| 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 | 2 |
| GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 2 |
| GO:0031464 | Cul4A-RING E3 ubiquitin ligase complex | 6 | 2 |
| GO:0032991 | protein-containing complex | 1 | 2 |
| GO:0080008 | Cul4-RING E3 ubiquitin ligase complex | 5 | 2 |
| GO:0140535 | intracellular protein-containing complex | 2 | 2 |
| GO:1902494 | catalytic complex | 2 | 2 |
| GO:1990234 | transferase complex | 3 | 2 |
Related structures:
AlphaFold database: Q4QHW7
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
| GO:0008152 | metabolic process | 1 | 2 |
| GO:0016567 | protein ubiquitination | 7 | 2 |
| GO:0019538 | protein metabolic process | 3 | 2 |
| GO:0032446 | protein modification by small protein conjugation | 6 | 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: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 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 123 | 127 | PF00656 | 0.674 |
| CLV_C14_Caspase3-7 | 315 | 319 | PF00656 | 0.843 |
| CLV_C14_Caspase3-7 | 430 | 434 | PF00656 | 0.648 |
| CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.672 |
| CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.754 |
| CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.650 |
| CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.518 |
| CLV_NRD_NRD_1 | 391 | 393 | PF00675 | 0.523 |
| CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.495 |
| CLV_PCSK_FUR_1 | 379 | 383 | PF00082 | 0.531 |
| CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.672 |
| CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.523 |
| CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.517 |
| CLV_PCSK_KEX2_1 | 391 | 393 | PF00082 | 0.515 |
| CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.499 |
| CLV_PCSK_PC1ET2_1 | 384 | 386 | PF00082 | 0.522 |
| DEG_APCC_DBOX_1 | 79 | 87 | PF00400 | 0.481 |
| DEG_SCF_FBW7_2 | 95 | 101 | PF00400 | 0.683 |
| DEG_SPOP_SBC_1 | 155 | 159 | PF00917 | 0.626 |
| DEG_SPOP_SBC_1 | 261 | 265 | PF00917 | 0.809 |
| DOC_ANK_TNKS_1 | 279 | 286 | PF00023 | 0.758 |
| DOC_CDC14_PxL_1 | 420 | 428 | PF14671 | 0.580 |
| DOC_CKS1_1 | 95 | 100 | PF01111 | 0.558 |
| DOC_MAPK_gen_1 | 391 | 397 | PF00069 | 0.534 |
| DOC_MAPK_gen_1 | 79 | 86 | PF00069 | 0.465 |
| DOC_MAPK_MEF2A_6 | 85 | 92 | PF00069 | 0.473 |
| DOC_PP1_RVXF_1 | 369 | 376 | PF00149 | 0.628 |
| DOC_PP2B_LxvP_1 | 160 | 163 | PF13499 | 0.637 |
| DOC_PP2B_LxvP_1 | 297 | 300 | PF13499 | 0.838 |
| DOC_PP2B_LxvP_1 | 395 | 398 | PF13499 | 0.531 |
| DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.702 |
| DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.674 |
| DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.610 |
| DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.806 |
| DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.847 |
| DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.609 |
| DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.818 |
| DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.726 |
| DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.687 |
| DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.438 |
| DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.475 |
| DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.805 |
| DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.542 |
| DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.722 |
| DOC_WW_Pin1_4 | 344 | 349 | PF00397 | 0.545 |
| DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.572 |
| DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.573 |
| DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.707 |
| LIG_14-3-3_CanoR_1 | 153 | 163 | PF00244 | 0.617 |
| LIG_14-3-3_CanoR_1 | 243 | 249 | PF00244 | 0.586 |
| LIG_14-3-3_CanoR_1 | 391 | 396 | PF00244 | 0.539 |
| LIG_14-3-3_CanoR_1 | 454 | 460 | PF00244 | 0.496 |
| LIG_14-3-3_CanoR_1 | 94 | 98 | PF00244 | 0.728 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.805 |
| LIG_BIR_III_4 | 148 | 152 | PF00653 | 0.778 |
| LIG_BRCT_BRCA1_1 | 431 | 435 | PF00533 | 0.640 |
| LIG_EH1_1 | 363 | 371 | PF00400 | 0.625 |
| LIG_EH1_1 | 413 | 421 | PF00400 | 0.592 |
| LIG_eIF4E_1 | 364 | 370 | PF01652 | 0.517 |
| LIG_FHA_1 | 18 | 24 | PF00498 | 0.483 |
| LIG_FHA_1 | 223 | 229 | PF00498 | 0.579 |
| LIG_FHA_1 | 388 | 394 | PF00498 | 0.603 |
| LIG_FHA_1 | 434 | 440 | PF00498 | 0.608 |
| LIG_FHA_2 | 243 | 249 | PF00498 | 0.586 |
| LIG_FHA_2 | 313 | 319 | PF00498 | 0.845 |
| LIG_LIR_Gen_1 | 35 | 45 | PF02991 | 0.518 |
| LIG_LIR_Gen_1 | 412 | 421 | PF02991 | 0.579 |
| LIG_LIR_Nem_3 | 178 | 183 | PF02991 | 0.462 |
| LIG_LIR_Nem_3 | 347 | 353 | PF02991 | 0.503 |
| LIG_LIR_Nem_3 | 35 | 40 | PF02991 | 0.467 |
| LIG_LIR_Nem_3 | 408 | 413 | PF02991 | 0.562 |
| LIG_PTAP_UEV_1 | 269 | 274 | PF05743 | 0.763 |
| LIG_SH2_CRK | 421 | 425 | PF00017 | 0.609 |
| LIG_SH2_PTP2 | 89 | 92 | PF00017 | 0.417 |
| LIG_SH2_STAP1 | 183 | 187 | PF00017 | 0.450 |
| LIG_SH2_STAP1 | 54 | 58 | PF00017 | 0.528 |
| LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.417 |
| LIG_SH3_1 | 421 | 427 | PF00018 | 0.668 |
| LIG_SH3_3 | 2 | 8 | PF00018 | 0.628 |
| LIG_SH3_3 | 225 | 231 | PF00018 | 0.581 |
| LIG_SH3_3 | 264 | 270 | PF00018 | 0.758 |
| LIG_SH3_3 | 359 | 365 | PF00018 | 0.617 |
| LIG_SH3_3 | 421 | 427 | PF00018 | 0.668 |
| LIG_SH3_3 | 92 | 98 | PF00018 | 0.462 |
| LIG_SUMO_SIM_anti_2 | 19 | 25 | PF11976 | 0.458 |
| LIG_TRAF2_1 | 236 | 239 | PF00917 | 0.842 |
| LIG_TRAF2_1 | 41 | 44 | PF00917 | 0.558 |
| MOD_CDK_SPK_2 | 94 | 99 | PF00069 | 0.501 |
| MOD_CK1_1 | 303 | 309 | PF00069 | 0.755 |
| MOD_CK1_1 | 312 | 318 | PF00069 | 0.694 |
| MOD_CK1_1 | 4 | 10 | PF00069 | 0.804 |
| MOD_CK1_1 | 434 | 440 | PF00069 | 0.517 |
| MOD_CK1_1 | 472 | 478 | PF00069 | 0.692 |
| MOD_CK1_1 | 479 | 485 | PF00069 | 0.799 |
| MOD_CK2_1 | 161 | 167 | PF00069 | 0.521 |
| MOD_CK2_1 | 303 | 309 | PF00069 | 0.726 |
| MOD_CK2_1 | 481 | 487 | PF00069 | 0.773 |
| MOD_DYRK1A_RPxSP_1 | 94 | 98 | PF00069 | 0.528 |
| MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.745 |
| MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.599 |
| MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.618 |
| MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.687 |
| MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.819 |
| MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.735 |
| MOD_GlcNHglycan | 323 | 328 | PF01048 | 0.778 |
| MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.721 |
| MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.630 |
| MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.466 |
| MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.489 |
| MOD_GSK3_1 | 116 | 123 | PF00069 | 0.672 |
| MOD_GSK3_1 | 13 | 20 | PF00069 | 0.607 |
| MOD_GSK3_1 | 167 | 174 | PF00069 | 0.572 |
| MOD_GSK3_1 | 216 | 223 | PF00069 | 0.703 |
| MOD_GSK3_1 | 244 | 251 | PF00069 | 0.761 |
| MOD_GSK3_1 | 3 | 10 | PF00069 | 0.713 |
| MOD_GSK3_1 | 300 | 307 | PF00069 | 0.819 |
| MOD_GSK3_1 | 308 | 315 | PF00069 | 0.723 |
| MOD_GSK3_1 | 353 | 360 | PF00069 | 0.355 |
| MOD_GSK3_1 | 387 | 394 | PF00069 | 0.594 |
| MOD_GSK3_1 | 429 | 436 | PF00069 | 0.688 |
| MOD_GSK3_1 | 437 | 444 | PF00069 | 0.585 |
| MOD_GSK3_1 | 469 | 476 | PF00069 | 0.574 |
| MOD_N-GLC_1 | 188 | 193 | PF02516 | 0.413 |
| MOD_N-GLC_1 | 473 | 478 | PF02516 | 0.660 |
| MOD_N-GLC_1 | 62 | 67 | PF02516 | 0.550 |
| MOD_NEK2_1 | 25 | 30 | PF00069 | 0.399 |
| MOD_NEK2_1 | 400 | 405 | PF00069 | 0.520 |
| MOD_NEK2_2 | 156 | 161 | PF00069 | 0.684 |
| MOD_NEK2_2 | 168 | 173 | PF00069 | 0.406 |
| MOD_NEK2_2 | 88 | 93 | PF00069 | 0.492 |
| MOD_PIKK_1 | 255 | 261 | PF00454 | 0.744 |
| MOD_PKA_1 | 391 | 397 | PF00069 | 0.534 |
| MOD_PKA_2 | 242 | 248 | PF00069 | 0.663 |
| MOD_PKA_2 | 391 | 397 | PF00069 | 0.506 |
| MOD_PKA_2 | 400 | 406 | PF00069 | 0.520 |
| MOD_PKA_2 | 93 | 99 | PF00069 | 0.608 |
| MOD_Plk_1 | 175 | 181 | PF00069 | 0.466 |
| MOD_Plk_1 | 323 | 329 | PF00069 | 0.724 |
| MOD_Plk_2-3 | 304 | 310 | PF00069 | 0.840 |
| MOD_Plk_4 | 161 | 167 | PF00069 | 0.568 |
| MOD_Plk_4 | 168 | 174 | PF00069 | 0.499 |
| MOD_Plk_4 | 175 | 181 | PF00069 | 0.418 |
| MOD_Plk_4 | 309 | 315 | PF00069 | 0.603 |
| MOD_Plk_4 | 32 | 38 | PF00069 | 0.517 |
| MOD_Plk_4 | 365 | 371 | PF00069 | 0.525 |
| MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.805 |
| MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.525 |
| MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.724 |
| MOD_ProDKin_1 | 344 | 350 | PF00069 | 0.537 |
| MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.564 |
| MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.713 |
| TRG_DiLeu_BaLyEn_6 | 421 | 426 | PF01217 | 0.575 |
| TRG_ENDOCYTIC_2 | 413 | 416 | PF00928 | 0.571 |
| TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.417 |
| TRG_ER_diArg_1 | 211 | 213 | PF00400 | 0.626 |
| TRG_ER_diArg_1 | 379 | 382 | PF00400 | 0.537 |
| TRG_ER_diArg_1 | 383 | 386 | PF00400 | 0.502 |
| TRG_ER_diArg_1 | 391 | 393 | PF00400 | 0.496 |
| TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.495 |
| TRG_ER_FFAT_2 | 430 | 440 | PF00635 | 0.459 |
| TRG_NLS_MonoExtN_4 | 230 | 236 | PF00514 | 0.795 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P5U2 | Leptomonas seymouri | 40% | 100% |
| A0A3S7WQQ0 | Leishmania donovani | 91% | 100% |
| A4H5N4 | Leishmania braziliensis | 70% | 99% |
| A4HTX8 | Leishmania infantum | 91% | 100% |
| E9AMQ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |