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: 0 |
Pissara et al. | yes | yes: 15 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: E9AK14
Term | Name | Level | Count |
---|---|---|---|
GO:0005975 | carbohydrate metabolic process | 3 | 7 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004553 | hydrolase activity, hydrolyzing O-glycosyl compounds | 4 | 7 |
GO:0016787 | hydrolase activity | 2 | 8 |
GO:0016798 | hydrolase activity, acting on glycosyl bonds | 3 | 8 |
GO:0004564 | beta-fructofuranosidase activity | 5 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.495 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.470 |
DEG_APCC_DBOX_1 | 279 | 287 | PF00400 | 0.441 |
DEG_COP1_1 | 176 | 186 | PF00400 | 0.391 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.279 |
DOC_MAPK_gen_1 | 124 | 134 | PF00069 | 0.541 |
DOC_MAPK_HePTP_8 | 353 | 365 | PF00069 | 0.387 |
DOC_MAPK_MEF2A_6 | 356 | 365 | PF00069 | 0.387 |
DOC_PP1_RVXF_1 | 258 | 264 | PF00149 | 0.441 |
DOC_PP4_FxxP_1 | 2 | 5 | PF00568 | 0.477 |
DOC_PP4_FxxP_1 | 68 | 71 | PF00568 | 0.495 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.368 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.491 |
DOC_USP7_UBL2_3 | 260 | 264 | PF12436 | 0.441 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.553 |
LIG_14-3-3_CanoR_1 | 162 | 166 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 52 | 57 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 75 | 79 | PF00244 | 0.225 |
LIG_Actin_WH2_2 | 3 | 21 | PF00022 | 0.447 |
LIG_APCC_ABBA_1 | 316 | 321 | PF00400 | 0.340 |
LIG_APCC_ABBA_1 | 325 | 330 | PF00400 | 0.340 |
LIG_BRCT_BRCA1_1 | 248 | 252 | PF00533 | 0.481 |
LIG_BRCT_BRCA1_1 | 52 | 56 | PF00533 | 0.425 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.380 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.558 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.459 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.398 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.516 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.365 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.365 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.365 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.613 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.559 |
LIG_FHA_2 | 162 | 168 | PF00498 | 0.510 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.420 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.481 |
LIG_FHA_2 | 389 | 395 | PF00498 | 0.405 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.456 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.337 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.252 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.320 |
LIG_LIR_Apic_2 | 371 | 377 | PF02991 | 0.524 |
LIG_LIR_Apic_2 | 67 | 71 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 15 | 24 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 154 | 163 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 197 | 207 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 388 | 397 | PF02991 | 0.613 |
LIG_LIR_Gen_1 | 41 | 50 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 51 | 62 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 15 | 20 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 154 | 159 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 197 | 202 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 221 | 226 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 28 | 32 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 388 | 393 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 41 | 47 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 58 | 62 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 6 | 10 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.436 |
LIG_LYPXL_yS_3 | 223 | 226 | PF13949 | 0.441 |
LIG_NRBOX | 388 | 394 | PF00104 | 0.564 |
LIG_PCNA_yPIPBox_3 | 100 | 114 | PF02747 | 0.441 |
LIG_PDZ_Class_2 | 394 | 399 | PF00595 | 0.670 |
LIG_PTB_Apo_2 | 384 | 391 | PF02174 | 0.556 |
LIG_PTB_Phospho_1 | 384 | 390 | PF10480 | 0.557 |
LIG_REV1ctd_RIR_1 | 5 | 15 | PF16727 | 0.441 |
LIG_SH2_CRK | 199 | 203 | PF00017 | 0.391 |
LIG_SH2_CRK | 69 | 73 | PF00017 | 0.447 |
LIG_SH2_GRB2like | 199 | 202 | PF00017 | 0.225 |
LIG_SH2_NCK_1 | 199 | 203 | PF00017 | 0.391 |
LIG_SH2_PTP2 | 44 | 47 | PF00017 | 0.468 |
LIG_SH2_SRC | 69 | 72 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 354 | 358 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 368 | 371 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.447 |
LIG_SH3_1 | 264 | 270 | PF00018 | 0.225 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.365 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.384 |
LIG_SH3_3 | 276 | 282 | PF00018 | 0.340 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.441 |
LIG_SUMO_SIM_par_1 | 361 | 366 | PF11976 | 0.376 |
LIG_TYR_ITSM | 152 | 159 | PF00017 | 0.525 |
LIG_TYR_ITSM | 65 | 72 | PF00017 | 0.495 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.444 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.482 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.494 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.420 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.441 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.398 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.252 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.447 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.240 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.420 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.457 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.360 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.379 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.299 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.365 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.597 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.451 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.447 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.353 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.423 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.599 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.491 |
MOD_N-GLC_1 | 151 | 156 | PF02516 | 0.547 |
MOD_N-GLC_1 | 200 | 205 | PF02516 | 0.490 |
MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.395 |
MOD_N-GLC_1 | 241 | 246 | PF02516 | 0.378 |
MOD_N-GLC_1 | 37 | 42 | PF02516 | 0.397 |
MOD_N-GLC_1 | 383 | 388 | PF02516 | 0.569 |
MOD_N-GLC_2 | 257 | 259 | PF02516 | 0.441 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.441 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.447 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.382 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.172 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.298 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.447 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.513 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.559 |
MOD_NEK2_2 | 64 | 69 | PF00069 | 0.495 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.441 |
MOD_PIKK_1 | 194 | 200 | PF00454 | 0.495 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.441 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.333 |
MOD_PKB_1 | 288 | 296 | PF00069 | 0.225 |
MOD_Plk_1 | 151 | 157 | PF00069 | 0.523 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.468 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.369 |
MOD_Plk_1 | 320 | 326 | PF00069 | 0.340 |
MOD_Plk_2-3 | 248 | 254 | PF00069 | 0.225 |
MOD_Plk_2-3 | 366 | 372 | PF00069 | 0.446 |
MOD_Plk_2-3 | 6 | 12 | PF00069 | 0.252 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.564 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.441 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.340 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.446 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.664 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.645 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.447 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.530 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.478 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.558 |
MOD_SUMO_for_1 | 328 | 331 | PF00179 | 0.441 |
MOD_SUMO_rev_2 | 109 | 115 | PF00179 | 0.452 |
MOD_SUMO_rev_2 | 129 | 137 | PF00179 | 0.268 |
TRG_DiLeu_BaEn_2 | 314 | 320 | PF01217 | 0.441 |
TRG_DiLeu_BaLyEn_6 | 279 | 284 | PF01217 | 0.468 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 223 | 226 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.610 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.398 |
TRG_NES_CRM1_1 | 129 | 141 | PF08389 | 0.323 |
TRG_NES_CRM1_1 | 331 | 343 | PF08389 | 0.441 |
TRG_Pf-PMV_PEXEL_1 | 124 | 129 | PF00026 | 0.439 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4P1 | Leptomonas seymouri | 49% | 100% |
A0A0S4J9J2 | Bodo saltans | 32% | 88% |
A0A1X0NKQ8 | Trypanosomatidae | 34% | 100% |
A0A1X0NYR4 | Trypanosomatidae | 35% | 73% |
A0A3S5H596 | Leishmania donovani | 90% | 91% |
A4HS27 | Leishmania infantum | 90% | 82% |
P49174 | Zea mays | 28% | 68% |
Q9XZX0 | Leishmania major | 90% | 100% |