| 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: 3 |
| 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: 8 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 11 |
| NetGPI | no | yes: 0, no: 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HH14
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006082 | organic acid metabolic process | 3 | 12 |
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
| GO:0006399 | tRNA metabolic process | 7 | 12 |
| GO:0006418 | tRNA aminoacylation for protein translation | 6 | 12 |
| GO:0006436 | tryptophanyl-tRNA aminoacylation | 7 | 12 |
| GO:0006520 | amino acid metabolic process | 3 | 12 |
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
| GO:0008152 | metabolic process | 1 | 12 |
| GO:0009987 | cellular process | 1 | 12 |
| GO:0016070 | RNA metabolic process | 5 | 12 |
| GO:0019752 | carboxylic acid metabolic process | 5 | 12 |
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
| GO:0034660 | ncRNA metabolic process | 6 | 12 |
| GO:0043038 | amino acid activation | 4 | 12 |
| GO:0043039 | tRNA aminoacylation | 5 | 12 |
| GO:0043170 | macromolecule metabolic process | 3 | 12 |
| GO:0043436 | oxoacid metabolic process | 4 | 12 |
| GO:0044237 | cellular metabolic process | 2 | 12 |
| GO:0044238 | primary metabolic process | 2 | 12 |
| GO:0044281 | small molecule metabolic process | 2 | 12 |
| GO:0046483 | heterocycle metabolic process | 3 | 12 |
| GO:0071704 | organic substance metabolic process | 2 | 12 |
| GO:0090304 | nucleic acid metabolic process | 4 | 12 |
| GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000166 | nucleotide binding | 3 | 12 |
| GO:0003824 | catalytic activity | 1 | 12 |
| GO:0004812 | aminoacyl-tRNA ligase activity | 4 | 12 |
| GO:0004830 | tryptophan-tRNA ligase activity | 5 | 12 |
| GO:0005488 | binding | 1 | 12 |
| GO:0005524 | ATP binding | 5 | 12 |
| GO:0016874 | ligase activity | 2 | 12 |
| GO:0016875 | ligase activity, forming carbon-oxygen bonds | 3 | 12 |
| GO:0017076 | purine nucleotide binding | 4 | 12 |
| GO:0030554 | adenyl nucleotide binding | 5 | 12 |
| GO:0032553 | ribonucleotide binding | 3 | 12 |
| GO:0032555 | purine ribonucleotide binding | 4 | 12 |
| GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
| GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
| GO:0036094 | small molecule binding | 2 | 12 |
| GO:0043167 | ion binding | 2 | 12 |
| GO:0043168 | anion binding | 3 | 12 |
| GO:0097159 | organic cyclic compound binding | 2 | 12 |
| GO:0097367 | carbohydrate derivative binding | 2 | 12 |
| GO:0140098 | catalytic activity, acting on RNA | 3 | 12 |
| GO:0140101 | catalytic activity, acting on a tRNA | 4 | 12 |
| GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
| GO:1901265 | nucleoside phosphate binding | 3 | 12 |
| GO:1901363 | heterocyclic compound binding | 2 | 12 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 450 | 454 | PF00656 | 0.297 |
| CLV_C14_Caspase3-7 | 55 | 59 | PF00656 | 0.405 |
| CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.323 |
