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 | no | yes: 11, no: 5 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4IAW1
Term | Name | Level | Count |
---|---|---|---|
GO:0005975 | carbohydrate metabolic process | 3 | 17 |
GO:0008152 | metabolic process | 1 | 17 |
GO:0044238 | primary metabolic process | 2 | 17 |
GO:0071704 | organic substance metabolic process | 2 | 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 17 |
GO:0004553 | hydrolase activity, hydrolyzing O-glycosyl compounds | 4 | 17 |
GO:0004564 | beta-fructofuranosidase activity | 5 | 9 |
GO:0016787 | hydrolase activity | 2 | 17 |
GO:0016798 | hydrolase activity, acting on glycosyl bonds | 3 | 17 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 462 | 466 | PF00656 | 0.174 |
CLV_C14_Caspase3-7 | 64 | 68 | PF00656 | 0.167 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.356 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.356 |
CLV_PCSK_PC1ET2_1 | 200 | 202 | PF00082 | 0.462 |
CLV_PCSK_PC1ET2_1 | 366 | 368 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.497 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.489 |
DEG_SCF_FBW7_1 | 141 | 148 | PF00400 | 0.156 |
DEG_SCF_FBW7_1 | 70 | 77 | PF00400 | 0.158 |
DEG_SPOP_SBC_1 | 23 | 27 | PF00917 | 0.465 |
DEG_SPOP_SBC_1 | 54 | 58 | PF00917 | 0.167 |
DOC_CKS1_1 | 142 | 147 | PF01111 | 0.156 |
DOC_MAPK_HePTP_8 | 423 | 435 | PF00069 | 0.226 |
DOC_MAPK_MEF2A_6 | 426 | 435 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 451 | 459 | PF00069 | 0.220 |
DOC_PP1_RVXF_1 | 199 | 206 | PF00149 | 0.156 |
DOC_PP2B_LxvP_1 | 639 | 642 | PF13499 | 0.162 |
DOC_PP2B_PxIxI_1 | 438 | 444 | PF00149 | 0.220 |
DOC_PP4_FxxP_1 | 229 | 232 | PF00568 | 0.242 |
DOC_PP4_FxxP_1 | 294 | 297 | PF00568 | 0.360 |
DOC_PP4_FxxP_1 | 360 | 363 | PF00568 | 0.361 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.293 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.167 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.160 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.424 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.351 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.240 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.200 |
DOC_WW_Pin1_4 | 435 | 440 | PF00397 | 0.434 |
DOC_WW_Pin1_4 | 550 | 555 | PF00397 | 0.373 |
DOC_WW_Pin1_4 | 600 | 605 | PF00397 | 0.371 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.159 |
LIG_14-3-3_CanoR_1 | 201 | 206 | PF00244 | 0.195 |
LIG_14-3-3_CanoR_1 | 30 | 35 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 344 | 349 | PF00244 | 0.282 |
LIG_14-3-3_CanoR_1 | 419 | 427 | PF00244 | 0.278 |
LIG_14-3-3_CanoR_1 | 543 | 549 | PF00244 | 0.177 |
LIG_Actin_WH2_2 | 295 | 313 | PF00022 | 0.251 |
LIG_APCC_ABBA_1 | 615 | 620 | PF00400 | 0.257 |
LIG_APCC_ABBA_1 | 624 | 629 | PF00400 | 0.257 |
LIG_APCC_ABBAyCdc20_2 | 614 | 620 | PF00400 | 0.162 |
LIG_BRCT_BRCA1_1 | 344 | 348 | PF00533 | 0.315 |
LIG_BRCT_BRCA1_1 | 356 | 360 | PF00533 | 0.311 |
LIG_Clathr_ClatBox_1 | 432 | 436 | PF01394 | 0.226 |
LIG_Clathr_ClatBox_1 | 582 | 586 | PF01394 | 0.156 |
LIG_deltaCOP1_diTrp_1 | 151 | 157 | PF00928 | 0.351 |
LIG_EH1_1 | 31 | 39 | PF00400 | 0.419 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.323 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.491 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.306 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.222 |
LIG_FHA_1 | 436 | 442 | PF00498 | 0.363 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.275 |
LIG_FHA_1 | 494 | 500 | PF00498 | 0.358 |
LIG_FHA_1 | 555 | 561 | PF00498 | 0.327 |
LIG_FHA_1 | 575 | 581 | PF00498 | 0.167 |
LIG_FHA_1 | 634 | 640 | PF00498 | 0.275 |
LIG_FHA_1 | 655 | 661 | PF00498 | 0.353 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.216 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.255 |
LIG_FHA_2 | 146 | 152 | PF00498 | 0.302 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.300 |
