An expanded and variable family of glycosidases. Some Leishmaniid members even incorporate an extra N-terminal fructofuronidase domain after the signal peptide.. Seems to be evolving rapidly for unclear reasons
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: 4 |
Pissara et al. | no | yes: 28 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 11, no: 6 |
NetGPI | no | yes: 0, no: 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S5H595
Term | Name | Level | Count |
---|---|---|---|
GO:0005975 | carbohydrate metabolic process | 3 | 18 |
GO:0008152 | metabolic process | 1 | 18 |
GO:0044238 | primary metabolic process | 2 | 18 |
GO:0071704 | organic substance metabolic process | 2 | 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 18 |
GO:0004553 | hydrolase activity, hydrolyzing O-glycosyl compounds | 4 | 18 |
GO:0004564 | beta-fructofuranosidase activity | 5 | 10 |
GO:0016787 | hydrolase activity | 2 | 18 |
GO:0016798 | hydrolase activity, acting on glycosyl bonds | 3 | 18 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 476 | 480 | PF00656 | 0.229 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.587 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.338 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.608 |
CLV_PCSK_PC1ET2_1 | 152 | 154 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 627 | 631 | PF00082 | 0.624 |
DEG_APCC_DBOX_1 | 523 | 531 | PF00400 | 0.440 |
DEG_COP1_1 | 419 | 430 | PF00400 | 0.357 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.574 |
DOC_CYCLIN_yClb3_PxF_3 | 33 | 41 | PF00134 | 0.246 |
DOC_MAPK_gen_1 | 368 | 378 | PF00069 | 0.474 |
DOC_MAPK_gen_1 | 7 | 15 | PF00069 | 0.602 |
DOC_MAPK_gen_1 | 90 | 100 | PF00069 | 0.406 |
DOC_MAPK_HePTP_8 | 597 | 609 | PF00069 | 0.393 |
DOC_MAPK_MEF2A_6 | 160 | 167 | PF00069 | 0.273 |
DOC_MAPK_MEF2A_6 | 600 | 609 | PF00069 | 0.393 |
DOC_MAPK_MEF2A_6 | 7 | 15 | PF00069 | 0.622 |
DOC_MAPK_NFAT4_5 | 8 | 16 | PF00069 | 0.600 |
DOC_PP1_RVXF_1 | 502 | 508 | PF00149 | 0.415 |
DOC_PP4_FxxP_1 | 181 | 184 | PF00568 | 0.291 |
DOC_PP4_FxxP_1 | 246 | 249 | PF00568 | 0.442 |
DOC_PP4_FxxP_1 | 312 | 315 | PF00568 | 0.444 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 474 | 478 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 511 | 515 | PF00917 | 0.305 |
DOC_USP7_UBL2_3 | 104 | 108 | PF12436 | 0.363 |
DOC_USP7_UBL2_3 | 504 | 508 | PF12436 | 0.430 |
DOC_WW_Pin1_4 | 383 | 388 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 551 | 556 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 619 | 624 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 93 | 98 | PF00397 | 0.430 |
LIG_14-3-3_CanoR_1 | 296 | 301 | PF00244 | 0.350 |
LIG_14-3-3_CanoR_1 | 406 | 410 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 459 | 467 | PF00244 | 0.310 |
LIG_Actin_WH2_2 | 247 | 265 | PF00022 | 0.310 |
LIG_Actin_WH2_2 | 443 | 461 | PF00022 | 0.229 |
LIG_APCC_ABBA_1 | 560 | 565 | PF00400 | 0.319 |
LIG_APCC_ABBA_1 | 569 | 574 | PF00400 | 0.319 |
LIG_APCC_ABBAyCdc20_2 | 286 | 292 | PF00400 | 0.229 |
LIG_BRCT_BRCA1_1 | 296 | 300 | PF00533 | 0.389 |
LIG_BRCT_BRCA1_1 | 308 | 312 | PF00533 | 0.389 |
LIG_BRCT_BRCA1_1 | 492 | 496 | PF00533 | 0.437 |
LIG_deltaCOP1_diTrp_1 | 103 | 109 | PF00928 | 0.430 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.373 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.489 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.267 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.441 |
LIG_FHA_1 | 500 | 506 | PF00498 | 0.380 |
LIG_FHA_1 | 539 | 545 | PF00498 | 0.427 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.398 |
LIG_FHA_1 | 579 | 585 | PF00498 | 0.332 |
LIG_FHA_1 | 590 | 596 | PF00498 | 0.332 |
LIG_FHA_1 | 604 | 610 | PF00498 | 0.404 |
LIG_FHA_1 | 628 | 634 | PF00498 | 0.606 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.395 |
