| 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:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
| GO:0031464 | Cul4A-RING E3 ubiquitin ligase complex | 6 | 1 |
| GO:0032991 | protein-containing complex | 1 | 1 |
| GO:0080008 | Cul4-RING E3 ubiquitin ligase complex | 5 | 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: A4H5N4
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
| GO:0008152 | metabolic process | 1 | 1 |
| GO:0016567 | protein ubiquitination | 7 | 1 |
| GO:0019538 | protein metabolic process | 3 | 1 |
| GO:0032446 | protein modification by small protein conjugation | 6 | 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: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 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 227 | 231 | PF00656 | 0.549 |
| CLV_C14_Caspase3-7 | 319 | 323 | PF00656 | 0.702 |
| CLV_C14_Caspase3-7 | 402 | 406 | PF00656 | 0.357 |
| CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.560 |
| CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.476 |
| CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.426 |
| CLV_PCSK_FUR_1 | 214 | 218 | PF00082 | 0.422 |
| CLV_PCSK_FUR_1 | 382 | 386 | PF00082 | 0.438 |
| CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.701 |
| CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.429 |
| CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.428 |
| CLV_PCSK_PC1ET2_1 | 387 | 389 | PF00082 | 0.432 |
| CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.347 |
| DEG_APCC_DBOX_1 | 396 | 404 | PF00400 | 0.346 |
| DEG_APCC_DBOX_1 | 81 | 89 | PF00400 | 0.387 |
| DEG_SCF_FBW7_1 | 86 | 93 | PF00400 | 0.296 |
| DEG_SPOP_SBC_1 | 255 | 259 | PF00917 | 0.615 |
| DOC_CKS1_1 | 424 | 429 | PF01111 | 0.393 |
| DOC_CYCLIN_RxL_1 | 394 | 402 | PF00134 | 0.353 |
| DOC_MAPK_MEF2A_6 | 87 | 94 | PF00069 | 0.415 |
| DOC_PP1_RVXF_1 | 372 | 379 | PF00149 | 0.502 |
| DOC_PP2B_LxvP_1 | 162 | 165 | PF13499 | 0.506 |
| DOC_PP2B_LxvP_1 | 300 | 303 | PF13499 | 0.710 |
| DOC_PP4_FxxP_1 | 429 | 432 | PF00568 | 0.479 |
| DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.579 |
| DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.671 |
| DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.789 |
| DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.625 |
| DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.703 |
| DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.619 |
| DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.354 |
| DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.421 |
| DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.495 |
| DOC_USP7_MATH_2 | 262 | 268 | PF00917 | 0.531 |
| DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.768 |
| DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.609 |
| DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.658 |
| DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.523 |
| DOC_WW_Pin1_4 | 423 | 428 | PF00397 | 0.364 |
| DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.475 |
| DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.498 |
| LIG_14-3-3_CanoR_1 | 214 | 224 | PF00244 | 0.484 |
| LIG_14-3-3_CanoR_1 | 292 | 300 | PF00244 | 0.625 |
| LIG_14-3-3_CanoR_1 | 471 | 481 | PF00244 | 0.448 |
| LIG_14-3-3_CanoR_1 | 96 | 100 | PF00244 | 0.646 |
| LIG_Actin_WH2_2 | 202 | 218 | PF00022 | 0.345 |
| LIG_APCC_ABBA_1 | 60 | 65 | PF00400 | 0.362 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.663 |
| LIG_BIR_III_4 | 150 | 154 | PF00653 | 0.662 |
| LIG_CtBP_PxDLS_1 | 5 | 9 | PF00389 | 0.512 |
| LIG_EH1_1 | 366 | 374 | PF00400 | 0.496 |
| LIG_EH1_1 | 416 | 424 | PF00400 | 0.467 |
| LIG_eIF4E_1 | 367 | 373 | PF01652 | 0.416 |
| LIG_FHA_1 | 315 | 321 | PF00498 | 0.565 |
| LIG_FHA_1 | 391 | 397 | PF00498 | 0.492 |
| LIG_FHA_1 | 441 | 447 | PF00498 | 0.575 |
| LIG_FHA_1 | 87 | 93 | PF00498 | 0.359 |
| LIG_FHA_2 | 225 | 231 | PF00498 | 0.507 |
| LIG_FHA_2 | 317 | 323 | PF00498 | 0.704 |
| LIG_LIR_Apic_2 | 426 | 432 | PF02991 | 0.444 |
| LIG_LIR_Gen_1 | 37 | 47 | PF02991 | 0.414 |
| LIG_LIR_Gen_1 | 411 | 419 | PF02991 | 0.448 |
| LIG_LIR_Gen_1 | 89 | 99 | PF02991 | 0.355 |
| LIG_LIR_Nem_3 | 180 | 185 | PF02991 | 0.404 |
| LIG_LIR_Nem_3 | 352 | 356 | PF02991 | 0.365 |
| LIG_LIR_Nem_3 | 37 | 42 | PF02991 | 0.368 |
| LIG_LIR_Nem_3 | 411 | 416 | PF02991 | 0.483 |
| LIG_LIR_Nem_3 | 89 | 94 | PF02991 | 0.305 |
| LIG_SH2_CRK | 424 | 428 | PF00017 | 0.510 |
| LIG_SH2_GRB2like | 413 | 416 | PF00017 | 0.336 |
| LIG_SH2_PTP2 | 91 | 94 | PF00017 | 0.357 |
| LIG_SH2_STAP1 | 185 | 189 | PF00017 | 0.348 |
| LIG_SH2_STAP1 | 56 | 60 | PF00017 | 0.426 |
| LIG_SH2_STAT5 | 314 | 317 | PF00017 | 0.561 |
| LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.357 |
| LIG_SH3_1 | 424 | 430 | PF00018 | 0.555 |
| LIG_SH3_3 | 120 | 126 | PF00018 | 0.514 |
| LIG_SH3_3 | 14 | 20 | PF00018 | 0.518 |
| LIG_SH3_3 | 142 | 148 | PF00018 | 0.552 |
| LIG_SH3_3 | 362 | 368 | PF00018 | 0.483 |
| LIG_SH3_3 | 424 | 430 | PF00018 | 0.555 |
| LIG_SH3_3 | 439 | 445 | PF00018 | 0.477 |
| LIG_SUMO_SIM_par_1 | 267 | 273 | PF11976 | 0.535 |
| LIG_TRAF2_1 | 238 | 241 | PF00917 | 0.650 |
| LIG_TRAF2_2 | 135 | 140 | PF00917 | 0.542 |
| LIG_TRAF2_2 | 145 | 150 | PF00917 | 0.529 |
| LIG_TYR_ITSM | 87 | 94 | PF00017 | 0.300 |
| MOD_CDK_SPK_2 | 13 | 18 | PF00069 | 0.510 |
| MOD_CK1_1 | 177 | 183 | PF00069 | 0.300 |
| MOD_CK1_1 | 218 | 224 | PF00069 | 0.499 |
| MOD_CK1_1 | 225 | 231 | PF00069 | 0.514 |
| MOD_CK1_1 | 298 | 304 | PF00069 | 0.701 |
| MOD_CK1_1 | 316 | 322 | PF00069 | 0.588 |
| MOD_CK1_1 | 323 | 329 | PF00069 | 0.599 |
| MOD_CK1_1 | 4 | 10 | PF00069 | 0.770 |
| MOD_CK1_1 | 435 | 441 | PF00069 | 0.537 |
| MOD_CK1_1 | 475 | 481 | PF00069 | 0.571 |
| MOD_CK1_1 | 98 | 104 | PF00069 | 0.585 |
| MOD_CK2_1 | 220 | 226 | PF00069 | 0.499 |
| MOD_CK2_1 | 486 | 492 | PF00069 | 0.706 |
| MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.638 |
| MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.584 |
| MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.360 |
| MOD_GlcNHglycan | 219 | 223 | PF01048 | 0.609 |
| MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.637 |
| MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.735 |
| MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.691 |
| MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.490 |
| MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.602 |
| MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.413 |
| MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.538 |
| MOD_GSK3_1 | 169 | 176 | PF00069 | 0.513 |
| MOD_GSK3_1 | 218 | 225 | PF00069 | 0.632 |
| MOD_GSK3_1 | 250 | 257 | PF00069 | 0.587 |
| MOD_GSK3_1 | 291 | 298 | PF00069 | 0.620 |
| MOD_GSK3_1 | 308 | 315 | PF00069 | 0.632 |
| MOD_GSK3_1 | 316 | 323 | PF00069 | 0.587 |
| MOD_GSK3_1 | 431 | 438 | PF00069 | 0.608 |
| MOD_GSK3_1 | 440 | 447 | PF00069 | 0.562 |
| MOD_GSK3_1 | 481 | 488 | PF00069 | 0.681 |
| MOD_GSK3_1 | 7 | 14 | PF00069 | 0.589 |
| MOD_GSK3_1 | 86 | 93 | PF00069 | 0.296 |
| MOD_GSK3_1 | 95 | 102 | PF00069 | 0.423 |
| MOD_N-GLC_1 | 323 | 328 | PF02516 | 0.549 |
| MOD_N-GLC_1 | 481 | 486 | PF02516 | 0.585 |
| MOD_NEK2_1 | 224 | 229 | PF00069 | 0.505 |
| MOD_NEK2_1 | 343 | 348 | PF00069 | 0.419 |
| MOD_NEK2_2 | 158 | 163 | PF00069 | 0.562 |
| MOD_NEK2_2 | 90 | 95 | PF00069 | 0.402 |
| MOD_PIKK_1 | 109 | 115 | PF00454 | 0.547 |
| MOD_PIKK_1 | 257 | 263 | PF00454 | 0.622 |
| MOD_PKA_2 | 116 | 122 | PF00069 | 0.565 |
| MOD_PKA_2 | 215 | 221 | PF00069 | 0.556 |
| MOD_PKA_2 | 291 | 297 | PF00069 | 0.619 |
| MOD_PKA_2 | 403 | 409 | PF00069 | 0.550 |
| MOD_PKA_2 | 432 | 438 | PF00069 | 0.538 |
| MOD_PKA_2 | 95 | 101 | PF00069 | 0.570 |
| MOD_Plk_1 | 177 | 183 | PF00069 | 0.363 |
| MOD_Plk_2-3 | 308 | 314 | PF00069 | 0.706 |
| MOD_Plk_4 | 177 | 183 | PF00069 | 0.325 |
| MOD_Plk_4 | 34 | 40 | PF00069 | 0.409 |
| MOD_Plk_4 | 368 | 374 | PF00069 | 0.426 |
| MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.768 |
| MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.601 |
| MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.663 |
| MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.523 |
| MOD_ProDKin_1 | 423 | 429 | PF00069 | 0.374 |
| MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.464 |
| MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.496 |
| TRG_ENDOCYTIC_2 | 413 | 416 | PF00928 | 0.464 |
| TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.357 |
| TRG_ER_diArg_1 | 214 | 217 | PF00400 | 0.561 |
| TRG_ER_diArg_1 | 382 | 385 | PF00400 | 0.442 |
| TRG_ER_diArg_1 | 386 | 389 | PF00400 | 0.413 |
| TRG_NLS_Bipartite_1 | 216 | 238 | PF00514 | 0.495 |
| TRG_NLS_MonoExtN_4 | 232 | 238 | PF00514 | 0.639 |
| TRG_NLS_MonoExtN_4 | 384 | 390 | PF00514 | 0.350 |
| TRG_Pf-PMV_PEXEL_1 | 275 | 279 | PF00026 | 0.526 |
| TRG_Pf-PMV_PEXEL_1 | 397 | 402 | PF00026 | 0.356 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P5U2 | Leptomonas seymouri | 40% | 100% |
| A0A3S7WQQ0 | Leishmania donovani | 71% | 100% |
| A4HTX8 | Leishmania infantum | 71% | 100% |
| E9AMQ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
| Q4QHW7 | Leishmania major | 70% | 99% |