LIG_FHA_2 | 345 | 351 | PF00498 | 0.277 |
LIG_FHA_2 | 357 | 363 | PF00498 | 0.251 |
LIG_FHA_2 | 372 | 378 | PF00498 | 0.361 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.466 |
LIG_FHA_2 | 485 | 491 | PF00498 | 0.373 |
LIG_LIR_Apic_2 | 233 | 239 | PF02991 | 0.218 |
LIG_LIR_Apic_2 | 291 | 297 | PF02991 | 0.357 |
LIG_LIR_Apic_2 | 357 | 363 | PF02991 | 0.361 |
LIG_LIR_Apic_2 | 421 | 427 | PF02991 | 0.232 |
LIG_LIR_Gen_1 | 25 | 36 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 307 | 316 | PF02991 | 0.271 |
LIG_LIR_Gen_1 | 333 | 343 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 345 | 354 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 399 | 407 | PF02991 | 0.297 |
LIG_LIR_Gen_1 | 492 | 502 | PF02991 | 0.245 |
LIG_LIR_Gen_1 | 690 | 700 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 9 | 19 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 125 | 131 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 155 | 160 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 25 | 31 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 298 | 302 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 307 | 312 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 320 | 324 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 333 | 339 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 345 | 351 | PF02991 | 0.173 |
LIG_LIR_Nem_3 | 359 | 364 | PF02991 | 0.235 |
LIG_LIR_Nem_3 | 385 | 391 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 399 | 403 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 492 | 497 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 5 | 11 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 515 | 521 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 688 | 694 | PF02991 | 0.350 |
LIG_LRP6_Inhibitor_1 | 679 | 685 | PF00058 | 0.503 |
LIG_Pex14_1 | 245 | 249 | PF04695 | 0.247 |
LIG_PTB_Apo_2 | 163 | 170 | PF02174 | 0.278 |
LIG_PTB_Apo_2 | 686 | 693 | PF02174 | 0.431 |
LIG_PTB_Phospho_1 | 163 | 169 | PF10480 | 0.278 |
LIG_PTB_Phospho_1 | 686 | 692 | PF10480 | 0.433 |
LIG_REV1ctd_RIR_1 | 203 | 209 | PF16727 | 0.156 |
LIG_REV1ctd_RIR_1 | 297 | 307 | PF16727 | 0.262 |
LIG_SH2_CRK | 11 | 15 | PF00017 | 0.471 |
LIG_SH2_CRK | 361 | 365 | PF00017 | 0.257 |
LIG_SH2_CRK | 494 | 498 | PF00017 | 0.360 |
LIG_SH2_CRK | 692 | 696 | PF00017 | 0.314 |
LIG_SH2_GRB2like | 687 | 690 | PF00017 | 0.275 |
LIG_SH2_GRB2like | 691 | 694 | PF00017 | 0.261 |
LIG_SH2_NCK_1 | 400 | 404 | PF00017 | 0.302 |
LIG_SH2_NCK_1 | 424 | 428 | PF00017 | 0.224 |
LIG_SH2_NCK_1 | 494 | 498 | PF00017 | 0.360 |
LIG_SH2_PTP2 | 336 | 339 | PF00017 | 0.360 |
LIG_SH2_SRC | 361 | 364 | PF00017 | 0.269 |
LIG_SH2_SRC | 640 | 643 | PF00017 | 0.191 |
LIG_SH2_STAP1 | 149 | 153 | PF00017 | 0.156 |
LIG_SH2_STAP1 | 32 | 36 | PF00017 | 0.412 |
LIG_SH2_STAP1 | 473 | 477 | PF00017 | 0.156 |
LIG_SH2_STAP1 | 687 | 691 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.242 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.240 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.261 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.254 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.189 |
LIG_SH2_STAT5 | 473 | 476 | PF00017 | 0.223 |
LIG_SH2_STAT5 | 494 | 497 | PF00017 | 0.257 |
LIG_SH2_STAT5 | 550 | 553 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 640 | 643 | PF00017 | 0.257 |
LIG_SH2_STAT5 | 687 | 690 | PF00017 | 0.275 |
LIG_SH3_2 | 98 | 103 | PF14604 | 0.251 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.150 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.351 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.496 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.210 |
LIG_SH3_3 | 236 | 242 | PF00018 | 0.352 |
LIG_SH3_3 | 496 | 502 | PF00018 | 0.261 |
LIG_SH3_3 | 575 | 581 | PF00018 | 0.262 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.208 |
LIG_SUMO_SIM_anti_2 | 428 | 436 | PF11976 | 0.319 |
