Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 23 |
NetGPI | no | yes: 0, no: 23 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005874 | microtubule | 6 | 9 |
GO:0099080 | supramolecular complex | 2 | 9 |
GO:0099081 | supramolecular polymer | 3 | 9 |
GO:0099512 | supramolecular fiber | 4 | 9 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005737 | cytoplasm | 2 | 3 |
GO:0005871 | kinesin complex | 3 | 1 |
GO:0005875 | microtubule associated complex | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
Related structures:
AlphaFold database: E9B687
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 24 |
GO:0007018 | microtubule-based movement | 3 | 24 |
GO:0009987 | cellular process | 1 | 24 |
GO:0006810 | transport | 3 | 1 |
GO:0030705 | cytoskeleton-dependent intracellular transport | 4 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 24 |
GO:0003774 | cytoskeletal motor activity | 1 | 24 |
GO:0003777 | microtubule motor activity | 2 | 24 |
GO:0005488 | binding | 1 | 24 |
GO:0005515 | protein binding | 2 | 24 |
GO:0005524 | ATP binding | 5 | 24 |
GO:0008017 | microtubule binding | 5 | 24 |
GO:0008092 | cytoskeletal protein binding | 3 | 24 |
GO:0015631 | tubulin binding | 4 | 24 |
GO:0017076 | purine nucleotide binding | 4 | 24 |
GO:0030554 | adenyl nucleotide binding | 5 | 24 |
GO:0032553 | ribonucleotide binding | 3 | 24 |
GO:0032555 | purine ribonucleotide binding | 4 | 24 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 24 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 24 |
GO:0036094 | small molecule binding | 2 | 24 |
GO:0043167 | ion binding | 2 | 24 |
GO:0043168 | anion binding | 3 | 24 |
GO:0097159 | organic cyclic compound binding | 2 | 24 |
GO:0097367 | carbohydrate derivative binding | 2 | 24 |
GO:0140657 | ATP-dependent activity | 1 | 24 |
GO:1901265 | nucleoside phosphate binding | 3 | 24 |
GO:1901363 | heterocyclic compound binding | 2 | 24 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0008574 | plus-end-directed microtubule motor activity | 3 | 1 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 1 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
GO:0016887 | ATP hydrolysis activity | 7 | 1 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 83 | 87 | PF00656 | 0.271 |
CLV_MEL_PAP_1 | 358 | 364 | PF00089 | 0.212 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.287 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 484 | 486 | PF00675 | 0.503 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 484 | 486 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 645 | 647 | PF00082 | 0.436 |
CLV_PCSK_PC1ET2_1 | 645 | 647 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 144 | 148 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.233 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.190 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 475 | 479 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 539 | 543 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 633 | 637 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 645 | 649 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 658 | 662 | PF00082 | 0.424 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 361 | 369 | PF00134 | 0.268 |
DOC_MAPK_gen_1 | 144 | 154 | PF00069 | 0.275 |
DOC_MAPK_gen_1 | 472 | 481 | PF00069 | 0.679 |
DOC_MAPK_gen_1 | 510 | 518 | PF00069 | 0.524 |
DOC_MAPK_MEF2A_6 | 147 | 156 | PF00069 | 0.224 |
DOC_MAPK_MEF2A_6 | 472 | 481 | PF00069 | 0.596 |
DOC_MAPK_MEF2A_6 | 8 | 15 | PF00069 | 0.309 |
DOC_PP1_RVXF_1 | 419 | 425 | PF00149 | 0.472 |
DOC_PP4_FxxP_1 | 297 | 300 | PF00568 | 0.434 |
