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: A4H3V1
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_C14_Caspase3-7 | 206 | 210 | PF00656 | 0.232 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.575 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 317 | 319 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.581 |
CLV_PCSK_PC1ET2_1 | 150 | 152 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 625 | 629 | PF00082 | 0.661 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.353 |
DEG_APCC_DBOX_1 | 521 | 529 | PF00400 | 0.473 |
DEG_APCC_DBOX_1 | 8 | 16 | PF00400 | 0.358 |
DEG_COP1_1 | 418 | 428 | PF00400 | 0.374 |
DOC_CKS1_1 | 471 | 476 | PF01111 | 0.224 |
DOC_CYCLIN_yCln2_LP_2 | 407 | 413 | PF00134 | 0.224 |
DOC_MAPK_gen_1 | 7 | 15 | PF00069 | 0.567 |
DOC_MAPK_HePTP_8 | 5 | 17 | PF00069 | 0.361 |
DOC_MAPK_HePTP_8 | 595 | 607 | PF00069 | 0.371 |
DOC_MAPK_MEF2A_6 | 598 | 607 | PF00069 | 0.371 |
DOC_MAPK_MEF2A_6 | 7 | 15 | PF00069 | 0.591 |
DOC_MAPK_NFAT4_5 | 8 | 16 | PF00069 | 0.565 |
DOC_PP2B_PxIxI_1 | 465 | 471 | PF00149 | 0.370 |
DOC_PP4_FxxP_1 | 179 | 182 | PF00568 | 0.311 |
DOC_PP4_FxxP_1 | 244 | 247 | PF00568 | 0.456 |
DOC_PP4_FxxP_1 | 310 | 313 | PF00568 | 0.477 |
DOC_PP4_FxxP_1 | 471 | 474 | PF00568 | 0.384 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.227 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 453 | 457 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.469 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.245 |
DOC_WW_Pin1_4 | 381 | 386 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.228 |
DOC_WW_Pin1_4 | 470 | 475 | PF00397 | 0.183 |
DOC_WW_Pin1_4 | 549 | 554 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 617 | 622 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.467 |
LIG_14-3-3_CanoR_1 | 294 | 299 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 317 | 321 | PF00244 | 0.249 |
LIG_14-3-3_CanoR_1 | 404 | 408 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 433 | 439 | PF00244 | 0.266 |
LIG_Actin_WH2_2 | 245 | 263 | PF00022 | 0.329 |
LIG_APCC_ABBA_1 | 558 | 563 | PF00400 | 0.327 |
LIG_APCC_ABBA_1 | 567 | 572 | PF00400 | 0.327 |
LIG_BRCT_BRCA1_1 | 294 | 298 | PF00533 | 0.409 |
LIG_BRCT_BRCA1_1 | 306 | 310 | PF00533 | 0.313 |
LIG_BRCT_BRCA1_1 | 490 | 494 | PF00533 | 0.503 |
LIG_Clathr_ClatBox_1 | 173 | 177 | PF01394 | 0.224 |
LIG_deltaCOP1_diTrp_1 | 101 | 107 | PF00928 | 0.461 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.393 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.512 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.474 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.455 |
LIG_FHA_1 | 537 | 543 | PF00498 | 0.396 |
LIG_FHA_1 | 55 | 61 | PF00498 | 0.423 |
LIG_FHA_1 | 577 | 583 | PF00498 | 0.351 |
LIG_FHA_1 | 588 | 594 | PF00498 | 0.351 |
LIG_FHA_1 | 600 | 606 | PF00498 | 0.428 |
LIG_FHA_1 | 626 | 632 | PF00498 | 0.638 |
LIG_FHA_2 | 125 | 131 | PF00498 | 0.420 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.347 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.374 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.458 |
LIG_FHA_2 | 404 | 410 | PF00498 | 0.437 |
LIG_FHA_2 | 416 | 422 | PF00498 | 0.441 |
LIG_FHA_2 | 491 | 497 | PF00498 | 0.333 |
LIG_FHA_2 | 518 | 524 | PF00498 | 0.464 |
LIG_FHA_2 | 635 | 641 | PF00498 | 0.573 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.311 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.311 |
LIG_LIR_Apic_2 | 177 | 182 | PF02991 | 0.327 |
LIG_LIR_Apic_2 | 183 | 189 | PF02991 | 0.275 |
LIG_LIR_Apic_2 | 241 | 247 | PF02991 | 0.432 |
LIG_LIR_Apic_2 | 307 | 313 | PF02991 | 0.477 |
LIG_LIR_Apic_2 | 613 | 619 | PF02991 | 0.573 |
LIG_LIR_Gen_1 | 257 | 266 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 283 | 292 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 293 | 304 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 347 | 357 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 396 | 405 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 630 | 639 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 105 | 110 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 248 | 252 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 257 | 262 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 270 | 274 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 283 | 289 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 293 | 299 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 300 | 304 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 309 | 314 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 347 | 353 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 396 | 401 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 463 | 468 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 630 | 635 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.326 |
LIG_LYPXL_yS_3 | 465 | 468 | PF13949 | 0.404 |
LIG_NRBOX | 630 | 636 | PF00104 | 0.610 |
LIG_PCNA_yPIPBox_3 | 342 | 356 | PF02747 | 0.404 |
LIG_PDZ_Class_2 | 636 | 641 | PF00595 | 0.569 |
LIG_Pex14_1 | 195 | 199 | PF04695 | 0.322 |
LIG_PTB_Apo_2 | 113 | 120 | PF02174 | 0.347 |
LIG_PTB_Apo_2 | 626 | 633 | PF02174 | 0.600 |
LIG_PTB_Phospho_1 | 113 | 119 | PF10480 | 0.347 |
LIG_PTB_Phospho_1 | 626 | 632 | PF10480 | 0.602 |
LIG_SH2_CRK | 301 | 305 | PF00017 | 0.384 |
LIG_SH2_CRK | 311 | 315 | PF00017 | 0.347 |
LIG_SH2_CRK | 441 | 445 | PF00017 | 0.439 |
LIG_SH2_NCK_1 | 32 | 36 | PF00017 | 0.504 |
LIG_SH2_NCK_1 | 350 | 354 | PF00017 | 0.395 |
LIG_SH2_NCK_1 | 441 | 445 | PF00017 | 0.439 |
LIG_SH2_PTP2 | 286 | 289 | PF00017 | 0.476 |
LIG_SH2_SRC | 311 | 314 | PF00017 | 0.355 |
LIG_SH2_SRC | 32 | 35 | PF00017 | 0.508 |
LIG_SH2_STAP1 | 234 | 238 | PF00017 | 0.335 |
LIG_SH2_STAP1 | 596 | 600 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 492 | 495 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 527 | 530 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 583 | 586 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 610 | 613 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.311 |
LIG_SH3_2 | 189 | 194 | PF14604 | 0.455 |
LIG_SH3_2 | 48 | 53 | PF14604 | 0.323 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.300 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.463 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.450 |
LIG_SH3_3 | 286 | 292 | PF00018 | 0.475 |
LIG_SH3_3 | 443 | 449 | PF00018 | 0.333 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.261 |
LIG_SH3_3 | 518 | 524 | PF00018 | 0.338 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.176 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.467 |
LIG_SUMO_SIM_par_1 | 120 | 127 | PF11976 | 0.441 |
LIG_SUMO_SIM_par_1 | 172 | 177 | PF11976 | 0.224 |
LIG_SUMO_SIM_par_1 | 601 | 606 | PF11976 | 0.505 |
LIG_TYR_ITIM | 299 | 304 | PF00017 | 0.370 |
LIG_TYR_ITIM | 30 | 35 | PF00017 | 0.535 |
LIG_TYR_ITIM | 348 | 353 | PF00017 | 0.384 |
LIG_TYR_ITSM | 307 | 314 | PF00017 | 0.420 |
LIG_TYR_ITSM | 394 | 401 | PF00017 | 0.552 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.482 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.492 |
MOD_CK1_1 | 456 | 462 | PF00069 | 0.484 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.420 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.477 |
MOD_CK2_1 | 451 | 457 | PF00069 | 0.500 |
MOD_CK2_1 | 490 | 496 | PF00069 | 0.383 |
MOD_CK2_1 | 517 | 523 | PF00069 | 0.514 |
MOD_CK2_1 | 562 | 568 | PF00069 | 0.439 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.458 |
MOD_Cter_Amidation | 148 | 151 | PF01082 | 0.339 |
