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: 32 |
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: 10, no: 9 |
NetGPI | no | yes: 0, no: 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: Q9XZX0
Term | Name | Level | Count |
---|---|---|---|
GO:0005975 | carbohydrate metabolic process | 3 | 19 |
GO:0008152 | metabolic process | 1 | 20 |
GO:0044238 | primary metabolic process | 2 | 19 |
GO:0071704 | organic substance metabolic process | 2 | 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 20 |
GO:0004553 | hydrolase activity, hydrolyzing O-glycosyl compounds | 4 | 19 |
GO:0004564 | beta-fructofuranosidase activity | 5 | 10 |
GO:0016787 | hydrolase activity | 2 | 20 |
GO:0016798 | hydrolase activity, acting on glycosyl bonds | 3 | 20 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.670 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 470 | 474 | PF00082 | 0.624 |
DEG_APCC_DBOX_1 | 366 | 374 | PF00400 | 0.471 |
DEG_COP1_1 | 263 | 273 | PF00400 | 0.402 |
DEG_SCF_FBW7_1 | 20 | 25 | PF00400 | 0.484 |
DOC_CYCLIN_RxL_1 | 10 | 21 | PF00134 | 0.498 |
DOC_MAPK_gen_1 | 10 | 18 | PF00069 | 0.494 |
DOC_MAPK_gen_1 | 211 | 221 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 35 | 44 | PF00069 | 0.596 |
DOC_MAPK_HePTP_8 | 440 | 452 | PF00069 | 0.427 |
DOC_MAPK_MEF2A_6 | 443 | 452 | PF00069 | 0.427 |
DOC_PP1_RVXF_1 | 345 | 351 | PF00149 | 0.462 |
DOC_PP4_FxxP_1 | 155 | 158 | PF00568 | 0.475 |
DOC_PP4_FxxP_1 | 89 | 92 | PF00568 | 0.458 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.359 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.331 |
DOC_USP7_UBL2_3 | 347 | 351 | PF12436 | 0.490 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.785 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 462 | 467 | PF00397 | 0.664 |
LIG_14-3-3_CanoR_1 | 139 | 144 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 249 | 253 | PF00244 | 0.469 |
LIG_Actin_WH2_2 | 90 | 108 | PF00022 | 0.353 |
LIG_APCC_ABBA_1 | 403 | 408 | PF00400 | 0.328 |
LIG_APCC_ABBA_1 | 412 | 417 | PF00400 | 0.328 |
LIG_BRCT_BRCA1_1 | 139 | 143 | PF00533 | 0.411 |
LIG_BRCT_BRCA1_1 | 151 | 155 | PF00533 | 0.374 |
LIG_BRCT_BRCA1_1 | 335 | 339 | PF00533 | 0.495 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.374 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.511 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.470 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.462 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.388 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.509 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.350 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.350 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.373 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.570 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.362 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.321 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.366 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.437 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.464 |
LIG_LIR_Apic_2 | 152 | 158 | PF02991 | 0.474 |
LIG_LIR_Apic_2 | 458 | 464 | PF02991 | 0.626 |
LIG_LIR_Apic_2 | 86 | 92 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 102 | 111 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 128 | 138 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 140 | 149 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 241 | 250 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 284 | 294 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 474 | 485 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 102 | 107 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 115 | 119 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 154 | 159 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 241 | 246 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 284 | 289 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 308 | 313 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 474 | 480 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 93 | 97 | PF02991 | 0.356 |
LIG_LYPXL_yS_3 | 310 | 313 | PF13949 | 0.469 |
LIG_NRBOX | 475 | 481 | PF00104 | 0.594 |
LIG_PCNA_yPIPBox_3 | 187 | 201 | PF02747 | 0.469 |
LIG_PDZ_Class_2 | 481 | 486 | PF00595 | 0.565 |
LIG_REV1ctd_RIR_1 | 92 | 102 | PF16727 | 0.360 |
LIG_SH2_CRK | 156 | 160 | PF00017 | 0.365 |
LIG_SH2_CRK | 286 | 290 | PF00017 | 0.418 |
LIG_SH2_NCK_1 | 286 | 290 | PF00017 | 0.418 |
LIG_SH2_PTP2 | 131 | 134 | PF00017 | 0.474 |
LIG_SH2_SRC | 156 | 159 | PF00017 | 0.382 |
LIG_SH2_STAP1 | 441 | 445 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.470 |
LIG_SH3_1 | 14 | 20 | PF00018 | 0.495 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.472 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.345 |
