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. | no | yes: 30 |
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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005871 | kinesin complex | 3 | 1 |
GO:0005874 | microtubule | 6 | 1 |
GO:0005875 | microtubule associated complex | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0051286 | cell tip | 3 | 1 |
GO:0060187 | cell pole | 2 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
GO:0099081 | supramolecular polymer | 3 | 1 |
GO:0099512 | supramolecular fiber | 4 | 1 |
GO:0099513 | polymeric cytoskeletal fiber | 5 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7X2P9
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 14 |
GO:0007018 | microtubule-based movement | 3 | 14 |
GO:0009987 | cellular process | 1 | 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 14 |
GO:0003774 | cytoskeletal motor activity | 1 | 14 |
GO:0003777 | microtubule motor activity | 2 | 14 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0005488 | binding | 1 | 14 |
GO:0005515 | protein binding | 2 | 14 |
GO:0005524 | ATP binding | 5 | 14 |
GO:0008017 | microtubule binding | 5 | 14 |
GO:0008092 | cytoskeletal protein binding | 3 | 14 |
GO:0015631 | tubulin binding | 4 | 14 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 14 |
GO:0030554 | adenyl nucleotide binding | 5 | 14 |
GO:0032553 | ribonucleotide binding | 3 | 14 |
GO:0032555 | purine ribonucleotide binding | 4 | 14 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 14 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 14 |
GO:0036094 | small molecule binding | 2 | 14 |
GO:0043167 | ion binding | 2 | 14 |
GO:0043168 | anion binding | 3 | 14 |
GO:0097159 | organic cyclic compound binding | 2 | 14 |
GO:0097367 | carbohydrate derivative binding | 2 | 14 |
GO:0140657 | ATP-dependent activity | 1 | 14 |
GO:1901265 | nucleoside phosphate binding | 3 | 14 |
GO:1901363 | heterocyclic compound binding | 2 | 14 |
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 | 398 | 402 | PF00656 | 0.436 |
CLV_C14_Caspase3-7 | 413 | 417 | PF00656 | 0.353 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.279 |
CLV_NRD_NRD_1 | 554 | 556 | PF00675 | 0.374 |
CLV_PCSK_FUR_1 | 45 | 49 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.339 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 554 | 556 | PF00082 | 0.374 |
CLV_PCSK_PC1ET2_1 | 47 | 49 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 523 | 527 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 554 | 558 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.267 |
DEG_SCF_FBW7_1 | 524 | 530 | PF00400 | 0.435 |
DOC_CKS1_1 | 524 | 529 | PF01111 | 0.436 |
DOC_CYCLIN_RxL_1 | 112 | 120 | PF00134 | 0.440 |
DOC_CYCLIN_RxL_1 | 391 | 401 | PF00134 | 0.420 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 475 | 484 | PF00134 | 0.516 |
DOC_MAPK_gen_1 | 19 | 30 | PF00069 | 0.515 |
DOC_MAPK_gen_1 | 6 | 15 | PF00069 | 0.538 |
DOC_MAPK_MEF2A_6 | 213 | 222 | PF00069 | 0.305 |
DOC_MAPK_MEF2A_6 | 6 | 15 | PF00069 | 0.406 |
DOC_PP2B_LxvP_1 | 150 | 153 | PF13499 | 0.305 |
DOC_PP2B_LxvP_1 | 462 | 465 | PF13499 | 0.442 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.291 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 453 | 457 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 527 | 531 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 573 | 577 | PF00917 | 0.531 |
DOC_USP7_UBL2_3 | 537 | 541 | PF12436 | 0.420 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.321 |
DOC_WW_Pin1_4 | 523 | 528 | PF00397 | 0.423 |
LIG_14-3-3_CanoR_1 | 176 | 181 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 200 | 207 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 23 | 30 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 274 | 280 | PF00244 | 0.305 |
LIG_14-3-3_CanoR_1 | 554 | 564 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 8 | 14 | PF00244 | 0.435 |
LIG_14-3-3_CterR_2 | 585 | 588 | PF00244 | 0.529 |
LIG_Actin_WH2_2 | 60 | 75 | PF00022 | 0.266 |
LIG_APCC_ABBA_1 | 140 | 145 | PF00400 | 0.305 |
LIG_APCC_ABBA_1 | 163 | 168 | PF00400 | 0.305 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.611 |
LIG_BRCT_BRCA1_1 | 222 | 226 | PF00533 | 0.440 |
LIG_BRCT_BRCA1_1 | 284 | 288 | PF00533 | 0.420 |
LIG_BRCT_BRCA1_1 | 300 | 304 | PF00533 | 0.305 |
LIG_BRCT_BRCA1_1 | 512 | 516 | PF00533 | 0.463 |
LIG_EH1_1 | 456 | 464 | PF00400 | 0.490 |
LIG_eIF4E_1 | 457 | 463 | PF01652 | 0.494 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.436 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.559 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.305 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.305 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.305 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.259 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.389 |
LIG_FHA_1 | 505 | 511 | PF00498 | 0.490 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.440 |
LIG_FHA_1 | 548 | 554 | PF00498 | 0.404 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.305 |
LIG_FHA_2 | 248 | 254 | PF00498 | 0.391 |
LIG_FHA_2 | 396 | 402 | PF00498 | 0.420 |
LIG_FHA_2 | 411 | 417 | PF00498 | 0.603 |
LIG_LIR_Gen_1 | 223 | 234 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 285 | 296 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 351 | 360 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 560 | 569 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 62 | 72 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 94 | 101 | PF02991 | 0.391 |
LIG_LIR_LC3C_4 | 461 | 464 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 223 | 229 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 285 | 291 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 351 | 357 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 560 | 566 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 62 | 67 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 74 | 79 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 94 | 98 | PF02991 | 0.210 |
LIG_NRBOX | 295 | 301 | PF00104 | 0.339 |
LIG_NRBOX | 479 | 485 | PF00104 | 0.337 |
LIG_Pex14_2 | 52 | 56 | PF04695 | 0.294 |
LIG_PTB_Apo_2 | 532 | 539 | PF02174 | 0.481 |
LIG_Rb_pABgroove_1 | 112 | 120 | PF01858 | 0.440 |
LIG_Rb_pABgroove_1 | 461 | 469 | PF01858 | 0.433 |
LIG_SH2_CRK | 467 | 471 | PF00017 | 0.523 |
LIG_SH2_CRK | 95 | 99 | PF00017 | 0.440 |
LIG_SH2_NCK_1 | 467 | 471 | PF00017 | 0.570 |
LIG_SH2_SRC | 363 | 366 | PF00017 | 0.345 |
LIG_SH2_STAP1 | 332 | 336 | PF00017 | 0.303 |
LIG_SH2_STAP1 | 354 | 358 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 378 | 382 | PF00017 | 0.407 |
LIG_SH2_STAT3 | 378 | 381 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 363 | 366 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 544 | 547 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 563 | 566 | PF00017 | 0.441 |
LIG_SH3_3 | 467 | 473 | PF00018 | 0.593 |
LIG_SH3_3 | 521 | 527 | PF00018 | 0.455 |
LIG_SUMO_SIM_anti_2 | 489 | 495 | PF11976 | 0.457 |
LIG_SUMO_SIM_par_1 | 235 | 242 | PF11976 | 0.339 |
LIG_SUMO_SIM_par_1 | 395 | 402 | PF11976 | 0.543 |
LIG_SUMO_SIM_par_1 | 489 | 495 | PF11976 | 0.462 |
LIG_TYR_ITIM | 352 | 357 | PF00017 | 0.526 |
LIG_TYR_ITIM | 561 | 566 | PF00017 | 0.438 |
LIG_UBA3_1 | 189 | 195 | PF00899 | 0.339 |
LIG_WRC_WIRS_1 | 276 | 281 | PF05994 | 0.291 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.289 |
MOD_CK1_1 | 294 | 300 | PF00069 | 0.302 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.416 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.488 |
MOD_CK1_1 | 448 | 454 | PF00069 | 0.410 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.339 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.305 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.290 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.472 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.519 |
MOD_DYRK1A_RPxSP_1 | 523 | 527 | PF00069 | 0.428 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.440 |
MOD_GlcNHglycan | 253 | 257 | PF01048 | 0.423 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.542 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.392 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.496 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.339 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.369 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.304 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.288 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.305 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.313 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.291 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.514 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.532 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.408 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.454 |
MOD_N-GLC_1 | 207 | 212 | PF02516 | 0.291 |
MOD_N-GLC_1 | 265 | 270 | PF02516 | 0.305 |
MOD_N-GLC_1 | 321 | 326 | PF02516 | 0.305 |
MOD_N-GLC_1 | 345 | 350 | PF02516 | 0.465 |
MOD_N-GLC_1 | 399 | 404 | PF02516 | 0.583 |
MOD_N-GLC_2 | 80 | 82 | PF02516 | 0.305 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.305 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.305 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.305 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.305 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.295 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.300 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.446 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.571 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.515 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.425 |
MOD_NEK2_2 | 129 | 134 | PF00069 | 0.440 |
MOD_NEK2_2 | 287 | 292 | PF00069 | 0.278 |
MOD_OFUCOSY | 440 | 445 | PF10250 | 0.424 |
MOD_PIKK_1 | 220 | 226 | PF00454 | 0.305 |
MOD_PIKK_1 | 377 | 383 | PF00454 | 0.552 |
MOD_PIKK_1 | 399 | 405 | PF00454 | 0.602 |
MOD_PK_1 | 176 | 182 | PF00069 | 0.440 |
MOD_PKA_1 | 282 | 288 | PF00069 | 0.420 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.339 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.475 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.290 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.305 |
MOD_PKA_2 | 510 | 516 | PF00069 | 0.469 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.440 |
MOD_Plk_1 | 265 | 271 | PF00069 | 0.305 |
MOD_Plk_1 | 399 | 405 | PF00069 | 0.496 |
MOD_Plk_1 | 573 | 579 | PF00069 | 0.653 |
MOD_Plk_2-3 | 159 | 165 | PF00069 | 0.336 |
MOD_Plk_2-3 | 395 | 401 | PF00069 | 0.417 |
MOD_Plk_2-3 | 410 | 416 | PF00069 | 0.606 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.305 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.353 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.305 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.305 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.372 |
MOD_Plk_4 | 510 | 516 | PF00069 | 0.408 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.304 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.321 |
MOD_ProDKin_1 | 523 | 529 | PF00069 | 0.421 |
MOD_SUMO_rev_2 | 2 | 7 | PF00179 | 0.461 |
MOD_SUMO_rev_2 | 255 | 265 | PF00179 | 0.298 |
MOD_SUMO_rev_2 | 278 | 285 | PF00179 | 0.441 |
MOD_SUMO_rev_2 | 290 | 297 | PF00179 | 0.436 |
TRG_DiLeu_BaEn_1 | 353 | 358 | PF01217 | 0.562 |
TRG_DiLeu_BaEn_1 | 414 | 419 | PF01217 | 0.490 |
TRG_DiLeu_BaEn_1 | 458 | 463 | PF01217 | 0.489 |
TRG_DiLeu_BaLyEn_6 | 295 | 300 | PF01217 | 0.339 |
TRG_DiLeu_BaLyEn_6 | 471 | 476 | PF01217 | 0.408 |
