| 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: 9 |
| NetGPI | no | yes: 0, no: 9 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005634 | nucleus | 5 | 1 |
| GO:0005654 | nucleoplasm | 2 | 1 |
| GO:0005730 | nucleolus | 5 | 1 |
| GO:0005737 | cytoplasm | 2 | 1 |
| GO:0043226 | organelle | 2 | 1 |
| GO:0043227 | membrane-bounded organelle | 3 | 1 |
| GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
| GO:0043229 | intracellular organelle | 3 | 1 |
| GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
| GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AMG2
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006479 | protein methylation | 4 | 1 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
| GO:0008152 | metabolic process | 1 | 3 |
| GO:0008213 | protein alkylation | 5 | 1 |
| GO:0009987 | cellular process | 1 | 1 |
| GO:0016570 | histone modification | 5 | 1 |
| GO:0016571 | histone methylation | 5 | 1 |
| GO:0018022 | peptidyl-lysine methylation | 5 | 1 |
| GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
| GO:0018205 | peptidyl-lysine modification | 6 | 1 |
| GO:0019538 | protein metabolic process | 3 | 1 |
| GO:0032259 | methylation | 2 | 3 |
| GO:0034968 | histone lysine methylation | 6 | 1 |
| GO:0036211 | protein modification process | 4 | 1 |
| GO:0043170 | macromolecule metabolic process | 3 | 1 |
| GO:0043412 | macromolecule modification | 4 | 1 |
| GO:0043414 | macromolecule methylation | 3 | 1 |
| GO:0044237 | cellular metabolic process | 2 | 1 |
| GO:0044238 | primary metabolic process | 2 | 1 |
| GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 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 | 3 |
| GO:0008168 | methyltransferase activity | 4 | 3 |
| GO:0008170 | N-methyltransferase activity | 5 | 1 |
| GO:0008276 | protein methyltransferase activity | 3 | 1 |
| GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 1 |
| GO:0016278 | lysine N-methyltransferase activity | 6 | 1 |
| GO:0016279 | protein-lysine N-methyltransferase activity | 4 | 1 |
| GO:0016740 | transferase activity | 2 | 3 |
| GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 3 |
| GO:0018024 | obsolete histone lysine N-methyltransferase activity | 5 | 1 |
| GO:0042054 | histone methyltransferase activity | 4 | 1 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 382 | 386 | PF00656 | 0.557 |
| CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.788 |
| CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.654 |
| CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.519 |
| CLV_NRD_NRD_1 | 414 | 416 | PF00675 | 0.401 |
| CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.732 |
| CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.645 |
| CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.652 |
| CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.522 |
| CLV_PCSK_KEX2_1 | 414 | 416 | PF00082 | 0.357 |
| CLV_PCSK_PC1ET2_1 | 174 | 176 | PF00082 | 0.715 |
| CLV_PCSK_PC1ET2_1 | 28 | 30 | PF00082 | 0.701 |
| CLV_PCSK_PC7_1 | 170 | 176 | PF00082 | 0.723 |
| CLV_PCSK_SKI1_1 | 480 | 484 | PF00082 | 0.466 |
| DEG_APCC_DBOX_1 | 182 | 190 | PF00400 | 0.545 |
| DEG_SCF_TRCP1_1 | 146 | 152 | PF00400 | 0.527 |
| DEG_SPOP_SBC_1 | 107 | 111 | PF00917 | 0.690 |
| DEG_SPOP_SBC_1 | 427 | 431 | PF00917 | 0.563 |
| DEG_SPOP_SBC_1 | 434 | 438 | PF00917 | 0.524 |
| DOC_CYCLIN_RxL_1 | 477 | 484 | PF00134 | 0.457 |