| CLV_NRD_NRD_1 | 445 | 447 | PF00675 | 0.407 |
| CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.348 |
| CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.300 |
| CLV_PCSK_KEX2_1 | 447 | 449 | PF00082 | 0.410 |
| CLV_PCSK_PC1ET2_1 | 411 | 413 | PF00082 | 0.300 |
| CLV_PCSK_PC1ET2_1 | 447 | 449 | PF00082 | 0.410 |
| CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.423 |
| CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.330 |
| CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.285 |
| CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.258 |
| CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.250 |
| CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.250 |
| CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.336 |
| CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.119 |
| CLV_PCSK_SKI1_1 | 428 | 432 | PF00082 | 0.245 |
| CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.411 |
| DOC_AGCK_PIF_2 | 235 | 240 | PF00069 | 0.450 |
| DOC_CKS1_1 | 88 | 93 | PF01111 | 0.451 |
| DOC_MAPK_gen_1 | 381 | 387 | PF00069 | 0.555 |
| DOC_PP1_RVXF_1 | 132 | 139 | PF00149 | 0.331 |
| DOC_PP2B_LxvP_1 | 4 | 7 | PF13499 | 0.416 |
| DOC_PP4_FxxP_1 | 187 | 190 | PF00568 | 0.450 |
| DOC_PP4_FxxP_1 | 327 | 330 | PF00568 | 0.405 |
| DOC_PP4_FxxP_1 | 9 | 12 | PF00568 | 0.380 |
| DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.450 |
| DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.365 |
| DOC_USP7_UBL2_3 | 200 | 204 | PF12436 | 0.498 |
| DOC_USP7_UBL2_3 | 411 | 415 | PF12436 | 0.500 |
| DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.369 |
| DOC_WW_Pin1_4 | 358 | 363 | PF00397 | 0.512 |
| DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.407 |
| DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.454 |
| LIG_14-3-3_CanoR_1 | 162 | 171 | PF00244 | 0.450 |
| LIG_14-3-3_CanoR_1 | 446 | 456 | PF00244 | 0.423 |
| LIG_Actin_WH2_2 | 204 | 222 | PF00022 | 0.536 |
| LIG_Actin_WH2_2 | 314 | 331 | PF00022 | 0.450 |
| LIG_BRCT_BRCA1_1 | 12 | 16 | PF00533 | 0.365 |
| LIG_BRCT_BRCA1_1 | 286 | 290 | PF00533 | 0.450 |
| LIG_BRCT_BRCA1_1 | 334 | 338 | PF00533 | 0.450 |
| LIG_deltaCOP1_diTrp_1 | 58 | 67 | PF00928 | 0.401 |
| LIG_EH1_1 | 32 | 40 | PF00400 | 0.329 |
| LIG_eIF4E_1 | 33 | 39 | PF01652 | 0.330 |
| LIG_EVH1_1 | 4 | 8 | PF00568 | 0.427 |
| LIG_FHA_1 | 178 | 184 | PF00498 | 0.448 |
| LIG_FHA_1 | 214 | 220 | PF00498 | 0.441 |
| LIG_FHA_1 | 316 | 322 | PF00498 | 0.449 |
| LIG_FHA_1 | 34 | 40 | PF00498 | 0.325 |
| LIG_FHA_1 | 422 | 428 | PF00498 | 0.457 |
| LIG_FHA_1 | 434 | 440 | PF00498 | 0.436 |
| LIG_FHA_1 | 52 | 58 | PF00498 | 0.350 |
| LIG_FHA_2 | 194 | 200 | PF00498 | 0.450 |
| LIG_FHA_2 | 205 | 211 | PF00498 | 0.501 |
| LIG_FHA_2 | 389 | 395 | PF00498 | 0.487 |
| LIG_FHA_2 | 439 | 445 | PF00498 | 0.382 |
| LIG_FHA_2 | 448 | 454 | PF00498 | 0.409 |
| LIG_LIR_Apic_2 | 185 | 190 | PF02991 | 0.450 |
| LIG_LIR_Gen_1 | 237 | 245 | PF02991 | 0.475 |
| LIG_LIR_Gen_1 | 455 | 465 | PF02991 | 0.508 |
| LIG_LIR_Gen_1 | 75 | 83 | PF02991 | 0.672 |
| LIG_LIR_Gen_1 | 97 | 107 | PF02991 | 0.413 |