TRG_ENDOCYTIC_2 | 354 | 357 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 563 | 566 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.173 |
TRG_ER_diArg_1 | 13 | 16 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 153 | 156 | PF00400 | 0.305 |
TRG_ER_diArg_1 | 171 | 173 | PF00400 | 0.339 |
TRG_ER_diArg_1 | 358 | 361 | PF00400 | 0.538 |
TRG_ER_diArg_1 | 553 | 555 | PF00400 | 0.366 |
TRG_NES_CRM1_1 | 233 | 247 | PF08389 | 0.353 |
TRG_Pf-PMV_PEXEL_1 | 115 | 119 | PF00026 | 0.440 |
TRG_Pf-PMV_PEXEL_1 | 298 | 302 | PF00026 | 0.305 |
TRG_Pf-PMV_PEXEL_1 | 372 | 376 | PF00026 | 0.498 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P569 | Leptomonas seymouri | 27% | 67% |
A0A0N1I0Y5 | Leptomonas seymouri | 29% | 96% |
A0A0N1PDD6 | Leptomonas seymouri | 31% | 77% |
A0A0S4IP49 | Bodo saltans | 27% | 73% |
A0A0S4J0Q2 | Bodo saltans | 35% | 71% |
A0A0S4JEF6 | Bodo saltans | 28% | 88% |
A0A0S4JJ54 | Bodo saltans | 32% | 84% |
A0A0S4JLW3 | Bodo saltans | 32% | 100% |
A0A0S4JXY6 | Bodo saltans | 31% | 68% |
A0A0S4KL43 | Bodo saltans | 29% | 100% |
A0A1X0NQ03 | Trypanosomatidae | 28% | 71% |
A0A1X0P0C2 | Trypanosomatidae | 32% | 72% |
A0A1X0P2B6 | Trypanosomatidae | 30% | 96% |
A0A1X0P728 | Trypanosomatidae | 27% | 66% |
A0A1X0P9E3 | Trypanosomatidae | 60% | 99% |
A0A1X0P9H3 | Trypanosomatidae | 33% | 68% |
A0A1X0P9T0 | Trypanosomatidae | 32% | 100% |
A0A1X0PAG9 | Trypanosomatidae | 50% | 99% |
A0A3Q8IHG6 | Leishmania donovani | 98% | 100% |
A0A3R7LY66 | Trypanosoma rangeli | 32% | 72% |
A0A3R7MDH9 | Trypanosoma rangeli | 28% | 83% |
A0A3R7R330 | Trypanosoma rangeli | 62% | 100% |
A0A3R7RD86 | Trypanosoma rangeli | 34% | 73% |
A0A422NE49 | Trypanosoma rangeli | 31% | 66% |
A0A422NEQ8 | Trypanosoma rangeli | 32% | 78% |
A4H4R6 | Leishmania braziliensis | 29% | 67% |
A4HAQ7 | Leishmania braziliensis | 27% | 100% |
A4HHN7 | Leishmania braziliensis | 88% | 100% |
A4HHY2 | Leishmania braziliensis | 28% | 100% |
A4HSA6 | Leishmania infantum | 33% | 100% |
A4I4V2 | Leishmania infantum | 98% | 100% |
B9G2X9 | Oryza sativa subsp. japonica | 33% | 97% |
C9ZK93 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 79% |
C9ZL08 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 99% |
C9ZL09 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
C9ZQI8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 94% |
C9ZU98 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 73% |
C9ZV26 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 78% |
E9AEA0 | Leishmania major | 95% | 100% |
E9ALI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9ALI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
E9B0F9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
P46870 | Chlamydomonas reinhardtii | 30% | 76% |
Q10E64 | Oryza sativa subsp. japonica | 34% | 80% |
Q1MTQ7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 93% |
Q29DY1 | Drosophila pseudoobscura pseudoobscura | 35% | 74% |
Q2R2P7 | Oryza sativa subsp. japonica | 33% | 92% |
Q4QJ61 | Leishmania major | 26% | 100% |
Q5E913 | Arabidopsis thaliana | 27% | 94% |
Q5XI51 | Rattus norvegicus | 30% | 89% |
Q651Z7 | Oryza sativa subsp. japonica | 30% | 68% |
Q6H638 | Oryza sativa subsp. japonica | 31% | 67% |
Q7ZYL5 | Xenopus laevis | 28% | 90% |
Q8VWI7 | Arabidopsis thaliana | 28% | 68% |
Q8W5R6 | Arabidopsis thaliana | 30% | 66% |
Q965T6 | Caenorhabditis elegans | 35% | 91% |
Q9I869 | Xenopus laevis | 29% | 90% |
Q9SCJ4 | Arabidopsis thaliana | 33% | 72% |
Q9V877 | Drosophila melanogaster | 28% | 94% |
V5B8X9 | Trypanosoma cruzi | 28% | 84% |
V5BIC1 | Trypanosoma cruzi | 32% | 92% |
V5BK25 | Trypanosoma cruzi | 29% | 82% |
V5BMP0 | Trypanosoma cruzi | 32% | 76% |
V5D4P5 | Trypanosoma cruzi | 30% | 95% |
V5D733 | Trypanosoma cruzi | 32% | 78% |
V5DFA7 | Trypanosoma cruzi | 32% | 100% |
V5DTU1 | Trypanosoma cruzi | 49% | 100% |