| 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: E9AUV2
| 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_C14_Caspase3-7 | 129 | 133 | PF00656 | 0.617 |
| CLV_C14_Caspase3-7 | 594 | 598 | PF00656 | 0.636 |
| CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.626 |
| CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.325 |
| CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.298 |
| CLV_NRD_NRD_1 | 441 | 443 | PF00675 | 0.372 |
| CLV_NRD_NRD_1 | 504 | 506 | PF00675 | 0.284 |
| CLV_NRD_NRD_1 | 561 | 563 | PF00675 | 0.460 |
| CLV_PCSK_FUR_1 | 151 | 155 | PF00082 | 0.403 |
| CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.602 |
| CLV_PCSK_KEX2_1 | 153 | 155 | PF00082 | 0.451 |
| CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.287 |
| 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 | 0.460 |
| CLV_PCSK_PC1ET2_1 | 123 | 125 | PF00082 | 0.588 |
| CLV_PCSK_PC1ET2_1 | 153 | 155 | PF00082 | 0.451 |
| CLV_PCSK_PC1ET2_1 | 425 | 427 | PF00082 | 0.269 |
| CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.349 |
| CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.271 |
| DEG_APCC_DBOX_1 | 153 | 161 | PF00400 | 0.417 |
| DEG_APCC_DBOX_1 | 306 | 314 | PF00400 | 0.485 |
| DEG_SCF_FBW7_2 | 382 | 388 | PF00400 | 0.334 |
| DEG_SPOP_SBC_1 | 295 | 299 | PF00917 | 0.421 |
| DOC_CDC14_PxL_1 | 357 | 365 | PF14671 | 0.425 |
| DOC_CKS1_1 | 382 | 387 | PF01111 | 0.334 |
| DOC_CKS1_1 | 81 | 86 | PF01111 | 0.523 |
| DOC_CYCLIN_yCln2_LP_2 | 182 | 188 | PF00134 | 0.232 |
| DOC_MAPK_gen_1 | 151 | 159 | PF00069 | 0.313 |
| DOC_MAPK_gen_1 | 422 | 432 | PF00069 | 0.255 |
| DOC_MAPK_MEF2A_6 | 191 | 198 | PF00069 | 0.323 |
| DOC_MAPK_MEF2A_6 | 425 | 432 | PF00069 | 0.255 |
| DOC_MAPK_MEF2A_6 | 475 | 482 | PF00069 | 0.386 |
| DOC_PP2B_LxvP_1 | 350 | 353 | PF13499 | 0.420 |
| DOC_PP2B_LxvP_1 | 482 | 485 | PF13499 | 0.255 |
| DOC_PP2B_LxvP_1 | 5 | 8 | PF13499 | 0.598 |
| DOC_PP4_FxxP_1 | 81 | 84 | PF00568 | 0.489 |
| DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.393 |
| DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.423 |
| DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.426 |
| DOC_USP7_MATH_1 | 570 | 574 | PF00917 | 0.514 |
| DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.480 |
| DOC_USP7_UBL2_3 | 119 | 123 | PF12436 | 0.623 |
| DOC_USP7_UBL2_3 | 43 | 47 | PF12436 | 0.531 |
| DOC_USP7_UBL2_3 | 525 | 529 | PF12436 | 0.255 |
| DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.351 |
| DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.475 |
| DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.252 |
| DOC_WW_Pin1_4 | 381 | 386 | PF00397 | 0.255 |
| DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.535 |
| DOC_WW_Pin1_4 | 531 | 536 | PF00397 | 0.330 |
| DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.533 |
| LIG_14-3-3_CanoR_1 | 102 | 111 | PF00244 | 0.529 |
| LIG_AP2alpha_1 | 174 | 178 | PF02296 | 0.397 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.665 |
| LIG_BIR_III_4 | 597 | 601 | PF00653 | 0.587 |
| LIG_BRCT_BRCA1_1 | 196 | 200 | PF00533 | 0.391 |
