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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000151 | ubiquitin ligase complex | 3 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0110165 | cellular anatomical entity | 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: A4HIE9
Term | Name | Level | Count |
---|---|---|---|
GO:0000209 | protein polyubiquitination | 8 | 1 |
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009894 | regulation of catabolic process | 4 | 1 |
GO:0009896 | positive regulation of catabolic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0030162 | regulation of proteolysis | 6 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031329 | regulation of cellular catabolic process | 5 | 1 |
GO:0031331 | positive regulation of cellular catabolic process | 6 | 1 |
GO:0032434 | regulation of proteasomal ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0032436 | positive regulation of proteasomal ubiquitin-dependent protein catabolic process | 8 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0042176 | regulation of protein catabolic process | 5 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 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:0045732 | positive regulation of protein catabolic process | 6 | 1 |
GO:0045862 | positive regulation of proteolysis | 7 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051246 | regulation of protein metabolic process | 5 | 1 |
GO:0051247 | positive regulation of protein metabolic process | 6 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0061136 | regulation of proteasomal protein catabolic process | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:1901800 | positive regulation of proteasomal protein catabolic process | 7 | 1 |
GO:1903050 | regulation of proteolysis involved in protein catabolic process | 7 | 1 |
GO:1903052 | positive regulation of proteolysis involved in protein catabolic process | 8 | 1 |
GO:2000058 | regulation of ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:2000060 | positive regulation of ubiquitin-dependent protein catabolic process | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 7 |
GO:0005488 | binding | 1 | 6 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 7 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043169 | cation binding | 3 | 6 |
GO:0046872 | metal ion binding | 4 | 6 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:0005515 | protein binding | 2 | 1 |
GO:0019899 | enzyme binding | 3 | 1 |
GO:0031624 | ubiquitin conjugating enzyme binding | 5 | 1 |
GO:0044390 | ubiquitin-like protein conjugating enzyme binding | 4 | 1 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 1 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 21 | 25 | PF00656 | 0.519 |
CLV_C14_Caspase3-7 | 355 | 359 | PF00656 | 0.478 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.365 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.427 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 407 | 409 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.427 |
CLV_PCSK_PC1ET2_1 | 361 | 363 | PF00082 | 0.432 |
CLV_PCSK_PC1ET2_1 | 407 | 409 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 489 | 493 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.291 |
DEG_APCC_DBOX_1 | 393 | 401 | PF00400 | 0.349 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.501 |
DOC_CDC14_PxL_1 | 239 | 247 | PF14671 | 0.365 |
DOC_CYCLIN_RxL_1 | 185 | 195 | PF00134 | 0.280 |
DOC_CYCLIN_RxL_1 | 437 | 447 | PF00134 | 0.280 |
DOC_CYCLIN_yCln2_LP_2 | 238 | 244 | PF00134 | 0.208 |
DOC_MAPK_gen_1 | 81 | 91 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 431 | 438 | PF00069 | 0.311 |
DOC_MAPK_RevD_3 | 66 | 82 | PF00069 | 0.385 |
DOC_PP2B_LxvP_1 | 238 | 241 | PF13499 | 0.208 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.451 |
DOC_USP7_UBL2_3 | 193 | 197 | PF12436 | 0.382 |
DOC_USP7_UBL2_3 | 305 | 309 | PF12436 | 0.326 |
LIG_14-3-3_CanoR_1 | 262 | 266 | PF00244 | 0.289 |
LIG_14-3-3_CanoR_1 | 269 | 276 | PF00244 | 0.289 |
