| 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:0005737 | cytoplasm | 2 | 2 |
| GO:0008180 | COP9 signalosome | 3 | 7 |
| GO:0032991 | protein-containing complex | 1 | 7 |
| GO:0110165 | cellular anatomical entity | 1 | 2 |
| GO:0140513 | nuclear protein-containing complex | 2 | 7 |
Related structures:
AlphaFold database: Q4QET4
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000338 | protein deneddylation | 6 | 2 |
| GO:0006508 | proteolysis | 4 | 7 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
| GO:0008152 | metabolic process | 1 | 7 |
| GO:0019538 | protein metabolic process | 3 | 7 |
| GO:0036211 | protein modification process | 4 | 2 |
| GO:0043170 | macromolecule metabolic process | 3 | 7 |
| GO:0043412 | macromolecule modification | 4 | 2 |
| GO:0044238 | primary metabolic process | 2 | 7 |
| 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 | 7 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 7 |
| GO:0004175 | endopeptidase activity | 4 | 7 |
| GO:0004222 | metalloendopeptidase activity | 5 | 7 |
| GO:0005488 | binding | 1 | 7 |
| GO:0008233 | peptidase activity | 3 | 7 |
| GO:0008237 | metallopeptidase activity | 4 | 7 |
| GO:0016787 | hydrolase activity | 2 | 7 |
| GO:0019783 | ubiquitin-like protein peptidase activity | 4 | 2 |
| GO:0019784 | deNEDDylase activity | 5 | 2 |
| GO:0043167 | ion binding | 2 | 7 |
| GO:0043169 | cation binding | 3 | 7 |
| GO:0046872 | metal ion binding | 4 | 7 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 230 | 234 | PF00656 | 0.590 |
| CLV_C14_Caspase3-7 | 281 | 285 | PF00656 | 0.402 |
| CLV_C14_Caspase3-7 | 372 | 376 | PF00656 | 0.654 |
| CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.302 |
| CLV_NRD_NRD_1 | 449 | 451 | PF00675 | 0.573 |
| CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.302 |
| CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.763 |
| CLV_PCSK_PC1ET2_1 | 436 | 438 | PF00082 | 0.631 |
| CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.363 |
| CLV_Separin_Metazoa | 396 | 400 | PF03568 | 0.458 |
| DEG_SCF_FBW7_1 | 20 | 26 | PF00400 | 0.581 |
| DOC_CKS1_1 | 20 | 25 | PF01111 | 0.763 |
| DOC_CKS1_1 | 43 | 48 | PF01111 | 0.435 |
| DOC_CYCLIN_yCln2_LP_2 | 302 | 308 | PF00134 | 0.481 |
| DOC_MAPK_gen_1 | 58 | 67 | PF00069 | 0.389 |
| DOC_MAPK_HePTP_8 | 290 | 302 | PF00069 | 0.497 |
| DOC_MAPK_MEF2A_6 | 270 | 278 | PF00069 | 0.373 |
| DOC_MAPK_MEF2A_6 | 293 | 302 | PF00069 | 0.496 |
| DOC_PP4_FxxP_1 | 120 | 123 | PF00568 | 0.302 |
| DOC_PP4_FxxP_1 | 247 | 250 | PF00568 | 0.514 |
| DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.684 |
| DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.649 |
| DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.524 |
| DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.362 |
| DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.305 |
| DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.633 |
| DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.681 |
| DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.554 |
| DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.613 |
| DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.619 |
| DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.507 |
| LIG_14-3-3_CanoR_1 | 223 | 232 | PF00244 | 0.583 |
| LIG_14-3-3_CanoR_1 | 277 | 287 | PF00244 | 0.408 |
| LIG_14-3-3_CanoR_1 | 437 | 445 | PF00244 | 0.604 |
| LIG_AP2alpha_2 | 188 | 190 | PF02296 | 0.362 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.655 |
| LIG_BRCT_BRCA1_1 | 300 | 304 | PF00533 | 0.439 |
| LIG_BRCT_BRCA1_1 | 455 | 459 | PF00533 | 0.609 |
| LIG_BRCT_BRCA1_1 | 63 | 67 | PF00533 | 0.415 |
| LIG_CtBP_PxDLS_1 | 297 | 301 | PF00389 | 0.427 |
| LIG_deltaCOP1_diTrp_1 | 41 | 48 | PF00928 | 0.467 |
| LIG_EH1_1 | 98 | 106 | PF00400 | 0.302 |
| LIG_FHA_1 | 392 | 398 | PF00498 | 0.508 |
| LIG_FHA_2 | 246 | 252 | PF00498 | 0.609 |
| LIG_FHA_2 | 439 | 445 | PF00498 | 0.537 |
| LIG_HP1_1 | 189 | 193 | PF01393 | 0.346 |
| LIG_LIR_Apic_2 | 117 | 123 | PF02991 | 0.302 |
| LIG_LIR_Apic_2 | 245 | 250 | PF02991 | 0.613 |
| LIG_LIR_Apic_2 | 251 | 256 | PF02991 | 0.564 |
| LIG_LIR_Apic_2 | 40 | 46 | PF02991 | 0.402 |
| LIG_LIR_Gen_1 | 188 | 198 | PF02991 | 0.399 |
| LIG_LIR_Gen_1 | 403 | 413 | PF02991 | 0.578 |
| LIG_LIR_Gen_1 | 45 | 54 | PF02991 | 0.520 |
| LIG_LIR_Gen_1 | 452 | 459 | PF02991 | 0.598 |
| LIG_LIR_Gen_1 | 64 | 75 | PF02991 | 0.196 |
| LIG_LIR_Nem_3 | 188 | 193 | PF02991 | 0.375 |
| LIG_LIR_Nem_3 | 403 | 408 | PF02991 | 0.562 |
| LIG_LIR_Nem_3 | 452 | 458 | PF02991 | 0.594 |
| LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.405 |
| LIG_MLH1_MIPbox_1 | 63 | 67 | PF16413 | 0.415 |
| LIG_PCNA_PIPBox_1 | 102 | 111 | PF02747 | 0.302 |
| LIG_Pex14_1 | 44 | 48 | PF04695 | 0.468 |
| LIG_Pex14_2 | 455 | 459 | PF04695 | 0.609 |
| LIG_Pex14_2 | 62 | 66 | PF04695 | 0.393 |
| LIG_SH2_CRK | 253 | 257 | PF00017 | 0.547 |
| LIG_SH2_STAP1 | 168 | 172 | PF00017 | 0.302 |
| LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.311 |
| LIG_SH3_3 | 191 | 197 | PF00018 | 0.341 |
| LIG_SH3_3 | 2 | 8 | PF00018 | 0.562 |
| LIG_SH3_3 | 302 | 308 | PF00018 | 0.520 |
| LIG_SUMO_SIM_par_1 | 296 | 301 | PF11976 | 0.429 |
| LIG_SUMO_SIM_par_1 | 389 | 394 | PF11976 | 0.554 |
| LIG_TRAF2_1 | 466 | 469 | PF00917 | 0.662 |
| MOD_CDK_SPxxK_3 | 4 | 11 | PF00069 | 0.620 |
| MOD_CK1_1 | 13 | 19 | PF00069 | 0.588 |
| MOD_CK1_1 | 4 | 10 | PF00069 | 0.619 |
| MOD_CK1_1 | 439 | 445 | PF00069 | 0.735 |
| MOD_CK1_1 | 454 | 460 | PF00069 | 0.499 |
| MOD_CK2_1 | 107 | 113 | PF00069 | 0.318 |
| MOD_CK2_1 | 124 | 130 | PF00069 | 0.325 |
| MOD_CK2_1 | 438 | 444 | PF00069 | 0.536 |
| MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.532 |
| MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.302 |
| MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.636 |
| MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.661 |
| MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.541 |
| MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.453 |
| MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.576 |
| MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.541 |
| MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.636 |
| MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.586 |
| MOD_GlcNHglycan | 375 | 379 | PF01048 | 0.516 |
| MOD_GSK3_1 | 114 | 121 | PF00069 | 0.302 |
| MOD_GSK3_1 | 166 | 173 | PF00069 | 0.302 |
| MOD_GSK3_1 | 176 | 183 | PF00069 | 0.302 |
| MOD_GSK3_1 | 18 | 25 | PF00069 | 0.607 |
| MOD_GSK3_1 | 200 | 207 | PF00069 | 0.439 |
| MOD_GSK3_1 | 221 | 228 | PF00069 | 0.727 |
| MOD_GSK3_1 | 296 | 303 | PF00069 | 0.481 |
| MOD_GSK3_1 | 333 | 340 | PF00069 | 0.552 |
| MOD_GSK3_1 | 453 | 460 | PF00069 | 0.545 |
| MOD_GSK3_1 | 66 | 73 | PF00069 | 0.320 |
| MOD_GSK3_1 | 9 | 16 | PF00069 | 0.614 |
| MOD_N-GLC_1 | 242 | 247 | PF02516 | 0.552 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.620 |
| MOD_NEK2_1 | 116 | 121 | PF00069 | 0.302 |
| MOD_NEK2_1 | 298 | 303 | PF00069 | 0.481 |
| MOD_NEK2_1 | 32 | 37 | PF00069 | 0.556 |
| MOD_NEK2_1 | 358 | 363 | PF00069 | 0.626 |
| MOD_NEK2_1 | 458 | 463 | PF00069 | 0.618 |
| MOD_NEK2_1 | 66 | 71 | PF00069 | 0.375 |
| MOD_NEK2_1 | 74 | 79 | PF00069 | 0.265 |
| MOD_NEK2_1 | 82 | 87 | PF00069 | 0.234 |
| MOD_NEK2_2 | 166 | 171 | PF00069 | 0.302 |
| MOD_NEK2_2 | 204 | 209 | PF00069 | 0.423 |
| MOD_PIKK_1 | 13 | 19 | PF00454 | 0.620 |
| MOD_PIKK_1 | 134 | 140 | PF00454 | 0.302 |
| MOD_PIKK_1 | 176 | 182 | PF00454 | 0.302 |
| MOD_PIKK_1 | 89 | 95 | PF00454 | 0.302 |
| MOD_PKA_1 | 436 | 442 | PF00069 | 0.574 |
| MOD_PKA_2 | 10 | 16 | PF00069 | 0.630 |
| MOD_PKA_2 | 436 | 442 | PF00069 | 0.608 |
| MOD_PKB_1 | 223 | 231 | PF00069 | 0.580 |
| MOD_PKB_1 | 399 | 407 | PF00069 | 0.497 |
| MOD_Plk_1 | 129 | 135 | PF00069 | 0.300 |
| MOD_Plk_1 | 242 | 248 | PF00069 | 0.563 |
| MOD_Plk_1 | 451 | 457 | PF00069 | 0.626 |
| MOD_Plk_4 | 454 | 460 | PF00069 | 0.605 |
| MOD_Plk_4 | 61 | 67 | PF00069 | 0.435 |
| MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.677 |
| MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.556 |
| MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.613 |
| MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.619 |
| MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.510 |
| TRG_AP2beta_CARGO_1 | 452 | 462 | PF09066 | 0.571 |
| TRG_DiLeu_BaEn_1 | 100 | 105 | PF01217 | 0.302 |
| TRG_DiLeu_BaEn_1 | 403 | 408 | PF01217 | 0.500 |
| TRG_DiLeu_BaLyEn_6 | 353 | 358 | PF01217 | 0.532 |
| TRG_DiLeu_BaLyEn_6 | 386 | 391 | PF01217 | 0.572 |
| TRG_ENDOCYTIC_2 | 168 | 171 | PF00928 | 0.352 |
| TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.355 |
| TRG_ER_diArg_1 | 149 | 151 | PF00400 | 0.302 |
| TRG_ER_diArg_1 | 398 | 401 | PF00400 | 0.473 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PD30 | Leptomonas seymouri | 58% | 100% |
| A0A3Q8IAE8 | Leishmania donovani | 94% | 97% |
| A4H8K9 | Leishmania braziliensis | 78% | 100% |
| A4HWY1 | Leishmania infantum | 94% | 100% |
| E9AQP4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |