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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 12 |
GO:0008180 | COP9 signalosome | 3 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0140513 | nuclear protein-containing complex | 2 | 12 |
GO:0000502 | proteasome complex | 3 | 3 |
GO:0140535 | intracellular protein-containing complex | 2 | 3 |
GO:1902494 | catalytic complex | 2 | 3 |
GO:1905368 | peptidase complex | 3 | 3 |
GO:1905369 | endopeptidase complex | 4 | 3 |
Related structures:
AlphaFold database: A4HEC5
Term | Name | Level | Count |
---|---|---|---|
GO:0000338 | protein deneddylation | 6 | 1 |
GO:0006508 | proteolysis | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0070646 | protein modification by small protein removal | 5 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.387 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.342 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.431 |
DEG_COP1_1 | 141 | 151 | PF00400 | 0.438 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.608 |
DOC_CYCLIN_RxL_1 | 194 | 202 | PF00134 | 0.498 |
DOC_CYCLIN_yCln2_LP_2 | 327 | 333 | PF00134 | 0.514 |
DOC_MAPK_DCC_7 | 222 | 232 | PF00069 | 0.572 |
DOC_MAPK_gen_1 | 125 | 133 | PF00069 | 0.497 |
DOC_MAPK_gen_1 | 153 | 159 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 125 | 133 | PF00069 | 0.459 |
DOC_PP1_RVXF_1 | 404 | 411 | PF00149 | 0.571 |
DOC_PP1_RVXF_1 | 90 | 97 | PF00149 | 0.425 |
DOC_PP2B_LxvP_1 | 327 | 330 | PF13499 | 0.548 |
DOC_PP4_FxxP_1 | 96 | 99 | PF00568 | 0.519 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.284 |
DOC_USP7_UBL2_3 | 108 | 112 | PF12436 | 0.401 |
DOC_USP7_UBL2_3 | 64 | 68 | PF12436 | 0.330 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.505 |
LIG_14-3-3_CanoR_1 | 125 | 130 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 153 | 158 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 255 | 260 | PF00244 | 0.275 |
LIG_14-3-3_CanoR_1 | 412 | 418 | PF00244 | 0.600 |
LIG_Actin_WH2_2 | 200 | 216 | PF00022 | 0.255 |
LIG_APCC_ABBA_1 | 342 | 347 | PF00400 | 0.509 |
LIG_APCC_ABBAyCdc20_2 | 154 | 160 | PF00400 | 0.485 |
LIG_BRCT_BRCA1_1 | 361 | 365 | PF00533 | 0.561 |
LIG_deltaCOP1_diTrp_1 | 247 | 257 | PF00928 | 0.380 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.435 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.400 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.596 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.560 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.506 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.542 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.582 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.531 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.318 |
LIG_FHA_2 | 335 | 341 | PF00498 | 0.454 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.510 |
LIG_GBD_Chelix_1 | 316 | 324 | PF00786 | 0.180 |
LIG_IRF3_LxIS_1 | 315 | 321 | PF10401 | 0.446 |
LIG_LIR_Gen_1 | 208 | 218 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 321 | 331 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 87 | 96 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 141 | 146 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 202 | 207 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 208 | 213 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 321 | 326 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 339 | 345 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 362 | 368 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 66 | 70 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 87 | 93 | PF02991 | 0.439 |
LIG_RPA_C_Fungi | 250 | 262 | PF08784 | 0.504 |
LIG_SH2_CRK | 204 | 208 | PF00017 | 0.419 |
LIG_SH2_CRK | 273 | 277 | PF00017 | 0.445 |
LIG_SH2_CRK | 90 | 94 | PF00017 | 0.412 |
LIG_SH2_GRB2like | 17 | 20 | PF00017 | 0.695 |
LIG_SH2_PTP2 | 278 | 281 | PF00017 | 0.421 |
LIG_SH2_PTP2 | 345 | 348 | PF00017 | 0.454 |
LIG_SH2_SRC | 164 | 167 | PF00017 | 0.403 |
LIG_SH2_SRC | 17 | 20 | PF00017 | 0.680 |
LIG_SH2_SRC | 34 | 37 | PF00017 | 0.468 |
LIG_SH2_SRC | 345 | 348 | PF00017 | 0.421 |
LIG_SH2_SRC | 357 | 360 | PF00017 | 0.365 |
LIG_SH2_STAP1 | 13 | 17 | PF00017 | 0.501 |
LIG_SH2_STAP1 | 164 | 168 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 361 | 365 | PF00017 | 0.400 |
LIG_SH2_STAP1 | 90 | 94 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.327 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.528 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.524 |
