Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 1 |
Forrest at al. (metacyclic) | no | yes: 3 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 36 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 93 |
NetGPI | no | yes: 0, no: 94 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
GO:0005737 | cytoplasm | 2 | 3 |
GO:0005930 | axoneme | 2 | 1 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0005856 | cytoskeleton | 5 | 1 |
GO:0020016 | ciliary pocket | 2 | 1 |
GO:0020038 | subpellicular network | 2 | 1 |
GO:0030863 | cortical cytoskeleton | 6 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: E9AXM9
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 95 |
GO:0006807 | nitrogen compound metabolic process | 2 | 95 |
GO:0008152 | metabolic process | 1 | 95 |
GO:0019538 | protein metabolic process | 3 | 95 |
GO:0043170 | macromolecule metabolic process | 3 | 95 |
GO:0044238 | primary metabolic process | 2 | 95 |
GO:0071704 | organic substance metabolic process | 2 | 95 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 95 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 95 |
GO:0004175 | endopeptidase activity | 4 | 95 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 95 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 95 |
GO:0008233 | peptidase activity | 3 | 95 |
GO:0008234 | cysteine-type peptidase activity | 4 | 95 |
GO:0016787 | hydrolase activity | 2 | 95 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 95 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 184 | 188 | PF00656 | 0.518 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.340 |
CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 603 | 605 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 611 | 613 | PF00675 | 0.371 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.487 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.343 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 493 | 495 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 611 | 613 | PF00082 | 0.448 |
CLV_PCSK_PC1ET2_1 | 191 | 193 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.286 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.201 |
CLV_PCSK_SKI1_1 | 611 | 615 | PF00082 | 0.497 |
CLV_Separin_Metazoa | 73 | 77 | PF03568 | 0.203 |
DEG_MDM2_SWIB_1 | 474 | 481 | PF02201 | 0.495 |
DEG_SCF_TRCP1_1 | 79 | 84 | PF00400 | 0.208 |
DOC_CKS1_1 | 380 | 385 | PF01111 | 0.506 |
DOC_CYCLIN_RxL_1 | 359 | 367 | PF00134 | 0.583 |
DOC_MAPK_gen_1 | 122 | 131 | PF00069 | 0.357 |
DOC_MAPK_gen_1 | 207 | 215 | PF00069 | 0.613 |
DOC_MAPK_gen_1 | 374 | 380 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 599 | 609 | PF00069 | 0.536 |
DOC_MAPK_gen_1 | 623 | 630 | PF00069 | 0.425 |
DOC_MAPK_MEF2A_6 | 207 | 215 | PF00069 | 0.573 |
DOC_MAPK_MEF2A_6 | 551 | 559 | PF00069 | 0.368 |
DOC_PP2B_LxvP_1 | 607 | 610 | PF13499 | 0.395 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 573 | 577 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.409 |
DOC_USP7_UBL2_3 | 12 | 16 | PF12436 | 0.497 |
DOC_USP7_UBL2_3 | 122 | 126 | PF12436 | 0.491 |
DOC_USP7_UBL2_3 | 140 | 144 | PF12436 | 0.590 |
DOC_USP7_UBL2_3 | 208 | 212 | PF12436 | 0.401 |
DOC_USP7_UBL2_3 | 249 | 253 | PF12436 | 0.629 |
DOC_USP7_UBL2_3 | 315 | 319 | PF12436 | 0.505 |
DOC_USP7_UBL2_3 | 385 | 389 | PF12436 | 0.401 |
DOC_USP7_UBL2_3 | 95 | 99 | PF12436 | 0.426 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 448 | 453 | PF00397 | 0.527 |