LIG_FHA_2 | 297 | 303 | PF00498 | 0.323 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.310 |
LIG_FHA_2 | 324 | 330 | PF00498 | 0.444 |
LIG_FHA_2 | 384 | 390 | PF00498 | 0.483 |
LIG_FHA_2 | 406 | 412 | PF00498 | 0.410 |
LIG_FHA_2 | 520 | 526 | PF00498 | 0.423 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.279 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.279 |
LIG_LIR_Apic_2 | 179 | 184 | PF02991 | 0.308 |
LIG_LIR_Apic_2 | 185 | 191 | PF02991 | 0.253 |
LIG_LIR_Apic_2 | 243 | 249 | PF02991 | 0.438 |
LIG_LIR_Apic_2 | 309 | 315 | PF02991 | 0.443 |
LIG_LIR_Apic_2 | 615 | 621 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 259 | 268 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 285 | 295 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 297 | 306 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 398 | 407 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 441 | 451 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 631 | 642 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 107 | 112 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 250 | 254 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 259 | 264 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 272 | 276 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 285 | 291 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 297 | 303 | PF02991 | 0.247 |
LIG_LIR_Nem_3 | 311 | 316 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 398 | 403 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 441 | 446 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 464 | 470 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 631 | 637 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 77 | 83 | PF02991 | 0.305 |
LIG_LYPXL_yS_3 | 467 | 470 | PF13949 | 0.437 |
LIG_NRBOX | 632 | 638 | PF00104 | 0.587 |
LIG_PCNA_yPIPBox_3 | 344 | 358 | PF02747 | 0.437 |
LIG_PDZ_Class_2 | 638 | 643 | PF00595 | 0.554 |
LIG_Pex14_1 | 197 | 201 | PF04695 | 0.302 |
LIG_PTB_Apo_2 | 115 | 122 | PF02174 | 0.360 |
LIG_PTB_Phospho_1 | 115 | 121 | PF10480 | 0.360 |
LIG_REV1ctd_RIR_1 | 249 | 259 | PF16727 | 0.328 |
LIG_SH2_CRK | 313 | 317 | PF00017 | 0.319 |
LIG_SH2_CRK | 443 | 447 | PF00017 | 0.442 |
LIG_SH2_NCK_1 | 34 | 38 | PF00017 | 0.482 |
LIG_SH2_NCK_1 | 443 | 447 | PF00017 | 0.442 |
LIG_SH2_PTP2 | 288 | 291 | PF00017 | 0.442 |
LIG_SH2_SRC | 313 | 316 | PF00017 | 0.335 |
LIG_SH2_SRC | 34 | 37 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 598 | 602 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.251 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 443 | 446 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 494 | 497 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 529 | 532 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 585 | 588 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 612 | 615 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.291 |
LIG_SH3_2 | 191 | 196 | PF14604 | 0.426 |
LIG_SH3_2 | 50 | 55 | PF14604 | 0.304 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.432 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.441 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.441 |
LIG_SH3_3 | 445 | 451 | PF00018 | 0.312 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.237 |
LIG_SH3_3 | 520 | 526 | PF00018 | 0.326 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.131 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.430 |
LIG_SUMO_SIM_par_1 | 122 | 129 | PF11976 | 0.414 |
LIG_SUMO_SIM_par_1 | 373 | 380 | PF11976 | 0.345 |
LIG_SUMO_SIM_par_1 | 605 | 610 | PF11976 | 0.460 |
LIG_TYR_ITIM | 32 | 37 | PF00017 | 0.514 |
LIG_TYR_ITSM | 309 | 316 | PF00017 | 0.459 |
LIG_TYR_ITSM | 396 | 403 | PF00017 | 0.528 |
