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: 0, no: 30 |
NetGPI | no | yes: 0, no: 30 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 31 |
GO:0042995 | cell projection | 2 | 31 |
GO:0043226 | organelle | 2 | 31 |
GO:0043227 | membrane-bounded organelle | 3 | 31 |
GO:0110165 | cellular anatomical entity | 1 | 31 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 31 |
GO:0005743 | mitochondrial inner membrane | 5 | 2 |
GO:0016020 | membrane | 2 | 2 |
GO:0019866 | organelle inner membrane | 4 | 2 |
GO:0031090 | organelle membrane | 3 | 2 |
GO:0031966 | mitochondrial membrane | 4 | 2 |
GO:0000151 | ubiquitin ligase complex | 3 | 1 |
GO:0019005 | SCF ubiquitin ligase complex | 5 | 1 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: A4HCY0
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 3 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 3 |
GO:0008152 | metabolic process | 1 | 4 |
GO:0009987 | cellular process | 1 | 4 |
GO:0016310 | phosphorylation | 5 | 3 |
GO:0044237 | cellular metabolic process | 2 | 4 |
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0031146 | SCF-dependent proteasomal ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
GO:0003824 | catalytic activity | 1 | 5 |
GO:0016301 | kinase activity | 4 | 3 |
GO:0016740 | transferase activity | 2 | 3 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 3 |
GO:0016787 | hydrolase activity | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.535 |
CLV_PCSK_KEX2_1 | 380 | 382 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 9 | 13 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.338 |
DEG_APCC_DBOX_1 | 7 | 15 | PF00400 | 0.535 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.428 |
DEG_SCF_FBW7_1 | 243 | 250 | PF00400 | 0.473 |
DOC_CKS1_1 | 244 | 249 | PF01111 | 0.216 |
DOC_CYCLIN_RxL_1 | 158 | 171 | PF00134 | 0.378 |
DOC_MAPK_gen_1 | 135 | 144 | PF00069 | 0.386 |
DOC_MAPK_gen_1 | 158 | 167 | PF00069 | 0.337 |
DOC_MAPK_gen_1 | 262 | 269 | PF00069 | 0.208 |
DOC_MAPK_MEF2A_6 | 137 | 146 | PF00069 | 0.419 |
DOC_PP1_RVXF_1 | 284 | 290 | PF00149 | 0.426 |
DOC_PP2B_LxvP_1 | 241 | 244 | PF13499 | 0.445 |
DOC_PP4_FxxP_1 | 106 | 109 | PF00568 | 0.487 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.354 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.454 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.394 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.500 |
LIG_14-3-3_CanoR_1 | 125 | 131 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 19 | 28 | PF00244 | 0.657 |
LIG_14-3-3_CanoR_1 | 294 | 298 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 71 | 81 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 8 | 17 | PF00244 | 0.541 |
LIG_Actin_WH2_2 | 412 | 428 | PF00022 | 0.347 |
LIG_APCC_ABBA_1 | 188 | 193 | PF00400 | 0.477 |
LIG_BRCT_BRCA1_1 | 17 | 21 | PF00533 | 0.648 |
LIG_BRCT_BRCA1_1 | 201 | 205 | PF00533 | 0.426 |
LIG_BRCT_BRCA1_1 | 321 | 325 | PF00533 | 0.369 |
LIG_BRCT_BRCA1_2 | 321 | 327 | PF00533 | 0.371 |
LIG_Clathr_ClatBox_1 | 347 | 351 | PF01394 | 0.346 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.351 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.481 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.454 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.371 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.464 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.356 |
LIG_IRF3_LxIS_1 | 361 | 368 | PF10401 | 0.260 |
LIG_LIR_Apic_2 | 103 | 109 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 343 | 350 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 105 | 110 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 143 | 149 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 343 | 348 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 59 | 64 | PF02991 | 0.516 |
LIG_MLH1_MIPbox_1 | 202 | 206 | PF16413 | 0.246 |
LIG_NRBOX | 237 | 243 | PF00104 | 0.461 |
LIG_PCNA_yPIPBox_3 | 437 | 446 | PF02747 | 0.288 |
LIG_PTB_Apo_2 | 101 | 108 | PF02174 | 0.294 |
LIG_SH2_CRK | 345 | 349 | PF00017 | 0.505 |
LIG_SH2_CRK | 84 | 88 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 3 | 6 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.467 |
LIG_SH3_3 | 14 | 20 | PF00018 | 0.557 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.366 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.516 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.458 |
LIG_SUMO_SIM_anti_2 | 118 | 123 | PF11976 | 0.431 |
LIG_SUMO_SIM_anti_2 | 140 | 146 | PF11976 | 0.423 |
LIG_SUMO_SIM_anti_2 | 293 | 300 | PF11976 | 0.272 |
LIG_SUMO_SIM_anti_2 | 447 | 455 | PF11976 | 0.505 |
LIG_SUMO_SIM_par_1 | 357 | 362 | PF11976 | 0.307 |
LIG_TRAF2_1 | 402 | 405 | PF00917 | 0.491 |
LIG_TRAF2_1 | 455 | 458 | PF00917 | 0.387 |