| LIG_Clathr_ClatBox_1 | 26 | 30 | PF01394 | 0.538 |
| LIG_FHA_1 | 181 | 187 | PF00498 | 0.443 |
| LIG_FHA_1 | 204 | 210 | PF00498 | 0.435 |
| LIG_FHA_1 | 218 | 224 | PF00498 | 0.323 |
| LIG_FHA_1 | 297 | 303 | PF00498 | 0.412 |
| LIG_FHA_1 | 329 | 335 | PF00498 | 0.332 |
| LIG_FHA_1 | 362 | 368 | PF00498 | 0.299 |
| 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 | 136 | 142 | PF00498 | 0.509 |
| LIG_FHA_2 | 225 | 231 | PF00498 | 0.441 |
| LIG_FHA_2 | 360 | 366 | PF00498 | 0.306 |
| LIG_FHA_2 | 403 | 409 | PF00498 | 0.255 |
| LIG_FHA_2 | 448 | 454 | PF00498 | 0.282 |
| LIG_FHA_2 | 532 | 538 | PF00498 | 0.282 |
| LIG_FHA_2 | 592 | 598 | PF00498 | 0.654 |
| LIG_FHA_2 | 81 | 87 | PF00498 | 0.505 |
| LIG_Integrin_RGD_1 | 475 | 477 | PF01839 | 0.331 |
| LIG_LIR_Apic_2 | 355 | 361 | PF02991 | 0.467 |
| LIG_LIR_Gen_1 | 138 | 145 | PF02991 | 0.495 |
| LIG_LIR_Gen_1 | 263 | 273 | PF02991 | 0.450 |
| LIG_LIR_Gen_1 | 33 | 41 | PF02991 | 0.522 |
| LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.434 |
| LIG_LIR_Nem_3 | 176 | 181 | PF02991 | 0.338 |
| LIG_LIR_Nem_3 | 253 | 257 | PF02991 | 0.353 |
| LIG_LIR_Nem_3 | 263 | 268 | PF02991 | 0.426 |
| LIG_LIR_Nem_3 | 271 | 277 | PF02991 | 0.434 |
| LIG_LIR_Nem_3 | 33 | 38 | PF02991 | 0.530 |
| LIG_LIR_Nem_3 | 377 | 382 | PF02991 | 0.255 |
| LIG_PCNA_yPIPBox_3 | 486 | 497 | PF02747 | 0.331 |
| LIG_PCNA_yPIPBox_3 | 54 | 66 | PF02747 | 0.677 |
| LIG_Pex14_2 | 174 | 178 | PF04695 | 0.493 |
| LIG_PTB_Apo_2 | 448 | 455 | PF02174 | 0.255 |
| LIG_SH2_CRK | 35 | 39 | PF00017 | 0.518 |
| LIG_SH2_CRK | 358 | 362 | PF00017 | 0.444 |
| LIG_SH2_NCK_1 | 35 | 39 | PF00017 | 0.518 |
| LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.421 |
| LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.255 |
| LIG_SH3_1 | 54 | 60 | PF00018 | 0.671 |
| LIG_SH3_3 | 379 | 385 | PF00018 | 0.358 |
| LIG_SH3_3 | 478 | 484 | PF00018 | 0.188 |
| LIG_SH3_3 | 54 | 60 | PF00018 | 0.582 |
| LIG_SH3_4 | 525 | 532 | PF00018 | 0.273 |
| LIG_SUMO_SIM_anti_2 | 477 | 483 | PF11976 | 0.296 |
| LIG_SUMO_SIM_anti_2 | 554 | 560 | PF11976 | 0.255 |
| LIG_SUMO_SIM_par_1 | 404 | 411 | PF11976 | 0.340 |
| LIG_SUMO_SIM_par_1 | 477 | 483 | PF11976 | 0.257 |
| LIG_SUMO_SIM_par_1 | 554 | 560 | PF11976 | 0.334 |
| LIG_SUMO_SIM_par_1 | 580 | 585 | PF11976 | 0.444 |
| LIG_TRAF2_1 | 315 | 318 | PF00917 | 0.355 |
| LIG_TRAF2_1 | 9 | 12 | PF00917 | 0.744 |
| LIG_TRFH_1 | 372 | 376 | PF08558 | 0.255 |
| LIG_TRFH_1 | 544 | 548 | PF08558 | 0.149 |
| LIG_UBA3_1 | 61 | 70 | PF00899 | 0.520 |
| LIG_WW_3 | 483 | 487 | PF00397 | 0.255 |
| MOD_CDK_SPxxK_3 | 80 | 87 | PF00069 | 0.544 |
| MOD_CK1_1 | 135 | 141 | PF00069 | 0.419 |
| MOD_CK1_1 | 184 | 190 | PF00069 | 0.439 |
| MOD_CK1_1 | 232 | 238 | PF00069 | 0.294 |
| MOD_CK1_1 | 401 | 407 | PF00069 | 0.386 |
| MOD_CK1_1 | 465 | 471 | PF00069 | 0.344 |
| MOD_CK2_1 | 135 | 141 | PF00069 | 0.471 |
| MOD_CK2_1 | 212 | 218 | PF00069 | 0.536 |
| MOD_CK2_1 | 359 | 365 | PF00069 | 0.310 |
| MOD_CK2_1 | 447 | 453 | PF00069 | 0.440 |
| MOD_CK2_1 | 531 | 537 | PF00069 | 0.282 |
