| 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: 5 |
| NetGPI | no | yes: 0, no: 5 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005634 | nucleus | 5 | 1 |
| GO:0016020 | membrane | 2 | 2 |
| GO:0043226 | organelle | 2 | 1 |
| GO:0043227 | membrane-bounded organelle | 3 | 1 |
| GO:0043229 | intracellular organelle | 3 | 1 |
| GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9AKJ9
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000209 | protein polyubiquitination | 8 | 1 |
| 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 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 2 |
| GO:0004842 | ubiquitin-protein transferase activity | 4 | 1 |
| GO:0016740 | transferase activity | 2 | 1 |
| GO:0016874 | ligase activity | 2 | 2 |
| GO:0019787 | ubiquitin-like protein transferase activity | 3 | 1 |
| GO:0061631 | ubiquitin conjugating enzyme activity | 5 | 1 |
| GO:0061650 | ubiquitin-like protein conjugating enzyme activity | 4 | 1 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 454 | 456 | PF00675 | 0.362 |
| CLV_PCSK_KEX2_1 | 454 | 456 | PF00082 | 0.362 |
| CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.265 |
| CLV_PCSK_PC1ET2_1 | 9 | 11 | PF00082 | 0.310 |
| DEG_APCC_DBOX_1 | 453 | 461 | PF00400 | 0.362 |
| DEG_SCF_FBW7_1 | 217 | 223 | PF00400 | 0.645 |
| DEG_SCF_FBW7_1 | 361 | 368 | PF00400 | 0.613 |
| DEG_SPOP_SBC_1 | 227 | 231 | PF00917 | 0.620 |
| DOC_CKS1_1 | 217 | 222 | PF01111 | 0.621 |
| DOC_CKS1_1 | 319 | 324 | PF01111 | 0.742 |
| DOC_CKS1_1 | 362 | 367 | PF01111 | 0.616 |
| DOC_CYCLIN_yCln2_LP_2 | 237 | 243 | PF00134 | 0.666 |
| DOC_MAPK_MEF2A_6 | 420 | 427 | PF00069 | 0.569 |
| DOC_MAPK_RevD_3 | 441 | 455 | PF00069 | 0.362 |
| DOC_PP2B_LxvP_1 | 187 | 190 | PF13499 | 0.804 |
| DOC_PP2B_LxvP_1 | 73 | 76 | PF13499 | 0.510 |
| DOC_SPAK_OSR1_1 | 86 | 90 | PF12202 | 0.465 |
| DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.675 |
| DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.656 |
| DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.478 |
| DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.644 |
| DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.740 |
| DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.685 |
| DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.636 |
| DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.732 |
| DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.662 |
| DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.634 |
| DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.671 |
| DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.725 |
| DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.670 |
| DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.718 |
| DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.703 |
| DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.617 |
| DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.701 |
| LIG_Actin_WH2_2 | 440 | 456 | PF00022 | 0.308 |