| DOC_MAPK_gen_1 | 28 | 40 | PF00069 | 0.607 |
| DOC_MAPK_gen_1 | 340 | 348 | PF00069 | 0.459 |
| DOC_PP2B_LxvP_1 | 135 | 138 | PF13499 | 0.502 |
| DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.769 |
| DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.654 |
| DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.589 |
| DOC_WW_Pin1_4 | 103 | 108 | PF00397 | 0.698 |
| DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.551 |
| DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.553 |
| DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.396 |
| DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.389 |
| LIG_14-3-3_CanoR_1 | 175 | 180 | PF00244 | 0.560 |
| LIG_14-3-3_CanoR_1 | 236 | 242 | PF00244 | 0.592 |
| LIG_14-3-3_CanoR_1 | 263 | 269 | PF00244 | 0.477 |
| LIG_14-3-3_CanoR_1 | 326 | 332 | PF00244 | 0.568 |
| LIG_14-3-3_CanoR_1 | 33 | 39 | PF00244 | 0.549 |
| LIG_14-3-3_CanoR_1 | 396 | 405 | PF00244 | 0.578 |
| LIG_14-3-3_CanoR_1 | 414 | 424 | PF00244 | 0.587 |
| LIG_14-3-3_CanoR_1 | 425 | 435 | PF00244 | 0.446 |
| LIG_14-3-3_CanoR_1 | 487 | 496 | PF00244 | 0.514 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.743 |
| LIG_BRCT_BRCA1_1 | 344 | 348 | PF00533 | 0.500 |
| LIG_FHA_1 | 155 | 161 | PF00498 | 0.688 |
| LIG_FHA_1 | 212 | 218 | PF00498 | 0.386 |
| LIG_FHA_1 | 35 | 41 | PF00498 | 0.527 |
| LIG_FHA_1 | 450 | 456 | PF00498 | 0.578 |
| LIG_FHA_1 | 489 | 495 | PF00498 | 0.489 |
| LIG_FHA_2 | 427 | 433 | PF00498 | 0.557 |
| LIG_LIR_Apic_2 | 2 | 7 | PF02991 | 0.658 |
| LIG_LIR_Gen_1 | 213 | 223 | PF02991 | 0.377 |
| LIG_LIR_Gen_1 | 330 | 339 | PF02991 | 0.525 |
| LIG_LIR_Gen_1 | 462 | 471 | PF02991 | 0.541 |
| LIG_LIR_Nem_3 | 213 | 219 | PF02991 | 0.389 |
| LIG_LIR_Nem_3 | 330 | 334 | PF02991 | 0.539 |
| LIG_LIR_Nem_3 | 462 | 468 | PF02991 | 0.467 |
| LIG_LIR_Nem_3 | 484 | 489 | PF02991 | 0.409 |
| LIG_NRP_CendR_1 | 502 | 503 | PF00754 | 0.564 |
| LIG_RPA_C_Fungi | 391 | 403 | PF08784 | 0.188 |
| LIG_SH2_CRK | 125 | 129 | PF00017 | 0.503 |
| LIG_SH2_CRK | 200 | 204 | PF00017 | 0.495 |
| LIG_SH2_CRK | 486 | 490 | PF00017 | 0.413 |
| LIG_SH2_PTP2 | 4 | 7 | PF00017 | 0.662 |
| LIG_SH2_PTP2 | 465 | 468 | PF00017 | 0.412 |
| LIG_SH2_SRC | 4 | 7 | PF00017 | 0.662 |
| LIG_SH2_STAP1 | 435 | 439 | PF00017 | 0.372 |
| LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.498 |
| LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.453 |
| LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.415 |
| LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.662 |
| LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.421 |
| LIG_SH3_3 | 118 | 124 | PF00018 | 0.436 |
| LIG_SH3_3 | 318 | 324 | PF00018 | 0.623 |
| LIG_SUMO_SIM_par_1 | 376 | 383 | PF11976 | 0.422 |
| LIG_TRAF2_1 | 19 | 22 | PF00917 | 0.594 |
| LIG_TRAF2_1 | 457 | 460 | PF00917 | 0.312 |
| LIG_TYR_ITIM | 463 | 468 | PF00017 | 0.425 |
| LIG_WRC_WIRS_1 | 265 | 270 | PF05994 | 0.460 |
| LIG_WW_1 | 324 | 327 | PF00397 | 0.497 |
| LIG_WW_3 | 323 | 327 | PF00397 | 0.523 |
| MOD_CDK_SPxxK_3 | 55 | 62 | PF00069 | 0.405 |
| MOD_CK1_1 | 105 | 111 | PF00069 | 0.729 |
| MOD_CK1_1 | 112 | 118 | PF00069 | 0.708 |
| MOD_CK1_1 | 154 | 160 | PF00069 | 0.744 |
| MOD_CK1_1 | 246 | 252 | PF00069 | 0.589 |
| MOD_CK1_1 | 430 | 436 | PF00069 | 0.395 |
| MOD_CK2_1 | 426 | 432 | PF00069 | 0.454 |
| MOD_Cter_Amidation | 172 | 175 | PF01082 | 0.624 |
| MOD_Cter_Amidation | 30 | 33 | PF01082 | 0.596 |
| MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.513 |
| MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.606 |
| MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.732 |
| MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.772 |
| MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.473 |
| MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.429 |
| MOD_GSK3_1 | 101 | 108 | PF00069 | 0.655 |
| MOD_GSK3_1 | 150 | 157 | PF00069 | 0.575 |
| MOD_GSK3_1 | 199 | 206 | PF00069 | 0.415 |
| MOD_GSK3_1 | 271 | 278 | PF00069 | 0.635 |
| MOD_GSK3_1 | 334 | 341 | PF00069 | 0.354 |
| MOD_GSK3_1 | 349 | 356 | PF00069 | 0.464 |
| MOD_GSK3_1 | 426 | 433 | PF00069 | 0.458 |
| MOD_GSK3_1 | 435 | 442 | PF00069 | 0.342 |
| MOD_N-GLC_1 | 211 | 216 | PF02516 | 0.521 |
| MOD_N-GLC_1 | 243 | 248 | PF02516 | 0.554 |
| MOD_N-GLC_1 | 367 | 372 | PF02516 | 0.312 |
| MOD_NEK2_1 | 144 | 149 | PF00069 | 0.510 |
| MOD_NEK2_1 | 229 | 234 | PF00069 | 0.398 |
| MOD_NEK2_1 | 334 | 339 | PF00069 | 0.382 |
| MOD_NEK2_1 | 360 | 365 | PF00069 | 0.380 |
| MOD_NEK2_1 | 367 | 372 | PF00069 | 0.446 |
| MOD_OFUCOSY | 365 | 371 | PF10250 | 0.312 |
| MOD_PIKK_1 | 406 | 412 | PF00454 | 0.372 |
| MOD_PIKK_1 | 497 | 503 | PF00454 | 0.478 |
| MOD_PIKK_1 | 5 | 11 | PF00454 | 0.728 |
| MOD_PK_1 | 175 | 181 | PF00069 | 0.652 |
| MOD_PK_1 | 342 | 348 | PF00069 | 0.432 |
| MOD_PKA_1 | 174 | 180 | PF00069 | 0.420 |
| MOD_PKA_1 | 415 | 421 | PF00069 | 0.438 |
| MOD_PKA_2 | 174 | 180 | PF00069 | 0.460 |
| MOD_PKA_2 | 314 | 320 | PF00069 | 0.681 |
| MOD_PKA_2 | 334 | 340 | PF00069 | 0.213 |
| MOD_PKB_1 | 340 | 348 | PF00069 | 0.510 |
| MOD_Plk_1 | 243 | 249 | PF00069 | 0.565 |
| MOD_Plk_1 | 367 | 373 | PF00069 | 0.337 |
| MOD_Plk_1 | 459 | 465 | PF00069 | 0.324 |
| MOD_Plk_2-3 | 467 | 473 | PF00069 | 0.580 |
| MOD_Plk_4 | 175 | 181 | PF00069 | 0.633 |
| MOD_Plk_4 | 334 | 340 | PF00069 | 0.430 |
| MOD_ProDKin_1 | 103 | 109 | PF00069 | 0.697 |
| MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.429 |
| MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.432 |
| MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.391 |
| MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.385 |
| TRG_DiLeu_BaEn_2 | 483 | 489 | PF01217 | 0.410 |
| TRG_DiLeu_BaLyEn_6 | 162 | 167 | PF01217 | 0.568 |
| TRG_DiLeu_BaLyEn_6 | 185 | 190 | PF01217 | 0.429 |
| TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.453 |
| TRG_ENDOCYTIC_2 | 465 | 468 | PF00928 | 0.421 |
| TRG_ENDOCYTIC_2 | 486 | 489 | PF00928 | 0.399 |
| TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.384 |
| TRG_ER_diArg_1 | 312 | 315 | PF00400 | 0.606 |
| TRG_ER_diArg_1 | 32 | 34 | PF00400 | 0.538 |
| TRG_ER_diArg_1 | 339 | 342 | PF00400 | 0.492 |
| TRG_ER_diArg_1 | 496 | 499 | PF00400 | 0.519 |
| TRG_NLS_MonoExtC_3 | 27 | 32 | PF00514 | 0.677 |
| TRG_NLS_MonoExtN_4 | 25 | 32 | PF00514 | 0.693 |
| TRG_Pf-PMV_PEXEL_1 | 480 | 484 | PF00026 | 0.431 |
| TRG_Pf-PMV_PEXEL_1 | 67 | 72 | PF00026 | 0.512 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P3I8 | Leptomonas seymouri | 49% | 91% |
| A0A1X0NPE5 | Trypanosomatidae | 26% | 100% |
| A0A3S5H671 | Leishmania donovani | 91% | 78% |
| A0A3S5IRB9 | Trypanosoma rangeli | 27% | 100% |
| A4H6C5 | Leishmania braziliensis | 87% | 100% |
| A4HTM8 | Leishmania infantum | 91% | 99% |
| C9ZPC4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
| Q4QI81 | Leishmania major | 93% | 100% |