| 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: 10 |
| NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9AIL9
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
| GO:0006396 | RNA processing | 6 | 11 |
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
| GO:0008152 | metabolic process | 1 | 11 |
| GO:0009987 | cellular process | 1 | 11 |
| GO:0016070 | RNA metabolic process | 5 | 11 |
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
| GO:0043170 | macromolecule metabolic process | 3 | 11 |
| GO:0044237 | cellular metabolic process | 2 | 11 |
| GO:0044238 | primary metabolic process | 2 | 11 |
| GO:0046483 | heterocycle metabolic process | 3 | 11 |
| GO:0071704 | organic substance metabolic process | 2 | 11 |
| GO:0090304 | nucleic acid metabolic process | 4 | 11 |
| GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 11 |
| GO:0008168 | methyltransferase activity | 4 | 11 |
| GO:0008173 | RNA methyltransferase activity | 4 | 11 |
| GO:0016740 | transferase activity | 2 | 11 |
| GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 11 |
| GO:0140098 | catalytic activity, acting on RNA | 3 | 11 |
| GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.318 |
| CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.296 |
| CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.452 |
| CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.424 |
| CLV_NRD_NRD_1 | 441 | 443 | PF00675 | 0.373 |
| CLV_NRD_NRD_1 | 504 | 506 | PF00675 | 0.284 |
| CLV_NRD_NRD_1 | 561 | 563 | PF00675 | 0.469 |
| CLV_PCSK_FUR_1 | 151 | 155 | PF00082 | 0.397 |
| CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.591 |
| CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.445 |
| CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.531 |
| CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.288 |
| CLV_PCSK_KEX2_1 | 441 | 443 | PF00082 | 0.190 |
| CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.284 |
| CLV_PCSK_KEX2_1 | 561 | 563 | PF00082 | 0.469 |
| CLV_PCSK_PC1ET2_1 | 123 | 125 | PF00082 | 0.577 |
| CLV_PCSK_PC1ET2_1 | 153 | 155 | PF00082 | 0.445 |
| CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.394 |
| CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.346 |
| CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.382 |
| DEG_APCC_DBOX_1 | 153 | 161 | PF00400 | 0.414 |
| DEG_APCC_DBOX_1 | 306 | 314 | PF00400 | 0.491 |
| DEG_SCF_FBW7_1 | 357 | 364 | PF00400 | 0.331 |
| DEG_SCF_FBW7_2 | 382 | 388 | PF00400 | 0.334 |
| DEG_SPOP_SBC_1 | 295 | 299 | PF00917 | 0.410 |
| DOC_CKS1_1 | 358 | 363 | PF01111 | 0.335 |
| DOC_CKS1_1 | 382 | 387 | PF01111 | 0.334 |
| DOC_CKS1_1 | 81 | 86 | PF01111 | 0.432 |
| DOC_MAPK_gen_1 | 151 | 159 | PF00069 | 0.307 |
| DOC_MAPK_gen_1 | 307 | 313 | PF00069 | 0.236 |
