Structural Proteins, Kinesin-like
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | yes | yes: 4 |
Forrest at al. (procyclic) | yes | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 31 |
NetGPI | no | yes: 0, no: 31 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005874 | microtubule | 6 | 15 |
GO:0099080 | supramolecular complex | 2 | 15 |
GO:0099081 | supramolecular polymer | 3 | 15 |
GO:0099512 | supramolecular fiber | 4 | 15 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 15 |
GO:0110165 | cellular anatomical entity | 1 | 19 |
GO:0005737 | cytoplasm | 2 | 6 |
GO:0005871 | kinesin complex | 3 | 2 |
GO:0005875 | microtubule associated complex | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4IBA7
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 32 |
GO:0007018 | microtubule-based movement | 3 | 32 |
GO:0009987 | cellular process | 1 | 32 |
GO:0006810 | transport | 3 | 2 |
GO:0030705 | cytoskeleton-dependent intracellular transport | 4 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 32 |
GO:0003774 | cytoskeletal motor activity | 1 | 32 |
GO:0003777 | microtubule motor activity | 2 | 32 |
GO:0003824 | catalytic activity | 1 | 14 |
GO:0005488 | binding | 1 | 32 |
GO:0005515 | protein binding | 2 | 32 |
GO:0005524 | ATP binding | 5 | 32 |
GO:0008017 | microtubule binding | 5 | 32 |
GO:0008092 | cytoskeletal protein binding | 3 | 32 |
GO:0015631 | tubulin binding | 4 | 32 |
GO:0016787 | hydrolase activity | 2 | 14 |
GO:0017076 | purine nucleotide binding | 4 | 32 |
GO:0030554 | adenyl nucleotide binding | 5 | 32 |
GO:0032553 | ribonucleotide binding | 3 | 32 |
GO:0032555 | purine ribonucleotide binding | 4 | 32 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 32 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 32 |
GO:0036094 | small molecule binding | 2 | 32 |
GO:0043167 | ion binding | 2 | 32 |
GO:0043168 | anion binding | 3 | 32 |
GO:0097159 | organic cyclic compound binding | 2 | 32 |
GO:0097367 | carbohydrate derivative binding | 2 | 32 |
GO:0140657 | ATP-dependent activity | 1 | 32 |
GO:1901265 | nucleoside phosphate binding | 3 | 32 |
GO:1901363 | heterocyclic compound binding | 2 | 32 |
GO:0008574 | plus-end-directed microtubule motor activity | 3 | 2 |
GO:0016462 | pyrophosphatase activity | 5 | 2 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 2 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 2 |
GO:0016887 | ATP hydrolysis activity | 7 | 2 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 83 | 87 | PF00656 | 0.275 |
CLV_MEL_PAP_1 | 365 | 371 | PF00089 | 0.217 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.334 |
CLV_NRD_NRD_1 | 462 | 464 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.461 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 462 | 464 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 652 | 654 | PF00082 | 0.449 |
CLV_PCSK_PC1ET2_1 | 278 | 280 | PF00082 | 0.492 |
CLV_PCSK_PC1ET2_1 | 652 | 654 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 144 | 148 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.220 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 482 | 486 | PF00082 | 0.656 |
CLV_PCSK_SKI1_1 | 640 | 644 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 652 | 656 | PF00082 | 0.396 |
DEG_SCF_FBW7_1 | 624 | 631 | PF00400 | 0.427 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 368 | 376 | PF00134 | 0.287 |
DOC_MAPK_gen_1 | 144 | 154 | PF00069 | 0.262 |
DOC_MAPK_gen_1 | 479 | 488 | PF00069 | 0.661 |
DOC_MAPK_gen_1 | 517 | 525 | PF00069 | 0.590 |
DOC_MAPK_MEF2A_6 | 147 | 156 | PF00069 | 0.237 |
DOC_MAPK_MEF2A_6 | 8 | 15 | PF00069 | 0.310 |
