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: A4HS27
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_C14_Caspase3-7 | 318 | 322 | PF00656 | 0.272 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.651 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 469 | 473 | PF00082 | 0.612 |
DEG_APCC_DBOX_1 | 365 | 373 | PF00400 | 0.487 |
DEG_COP1_1 | 261 | 272 | PF00400 | 0.420 |
DOC_MAPK_gen_1 | 210 | 220 | PF00069 | 0.527 |
DOC_MAPK_gen_1 | 34 | 43 | PF00069 | 0.481 |
DOC_MAPK_HePTP_8 | 439 | 451 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 442 | 451 | PF00069 | 0.442 |
DOC_PP1_RVXF_1 | 344 | 350 | PF00149 | 0.477 |
DOC_PP2B_LxvP_1 | 12 | 15 | PF13499 | 0.566 |
DOC_PP4_FxxP_1 | 154 | 157 | PF00568 | 0.490 |
DOC_PP4_FxxP_1 | 88 | 91 | PF00568 | 0.473 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.375 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.346 |
DOC_USP7_UBL2_3 | 346 | 350 | PF12436 | 0.505 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 393 | 398 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.661 |
LIG_14-3-3_CanoR_1 | 138 | 143 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 248 | 252 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 301 | 309 | PF00244 | 0.379 |
LIG_Actin_WH2_2 | 285 | 303 | PF00022 | 0.272 |
LIG_Actin_WH2_2 | 89 | 107 | PF00022 | 0.369 |
LIG_APCC_ABBA_1 | 402 | 407 | PF00400 | 0.344 |
LIG_APCC_ABBA_1 | 411 | 416 | PF00400 | 0.344 |
LIG_APCC_ABBAyCdc20_2 | 128 | 134 | PF00400 | 0.272 |
LIG_BRCT_BRCA1_1 | 138 | 142 | PF00533 | 0.427 |
LIG_BRCT_BRCA1_1 | 150 | 154 | PF00533 | 0.389 |
LIG_BRCT_BRCA1_1 | 334 | 338 | PF00533 | 0.510 |
LIG_deltaCOP1_diTrp_1 | 37 | 43 | PF00928 | 0.233 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.389 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.530 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.311 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.485 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.404 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.525 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.365 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.365 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.344 |
LIG_FHA_1 | 470 | 476 | PF00498 | 0.563 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.378 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.336 |
LIG_FHA_2 | 166 | 172 | PF00498 | 0.382 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.543 |
LIG_FHA_2 | 248 | 254 | PF00498 | 0.453 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.480 |
LIG_LIR_Apic_2 | 151 | 157 | PF02991 | 0.489 |
LIG_LIR_Apic_2 | 457 | 463 | PF02991 | 0.631 |
LIG_LIR_Apic_2 | 85 | 91 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 101 | 110 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 127 | 136 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 137 | 148 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 240 | 249 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 283 | 293 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 473 | 484 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 101 | 106 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 114 | 118 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 127 | 133 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 137 | 143 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 144 | 148 | PF02991 | 0.256 |
LIG_LIR_Nem_3 | 153 | 158 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 240 | 245 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 283 | 288 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 306 | 312 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 473 | 479 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 92 | 96 | PF02991 | 0.371 |
LIG_LYPXL_yS_3 | 309 | 312 | PF13949 | 0.484 |
LIG_NRBOX | 474 | 480 | PF00104 | 0.586 |
LIG_PCNA_yPIPBox_3 | 186 | 200 | PF02747 | 0.484 |
LIG_PDZ_Class_2 | 480 | 485 | PF00595 | 0.566 |
LIG_Pex14_1 | 39 | 43 | PF04695 | 0.359 |
LIG_REV1ctd_RIR_1 | 91 | 101 | PF16727 | 0.375 |
LIG_SH2_CRK | 155 | 159 | PF00017 | 0.380 |
LIG_SH2_CRK | 285 | 289 | PF00017 | 0.433 |
LIG_SH2_NCK_1 | 285 | 289 | PF00017 | 0.433 |
LIG_SH2_PTP2 | 130 | 133 | PF00017 | 0.489 |
LIG_SH2_SRC | 155 | 158 | PF00017 | 0.397 |
LIG_SH2_STAP1 | 440 | 444 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 263 | 266 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 427 | 430 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 454 | 457 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.485 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.483 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.694 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.488 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.789 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.360 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.351 |