LIG_UBA3_1 | 37 | 44 | PF00899 | 0.185 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.424 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.403 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.395 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.444 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.471 |
MOD_CK2_1 | 519 | 525 | PF00069 | 0.470 |
MOD_CK2_1 | 564 | 570 | PF00069 | 0.442 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.428 |
MOD_Cter_Amidation | 150 | 153 | PF01082 | 0.320 |
MOD_DYRK1A_RPxSP_1 | 93 | 97 | PF00069 | 0.428 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.304 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.374 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.408 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.310 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.445 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.456 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.351 |
MOD_GlcNHglycan | 534 | 537 | PF01048 | 0.263 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.384 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.360 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.322 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.515 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.436 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.298 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.472 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.358 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.422 |
MOD_N-GLC_1 | 119 | 124 | PF02516 | 0.420 |
MOD_N-GLC_1 | 281 | 286 | PF02516 | 0.343 |
MOD_N-GLC_1 | 395 | 400 | PF02516 | 0.517 |
MOD_N-GLC_1 | 438 | 443 | PF02516 | 0.431 |
MOD_N-GLC_1 | 479 | 484 | PF02516 | 0.395 |
MOD_N-GLC_1 | 627 | 632 | PF02516 | 0.621 |
MOD_N-GLC_2 | 501 | 503 | PF02516 | 0.360 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.274 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.273 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.321 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.310 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.310 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.398 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.451 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.447 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.325 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.326 |
MOD_NEK2_1 | 629 | 634 | PF00069 | 0.593 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.510 |
MOD_NEK2_2 | 308 | 313 | PF00069 | 0.444 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.450 |
MOD_PIKK_1 | 438 | 444 | PF00454 | 0.435 |
MOD_PIKK_1 | 530 | 536 | PF00454 | 0.400 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.423 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.437 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.433 |
MOD_Plk_1 | 395 | 401 | PF00069 | 0.532 |
MOD_Plk_1 | 438 | 444 | PF00069 | 0.442 |
MOD_Plk_1 | 564 | 570 | PF00069 | 0.319 |
MOD_Plk_2-3 | 610 | 616 | PF00069 | 0.408 |
MOD_Plk_4 | 112 | 118 | PF00069 | 0.392 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.375 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.445 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.554 |
MOD_Plk_4 | 417 | 423 | PF00069 | 0.420 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.381 |
MOD_Plk_4 | 564 | 570 | PF00069 | 0.332 |
MOD_Plk_4 | 613 | 619 | PF00069 | 0.408 |
MOD_Plk_4 | 629 | 635 | PF00069 | 0.627 |
MOD_Plk_4 | 636 | 642 | PF00069 | 0.529 |
MOD_ProDKin_1 | 383 | 389 | PF00069 | 0.548 |
MOD_ProDKin_1 | 551 | 557 | PF00069 | 0.442 |
MOD_ProDKin_1 | 619 | 625 | PF00069 | 0.629 |
MOD_ProDKin_1 | 93 | 99 | PF00069 | 0.430 |
MOD_SUMO_for_1 | 572 | 575 | PF00179 | 0.426 |
MOD_SUMO_rev_2 | 353 | 359 | PF00179 | 0.419 |
TRG_DiLeu_BaEn_2 | 558 | 564 | PF01217 | 0.426 |
