Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 20 |
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: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005871 | kinesin complex | 3 | 2 |
GO:0005874 | microtubule | 6 | 6 |
GO:0005875 | microtubule associated complex | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0051286 | cell tip | 3 | 2 |
GO:0060187 | cell pole | 2 | 2 |
GO:0099080 | supramolecular complex | 2 | 6 |
GO:0099081 | supramolecular polymer | 3 | 6 |
GO:0099512 | supramolecular fiber | 4 | 6 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: E9AEA1
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 15 |
GO:0007018 | microtubule-based movement | 3 | 15 |
GO:0009987 | cellular process | 1 | 15 |
GO:0006810 | transport | 3 | 1 |
GO:0010970 | transport along microtubule | 4 | 1 |
GO:0030705 | cytoskeleton-dependent intracellular transport | 4 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0047496 | vesicle transport along microtubule | 5 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051640 | organelle localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051648 | vesicle localization | 3 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0051650 | establishment of vesicle localization | 4 | 1 |
GO:0051656 | establishment of organelle localization | 3 | 1 |
GO:0072383 | plus-end-directed vesicle transport along microtubule | 6 | 1 |
GO:0072384 | organelle transport along microtubule | 4 | 1 |
GO:0072386 | plus-end-directed organelle transport along microtubule | 5 | 1 |
GO:0099111 | microtubule-based transport | 4 | 1 |
GO:0099518 | vesicle cytoskeletal trafficking | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 15 |
GO:0003774 | cytoskeletal motor activity | 1 | 15 |
GO:0003777 | microtubule motor activity | 2 | 15 |
GO:0003824 | catalytic activity | 1 | 5 |
GO:0005488 | binding | 1 | 15 |
GO:0005515 | protein binding | 2 | 15 |
GO:0005524 | ATP binding | 5 | 15 |
GO:0008017 | microtubule binding | 5 | 15 |
GO:0008092 | cytoskeletal protein binding | 3 | 15 |
GO:0015631 | tubulin binding | 4 | 15 |
GO:0016462 | pyrophosphatase activity | 5 | 2 |
GO:0016787 | hydrolase activity | 2 | 5 |
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 | 15 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 2 |
GO:0030554 | adenyl nucleotide binding | 5 | 15 |
GO:0032553 | ribonucleotide binding | 3 | 15 |
GO:0032555 | purine ribonucleotide binding | 4 | 15 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 15 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 15 |
GO:0036094 | small molecule binding | 2 | 15 |
GO:0043167 | ion binding | 2 | 15 |
GO:0043168 | anion binding | 3 | 15 |
GO:0097159 | organic cyclic compound binding | 2 | 15 |
GO:0097367 | carbohydrate derivative binding | 2 | 15 |
GO:0140657 | ATP-dependent activity | 1 | 15 |
GO:1901265 | nucleoside phosphate binding | 3 | 15 |
GO:1901363 | heterocyclic compound binding | 2 | 15 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.537 |
CLV_PCSK_FUR_1 | 45 | 49 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 559 | 561 | PF00082 | 0.592 |
CLV_PCSK_PC1ET2_1 | 432 | 434 | PF00082 | 0.685 |
CLV_PCSK_PC1ET2_1 | 463 | 465 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 47 | 49 | PF00082 | 0.469 |
CLV_PCSK_PC1ET2_1 | 559 | 561 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.574 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 540 | 544 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.352 |
CLV_Separin_Metazoa | 191 | 195 | PF03568 | 0.410 |
DEG_APCC_DBOX_1 | 559 | 567 | PF00400 | 0.587 |
DEG_SPOP_SBC_1 | 477 | 481 | PF00917 | 0.452 |
DOC_CYCLIN_RxL_1 | 112 | 120 | PF00134 | 0.455 |
DOC_CYCLIN_RxL_1 | 344 | 356 | PF00134 | 0.584 |
DOC_MAPK_gen_1 | 19 | 30 | PF00069 | 0.545 |
DOC_MAPK_gen_1 | 448 | 455 | PF00069 | 0.493 |
DOC_MAPK_gen_1 | 463 | 470 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 505 | 513 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 6 | 15 | PF00069 | 0.566 |
