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: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005874 | microtubule | 6 | 11 |
GO:0099080 | supramolecular complex | 2 | 11 |
GO:0099081 | supramolecular polymer | 3 | 11 |
GO:0099512 | supramolecular fiber | 4 | 11 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005871 | kinesin complex | 3 | 1 |
GO:0005875 | microtubule associated complex | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
Related structures:
AlphaFold database: A4HHY2
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 12 |
GO:0007018 | microtubule-based movement | 3 | 12 |
GO:0009987 | cellular process | 1 | 12 |
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 | 12 |
GO:0003774 | cytoskeletal motor activity | 1 | 12 |
GO:0003777 | microtubule motor activity | 2 | 12 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0005488 | binding | 1 | 12 |
GO:0005515 | protein binding | 2 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008017 | microtubule binding | 5 | 12 |
GO:0008092 | cytoskeletal protein binding | 3 | 12 |
GO:0015631 | tubulin binding | 4 | 12 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
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 | 597 | 601 | PF00656 | 0.402 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 519 | 521 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 603 | 605 | PF00675 | 0.647 |
CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 519 | 521 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 360 | 362 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.652 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 484 | 488 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.213 |
DEG_APCC_DBOX_1 | 255 | 263 | PF00400 | 0.383 |
DEG_APCC_DBOX_1 | 481 | 489 | PF00400 | 0.533 |
DEG_SCF_TRCP1_1 | 245 | 250 | PF00400 | 0.201 |
DOC_CYCLIN_RxL_1 | 283 | 290 | PF00134 | 0.423 |
DOC_MAPK_gen_1 | 161 | 169 | PF00069 | 0.327 |
DOC_MAPK_gen_1 | 233 | 242 | PF00069 | 0.321 |
DOC_MAPK_gen_1 | 482 | 489 | PF00069 | 0.516 |
DOC_MAPK_gen_1 | 586 | 594 | PF00069 | 0.607 |
DOC_MAPK_MEF2A_6 | 161 | 169 | PF00069 | 0.355 |
DOC_MAPK_MEF2A_6 | 482 | 489 | PF00069 | 0.556 |
DOC_MAPK_NFAT4_5 | 482 | 490 | PF00069 | 0.626 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.589 |
DOC_USP7_UBL2_3 | 356 | 360 | PF12436 | 0.439 |
DOC_USP7_UBL2_3 | 51 | 55 | PF12436 | 0.354 |
DOC_USP7_UBL2_3 | 9 | 13 | PF12436 | 0.560 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.309 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 545 | 550 | PF00397 | 0.614 |
LIG_14-3-3_CanoR_1 | 222 | 227 | PF00244 | 0.270 |
LIG_14-3-3_CanoR_1 | 286 | 292 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 3 | 12 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 400 | 405 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 44 | 49 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 593 | 603 | PF00244 | 0.398 |
LIG_Actin_WH2_2 | 422 | 437 | PF00022 | 0.656 |
LIG_Actin_WH2_2 | 460 | 478 | PF00022 | 0.568 |
LIG_Actin_WH2_2 | 588 | 606 | PF00022 | 0.524 |
LIG_APCC_ABBA_1 | 147 | 152 | PF00400 | 0.314 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.681 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.328 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.579 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.323 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.363 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.367 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.311 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.314 |
LIG_FHA_1 | 523 | 529 | PF00498 | 0.523 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.488 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.374 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.313 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.572 |
LIG_FHA_2 | 434 | 440 | PF00498 | 0.460 |
LIG_FHA_2 | 475 | 481 | PF00498 | 0.391 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.388 |
LIG_HCF-1_HBM_1 | 137 | 140 | PF13415 | 0.323 |
LIG_IRF3_LxIS_1 | 226 | 232 | PF10401 | 0.183 |
LIG_LIR_Gen_1 | 127 | 133 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 143 | 154 | PF02991 | 0.153 |
LIG_LIR_Gen_1 | 16 | 26 | PF02991 | 0.223 |
LIG_LIR_Gen_1 | 340 | 348 | PF02991 | 0.201 |
LIG_LIR_Gen_1 | 559 | 567 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 75 | 85 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 143 | 149 | PF02991 | 0.212 |
LIG_LIR_Nem_3 | 16 | 21 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 340 | 346 | PF02991 | 0.201 |
LIG_LIR_Nem_3 | 366 | 370 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 559 | 564 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 75 | 80 | PF02991 | 0.332 |
LIG_NRBOX | 153 | 159 | PF00104 | 0.309 |