| DOC_MAPK_gen_1 | 422 | 432 | PF00069 | 0.255 |
| DOC_MAPK_MEF2A_6 | 191 | 198 | PF00069 | 0.323 |
| DOC_MAPK_MEF2A_6 | 284 | 293 | PF00069 | 0.346 |
| DOC_MAPK_MEF2A_6 | 425 | 432 | PF00069 | 0.255 |
| DOC_MAPK_MEF2A_6 | 475 | 482 | PF00069 | 0.387 |
| DOC_MAPK_MEF2A_6 | 70 | 79 | PF00069 | 0.297 |
| DOC_PP1_RVXF_1 | 352 | 359 | PF00149 | 0.278 |
| DOC_PP2B_LxvP_1 | 482 | 485 | PF13499 | 0.255 |
| DOC_PP4_FxxP_1 | 182 | 185 | PF00568 | 0.277 |
| DOC_PP4_FxxP_1 | 350 | 353 | PF00568 | 0.363 |
| DOC_PP4_FxxP_1 | 358 | 361 | PF00568 | 0.282 |
| DOC_PP4_FxxP_1 | 81 | 84 | PF00568 | 0.401 |
| DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.344 |
| DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.424 |
| DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.586 |
| DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.433 |
| DOC_USP7_UBL2_3 | 119 | 123 | PF12436 | 0.610 |
| DOC_USP7_UBL2_3 | 43 | 47 | PF12436 | 0.458 |
| DOC_USP7_UBL2_3 | 525 | 529 | PF12436 | 0.255 |
| DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.512 |
| DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.343 |
| DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.331 |
| DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.253 |
| DOC_WW_Pin1_4 | 381 | 386 | PF00397 | 0.255 |
| DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.437 |
| LIG_14-3-3_CanoR_1 | 154 | 160 | PF00244 | 0.310 |
| LIG_14-3-3_CanoR_1 | 87 | 97 | PF00244 | 0.513 |
| LIG_Actin_WH2_2 | 174 | 189 | PF00022 | 0.241 |
| LIG_AP2alpha_1 | 174 | 178 | PF02296 | 0.390 |
| LIG_BRCT_BRCA1_1 | 196 | 200 | PF00533 | 0.387 |
| LIG_BRCT_BRCA1_1 | 346 | 350 | PF00533 | 0.410 |
| LIG_Clathr_ClatBox_1 | 26 | 30 | PF01394 | 0.373 |
| LIG_EH_1 | 533 | 537 | PF12763 | 0.174 |
| LIG_FHA_1 | 181 | 187 | PF00498 | 0.439 |
| LIG_FHA_1 | 204 | 210 | PF00498 | 0.426 |
| LIG_FHA_1 | 218 | 224 | PF00498 | 0.311 |
| LIG_FHA_1 | 297 | 303 | PF00498 | 0.402 |
| LIG_FHA_1 | 329 | 335 | PF00498 | 0.329 |
| LIG_FHA_1 | 358 | 364 | PF00498 | 0.323 |
| LIG_FHA_1 | 402 | 408 | PF00498 | 0.337 |
| LIG_FHA_1 | 411 | 417 | PF00498 | 0.293 |
| LIG_FHA_1 | 548 | 554 | PF00498 | 0.255 |
| LIG_FHA_2 | 296 | 302 | PF00498 | 0.472 |
| LIG_FHA_2 | 313 | 319 | PF00498 | 0.279 |
| LIG_FHA_2 | 360 | 366 | PF00498 | 0.307 |
| LIG_FHA_2 | 403 | 409 | PF00498 | 0.255 |
| LIG_FHA_2 | 580 | 586 | PF00498 | 0.558 |
| LIG_FHA_2 | 81 | 87 | PF00498 | 0.417 |
| LIG_IBAR_NPY_1 | 74 | 76 | PF08397 | 0.282 |
| LIG_Integrin_RGD_1 | 475 | 477 | PF01839 | 0.331 |
| LIG_LIR_Apic_2 | 347 | 353 | PF02991 | 0.402 |
| LIG_LIR_Apic_2 | 355 | 361 | PF02991 | 0.466 |
| LIG_LIR_Gen_1 | 263 | 273 | PF02991 | 0.447 |
| LIG_LIR_Gen_1 | 301 | 311 | PF02991 | 0.438 |
| LIG_LIR_Gen_1 | 33 | 41 | PF02991 | 0.433 |