LIG_SH3_3 | 363 | 369 | PF00018 | 0.336 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.627 |
LIG_SUMO_SIM_par_1 | 446 | 451 | PF11976 | 0.496 |
LIG_TYR_ITSM | 152 | 159 | PF00017 | 0.491 |
LIG_TYR_ITSM | 239 | 246 | PF00017 | 0.472 |
LIG_WW_3 | 10 | 14 | PF00397 | 0.506 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.407 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.477 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.445 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.503 |
MOD_CK2_1 | 407 | 413 | PF00069 | 0.418 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.341 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.448 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.450 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.408 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.360 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.281 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.417 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.353 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.481 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.538 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.332 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.399 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.372 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.407 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.410 |
MOD_N-GLC_1 | 124 | 129 | PF02516 | 0.373 |
MOD_N-GLC_1 | 238 | 243 | PF02516 | 0.397 |
MOD_N-GLC_1 | 281 | 286 | PF02516 | 0.461 |
MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.378 |
MOD_N-GLC_1 | 342 | 347 | PF02516 | 0.205 |
MOD_N-GLC_1 | 470 | 475 | PF02516 | 0.621 |
MOD_N-GLC_2 | 344 | 346 | PF02516 | 0.395 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.353 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.353 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.421 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.418 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.456 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.328 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.354 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.495 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.349 |
MOD_NEK2_2 | 151 | 156 | PF00069 | 0.475 |
MOD_PIKK_1 | 126 | 132 | PF00454 | 0.493 |
MOD_PIKK_1 | 201 | 207 | PF00454 | 0.481 |
MOD_PIKK_1 | 228 | 234 | PF00454 | 0.542 |
MOD_PIKK_1 | 281 | 287 | PF00454 | 0.467 |
MOD_PIKK_1 | 373 | 379 | PF00454 | 0.423 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.469 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.417 |
MOD_Plk_1 | 281 | 287 | PF00069 | 0.473 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.306 |
MOD_Plk_1 | 407 | 413 | PF00069 | 0.328 |
MOD_Plk_2-3 | 453 | 459 | PF00069 | 0.446 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.446 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.473 |
MOD_Plk_4 | 335 | 341 | PF00069 | 0.464 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.339 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.458 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.534 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.406 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.786 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.535 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.473 |
MOD_ProDKin_1 | 462 | 468 | PF00069 | 0.664 |
MOD_SUMO_for_1 | 415 | 418 | PF00179 | 0.459 |
MOD_SUMO_rev_2 | 196 | 202 | PF00179 | 0.426 |
TRG_DiLeu_BaEn_2 | 401 | 407 | PF01217 | 0.459 |
TRG_DiLeu_BaLyEn_6 | 366 | 371 | PF01217 | 0.472 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.458 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 477 | 480 | PF00928 | 0.570 |
TRG_ER_diArg_1 | 12 | 14 | PF00400 | 0.505 |
TRG_NES_CRM1_1 | 418 | 430 | PF08389 | 0.459 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4P1 | Leptomonas seymouri | 48% | 100% |
A0A0N1PBT6 | Leptomonas seymouri | 74% | 75% |
A0A0S4J9J2 | Bodo saltans | 32% | 100% |
A0A1X0NTL0 | Trypanosomatidae | 35% | 77% |
A0A1X0NTM3 | Trypanosomatidae | 37% | 77% |
A0A1X0NY19 | Trypanosomatidae | 38% | 77% |
A0A1X0NYR4 | Trypanosomatidae | 36% | 89% |
A0A1X0P322 | Trypanosomatidae | 36% | 77% |
A0A1X0P5Y7 | Trypanosomatidae | 37% | 76% |
A0A3S5H595 | Leishmania donovani | 93% | 76% |
A0A3S5H596 | Leishmania donovani | 95% | 100% |
A4H3V1 | Leishmania braziliensis | 81% | 76% |
A4HS26 | Leishmania infantum | 93% | 76% |
A4HS27 | Leishmania infantum | 93% | 100% |
A4IAW1 | Leishmania infantum | 61% | 69% |
E9AK13 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 76% |
E9AK14 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
P49174 | Zea mays | 28% | 82% |
P49175 | Zea mays | 26% | 73% |
Q39041 | Arabidopsis thaliana | 24% | 73% |
Q9XTP3 | Leishmania major | 98% | 100% |