LIG_PCNA_yPIPBox_3 | 151 | 164 | PF02747 | 0.309 |
LIG_PCNA_yPIPBox_3 | 459 | 468 | PF02747 | 0.634 |
LIG_Pex14_2 | 63 | 67 | PF04695 | 0.314 |
LIG_PTB_Apo_2 | 61 | 68 | PF02174 | 0.352 |
LIG_REV1ctd_RIR_1 | 199 | 207 | PF16727 | 0.238 |
LIG_SH2_CRK | 367 | 371 | PF00017 | 0.482 |
LIG_SH2_PTP2 | 146 | 149 | PF00017 | 0.309 |
LIG_SH2_STAP1 | 140 | 144 | PF00017 | 0.328 |
LIG_SH2_STAP1 | 77 | 81 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 536 | 539 | PF00017 | 0.533 |
LIG_SH3_1 | 20 | 26 | PF00018 | 0.352 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.329 |
LIG_SH3_3 | 546 | 552 | PF00018 | 0.716 |
LIG_SH3_3 | 63 | 69 | PF00018 | 0.354 |
LIG_SUMO_SIM_anti_2 | 176 | 184 | PF11976 | 0.232 |
LIG_SUMO_SIM_par_1 | 176 | 184 | PF11976 | 0.309 |
LIG_SUMO_SIM_par_1 | 249 | 254 | PF11976 | 0.392 |
LIG_TRAF2_1 | 389 | 392 | PF00917 | 0.633 |
LIG_TRAF2_1 | 460 | 463 | PF00917 | 0.426 |
LIG_TYR_ITIM | 144 | 149 | PF00017 | 0.309 |
LIG_TYR_ITIM | 365 | 370 | PF00017 | 0.468 |
LIG_UBA3_1 | 153 | 162 | PF00899 | 0.328 |
LIG_UBA3_1 | 288 | 293 | PF00899 | 0.309 |
LIG_UBA3_1 | 374 | 381 | PF00899 | 0.509 |
LIG_WRC_WIRS_1 | 540 | 545 | PF05994 | 0.679 |
MOD_CDK_SPK_2 | 548 | 553 | PF00069 | 0.597 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.296 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.388 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.297 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.260 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.397 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.310 |
MOD_CK1_1 | 545 | 551 | PF00069 | 0.614 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.632 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.290 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.309 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.580 |
MOD_CK2_1 | 474 | 480 | PF00069 | 0.426 |
MOD_CK2_1 | 553 | 559 | PF00069 | 0.478 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.272 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.298 |
MOD_GlcNHglycan | 182 | 186 | PF01048 | 0.229 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.238 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.342 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.721 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.515 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.578 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.610 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.646 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.305 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.333 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.325 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.283 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.367 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.298 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.341 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.622 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.483 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.503 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.635 |
MOD_LATS_1 | 27 | 33 | PF00433 | 0.201 |
MOD_N-GLC_1 | 133 | 138 | PF02516 | 0.386 |
MOD_N-GLC_1 | 195 | 200 | PF02516 | 0.201 |
MOD_N-GLC_1 | 216 | 221 | PF02516 | 0.309 |
MOD_N-GLC_1 | 229 | 234 | PF02516 | 0.309 |
MOD_N-GLC_1 | 284 | 289 | PF02516 | 0.314 |
MOD_N-GLC_1 | 324 | 329 | PF02516 | 0.314 |
MOD_N-GLC_1 | 330 | 335 | PF02516 | 0.302 |
MOD_N-GLC_1 | 34 | 39 | PF02516 | 0.348 |
MOD_N-GLC_1 | 69 | 74 | PF02516 | 0.394 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.408 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.367 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.304 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.250 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.319 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.331 |
MOD_NEK2_1 | 543 | 548 | PF00069 | 0.690 |
MOD_PIKK_1 | 350 | 356 | PF00454 | 0.423 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.352 |
MOD_PK_1 | 13 | 19 | PF00069 | 0.308 |
MOD_PKA_1 | 50 | 56 | PF00069 | 0.291 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.323 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.314 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.308 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.423 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.334 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.332 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.323 |
MOD_Plk_1 | 339 | 345 | PF00069 | 0.268 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.346 |
MOD_Plk_1 | 382 | 388 | PF00069 | 0.593 |
MOD_Plk_1 | 543 | 549 | PF00069 | 0.599 |
MOD_Plk_2-3 | 274 | 280 | PF00069 | 0.328 |
