| 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. | no | yes: 0 |
| 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: 18 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 10 |
| NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9ASC1
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006040 | amino sugar metabolic process | 4 | 1 |
| GO:0006044 | N-acetylglucosamine metabolic process | 6 | 1 |
| GO:0006046 | N-acetylglucosamine catabolic process | 7 | 1 |
| GO:0008152 | metabolic process | 1 | 1 |
| GO:0009056 | catabolic process | 2 | 1 |
| GO:0046348 | amino sugar catabolic process | 5 | 1 |
| GO:0071704 | organic substance metabolic process | 2 | 1 |
| GO:1901071 | glucosamine-containing compound metabolic process | 5 | 1 |
| GO:1901072 | glucosamine-containing compound catabolic process | 6 | 1 |
| GO:1901135 | carbohydrate derivative metabolic process | 3 | 1 |
| GO:1901136 | carbohydrate derivative catabolic process | 4 | 1 |
| GO:1901575 | organic substance catabolic process | 3 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 11 |
| GO:0016787 | hydrolase activity | 2 | 11 |
| GO:0016810 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds | 3 | 11 |
| GO:0008448 | N-acetylglucosamine-6-phosphate deacetylase activity | 4 | 2 |
| GO:0016811 | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides | 4 | 2 |
| GO:0019213 | deacetylase activity | 3 | 2 |
| GO:0047419 | N-acetylgalactosamine-6-phosphate deacetylase activity | 4 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 121 | 125 | PF00656 | 0.506 |
| CLV_MEL_PAP_1 | 126 | 132 | PF00089 | 0.272 |
| CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.556 |
| CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.289 |
| CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.362 |
| CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.366 |
| CLV_PCSK_PC1ET2_1 | 128 | 130 | PF00082 | 0.289 |
| CLV_PCSK_PC1ET2_1 | 169 | 171 | PF00082 | 0.362 |
| CLV_PCSK_PC1ET2_1 | 409 | 411 | PF00082 | 0.366 |
| CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.282 |
| CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.259 |
| CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.259 |
| CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.258 |
| CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.229 |
| DEG_APCC_DBOX_1 | 40 | 48 | PF00400 | 0.506 |
| DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.300 |
| DOC_MAPK_DCC_7 | 267 | 276 | PF00069 | 0.497 |
| DOC_MAPK_gen_1 | 201 | 208 | PF00069 | 0.517 |
| DOC_MAPK_gen_1 | 267 | 276 | PF00069 | 0.506 |
| DOC_MAPK_gen_1 | 393 | 400 | PF00069 | 0.461 |
| DOC_MAPK_MEF2A_6 | 201 | 208 | PF00069 | 0.382 |
| DOC_MAPK_MEF2A_6 | 267 | 276 | PF00069 | 0.506 |
| DOC_PP4_FxxP_1 | 64 | 67 | PF00568 | 0.459 |
| DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.562 |
| DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.459 |
| LIG_14-3-3_CanoR_1 | 170 | 176 | PF00244 | 0.415 |
| LIG_14-3-3_CanoR_1 | 247 | 252 | PF00244 | 0.504 |
| LIG_14-3-3_CanoR_1 | 339 | 345 | PF00244 | 0.506 |
| LIG_APCC_ABBA_1 | 183 | 188 | PF00400 | 0.472 |
| LIG_BRCT_BRCA1_1 | 107 | 111 | PF00533 | 0.459 |
| LIG_Clathr_ClatBox_1 | 280 | 284 | PF01394 | 0.511 |
| LIG_Clathr_ClatBox_1 | 397 | 401 | PF01394 | 0.562 |
| LIG_FHA_1 | 118 | 124 | PF00498 | 0.512 |
| LIG_FHA_1 | 12 | 18 | PF00498 | 0.467 |
| LIG_FHA_1 | 271 | 277 | PF00498 | 0.482 |
| LIG_FHA_1 | 302 | 308 | PF00498 | 0.472 |
| LIG_FHA_1 | 346 | 352 | PF00498 | 0.468 |
| LIG_FHA_1 | 371 | 377 | PF00498 | 0.517 |
| LIG_FHA_2 | 213 | 219 | PF00498 | 0.382 |
| LIG_FHA_2 | 56 | 62 | PF00498 | 0.519 |
| LIG_Integrin_isoDGR_2 | 319 | 321 | PF01839 | 0.259 |
| LIG_LIR_Apic_2 | 61 | 67 | PF02991 | 0.312 |
| LIG_LIR_Gen_1 | 353 | 362 | PF02991 | 0.459 |
| LIG_LIR_Nem_3 | 166 | 171 | PF02991 | 0.457 |