DOC_PP1_RVXF_1 | 426 | 432 | PF00149 | 0.472 |
DOC_PP4_FxxP_1 | 304 | 307 | PF00568 | 0.350 |
DOC_PP4_FxxP_1 | 380 | 383 | PF00568 | 0.260 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.379 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 484 | 488 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 495 | 499 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.287 |
DOC_USP7_UBL2_3 | 485 | 489 | PF12436 | 0.534 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.279 |
DOC_WW_Pin1_4 | 624 | 629 | PF00397 | 0.453 |
LIG_14-3-3_CanoR_1 | 133 | 141 | PF00244 | 0.291 |
LIG_14-3-3_CanoR_1 | 491 | 500 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 653 | 658 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 8 | 14 | PF00244 | 0.382 |
LIG_Actin_WH2_2 | 362 | 379 | PF00022 | 0.417 |
LIG_Actin_WH2_2 | 535 | 551 | PF00022 | 0.472 |
LIG_Actin_WH2_2 | 6 | 22 | PF00022 | 0.273 |
LIG_APCC_ABBA_1 | 159 | 164 | PF00400 | 0.269 |
LIG_APCC_ABBA_1 | 74 | 79 | PF00400 | 0.260 |
LIG_APCC_ABBAyCdc20_2 | 468 | 474 | PF00400 | 0.463 |
LIG_BIR_III_4 | 496 | 500 | PF00653 | 0.396 |
LIG_BRCT_BRCA1_1 | 127 | 131 | PF00533 | 0.254 |
LIG_BRCT_BRCA1_1 | 57 | 61 | PF00533 | 0.279 |
LIG_Clathr_ClatBox_1 | 234 | 238 | PF01394 | 0.260 |
LIG_Clathr_ClatBox_1 | 60 | 64 | PF01394 | 0.399 |
LIG_CSK_EPIYA_1 | 311 | 315 | PF00017 | 0.343 |
LIG_deltaCOP1_diTrp_1 | 294 | 299 | PF00928 | 0.441 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.269 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.414 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.279 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.584 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.392 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.197 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.219 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.452 |
LIG_FHA_2 | 625 | 631 | PF00498 | 0.674 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.303 |
LIG_LIR_Apic_2 | 294 | 298 | PF02991 | 0.618 |
LIG_LIR_Apic_2 | 302 | 307 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 107 | 116 | PF02991 | 0.249 |
LIG_LIR_Gen_1 | 128 | 139 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 584 | 594 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 62 | 67 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 663 | 672 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 107 | 111 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 361 | 367 | PF02991 | 0.252 |
LIG_LIR_Nem_3 | 62 | 66 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 663 | 667 | PF02991 | 0.568 |
LIG_NRBOX | 371 | 377 | PF00104 | 0.261 |
LIG_PCNA_yPIPBox_3 | 163 | 173 | PF02747 | 0.415 |
LIG_Pex14_1 | 295 | 299 | PF04695 | 0.448 |
LIG_Pex14_2 | 63 | 67 | PF04695 | 0.296 |
LIG_SH2_CRK | 440 | 444 | PF00017 | 0.479 |
LIG_SH2_CRK | 664 | 668 | PF00017 | 0.455 |
LIG_SH2_SRC | 191 | 194 | PF00017 | 0.329 |
LIG_SH2_SRC | 77 | 80 | PF00017 | 0.297 |
LIG_SH2_STAP1 | 314 | 318 | PF00017 | 0.423 |
LIG_SH2_STAP1 | 440 | 444 | PF00017 | 0.418 |
LIG_SH2_STAP1 | 473 | 477 | PF00017 | 0.627 |
LIG_SH2_STAP1 | 77 | 81 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 314 | 317 | PF00017 | 0.201 |
LIG_SH2_STAT5 | 593 | 596 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.403 |
LIG_SH3_2 | 52 | 57 | PF14604 | 0.308 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.256 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.588 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.329 |
LIG_SUMO_SIM_anti_2 | 236 | 241 | PF11976 | 0.370 |
LIG_SUMO_SIM_anti_2 | 250 | 255 | PF11976 | 0.383 |
LIG_SUMO_SIM_anti_2 | 384 | 391 | PF11976 | 0.243 |
LIG_SUMO_SIM_anti_2 | 521 | 527 | PF11976 | 0.301 |
LIG_UBA3_1 | 511 | 519 | PF00899 | 0.346 |
LIG_UBA3_1 | 589 | 595 | PF00899 | 0.316 |
LIG_WRC_WIRS_1 | 60 | 65 | PF05994 | 0.280 |
LIG_WRC_WIRS_1 | 654 | 659 | PF05994 | 0.330 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.287 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.279 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.268 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.603 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.281 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.327 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.282 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.286 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.537 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.278 |
MOD_CK1_1 | 606 | 612 | PF00069 | 0.481 |
MOD_CK1_1 | 644 | 650 | PF00069 | 0.512 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.241 |
MOD_CK2_1 | 355 | 361 | PF00069 | 0.252 |
MOD_CK2_1 | 396 | 402 | PF00069 | 0.263 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.466 |
MOD_CK2_1 | 526 | 532 | PF00069 | 0.502 |
MOD_CK2_1 | 607 | 613 | PF00069 | 0.435 |
MOD_CK2_1 | 624 | 630 | PF00069 | 0.593 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.286 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.300 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.243 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.490 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.367 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.488 |
MOD_GlcNHglycan | 284 | 287 | PF01048 | 0.639 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.284 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.483 |
MOD_GlcNHglycan | 474 | 478 | PF01048 | 0.656 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.584 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.610 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.545 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.439 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.300 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.285 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.268 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.281 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.271 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.495 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.307 |
MOD_GSK3_1 | 603 | 610 | PF00069 | 0.337 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.627 |
MOD_N-GLC_1 | 345 | 350 | PF02516 | 0.274 |
MOD_N-GLC_1 | 370 | 375 | PF02516 | 0.292 |
MOD_N-GLC_1 | 628 | 633 | PF02516 | 0.703 |
MOD_N-GLC_1 | 674 | 679 | PF02516 | 0.561 |
MOD_N-GLC_1 | 92 | 97 | PF02516 | 0.249 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.358 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.543 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.462 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.253 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.412 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.471 |
MOD_NEK2_1 | 568 | 573 | PF00069 | 0.475 |
MOD_NEK2_2 | 41 | 46 | PF00069 | 0.301 |
MOD_NEK2_2 | 484 | 489 | PF00069 | 0.597 |
MOD_PIKK_1 | 223 | 229 | PF00454 | 0.394 |
MOD_PIKK_1 | 393 | 399 | PF00454 | 0.285 |
MOD_PIKK_1 | 451 | 457 | PF00454 | 0.550 |
MOD_PIKK_1 | 561 | 567 | PF00454 | 0.516 |
MOD_PIKK_1 | 613 | 619 | PF00454 | 0.556 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.262 |
MOD_PKA_1 | 216 | 222 | PF00069 | 0.260 |
MOD_PKA_1 | 491 | 497 | PF00069 | 0.560 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.264 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.299 |
