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: 35 |
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: 17 |
NetGPI | no | yes: 0, no: 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005871 | kinesin complex | 3 | 2 |
GO:0005874 | microtubule | 6 | 4 |
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 | 4 |
GO:0099081 | supramolecular polymer | 3 | 4 |
GO:0099512 | supramolecular fiber | 4 | 4 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: E9AEA0
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 18 |
GO:0007018 | microtubule-based movement | 3 | 18 |
GO:0009987 | cellular process | 1 | 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 18 |
GO:0003774 | cytoskeletal motor activity | 1 | 18 |
GO:0003777 | microtubule motor activity | 2 | 18 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0005488 | binding | 1 | 18 |
GO:0005515 | protein binding | 2 | 18 |
GO:0005524 | ATP binding | 5 | 18 |
GO:0008017 | microtubule binding | 5 | 18 |
GO:0008092 | cytoskeletal protein binding | 3 | 18 |
GO:0015631 | tubulin binding | 4 | 18 |
GO:0016462 | pyrophosphatase activity | 5 | 2 |
GO:0016787 | hydrolase activity | 2 | 9 |
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 | 18 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 2 |
GO:0030554 | adenyl nucleotide binding | 5 | 18 |
GO:0032553 | ribonucleotide binding | 3 | 18 |
GO:0032555 | purine ribonucleotide binding | 4 | 18 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 18 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 18 |
GO:0036094 | small molecule binding | 2 | 18 |
GO:0043167 | ion binding | 2 | 18 |
GO:0043168 | anion binding | 3 | 18 |
GO:0097159 | organic cyclic compound binding | 2 | 18 |
GO:0097367 | carbohydrate derivative binding | 2 | 18 |
GO:0140657 | ATP-dependent activity | 1 | 18 |
GO:1901265 | nucleoside phosphate binding | 3 | 18 |
GO:1901363 | heterocyclic compound binding | 2 | 18 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 415 | 419 | PF00656 | 0.469 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.329 |
CLV_NRD_NRD_1 | 556 | 558 | PF00675 | 0.420 |
CLV_PCSK_FUR_1 | 47 | 51 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.420 |
CLV_PCSK_PC1ET2_1 | 49 | 51 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 525 | 529 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.335 |
CLV_Separin_Metazoa | 193 | 197 | PF03568 | 0.455 |
DEG_SCF_FBW7_1 | 526 | 532 | PF00400 | 0.445 |
DOC_CKS1_1 | 526 | 531 | PF01111 | 0.475 |
DOC_CYCLIN_RxL_1 | 114 | 122 | PF00134 | 0.474 |
DOC_CYCLIN_RxL_1 | 393 | 400 | PF00134 | 0.425 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 477 | 486 | PF00134 | 0.400 |
DOC_MAPK_MEF2A_6 | 10 | 17 | PF00069 | 0.427 |
DOC_MAPK_MEF2A_6 | 215 | 224 | PF00069 | 0.347 |
DOC_PP2B_LxvP_1 | 152 | 155 | PF13499 | 0.360 |
DOC_PP2B_LxvP_1 | 464 | 467 | PF13499 | 0.479 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.345 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 529 | 533 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 575 | 579 | PF00917 | 0.544 |
DOC_USP7_UBL2_3 | 22 | 26 | PF12436 | 0.204 |
DOC_USP7_UBL2_3 | 539 | 543 | PF12436 | 0.572 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.346 |
DOC_WW_Pin1_4 | 525 | 530 | PF00397 | 0.450 |
LIG_14-3-3_CanoR_1 | 10 | 16 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 178 | 183 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 202 | 209 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 276 | 282 | PF00244 | 0.346 |
LIG_14-3-3_CanoR_1 | 556 | 566 | PF00244 | 0.522 |
LIG_14-3-3_CterR_2 | 587 | 590 | PF00244 | 0.560 |
LIG_Actin_WH2_2 | 62 | 77 | PF00022 | 0.335 |
LIG_APCC_ABBA_1 | 142 | 147 | PF00400 | 0.335 |
LIG_APCC_ABBA_1 | 165 | 170 | PF00400 | 0.351 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.697 |
LIG_BRCT_BRCA1_1 | 224 | 228 | PF00533 | 0.474 |
LIG_BRCT_BRCA1_1 | 286 | 290 | PF00533 | 0.432 |
LIG_BRCT_BRCA1_1 | 302 | 306 | PF00533 | 0.264 |