| LIG_LIR_Nem_3 | 353 | 358 | PF02991 | 0.459 |
| LIG_PTB_Apo_2 | 86 | 93 | PF02174 | 0.472 |
| LIG_PTB_Phospho_1 | 86 | 92 | PF10480 | 0.489 |
| LIG_SH2_CRK | 422 | 426 | PF00017 | 0.415 |
| LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.489 |
| LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.489 |
| LIG_SH3_3 | 255 | 261 | PF00018 | 0.562 |
| LIG_Sin3_3 | 395 | 402 | PF02671 | 0.506 |
| LIG_SUMO_SIM_anti_2 | 2 | 8 | PF11976 | 0.365 |
| LIG_SUMO_SIM_anti_2 | 273 | 279 | PF11976 | 0.511 |
| LIG_SUMO_SIM_anti_2 | 298 | 305 | PF11976 | 0.473 |
| LIG_SUMO_SIM_par_1 | 22 | 28 | PF11976 | 0.412 |
| LIG_TRAF2_1 | 227 | 230 | PF00917 | 0.501 |
| LIG_TRAF2_1 | 58 | 61 | PF00917 | 0.451 |
| LIG_UBA3_1 | 219 | 224 | PF00899 | 0.459 |
| LIG_UBA3_1 | 357 | 364 | PF00899 | 0.551 |
| LIG_WRC_WIRS_1 | 241 | 246 | PF05994 | 0.472 |
| MOD_CK1_1 | 161 | 167 | PF00069 | 0.543 |
| MOD_CK1_1 | 174 | 180 | PF00069 | 0.553 |
| MOD_CK1_1 | 290 | 296 | PF00069 | 0.426 |
| MOD_CK2_1 | 129 | 135 | PF00069 | 0.527 |
| MOD_CK2_1 | 212 | 218 | PF00069 | 0.493 |
| MOD_CK2_1 | 225 | 231 | PF00069 | 0.424 |
| MOD_CK2_1 | 55 | 61 | PF00069 | 0.543 |
| MOD_CK2_1 | 85 | 91 | PF00069 | 0.472 |
| MOD_Cter_Amidation | 391 | 394 | PF01082 | 0.245 |
| MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.323 |
| MOD_GSK3_1 | 101 | 108 | PF00069 | 0.466 |
| MOD_GSK3_1 | 287 | 294 | PF00069 | 0.506 |
| MOD_GSK3_1 | 301 | 308 | PF00069 | 0.397 |
| MOD_LATS_1 | 115 | 121 | PF00433 | 0.529 |
| MOD_LATS_1 | 210 | 216 | PF00433 | 0.459 |
| MOD_N-GLC_1 | 2 | 7 | PF02516 | 0.468 |
| MOD_N-GLC_1 | 239 | 244 | PF02516 | 0.321 |
| MOD_N-GLC_1 | 35 | 40 | PF02516 | 0.381 |
| MOD_NEK2_1 | 111 | 116 | PF00069 | 0.538 |
| MOD_NEK2_1 | 171 | 176 | PF00069 | 0.459 |
| MOD_NEK2_1 | 233 | 238 | PF00069 | 0.448 |
| MOD_NEK2_1 | 29 | 34 | PF00069 | 0.449 |
| MOD_NEK2_1 | 333 | 338 | PF00069 | 0.513 |
| MOD_NEK2_1 | 47 | 52 | PF00069 | 0.521 |
| MOD_NEK2_2 | 90 | 95 | PF00069 | 0.456 |
| MOD_PKA_2 | 246 | 252 | PF00069 | 0.531 |
| MOD_PKA_2 | 320 | 326 | PF00069 | 0.466 |
| MOD_PKA_2 | 338 | 344 | PF00069 | 0.415 |
| MOD_Plk_1 | 161 | 167 | PF00069 | 0.562 |
| MOD_Plk_1 | 2 | 8 | PF00069 | 0.470 |
| MOD_Plk_1 | 239 | 245 | PF00069 | 0.552 |
| MOD_Plk_1 | 35 | 41 | PF00069 | 0.388 |
| MOD_Plk_1 | 90 | 96 | PF00069 | 0.472 |
| MOD_Plk_2-3 | 403 | 409 | PF00069 | 0.571 |
| MOD_Plk_4 | 105 | 111 | PF00069 | 0.459 |
| MOD_Plk_4 | 2 | 8 | PF00069 | 0.444 |
| MOD_Plk_4 | 247 | 253 | PF00069 | 0.459 |
| MOD_Plk_4 | 287 | 293 | PF00069 | 0.511 |
| MOD_Plk_4 | 320 | 326 | PF00069 | 0.497 |
| MOD_Plk_4 | 346 | 352 | PF00069 | 0.502 |
| MOD_Plk_4 | 35 | 41 | PF00069 | 0.291 |
| MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.459 |
| MOD_SUMO_rev_2 | 152 | 161 | PF00179 | 0.523 |
| MOD_SUMO_rev_2 | 162 | 171 | PF00179 | 0.489 |
| MOD_SUMO_rev_2 | 228 | 233 | PF00179 | 0.545 |
| TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.459 |
| TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.388 |
| TRG_NES_CRM1_1 | 279 | 289 | PF08389 | 0.538 |
| TRG_NLS_MonoExtC_3 | 200 | 205 | PF00514 | 0.354 |
| TRG_NLS_MonoExtN_4 | 201 | 206 | PF00514 | 0.354 |
| TRG_Pf-PMV_PEXEL_1 | 42 | 46 | PF00026 | 0.511 |
| TRG_PTS1 | 429 | 432 | PF00515 | 0.474 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PAM2 | Leptomonas seymouri | 78% | 100% |
| A0A0S4JIK6 | Bodo saltans | 53% | 98% |
| A0A1X0NNC6 | Trypanosomatidae | 60% | 100% |
| A0A3R7KWA9 | Trypanosoma rangeli | 58% | 100% |
| A0A3S7XA87 | Leishmania donovani | 94% | 100% |
| A4HNK9 | Leishmania braziliensis | 87% | 100% |
| A4ICY4 | Leishmania infantum | 94% | 100% |
| O34450 | Bacillus subtilis (strain 168) | 27% | 100% |
| Q4Q275 | Leishmania major | 93% | 100% |
| Q8XAC3 | Escherichia coli O157:H7 | 27% | 100% |
| Q9VR81 | Drosophila melanogaster | 24% | 100% |
| V5C012 | Trypanosoma cruzi | 58% | 100% |