TRG_DiLeu_BaLyEn_6 | 523 | 528 | PF01217 | 0.441 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 288 | 291 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.254 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.262 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 443 | 446 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 634 | 637 | PF00928 | 0.603 |
TRG_ER_diArg_1 | 6 | 8 | PF00400 | 0.609 |
TRG_NES_CRM1_1 | 575 | 587 | PF08389 | 0.426 |
TRG_Pf-PMV_PEXEL_1 | 368 | 373 | PF00026 | 0.373 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBT6 | Leptomonas seymouri | 77% | 100% |
A0A0S4J9J2 | Bodo saltans | 31% | 100% |
A0A1X0NFY9 | Trypanosomatidae | 41% | 100% |
A0A1X0NTL0 | Trypanosomatidae | 40% | 100% |
A0A1X0NTM3 | Trypanosomatidae | 41% | 100% |
A0A1X0NY19 | Trypanosomatidae | 42% | 100% |
A0A1X0NYR4 | Trypanosomatidae | 37% | 100% |
A0A1X0P322 | Trypanosomatidae | 37% | 100% |
A0A1X0P5Y7 | Trypanosomatidae | 41% | 100% |
A0A3Q8IB13 | Leishmania donovani | 26% | 100% |
A0A3Q8IFU7 | Leishmania donovani | 27% | 100% |
A0A3S5H596 | Leishmania donovani | 100% | 100% |
A0A3S7WXQ4 | Leishmania donovani | 27% | 100% |
A0A3S7WXS2 | Leishmania donovani | 27% | 100% |
A2YZ01 | Oryza sativa subsp. indica | 28% | 100% |
A4H3V1 | Leishmania braziliensis | 84% | 100% |
A4HCV9 | Leishmania braziliensis | 24% | 100% |
A4HCW0 | Leishmania braziliensis | 27% | 100% |
A4HG14 | Leishmania braziliensis | 24% | 100% |
A4HS26 | Leishmania infantum | 100% | 100% |
A4HS27 | Leishmania infantum | 99% | 100% |
A4I0D9 | Leishmania infantum | 27% | 100% |
A4I0E0 | Leishmania infantum | 26% | 100% |
A4IAW1 | Leishmania infantum | 65% | 100% |
B6DXP5 | Leymus chinensis | 29% | 100% |
B6DZC8 | Triticum aestivum | 30% | 100% |
B6DZD0 | Triticum urartu | 30% | 100% |
B6DZD1 | Aegilops speltoides | 31% | 100% |
B6DZD2 | Aegilops tauschii | 30% | 100% |
D2IGW7 | Bromus pictus | 29% | 100% |
E8NHF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E8NHF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9ACV4 | Leishmania major | 23% | 100% |
E9AK13 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
E9AZE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
H2DF88 | Rosa hybrid cultivar | 30% | 100% |
O07003 | Bacillus subtilis (strain 168) | 22% | 100% |
O24509 | Phaseolus vulgaris | 30% | 99% |
O33833 | Thermotoga maritima (strain ATCC 43589 / DSM 3109 / JCM 10099 / NBRC 100826 / MSB8) | 25% | 100% |
P05656 | Bacillus subtilis (strain 168) | 23% | 95% |
P10596 | Saccharomyces cerevisiae | 24% | 100% |
P26792 | Daucus carota | 30% | 100% |
P29000 | Solanum lycopersicum | 29% | 100% |
P29001 | Vigna radiata var. radiata | 31% | 99% |
P80065 | Daucus carota | 28% | 97% |
P92916 | Allium cepa | 26% | 100% |
P93761 | Capsicum annuum | 28% | 100% |
Q01IS7 | Oryza sativa subsp. indica | 29% | 100% |
Q01IS8 | Oryza sativa subsp. indica | 29% | 100% |
Q0J360 | Oryza sativa subsp. japonica | 28% | 100% |
Q0JDC5 | Oryza sativa subsp. japonica | 29% | 100% |
Q0JDC6 | Oryza sativa subsp. japonica | 29% | 100% |
Q1PEF8 | Arabidopsis thaliana | 29% | 100% |
Q2UXF7 | Triticum aestivum | 30% | 100% |
Q39693 | Daucus carota | 30% | 100% |
Q43089 | Pisum sativum | 29% | 100% |
Q43857 | Vicia faba | 31% | 100% |
Q43866 | Arabidopsis thaliana | 32% | 100% |
Q4QB75 | Leishmania major | 27% | 100% |
Q4QB76 | Leishmania major | 25% | 100% |
Q56UD0 | Oryza sativa subsp. japonica | 29% | 100% |
Q56UD1 | Oryza sativa subsp. japonica | 25% | 100% |
Q5FC15 | Asparagus officinalis | 30% | 100% |
Q5JJV0 | Oryza sativa subsp. japonica | 30% | 100% |
Q67XZ3 | Arabidopsis thaliana | 30% | 100% |
Q70AT7 | Hordeum vulgare | 29% | 100% |
Q70XE6 | Beta vulgaris | 28% | 100% |
Q84LA1 | Triticum aestivum | 29% | 100% |
Q84PN8 | Triticum aestivum | 29% | 100% |
Q8W4S6 | Arabidopsis thaliana | 28% | 100% |
Q9FSV7 | Festuca arundinacea | 29% | 98% |
Q9LIB9 | Arabidopsis thaliana | 28% | 100% |
Q9XTP3 | Leishmania major | 94% | 100% |
Q9XZX0 | Leishmania major | 93% | 100% |