LIG_BRCT_BRCA1_1 | 514 | 518 | PF00533 | 0.507 |
LIG_EH1_1 | 458 | 466 | PF00400 | 0.533 |
LIG_eIF4E_1 | 459 | 465 | PF01652 | 0.537 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.474 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.324 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.324 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.360 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.413 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.489 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.478 |
LIG_FHA_1 | 550 | 556 | PF00498 | 0.483 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.526 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.351 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.450 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.423 |
LIG_LIR_Gen_1 | 225 | 236 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 287 | 298 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 353 | 362 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 562 | 571 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 64 | 74 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 96 | 103 | PF02991 | 0.393 |
LIG_LIR_LC3C_4 | 463 | 466 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 225 | 231 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 287 | 293 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 353 | 359 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 562 | 568 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 64 | 69 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 76 | 81 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 96 | 100 | PF02991 | 0.351 |
LIG_NRBOX | 297 | 303 | PF00104 | 0.393 |
LIG_NRBOX | 481 | 487 | PF00104 | 0.366 |
LIG_Pex14_2 | 54 | 58 | PF04695 | 0.337 |
LIG_PTB_Apo_2 | 534 | 541 | PF02174 | 0.524 |
LIG_Rb_LxCxE_1 | 98 | 121 | PF01857 | 0.249 |
LIG_Rb_pABgroove_1 | 114 | 122 | PF01858 | 0.474 |
LIG_Rb_pABgroove_1 | 463 | 471 | PF01858 | 0.450 |
LIG_SH2_CRK | 469 | 473 | PF00017 | 0.570 |
LIG_SH2_CRK | 97 | 101 | PF00017 | 0.470 |
LIG_SH2_NCK_1 | 469 | 473 | PF00017 | 0.613 |
LIG_SH2_STAP1 | 334 | 338 | PF00017 | 0.341 |
LIG_SH2_STAP1 | 356 | 360 | PF00017 | 0.623 |
LIG_SH2_STAP1 | 380 | 384 | PF00017 | 0.568 |
LIG_SH2_STAT3 | 380 | 383 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 546 | 549 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 565 | 568 | PF00017 | 0.487 |
LIG_SH3_3 | 469 | 475 | PF00018 | 0.491 |
LIG_SH3_3 | 523 | 529 | PF00018 | 0.506 |
LIG_SUMO_SIM_anti_2 | 491 | 497 | PF11976 | 0.502 |
LIG_SUMO_SIM_par_1 | 237 | 244 | PF11976 | 0.393 |
LIG_SUMO_SIM_par_1 | 491 | 497 | PF11976 | 0.508 |
LIG_TYR_ITIM | 354 | 359 | PF00017 | 0.562 |
LIG_TYR_ITIM | 563 | 568 | PF00017 | 0.491 |
LIG_UBA3_1 | 191 | 197 | PF00899 | 0.393 |
LIG_WRC_WIRS_1 | 278 | 283 | PF05994 | 0.360 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.320 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.335 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.438 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.520 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.457 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.360 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.346 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.328 |
MOD_CK2_1 | 289 | 295 | PF00069 | 0.495 |
MOD_CK2_1 | 401 | 407 | PF00069 | 0.554 |
MOD_DYRK1A_RPxSP_1 | 525 | 529 | PF00069 | 0.441 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.679 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.474 |
MOD_GlcNHglycan | 255 | 259 | PF01048 | 0.468 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.425 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.455 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.631 |
