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. | yes | 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. | yes | 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: Q9XTP3
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_NRD_NRD_1 | 316 | 318 | PF00675 | 0.534 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.473 |
CLV_PCSK_PC1ET2_1 | 149 | 151 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 624 | 628 | PF00082 | 0.711 |
DEG_APCC_DBOX_1 | 520 | 528 | PF00400 | 0.530 |
DEG_COP1_1 | 417 | 427 | PF00400 | 0.432 |
DOC_MAPK_gen_1 | 365 | 375 | PF00069 | 0.537 |
DOC_MAPK_gen_1 | 87 | 97 | PF00069 | 0.489 |
DOC_MAPK_HePTP_8 | 594 | 606 | PF00069 | 0.458 |
DOC_MAPK_MEF2A_6 | 157 | 164 | PF00069 | 0.354 |
DOC_MAPK_MEF2A_6 | 597 | 606 | PF00069 | 0.458 |
DOC_MAPK_MEF2A_6 | 7 | 14 | PF00069 | 0.662 |
DOC_PP1_RVXF_1 | 499 | 505 | PF00149 | 0.501 |
DOC_PP4_FxxP_1 | 178 | 181 | PF00568 | 0.369 |
DOC_PP4_FxxP_1 | 243 | 246 | PF00568 | 0.533 |
DOC_PP4_FxxP_1 | 309 | 312 | PF00568 | 0.534 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 471 | 475 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 476 | 480 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 508 | 512 | PF00917 | 0.382 |
DOC_USP7_UBL2_3 | 501 | 505 | PF12436 | 0.518 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 548 | 553 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 616 | 621 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.518 |
LIG_14-3-3_CanoR_1 | 150 | 156 | PF00244 | 0.301 |
LIG_14-3-3_CanoR_1 | 293 | 298 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 403 | 407 | PF00244 | 0.496 |
LIG_Actin_WH2_2 | 244 | 262 | PF00022 | 0.388 |
LIG_APCC_ABBA_1 | 557 | 562 | PF00400 | 0.396 |
LIG_APCC_ABBA_1 | 566 | 571 | PF00400 | 0.396 |
LIG_BRCT_BRCA1_1 | 293 | 297 | PF00533 | 0.470 |
LIG_BRCT_BRCA1_1 | 305 | 309 | PF00533 | 0.470 |
LIG_BRCT_BRCA1_1 | 489 | 493 | PF00533 | 0.496 |
LIG_deltaCOP1_diTrp_1 | 100 | 106 | PF00928 | 0.518 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.453 |
LIG_FHA_1 | 383 | 389 | PF00498 | 0.567 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.531 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.518 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.460 |
LIG_FHA_1 | 536 | 542 | PF00498 | 0.487 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.481 |
LIG_FHA_1 | 576 | 582 | PF00498 | 0.410 |
LIG_FHA_1 | 587 | 593 | PF00498 | 0.410 |
LIG_FHA_1 | 599 | 605 | PF00498 | 0.505 |
LIG_FHA_1 | 625 | 631 | PF00498 | 0.688 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.451 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.401 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.388 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.534 |
LIG_FHA_2 | 403 | 409 | PF00498 | 0.494 |
LIG_FHA_2 | 517 | 523 | PF00498 | 0.509 |
LIG_FHA_2 | 79 | 85 | PF00498 | 0.369 |
LIG_FHA_2 | 87 | 93 | PF00498 | 0.369 |
LIG_LIR_Apic_2 | 176 | 181 | PF02991 | 0.385 |
LIG_LIR_Apic_2 | 182 | 188 | PF02991 | 0.333 |
LIG_LIR_Apic_2 | 240 | 246 | PF02991 | 0.528 |
LIG_LIR_Apic_2 | 306 | 312 | PF02991 | 0.534 |
LIG_LIR_Apic_2 | 612 | 618 | PF02991 | 0.633 |
LIG_LIR_Gen_1 | 256 | 265 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 282 | 292 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 294 | 303 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 395 | 404 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 438 | 448 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 628 | 639 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 104 | 109 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 247 | 251 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 256 | 261 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 269 | 273 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 282 | 288 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 294 | 300 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 308 | 313 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 395 | 400 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 438 | 443 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 462 | 467 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 628 | 634 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 74 | 80 | PF02991 | 0.384 |
LIG_LYPXL_yS_3 | 464 | 467 | PF13949 | 0.496 |
LIG_NRBOX | 629 | 635 | PF00104 | 0.660 |
LIG_PCNA_yPIPBox_3 | 341 | 355 | PF02747 | 0.496 |
LIG_PDZ_Class_2 | 635 | 640 | PF00595 | 0.623 |
LIG_Pex14_1 | 194 | 198 | PF04695 | 0.380 |
