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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005871 | kinesin complex | 3 | 2 |
GO:0005874 | microtubule | 6 | 11 |
GO:0005875 | microtubule associated complex | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
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 |
Related structures:
AlphaFold database: Q4Q7S4
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0007017 | microtubule-based process | 2 | 11 |
GO:0007018 | microtubule-based movement | 3 | 11 |
GO:0009987 | cellular process | 1 | 11 |
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 | 11 |
GO:0003774 | cytoskeletal motor activity | 1 | 11 |
GO:0003777 | microtubule motor activity | 2 | 11 |
GO:0003824 | catalytic activity | 1 | 6 |
GO:0005488 | binding | 1 | 11 |
GO:0005515 | protein binding | 2 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0008017 | microtubule binding | 5 | 11 |
GO:0008092 | cytoskeletal protein binding | 3 | 11 |
GO:0008574 | plus-end-directed microtubule motor activity | 3 | 2 |
GO:0015631 | tubulin binding | 4 | 11 |
GO:0016462 | pyrophosphatase activity | 5 | 2 |
GO:0016787 | hydrolase activity | 2 | 6 |
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:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 2 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 39 | 43 | PF00656 | 0.282 |
CLV_C14_Caspase3-7 | 560 | 564 | PF00656 | 0.714 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.271 |
CLV_NRD_NRD_1 | 464 | 466 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.286 |
CLV_NRD_NRD_1 | 493 | 495 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 592 | 594 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 603 | 605 | PF00675 | 0.603 |
CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 493 | 495 | PF00082 | 0.501 |
CLV_PCSK_PC1ET2_1 | 360 | 362 | PF00082 | 0.376 |
CLV_PCSK_PC1ET2_1 | 493 | 495 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 190 | 194 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 484 | 488 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 594 | 598 | PF00082 | 0.441 |
DEG_APCC_DBOX_1 | 255 | 263 | PF00400 | 0.365 |
DEG_APCC_DBOX_1 | 481 | 489 | PF00400 | 0.419 |
DOC_CYCLIN_RxL_1 | 283 | 290 | PF00134 | 0.386 |
DOC_MAPK_gen_1 | 233 | 242 | PF00069 | 0.273 |
DOC_MAPK_gen_1 | 482 | 489 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 572 | 581 | PF00069 | 0.575 |
DOC_MAPK_MEF2A_6 | 162 | 169 | PF00069 | 0.295 |
DOC_MAPK_MEF2A_6 | 233 | 242 | PF00069 | 0.374 |
DOC_MAPK_MEF2A_6 | 482 | 489 | PF00069 | 0.443 |
DOC_MAPK_MEF2A_6 | 575 | 583 | PF00069 | 0.395 |
DOC_MAPK_NFAT4_5 | 482 | 490 | PF00069 | 0.533 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.367 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.236 |
DOC_USP7_MATH_1 | 539 | 543 | PF00917 | 0.453 |
DOC_USP7_UBL2_3 | 356 | 360 | PF12436 | 0.378 |
DOC_USP7_UBL2_3 | 51 | 55 | PF12436 | 0.300 |
DOC_USP7_UBL2_3 | 9 | 13 | PF12436 | 0.499 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.254 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 545 | 550 | PF00397 | 0.596 |
LIG_14-3-3_CanoR_1 | 131 | 140 | PF00244 | 0.186 |
LIG_14-3-3_CanoR_1 | 286 | 292 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 3 | 12 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 400 | 408 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 68 | 77 | PF00244 | 0.282 |
LIG_Actin_WH2_2 | 422 | 437 | PF00022 | 0.582 |
LIG_Actin_WH2_2 | 460 | 478 | PF00022 | 0.486 |
LIG_APCC_ABBA_1 | 147 | 152 | PF00400 | 0.254 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.654 |
LIG_BIR_III_4 | 160 | 164 | PF00653 | 0.186 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.273 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.267 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.333 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.385 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.254 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.254 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.267 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.464 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.322 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.265 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.273 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.513 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.340 |
LIG_Integrin_RGD_1 | 174 | 176 | PF01839 | 0.251 |
LIG_LIR_Gen_1 | 127 | 137 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 143 | 154 | PF02991 | 0.177 |
LIG_LIR_Gen_1 | 32 | 38 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 454 | 464 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 60 | 71 | PF02991 | 0.212 |
LIG_LIR_Gen_1 | 75 | 85 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.254 |
LIG_LIR_Nem_3 | 143 | 149 | PF02991 | 0.254 |
LIG_LIR_Nem_3 | 32 | 36 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 366 | 370 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 454 | 460 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.212 |
