.293 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.375 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.400 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.514 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.610 |
MOD_GSK3_1 | 621 | 628 | PF00069 | 0.759 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.541 |
MOD_N-GLC_1 | 262 | 267 | PF02516 | 0.395 |
MOD_N-GLC_1 | 448 | 453 | PF02516 | 0.254 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.495 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.453 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.342 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.335 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.332 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.286 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.357 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.309 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.545 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.362 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.346 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.353 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.301 |
MOD_NEK2_1 | 567 | 572 | PF00069 | 0.457 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.479 |
MOD_NEK2_2 | 370 | 375 | PF00069 | 0.462 |
MOD_NEK2_2 | 464 | 469 | PF00069 | 0.369 |
MOD_PK_1 | 262 | 268 | PF00069 | 0.381 |
MOD_PKA_2 | 590 | 596 | PF00069 | 0.400 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.407 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.519 |
MOD_Plk_1 | 262 | 268 | PF00069 | 0.460 |
MOD_Plk_1 | 448 | 454 | PF00069 | 0.454 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.347 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.337 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.502 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.391 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.338 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.363 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.231 |
MOD_Plk_4 | 464 | 470 | PF00069 | 0.320 |
MOD_Plk_4 | 519 | 525 | PF00069 | 0.516 |
MOD_Plk_4 | 527 | 533 | PF00069 | 0.358 |
MOD_Plk_4 | 546 | 552 | PF00069 | 0.299 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.444 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.755 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.502 |
MOD_ProDKin_1 | 572 | 578 | PF00069 | 0.414 |
MOD_SUMO_for_1 | 253 | 256 | PF00179 | 0.560 |
MOD_SUMO_rev_2 | 251 | 255 | PF00179 | 0.411 |
MOD_SUMO_rev_2 | 275 | 284 | PF00179 | 0.547 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 329 | 332 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.594 |
TRG_ENDOCYTIC_2 | 395 | 398 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 452 | 455 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 544 | 547 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 584 | 587 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.480 |
TRG_ER_diArg_1 | 179 | 182 | PF00400 | 0.437 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2U2 | Leptomonas seymouri | 42% | 89% |
A0A0N1HY49 | Leptomonas seymouri | 39% | 93% |
A0A0N1HZ06 | Leptomonas seymouri | 59% | 100% |
A0A0N1IHL1 | Leptomonas seymouri | 37% | 88% |
A0A0N1PAY4 | Leptomonas seymouri | 38% | 71% |
A0A0N1PB77 | Leptomonas seymouri | 69% | 97% |
A0A0N1PBZ2 | Leptomonas seymouri | 36% | 93% |
A0A0N1PCC1 | Leptomonas seymouri | 37% | 94% |
A0A0S4INN8 | Bodo saltans | 28% | 97% |
A0A381MBI0 | Leishmania infantum | 39% | 95% |
A0A3Q8I8X7 | Leishmania donovani | 39% | 95% |
A0A3Q8IAZ0 | Leishmania donovani | 36% | 90% |
A0A3Q8IH50 | Leishmania donovani | 37% | 87% |
A0A3Q8IVN0 | Leishmania donovani | 85% | 100% |
A0A3R7M4J1 | Trypanosoma rangeli | 39% | 98% |
A0A3S5H5P4 | Leishmania donovani | 39% | 93% |
A0A3S5H5V2 | Leishmania donovani | 44% | 96% |
A0A3S5H6F6 | Leishmania donovani | 36% | 90% |
A0A3S5H763 | Leishmania donovani | 40% | 93% |
A0A3S7WR10 | Leishmania donovani | 39% | 84% |
A0A3S7WR14 | Leishmania donovani | 36% | 92% |
A0A3S7WR15 | Leishmania donovani | 35% | 74% |
A0A3S7WR24 | Leishmania donovani | 37% | 89% |
A4H4T8 | Leishmania braziliensis | 43% | 100% |
A4H5Y4 | Leishmania braziliensis | 39% | 100% |
A4H617 | Leishmania braziliensis | 36% | 100% |
A4H618 | Leishmania braziliensis | 36% | 100% |
A4H619 | Leishmania braziliensis | 36% | 100% |
A4H620 | Leishmania braziliensis | 38% | 100% |
A4H6C3 | Leishmania braziliensis | 39% | 100% |
A4HSS2 | Leishmania infantum | 39% | 93% |
A4HUE4 | Leishmania infantum | 39% | 84% |
A4HUE5 | Leishmania infantum | 35% | 91% |
A4HUE6 | Leishmania infantum | 36% | 92% |
A4HUE7 | Leishmania infantum | 36% | 90% |
A4HUE8 | Leishmania infantum | 37% | 89% |
A4HUF4 | Leishmania infantum | 36% | 90% |
A4HUF5 | Leishmania infantum | 37% | 95% |
A4HYA9 | Leishmania infantum | 41% | 93% |
A4IC33 | Leishmania infantum | 84% | 99% |
C9ZIK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 96% |
C9ZIK3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 96% |
C9ZVE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 99% |
C9ZVE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 99% |
C9ZVF1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 99% |
D0A423 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 98% |
E8NHQ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 90% |
E9AG72 | Leishmania infantum | 44% | 96% |
E9AI40 | Leishmania braziliensis | 35% | 92% |
E9AJY4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 100% |
E9AKQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 93% |
E9AL06 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 96% |
E9AN44 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 84% |
E9AN45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 96% |
E9AN46 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9AN47 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 88% |
E9ANE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 95% |
E9AS42 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 40% | 93% |
E9B741 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4QDC4 | Leishmania major | 40% | 100% |
Q4QH81 | Leishmania major | 38% | 100% |
Q4QHH7 | Leishmania major | 37% | 100% |
Q4QHH8 | Leishmania major | 36% | 100% |
Q4QHH9 | Leishmania major | 36% | 100% |
Q4QHI0 | Leishmania major | 35% | 100% |
Q4QHI1 | Leishmania major | 37% | 100% |
Q4QHI2 | Leishmania major | 35% | 100% |
Q4QIU9 | Leishmania major | 44% | 100% |
Q4QJ48 | Leishmania major | 39% | 100% |
Q7KIP2 | Leishmania major | 82% | 100% |