LIG_PTB_Apo_2 | 112 | 119 | PF02174 | 0.430 |
LIG_PTB_Phospho_1 | 112 | 118 | PF10480 | 0.430 |
LIG_REV1ctd_RIR_1 | 246 | 256 | PF16727 | 0.406 |
LIG_SH2_CRK | 310 | 314 | PF00017 | 0.397 |
LIG_SH2_CRK | 440 | 444 | PF00017 | 0.533 |
LIG_SH2_NCK_1 | 31 | 35 | PF00017 | 0.570 |
LIG_SH2_NCK_1 | 440 | 444 | PF00017 | 0.533 |
LIG_SH2_PTP2 | 285 | 288 | PF00017 | 0.533 |
LIG_SH2_SRC | 31 | 34 | PF00017 | 0.575 |
LIG_SH2_SRC | 310 | 313 | PF00017 | 0.413 |
LIG_SH2_STAP1 | 595 | 599 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 526 | 529 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 582 | 585 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 609 | 612 | PF00017 | 0.583 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.369 |
LIG_SH3_2 | 188 | 193 | PF14604 | 0.513 |
LIG_SH3_2 | 47 | 52 | PF14604 | 0.382 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.520 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.511 |
LIG_SH3_3 | 285 | 291 | PF00018 | 0.532 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.318 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.390 |
LIG_SH3_3 | 517 | 523 | PF00018 | 0.404 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.231 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.518 |
LIG_SUMO_SIM_par_1 | 600 | 605 | PF11976 | 0.561 |
LIG_TYR_ITIM | 29 | 34 | PF00017 | 0.601 |
LIG_TYR_ITSM | 306 | 313 | PF00017 | 0.515 |
LIG_TYR_ITSM | 393 | 400 | PF00017 | 0.532 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.485 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.486 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.478 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.534 |
MOD_CK2_1 | 516 | 522 | PF00069 | 0.567 |
MOD_CK2_1 | 561 | 567 | PF00069 | 0.533 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.515 |
MOD_Cter_Amidation | 147 | 150 | PF01082 | 0.397 |
MOD_DYRK1A_RPxSP_1 | 90 | 94 | PF00069 | 0.515 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.382 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.454 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.492 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.388 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.563 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.537 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.549 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.433 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.395 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.367 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.479 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.492 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.399 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.602 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.378 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.459 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.437 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.508 |
MOD_N-GLC_1 | 116 | 121 | PF02516 | 0.518 |
MOD_N-GLC_1 | 278 | 283 | PF02516 | 0.421 |
MOD_N-GLC_1 | 392 | 397 | PF02516 | 0.476 |
MOD_N-GLC_1 | 435 | 440 | PF02516 | 0.491 |
MOD_N-GLC_1 | 476 | 481 | PF02516 | 0.477 |
MOD_N-GLC_1 | 496 | 501 | PF02516 | 0.301 |
MOD_N-GLC_1 | 624 | 629 | PF02516 | 0.708 |
MOD_N-GLC_2 | 498 | 500 | PF02516 | 0.430 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.363 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.354 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.398 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.388 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.388 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.480 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.544 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.539 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.403 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.403 |
MOD_NEK2_1 | 633 | 638 | PF00069 | 0.575 |
MOD_NEK2_2 | 305 | 310 | PF00069 | 0.534 |
MOD_PIKK_1 | 280 | 286 | PF00454 | 0.558 |
MOD_PIKK_1 | 355 | 361 | PF00454 | 0.542 |
MOD_PIKK_1 | 382 | 388 | PF00454 | 0.599 |
MOD_PIKK_1 | 435 | 441 | PF00454 | 0.525 |
MOD_PIKK_1 | 527 | 533 | PF00454 | 0.464 |
MOD_PIKK_1 | 79 | 85 | PF00454 | 0.288 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.496 |
MOD_Plk_1 | 392 | 398 | PF00069 | 0.506 |
MOD_Plk_1 | 435 | 441 | PF00069 | 0.532 |
MOD_Plk_1 | 561 | 567 | PF00069 | 0.396 |