LIG_14-3-3_CanoR_1 | 592 | 597 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 611 | 621 | PF00244 | 0.474 |
LIG_Actin_WH2_2 | 373 | 391 | PF00022 | 0.574 |
LIG_BRCT_BRCA1_1 | 481 | 485 | PF00533 | 0.503 |
LIG_BRCT_BRCA1_1 | 488 | 492 | PF00533 | 0.487 |
LIG_CNOT1_NIM_1 | 498 | 507 | PF04054 | 0.253 |
LIG_deltaCOP1_diTrp_1 | 307 | 312 | PF00928 | 0.575 |
LIG_deltaCOP1_diTrp_1 | 42 | 46 | PF00928 | 0.279 |
LIG_deltaCOP1_diTrp_1 | 442 | 447 | PF00928 | 0.502 |
LIG_deltaCOP1_diTrp_1 | 477 | 485 | PF00928 | 0.514 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.517 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.364 |
LIG_FHA_1 | 582 | 588 | PF00498 | 0.576 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.460 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.374 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.496 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.488 |
LIG_IRF3_LxIS_1 | 272 | 277 | PF10401 | 0.405 |
LIG_LIR_Apic_2 | 195 | 201 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 307 | 317 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 323 | 332 | PF02991 | 0.510 |
LIG_LIR_Gen_1 | 50 | 60 | PF02991 | 0.286 |
LIG_LIR_Gen_1 | 509 | 518 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 549 | 559 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 700 | 705 | PF02991 | 0.618 |
LIG_LIR_LC3C_4 | 700 | 705 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 277 | 283 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 307 | 312 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 323 | 327 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 340 | 345 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 42 | 47 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 451 | 457 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 477 | 481 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 50 | 56 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 500 | 504 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 509 | 513 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 526 | 532 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 549 | 555 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 595 | 600 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 700 | 704 | PF02991 | 0.566 |
LIG_LYPXL_yS_3 | 457 | 460 | PF13949 | 0.463 |
LIG_MLH1_MIPbox_1 | 481 | 485 | PF16413 | 0.555 |
LIG_PCNA_yPIPBox_3 | 266 | 280 | PF02747 | 0.486 |
LIG_PDZ_Class_2 | 700 | 705 | PF00595 | 0.633 |
LIG_Pex14_2 | 347 | 351 | PF04695 | 0.500 |
LIG_Pex14_2 | 474 | 478 | PF04695 | 0.504 |
LIG_SH2_CRK | 110 | 114 | PF00017 | 0.436 |
LIG_SH2_CRK | 324 | 328 | PF00017 | 0.502 |
LIG_SH2_CRK | 504 | 508 | PF00017 | 0.386 |
LIG_SH2_CRK | 53 | 57 | PF00017 | 0.189 |
LIG_SH2_CRK | 552 | 556 | PF00017 | 0.429 |
LIG_SH2_NCK_1 | 317 | 321 | PF00017 | 0.526 |
LIG_SH2_PTP2 | 532 | 535 | PF00017 | 0.423 |
LIG_SH2_SRC | 288 | 291 | PF00017 | 0.519 |
LIG_SH2_SRC | 626 | 629 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 317 | 321 | PF00017 | 0.518 |
LIG_SH2_STAP1 | 502 | 506 | PF00017 | 0.364 |
LIG_SH2_STAP1 | 552 | 556 | PF00017 | 0.340 |
LIG_SH2_STAT3 | 331 | 334 | PF00017 | 0.571 |
LIG_SH2_STAT3 | 586 | 589 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 586 | 589 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 606 | 609 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 626 | 629 | PF00017 | 0.385 |