MOD_GlcNHglycan | 572 | 575 | PF01048 | 0.492 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.430 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.349 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.439 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.360 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.335 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.351 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.355 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.342 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.542 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.571 |
MOD_GSK3_1 | 443 | 450 | PF00069 | 0.433 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.478 |
MOD_N-GLC_1 | 209 | 214 | PF02516 | 0.347 |
MOD_N-GLC_1 | 267 | 272 | PF02516 | 0.335 |
MOD_N-GLC_1 | 323 | 328 | PF02516 | 0.360 |
MOD_N-GLC_1 | 347 | 352 | PF02516 | 0.481 |
MOD_N-GLC_1 | 401 | 406 | PF02516 | 0.613 |
MOD_N-GLC_2 | 82 | 84 | PF02516 | 0.330 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.344 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.327 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.340 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.326 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.335 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.336 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.471 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.426 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.517 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.474 |
MOD_NEK2_2 | 131 | 136 | PF00069 | 0.474 |
MOD_NEK2_2 | 289 | 294 | PF00069 | 0.335 |
MOD_NEK2_2 | 447 | 452 | PF00069 | 0.576 |
MOD_OFUCOSY | 442 | 447 | PF10250 | 0.472 |
MOD_PIKK_1 | 222 | 228 | PF00454 | 0.346 |
MOD_PIKK_1 | 379 | 385 | PF00454 | 0.556 |
MOD_PIKK_1 | 401 | 407 | PF00454 | 0.621 |
MOD_PIKK_1 | 423 | 429 | PF00454 | 0.572 |
MOD_PK_1 | 178 | 184 | PF00069 | 0.474 |
MOD_PKA_1 | 284 | 290 | PF00069 | 0.464 |
MOD_PKA_2 | 201 | 207 | PF00069 | 0.353 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.346 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.329 |
MOD_PKA_2 | 512 | 518 | PF00069 | 0.489 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.474 |
MOD_Plk_1 | 267 | 273 | PF00069 | 0.335 |
MOD_Plk_1 | 401 | 407 | PF00069 | 0.644 |
MOD_Plk_1 | 575 | 581 | PF00069 | 0.696 |
MOD_Plk_2-3 | 161 | 167 | PF00069 | 0.393 |
MOD_Plk_2-3 | 412 | 418 | PF00069 | 0.470 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.346 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.392 |
MOD_Plk_4 | 267 | 273 | PF00069 | 0.347 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.346 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.294 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.451 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.458 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.335 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.346 |
MOD_ProDKin_1 | 525 | 531 | PF00069 | 0.448 |
MOD_SUMO_rev_2 | 257 | 267 | PF00179 | 0.342 |
MOD_SUMO_rev_2 | 280 | 287 | PF00179 | 0.477 |
MOD_SUMO_rev_2 | 292 | 299 | PF00179 | 0.490 |
TRG_DiLeu_BaEn_1 | 355 | 360 | PF01217 | 0.595 |
TRG_DiLeu_BaEn_1 | 416 | 421 | PF01217 | 0.523 |
TRG_DiLeu_BaEn_1 | 460 | 465 | PF01217 | 0.530 |
TRG_DiLeu_BaEn_2 | 553 | 559 | PF01217 | 0.333 |
TRG_DiLeu_BaLyEn_6 | 297 | 302 | PF01217 | 0.393 |
TRG_DiLeu_BaLyEn_6 | 473 | 478 | PF01217 | 0.452 |
TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.539 |
TRG_ENDOCYTIC_2 | 469 | 472 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 565 | 568 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.393 |
TRG_ER_diArg_1 | 15 | 18 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 155 | 158 | PF00400 | 0.346 |
TRG_ER_diArg_1 | 173 | 175 | PF00400 | 0.299 |
TRG_ER_diArg_1 | 360 | 363 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 555 | 557 | PF00400 | 0.415 |
TRG_NES_CRM1_1 | 235 | 249 | PF08389 | 0.409 |
TRG_Pf-PMV_PEXEL_1 | 117 | 121 | PF00026 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 300 | 304 | PF00026 | 0.360 |
TRG_Pf-PMV_PEXEL_1 | 374 | 378 | PF00026 | 0.514 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P569 | Leptomonas seymouri | 27% | 67% |