MOD_PKA_2 | 491 | 497 | PF00069 | 0.521 |
MOD_PKA_2 | 622 | 628 | PF00069 | 0.625 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.360 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.266 |
MOD_Plk_1 | 340 | 346 | PF00069 | 0.282 |
MOD_Plk_1 | 370 | 376 | PF00069 | 0.282 |
MOD_Plk_1 | 400 | 406 | PF00069 | 0.244 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.251 |
MOD_Plk_1 | 521 | 527 | PF00069 | 0.527 |
MOD_Plk_1 | 603 | 609 | PF00069 | 0.427 |
MOD_Plk_1 | 674 | 680 | PF00069 | 0.556 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.260 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.245 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.275 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.463 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.632 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.296 |
MOD_Plk_4 | 585 | 591 | PF00069 | 0.486 |
MOD_Plk_4 | 674 | 680 | PF00069 | 0.537 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.254 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.279 |
MOD_ProDKin_1 | 624 | 630 | PF00069 | 0.448 |
MOD_SUMO_for_1 | 45 | 48 | PF00179 | 0.307 |
MOD_SUMO_rev_2 | 136 | 143 | PF00179 | 0.279 |
MOD_SUMO_rev_2 | 257 | 266 | PF00179 | 0.558 |
MOD_SUMO_rev_2 | 268 | 274 | PF00179 | 0.518 |
MOD_SUMO_rev_2 | 544 | 551 | PF00179 | 0.459 |
MOD_SUMO_rev_2 | 633 | 642 | PF00179 | 0.660 |
MOD_SUMO_rev_2 | 693 | 698 | PF00179 | 0.627 |
TRG_DiLeu_BaEn_1 | 507 | 512 | PF01217 | 0.515 |
TRG_DiLeu_BaEn_3 | 584 | 590 | PF01217 | 0.495 |
TRG_DiLeu_BaLyEn_6 | 371 | 376 | PF01217 | 0.260 |
TRG_ENDOCYTIC_2 | 440 | 443 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 664 | 667 | PF00928 | 0.478 |
TRG_ER_diArg_1 | 13 | 16 | PF00400 | 0.291 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 461 | 463 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 491 | 493 | PF00400 | 0.626 |
TRG_NLS_MonoExtC_3 | 681 | 687 | PF00514 | 0.322 |
TRG_NLS_MonoExtN_4 | 680 | 686 | PF00514 | 0.334 |
TRG_Pf-PMV_PEXEL_1 | 133 | 137 | PF00026 | 0.231 |
TRG_Pf-PMV_PEXEL_1 | 463 | 467 | PF00026 | 0.672 |
TRG_Pf-PMV_PEXEL_1 | 491 | 496 | PF00026 | 0.653 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P672 | Leptomonas seymouri | 34% | 66% |
A0A0N1HVM1 | Leptomonas seymouri | 29% | 75% |
A0A0N1IM30 | Leptomonas seymouri | 73% | 100% |
A0A0S4IXS6 | Bodo saltans | 39% | 68% |
A0A0S4JN49 | Bodo saltans | 50% | 96% |
A0A1X0NQ03 | Trypanosomatidae | 24% | 84% |
A0A1X0P5Y8 | Trypanosomatidae | 60% | 100% |
A0A3Q8IBS7 | Leishmania donovani | 24% | 100% |
A0A3Q8IG88 | Leishmania donovani | 100% | 100% |
A0A3S7WX05 | Leishmania donovani | 30% | 79% |
A0A422MZ05 | Trypanosoma rangeli | 57% | 100% |
A0A422NEF2 | Trypanosoma rangeli | 36% | 69% |
A4HAQ7 | Leishmania braziliensis | 27% | 100% |
A4HHY2 | Leishmania braziliensis | 26% | 100% |
A4HMM9 | Leishmania braziliensis | 76% | 100% |
A4HZT3 | Leishmania infantum | 30% | 79% |
A4I562 | Leishmania infantum | 24% | 100% |
C9ZU98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 86% |
C9ZV26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 93% |
C9ZVT5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 69% |
C9ZZN5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
E9AF32 | Leishmania major | 92% | 100% |
E9B0F9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B687 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 99% |
Q4Q7S4 | Leishmania major | 27% | 100% |
Q4QBU1 | Leishmania major | 31% | 78% |
V5B8X9 | Trypanosoma cruzi | 58% | 99% |
V5D733 | Trypanosoma cruzi | 25% | 93% |
V5DFA7 | Trypanosoma cruzi | 28% | 100% |
V5DQN8 | Trypanosoma cruzi | 32% | 67% |