LIG_SH3_3 | 576 | 582 | PF00018 | 0.502 |
LIG_SH3_4 | 12 | 19 | PF00018 | 0.550 |
LIG_SUMO_SIM_anti_2 | 516 | 524 | PF11976 | 0.348 |
LIG_SUMO_SIM_par_1 | 281 | 287 | PF11976 | 0.487 |
LIG_SUMO_SIM_par_1 | 516 | 524 | PF11976 | 0.423 |
LIG_SUMO_SIM_par_1 | 555 | 561 | PF11976 | 0.401 |
LIG_SUMO_SIM_par_1 | 626 | 632 | PF11976 | 0.470 |
LIG_TYR_ITIM | 108 | 113 | PF00017 | 0.217 |
LIG_UBA3_1 | 215 | 222 | PF00899 | 0.405 |
LIG_UBA3_1 | 35 | 40 | PF00899 | 0.381 |
LIG_UBA3_1 | 377 | 385 | PF00899 | 0.575 |
LIG_UBA3_1 | 519 | 525 | PF00899 | 0.519 |
LIG_WRC_WIRS_1 | 507 | 512 | PF05994 | 0.269 |
LIG_WRC_WIRS_1 | 658 | 663 | PF05994 | 0.463 |
MOD_CDK_SPK_2 | 217 | 222 | PF00069 | 0.575 |
MOD_CDK_SPxK_1 | 379 | 385 | PF00069 | 0.525 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.485 |
MOD_CK1_1 | 524 | 530 | PF00069 | 0.502 |
MOD_CK1_1 | 668 | 674 | PF00069 | 0.499 |
MOD_CK2_1 | 308 | 314 | PF00069 | 0.489 |
MOD_CK2_1 | 436 | 442 | PF00069 | 0.509 |
MOD_CK2_1 | 555 | 561 | PF00069 | 0.415 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.330 |
MOD_CMANNOS | 475 | 478 | PF00535 | 0.304 |
MOD_Cter_Amidation | 161 | 164 | PF01082 | 0.313 |
MOD_Cter_Amidation | 692 | 695 | PF01082 | 0.597 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.452 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.552 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.358 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.318 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.302 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.268 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.384 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.495 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.475 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.368 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.537 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.530 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.391 |
MOD_GSK3_1 | 631 | 638 | PF00069 | 0.512 |
MOD_GSK3_1 | 664 | 671 | PF00069 | 0.417 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.387 |
MOD_N-GLC_1 | 217 | 222 | PF02516 | 0.205 |
MOD_N-GLC_1 | 274 | 279 | PF02516 | 0.314 |
MOD_N-GLC_1 | 47 | 52 | PF02516 | 0.351 |
MOD_N-GLC_1 | 564 | 569 | PF02516 | 0.511 |
MOD_N-GLC_1 | 573 | 578 | PF02516 | 0.456 |
MOD_N-GLC_1 | 77 | 82 | PF02516 | 0.368 |
MOD_N-GLC_2 | 3 | 5 | PF02516 | 0.459 |
MOD_N-GLC_2 | 398 | 400 | PF02516 | 0.257 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.516 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.505 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.558 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.511 |
MOD_NEK2_1 | 484 | 489 | PF00069 | 0.497 |
MOD_NEK2_1 | 588 | 593 | PF00069 | 0.445 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.526 |
MOD_NEK2_2 | 531 | 536 | PF00069 | 0.475 |
MOD_NEK2_2 | 85 | 90 | PF00069 | 0.341 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.550 |
MOD_PIKK_1 | 171 | 177 | PF00454 | 0.566 |
MOD_PIKK_1 | 222 | 228 | PF00454 | 0.543 |
MOD_PIKK_1 | 259 | 265 | PF00454 | 0.460 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.571 |
MOD_PIKK_1 | 47 | 53 | PF00454 | 0.404 |
MOD_PIKK_1 | 524 | 530 | PF00454 | 0.456 |
MOD_PIKK_1 | 564 | 570 | PF00454 | 0.574 |
MOD_PIKK_1 | 629 | 635 | PF00454 | 0.544 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.505 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.513 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.572 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.373 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.517 |
MOD_Plk_4 | 592 | 598 | PF00069 | 0.447 |
MOD_Plk_4 | 668 | 674 | PF00069 | 0.528 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.380 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.489 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.389 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.519 |
MOD_ProDKin_1 | 448 | 454 | PF00069 | 0.527 |
MOD_SUMO_for_1 | 11 | 14 | PF00179 | 0.502 |
MOD_SUMO_rev_2 | 10 | 17 | PF00179 | 0.539 |
MOD_SUMO_rev_2 | 367 | 377 | PF00179 | 0.573 |
MOD_SUMO_rev_2 | 416 | 423 | PF00179 | 0.552 |
MOD_SUMO_rev_2 | 547 | 553 | PF00179 | 0.455 |
MOD_SUMO_rev_2 | 88 | 97 | PF00179 | 0.382 |
TRG_DiLeu_BaEn_1 | 373 | 378 | PF01217 | 0.587 |
TRG_DiLeu_BaLyEn_6 | 150 | 155 | PF01217 | 0.313 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 324 | 327 | PF00928 | 0.500 |
TRG_ENDOCYTIC_2 | 415 | 418 | PF00928 | 0.527 |
TRG_ENDOCYTIC_2 | 457 | 460 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 504 | 507 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 53 | 56 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 532 | 535 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 552 | 555 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 597 | 600 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 606 | 609 | PF00928 | 0.356 |
TRG_ER_diArg_1 | 198 | 200 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 492 | 494 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 610 | 612 | PF00400 | 0.493 |
TRG_NLS_Bipartite_1 | 611 | 627 | PF00514 | 0.552 |
TRG_NLS_MonoExtC_3 | 159 | 164 | PF00514 | 0.310 |
TRG_NLS_MonoExtN_4 | 159 | 164 | PF00514 | 0.594 |
TRG_NLS_MonoExtN_4 | 622 | 627 | PF00514 | 0.530 |
TRG_Pf-PMV_PEXEL_1 | 139 | 143 | PF00026 | 0.589 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 36% | 100% |
A0A0N1I8N2 | Leptomonas seymouri | 26% | 72% |
A0A0N1IGQ2 | Leptomonas seymouri | 69% | 100% |
A0A0N1ILF1 | Leptomonas seymouri | 34% | 100% |
A0A0N1IMH1 | Leptomonas seymouri | 32% | 90% |
A0A0N1P9P1 | Leptomonas seymouri | 32% | 83% |
A0A0N1PCA9 | Leptomonas seymouri | 28% | 96% |
A0A0N1PE91 | Leptomonas seymouri | 23% | 79% |
A0A0N1PFI4 | Leptomonas seymouri | 32% | 91% |
A0A0S4JLK6 | Bodo saltans | 34% | 87% |
A0A0S4JS70 | Bodo saltans | 24% | 92% |
A0A0S4KGT2 | Bodo saltans | 38% | 93% |
A0A1X0NJ61 | Trypanosomatidae | 45% | 100% |
A0A1X0NJK2 | Trypanosomatidae | 32% | 93% |
A0A1X0NJX8 | Trypanosomatidae | 34% | 91% |
A0A1X0NKT7 | Trypanosomatidae | 28% | 89% |
A0A1X0NKX8 | Trypanosomatidae | 31% | 86% |
A0A1X0NMT3 | Trypanosomatidae | 32% | 83% |
A0A1X0NW84 | Trypanosomatidae | 34% | 100% |
A0A1X0NW85 | Trypanosomatidae | 31% | 100% |
A0A1X0NW89 | Trypanosomatidae | 34% | 82% |
A0A1X0NWA6 | Trypanosomatidae | 28% | 81% |
A0A1X0NWW1 | Trypanosomatidae | 34% | 98% |
A0A3Q8IBS3 | Leishmania donovani | 34% | 77% |
A0A3Q8IDD4 | Leishmania donovani | 92% | 100% |
A0A3Q8IJT4 | Leishmania donovani | 24% | 94% |
A0A3S5H5A5 | Leishmania donovani | 31% | 82% |
A0A3S5ISG2 | Trypanosoma rangeli | 31% | 91% |
A0A3S7WW18 | Leishmania donovani | 34% | 86% |
A0A3S7WW41 | Leishmania donovani | 28% | 95% |
A0A3S7WW71 | Leishmania donovani | 35% | 100% |
A0A3S7X430 | Leishmania donovani | 32% | 90% |
A0A3S7X438 | Leishmania donovani | 28% | 75% |