| LIG_LIR_Nem_3 | 176 | 181 | PF02991 | 0.332 |
| LIG_LIR_Nem_3 | 263 | 268 | PF02991 | 0.423 |
| LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.432 |
| LIG_LIR_Nem_3 | 301 | 306 | PF02991 | 0.436 |
| LIG_LIR_Nem_3 | 33 | 38 | PF02991 | 0.433 |
| LIG_LIR_Nem_3 | 377 | 382 | PF02991 | 0.255 |
| LIG_MYND_1 | 575 | 579 | PF01753 | 0.471 |
| LIG_NRBOX | 61 | 67 | PF00104 | 0.430 |
| LIG_PCNA_yPIPBox_3 | 486 | 497 | PF02747 | 0.331 |
| LIG_PCNA_yPIPBox_3 | 54 | 66 | PF02747 | 0.589 |
| LIG_Pex14_2 | 174 | 178 | PF04695 | 0.487 |
| LIG_PTB_Apo_2 | 448 | 455 | PF02174 | 0.255 |
| LIG_SH2_CRK | 35 | 39 | PF00017 | 0.446 |
| LIG_SH2_NCK_1 | 35 | 39 | PF00017 | 0.446 |
| LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.426 |
| LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.255 |
| LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.408 |
| LIG_SH3_3 | 2 | 8 | PF00018 | 0.764 |
| LIG_SH3_3 | 379 | 385 | PF00018 | 0.359 |
| LIG_SH3_3 | 575 | 581 | PF00018 | 0.473 |
| LIG_SH3_3 | 69 | 75 | PF00018 | 0.324 |
| LIG_SH3_4 | 525 | 532 | PF00018 | 0.274 |
| LIG_SUMO_SIM_anti_2 | 477 | 483 | PF11976 | 0.297 |
| LIG_SUMO_SIM_anti_2 | 554 | 560 | PF11976 | 0.255 |
| LIG_SUMO_SIM_par_1 | 309 | 318 | PF11976 | 0.294 |
| LIG_SUMO_SIM_par_1 | 404 | 411 | PF11976 | 0.341 |
| LIG_SUMO_SIM_par_1 | 477 | 483 | PF11976 | 0.257 |
| LIG_SUMO_SIM_par_1 | 554 | 560 | PF11976 | 0.334 |
| LIG_TRAF2_1 | 144 | 147 | PF00917 | 0.295 |
| LIG_TRFH_1 | 372 | 376 | PF08558 | 0.255 |
| LIG_UBA3_1 | 26 | 34 | PF00899 | 0.373 |
| LIG_UBA3_1 | 61 | 70 | PF00899 | 0.420 |
| LIG_WW_3 | 483 | 487 | PF00397 | 0.255 |
| MOD_CDC14_SPxK_1 | 184 | 187 | PF00782 | 0.253 |
| MOD_CDK_SPxK_1 | 181 | 187 | PF00069 | 0.243 |
| MOD_CDK_SPxxK_3 | 80 | 87 | PF00069 | 0.449 |
| MOD_CK1_1 | 108 | 114 | PF00069 | 0.527 |
| MOD_CK1_1 | 401 | 407 | PF00069 | 0.387 |
| MOD_CK1_1 | 465 | 471 | PF00069 | 0.345 |
| MOD_CK1_1 | 583 | 589 | PF00069 | 0.551 |
| MOD_CK1_1 | 9 | 15 | PF00069 | 0.621 |
| MOD_CK2_1 | 141 | 147 | PF00069 | 0.462 |
| MOD_CK2_1 | 212 | 218 | PF00069 | 0.536 |
| MOD_CK2_1 | 295 | 301 | PF00069 | 0.325 |
| MOD_CK2_1 | 312 | 318 | PF00069 | 0.341 |
| MOD_CK2_1 | 359 | 365 | PF00069 | 0.311 |
| MOD_CK2_1 | 579 | 585 | PF00069 | 0.485 |
| MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.340 |
| MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.397 |
| MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.391 |
| MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.255 |
| MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.384 |
| MOD_GlcNHglycan | 582 | 585 | PF01048 | 0.710 |
| MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.712 |
| MOD_GSK3_1 | 340 | 347 | PF00069 | 0.383 |