| MOD_CK2_1 | 6 | 12 | PF00069 | 0.775 |
| MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.441 |
| MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.401 |
| MOD_GlcNHglycan | 399 | 403 | PF01048 | 0.438 |
| MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.391 |
| MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.255 |
| MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.384 |
| MOD_GlcNHglycan | 564 | 567 | PF01048 | 0.654 |
| MOD_GlcNHglycan | 572 | 575 | PF01048 | 0.695 |
| MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.511 |
| MOD_GSK3_1 | 131 | 138 | PF00069 | 0.670 |
| MOD_GSK3_1 | 180 | 187 | PF00069 | 0.348 |
| MOD_GSK3_1 | 199 | 206 | PF00069 | 0.289 |
| MOD_GSK3_1 | 324 | 331 | PF00069 | 0.362 |
| MOD_GSK3_1 | 33 | 40 | PF00069 | 0.582 |
| MOD_GSK3_1 | 340 | 347 | PF00069 | 0.387 |
| MOD_GSK3_1 | 398 | 405 | PF00069 | 0.324 |
| MOD_GSK3_1 | 408 | 415 | PF00069 | 0.278 |
| MOD_GSK3_1 | 521 | 528 | PF00069 | 0.274 |
| MOD_N-GLC_1 | 194 | 199 | PF02516 | 0.384 |
| MOD_N-GLC_1 | 489 | 494 | PF02516 | 0.331 |
| MOD_NEK2_1 | 1 | 6 | PF00069 | 0.698 |
| MOD_NEK2_1 | 114 | 119 | PF00069 | 0.516 |
| 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_2 | 107 | 112 | PF00069 | 0.353 |
| MOD_NEK2_2 | 499 | 504 | PF00069 | 0.299 |
| MOD_PIKK_1 | 135 | 141 | PF00454 | 0.419 |
| MOD_PKB_1 | 100 | 108 | PF00069 | 0.472 |
| MOD_Plk_1 | 105 | 111 | PF00069 | 0.467 |
| MOD_Plk_1 | 194 | 200 | PF00069 | 0.461 |
| MOD_Plk_1 | 229 | 235 | PF00069 | 0.360 |
| MOD_Plk_1 | 489 | 495 | PF00069 | 0.331 |
| MOD_Plk_1 | 591 | 597 | PF00069 | 0.578 |
| MOD_Plk_2-3 | 591 | 597 | PF00069 | 0.578 |
| MOD_Plk_4 | 212 | 218 | PF00069 | 0.493 |
| MOD_Plk_4 | 229 | 235 | PF00069 | 0.324 |
| MOD_Plk_4 | 386 | 392 | PF00069 | 0.376 |
| MOD_Plk_4 | 402 | 408 | PF00069 | 0.241 |
| MOD_Plk_4 | 462 | 468 | PF00069 | 0.343 |
| MOD_Plk_4 | 489 | 495 | PF00069 | 0.264 |
| MOD_Plk_4 | 93 | 99 | PF00069 | 0.458 |
| MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.351 |
| MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.467 |
| MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.252 |
| MOD_ProDKin_1 | 381 | 387 | PF00069 | 0.255 |
| MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.538 |
| MOD_ProDKin_1 | 531 | 537 | PF00069 | 0.330 |
| MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.531 |
| MOD_SUMO_for_1 | 283 | 286 | PF00179 | 0.462 |
| MOD_SUMO_rev_2 | 510 | 516 | PF00179 | 0.245 |
| TRG_DiLeu_BaLyEn_6 | 57 | 62 | PF01217 | 0.644 |
| TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.515 |
| TRG_ENDOCYTIC_2 | 171 | 174 | PF00928 | 0.411 |
| TRG_ENDOCYTIC_2 | 35 | 38 | PF00928 | 0.520 |
| TRG_ER_diArg_1 | 100 | 103 | PF00400 | 0.533 |
| TRG_ER_diArg_1 | 124 | 126 | PF00400 | 0.643 |
| TRG_ER_diArg_1 | 306 | 309 | PF00400 | 0.472 |
| TRG_ER_diArg_1 | 503 | 505 | PF00400 | 0.284 |
| TRG_ER_diArg_1 | 561 | 563 | PF00400 | 0.462 |
| TRG_NLS_MonoExtN_4 | 151 | 156 | PF00514 | 0.394 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I1V8 | Leptomonas seymouri | 76% | 100% |