A0A3S7X460 | Leishmania donovani | 35% | 91% |
A0A3S7X463 | Leishmania donovani | 28% | 75% |
A0A3S7X470 | Leishmania donovani | 32% | 97% |
A0A422MYU1 | Trypanosoma rangeli | 33% | 77% |
A0A422MYX0 | Trypanosoma rangeli | 33% | 97% |
A4H3W4 | Leishmania braziliensis | 32% | 100% |
A4HE81 | Leishmania braziliensis | 82% | 100% |
A4HJ14 | Leishmania braziliensis | 33% | 100% |
A4HJ21 | Leishmania braziliensis | 24% | 79% |
A4HJ22 | Leishmania braziliensis | 29% | 100% |
A4HJ23 | Leishmania braziliensis | 32% | 96% |
A4HJ24 | Leishmania braziliensis | 36% | 100% |
A4HS39 | Leishmania infantum | 32% | 82% |
A4HYN0 | Leishmania infantum | 34% | 86% |
A4HYW1 | Leishmania infantum | 34% | 70% |
A4HYW2 | Leishmania infantum | 34% | 100% |
A4HYW3 | Leishmania infantum | 28% | 95% |
A4HYW4 | Leishmania infantum | 25% | 71% |
A4I1J4 | Leishmania infantum | 93% | 100% |
A4I6E4 | Leishmania infantum | 32% | 97% |
A4I6E6 | Leishmania infantum | 35% | 91% |
A4I6F0 | Leishmania infantum | 28% | 75% |
A4I6K4 | Leishmania infantum | 32% | 90% |
A4I6K5 | Leishmania infantum | 28% | 75% |
A4I6K6 | Leishmania infantum | 24% | 94% |
C9ZIE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
C9ZIE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 96% |
C9ZN52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 89% |
C9ZN53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 83% |
C9ZWY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 88% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 82% |
E8NHF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 39% | 100% |
E8NHG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E8NHG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E8NHG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E8NHM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E8NHM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E8NHM8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9AIH1 | Leishmania braziliensis | 34% | 100% |
E9AIH3 | Leishmania braziliensis | 33% | 100% |
E9AIH4 | Leishmania braziliensis | 29% | 100% |
E9AIH6 | Leishmania braziliensis | 25% | 99% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AUQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AUR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 99% |
E9B1J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 90% |
E9B1J1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 75% |
E9B1J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 94% |
E9B1J6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
Q22036 | Caenorhabditis elegans | 27% | 100% |
Q4Q6L7 | Leishmania major | 34% | 100% |
Q4Q6L9 | Leishmania major | 32% | 100% |
Q4Q6M0 | Leishmania major | 29% | 100% |
Q4Q6M2 | Leishmania major | 21% | 100% |
Q4Q6M3 | Leishmania major | 27% | 76% |
Q4Q6M4 | Leishmania major | 32% | 100% |
Q4Q9U3 | Leishmania major | 92% | 100% |
Q4QCS6 | Leishmania major | 29% | 100% |
Q4QCS7 | Leishmania major | 34% | 100% |
Q4QCS8 | Leishmania major | 34% | 100% |
Q4QCS9 | Leishmania major | 34% | 100% |
Q9U0T9 | Leishmania major | 31% | 100% |
V5AYJ1 | Trypanosoma cruzi | 35% | 99% |
V5B5I4 | Trypanosoma cruzi | 33% | 84% |
V5BA05 | Trypanosoma cruzi | 33% | 100% |
V5BEL3 | Trypanosoma cruzi | 34% | 100% |
V5BN20 | Trypanosoma cruzi | 33% | 91% |
V5D5V8 | Trypanosoma cruzi | 29% | 95% |
V5D9Y2 | Trypanosoma cruzi | 31% | 83% |
V5DES7 | Trypanosoma cruzi | 31% | 89% |