| MOD_GSK3_1 | 357 | 364 | PF00069 | 0.233 |
| MOD_GSK3_1 | 398 | 405 | PF00069 | 0.325 |
| MOD_GSK3_1 | 408 | 415 | PF00069 | 0.278 |
| MOD_GSK3_1 | 521 | 528 | PF00069 | 0.275 |
| MOD_GSK3_1 | 579 | 586 | PF00069 | 0.544 |
| MOD_GSK3_1 | 89 | 96 | PF00069 | 0.385 |
| MOD_LATS_1 | 32 | 38 | PF00433 | 0.310 |
| MOD_N-GLC_1 | 194 | 199 | PF02516 | 0.381 |
| MOD_N-GLC_1 | 489 | 494 | PF02516 | 0.331 |
| MOD_N-GLC_2 | 249 | 251 | PF02516 | 0.218 |
| MOD_N-GLC_2 | 600 | 602 | PF02516 | 0.454 |
| MOD_NEK2_1 | 105 | 110 | PF00069 | 0.429 |
| MOD_NEK2_1 | 114 | 119 | PF00069 | 0.481 |
| MOD_NEK2_1 | 418 | 423 | PF00069 | 0.376 |
| MOD_NEK2_1 | 432 | 437 | PF00069 | 0.178 |
| MOD_NEK2_1 | 536 | 541 | PF00069 | 0.327 |
| MOD_NEK2_1 | 570 | 575 | PF00069 | 0.688 |
| MOD_NEK2_1 | 93 | 98 | PF00069 | 0.338 |
| MOD_NEK2_2 | 499 | 504 | PF00069 | 0.299 |
| MOD_PKA_2 | 521 | 527 | PF00069 | 0.213 |
| MOD_Plk_1 | 105 | 111 | PF00069 | 0.420 |
| MOD_Plk_1 | 194 | 200 | PF00069 | 0.459 |
| MOD_Plk_1 | 489 | 495 | PF00069 | 0.331 |
| MOD_Plk_2-3 | 141 | 147 | PF00069 | 0.336 |
| MOD_Plk_4 | 155 | 161 | PF00069 | 0.244 |
| MOD_Plk_4 | 212 | 218 | PF00069 | 0.493 |
| MOD_Plk_4 | 386 | 392 | PF00069 | 0.376 |
| MOD_Plk_4 | 402 | 408 | PF00069 | 0.242 |
| MOD_Plk_4 | 462 | 468 | PF00069 | 0.343 |
| MOD_Plk_4 | 489 | 495 | PF00069 | 0.264 |
| MOD_Plk_4 | 89 | 95 | PF00069 | 0.309 |
| MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.510 |
| MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.346 |
| MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.324 |
| MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.253 |
| MOD_ProDKin_1 | 381 | 387 | PF00069 | 0.255 |
| MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.433 |
| MOD_SUMO_for_1 | 283 | 286 | PF00179 | 0.459 |
| MOD_SUMO_rev_2 | 510 | 516 | PF00179 | 0.245 |
| TRG_DiLeu_BaLyEn_6 | 57 | 62 | PF01217 | 0.548 |
| TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.505 |
| TRG_ENDOCYTIC_2 | 171 | 174 | PF00928 | 0.402 |
| TRG_ENDOCYTIC_2 | 35 | 38 | PF00928 | 0.442 |
| TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.506 |
| TRG_ER_diArg_1 | 100 | 103 | PF00400 | 0.487 |
| TRG_ER_diArg_1 | 306 | 309 | PF00400 | 0.476 |
| TRG_ER_diArg_1 | 424 | 426 | PF00400 | 0.174 |
| TRG_ER_diArg_1 | 503 | 505 | PF00400 | 0.284 |
| TRG_ER_diArg_1 | 561 | 563 | PF00400 | 0.471 |
| TRG_NLS_MonoExtN_4 | 151 | 156 | PF00514 | 0.388 |
| TRG_Pf-PMV_PEXEL_1 | 308 | 312 | PF00026 | 0.240 |
| TRG_Pf-PMV_PEXEL_1 | 54 | 58 | PF00026 | 0.425 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I1V8 | Leptomonas seymouri | 75% | 100% |
| A0A1X0NXG3 | Trypanosomatidae | 59% | 100% |
| A0A3Q8IAY6 | Leishmania donovani | 85% | 100% |
| A0A3R7L6W3 | Trypanosoma rangeli | 63% | 100% |