LIG_SUMO_SIM_par_1 | 170 | 177 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 428 | 436 | PF11976 | 0.260 |
LIG_SxIP_EBH_1 | 50 | 59 | PF03271 | 0.356 |
LIG_TYR_ITIM | 398 | 403 | PF00017 | 0.294 |
LIG_TYR_ITSM | 357 | 364 | PF00017 | 0.320 |
LIG_WRC_WIRS_1 | 456 | 461 | PF05994 | 0.162 |
LIG_WRC_WIRS_1 | 464 | 469 | PF05994 | 0.191 |
MOD_CDC14_SPxK_1 | 603 | 606 | PF00782 | 0.214 |
MOD_CDK_SPxK_1 | 600 | 606 | PF00069 | 0.214 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.309 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.305 |
MOD_CK1_1 | 492 | 498 | PF00069 | 0.337 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.314 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.167 |
MOD_CK1_1 | 553 | 559 | PF00069 | 0.265 |
MOD_CK1_1 | 592 | 598 | PF00069 | 0.169 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.158 |
MOD_CK1_1 | 654 | 660 | PF00069 | 0.230 |
MOD_CK1_1 | 670 | 676 | PF00069 | 0.294 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.321 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.156 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.469 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.361 |
MOD_CK2_1 | 422 | 428 | PF00069 | 0.255 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.166 |
MOD_CK2_1 | 619 | 625 | PF00069 | 0.366 |
MOD_Cter_Amidation | 198 | 201 | PF01082 | 0.462 |
MOD_GlcNHglycan | 160 | 163 | PF01048 | 0.451 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.535 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.451 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.518 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.560 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.583 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.493 |
MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.475 |
MOD_GlcNHglycan | 664 | 667 | PF01048 | 0.429 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.158 |
MOD_GlcNHglycan | 672 | 675 | PF01048 | 0.419 |
MOD_GlcNHglycan | 695 | 698 | PF01048 | 0.455 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.343 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.228 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.319 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.329 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.277 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.166 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.315 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.458 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.342 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.252 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.358 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.248 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.241 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.290 |
MOD_GSK3_1 | 654 | 661 | PF00069 | 0.241 |
MOD_GSK3_1 | 683 | 690 | PF00069 | 0.331 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.406 |
MOD_LATS_1 | 87 | 93 | PF00433 | 0.161 |
MOD_N-GLC_1 | 167 | 172 | PF02516 | 0.551 |
MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.268 |
MOD_N-GLC_1 | 447 | 452 | PF02516 | 0.515 |
MOD_N-GLC_1 | 533 | 538 | PF02516 | 0.526 |
MOD_N-GLC_1 | 569 | 574 | PF02516 | 0.372 |
MOD_N-GLC_2 | 46 | 48 | PF02516 | 0.249 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.238 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.281 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.269 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.318 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.263 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.225 |
MOD_NEK2_1 | 484 | 489 | PF00069 | 0.238 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.268 |
MOD_NEK2_1 | 683 | 688 | PF00069 | 0.476 |
MOD_NEK2_2 | 356 | 361 | PF00069 | 0.363 |
MOD_OFUCOSY | 539 | 545 | PF10250 | 0.362 |
MOD_PIKK_1 | 240 | 246 | PF00454 | 0.186 |
MOD_PIKK_1 | 382 | 388 | PF00454 | 0.209 |