MOD_Plk_2-3 | 607 | 613 | PF00069 | 0.483 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.518 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.341 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.455 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.536 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.532 |
MOD_Plk_4 | 489 | 495 | PF00069 | 0.462 |
MOD_Plk_4 | 561 | 567 | PF00069 | 0.410 |
MOD_Plk_4 | 610 | 616 | PF00069 | 0.483 |
MOD_Plk_4 | 633 | 639 | PF00069 | 0.596 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.637 |
MOD_ProDKin_1 | 548 | 554 | PF00069 | 0.532 |
MOD_ProDKin_1 | 616 | 622 | PF00069 | 0.717 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.518 |
MOD_SUMO_for_1 | 569 | 572 | PF00179 | 0.486 |
MOD_SUMO_rev_2 | 350 | 356 | PF00179 | 0.505 |
TRG_DiLeu_BaEn_2 | 555 | 561 | PF01217 | 0.486 |
TRG_DiLeu_BaLyEn_6 | 520 | 525 | PF01217 | 0.532 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.523 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 31 | 34 | PF00928 | 0.575 |
TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 440 | 443 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 464 | 467 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 631 | 634 | PF00928 | 0.678 |
TRG_NES_CRM1_1 | 572 | 584 | PF08389 | 0.486 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBT6 | Leptomonas seymouri | 76% | 99% |
A0A0S4J9J2 | Bodo saltans | 31% | 100% |
A0A1X0NFY9 | Trypanosomatidae | 42% | 100% |
A0A1X0NTL0 | Trypanosomatidae | 40% | 100% |
A0A1X0NTM3 | Trypanosomatidae | 41% | 100% |
A0A1X0NY19 | Trypanosomatidae | 41% | 100% |
A0A1X0NYR4 | Trypanosomatidae | 38% | 100% |
A0A1X0P322 | Trypanosomatidae | 38% | 100% |
A0A1X0P5Y7 | Trypanosomatidae | 41% | 100% |
A0A3Q8IB13 | Leishmania donovani | 27% | 100% |
A0A3Q8IFU7 | Leishmania donovani | 26% | 100% |
A0A3S5H595 | Leishmania donovani | 94% | 100% |
A0A3S5H596 | Leishmania donovani | 93% | 100% |
A0A3S5H7I4 | Leishmania donovani | 23% | 100% |
A0A3S7WXQ4 | Leishmania donovani | 27% | 100% |
A0A3S7WXS2 | Leishmania donovani | 26% | 100% |
A2YZ01 | Oryza sativa subsp. indica | 28% | 100% |
A4H3V1 | Leishmania braziliensis | 83% | 100% |
A4HCV9 | Leishmania braziliensis | 24% | 100% |
A4HCW0 | Leishmania braziliensis | 26% | 100% |
A4HG14 | Leishmania braziliensis | 24% | 100% |
A4HS26 | Leishmania infantum | 94% | 100% |
A4HS27 | Leishmania infantum | 93% | 100% |
A4I0D9 | Leishmania infantum | 27% | 100% |
A4I0E0 | Leishmania infantum | 26% | 100% |
A4IAW1 | Leishmania infantum | 65% | 91% |
B6DXP5 | Leymus chinensis | 28% | 100% |
B6DZC8 | Triticum aestivum | 29% | 100% |
B6DZD0 | Triticum urartu | 29% | 100% |
B6DZD1 | Aegilops speltoides | 30% | 100% |
B6DZD2 | Aegilops tauschii | 29% | 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) | 91% | 100% |
H2DF88 | Rosa hybrid cultivar | 29% | 100% |
O07003 | Bacillus subtilis (strain 168) | 21% | 100% |
O24509 | Phaseolus vulgaris | 26% | 98% |
P05656 | Bacillus subtilis (strain 168) | 24% | 95% |
P10596 | Saccharomyces cerevisiae | 25% | 100% |
P26792 | Daucus carota | 28% | 100% |
P29000 | Solanum lycopersicum | 28% | 100% |
P29001 | Vigna radiata var. radiata | 27% | 99% |
P49174 | Zea mays | 28% | 100% |
P49175 | Zea mays | 30% | 96% |
P80065 | Daucus carota | 28% | 97% |
P92916 | Allium cepa | 26% | 100% |
P93761 | Capsicum annuum | 27% | 100% |
Q01IS7 | Oryza sativa subsp. indica | 30% | 100% |
Q01IS8 | Oryza sativa subsp. indica | 30% | 100% |
Q0J360 | Oryza sativa subsp. japonica | 28% | 100% |
Q0JDC5 | Oryza sativa subsp. japonica | 30% | 100% |
Q0JDC6 | Oryza sativa subsp. japonica | 30% | 100% |
Q1PEF8 | Arabidopsis thaliana | 30% | 100% |
Q2UXF7 | Triticum aestivum | 30% | 100% |
Q39041 | Arabidopsis thaliana | 26% | 96% |
Q39693 | Daucus carota | 30% | 100% |
Q43089 | Pisum sativum | 29% | 100% |
Q43857 | Vicia faba | 30% | 100% |
Q43866 | Arabidopsis thaliana | 32% | 100% |
Q4QB75 | Leishmania major | 27% | 100% |
Q4QB76 | Leishmania major | 25% | 100% |
Q56UD0 | Oryza sativa subsp. japonica | 28% | 100% |
Q56UD1 | Oryza sativa subsp. japonica | 25% | 100% |
Q5FC15 | Asparagus officinalis | 29% | 100% |
Q5JJV0 | Oryza sativa subsp. japonica | 30% | 100% |
Q67XZ3 | Arabidopsis thaliana | 31% | 100% |
Q70AT7 | Hordeum vulgare | 28% | 100% |
Q70XE6 | Beta vulgaris | 27% | 100% |
Q84LA1 | Triticum aestivum | 28% | 100% |
Q84PN8 | Triticum aestivum | 29% | 100% |
Q8W413 | Arabidopsis thaliana | 29% | 100% |
Q8W4S6 | Arabidopsis thaliana | 27% | 100% |
Q9LIB9 | Arabidopsis thaliana | 28% | 100% |
Q9XZX0 | Leishmania major | 98% | 100% |