| A0A1X0NXG3 | Trypanosomatidae | 58% | 100% |
| A0A3Q8IAY6 | Leishmania donovani | 94% | 100% |
| A0A3R7L6W3 | Trypanosoma rangeli | 62% | 100% |
| A4HZ00 | Leishmania infantum | 94% | 100% |
| A4QP75 | Danio rerio | 31% | 100% |
| C9ZIM3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
| E9AIL9 | Leishmania braziliensis | 84% | 100% |
| O31503 | Bacillus subtilis (strain 168) | 26% | 100% |
| P73374 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 25% | 100% |
| Q02I93 | Pseudomonas aeruginosa (strain UCBPP-PA14) | 27% | 100% |
| Q4QCN1 | Leishmania major | 92% | 100% |
| Q5HEM5 | Staphylococcus aureus (strain COL) | 26% | 100% |
| Q6G836 | Staphylococcus aureus (strain MSSA476) | 26% | 100% |
| Q6GFG0 | Staphylococcus aureus (strain MRSA252) | 26% | 100% |
| Q71YR7 | Listeria monocytogenes serotype 4b (strain F2365) | 27% | 100% |
| Q72DK5 | Desulfovibrio vulgaris (strain ATCC 29579 / DSM 644 / NCIMB 8303 / VKM B-1760 / Hildenborough) | 28% | 100% |
| Q73E18 | Bacillus cereus (strain ATCC 10987 / NRS 248) | 26% | 100% |
| Q73EJ5 | Bacillus cereus (strain ATCC 10987 / NRS 248) | 28% | 100% |
| Q7A4Q9 | Staphylococcus aureus (strain N315) | 26% | 100% |
| Q7MVG9 | Porphyromonas gingivalis (strain ATCC BAA-308 / W83) | 27% | 100% |
| Q7NGN4 | Gloeobacter violaceus (strain ATCC 29082 / PCC 7421) | 28% | 100% |
| Q814A6 | Bacillus cereus (strain ATCC 14579 / DSM 31 / CCUG 7414 / JCM 2152 / NBRC 15305 / NCIMB 9373 / NCTC 2599 / NRRL B-3711) | 28% | 100% |
| Q81Z48 | Bacillus anthracis | 26% | 100% |
| Q81ZD6 | Bacillus anthracis | 28% | 100% |
| Q830R6 | Enterococcus faecalis (strain ATCC 700802 / V583) | 27% | 100% |
| Q891A0 | Clostridium tetani (strain Massachusetts / E88) | 25% | 100% |
| Q892Z2 | Clostridium tetani (strain Massachusetts / E88) | 27% | 100% |
| Q8BNV1 | Mus musculus | 32% | 99% |
| Q8IZ69 | Homo sapiens | 31% | 97% |
| Q8KGF9 | Chlorobaculum tepidum (strain ATCC 49652 / DSM 12025 / NBRC 103806 / TLS) | 27% | 100% |
| Q8NVT4 | Staphylococcus aureus (strain MW2) | 26% | 100% |
| Q8R5Z8 | Fusobacterium nucleatum subsp. nucleatum (strain ATCC 25586 / DSM 15643 / BCRC 10681 / CIP 101130 / JCM 8532 / KCTC 2640 / LMG 13131 / VPI 4355) | 24% | 100% |
| Q8R933 | Caldanaerobacter subterraneus subsp. tengcongensis (strain DSM 15242 / JCM 11007 / NBRC 100824 / MB4) | 31% | 100% |
| Q8Y6D6 | Listeria monocytogenes serovar 1/2a (strain ATCC BAA-679 / EGD-e) | 27% | 100% |
| Q8YR05 | Nostoc sp. (strain PCC 7120 / SAG 25.82 / UTEX 2576) | 28% | 100% |
| Q97J51 | Clostridium acetobutylicum (strain ATCC 824 / DSM 792 / JCM 1419 / LMG 5710 / VKM B-1787) | 28% | 100% |
| Q97LN4 | Clostridium acetobutylicum (strain ATCC 824 / DSM 792 / JCM 1419 / LMG 5710 / VKM B-1787) | 27% | 100% |
| Q99SY9 | Staphylococcus aureus (strain Mu50 / ATCC 700699) | 26% | 100% |
| Q9CDP0 | Lactococcus lactis subsp. lactis (strain IL1403) | 25% | 100% |
| Q9CGB9 | Lactococcus lactis subsp. lactis (strain IL1403) | 26% | 100% |
| Q9I525 | Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) | 27% | 100% |
| V5ASX3 | Trypanosoma cruzi | 60% | 100% |