MOD_Plk_2-3 | 336 | 342 | PF00069 | 0.328 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.309 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.314 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.331 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.338 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.309 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.687 |
MOD_ProDKin_1 | 545 | 551 | PF00069 | 0.615 |
MOD_SUMO_for_1 | 115 | 118 | PF00179 | 0.238 |
MOD_SUMO_rev_2 | 111 | 117 | PF00179 | 0.298 |
MOD_SUMO_rev_2 | 269 | 278 | PF00179 | 0.330 |
MOD_SUMO_rev_2 | 363 | 370 | PF00179 | 0.466 |
MOD_SUMO_rev_2 | 466 | 475 | PF00179 | 0.502 |
TRG_DiLeu_BaEn_1 | 577 | 582 | PF01217 | 0.563 |
TRG_DiLeu_BaEn_4 | 413 | 419 | PF01217 | 0.600 |
TRG_DiLeu_BaEn_4 | 480 | 486 | PF01217 | 0.403 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 318 | 321 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 371 | 374 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 561 | 564 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.293 |
TRG_ER_diArg_1 | 20 | 23 | PF00400 | 0.318 |
TRG_ER_diArg_1 | 482 | 485 | PF00400 | 0.625 |
TRG_NES_CRM1_1 | 399 | 414 | PF08389 | 0.613 |
TRG_Pf-PMV_PEXEL_1 | 276 | 280 | PF00026 | 0.328 |
TRG_Pf-PMV_PEXEL_1 | 409 | 413 | PF00026 | 0.458 |
TRG_Pf-PMV_PEXEL_1 | 476 | 480 | PF00026 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 572 | 577 | PF00026 | 0.557 |
TRG_Pf-PMV_PEXEL_1 | 593 | 598 | PF00026 | 0.523 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P569 | Leptomonas seymouri | 25% | 69% |
A0A0N1I0Y5 | Leptomonas seymouri | 74% | 99% |
A0A0S4IP49 | Bodo saltans | 25% | 75% |
A0A0S4IR67 | Bodo saltans | 26% | 78% |
A0A0S4JEF6 | Bodo saltans | 52% | 90% |
A0A0S4JJ54 | Bodo saltans | 25% | 87% |
A0A1X0NQ03 | Trypanosomatidae | 23% | 73% |
A0A1X0P2B6 | Trypanosomatidae | 59% | 99% |
A0A1X0P9E3 | Trypanosomatidae | 29% | 100% |
A0A1X0P9H3 | Trypanosomatidae | 31% | 70% |
A0A1X0P9T0 | Trypanosomatidae | 31% | 100% |
A0A3Q8IBS7 | Leishmania donovani | 76% | 100% |
A0A3Q8IEL2 | Leishmania donovani | 29% | 100% |
A0A3Q8IG88 | Leishmania donovani | 26% | 87% |
A0A3Q8IHG6 | Leishmania donovani | 29% | 100% |
A0A3R7KSK0 | Trypanosoma rangeli | 28% | 82% |
A0A3R7LER1 | Trypanosoma rangeli | 26% | 66% |
A0A3R7MDH9 | Trypanosoma rangeli | 28% | 85% |
A0A3R7R330 | Trypanosoma rangeli | 31% | 100% |
A0A3S5IRH3 | Trypanosoma rangeli | 57% | 100% |
A0A3S7WPL3 | Leishmania donovani | 26% | 68% |
A0A3S7X2P9 | Leishmania donovani | 28% | 100% |
A0A3S7X9Y1 | Leishmania donovani | 28% | 100% |
A0A422MZ05 | Trypanosoma rangeli | 29% | 90% |
A2ZRG4 | Oryza sativa subsp. japonica | 31% | 73% |
A4H4R6 | Leishmania braziliensis | 25% | 69% |
A4HAQ7 | Leishmania braziliensis | 26% | 100% |
A4HCA1 | Leishmania braziliensis | 25% | 68% |
A4HHN8 | Leishmania braziliensis | 30% | 100% |
A4HMM9 | Leishmania braziliensis | 27% | 87% |
A4HND6 | Leishmania braziliensis | 26% | 100% |
A4HSA6 | Leishmania infantum | 35% | 100% |
A4HSZ5 | Leishmania infantum | 26% | 68% |
A4I4V2 | Leishmania infantum | 29% | 100% |
A4I4V3 | Leishmania infantum | 29% | 100% |
A4I562 | Leishmania infantum | 76% | 100% |
A4IBA7 | Leishmania infantum | 26% | 87% |
A4IC09 | Leishmania infantum | 28% | 100% |
B9G2X9 | Oryza sativa subsp. japonica | 34% | 100% |
C9ZQI8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 97% |
C9ZV26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 81% |
C9ZZN5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 89% |
E9AEA1 | Leishmania major | 29% | 100% |
E9AF32 | Leishmania major | 27% | 87% |
E9AFU7 | Leishmania major | 28% | 100% |
E9AKP6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 92% |
E9AKY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 68% |
E9ALI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B0F9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
E9B6Z9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
F4I1T9 | Arabidopsis thaliana | 29% | 71% |
P28743 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 86% |
P46870 | Chlamydomonas reinhardtii | 31% | 78% |
Q10E64 | Oryza sativa subsp. japonica | 31% | 83% |
Q1MTQ1 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 97% |
Q2R2P7 | Oryza sativa subsp. japonica | 33% | 95% |
Q4Q7S4 | Leishmania major | 74% | 100% |
Q4QJ61 | Leishmania major | 27% | 90% |
Q4R918 | Macaca fascicularis | 26% | 100% |
Q6H638 | Oryza sativa subsp. japonica | 30% | 69% |
Q965T6 | Caenorhabditis elegans | 32% | 94% |
Q96FN5 | Homo sapiens | 31% | 94% |
Q9HAQ2 | Homo sapiens | 29% | 77% |
Q9V877 | Drosophila melanogaster | 28% | 97% |
Q9WV04 | Mus musculus | 31% | 77% |
V5AP02 | Trypanosoma cruzi | 28% | 81% |
V5B8M1 | Trypanosoma cruzi | 29% | 99% |
V5BHY4 | Trypanosoma cruzi | 29% | 81% |
V5BK25 | Trypanosoma cruzi | 27% | 84% |
V5D733 | Trypanosoma cruzi | 28% | 81% |
V5DTU1 | Trypanosoma cruzi | 30% | 100% |