LIG_LIR_Nem_3 | 75 | 80 | PF02991 | 0.308 |
LIG_NRBOX | 153 | 159 | PF00104 | 0.254 |
LIG_PCNA_yPIPBox_3 | 151 | 164 | PF02747 | 0.254 |
LIG_PCNA_yPIPBox_3 | 419 | 429 | PF02747 | 0.542 |
LIG_PCNA_yPIPBox_3 | 459 | 468 | PF02747 | 0.500 |
LIG_Pex14_2 | 63 | 67 | PF04695 | 0.254 |
LIG_PTB_Apo_2 | 32 | 39 | PF02174 | 0.310 |
LIG_PTB_Apo_2 | 61 | 68 | PF02174 | 0.298 |
LIG_PTB_Phospho_1 | 32 | 38 | PF10480 | 0.310 |
LIG_SH2_CRK | 18 | 22 | PF00017 | 0.367 |
LIG_SH2_CRK | 367 | 371 | PF00017 | 0.429 |
LIG_SH2_PTP2 | 146 | 149 | PF00017 | 0.254 |
LIG_SH2_SRC | 38 | 41 | PF00017 | 0.210 |
LIG_SH2_SRC | 428 | 431 | PF00017 | 0.476 |
LIG_SH2_STAP1 | 140 | 144 | PF00017 | 0.273 |
LIG_SH2_STAP1 | 397 | 401 | PF00017 | 0.469 |
LIG_SH2_STAP1 | 77 | 81 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 18 | 21 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 536 | 539 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.367 |
LIG_SH3_1 | 20 | 26 | PF00018 | 0.298 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.271 |
LIG_SH3_3 | 546 | 552 | PF00018 | 0.744 |
LIG_SH3_3 | 63 | 69 | PF00018 | 0.298 |
LIG_SUMO_SIM_par_1 | 176 | 184 | PF11976 | 0.254 |
LIG_SUMO_SIM_par_1 | 236 | 241 | PF11976 | 0.227 |
LIG_SUMO_SIM_par_1 | 249 | 254 | PF11976 | 0.320 |
LIG_TRAF2_1 | 385 | 388 | PF00917 | 0.625 |
LIG_TRAF2_1 | 389 | 392 | PF00917 | 0.581 |
LIG_TYR_ITIM | 144 | 149 | PF00017 | 0.254 |
LIG_TYR_ITIM | 365 | 370 | PF00017 | 0.413 |
LIG_UBA3_1 | 153 | 162 | PF00899 | 0.273 |
LIG_UBA3_1 | 226 | 233 | PF00899 | 0.282 |
LIG_UBA3_1 | 288 | 293 | PF00899 | 0.254 |
LIG_UBA3_1 | 374 | 381 | PF00899 | 0.459 |
LIG_WRC_WIRS_1 | 503 | 508 | PF05994 | 0.476 |
LIG_WRC_WIRS_1 | 540 | 545 | PF05994 | 0.645 |
LIG_WRC_WIRS_1 | 77 | 82 | PF05994 | 0.305 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.254 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.340 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.262 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.406 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.261 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.585 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.653 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.627 |
MOD_CK2_1 | 108 | 114 | PF00069 | 0.403 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.355 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.292 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.585 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.254 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.287 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.506 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.680 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.623 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.236 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.559 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.637 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.692 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.254 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.294 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.286 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.298 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.294 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.257 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.478 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.530 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.460 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.526 |
MOD_N-GLC_1 | 216 | 221 | PF02516 | 0.254 |
MOD_N-GLC_1 | 284 | 289 | PF02516 | 0.254 |
MOD_N-GLC_1 | 324 | 329 | PF02516 | 0.260 |
MOD_N-GLC_1 | 330 | 335 | PF02516 | 0.248 |
MOD_N-GLC_1 | 34 | 39 | PF02516 | 0.294 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.674 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.365 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.253 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.270 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.312 |
MOD_NEK2_1 | 543 | 548 | PF00069 | 0.732 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.186 |
MOD_PIKK_1 | 1 | 7 | PF00454 | 0.568 |
MOD_PIKK_1 | 350 | 356 | PF00454 | 0.386 |
MOD_PIKK_1 | 515 | 521 | PF00454 | 0.528 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.298 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.254 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.294 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.395 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.538 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.279 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.298 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.273 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.268 |
MOD_Plk_1 | 339 | 345 | PF00069 | 0.219 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.291 |
MOD_Plk_1 | 382 | 388 | PF00069 | 0.554 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.248 |
MOD_Plk_2-3 | 274 | 280 | PF00069 | 0.273 |
MOD_Plk_2-3 | 336 | 342 | PF00069 | 0.273 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.254 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.264 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.299 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.289 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.231 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.254 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.580 |
MOD_ProDKin_1 | 545 | 551 | PF00069 | 0.597 |
MOD_SUMO_rev_2 | 189 | 198 | PF00179 | 0.387 |
MOD_SUMO_rev_2 | 269 | 278 | PF00179 | 0.273 |
MOD_SUMO_rev_2 | 363 | 370 | PF00179 | 0.405 |
MOD_SUMO_rev_2 | 402 | 411 | PF00179 | 0.565 |
TRG_DiLeu_BaEn_1 | 406 | 411 | PF01217 | 0.439 |
TRG_DiLeu_BaEn_1 | 577 | 582 | PF01217 | 0.508 |
TRG_DiLeu_BaEn_4 | 406 | 412 | PF01217 | 0.563 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.254 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.254 |
TRG_ENDOCYTIC_2 | 18 | 21 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 318 | 321 | PF00928 | 0.273 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 371 | 374 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.254 |
TRG_ER_diArg_1 | 20 | 23 | PF00400 | 0.258 |
TRG_ER_diArg_1 | 482 | 485 | PF00400 | 0.528 |
TRG_NES_CRM1_1 | 399 | 414 | PF08389 | 0.544 |
TRG_Pf-PMV_PEXEL_1 | 276 | 280 | PF00026 | 0.273 |
TRG_Pf-PMV_PEXEL_1 | 384 | 388 | PF00026 | 0.673 |
TRG_Pf-PMV_PEXEL_1 | 465 | 469 | PF00026 | 0.517 |
TRG_Pf-PMV_PEXEL_1 | 572 | 577 | PF00026 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 593 | 598 | PF00026 | 0.491 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P569 | Leptomonas seymouri | 25% | 69% |
A0A0N1HY56 | Leptomonas seymouri | 28% | 88% |
A0A0N1I0Y5 | Leptomonas seymouri | 72% | 99% |
A0A0N1I2F8 | Leptomonas seymouri | 26% | 72% |
A0A0S4IP49 | Bodo saltans | 27% | 75% |
A0A0S4IR67 | Bodo saltans | 27% | 78% |
A0A0S4JEF6 | Bodo saltans | 51% | 90% |
A0A0S4JUR0 | Bodo saltans | 30% | 69% |
A0A0S4JXY6 | Bodo saltans | 24% | 71% |
A0A1X0NNQ8 | Trypanosomatidae | 25% | 94% |
A0A1X0NQ03 | Trypanosomatidae | 24% | 73% |
A0A1X0NY69 | Trypanosomatidae | 30% | 80% |
A0A1X0P2B6 | Trypanosomatidae | 58% | 99% |
A0A1X0P9E3 | Trypanosomatidae | 29% | 100% |
A0A1X0P9T0 | Trypanosomatidae | 31% | 100% |
A0A3Q8IBS7 | Leishmania donovani | 92% | 100% |
A0A3Q8IG88 | Leishmania donovani | 26% | 87% |
A0A3R7KSK0 | Trypanosoma rangeli | 29% | 82% |
A0A3R7MDH9 | Trypanosoma rangeli | 27% | 85% |
A0A3R7R330 | Trypanosoma rangeli | 29% | 100% |
A0A3S5IRH3 | Trypanosoma rangeli | 56% | 100% |
A0A422N2N4 | Trypanosoma rangeli | 29% | 70% |
A2ZRG4 | Oryza sativa subsp. japonica | 33% | 73% |
A4H4I4 | Leishmania braziliensis | 26% | 92% |
A4HAQ7 | Leishmania braziliensis | 26% | 100% |
A4HHN7 | Leishmania braziliensis | 32% | 100% |
A4HHN8 | Leishmania braziliensis | 31% | 100% |
A4HHY2 | Leishmania braziliensis | 74% | 100% |
A4HSA6 | Leishmania infantum | 35% | 100% |
A4I562 | Leishmania infantum | 91% | 100% |
A4IBA7 | Leishmania infantum | 27% | 87% |
B9G2X9 | Oryza sativa subsp. japonica | 31% | 100% |
C9ZK93 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 81% |
C9ZL08 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZL09 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
C9ZQI8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 97% |
C9ZTM7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 95% |
C9ZV26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 81% |
C9ZZN5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 89% |
E9AEA0 | Leishmania major | 30% | 100% |
E9ALI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9AVN8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 68% |
E9B0F9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
F4I1T9 | Arabidopsis thaliana | 30% | 71% |
O59751 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 77% |
P46870 | Chlamydomonas reinhardtii | 30% | 78% |
Q1MTQ1 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 97% |
Q2NL05 | Bos taurus | 27% | 92% |
Q2R2P7 | Oryza sativa subsp. japonica | 33% | 95% |
Q4QEL8 | Leishmania major | 27% | 75% |
Q4QJ61 | Leishmania major | 27% | 90% |
Q4R918 | Macaca fascicularis | 27% | 100% |
Q75HV1 | Oryza sativa subsp. japonica | 31% | 72% |
Q86ZC1 | Botryotinia fuckeliana | 35% | 69% |
Q8NI77 | Homo sapiens | 30% | 68% |
Q8W0Y9 | Arabidopsis thaliana | 30% | 97% |
Q91WD7 | Mus musculus | 31% | 69% |
Q965T6 | Caenorhabditis elegans | 36% | 94% |
Q96FN5 | Homo sapiens | 31% | 94% |
Q9D2Z8 | Mus musculus | 32% | 95% |
Q9FZ06 | Arabidopsis thaliana | 34% | 66% |
Q9SCJ4 | Arabidopsis thaliana | 29% | 75% |
Q9UTL2 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 100% |
V5BHY4 | Trypanosoma cruzi | 30% | 81% |
V5BK25 | Trypanosoma cruzi | 28% | 84% |
V5BNJ8 | Trypanosoma cruzi | 27% | 100% |
V5DFA7 | Trypanosoma cruzi | 28% | 100% |
V5DTU1 | Trypanosoma cruzi | 32% | 100% |