A0A0N1HY56 | Leptomonas seymouri | 29% | 86% |
A0A0N1I2F8 | Leptomonas seymouri | 29% | 70% |
A0A0S4ILK1 | Bodo saltans | 32% | 69% |
A0A0S4IP49 | Bodo saltans | 27% | 73% |
A0A0S4J0Q2 | Bodo saltans | 34% | 71% |
A0A0S4JFN9 | Bodo saltans | 34% | 69% |
A0A0S4JJ54 | Bodo saltans | 33% | 84% |
A0A0S4JLW3 | Bodo saltans | 32% | 100% |
A0A0S4JXY6 | Bodo saltans | 31% | 69% |
A0A0S4KL43 | Bodo saltans | 29% | 100% |
A0A1X0NQ03 | Trypanosomatidae | 28% | 71% |
A0A1X0NWZ8 | Trypanosomatidae | 31% | 79% |
A0A1X0P0C2 | Trypanosomatidae | 32% | 72% |
A0A1X0P9E3 | Trypanosomatidae | 60% | 99% |
A0A1X0PAG9 | Trypanosomatidae | 50% | 99% |
A0A3Q8IBS7 | Leishmania donovani | 30% | 97% |
A0A3Q8IEL2 | Leishmania donovani | 70% | 100% |
A0A3Q8IHG6 | Leishmania donovani | 97% | 100% |
A0A3R7MDH9 | Trypanosoma rangeli | 28% | 83% |
A0A3R7R330 | Trypanosoma rangeli | 62% | 100% |
A0A3R7RD86 | Trypanosoma rangeli | 34% | 74% |
A0A3S7WPL3 | Leishmania donovani | 30% | 66% |
A0A3S7WU64 | Leishmania donovani | 32% | 68% |
A0A3S7X2P9 | Leishmania donovani | 95% | 100% |
A0A422MZ05 | Trypanosoma rangeli | 28% | 87% |
A0A422NE49 | Trypanosoma rangeli | 32% | 66% |
A0A422NEQ8 | Trypanosoma rangeli | 31% | 78% |
A4H4R6 | Leishmania braziliensis | 30% | 67% |
A4HAQ7 | Leishmania braziliensis | 27% | 100% |
A4HCT2 | Leishmania braziliensis | 31% | 82% |
A4HHN7 | Leishmania braziliensis | 87% | 100% |
A4HSA6 | Leishmania infantum | 34% | 100% |
A4HSZ5 | Leishmania infantum | 29% | 66% |
A4HX45 | Leishmania infantum | 32% | 74% |
A4I4V2 | Leishmania infantum | 97% | 100% |
A4I4V3 | Leishmania infantum | 85% | 100% |
A4I562 | Leishmania infantum | 30% | 97% |
B9G2X9 | Oryza sativa subsp. japonica | 34% | 98% |
C9ZI82 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 67% |
C9ZL08 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
C9ZL09 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
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) | 29% | 79% |
E9AKY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 66% |
E9ALI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
E9ALI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
E9B0F9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 97% |
O14782 | Homo sapiens | 33% | 74% |
O35066 | Mus musculus | 32% | 74% |
O55165 | Rattus norvegicus | 33% | 74% |
P46870 | Chlamydomonas reinhardtii | 30% | 76% |
P53086 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 73% |
Q10E64 | Oryza sativa subsp. japonica | 34% | 80% |
Q14807 | Homo sapiens | 30% | 89% |
Q1MTQ1 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 94% |
Q1MTQ7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 93% |
Q29DY1 | Drosophila pseudoobscura pseudoobscura | 34% | 74% |
Q2R2P7 | Oryza sativa subsp. japonica | 34% | 92% |
Q3V300 | Mus musculus | 30% | 89% |
Q4Q7S4 | Leishmania major | 30% | 97% |
Q4QEL8 | Leishmania major | 32% | 73% |
Q4QIX3 | Leishmania major | 29% | 67% |
Q4R918 | Macaca fascicularis | 28% | 100% |
Q5I0E8 | Rattus norvegicus | 30% | 90% |
Q5R706 | Pongo abelii | 33% | 74% |
Q5REP4 | Pongo abelii | 30% | 89% |
Q651Z7 | Oryza sativa subsp. japonica | 30% | 68% |
Q6H638 | Oryza sativa subsp. japonica | 31% | 67% |
Q7ZYL5 | Xenopus laevis | 29% | 91% |
Q8VWI7 | Arabidopsis thaliana | 27% | 68% |
Q8W5R6 | Arabidopsis thaliana | 30% | 66% |
Q9I869 | Xenopus laevis | 29% | 91% |
Q9S7P3 | Arabidopsis thaliana | 34% | 72% |
Q9SCJ4 | Arabidopsis thaliana | 33% | 73% |
Q9V877 | Drosophila melanogaster | 29% | 94% |
Q9WV04 | Mus musculus | 30% | 75% |
V5B325 | Trypanosoma cruzi | 28% | 71% |
V5B8M1 | Trypanosoma cruzi | 37% | 96% |
V5B8X9 | Trypanosoma cruzi | 28% | 84% |
V5BAA8 | Trypanosoma cruzi | 32% | 72% |
V5BCN9 | Trypanosoma cruzi | 27% | 83% |
V5BIC1 | Trypanosoma cruzi | 32% | 93% |
V5BK25 | Trypanosoma cruzi | 29% | 82% |
V5D733 | Trypanosoma cruzi | 32% | 79% |
V5DFA7 | Trypanosoma cruzi | 32% | 100% |
V5DTU1 | Trypanosoma cruzi | 62% | 100% |