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. | yes | 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: 7 |
NetGPI | no | yes: 0, no: 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AK13
Term | Name | Level | Count |
---|---|---|---|
GO:0005975 | carbohydrate metabolic process | 3 | 19 |
GO:0008152 | metabolic process | 1 | 19 |
GO:0044238 | primary metabolic process | 2 | 19 |
GO:0071704 | organic substance metabolic process | 2 | 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 19 |
GO:0004553 | hydrolase activity, hydrolyzing O-glycosyl compounds | 4 | 19 |
GO:0004564 | beta-fructofuranosidase activity | 5 | 10 |
GO:0016787 | hydrolase activity | 2 | 19 |
GO:0016798 | hydrolase activity, acting on glycosyl bonds | 3 | 19 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.489 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.416 |
CLV_PCSK_PC1ET2_1 | 145 | 147 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 289 | 293 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 620 | 624 | PF00082 | 0.669 |
DEG_APCC_DBOX_1 | 516 | 524 | PF00400 | 0.473 |
DEG_COP1_1 | 413 | 423 | PF00400 | 0.374 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.414 |
DOC_MAPK_gen_1 | 2 | 10 | PF00069 | 0.611 |
DOC_MAPK_gen_1 | 361 | 371 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 83 | 93 | PF00069 | 0.432 |
DOC_MAPK_HePTP_8 | 590 | 602 | PF00069 | 0.371 |
DOC_MAPK_MEF2A_6 | 153 | 160 | PF00069 | 0.282 |
DOC_MAPK_MEF2A_6 | 2 | 10 | PF00069 | 0.634 |
DOC_MAPK_MEF2A_6 | 593 | 602 | PF00069 | 0.371 |
DOC_MAPK_NFAT4_5 | 3 | 11 | PF00069 | 0.606 |
DOC_PP1_RVXF_1 | 495 | 501 | PF00149 | 0.461 |
DOC_PP4_FxxP_1 | 174 | 177 | PF00568 | 0.311 |
DOC_PP4_FxxP_1 | 239 | 242 | PF00568 | 0.456 |
DOC_PP4_FxxP_1 | 305 | 308 | PF00568 | 0.478 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.469 |
DOC_USP7_UBL2_3 | 497 | 501 | PF12436 | 0.497 |
DOC_USP7_UBL2_3 | 97 | 101 | PF12436 | 0.384 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 544 | 549 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 612 | 617 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.468 |
LIG_14-3-3_CanoR_1 | 289 | 294 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 312 | 316 | PF00244 | 0.249 |
LIG_14-3-3_CanoR_1 | 399 | 403 | PF00244 | 0.404 |
LIG_Actin_WH2_2 | 240 | 258 | PF00022 | 0.330 |
LIG_APCC_ABBA_1 | 553 | 558 | PF00400 | 0.327 |
LIG_APCC_ABBA_1 | 562 | 567 | PF00400 | 0.327 |
LIG_BRCT_BRCA1_1 | 289 | 293 | PF00533 | 0.409 |
LIG_BRCT_BRCA1_1 | 485 | 489 | PF00533 | 0.504 |
LIG_deltaCOP1_diTrp_1 | 96 | 102 | PF00928 | 0.461 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.394 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.515 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.456 |
LIG_FHA_1 | 493 | 499 | PF00498 | 0.403 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.423 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.396 |
LIG_FHA_1 | 572 | 578 | PF00498 | 0.352 |
LIG_FHA_1 | 583 | 589 | PF00498 | 0.352 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.381 |
LIG_FHA_1 | 621 | 627 | PF00498 | 0.648 |
LIG_FHA_2 | 120 | 126 | PF00498 | 0.420 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.445 |
LIG_FHA_2 | 290 | 296 | PF00498 | 0.347 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.374 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.458 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.510 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.437 |
LIG_FHA_2 | 486 | 492 | PF00498 | 0.333 |
LIG_FHA_2 | 513 | 519 | PF00498 | 0.464 |
LIG_FHA_2 | 626 | 632 | PF00498 | 0.585 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.311 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.311 |
LIG_LIR_Apic_2 | 172 | 177 | PF02991 | 0.327 |
LIG_LIR_Apic_2 | 178 | 184 | PF02991 | 0.275 |