DOC_PP4_FxxP_1 | 373 | 376 | PF00568 | 0.253 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.314 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 444 | 448 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.268 |
DOC_USP7_MATH_1 | 578 | 582 | PF00917 | 0.350 |
DOC_USP7_MATH_1 | 592 | 596 | PF00917 | 0.407 |
DOC_USP7_UBL2_3 | 478 | 482 | PF12436 | 0.532 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.241 |
DOC_WW_Pin1_4 | 621 | 626 | PF00397 | 0.558 |
LIG_14-3-3_CanoR_1 | 133 | 141 | PF00244 | 0.265 |
LIG_14-3-3_CanoR_1 | 455 | 459 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 646 | 651 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 8 | 14 | PF00244 | 0.350 |
LIG_Actin_WH2_2 | 355 | 372 | PF00022 | 0.393 |
LIG_Actin_WH2_2 | 6 | 22 | PF00022 | 0.253 |
LIG_APCC_ABBA_1 | 159 | 164 | PF00400 | 0.227 |
LIG_APCC_ABBA_1 | 74 | 79 | PF00400 | 0.240 |
LIG_APCC_ABBAyCdc20_2 | 461 | 467 | PF00400 | 0.443 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.549 |
LIG_BRCT_BRCA1_1 | 127 | 131 | PF00533 | 0.253 |
LIG_BRCT_BRCA1_1 | 57 | 61 | PF00533 | 0.253 |
LIG_BRCT_BRCA1_1 | 636 | 640 | PF00533 | 0.411 |
LIG_Clathr_ClatBox_1 | 234 | 238 | PF01394 | 0.253 |
LIG_Clathr_ClatBox_1 | 60 | 64 | PF01394 | 0.376 |
LIG_CSK_EPIYA_1 | 304 | 308 | PF00017 | 0.324 |
LIG_deltaCOP1_diTrp_1 | 287 | 292 | PF00928 | 0.445 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.213 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.415 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.238 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.399 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.570 |
LIG_FHA_1 | 533 | 539 | PF00498 | 0.378 |
LIG_FHA_1 | 544 | 550 | PF00498 | 0.325 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.340 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.183 |
LIG_FHA_2 | 390 | 396 | PF00498 | 0.201 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.445 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.254 |
LIG_LIR_Apic_2 | 287 | 291 | PF02991 | 0.654 |
LIG_LIR_Apic_2 | 295 | 300 | PF02991 | 0.639 |
LIG_LIR_Gen_1 | 107 | 116 | PF02991 | 0.246 |
LIG_LIR_Gen_1 | 128 | 139 | PF02991 | 0.260 |
LIG_LIR_Gen_1 | 577 | 587 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 62 | 67 | PF02991 | 0.286 |
LIG_LIR_Gen_1 | 637 | 648 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 107 | 111 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.254 |
LIG_LIR_Nem_3 | 354 | 360 | PF02991 | 0.231 |
LIG_LIR_Nem_3 | 62 | 66 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 637 | 643 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 656 | 660 | PF02991 | 0.600 |
LIG_NRBOX | 364 | 370 | PF00104 | 0.255 |
LIG_PALB2_WD40_1 | 635 | 643 | PF16756 | 0.276 |
LIG_PCNA_yPIPBox_3 | 163 | 173 | PF02747 | 0.389 |
LIG_Pex14_1 | 288 | 292 | PF04695 | 0.460 |
LIG_Pex14_2 | 63 | 67 | PF04695 | 0.240 |
LIG_SH2_CRK | 433 | 437 | PF00017 | 0.441 |
LIG_SH2_CRK | 657 | 661 | PF00017 | 0.478 |
LIG_SH2_GRB2like | 534 | 537 | PF00017 | 0.314 |
LIG_SH2_SRC | 77 | 80 | PF00017 | 0.278 |
LIG_SH2_STAP1 | 307 | 311 | PF00017 | 0.393 |
LIG_SH2_STAP1 | 433 | 437 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 466 | 470 | PF00017 | 0.540 |
LIG_SH2_STAP1 | 534 | 538 | PF00017 | 0.316 |
LIG_SH2_STAP1 | 77 | 81 | PF00017 | 0.255 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.189 |
LIG_SH2_STAT5 | 534 | 537 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 586 | 589 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.346 |
LIG_SH3_2 | 52 | 57 | PF14604 | 0.289 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.251 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.280 |
LIG_SUMO_SIM_anti_2 | 236 | 241 | PF11976 | 0.350 |