LIG_SUMO_SIM_par_1 | 215 | 222 | PF11976 | 0.388 |
LIG_SUMO_SIM_par_1 | 447 | 452 | PF11976 | 0.506 |
LIG_TYR_ITSM | 151 | 158 | PF00017 | 0.506 |
LIG_TYR_ITSM | 238 | 245 | PF00017 | 0.594 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.514 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.422 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.492 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.460 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.483 |
MOD_CK2_1 | 361 | 367 | PF00069 | 0.518 |
MOD_CK2_1 | 406 | 412 | PF00069 | 0.433 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.357 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.465 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.423 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.375 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.296 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.432 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.369 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.468 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.551 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.460 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.348 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.431 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.387 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.422 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.426 |
MOD_N-GLC_1 | 123 | 128 | PF02516 | 0.389 |
MOD_N-GLC_1 | 237 | 242 | PF02516 | 0.557 |
MOD_N-GLC_1 | 280 | 285 | PF02516 | 0.476 |
MOD_N-GLC_1 | 321 | 326 | PF02516 | 0.393 |
MOD_N-GLC_1 | 469 | 474 | PF02516 | 0.612 |
MOD_N-GLC_2 | 343 | 345 | PF02516 | 0.410 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.369 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.369 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.436 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.434 |
MOD_NEK2_1 | 315 | 320 | PF00069 | 0.471 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.344 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.370 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.584 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.487 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.364 |
MOD_NEK2_2 | 150 | 155 | PF00069 | 0.490 |
MOD_PIKK_1 | 200 | 206 | PF00454 | 0.497 |
MOD_PIKK_1 | 280 | 286 | PF00454 | 0.482 |
MOD_PIKK_1 | 372 | 378 | PF00454 | 0.438 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.470 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.484 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.489 |
MOD_Plk_1 | 237 | 243 | PF00069 | 0.562 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.488 |
MOD_Plk_1 | 406 | 412 | PF00069 | 0.344 |
MOD_Plk_2-3 | 452 | 458 | PF00069 | 0.457 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.461 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.619 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.464 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.479 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.354 |
MOD_Plk_4 | 455 | 461 | PF00069 | 0.470 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.592 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.527 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.421 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.669 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.550 |
MOD_ProDKin_1 | 393 | 399 | PF00069 | 0.488 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.660 |
MOD_SUMO_for_1 | 414 | 417 | PF00179 | 0.474 |
MOD_SUMO_rev_2 | 195 | 201 | PF00179 | 0.442 |
TRG_DiLeu_BaEn_2 | 400 | 406 | PF01217 | 0.474 |
TRG_DiLeu_BaLyEn_6 | 365 | 370 | PF01217 | 0.488 |
TRG_ENDOCYTIC_2 | 103 | 106 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 476 | 479 | PF00928 | 0.555 |
TRG_NES_CRM1_1 | 417 | 429 | PF08389 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 210 | 215 | PF00026 | 0.432 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4P1 | Leptomonas seymouri | 48% | 100% |
A0A0N1PBT6 | Leptomonas seymouri | 73% | 75% |
A0A0S4J9J2 | Bodo saltans | 32% | 100% |
A0A1X0NTL0 | Trypanosomatidae | 36% | 77% |
A0A1X0NTM3 | Trypanosomatidae | 38% | 77% |
A0A1X0NY19 | Trypanosomatidae | 38% | 77% |
A0A1X0NYR4 | Trypanosomatidae | 36% | 89% |
A0A1X0P322 | Trypanosomatidae | 36% | 77% |
A0A1X0P5Y7 | Trypanosomatidae | 37% | 75% |
A0A3S5H595 | Leishmania donovani | 99% | 75% |
A0A3S5H596 | Leishmania donovani | 100% | 100% |
A4H3V1 | Leishmania braziliensis | 81% | 100% |
A4HS26 | Leishmania infantum | 100% | 100% |
A4IAW1 | Leishmania infantum | 59% | 69% |
E9AK13 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
E9AK14 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q9XTP3 | Leishmania major | 93% | 100% |
Q9XZX0 | Leishmania major | 93% | 100% |