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: A4HNK9
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_MEL_PAP_1 | 126 | 132 | PF00089 | 0.239 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.315 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.323 |
CLV_PCSK_PC1ET2_1 | 128 | 130 | PF00082 | 0.278 |
CLV_PCSK_PC1ET2_1 | 169 | 171 | PF00082 | 0.294 |
CLV_PCSK_PC1ET2_1 | 409 | 411 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.233 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.233 |
DOC_CKS1_1 | 11 | 16 | PF01111 | 0.228 |
DOC_CYCLIN_RxL_1 | 194 | 201 | PF00134 | 0.474 |
DOC_MAPK_gen_1 | 202 | 208 | PF00069 | 0.492 |
DOC_MAPK_gen_1 | 393 | 400 | PF00069 | 0.428 |
DOC_PP4_FxxP_1 | 64 | 67 | PF00568 | 0.425 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.272 |
DOC_USP7_UBL2_3 | 42 | 46 | PF12436 | 0.391 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.222 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.425 |
LIG_14-3-3_CanoR_1 | 339 | 345 | PF00244 | 0.481 |
LIG_APCC_ABBA_1 | 183 | 188 | PF00400 | 0.439 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.304 |
LIG_BRCT_BRCA1_1 | 107 | 111 | PF00533 | 0.425 |
LIG_Clathr_ClatBox_1 | 280 | 284 | PF01394 | 0.481 |
LIG_Clathr_ClatBox_1 | 361 | 365 | PF01394 | 0.377 |
LIG_Clathr_ClatBox_1 | 397 | 401 | PF01394 | 0.494 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.483 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.471 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.439 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.447 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.489 |
LIG_FHA_2 | 48 | 54 | PF00498 | 0.322 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.482 |
LIG_Integrin_isoDGR_2 | 319 | 321 | PF01839 | 0.225 |
LIG_LIR_Apic_2 | 61 | 67 | PF02991 | 0.266 |
LIG_LIR_Gen_1 | 353 | 362 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 166 | 171 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 353 | 358 | PF02991 | 0.426 |
LIG_PTB_Apo_2 | 86 | 93 | PF02174 | 0.439 |
LIG_PTB_Phospho_1 | 86 | 92 | PF10480 | 0.457 |
LIG_SH2_CRK | 422 | 426 | PF00017 | 0.363 |
LIG_SH2_STAT3 | 92 | 95 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.478 |
LIG_SH3_3 | 255 | 261 | PF00018 | 0.494 |
LIG_SUMO_SIM_anti_2 | 2 | 8 | PF11976 | 0.312 |
LIG_SUMO_SIM_anti_2 | 273 | 279 | PF11976 | 0.481 |
LIG_SUMO_SIM_anti_2 | 299 | 305 | PF11976 | 0.438 |
LIG_SUMO_SIM_par_1 | 146 | 152 | PF11976 | 0.364 |
LIG_SUMO_SIM_par_1 | 22 | 28 | PF11976 | 0.372 |
LIG_TRAF2_1 | 227 | 230 | PF00917 | 0.481 |
LIG_TRAF2_1 | 58 | 61 | PF00917 | 0.393 |
LIG_TRAF2_1 | 93 | 96 | PF00917 | 0.364 |
LIG_UBA3_1 | 219 | 224 | PF00899 | 0.425 |
LIG_UBA3_1 | 361 | 368 | PF00899 | 0.468 |
LIG_WRC_WIRS_1 | 241 | 246 | PF05994 | 0.439 |
MOD_CDK_SPxK_1 | 10 | 16 | PF00069 | 0.325 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.524 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.494 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.315 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.487 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.477 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.406 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.483 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.445 |
MOD_Cter_Amidation | 391 | 394 | PF01082 | 0.213 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.297 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.449 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.476 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.324 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.394 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.377 |
MOD_LATS_1 | 210 | 216 | PF00433 | 0.425 |
MOD_LATS_1 | 245 | 251 | PF00433 | 0.366 |
MOD_N-GLC_1 | 239 | 244 | PF02516 | 0.322 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.517 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.425 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.425 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.466 |
MOD_NEK2_1 | 333 | 338 | PF00069 | 0.526 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.493 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.516 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.377 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.361 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.494 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.560 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.436 |
MOD_Plk_1 | 90 | 96 | PF00069 | 0.439 |
MOD_Plk_2-3 | 403 | 409 | PF00069 | 0.494 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.425 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.417 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.425 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.481 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.472 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.227 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.425 |
MOD_SUMO_rev_2 | 152 | 161 | PF00179 | 0.517 |
MOD_SUMO_rev_2 | 162 | 171 | PF00179 | 0.324 |
MOD_SUMO_rev_2 | 228 | 233 | PF00179 | 0.526 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.225 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.349 |
TRG_NES_CRM1_1 | 279 | 289 | PF08389 | 0.517 |
TRG_NES_CRM1_1 | 353 | 365 | PF08389 | 0.378 |
TRG_Pf-PMV_PEXEL_1 | 197 | 201 | PF00026 | 0.311 |
TRG_PTS1 | 429 | 432 | PF00515 | 0.415 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAM2 | Leptomonas seymouri | 78% | 100% |
A0A0S4JIK6 | Bodo saltans | 53% | 98% |
A0A1X0NNC6 | Trypanosomatidae | 59% | 100% |
A0A3R7KWA9 | Trypanosoma rangeli | 58% | 100% |
A0A3S7XA87 | Leishmania donovani | 88% | 100% |
A4ICY4 | Leishmania infantum | 88% | 100% |
E9ASC1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
O34450 | Bacillus subtilis (strain 168) | 26% | 100% |
Q4Q275 | Leishmania major | 87% | 100% |
Q8XAC3 | Escherichia coli O157:H7 | 25% | 100% |
Q9VR81 | Drosophila melanogaster | 25% | 100% |
V5C012 | Trypanosoma cruzi | 59% | 100% |