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. | no | 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: 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: A0A3S5H596
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 | 9 |
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 | 319 | 323 | PF00656 | 0.219 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.599 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.367 |
DEG_APCC_DBOX_1 | 366 | 374 | PF00400 | 0.434 |
DEG_COP1_1 | 262 | 273 | PF00400 | 0.351 |
DOC_MAPK_gen_1 | 211 | 221 | PF00069 | 0.499 |
DOC_MAPK_gen_1 | 35 | 44 | PF00069 | 0.428 |
DOC_PP1_RVXF_1 | 345 | 351 | PF00149 | 0.424 |
DOC_PP4_FxxP_1 | 155 | 158 | PF00568 | 0.437 |
DOC_PP4_FxxP_1 | 89 | 92 | PF00568 | 0.420 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.293 |
DOC_USP7_UBL2_3 | 347 | 351 | PF12436 | 0.452 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.435 |
LIG_14-3-3_CanoR_1 | 139 | 144 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 249 | 253 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 302 | 310 | PF00244 | 0.331 |
LIG_Actin_WH2_2 | 286 | 304 | PF00022 | 0.219 |
LIG_Actin_WH2_2 | 90 | 108 | PF00022 | 0.304 |
LIG_APCC_ABBA_1 | 403 | 408 | PF00400 | 0.301 |
LIG_APCC_ABBA_1 | 412 | 417 | PF00400 | 0.301 |
LIG_APCC_ABBAyCdc20_2 | 129 | 135 | PF00400 | 0.219 |
LIG_BRCT_BRCA1_1 | 139 | 143 | PF00533 | 0.374 |
LIG_BRCT_BRCA1_1 | 151 | 155 | PF00533 | 0.336 |
LIG_BRCT_BRCA1_1 | 335 | 339 | PF00533 | 0.457 |
LIG_deltaCOP1_diTrp_1 | 38 | 44 | PF00928 | 0.173 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.348 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.483 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.252 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.433 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.374 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.422 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.326 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.326 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.312 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.280 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.407 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.490 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.404 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.427 |
LIG_LIR_Apic_2 | 152 | 158 | PF02991 | 0.436 |
LIG_LIR_Apic_2 | 86 | 92 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 102 | 111 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 128 | 138 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 140 | 149 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 241 | 250 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 284 | 294 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 102 | 107 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 115 | 119 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.240 |
LIG_LIR_Nem_3 | 154 | 159 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 241 | 246 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 284 | 289 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 307 | 313 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 93 | 97 | PF02991 | 0.306 |
LIG_LYPXL_yS_3 | 310 | 313 | PF13949 | 0.432 |
LIG_PCNA_yPIPBox_3 | 187 | 201 | PF02747 | 0.432 |
LIG_PDZ_Class_2 | 435 | 440 | PF00595 | 0.156 |
LIG_Pex14_1 | 40 | 44 | PF04695 | 0.293 |
LIG_REV1ctd_RIR_1 | 92 | 102 | PF16727 | 0.322 |
LIG_SH2_CRK | 156 | 160 | PF00017 | 0.313 |
LIG_SH2_CRK | 286 | 290 | PF00017 | 0.405 |
LIG_SH2_NCK_1 | 286 | 290 | PF00017 | 0.405 |
LIG_SH2_PTP2 | 131 | 134 | PF00017 | 0.436 |
LIG_SH2_SRC | 156 | 159 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 104 | 107 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.239 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.432 |
LIG_SH3_1 | 14 | 20 | PF00018 | 0.469 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.484 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.435 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.756 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.307 |
LIG_SH3_3 | 363 | 369 | PF00018 | 0.310 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.488 |
LIG_SUMO_SIM_par_1 | 216 | 223 | PF11976 | 0.361 |
LIG_TYR_ITSM | 152 | 159 | PF00017 | 0.453 |
LIG_TYR_ITSM | 239 | 246 | PF00017 | 0.548 |
LIG_WW_3 | 10 | 14 | PF00397 | 0.486 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.466 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.369 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.440 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.437 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.447 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.465 |
MOD_CK2_1 | 407 | 413 | PF00069 | 0.405 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.304 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.419 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.404 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.338 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.250 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.379 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.304 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.526 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.431 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.286 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.389 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.337 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.368 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.373 |
MOD_N-GLC_1 | 124 | 129 | PF02516 | 0.321 |
MOD_N-GLC_1 | 238 | 243 | PF02516 | 0.525 |
MOD_N-GLC_1 | 281 | 286 | PF02516 | 0.423 |
MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.362 |
MOD_N-GLC_2 | 344 | 346 | PF02516 | 0.357 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.304 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.304 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.372 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.445 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.418 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.291 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.317 |
MOD_NEK2_1 | 74 | 79 | PF00069 | 0.300 |
MOD_NEK2_2 | 151 | 156 | PF00069 | 0.437 |
MOD_PIKK_1 | 201 | 207 | PF00454 | 0.444 |
MOD_PIKK_1 | 281 | 287 | PF00454 | 0.429 |
MOD_PIKK_1 | 373 | 379 | PF00454 | 0.385 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.418 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.432 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.436 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.538 |
MOD_Plk_1 | 281 | 287 | PF00069 | 0.435 |
MOD_Plk_1 | 407 | 413 | PF00069 | 0.301 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.408 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.570 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.411 |
MOD_Plk_4 | 335 | 341 | PF00069 | 0.431 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.313 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.368 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.492 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.540 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.435 |
MOD_SUMO_for_1 | 415 | 418 | PF00179 | 0.421 |
MOD_SUMO_rev_2 | 196 | 202 | PF00179 | 0.412 |
TRG_DiLeu_BaEn_2 | 401 | 407 | PF01217 | 0.421 |
TRG_DiLeu_BaLyEn_6 | 366 | 371 | PF01217 | 0.435 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.247 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.256 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 286 | 289 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 310 | 313 | PF00928 | 0.412 |
TRG_ER_diArg_1 | 12 | 14 | PF00400 | 0.471 |
TRG_NES_CRM1_1 | 418 | 430 | PF08389 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 211 | 216 | PF00026 | 0.404 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBT6 | Leptomonas seymouri | 72% | 68% |
A0A0S4J9J2 | Bodo saltans | 32% | 97% |
A0A1X0NFY9 | Trypanosomatidae | 36% | 92% |
A0A1X0NTL0 | Trypanosomatidae | 36% | 70% |
A0A1X0NTM3 | Trypanosomatidae | 38% | 70% |
A0A1X0NY19 | Trypanosomatidae | 39% | 70% |
A0A1X0NYR4 | Trypanosomatidae | 36% | 80% |
A0A1X0P322 | Trypanosomatidae | 36% | 70% |
A0A1X0P5Y7 | Trypanosomatidae | 38% | 68% |
A0A3S5H595 | Leishmania donovani | 100% | 68% |
A4H3V1 | Leishmania braziliensis | 80% | 69% |
A4HS26 | Leishmania infantum | 99% | 68% |
A4HS27 | Leishmania infantum | 100% | 100% |
E9AK13 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 69% |
E9AK14 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q8W4S6 | Arabidopsis thaliana | 25% | 80% |
Q9XTP3 | Leishmania major | 93% | 69% |
Q9XZX0 | Leishmania major | 95% | 100% |