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. | yes | yes: 15 |
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: 6, no: 4 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0017177 | glucosidase II complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140534 | endoplasmic reticulum protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
Related structures:
AlphaFold database: E9AY78
Term | Name | Level | Count |
---|---|---|---|
GO:0006491 | N-glycan processing | 5 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009100 | glycoprotein metabolic process | 4 | 8 |
GO:0009987 | cellular process | 1 | 10 |
GO:0019538 | protein metabolic process | 3 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 8 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 8 |
GO:0006793 | phosphorus metabolic process | 3 | 2 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 2 |
GO:0016310 | phosphorylation | 5 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016301 | kinase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 143 | 149 | PF00089 | 0.435 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 35 | 37 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.550 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.627 |
CLV_PCSK_PC1ET2_1 | 102 | 104 | PF00082 | 0.358 |
CLV_PCSK_PC1ET2_1 | 202 | 204 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.568 |
DOC_AGCK_PIF_1 | 235 | 240 | PF00069 | 0.368 |
DOC_CKS1_1 | 329 | 334 | PF01111 | 0.300 |
DOC_CYCLIN_RxL_1 | 203 | 216 | PF00134 | 0.301 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 217 | 226 | PF00134 | 0.220 |
DOC_PP4_FxxP_1 | 329 | 332 | PF00568 | 0.287 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.520 |
DOC_USP7_UBL2_3 | 170 | 174 | PF12436 | 0.687 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.300 |
LIG_14-3-3_CanoR_1 | 140 | 146 | PF00244 | 0.606 |
LIG_AP_GAE_1 | 64 | 70 | PF02883 | 0.516 |
LIG_Clathr_ClatBox_1 | 16 | 20 | PF01394 | 0.334 |
LIG_Clathr_ClatBox_1 | 314 | 318 | PF01394 | 0.343 |
LIG_deltaCOP1_diTrp_1 | 289 | 295 | PF00928 | 0.282 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.471 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.306 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.212 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.290 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.669 |
LIG_FHA_2 | 111 | 117 | PF00498 | 0.626 |
LIG_FHA_2 | 177 | 183 | PF00498 | 0.631 |
LIG_FHA_2 | 223 | 229 | PF00498 | 0.358 |
LIG_LIR_Gen_1 | 20 | 31 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 237 | 248 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 45 | 53 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 20 | 26 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 232 | 238 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 239 | 243 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 264 | 268 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 45 | 51 | PF02991 | 0.637 |
LIG_MYND_3 | 30 | 34 | PF01753 | 0.489 |
LIG_Pex14_2 | 231 | 235 | PF04695 | 0.368 |
LIG_SH2_CRK | 23 | 27 | PF00017 | 0.443 |
LIG_SH2_CRK | 240 | 244 | PF00017 | 0.335 |
LIG_SH2_CRK | 325 | 329 | PF00017 | 0.273 |
LIG_SH2_GRB2like | 288 | 291 | PF00017 | 0.368 |
LIG_SH2_SRC | 288 | 291 | PF00017 | 0.382 |
LIG_SH2_STAP1 | 23 | 27 | PF00017 | 0.443 |
LIG_SH2_STAP1 | 238 | 242 | PF00017 | 0.285 |
LIG_SH2_STAP1 | 273 | 277 | PF00017 | 0.340 |
LIG_SH2_STAP1 | 63 | 67 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.630 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.302 |
LIG_SH3_3 | 304 | 310 | PF00018 | 0.309 |
LIG_SH3_3 | 314 | 320 | PF00018 | 0.263 |
LIG_SUMO_SIM_par_1 | 15 | 22 | PF11976 | 0.424 |
LIG_SUMO_SIM_par_1 | 313 | 319 | PF11976 | 0.327 |
LIG_TRAF2_1 | 225 | 228 | PF00917 | 0.241 |
LIG_TRAF2_1 | 316 | 319 | PF00917 | 0.368 |
LIG_TYR_ITSM | 19 | 26 | PF00017 | 0.413 |
MOD_CDK_SPK_2 | 169 | 174 | PF00069 | 0.456 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.365 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.349 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.629 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.564 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.543 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.439 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.393 |
MOD_CMANNOS | 292 | 295 | PF00535 | 0.420 |
MOD_GlcNHglycan | 104 | 108 | PF01048 | 0.528 |
MOD_GlcNHglycan | 161 | 165 | PF01048 | 0.463 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.592 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.591 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.380 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.410 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.593 |
MOD_N-GLC_1 | 152 | 157 | PF02516 | 0.520 |
MOD_N-GLC_1 | 176 | 181 | PF02516 | 0.574 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.302 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.390 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.352 |
MOD_OFUCOSY | 149 | 156 | PF10250 | 0.432 |
MOD_PIKK_1 | 281 | 287 | PF00454 | 0.304 |
MOD_PKA_1 | 102 | 108 | PF00069 | 0.318 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.346 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.627 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.543 |
MOD_PKA_2 | 77 | 83 | PF00069 | 0.417 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.560 |
MOD_Plk_1 | 152 | 158 | PF00069 | 0.403 |
MOD_Plk_1 | 176 | 182 | PF00069 | 0.431 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.380 |
MOD_Plk_1 | 236 | 242 | PF00069 | 0.366 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.287 |
MOD_Plk_1 | 281 | 287 | PF00069 | 0.287 |
MOD_Plk_2-3 | 229 | 235 | PF00069 | 0.302 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.399 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.336 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.294 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.448 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.300 |
MOD_SUMO_rev_2 | 104 | 113 | PF00179 | 0.479 |
MOD_SUMO_rev_2 | 199 | 204 | PF00179 | 0.285 |
TRG_DiLeu_BaEn_4 | 228 | 234 | PF01217 | 0.220 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.441 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.287 |
TRG_ER_diArg_1 | 6 | 9 | PF00400 | 0.631 |
TRG_NLS_MonoExtC_3 | 193 | 199 | PF00514 | 0.304 |
TRG_NLS_MonoExtN_4 | 193 | 198 | PF00514 | 0.315 |
TRG_Pf-PMV_PEXEL_1 | 14 | 18 | PF00026 | 0.464 |
TRG_Pf-PMV_PEXEL_1 | 224 | 228 | PF00026 | 0.536 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4ILH9 | Bodo saltans | 32% | 70% |
A0A1X0NSB3 | Trypanosomatidae | 39% | 70% |
A0A3Q8IDT4 | Leishmania donovani | 87% | 100% |
A0A3R7L6D4 | Trypanosoma rangeli | 38% | 70% |
A4HEV5 | Leishmania braziliensis | 54% | 100% |
A4I229 | Leishmania infantum | 88% | 100% |
C9ZRX6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 70% |
Q4Q994 | Leishmania major | 82% | 100% |
V5DQZ5 | Trypanosoma cruzi | 36% | 70% |