| A4HZ00 | Leishmania infantum | 85% | 100% |
| A4QP75 | Danio rerio | 30% | 100% |
| A5IBU7 | Legionella pneumophila (strain Corby) | 25% | 100% |
| C9ZIM3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
| E9AUV2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
| O31545 | Bacillus subtilis (strain 168) | 26% | 100% |
| P0DG16 | Streptococcus pyogenes serotype M3 (strain ATCC BAA-595 / MGAS315) | 24% | 100% |
| P0DG17 | Streptococcus pyogenes serotype M3 (strain SSI-1) | 24% | 100% |
| Q4QCN1 | Leishmania major | 85% | 100% |
| Q5HEM5 | Staphylococcus aureus (strain COL) | 26% | 100% |
| Q5HN37 | Staphylococcus epidermidis (strain ATCC 35984 / RP62A) | 23% | 100% |
| Q5X5A8 | Legionella pneumophila (strain Paris) | 25% | 100% |
| Q5XAU1 | Streptococcus pyogenes serotype M6 (strain ATCC BAA-946 / MGAS10394) | 25% | 100% |
| Q6G836 | Staphylococcus aureus (strain MSSA476) | 26% | 100% |
| Q6GFG0 | Staphylococcus aureus (strain MRSA252) | 26% | 100% |
| Q73EJ5 | Bacillus cereus (strain ATCC 10987 / NRS 248) | 26% | 100% |
| Q7A4Q9 | Staphylococcus aureus (strain N315) | 26% | 100% |
| Q814A6 | Bacillus cereus (strain ATCC 14579 / DSM 31 / CCUG 7414 / JCM 2152 / NBRC 15305 / NCIMB 9373 / NCTC 2599 / NRRL B-3711) | 27% | 100% |
| Q81ZD6 | Bacillus anthracis | 27% | 100% |
| Q830R6 | Enterococcus faecalis (strain ATCC 700802 / V583) | 26% | 100% |
| Q88SY9 | Lactiplantibacillus plantarum (strain ATCC BAA-793 / NCIMB 8826 / WCFS1) | 29% | 100% |
| Q891A0 | Clostridium tetani (strain Massachusetts / E88) | 26% | 100% |
| Q892Z2 | Clostridium tetani (strain Massachusetts / E88) | 27% | 100% |
| Q8BNV1 | Mus musculus | 34% | 99% |
| Q8CRU6 | Staphylococcus epidermidis (strain ATCC 12228 / FDA PCI 1200) | 23% | 100% |
| Q8IZ69 | Homo sapiens | 34% | 97% |
| Q8KGF9 | Chlorobaculum tepidum (strain ATCC 49652 / DSM 12025 / NBRC 103806 / TLS) | 28% | 100% |
| Q8NVT4 | Staphylococcus aureus (strain MW2) | 26% | 100% |
| Q8P017 | Streptococcus pyogenes serotype M18 (strain MGAS8232) | 25% | 100% |
| Q8R933 | Caldanaerobacter subterraneus subsp. tengcongensis (strain DSM 15242 / JCM 11007 / NBRC 100824 / MB4) | 32% | 100% |
| Q8YR05 | Nostoc sp. (strain PCC 7120 / SAG 25.82 / UTEX 2576) | 28% | 100% |
| Q92AQ7 | Listeria innocua serovar 6a (strain ATCC BAA-680 / CLIP 11262) | 28% | 100% |
| Q97J51 | Clostridium acetobutylicum (strain ATCC 824 / DSM 792 / JCM 1419 / LMG 5710 / VKM B-1787) | 29% | 100% |
| Q99SY9 | Staphylococcus aureus (strain Mu50 / ATCC 700699) | 26% | 100% |
| Q99YP3 | Streptococcus pyogenes serotype M1 | 24% | 100% |
| Q9CDP0 | Lactococcus lactis subsp. lactis (strain IL1403) | 27% | 100% |
| Q9CGB9 | Lactococcus lactis subsp. lactis (strain IL1403) | 27% | 100% |
| V5ASX3 | Trypanosoma cruzi | 62% | 100% |