MOD_PIKK_1 | 48 | 54 | PF00454 | 0.488 |
MOD_PIKK_1 | 489 | 495 | PF00454 | 0.363 |
MOD_PIKK_1 | 643 | 649 | PF00454 | 0.177 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.284 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.162 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.469 |
MOD_Plk_1 | 489 | 495 | PF00069 | 0.359 |
MOD_Plk_1 | 514 | 520 | PF00069 | 0.156 |
MOD_Plk_1 | 541 | 547 | PF00069 | 0.178 |
MOD_Plk_1 | 619 | 625 | PF00069 | 0.257 |
MOD_Plk_2-3 | 399 | 405 | PF00069 | 0.162 |
MOD_Plk_2-3 | 667 | 673 | PF00069 | 0.325 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.351 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.250 |
MOD_Plk_4 | 279 | 285 | PF00069 | 0.321 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.469 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.363 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.326 |
MOD_Plk_4 | 619 | 625 | PF00069 | 0.273 |
MOD_Plk_4 | 687 | 693 | PF00069 | 0.477 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.351 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.240 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.200 |
MOD_ProDKin_1 | 435 | 441 | PF00069 | 0.434 |
MOD_ProDKin_1 | 550 | 556 | PF00069 | 0.373 |
MOD_ProDKin_1 | 600 | 606 | PF00069 | 0.371 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.159 |
MOD_SUMO_rev_2 | 399 | 407 | PF00179 | 0.328 |
MOD_SUMO_rev_2 | 77 | 84 | PF00179 | 0.281 |
TRG_DiLeu_BaLyEn_6 | 578 | 583 | PF01217 | 0.359 |
TRG_DiLeu_BaLyEn_6 | 595 | 600 | PF01217 | 0.156 |
TRG_ENDOCYTIC_2 | 11 | 14 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 336 | 339 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.220 |
TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 494 | 497 | PF00928 | 0.257 |
TRG_ENDOCYTIC_2 | 691 | 694 | PF00928 | 0.468 |
TRG_ER_diArg_1 | 367 | 369 | PF00400 | 0.333 |
TRG_ER_diArg_1 | 566 | 568 | PF00400 | 0.156 |
TRG_NLS_MonoExtN_4 | 363 | 370 | PF00514 | 0.156 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBT6 | Leptomonas seymouri | 64% | 100% |
A0A1X0NFY9 | Trypanosomatidae | 42% | 100% |
A0A1X0NTL0 | Trypanosomatidae | 42% | 100% |
A0A1X0NTM3 | Trypanosomatidae | 40% | 100% |
A0A1X0NY19 | Trypanosomatidae | 41% | 100% |
A0A1X0NYR4 | Trypanosomatidae | 38% | 100% |
A0A1X0P322 | Trypanosomatidae | 39% | 100% |
A0A1X0P5Y7 | Trypanosomatidae | 41% | 100% |
A0A3Q8IB13 | Leishmania donovani | 27% | 100% |
A0A3Q8IFU7 | Leishmania donovani | 27% | 100% |
A0A3S5H595 | Leishmania donovani | 65% | 100% |
A0A3S5H7I4 | Leishmania donovani | 26% | 100% |
A0A3S7WXQ4 | Leishmania donovani | 28% | 100% |
A0A3S7WXS2 | Leishmania donovani | 27% | 100% |
A4H3V1 | Leishmania braziliensis | 64% | 100% |
A4HCV9 | Leishmania braziliensis | 25% | 100% |
A4HG14 | Leishmania braziliensis | 27% | 100% |
A4HS26 | Leishmania infantum | 65% | 100% |
A4HS27 | Leishmania infantum | 59% | 100% |
A4I0D9 | Leishmania infantum | 27% | 100% |
A4I0E0 | Leishmania infantum | 27% | 100% |
A4I336 | Leishmania infantum | 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 | 26% | 100% |
E9AK13 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 100% |
E9AZE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
H2DF88 | Rosa hybrid cultivar | 27% | 100% |
P80065 | Daucus carota | 27% | 100% |
Q0J360 | Oryza sativa subsp. japonica | 29% | 100% |
Q0JDC5 | Oryza sativa subsp. japonica | 26% | 100% |
Q1PEF8 | Arabidopsis thaliana | 29% | 100% |
Q2UXF7 | Triticum aestivum | 28% | 100% |
Q43857 | Vicia faba | 26% | 100% |
Q43866 | Arabidopsis thaliana | 31% | 100% |
Q4QB75 | Leishmania major | 28% | 100% |
Q4QB76 | Leishmania major | 26% | 100% |
Q56UD0 | Oryza sativa subsp. japonica | 29% | 100% |
Q56UD1 | Oryza sativa subsp. japonica | 25% | 100% |
Q5FC15 | Asparagus officinalis | 28% | 100% |
Q9LIB9 | Arabidopsis thaliana | 29% | 100% |
Q9XTP3 | Leishmania major | 65% | 100% |
Q9XZX0 | Leishmania major | 61% | 100% |