LIG_LIR_Apic_2 | 236 | 242 | PF02991 | 0.432 |
LIG_LIR_Apic_2 | 304 | 308 | PF02991 | 0.478 |
LIG_LIR_Apic_2 | 608 | 614 | PF02991 | 0.572 |
LIG_LIR_Gen_1 | 252 | 261 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 278 | 287 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 288 | 299 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 391 | 400 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 434 | 444 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 625 | 634 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 100 | 105 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 243 | 247 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 252 | 257 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 265 | 269 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 278 | 284 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 288 | 294 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 295 | 299 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 304 | 309 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 391 | 396 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 434 | 439 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 458 | 463 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 625 | 630 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 70 | 76 | PF02991 | 0.326 |
LIG_LYPXL_yS_3 | 460 | 463 | PF13949 | 0.404 |
LIG_NRBOX | 625 | 631 | PF00104 | 0.625 |
LIG_PCNA_yPIPBox_3 | 337 | 351 | PF02747 | 0.404 |
LIG_PDZ_Class_2 | 631 | 636 | PF00595 | 0.583 |
LIG_Pex14_1 | 190 | 194 | PF04695 | 0.322 |
LIG_PTB_Apo_2 | 108 | 115 | PF02174 | 0.347 |
LIG_PTB_Apo_2 | 621 | 628 | PF02174 | 0.610 |
LIG_PTB_Phospho_1 | 108 | 114 | PF10480 | 0.347 |
LIG_PTB_Phospho_1 | 621 | 627 | PF10480 | 0.612 |
LIG_REV1ctd_RIR_1 | 242 | 252 | PF16727 | 0.347 |
LIG_SH2_CRK | 306 | 310 | PF00017 | 0.347 |
LIG_SH2_CRK | 436 | 440 | PF00017 | 0.439 |
LIG_SH2_GRB2like | 436 | 439 | PF00017 | 0.200 |
LIG_SH2_NCK_1 | 27 | 31 | PF00017 | 0.510 |
LIG_SH2_NCK_1 | 436 | 440 | PF00017 | 0.439 |
LIG_SH2_PTP2 | 281 | 284 | PF00017 | 0.476 |
LIG_SH2_SRC | 27 | 30 | PF00017 | 0.514 |
LIG_SH2_SRC | 306 | 309 | PF00017 | 0.355 |
LIG_SH2_STAP1 | 591 | 595 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 487 | 490 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 522 | 525 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 578 | 581 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 605 | 608 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 627 | 630 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.311 |
LIG_SH3_1 | 501 | 507 | PF00018 | 0.200 |
LIG_SH3_2 | 184 | 189 | PF14604 | 0.456 |
LIG_SH3_2 | 43 | 48 | PF14604 | 0.324 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.463 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.448 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.475 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.261 |
LIG_SH3_3 | 438 | 444 | PF00018 | 0.333 |
LIG_SH3_3 | 501 | 507 | PF00018 | 0.366 |
LIG_SH3_3 | 513 | 519 | PF00018 | 0.338 |
LIG_SH3_3 | 60 | 66 | PF00018 | 0.176 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.468 |
LIG_SUMO_SIM_par_1 | 115 | 122 | PF11976 | 0.441 |
LIG_SUMO_SIM_par_1 | 598 | 603 | PF11976 | 0.498 |
LIG_TYR_ITIM | 25 | 30 | PF00017 | 0.538 |
LIG_TYR_ITSM | 302 | 309 | PF00017 | 0.420 |
LIG_TYR_ITSM | 389 | 396 | PF00017 | 0.569 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.482 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.397 |
MOD_CK1_1 | 625 | 631 | PF00069 | 0.507 |
MOD_CK2_1 | 119 | 125 | PF00069 | 0.420 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.370 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.478 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.460 |