| LIG_APCC_ABBA_1 | 170 | 175 | PF00400 | 0.603 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.562 |
| LIG_BIR_III_2 | 379 | 383 | PF00653 | 0.715 |
| LIG_BRCT_BRCA1_1 | 83 | 87 | PF00533 | 0.465 |
| LIG_deltaCOP1_diTrp_1 | 144 | 153 | PF00928 | 0.569 |
| LIG_deltaCOP1_diTrp_1 | 39 | 42 | PF00928 | 0.465 |
| LIG_EVH1_1 | 187 | 191 | PF00568 | 0.790 |
| LIG_FHA_1 | 106 | 112 | PF00498 | 0.510 |
| LIG_FHA_1 | 160 | 166 | PF00498 | 0.564 |
| LIG_FHA_1 | 310 | 316 | PF00498 | 0.735 |
| LIG_FHA_1 | 379 | 385 | PF00498 | 0.712 |
| LIG_FHA_1 | 387 | 393 | PF00498 | 0.607 |
| LIG_LIR_Apic_2 | 27 | 32 | PF02991 | 0.465 |
| LIG_LIR_Nem_3 | 12 | 18 | PF02991 | 0.510 |
| LIG_LYPXL_S_1 | 172 | 176 | PF13949 | 0.296 |
| LIG_LYPXL_yS_3 | 173 | 176 | PF13949 | 0.490 |
| LIG_MYND_1 | 185 | 189 | PF01753 | 0.650 |
| LIG_MYND_1 | 269 | 273 | PF01753 | 0.619 |
| LIG_MYND_1 | 282 | 286 | PF01753 | 0.602 |
| LIG_NRBOX | 442 | 448 | PF00104 | 0.238 |
| LIG_NRBOX | 456 | 462 | PF00104 | 0.430 |
| LIG_Pex14_1 | 105 | 109 | PF04695 | 0.465 |
| LIG_Pex14_2 | 38 | 42 | PF04695 | 0.465 |
| LIG_PROFILIN_1 | 188 | 194 | PF00235 | 0.656 |
| LIG_PTAP_UEV_1 | 272 | 277 | PF05743 | 0.618 |
| LIG_REV1ctd_RIR_1 | 78 | 87 | PF16727 | 0.510 |
| LIG_SH2_CRK | 15 | 19 | PF00017 | 0.538 |
| LIG_SH2_PTP2 | 29 | 32 | PF00017 | 0.510 |
| LIG_SH2_SRC | 109 | 112 | PF00017 | 0.530 |
| LIG_SH2_STAP1 | 109 | 113 | PF00017 | 0.465 |
| LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.510 |
| LIG_SH3_1 | 186 | 192 | PF00018 | 0.669 |
| LIG_SH3_1 | 69 | 75 | PF00018 | 0.465 |
| LIG_SH3_3 | 182 | 188 | PF00018 | 0.685 |
| LIG_SH3_3 | 204 | 210 | PF00018 | 0.706 |
| LIG_SH3_3 | 214 | 220 | PF00018 | 0.706 |
| LIG_SH3_3 | 221 | 227 | PF00018 | 0.720 |
| LIG_SH3_3 | 266 | 272 | PF00018 | 0.636 |
| LIG_SH3_3 | 273 | 279 | PF00018 | 0.665 |
| LIG_SH3_3 | 280 | 286 | PF00018 | 0.615 |
| LIG_SH3_3 | 287 | 293 | PF00018 | 0.612 |
| LIG_SH3_3 | 316 | 322 | PF00018 | 0.691 |
| LIG_SH3_3 | 359 | 365 | PF00018 | 0.768 |
| LIG_SH3_3 | 367 | 373 | PF00018 | 0.748 |
| LIG_SH3_3 | 401 | 407 | PF00018 | 0.665 |
| LIG_SH3_3 | 409 | 415 | PF00018 | 0.662 |
| LIG_SH3_3 | 427 | 433 | PF00018 | 0.581 |
| LIG_SH3_3 | 69 | 75 | PF00018 | 0.465 |
| LIG_SUMO_SIM_par_1 | 136 | 142 | PF11976 | 0.545 |
| LIG_TRAF2_1 | 336 | 339 | PF00917 | 0.631 |
| LIG_TRFH_1 | 71 | 75 | PF08558 | 0.510 |
| LIG_UBA3_1 | 137 | 143 | PF00899 | 0.534 |
| LIG_WRC_WIRS_1 | 442 | 447 | PF05994 | 0.362 |
| MOD_CDC14_SPxK_1 | 177 | 180 | PF00782 | 0.629 |
| MOD_CDC14_SPxK_1 | 357 | 360 | PF00782 | 0.704 |
| MOD_CDK_SPK_2 | 286 | 291 | PF00069 | 0.628 |
| MOD_CDK_SPxK_1 | 174 | 180 | PF00069 | 0.620 |
| MOD_CDK_SPxK_1 | 354 | 360 | PF00069 | 0.704 |
| MOD_CK1_1 | 2 | 8 | PF00069 | 0.576 |
| MOD_CK1_1 | 223 | 229 | PF00069 | 0.708 |
| MOD_CK1_1 | 231 | 237 | PF00069 | 0.771 |
| MOD_CK1_1 | 262 | 268 | PF00069 | 0.675 |
| MOD_CK1_1 | 274 | 280 | PF00069 | 0.631 |
| MOD_CK1_1 | 386 | 392 | PF00069 | 0.609 |
| MOD_CK1_1 | 403 | 409 | PF00069 | 0.760 |