MOD_DYRK1A_RPxSP_1 | 91 | 95 | PF00069 | 0.458 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.323 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.411 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.329 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.438 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.346 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.364 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.278 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.293 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.403 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.404 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.329 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.548 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.382 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.248 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.313 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.363 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.454 |
MOD_N-GLC_1 | 117 | 122 | PF02516 | 0.461 |
MOD_N-GLC_1 | 393 | 398 | PF02516 | 0.519 |
MOD_N-GLC_1 | 434 | 439 | PF02516 | 0.385 |
MOD_N-GLC_1 | 499 | 504 | PF02516 | 0.329 |
MOD_N-GLC_1 | 625 | 630 | PF02516 | 0.658 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.328 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.330 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.432 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.410 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.496 |
MOD_NEK2_1 | 488 | 493 | PF00069 | 0.319 |
MOD_NEK2_1 | 528 | 533 | PF00069 | 0.345 |
MOD_NEK2_1 | 627 | 632 | PF00069 | 0.623 |
MOD_NEK2_1 | 634 | 639 | PF00069 | 0.518 |
MOD_NEK2_2 | 306 | 311 | PF00069 | 0.477 |
MOD_PIKK_1 | 328 | 334 | PF00454 | 0.233 |
MOD_PIKK_1 | 356 | 362 | PF00454 | 0.520 |
MOD_PIKK_1 | 379 | 385 | PF00454 | 0.551 |
MOD_PIKK_1 | 456 | 462 | PF00454 | 0.230 |
MOD_PIKK_1 | 528 | 534 | PF00454 | 0.376 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.452 |
MOD_PKA_2 | 403 | 409 | PF00069 | 0.404 |
MOD_PKA_2 | 494 | 500 | PF00069 | 0.348 |
MOD_Plk_1 | 292 | 298 | PF00069 | 0.270 |
MOD_Plk_1 | 393 | 399 | PF00069 | 0.537 |
MOD_Plk_1 | 415 | 421 | PF00069 | 0.366 |
MOD_Plk_1 | 434 | 440 | PF00069 | 0.466 |
MOD_Plk_1 | 499 | 505 | PF00069 | 0.232 |
MOD_Plk_1 | 562 | 568 | PF00069 | 0.327 |
MOD_Plk_2-3 | 490 | 496 | PF00069 | 0.404 |
MOD_Plk_2-3 | 608 | 614 | PF00069 | 0.423 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.469 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.284 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.399 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.467 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.576 |
MOD_Plk_4 | 499 | 505 | PF00069 | 0.352 |
MOD_Plk_4 | 562 | 568 | PF00069 | 0.338 |
MOD_Plk_4 | 611 | 617 | PF00069 | 0.411 |
MOD_Plk_4 | 627 | 633 | PF00069 | 0.663 |
MOD_Plk_4 | 634 | 640 | PF00069 | 0.540 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.245 |
MOD_ProDKin_1 | 381 | 387 | PF00069 | 0.565 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.228 |
MOD_ProDKin_1 | 470 | 476 | PF00069 | 0.183 |
MOD_ProDKin_1 | 549 | 555 | PF00069 | 0.475 |
MOD_ProDKin_1 | 617 | 623 | PF00069 | 0.667 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.467 |
MOD_SUMO_for_1 | 570 | 573 | PF00179 | 0.395 |
MOD_SUMO_rev_2 | 351 | 357 | PF00179 | 0.447 |
TRG_DiLeu_BaEn_2 | 556 | 562 | PF01217 | 0.395 |
TRG_DiLeu_BaLyEn_6 | 521 | 526 | PF01217 | 0.475 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.458 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 311 | 314 | PF00928 | 0.273 |
TRG_ENDOCYTIC_2 | 32 | 35 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 465 | 468 | PF00928 | 0.447 |
TRG_ENDOCYTIC_2 | 632 | 635 | PF00928 | 0.626 |
TRG_ER_diArg_1 | 6 | 9 | PF00400 | 0.577 |
TRG_NES_CRM1_1 | 573 | 585 | PF08389 | 0.395 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBT6 | Leptomonas seymouri | 75% | 100% |
A0A0S4J9J2 | Bodo saltans | 33% | 100% |
A0A1X0NFY9 | Trypanosomatidae | 41% | 100% |
A0A1X0NTL0 | Trypanosomatidae | 39% | 100% |
A0A1X0NTM3 | Trypanosomatidae | 41% | 100% |
A0A1X0NY19 | Trypanosomatidae | 41% | 100% |
A0A1X0NYR4 | Trypanosomatidae | 38% | 100% |
A0A1X0P322 | Trypanosomatidae | 39% | 100% |
A0A1X0P5Y7 | Trypanosomatidae | 42% | 100% |
A0A3Q8IB13 | Leishmania donovani | 26% | 100% |
A0A3Q8IFU7 | Leishmania donovani | 28% | 100% |
A0A3S5H595 | Leishmania donovani | 84% | 100% |
A0A3S5H596 | Leishmania donovani | 80% | 100% |
A0A3S7WXQ4 | Leishmania donovani | 28% | 100% |
A0A3S7WXS2 | Leishmania donovani | 28% | 100% |
A2R0E0 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 25% | 100% |
A2X5P7 | Oryza sativa subsp. indica | 32% | 100% |
A2YZ01 | Oryza sativa subsp. indica | 28% | 100% |
A4HCV9 | Leishmania braziliensis | 24% | 100% |
A4HCW0 | Leishmania braziliensis | 27% | 100% |
A4HG14 | Leishmania braziliensis | 27% | 100% |
A4HS26 | Leishmania infantum | 83% | 100% |
A4HS27 | Leishmania infantum | 81% | 100% |
A4I0D9 | Leishmania infantum | 26% | 100% |
A4I0E0 | Leishmania infantum | 28% | 100% |
A4IAW1 | Leishmania infantum | 64% | 91% |
B6DXP5 | Leymus chinensis | 28% | 100% |
B6DZC8 | Triticum aestivum | 29% | 100% |
B6DZD0 | Triticum urartu | 29% | 100% |
B6DZD1 | Aegilops speltoides | 30% | 100% |
B6DZD2 | Aegilops tauschii | 30% | 100% |
D2IGW7 | Bromus pictus | 30% | 100% |
E1ABX2 | Aspergillus ficuum | 26% | 100% |
E8NHF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E8NHF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9ACV4 | Leishmania major | 25% | 100% |
E9AK13 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
E9AZE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
H2DF88 | Rosa hybrid cultivar | 30% | 100% |
O24509 | Phaseolus vulgaris | 29% | 98% |
O33833 | Thermotoga maritima (strain ATCC 43589 / DSM 3109 / JCM 10099 / NBRC 100826 / MSB8) | 26% | 100% |
P05656 | Bacillus subtilis (strain 168) | 24% | 95% |
P26792 | Daucus carota | 30% | 100% |
P29000 | Solanum lycopersicum | 29% | 100% |
P29001 | Vigna radiata var. radiata | 31% | 99% |
P49174 | Zea mays | 30% | 100% |
P80065 | Daucus carota | 30% | 97% |
P92916 | Allium cepa | 28% | 100% |
P93761 | Capsicum annuum | 29% | 100% |
Q01IS7 | Oryza sativa subsp. indica | 29% | 100% |
Q01IS8 | Oryza sativa subsp. indica | 30% | 100% |
Q0E0P0 | Oryza sativa subsp. japonica | 31% | 100% |
Q0J360 | Oryza sativa subsp. japonica | 28% | 100% |
Q0JDC5 | Oryza sativa subsp. japonica | 29% | 100% |
Q0JDC6 | Oryza sativa subsp. japonica | 30% | 100% |
Q1PEF8 | Arabidopsis thaliana | 29% | 100% |
Q2UXF7 | Triticum aestivum | 29% | 100% |
Q39692 | Daucus carota | 28% | 100% |
Q39693 | Daucus carota | 29% | 100% |
Q43089 | Pisum sativum | 28% | 100% |
Q43857 | Vicia faba | 31% | 100% |
Q43866 | Arabidopsis thaliana | 31% | 100% |
Q4QB75 | Leishmania major | 27% | 100% |
Q4QB76 | Leishmania major | 26% | 100% |
Q56UD0 | Oryza sativa subsp. japonica | 30% | 100% |
Q56UD1 | Oryza sativa subsp. japonica | 26% | 100% |
Q5FC15 | Asparagus officinalis | 30% | 100% |
Q5JJV0 | Oryza sativa subsp. japonica | 30% | 100% |
Q67XZ3 | Arabidopsis thaliana | 29% | 100% |
Q70AT7 | Hordeum vulgare | 29% | 100% |
Q70XE6 | Beta vulgaris | 29% | 100% |
Q76HP6 | Aspergillus niger | 26% | 100% |
Q84LA1 | Triticum aestivum | 29% | 100% |
Q84PN8 | Triticum aestivum | 29% | 100% |
Q8W4S6 | Arabidopsis thaliana | 28% | 100% |
Q9LIB9 | Arabidopsis thaliana | 29% | 100% |
Q9XTP3 | Leishmania major | 83% | 100% |
Q9XZX0 | Leishmania major | 81% | 100% |