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: Q4Q9L6
Term | Name | Level | Count |
---|---|---|---|
GO:0000338 | protein deneddylation | 6 | 2 |
GO:0006508 | proteolysis | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0070646 | protein modification by small protein removal | 5 | 2 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 266 | 270 | PF00656 | 0.447 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.197 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.341 |
CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 68 | 72 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.445 |
DEG_COP1_1 | 141 | 151 | PF00400 | 0.424 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.603 |
DOC_CYCLIN_RxL_1 | 194 | 202 | PF00134 | 0.496 |
DOC_CYCLIN_RxL_1 | 400 | 414 | PF00134 | 0.532 |
DOC_MAPK_DCC_7 | 222 | 232 | PF00069 | 0.571 |
DOC_MAPK_gen_1 | 125 | 133 | PF00069 | 0.505 |
DOC_MAPK_gen_1 | 153 | 159 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 125 | 133 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 313 | 320 | PF00069 | 0.393 |
DOC_PP1_RVXF_1 | 404 | 411 | PF00149 | 0.570 |
DOC_PP2B_LxvP_1 | 327 | 330 | PF13499 | 0.547 |
DOC_PP2B_LxvP_1 | 368 | 371 | PF13499 | 0.519 |
DOC_PP4_FxxP_1 | 96 | 99 | PF00568 | 0.531 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.319 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.469 |
DOC_USP7_UBL2_3 | 108 | 112 | PF12436 | 0.401 |
LIG_14-3-3_CanoR_1 | 125 | 130 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 153 | 158 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 64 | 68 | PF00244 | 0.394 |
LIG_Actin_WH2_2 | 20 | 35 | PF00022 | 0.645 |
LIG_Actin_WH2_2 | 216 | 233 | PF00022 | 0.517 |
LIG_APCC_ABBA_1 | 342 | 347 | PF00400 | 0.516 |
LIG_APCC_ABBAyCdc20_2 | 154 | 160 | PF00400 | 0.477 |
LIG_BRCT_BRCA1_1 | 361 | 365 | PF00533 | 0.560 |
LIG_deltaCOP1_diTrp_1 | 247 | 257 | PF00928 | 0.382 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.470 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.392 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.561 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.623 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.450 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.450 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.570 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.423 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.541 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.584 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.510 |
LIG_IRF3_LxIS_1 | 316 | 321 | PF10401 | 0.446 |
LIG_LIR_Gen_1 | 321 | 330 | PF02991 | 0.495 |
LIG_LIR_Gen_1 | 88 | 97 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 141 | 146 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 202 | 207 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 321 | 326 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 339 | 345 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 362 | 368 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 66 | 70 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 88 | 93 | PF02991 | 0.424 |
LIG_Rb_pABgroove_1 | 77 | 85 | PF01858 | 0.449 |
LIG_RPA_C_Fungi | 250 | 262 | PF08784 | 0.508 |
LIG_SH2_CRK | 204 | 208 | PF00017 | 0.413 |
LIG_SH2_CRK | 273 | 277 | PF00017 | 0.477 |
LIG_SH2_CRK | 90 | 94 | PF00017 | 0.391 |
LIG_SH2_GRB2like | 17 | 20 | PF00017 | 0.682 |
LIG_SH2_PTP2 | 278 | 281 | PF00017 | 0.445 |
LIG_SH2_PTP2 | 345 | 348 | PF00017 | 0.454 |
LIG_SH2_SRC | 164 | 167 | PF00017 | 0.400 |
LIG_SH2_SRC | 17 | 20 | PF00017 | 0.722 |
LIG_SH2_SRC | 34 | 37 | PF00017 | 0.282 |
LIG_SH2_SRC | 345 | 348 | PF00017 | 0.428 |
LIG_SH2_SRC | 357 | 360 | PF00017 | 0.364 |
LIG_SH2_STAP1 | 164 | 168 | PF00017 | 0.465 |
LIG_SH2_STAP1 | 361 | 365 | PF00017 | 0.399 |
LIG_SH2_STAP1 | 83 | 87 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 90 | 94 | PF00017 | 0.359 |
LIG_SH2_STAT3 | 89 | 92 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.507 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.511 |
LIG_SUMO_SIM_anti_2 | 420 | 426 | PF11976 | 0.642 |
LIG_SUMO_SIM_par_1 | 131 | 137 | PF11976 | 0.514 |
LIG_SUMO_SIM_par_1 | 315 | 322 | PF11976 | 0.221 |
LIG_SUMO_SIM_par_1 | 366 | 372 | PF11976 | 0.389 |
LIG_TRAF2_1 | 294 | 297 | PF00917 | 0.541 |
LIG_TYR_ITIM | 276 | 281 | PF00017 | 0.343 |
LIG_WRC_WIRS_1 | 320 | 325 | PF05994 | 0.420 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.648 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.406 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.554 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.440 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.428 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.450 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.450 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.396 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.403 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.483 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.260 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.395 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.583 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.422 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.468 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.318 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.440 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.446 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.517 |
MOD_N-GLC_1 | 18 | 23 | PF02516 | 0.628 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.420 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.484 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.410 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.488 |
MOD_NEK2_2 | 63 | 68 | PF00069 | 0.376 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.509 |
MOD_PIKK_1 | 88 | 94 | PF00454 | 0.449 |
MOD_PKA_1 | 153 | 159 | PF00069 | 0.381 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.498 |
MOD_PKA_2 | 411 | 417 | PF00069 | 0.605 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.386 |
MOD_Plk_1 | 178 | 184 | PF00069 | 0.529 |
MOD_Plk_1 | 295 | 301 | PF00069 | 0.519 |
MOD_Plk_1 | 318 | 324 | PF00069 | 0.422 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.519 |
MOD_Plk_2-3 | 18 | 24 | PF00069 | 0.649 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.456 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.474 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.392 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.442 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.421 |
MOD_SUMO_for_1 | 162 | 165 | PF00179 | 0.413 |
MOD_SUMO_rev_2 | 26 | 35 | PF00179 | 0.528 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 217 | 220 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 273 | 276 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.376 |
TRG_ER_diArg_1 | 124 | 127 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 152 | 154 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 213 | 215 | PF00400 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 425 | 429 | PF00026 | 0.574 |
TRG_Pf-PMV_PEXEL_1 | 50 | 54 | PF00026 | 0.515 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKE5 | Leptomonas seymouri | 65% | 98% |
A0A0S4J4F8 | Bodo saltans | 27% | 96% |
A0A1X0NY12 | Trypanosomatidae | 32% | 99% |
A0A3S7WZD2 | Leishmania donovani | 92% | 100% |
A0A422P4P2 | Trypanosoma rangeli | 32% | 99% |
A4HEC5 | Leishmania braziliensis | 85% | 100% |
A4I1S0 | Leishmania infantum | 92% | 100% |
C9ZKC8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 99% |
E9AXV5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
O01422 | Caenorhabditis elegans | 21% | 88% |
P61201 | Homo sapiens | 23% | 99% |
P61202 | Mus musculus | 23% | 99% |
P61203 | Rattus norvegicus | 23% | 99% |
Q54HL6 | Dictyostelium discoideum | 22% | 97% |
Q5B3U7 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 21% | 86% |
Q6IQT4 | Danio rerio | 23% | 99% |
Q6IR75 | Xenopus laevis | 23% | 99% |
Q7SI58 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 22% | 89% |
Q8W207 | Arabidopsis thaliana | 22% | 100% |
Q94899 | Drosophila melanogaster | 22% | 98% |
Q9HFR0 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 100% |
V5BH20 | Trypanosoma cruzi | 31% | 99% |