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: A4HYV9
Term | Name | Level | Count |
---|---|---|---|
GO:0000272 | polysaccharide catabolic process | 5 | 4 |
GO:0005975 | carbohydrate metabolic process | 3 | 4 |
GO:0005976 | polysaccharide metabolic process | 4 | 4 |
GO:0008152 | metabolic process | 1 | 4 |
GO:0009056 | catabolic process | 2 | 4 |
GO:0009057 | macromolecule catabolic process | 4 | 4 |
GO:0009987 | cellular process | 1 | 4 |
GO:0010383 | cell wall polysaccharide metabolic process | 5 | 4 |
GO:0010410 | hemicellulose metabolic process | 6 | 4 |
GO:0016052 | carbohydrate catabolic process | 4 | 4 |
GO:0016998 | cell wall macromolecule catabolic process | 5 | 4 |
GO:0043170 | macromolecule metabolic process | 3 | 4 |
GO:0044036 | cell wall macromolecule metabolic process | 4 | 4 |
GO:0044237 | cellular metabolic process | 2 | 4 |
GO:0044238 | primary metabolic process | 2 | 4 |
GO:0044248 | cellular catabolic process | 3 | 4 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 4 |
GO:0044262 | obsolete cellular carbohydrate metabolic process | 3 | 4 |
GO:0044264 | obsolete cellular polysaccharide metabolic process | 4 | 4 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 4 |
GO:0044347 | cell wall polysaccharide catabolic process | 6 | 4 |
GO:0045491 | xylan metabolic process | 7 | 4 |
GO:0045493 | xylan catabolic process | 8 | 4 |
GO:0071704 | organic substance metabolic process | 2 | 4 |
GO:1901575 | organic substance catabolic process | 3 | 4 |
GO:2000895 | hemicellulose catabolic process | 7 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 4 |
GO:0004553 | hydrolase activity, hydrolyzing O-glycosyl compounds | 4 | 2 |
GO:0016787 | hydrolase activity | 2 | 4 |
GO:0016798 | hydrolase activity, acting on glycosyl bonds | 3 | 4 |
GO:0031176 | endo-1,4-beta-xylanase activity | 6 | 2 |
GO:0097599 | xylanase activity | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.456 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.399 |
DEG_SCF_FBW7_1 | 129 | 136 | PF00400 | 0.522 |
DOC_CKS1_1 | 130 | 135 | PF01111 | 0.463 |
DOC_CKS1_1 | 5 | 10 | PF01111 | 0.536 |
DOC_MAPK_gen_1 | 204 | 211 | PF00069 | 0.362 |
DOC_MAPK_gen_1 | 344 | 350 | PF00069 | 0.394 |
DOC_MAPK_MEF2A_6 | 204 | 211 | PF00069 | 0.387 |
DOC_MAPK_MEF2A_6 | 240 | 248 | PF00069 | 0.332 |
DOC_PP1_RVXF_1 | 353 | 359 | PF00149 | 0.363 |
DOC_PP1_RVXF_1 | 410 | 417 | PF00149 | 0.492 |
DOC_PP4_FxxP_1 | 27 | 30 | PF00568 | 0.594 |
DOC_PP4_FxxP_1 | 64 | 67 | PF00568 | 0.458 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.554 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.417 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.673 |
LIG_APCC_ABBA_1 | 276 | 281 | PF00400 | 0.332 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.643 |
LIG_eIF4E_1 | 206 | 212 | PF01652 | 0.387 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.466 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.375 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.335 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.477 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.484 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.387 |
LIG_FHA_2 | 284 | 290 | PF00498 | 0.387 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.387 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.440 |
LIG_FHA_2 | 49 | 55 | PF00498 | 0.463 |
LIG_LIR_Apic_2 | 26 | 30 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 328 | 333 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.510 |
LIG_LYPXL_yS_3 | 206 | 209 | PF13949 | 0.332 |
LIG_MYND_1 | 129 | 133 | PF01753 | 0.524 |
LIG_PCNA_yPIPBox_3 | 285 | 299 | PF02747 | 0.440 |
LIG_SH2_PTP2 | 148 | 151 | PF00017 | 0.390 |
LIG_SH2_PTP2 | 191 | 194 | PF00017 | 0.353 |
LIG_SH2_SRC | 148 | 151 | PF00017 | 0.390 |
LIG_SH2_SRC | 191 | 194 | PF00017 | 0.332 |
LIG_SH2_SRC | 65 | 68 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.213 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.533 |
LIG_SH3_2 | 153 | 158 | PF14604 | 0.466 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.546 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.333 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.403 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.624 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.526 |
LIG_SUMO_SIM_anti_2 | 242 | 251 | PF11976 | 0.387 |
LIG_SUMO_SIM_par_1 | 121 | 126 | PF11976 | 0.487 |
LIG_TRAF2_1 | 184 | 187 | PF00917 | 0.387 |
LIG_UBA3_1 | 244 | 249 | PF00899 | 0.440 |
LIG_WRC_WIRS_1 | 24 | 29 | PF05994 | 0.626 |
LIG_WW_1 | 193 | 196 | PF00397 | 0.332 |
MOD_CDK_SPxxK_3 | 11 | 18 | PF00069 | 0.628 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.440 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.440 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.643 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.353 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.387 |
MOD_CK2_1 | 48 | 54 | PF00069 | 0.460 |
MOD_CMANNOS | 396 | 399 | PF00535 | 0.320 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.693 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.518 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.440 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.432 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.332 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.661 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.522 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.375 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.302 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.468 |
MOD_N-GLC_1 | 56 | 61 | PF02516 | 0.513 |
MOD_N-GLC_2 | 157 | 159 | PF02516 | 0.559 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.440 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.330 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.380 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.690 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.539 |
MOD_Plk_1 | 412 | 418 | PF00069 | 0.541 |
MOD_Plk_2-3 | 270 | 276 | PF00069 | 0.387 |
MOD_Plk_2-3 | 48 | 54 | PF00069 | 0.460 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.554 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.442 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.631 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.412 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.671 |
MOD_SUMO_rev_2 | 233 | 242 | PF00179 | 0.387 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 318 | 321 | PF00928 | 0.357 |
TRG_ER_diArg_1 | 204 | 206 | PF00400 | 0.362 |
TRG_ER_diArg_1 | 343 | 345 | PF00400 | 0.362 |
TRG_ER_diArg_1 | 387 | 389 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 42 | 45 | PF00400 | 0.586 |
TRG_Pf-PMV_PEXEL_1 | 359 | 363 | PF00026 | 0.416 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM32 | Leptomonas seymouri | 60% | 100% |
A0A1X0NWX5 | Trypanosomatidae | 43% | 100% |
A0A3Q8IKN0 | Leishmania donovani | 98% | 100% |
E9AUQ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 99% |
P31471 | Escherichia coli (strain K12) | 25% | 100% |