LIG_SUMO_SIM_anti_2 | 250 | 255 | PF11976 | 0.415 |
LIG_SUMO_SIM_anti_2 | 377 | 384 | PF11976 | 0.240 |
LIG_SUMO_SIM_anti_2 | 513 | 520 | PF11976 | 0.472 |
LIG_UBA3_1 | 504 | 512 | PF00899 | 0.328 |
LIG_UBA3_1 | 584 | 591 | PF00899 | 0.524 |
LIG_WRC_WIRS_1 | 60 | 65 | PF05994 | 0.239 |
LIG_WRC_WIRS_1 | 647 | 652 | PF05994 | 0.337 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.238 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.247 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.219 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.266 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.270 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.245 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.250 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.542 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.254 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.508 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.234 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.231 |
MOD_CK2_1 | 389 | 395 | PF00069 | 0.257 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.460 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.279 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.254 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.240 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.459 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.508 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.623 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.255 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.531 |
MOD_GlcNHglycan | 467 | 471 | PF01048 | 0.575 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.441 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.390 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.255 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.277 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.248 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.252 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.218 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.589 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.471 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.336 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.235 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.462 |
MOD_N-GLC_1 | 260 | 265 | PF02516 | 0.600 |
MOD_N-GLC_1 | 338 | 343 | PF02516 | 0.240 |
MOD_N-GLC_1 | 363 | 368 | PF02516 | 0.254 |
MOD_N-GLC_1 | 92 | 97 | PF02516 | 0.239 |
MOD_N-GLC_2 | 663 | 665 | PF02516 | 0.286 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.549 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.526 |
MOD_NEK2_1 | 393 | 398 | PF00069 | 0.267 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.364 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.503 |
MOD_NEK2_1 | 541 | 546 | PF00069 | 0.396 |
MOD_NEK2_1 | 561 | 566 | PF00069 | 0.477 |
MOD_NEK2_1 | 661 | 666 | PF00069 | 0.477 |
MOD_NEK2_2 | 41 | 46 | PF00069 | 0.287 |
MOD_PIKK_1 | 223 | 229 | PF00454 | 0.372 |
MOD_PIKK_1 | 280 | 286 | PF00454 | 0.401 |
MOD_PIKK_1 | 386 | 392 | PF00454 | 0.272 |
MOD_PIKK_1 | 444 | 450 | PF00454 | 0.546 |
MOD_PIKK_1 | 554 | 560 | PF00454 | 0.515 |
MOD_PIKK_1 | 606 | 612 | PF00454 | 0.541 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.200 |
MOD_PKA_1 | 216 | 222 | PF00069 | 0.309 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.295 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.235 |
MOD_PKA_2 | 454 | 460 | PF00069 | 0.413 |
MOD_PKA_2 | 615 | 621 | PF00069 | 0.607 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.360 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.243 |