LIG_TYR_ITSM | 341 | 348 | PF00017 | 0.491 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.445 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.375 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.554 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.404 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.454 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.399 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.344 |
MOD_CK2_1 | 444 | 450 | PF00069 | 0.447 |
MOD_CK2_1 | 452 | 458 | PF00069 | 0.465 |
MOD_Cter_Amidation | 69 | 72 | PF01082 | 0.470 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.407 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.456 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.600 |
MOD_GlcNHglycan | 277 | 281 | PF01048 | 0.418 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.440 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.339 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.601 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.379 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.338 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.410 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.381 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.405 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.315 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.379 |
MOD_N-GLC_1 | 216 | 221 | PF02516 | 0.224 |
MOD_N-GLC_1 | 411 | 416 | PF02516 | 0.364 |
MOD_N-GLC_1 | 59 | 64 | PF02516 | 0.485 |
MOD_N-GLC_2 | 429 | 431 | PF02516 | 0.324 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.475 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.330 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.358 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.387 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.420 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.345 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.401 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.379 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.320 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.337 |
MOD_PKA_1 | 163 | 169 | PF00069 | 0.439 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.337 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.486 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.548 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.432 |
MOD_Plk_1 | 276 | 282 | PF00069 | 0.422 |
MOD_Plk_1 | 290 | 296 | PF00069 | 0.255 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.474 |
MOD_Plk_1 | 444 | 450 | PF00069 | 0.428 |
MOD_Plk_1 | 59 | 65 | PF00069 | 0.506 |
MOD_Plk_2-3 | 265 | 271 | PF00069 | 0.289 |
MOD_Plk_2-3 | 445 | 451 | PF00069 | 0.535 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.392 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.419 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.424 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.423 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.442 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.556 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.390 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.374 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.420 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.637 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.397 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.492 |
MOD_SUMO_rev_2 | 404 | 411 | PF00179 | 0.421 |
TRG_DiLeu_BaEn_4 | 273 | 279 | PF01217 | 0.299 |
TRG_DiLeu_BaEn_4 | 351 | 357 | PF01217 | 0.480 |
TRG_DiLeu_BaLyEn_6 | 439 | 444 | PF01217 | 0.536 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.527 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.529 |
TRG_ER_diArg_1 | 379 | 381 | PF00400 | 0.411 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2F4 | Leptomonas seymouri | 70% | 95% |
A0A0N0P8N9 | Leptomonas seymouri | 25% | 70% |
A0A0N1IGA0 | Leptomonas seymouri | 25% | 100% |
A0A0S4IRL6 | Bodo saltans | 24% | 100% |
A0A0S4IS80 | Bodo saltans | 30% | 90% |
A0A0S4JR29 | Bodo saltans | 26% | 91% |
A0A0S4JR64 | Bodo saltans | 23% | 71% |
A0A1X0NEN5 | Trypanosomatidae | 28% | 80% |
A0A1X0NG16 | Trypanosomatidae | 28% | 80% |
A0A1X0NXB3 | Trypanosomatidae | 55% | 95% |
A0A1X0P4M6 | Trypanosomatidae | 24% | 80% |
A0A3Q8IAE2 | Leishmania donovani | 26% | 74% |
A0A3S5H5M6 | Leishmania donovani | 26% | 87% |
A0A3S5H7C2 | Leishmania donovani | 90% | 95% |
A0A422NP39 | Trypanosoma rangeli | 52% | 95% |
A4HSP5 | Leishmania infantum | 26% | 87% |
A4I0G3 | Leishmania infantum | 90% | 95% |
C9ZS86 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 85% |
C9ZV75 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 95% |
D0A0X4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 69% |
E9AIU4 | Leishmania braziliensis | 25% | 84% |
E9AWC6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 95% |
Q4QB46 | Leishmania major | 89% | 100% |
Q4QD45 | Leishmania major | 26% | 69% |
Q4QFY4 | Leishmania major | 28% | 100% |
Q4QJ80 | Leishmania major | 26% | 81% |
V5BD47 | Trypanosoma cruzi | 24% | 100% |
V5BMQ2 | Trypanosoma cruzi | 27% | 83% |
V5DFL9 | Trypanosoma cruzi | 51% | 95% |