DOC_MAPK_MEF2A_6 | 213 | 222 | PF00069 | 0.361 |
DOC_MAPK_MEF2A_6 | 375 | 384 | PF00069 | 0.616 |
DOC_MAPK_MEF2A_6 | 389 | 396 | PF00069 | 0.439 |
DOC_MAPK_MEF2A_6 | 6 | 15 | PF00069 | 0.469 |
DOC_MAPK_NFAT4_5 | 389 | 397 | PF00069 | 0.605 |
DOC_PP1_RVXF_1 | 430 | 437 | PF00149 | 0.451 |
DOC_PP1_RVXF_1 | 503 | 510 | PF00149 | 0.481 |
DOC_PP2B_LxvP_1 | 150 | 153 | PF13499 | 0.361 |
DOC_PP4_FxxP_1 | 561 | 564 | PF00568 | 0.502 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.336 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.556 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.321 |
DOC_WW_Pin1_4 | 564 | 569 | PF00397 | 0.541 |
LIG_14-3-3_CanoR_1 | 176 | 181 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 200 | 207 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 274 | 280 | PF00244 | 0.335 |
LIG_14-3-3_CanoR_1 | 408 | 414 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 433 | 439 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 450 | 456 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 525 | 529 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 8 | 14 | PF00244 | 0.473 |
LIG_Actin_WH2_2 | 342 | 360 | PF00022 | 0.615 |
LIG_Actin_WH2_2 | 377 | 395 | PF00022 | 0.559 |
LIG_Actin_WH2_2 | 60 | 75 | PF00022 | 0.352 |
LIG_APCC_ABBA_1 | 140 | 145 | PF00400 | 0.321 |
LIG_APCC_ABBA_1 | 163 | 168 | PF00400 | 0.343 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.694 |
LIG_BRCT_BRCA1_1 | 222 | 226 | PF00533 | 0.455 |
LIG_BRCT_BRCA1_1 | 284 | 288 | PF00533 | 0.418 |
LIG_BRCT_BRCA1_1 | 300 | 304 | PF00533 | 0.243 |
LIG_BRCT_BRCA1_1 | 442 | 446 | PF00533 | 0.628 |
LIG_BRCT_BRCA1_1 | 505 | 509 | PF00533 | 0.487 |
LIG_BRCT_BRCA1_1 | 531 | 535 | PF00533 | 0.548 |
LIG_BRCT_BRCA1_2 | 442 | 448 | PF00533 | 0.607 |
LIG_Clathr_ClatBox_1 | 579 | 583 | PF01394 | 0.536 |
LIG_CtBP_PxDLS_1 | 499 | 503 | PF00389 | 0.599 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.427 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.634 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.311 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.311 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.311 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.468 |
LIG_FHA_1 | 574 | 580 | PF00498 | 0.496 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.352 |
LIG_FHA_2 | 248 | 254 | PF00498 | 0.453 |
LIG_FHA_2 | 492 | 498 | PF00498 | 0.578 |
LIG_FHA_2 | 544 | 550 | PF00498 | 0.593 |
LIG_GBD_Chelix_1 | 360 | 368 | PF00786 | 0.514 |
LIG_LIR_Gen_1 | 223 | 234 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 285 | 296 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 527 | 535 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 581 | 587 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 62 | 72 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 94 | 101 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 223 | 229 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 285 | 291 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 441 | 447 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 527 | 531 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 581 | 585 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 62 | 67 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 74 | 79 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 94 | 98 | PF02991 | 0.389 |
LIG_MAD2 | 512 | 520 | PF02301 | 0.539 |
LIG_MYND_1 | 564 | 568 | PF01753 | 0.570 |
LIG_NRBOX | 295 | 301 | PF00104 | 0.379 |
LIG_Pex14_2 | 52 | 56 | PF04695 | 0.361 |
LIG_Rb_LxCxE_1 | 96 | 119 | PF01857 | 0.235 |
LIG_Rb_pABgroove_1 | 112 | 120 | PF01858 | 0.469 |
LIG_Rb_pABgroove_1 | 529 | 537 | PF01858 | 0.573 |
LIG_RPA_C_Fungi | 421 | 433 | PF08784 | 0.650 |
LIG_SH2_CRK | 95 | 99 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 332 | 336 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 541 | 544 | PF00017 | 0.500 |
LIG_SUMO_SIM_anti_2 | 381 | 388 | PF11976 | 0.573 |
LIG_SUMO_SIM_par_1 | 235 | 242 | PF11976 | 0.361 |
LIG_UBA3_1 | 189 | 195 | PF00899 | 0.361 |