LIG_SUMO_SIM_anti_2 | 367 | 372 | PF11976 | 0.403 |
LIG_SUMO_SIM_anti_2 | 419 | 426 | PF11976 | 0.644 |
LIG_SUMO_SIM_par_1 | 131 | 137 | PF11976 | 0.524 |
LIG_SUMO_SIM_par_1 | 22 | 28 | PF11976 | 0.531 |
LIG_SUMO_SIM_par_1 | 366 | 372 | PF11976 | 0.390 |
LIG_TRAF2_1 | 294 | 297 | PF00917 | 0.573 |
LIG_TYR_ITIM | 276 | 281 | PF00017 | 0.345 |
LIG_WRC_WIRS_1 | 320 | 325 | PF05994 | 0.421 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.670 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.429 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.577 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.434 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.330 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.448 |
MOD_GlcNHglycan | 179 | 183 | PF01048 | 0.492 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.391 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.462 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.401 |
MOD_GlcNHglycan | 426 | 430 | PF01048 | 0.492 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.484 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.557 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.498 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.471 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.422 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.452 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.508 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.532 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.449 |
MOD_N-GLC_1 | 300 | 305 | PF02516 | 0.462 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.433 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.476 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.411 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.413 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.492 |
MOD_NEK2_2 | 63 | 68 | PF00069 | 0.391 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.516 |
MOD_PKA_1 | 153 | 159 | PF00069 | 0.389 |
MOD_PKA_1 | 205 | 211 | PF00069 | 0.269 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.506 |
MOD_PKA_2 | 411 | 417 | PF00069 | 0.605 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.447 |
MOD_Plk_1 | 295 | 301 | PF00069 | 0.566 |
MOD_Plk_1 | 318 | 324 | PF00069 | 0.423 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.438 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.465 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.395 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.379 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.452 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.439 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.428 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.370 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.510 |
MOD_SUMO_for_1 | 162 | 165 | PF00179 | 0.418 |
MOD_SUMO_rev_2 | 26 | 35 | PF00179 | 0.536 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 217 | 220 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.305 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.397 |
TRG_ER_diArg_1 | 124 | 127 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 152 | 154 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 213 | 215 | PF00400 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 309 | 313 | PF00026 | 0.460 |
TRG_Pf-PMV_PEXEL_1 | 50 | 54 | PF00026 | 0.549 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKE5 | Leptomonas seymouri | 62% | 99% |
A0A0S4J4F8 | Bodo saltans | 27% | 97% |
A0A1X0NY12 | Trypanosomatidae | 30% | 99% |
A0A3S7WZD2 | Leishmania donovani | 85% | 100% |
A0A422P4P2 | Trypanosoma rangeli | 30% | 99% |
A4I1S0 | Leishmania infantum | 85% | 100% |
C9ZKC8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AXV5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
O01422 | Caenorhabditis elegans | 21% | 89% |
P61201 | Homo sapiens | 22% | 99% |
P61202 | Mus musculus | 22% | 99% |
P61203 | Rattus norvegicus | 22% | 99% |
Q4Q9L6 | Leishmania major | 85% | 100% |
Q54HL6 | Dictyostelium discoideum | 21% | 98% |
Q5B3U7 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 22% | 87% |
Q6IQT4 | Danio rerio | 22% | 99% |
Q6IR75 | Xenopus laevis | 22% | 100% |
Q7SI58 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 20% | 90% |
Q8W207 | Arabidopsis thaliana | 21% | 100% |
Q94899 | Drosophila melanogaster | 20% | 99% |
Q9HFR0 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 21% | 100% |
V5BH20 | Trypanosoma cruzi | 30% | 99% |