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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 4 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A0A3Q8IKN0
Term | Name | Level | Count |
---|---|---|---|
GO:0000272 | polysaccharide catabolic process | 5 | 3 |
GO:0005975 | carbohydrate metabolic process | 3 | 3 |
GO:0005976 | polysaccharide metabolic process | 4 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009056 | catabolic process | 2 | 3 |
GO:0009057 | macromolecule catabolic process | 4 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0010383 | cell wall polysaccharide metabolic process | 5 | 3 |
GO:0010410 | hemicellulose metabolic process | 6 | 3 |
GO:0016052 | carbohydrate catabolic process | 4 | 3 |
GO:0016998 | cell wall macromolecule catabolic process | 5 | 3 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0044036 | cell wall macromolecule metabolic process | 4 | 3 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0044248 | cellular catabolic process | 3 | 3 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 3 |
GO:0044262 | obsolete cellular carbohydrate metabolic process | 3 | 3 |
GO:0044264 | obsolete cellular polysaccharide metabolic process | 4 | 3 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 3 |
GO:0044347 | cell wall polysaccharide catabolic process | 6 | 3 |
GO:0045491 | xylan metabolic process | 7 | 3 |
GO:0045493 | xylan catabolic process | 8 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:1901575 | organic substance catabolic process | 3 | 3 |
GO:2000895 | hemicellulose catabolic process | 7 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0016787 | hydrolase activity | 2 | 3 |
GO:0016798 | hydrolase activity, acting on glycosyl bonds | 3 | 3 |
GO:0004553 | hydrolase activity, hydrolyzing O-glycosyl compounds | 4 | 1 |
GO:0031176 | endo-1,4-beta-xylanase activity | 6 | 1 |
GO:0097599 | xylanase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 203 | 205 | PF00675 | 0.272 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.347 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.343 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.272 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.291 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.305 |
DEG_SCF_FBW7_1 | 128 | 135 | PF00400 | 0.339 |
DOC_CKS1_1 | 129 | 134 | PF01111 | 0.357 |
DOC_MAPK_gen_1 | 203 | 210 | PF00069 | 0.247 |
DOC_MAPK_gen_1 | 343 | 349 | PF00069 | 0.384 |
DOC_MAPK_MEF2A_6 | 203 | 210 | PF00069 | 0.274 |
DOC_MAPK_MEF2A_6 | 239 | 247 | PF00069 | 0.222 |
DOC_PP1_RVXF_1 | 352 | 358 | PF00149 | 0.249 |
DOC_PP1_RVXF_1 | 409 | 416 | PF00149 | 0.504 |
DOC_PP4_FxxP_1 | 27 | 30 | PF00568 | 0.490 |
DOC_PP4_FxxP_1 | 63 | 66 | PF00568 | 0.347 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.394 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.393 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.365 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.601 |
LIG_APCC_ABBA_1 | 275 | 280 | PF00400 | 0.222 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.555 |
LIG_eIF4E_1 | 205 | 211 | PF01652 | 0.274 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.398 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.260 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.337 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.460 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.463 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.274 |
LIG_FHA_2 | 283 | 289 | PF00498 | 0.274 |
LIG_FHA_2 | 308 | 314 | PF00498 | 0.274 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.251 |
LIG_FHA_2 | 48 | 54 | PF00498 | 0.470 |
LIG_LIR_Apic_2 | 26 | 30 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.226 |
LIG_LIR_Nem_3 | 327 | 332 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.327 |
LIG_LYPXL_yS_3 | 205 | 208 | PF13949 | 0.222 |
LIG_MYND_1 | 128 | 132 | PF01753 | 0.341 |
LIG_PCNA_yPIPBox_3 | 284 | 298 | PF02747 | 0.251 |
LIG_SH2_PTP2 | 147 | 150 | PF00017 | 0.285 |
LIG_SH2_PTP2 | 190 | 193 | PF00017 | 0.217 |
LIG_SH2_SRC | 147 | 150 | PF00017 | 0.285 |
LIG_SH2_SRC | 190 | 193 | PF00017 | 0.222 |
LIG_SH2_SRC | 64 | 67 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.195 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.134 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.244 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.455 |
LIG_SH3_2 | 152 | 157 | PF14604 | 0.352 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.518 |
LIG_SH3_3 | 126 | 132 | PF00018 | 0.368 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.307 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.323 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.623 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.507 |
LIG_SUMO_SIM_anti_2 | 241 | 250 | PF11976 | 0.274 |
LIG_SUMO_SIM_par_1 | 120 | 125 | PF11976 | 0.418 |
LIG_TRAF2_1 | 183 | 186 | PF00917 | 0.274 |
LIG_UBA3_1 | 243 | 248 | PF00899 | 0.251 |
LIG_WRC_WIRS_1 | 24 | 29 | PF05994 | 0.512 |
LIG_WW_1 | 192 | 195 | PF00397 | 0.222 |
MOD_CDK_SPxxK_3 | 11 | 18 | PF00069 | 0.517 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.251 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.562 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.251 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.523 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.217 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.274 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.471 |
MOD_CMANNOS | 395 | 398 | PF00535 | 0.250 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.531 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.429 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.251 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.247 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.298 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.625 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.412 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.260 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.222 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.401 |
MOD_N-GLC_1 | 54 | 59 | PF02516 | 0.381 |
MOD_N-GLC_2 | 156 | 158 | PF02516 | 0.391 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.304 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.241 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.328 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.546 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.478 |
MOD_Plk_1 | 411 | 417 | PF00069 | 0.388 |
MOD_Plk_1 | 54 | 60 | PF00069 | 0.296 |
MOD_Plk_2-3 | 269 | 275 | PF00069 | 0.274 |
MOD_Plk_2-3 | 47 | 53 | PF00069 | 0.341 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.453 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.332 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.532 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.359 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.600 |
MOD_SUMO_rev_2 | 232 | 241 | PF00179 | 0.274 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.222 |
TRG_ENDOCYTIC_2 | 317 | 320 | PF00928 | 0.357 |
TRG_ER_diArg_1 | 203 | 205 | PF00400 | 0.274 |
TRG_ER_diArg_1 | 342 | 344 | PF00400 | 0.347 |
TRG_ER_diArg_1 | 386 | 388 | PF00400 | 0.343 |
TRG_ER_diArg_1 | 41 | 44 | PF00400 | 0.524 |
TRG_Pf-PMV_PEXEL_1 | 358 | 362 | PF00026 | 0.305 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM32 | Leptomonas seymouri | 56% | 100% |
A0A1X0NWX5 | Trypanosomatidae | 42% | 100% |
A4HYV9 | Leishmania infantum | 98% | 100% |
E9AUQ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
P31471 | Escherichia coli (strain K12) | 25% | 100% |