LIG_WRC_WIRS_1 | 276 | 281 | PF05994 | 0.346 |
LIG_WRC_WIRS_1 | 579 | 584 | PF05994 | 0.503 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.299 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.320 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.433 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.608 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.333 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.333 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.334 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.471 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.568 |
MOD_CK2_1 | 491 | 497 | PF00069 | 0.599 |
MOD_CK2_1 | 542 | 548 | PF00069 | 0.549 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.486 |
MOD_GlcNHglycan | 253 | 257 | PF01048 | 0.422 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.427 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.333 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.425 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.340 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.333 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.360 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.330 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.315 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.502 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.630 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.471 |
MOD_N-GLC_1 | 207 | 212 | PF02516 | 0.347 |
MOD_N-GLC_1 | 265 | 270 | PF02516 | 0.311 |
MOD_N-GLC_1 | 321 | 326 | PF02516 | 0.361 |
MOD_N-GLC_2 | 80 | 82 | PF02516 | 0.333 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.343 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.290 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.343 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.299 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.298 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.312 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.415 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.595 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.542 |
MOD_NEK2_2 | 129 | 134 | PF00069 | 0.455 |
MOD_NEK2_2 | 287 | 292 | PF00069 | 0.333 |
MOD_NEK2_2 | 451 | 456 | PF00069 | 0.563 |
MOD_PIKK_1 | 220 | 226 | PF00454 | 0.333 |
MOD_PIKK_1 | 398 | 404 | PF00454 | 0.594 |
MOD_PK_1 | 176 | 182 | PF00069 | 0.455 |
MOD_PK_1 | 344 | 350 | PF00069 | 0.494 |
MOD_PKA_1 | 282 | 288 | PF00069 | 0.449 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.321 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.333 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.311 |
MOD_PKA_2 | 524 | 530 | PF00069 | 0.526 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.433 |
MOD_Plk_1 | 265 | 271 | PF00069 | 0.311 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.368 |
MOD_Plk_1 | 440 | 446 | PF00069 | 0.613 |
MOD_Plk_1 | 491 | 497 | PF00069 | 0.631 |
MOD_Plk_2-3 | 159 | 165 | PF00069 | 0.379 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.333 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.364 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.322 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.334 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.410 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.602 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.368 |
MOD_Plk_4 | 440 | 446 | PF00069 | 0.622 |
MOD_Plk_4 | 529 | 535 | PF00069 | 0.502 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.321 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.321 |
MOD_ProDKin_1 | 564 | 570 | PF00069 | 0.536 |
MOD_SUMO_rev_2 | 2 | 7 | PF00179 | 0.643 |
MOD_SUMO_rev_2 | 255 | 265 | PF00179 | 0.337 |
MOD_SUMO_rev_2 | 278 | 285 | PF00179 | 0.455 |
MOD_SUMO_rev_2 | 290 | 297 | PF00179 | 0.323 |
MOD_SUMO_rev_2 | 347 | 357 | PF00179 | 0.503 |
TRG_DiLeu_BaEn_4 | 387 | 393 | PF01217 | 0.545 |
TRG_DiLeu_BaLyEn_6 | 295 | 300 | PF01217 | 0.379 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.175 |