MOD_CK2_1 | 485 | 491 | PF00069 | 0.383 |
MOD_CK2_1 | 512 | 518 | PF00069 | 0.514 |
MOD_CK2_1 | 557 | 563 | PF00069 | 0.439 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.458 |
MOD_Cter_Amidation | 143 | 146 | PF01082 | 0.339 |
MOD_DYRK1A_RPxSP_1 | 86 | 90 | PF00069 | 0.458 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.324 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.396 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.411 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.330 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.326 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.513 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.455 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.438 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.364 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.279 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.293 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.403 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.405 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.330 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.447 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.549 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.457 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.440 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.396 |
MOD_GSK3_1 | 625 | 632 | PF00069 | 0.376 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.455 |
MOD_N-GLC_1 | 112 | 117 | PF02516 | 0.461 |
MOD_N-GLC_1 | 274 | 279 | PF02516 | 0.345 |
MOD_N-GLC_1 | 388 | 393 | PF02516 | 0.540 |
MOD_N-GLC_1 | 437 | 442 | PF02516 | 0.507 |
MOD_N-GLC_1 | 472 | 477 | PF02516 | 0.389 |
MOD_N-GLC_1 | 478 | 483 | PF02516 | 0.356 |
MOD_N-GLC_1 | 620 | 625 | PF02516 | 0.667 |
MOD_N-GLC_2 | 494 | 496 | PF02516 | 0.347 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.325 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.282 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.329 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.330 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.330 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.496 |
MOD_NEK2_1 | 466 | 471 | PF00069 | 0.454 |
MOD_NEK2_1 | 483 | 488 | PF00069 | 0.319 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.425 |
MOD_NEK2_1 | 622 | 627 | PF00069 | 0.633 |
MOD_NEK2_1 | 629 | 634 | PF00069 | 0.537 |
MOD_NEK2_2 | 301 | 306 | PF00069 | 0.478 |
MOD_PIKK_1 | 351 | 357 | PF00454 | 0.520 |
MOD_PIKK_1 | 431 | 437 | PF00454 | 0.468 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.452 |
MOD_PKA_2 | 398 | 404 | PF00069 | 0.404 |
MOD_PKB_1 | 525 | 533 | PF00069 | 0.200 |
MOD_Plk_1 | 388 | 394 | PF00069 | 0.555 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.475 |
MOD_Plk_1 | 478 | 484 | PF00069 | 0.222 |
MOD_Plk_1 | 557 | 563 | PF00069 | 0.327 |
MOD_Plk_2-3 | 243 | 249 | PF00069 | 0.387 |
MOD_Plk_2-3 | 485 | 491 | PF00069 | 0.405 |
MOD_Plk_2-3 | 603 | 609 | PF00069 | 0.425 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.470 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.284 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.399 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.467 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.594 |
MOD_Plk_4 | 485 | 491 | PF00069 | 0.470 |
MOD_Plk_4 | 557 | 563 | PF00069 | 0.338 |
MOD_Plk_4 | 606 | 612 | PF00069 | 0.412 |
MOD_Plk_4 | 622 | 628 | PF00069 | 0.673 |
MOD_Plk_4 | 629 | 635 | PF00069 | 0.558 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.567 |
MOD_ProDKin_1 | 544 | 550 | PF00069 | 0.475 |
MOD_ProDKin_1 | 612 | 618 | PF00069 | 0.663 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.468 |
MOD_SUMO_for_1 | 565 | 568 | PF00179 | 0.395 |
MOD_SUMO_rev_2 | 346 | 352 | PF00179 | 0.448 |