MOD_Plk_1 | 333 | 339 | PF00069 | 0.237 |
MOD_Plk_1 | 363 | 369 | PF00069 | 0.243 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.220 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.208 |
MOD_Plk_1 | 514 | 520 | PF00069 | 0.562 |
MOD_Plk_1 | 547 | 553 | PF00069 | 0.389 |
MOD_Plk_1 | 596 | 602 | PF00069 | 0.497 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.246 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.232 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.255 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.511 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.579 |
MOD_Plk_4 | 514 | 520 | PF00069 | 0.372 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.247 |
MOD_Plk_4 | 580 | 586 | PF00069 | 0.449 |
MOD_Plk_4 | 635 | 641 | PF00069 | 0.390 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.249 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.241 |
MOD_ProDKin_1 | 621 | 627 | PF00069 | 0.554 |
MOD_SUMO_for_1 | 45 | 48 | PF00179 | 0.287 |
MOD_SUMO_rev_2 | 136 | 143 | PF00179 | 0.263 |
MOD_SUMO_rev_2 | 533 | 541 | PF00179 | 0.461 |
MOD_SUMO_rev_2 | 626 | 635 | PF00179 | 0.604 |
TRG_DiLeu_BaEn_1 | 500 | 505 | PF01217 | 0.482 |
TRG_DiLeu_BaLyEn_6 | 364 | 369 | PF01217 | 0.268 |
TRG_ENDOCYTIC_2 | 433 | 436 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 657 | 660 | PF00928 | 0.502 |
TRG_ER_diArg_1 | 13 | 16 | PF00400 | 0.243 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 454 | 456 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 484 | 486 | PF00400 | 0.589 |
TRG_NES_CRM1_1 | 434 | 446 | PF08389 | 0.438 |
TRG_NLS_MonoExtC_3 | 674 | 680 | PF00514 | 0.597 |
TRG_NLS_MonoExtN_4 | 673 | 679 | PF00514 | 0.591 |
TRG_Pf-PMV_PEXEL_1 | 133 | 137 | PF00026 | 0.207 |
TRG_Pf-PMV_PEXEL_1 | 456 | 460 | PF00026 | 0.609 |
TRG_Pf-PMV_PEXEL_1 | 484 | 489 | PF00026 | 0.613 |
TRG_Pf-PMV_PEXEL_1 | 539 | 543 | PF00026 | 0.387 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P569 | Leptomonas seymouri | 25% | 79% |
A0A0N1HVM1 | Leptomonas seymouri | 29% | 74% |
A0A0N1IM30 | Leptomonas seymouri | 72% | 99% |
A0A0S4IR67 | Bodo saltans | 24% | 88% |
A0A0S4IXS6 | Bodo saltans | 34% | 67% |
A0A0S4JBC0 | Bodo saltans | 25% | 74% |
A0A0S4JN49 | Bodo saltans | 50% | 95% |
A0A1X0NJN6 | Trypanosomatidae | 23% | 100% |
A0A1X0NQ03 | Trypanosomatidae | 24% | 83% |
A0A1X0NWZ8 | Trypanosomatidae | 25% | 93% |
A0A1X0NY69 | Trypanosomatidae | 24% | 91% |
A0A1X0P5Y8 | Trypanosomatidae | 59% | 100% |
A0A3Q8IBS7 | Leishmania donovani | 24% | 100% |
A0A3Q8IG88 | Leishmania donovani | 91% | 99% |
A0A3S7WX05 | Leishmania donovani | 31% | 78% |
A0A422MZ05 | Trypanosoma rangeli | 57% | 100% |
A0A422NEF2 | Trypanosoma rangeli | 36% | 69% |
A0A422NEQ8 | Trypanosoma rangeli | 26% | 92% |
A4HAQ7 | Leishmania braziliensis | 27% | 100% |
A4HMM9 | Leishmania braziliensis | 75% | 99% |
A4HND6 | Leishmania braziliensis | 25% | 100% |
A4HZT3 | Leishmania infantum | 31% | 78% |
A4I562 | Leishmania infantum | 24% | 100% |
A4IBA7 | Leishmania infantum | 91% | 99% |
C9ZU98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 85% |
C9ZVT5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 68% |
C9ZZN5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
E9AF32 | Leishmania major | 87% | 100% |
E9B0F9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
Q4QBU1 | Leishmania major | 31% | 78% |
Q6FXI5 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 24% | 70% |
Q8J1G1 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 25% | 100% |
V5B8X9 | Trypanosoma cruzi | 57% | 98% |
V5D733 | Trypanosoma cruzi | 26% | 92% |
V5DFA7 | Trypanosoma cruzi | 29% | 100% |