| MOD_CK1_1 | 95 | 101 | PF00069 | 0.481 |
| MOD_CK2_1 | 333 | 339 | PF00069 | 0.778 |
| MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.581 |
| MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.443 |
| MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.453 |
| MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.496 |
| MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.573 |
| MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.449 |
| MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.286 |
| MOD_GSK3_1 | 147 | 154 | PF00069 | 0.546 |
| MOD_GSK3_1 | 216 | 223 | PF00069 | 0.715 |
| MOD_GSK3_1 | 226 | 233 | PF00069 | 0.740 |
| MOD_GSK3_1 | 271 | 278 | PF00069 | 0.635 |
| MOD_GSK3_1 | 294 | 301 | PF00069 | 0.654 |
| MOD_GSK3_1 | 303 | 310 | PF00069 | 0.697 |
| MOD_GSK3_1 | 361 | 368 | PF00069 | 0.636 |
| MOD_GSK3_1 | 378 | 385 | PF00069 | 0.713 |
| MOD_GSK3_1 | 92 | 99 | PF00069 | 0.498 |
| MOD_NEK2_1 | 113 | 118 | PF00069 | 0.510 |
| MOD_NEK2_1 | 153 | 158 | PF00069 | 0.575 |
| MOD_NEK2_1 | 383 | 388 | PF00069 | 0.617 |
| MOD_NEK2_1 | 428 | 433 | PF00069 | 0.726 |
| MOD_NEK2_1 | 65 | 70 | PF00069 | 0.585 |
| MOD_NEK2_1 | 81 | 86 | PF00069 | 0.418 |
| MOD_NEK2_2 | 4 | 9 | PF00069 | 0.457 |
| MOD_NEK2_2 | 40 | 45 | PF00069 | 0.510 |
| MOD_PIKK_1 | 262 | 268 | PF00454 | 0.642 |
| MOD_PKA_1 | 9 | 15 | PF00069 | 0.510 |
| MOD_PKA_2 | 9 | 15 | PF00069 | 0.522 |
| MOD_Plk_1 | 428 | 434 | PF00069 | 0.660 |
| MOD_Plk_1 | 50 | 56 | PF00069 | 0.552 |
| MOD_Plk_4 | 232 | 238 | PF00069 | 0.701 |
| MOD_Plk_4 | 388 | 394 | PF00069 | 0.659 |
| MOD_Plk_4 | 441 | 447 | PF00069 | 0.303 |
| MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.645 |
| MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.743 |
| MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.687 |
| MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.638 |
| MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.732 |
| MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.661 |
| MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.632 |
| MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.670 |
| MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.724 |
| MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.671 |
| MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.719 |
| MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.705 |
| MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.615 |
| MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.700 |
| MOD_SUMO_rev_2 | 164 | 172 | PF00179 | 0.478 |
| MOD_SUMO_rev_2 | 208 | 212 | PF00179 | 0.664 |
| TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.510 |
| TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.490 |
| TRG_ER_diArg_1 | 453 | 455 | PF00400 | 0.362 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A3S5H5K9 | Leishmania donovani | 68% | 100% |
| A4HSL5 | Leishmania infantum | 68% | 100% |
| Q4QJA9 | Leishmania major | 69% | 98% |
| V5B702 | Trypanosoma cruzi | 39% | 100% |