MOD_SUMO_rev_2 | 366 | 374 | PF00179 | 0.346 |
TRG_DiLeu_BaEn_2 | 551 | 557 | PF01217 | 0.395 |
TRG_DiLeu_BaLyEn_6 | 516 | 521 | PF01217 | 0.475 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.458 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 306 | 309 | PF00928 | 0.273 |
TRG_ENDOCYTIC_2 | 393 | 396 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 436 | 439 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 460 | 463 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 627 | 630 | PF00928 | 0.645 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.641 |
TRG_NES_CRM1_1 | 366 | 378 | PF08389 | 0.301 |
TRG_NES_CRM1_1 | 568 | 580 | PF08389 | 0.395 |
TRG_Pf-PMV_PEXEL_1 | 361 | 366 | PF00026 | 0.385 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBT6 | Leptomonas seymouri | 76% | 99% |
A0A0S4J9J2 | Bodo saltans | 32% | 100% |
A0A1X0NFY9 | Trypanosomatidae | 41% | 100% |
A0A1X0NTL0 | Trypanosomatidae | 41% | 100% |
A0A1X0NTM3 | Trypanosomatidae | 40% | 100% |
A0A1X0NY19 | Trypanosomatidae | 41% | 100% |
A0A1X0NYR4 | Trypanosomatidae | 38% | 100% |
A0A1X0P322 | Trypanosomatidae | 38% | 100% |
A0A1X0P5Y7 | Trypanosomatidae | 41% | 99% |
A0A3Q8IB13 | Leishmania donovani | 26% | 100% |
A0A3Q8IFU7 | Leishmania donovani | 27% | 100% |
A0A3S5H595 | Leishmania donovani | 92% | 99% |
A0A3S5H596 | Leishmania donovani | 91% | 100% |
A0A3S5H7I4 | Leishmania donovani | 24% | 100% |
A0A3S7WXQ4 | Leishmania donovani | 27% | 100% |
A0A3S7WXS2 | Leishmania donovani | 27% | 100% |
A2R0E0 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 24% | 100% |
A2YZ01 | Oryza sativa subsp. indica | 28% | 100% |
A4H3V1 | Leishmania braziliensis | 84% | 100% |
A4HCV9 | Leishmania braziliensis | 25% | 100% |
A4HCW0 | Leishmania braziliensis | 27% | 100% |
A4HG14 | Leishmania braziliensis | 26% | 100% |
A4HS26 | Leishmania infantum | 91% | 99% |
A4HS27 | Leishmania infantum | 89% | 100% |
A4I0D9 | Leishmania infantum | 26% | 100% |
A4I0E0 | Leishmania infantum | 27% | 100% |
A4I336 | Leishmania infantum | 24% | 100% |
A4IAW1 | Leishmania infantum | 64% | 91% |
B6DXP5 | Leymus chinensis | 27% | 100% |
B6DZC8 | Triticum aestivum | 28% | 100% |
B6DZD0 | Triticum urartu | 29% | 100% |
B6DZD1 | Aegilops speltoides | 29% | 100% |
B6DZD2 | Aegilops tauschii | 28% | 100% |
D2IGW7 | Bromus pictus | 30% | 100% |
E1ABX2 | Aspergillus ficuum | 24% | 100% |
E8NHF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E8NHF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9ACV4 | Leishmania major | 24% | 100% |
E9AZE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
O24509 | Phaseolus vulgaris | 30% | 98% |
P05656 | Bacillus subtilis (strain 168) | 24% | 94% |
P26792 | Daucus carota | 30% | 100% |
P29000 | Solanum lycopersicum | 29% | 100% |
P29001 | Vigna radiata var. radiata | 31% | 98% |
P49174 | Zea mays | 29% | 100% |
P49175 | Zea mays | 30% | 95% |
P80065 | Daucus carota | 28% | 96% |
P92916 | Allium cepa | 27% | 100% |
P93761 | Capsicum annuum | 28% | 99% |
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 | 29% | 100% |
Q39693 | Daucus carota | 30% | 100% |
Q43089 | Pisum sativum | 29% | 100% |
Q43857 | Vicia faba | 31% | 99% |
Q43866 | Arabidopsis thaliana | 30% | 100% |
Q4QB75 | Leishmania major | 29% | 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 | 29% | 100% |
Q67XZ3 | Arabidopsis thaliana | 30% | 100% |
Q70AT7 | Hordeum vulgare | 28% | 100% |
Q70XE6 | Beta vulgaris | 28% | 100% |
Q76HP6 | Aspergillus niger | 24% | 100% |
Q84LA1 | Triticum aestivum | 28% | 100% |
Q84PN8 | Triticum aestivum | 28% | 100% |
Q8W413 | Arabidopsis thaliana | 29% | 100% |
Q8W4S6 | Arabidopsis thaliana | 27% | 100% |
Q9LIB9 | Arabidopsis thaliana | 27% | 100% |
Q9XTP3 | Leishmania major | 91% | 100% |
Q9XZX0 | Leishmania major | 88% | 100% |