TRG_ER_diArg_1 | 13 | 16 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 153 | 156 | PF00400 | 0.354 |
TRG_ER_diArg_1 | 171 | 173 | PF00400 | 0.258 |
TRG_ER_diArg_1 | 22 | 25 | PF00400 | 0.632 |
TRG_ER_diArg_1 | 423 | 426 | PF00400 | 0.531 |
TRG_NES_CRM1_1 | 233 | 247 | PF08389 | 0.400 |
TRG_Pf-PMV_PEXEL_1 | 115 | 119 | PF00026 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 298 | 302 | PF00026 | 0.346 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P569 | Leptomonas seymouri | 27% | 67% |
A0A0N1HY56 | Leptomonas seymouri | 29% | 86% |
A0A0N1I0Y5 | Leptomonas seymouri | 30% | 96% |
A0A0N1PDD6 | Leptomonas seymouri | 30% | 77% |
A0A0S4IKE6 | Bodo saltans | 51% | 100% |
A0A0S4IP49 | Bodo saltans | 26% | 73% |
A0A0S4J0Q2 | Bodo saltans | 33% | 71% |
A0A0S4JEF6 | Bodo saltans | 29% | 88% |
A0A0S4JJ54 | Bodo saltans | 30% | 84% |
A0A0S4JXY6 | Bodo saltans | 30% | 68% |
A0A0S4KL43 | Bodo saltans | 29% | 100% |
A0A1X0NJN6 | Trypanosomatidae | 29% | 100% |
A0A1X0NNQ8 | Trypanosomatidae | 24% | 92% |
A0A1X0NP27 | Trypanosomatidae | 40% | 80% |
A0A1X0NQ03 | Trypanosomatidae | 27% | 71% |
A0A1X0NWZ8 | Trypanosomatidae | 31% | 79% |
A0A1X0P0C2 | Trypanosomatidae | 32% | 72% |
A0A1X0P2B6 | Trypanosomatidae | 31% | 96% |
A0A1X0P9E3 | Trypanosomatidae | 56% | 99% |
A0A1X0P9H3 | Trypanosomatidae | 32% | 68% |
A0A1X0P9T0 | Trypanosomatidae | 32% | 100% |
A0A1X0PAG9 | Trypanosomatidae | 59% | 99% |
A0A3Q8IEL2 | Leishmania donovani | 95% | 100% |
A0A3R7MDH9 | Trypanosoma rangeli | 28% | 83% |
A0A3S7WPL3 | Leishmania donovani | 30% | 66% |
A0A3S7WS99 | Leishmania donovani | 30% | 81% |
A0A422MZ05 | Trypanosoma rangeli | 28% | 87% |
A0A422N3U0 | Trypanosoma rangeli | 27% | 78% |
A0A422NE49 | Trypanosoma rangeli | 31% | 66% |
A0A422NEQ8 | Trypanosoma rangeli | 31% | 78% |
A0A422NXU3 | Trypanosoma rangeli | 59% | 100% |
A4H4I4 | Leishmania braziliensis | 28% | 89% |
A4H4R6 | Leishmania braziliensis | 30% | 67% |
A4HAQ7 | Leishmania braziliensis | 27% | 100% |
A4HCT2 | Leishmania braziliensis | 31% | 82% |
A4HHN8 | Leishmania braziliensis | 87% | 100% |
A4HHY2 | Leishmania braziliensis | 29% | 97% |
A4HSA6 | Leishmania infantum | 34% | 100% |
A4HSZ5 | Leishmania infantum | 29% | 66% |
A4HVE9 | Leishmania infantum | 30% | 81% |
A4I4V3 | Leishmania infantum | 95% | 100% |
C9ZK93 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 79% |
C9ZL08 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
C9ZQI8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 94% |
C9ZTV8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 66% |
C9ZU98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 73% |
C9ZV26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 79% |
E9AKY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 66% |
E9ALI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
E9AW71 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 90% |
E9B0F9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 97% |
F4I1T9 | Arabidopsis thaliana | 31% | 69% |
Q10E64 | Oryza sativa subsp. japonica | 33% | 80% |
Q1MTQ1 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 94% |
Q4QIX3 | Leishmania major | 29% | 66% |
Q5VQ09 | Oryza sativa subsp. japonica | 32% | 66% |
Q651Z7 | Oryza sativa subsp. japonica | 31% | 68% |
Q6H638 | Oryza sativa subsp. japonica | 32% | 67% |
Q8GW44 | Arabidopsis thaliana | 34% | 100% |
Q96FN5 | Homo sapiens | 32% | 91% |
Q9HAQ2 | Homo sapiens | 31% | 75% |
Q9NF78 | Leishmania major | 30% | 100% |
Q9SCJ4 | Arabidopsis thaliana | 32% | 72% |
Q9UTL2 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
Q9V877 | Drosophila melanogaster | 29% | 94% |
Q9WV04 | Mus musculus | 30% | 75% |
V5B8M1 | Trypanosoma cruzi | 34% | 96% |
V5B8X9 | Trypanosoma cruzi | 28% | 84% |
V5BAR9 | Trypanosoma cruzi | 33% | 92% |
V5BHY4 | Trypanosoma cruzi | 31% | 79% |
V5BIC1 | Trypanosoma cruzi | 32% | 92% |
V5BK25 | Trypanosoma cruzi | 29% | 82% |
V5DFA7 | Trypanosoma cruzi | 32% | 100% |
V5DMS2 | Trypanosoma cruzi | 36% | 100% |
V5DTU1 | Trypanosoma cruzi | 62% | 100% |