LIG_14-3-3_CanoR_1 | 277 | 283 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 362 | 366 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 369 | 373 | PF00244 | 0.314 |
LIG_14-3-3_CanoR_1 | 437 | 443 | PF00244 | 0.448 |
LIG_Actin_WH2_2 | 246 | 264 | PF00022 | 0.365 |
LIG_APCC_ABBAyCdc20_2 | 369 | 375 | PF00400 | 0.362 |
LIG_BIR_III_2 | 24 | 28 | PF00653 | 0.496 |
LIG_BRCT_BRCA1_1 | 320 | 324 | PF00533 | 0.208 |
LIG_BRCT_BRCA1_1 | 359 | 363 | PF00533 | 0.415 |
LIG_BRCT_BRCA1_1 | 498 | 502 | PF00533 | 0.293 |
LIG_deltaCOP1_diTrp_1 | 323 | 332 | PF00928 | 0.365 |
LIG_FHA_1 | 214 | 220 | PF00498 | 0.483 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.389 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.363 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.443 |
LIG_FHA_1 | 510 | 516 | PF00498 | 0.374 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.323 |
LIG_FHA_2 | 17 | 23 | PF00498 | 0.517 |
LIG_FHA_2 | 416 | 422 | PF00498 | 0.407 |
LIG_FHA_2 | 442 | 448 | PF00498 | 0.415 |
LIG_FHA_2 | 498 | 504 | PF00498 | 0.490 |
LIG_LIR_Apic_2 | 224 | 229 | PF02991 | 0.203 |
LIG_LIR_Gen_1 | 321 | 331 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 452 | 459 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 321 | 327 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 364 | 370 | PF02991 | 0.443 |
LIG_MAD2 | 402 | 410 | PF02301 | 0.384 |
LIG_MLH1_MIPbox_1 | 498 | 502 | PF16413 | 0.293 |
LIG_NRBOX | 164 | 170 | PF00104 | 0.274 |
LIG_PTB_Apo_2 | 253 | 260 | PF02174 | 0.365 |
LIG_PTB_Phospho_1 | 253 | 259 | PF10480 | 0.365 |
LIG_SH2_CRK | 239 | 243 | PF00017 | 0.365 |
LIG_SH2_NCK_1 | 239 | 243 | PF00017 | 0.365 |
LIG_SH2_SRC | 239 | 242 | PF00017 | 0.365 |
LIG_SH2_SRC | 265 | 268 | PF00017 | 0.365 |
LIG_SH2_STAP1 | 370 | 374 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 6 | 10 | PF00017 | 0.591 |
LIG_SH2_STAT3 | 20 | 23 | PF00017 | 0.794 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 18 | 21 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 458 | 461 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.444 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.294 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.312 |
LIG_SUMO_SIM_anti_2 | 420 | 428 | PF11976 | 0.384 |
LIG_TRAF2_1 | 19 | 22 | PF00917 | 0.604 |
LIG_TRAF2_1 | 352 | 355 | PF00917 | 0.728 |
LIG_TRAF2_1 | 418 | 421 | PF00917 | 0.360 |
LIG_TYR_ITIM | 237 | 242 | PF00017 | 0.365 |
LIG_UBA3_1 | 206 | 213 | PF00899 | 0.434 |
LIG_ULM_U2AF65_1 | 81 | 86 | PF00076 | 0.415 |
LIG_WRC_WIRS_1 | 498 | 503 | PF05994 | 0.430 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.468 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.329 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.315 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.461 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.516 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.251 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.404 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.326 |
MOD_GlcNHglycan | 308 | 312 | PF01048 | 0.292 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.646 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.475 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.405 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.682 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.393 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.436 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.343 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.629 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.398 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.345 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.542 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.407 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.527 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.482 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.389 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.447 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.412 |
MOD_LATS_1 | 211 | 217 | PF00433 | 0.341 |
MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.429 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.319 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.289 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.208 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.289 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.375 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.500 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.328 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.335 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.352 |
MOD_NEK2_1 | 483 | 488 | PF00069 | 0.473 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.422 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.365 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.396 |
MOD_NEK2_2 | 143 | 148 | PF00069 | 0.250 |
MOD_OFUCOSY | 313 | 318 | PF10250 | 0.289 |
MOD_PIKK_1 | 415 | 421 | PF00454 | 0.371 |
MOD_PIKK_1 | 493 | 499 | PF00454 | 0.482 |
MOD_PKA_1 | 361 | 367 | PF00069 | 0.480 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.409 |
MOD_PKA_2 | 361 | 367 | PF00069 | 0.429 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.445 |
MOD_PKA_2 | 436 | 442 | PF00069 | 0.457 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.513 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.305 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.516 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.423 |
MOD_Plk_2-3 | 109 | 115 | PF00069 | 0.447 |
MOD_Plk_2-3 | 16 | 22 | PF00069 | 0.516 |
MOD_Plk_2-3 | 45 | 51 | PF00069 | 0.477 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.272 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.629 |
MOD_Plk_4 | 254 | 260 | PF00069 | 0.208 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.351 |
MOD_Plk_4 | 438 | 444 | PF00069 | 0.368 |
MOD_Plk_4 | 449 | 455 | PF00069 | 0.311 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.541 |
MOD_Plk_4 | 497 | 503 | PF00069 | 0.412 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.309 |
MOD_SUMO_for_1 | 430 | 433 | PF00179 | 0.322 |
MOD_SUMO_rev_2 | 189 | 198 | PF00179 | 0.293 |
MOD_SUMO_rev_2 | 375 | 384 | PF00179 | 0.471 |
TRG_DiLeu_BaEn_1 | 420 | 425 | PF01217 | 0.391 |
TRG_DiLeu_BaEn_3 | 201 | 207 | PF01217 | 0.297 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.365 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.325 |
TRG_ER_diArg_1 | 80 | 82 | PF00400 | 0.417 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8P3 | Leptomonas seymouri | 51% | 100% |
A0A0S4JJP0 | Bodo saltans | 26% | 100% |
A0A1X0P1P5 | Trypanosomatidae | 26% | 100% |
A0A3Q8IEV4 | Leishmania donovani | 80% | 98% |
A0A3R7JXL5 | Trypanosoma rangeli | 29% | 100% |
A2VEA3 | Bos taurus | 26% | 93% |
A4I5P6 | Leishmania infantum | 81% | 98% |
B1H1E4 | Xenopus tropicalis | 26% | 98% |
C9ZR47 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9B0Z0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
O01965 | Caenorhabditis elegans | 25% | 100% |
O76924 | Drosophila melanogaster | 24% | 100% |
O95376 | Homo sapiens | 27% | 100% |
P0C8K8 | Arabidopsis thaliana | 27% | 94% |
P36113 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 94% |
Q22431 | Caenorhabditis elegans | 23% | 100% |
Q32NS4 | Xenopus laevis | 26% | 98% |
Q6NW85 | Danio rerio | 26% | 97% |
Q6PFJ9 | Danio rerio | 26% | 98% |
Q6T486 | Dictyostelium discoideum | 26% | 100% |
Q84RR0 | Arabidopsis thaliana | 31% | 92% |
Q84RR2 | Arabidopsis thaliana | 25% | 87% |
Q8L829 | Arabidopsis thaliana | 30% | 94% |
Q8W468 | Arabidopsis thaliana | 26% | 91% |
Q94981 | Drosophila melanogaster | 27% | 100% |
Q949V6 | Arabidopsis thaliana | 24% | 87% |
Q9LVW9 | Arabidopsis thaliana | 27% | 98% |
Q9LVX0 | Arabidopsis thaliana | 25% | 96% |
Q9NE54 | Leishmania major | 80% | 100% |
Q9P3U4 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 100% |
Q9SKC3 | Arabidopsis thaliana | 27% | 95% |
Q9SKC4 | Arabidopsis thaliana | 26% | 100% |
Q9Y4X5 | Homo sapiens | 26% | 93% |
Q9Z1K5 | Mus musculus | 26% | 93% |
Q9Z1K6 | Mus musculus | 27% | 100% |
V5AQL7 | Trypanosoma cruzi | 29% | 100% |