| LIG_LIR_Nem_3 | 13 | 19 | PF02991 | 0.581 |
| LIG_LIR_Nem_3 | 154 | 159 | PF02991 | 0.474 |
| LIG_LIR_Nem_3 | 232 | 238 | PF02991 | 0.450 |
| LIG_LIR_Nem_3 | 287 | 293 | PF02991 | 0.445 |
| LIG_LIR_Nem_3 | 312 | 317 | PF02991 | 0.462 |
| LIG_LIR_Nem_3 | 335 | 341 | PF02991 | 0.442 |
| LIG_LIR_Nem_3 | 455 | 460 | PF02991 | 0.510 |
| LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.415 |
| LIG_MLH1_MIPbox_1 | 334 | 338 | PF16413 | 0.450 |
| LIG_Pex14_1 | 399 | 403 | PF04695 | 0.450 |
| LIG_Pex14_2 | 286 | 290 | PF04695 | 0.450 |
| LIG_Pex14_2 | 72 | 76 | PF04695 | 0.518 |
| LIG_REV1ctd_RIR_1 | 135 | 145 | PF16727 | 0.332 |
| LIG_REV1ctd_RIR_1 | 199 | 208 | PF16727 | 0.491 |
| LIG_SH2_CRK | 100 | 104 | PF00017 | 0.407 |
| LIG_SH2_CRK | 245 | 249 | PF00017 | 0.450 |
| LIG_SH2_STAP1 | 100 | 104 | PF00017 | 0.396 |
| LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.450 |
| LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.355 |
| LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.511 |
| LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.536 |
| LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.569 |
| LIG_SH2_STAT5 | 314 | 317 | PF00017 | 0.448 |
| LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.396 |
| LIG_SH3_2 | 5 | 10 | PF14604 | 0.402 |
| LIG_SH3_3 | 2 | 8 | PF00018 | 0.431 |
| LIG_SH3_3 | 390 | 396 | PF00018 | 0.450 |
| LIG_SUMO_SIM_anti_2 | 36 | 43 | PF11976 | 0.331 |
| LIG_SUMO_SIM_par_1 | 36 | 43 | PF11976 | 0.331 |
| LIG_TRAF2_1 | 207 | 210 | PF00917 | 0.522 |
| LIG_TRAF2_1 | 441 | 444 | PF00917 | 0.458 |
| LIG_TRAF2_1 | 83 | 86 | PF00917 | 0.680 |
| LIG_TYR_ITIM | 98 | 103 | PF00017 | 0.416 |
| LIG_UBA3_1 | 174 | 181 | PF00899 | 0.462 |
| LIG_UBA3_1 | 293 | 298 | PF00899 | 0.444 |
| MOD_CDK_SPK_2 | 358 | 363 | PF00069 | 0.536 |
| MOD_CK1_1 | 165 | 171 | PF00069 | 0.451 |
| MOD_CK1_1 | 349 | 355 | PF00069 | 0.462 |
| MOD_CK2_1 | 193 | 199 | PF00069 | 0.450 |
| MOD_CK2_1 | 204 | 210 | PF00069 | 0.499 |
| MOD_CK2_1 | 438 | 444 | PF00069 | 0.311 |
| MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.292 |
| MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.250 |
| MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.242 |
| MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.367 |
| MOD_GSK3_1 | 433 | 440 | PF00069 | 0.536 |
| MOD_GSK3_1 | 47 | 54 | PF00069 | 0.593 |
| MOD_GSK3_1 | 56 | 63 | PF00069 | 0.531 |
| MOD_N-GLC_1 | 229 | 234 | PF02516 | 0.263 |
| MOD_NEK2_1 | 123 | 128 | PF00069 | 0.264 |
| MOD_NEK2_1 | 177 | 182 | PF00069 | 0.450 |
| MOD_NEK2_1 | 183 | 188 | PF00069 | 0.481 |
| MOD_NEK2_1 | 341 | 346 | PF00069 | 0.465 |
| MOD_NEK2_1 | 348 | 353 | PF00069 | 0.410 |
| MOD_NEK2_1 | 40 | 45 | PF00069 | 0.352 |
| MOD_NEK2_1 | 431 | 436 | PF00069 | 0.406 |
| MOD_NEK2_1 | 51 | 56 | PF00069 | 0.366 |
| MOD_NEK2_2 | 28 | 33 | PF00069 | 0.354 |
| MOD_PIKK_1 | 255 | 261 | PF00454 | 0.450 |
| MOD_PIKK_1 | 52 | 58 | PF00454 | 0.410 |
| MOD_PKA_1 | 447 | 453 | PF00069 | 0.500 |
| MOD_PKA_2 | 121 | 127 | PF00069 | 0.502 |
| MOD_PKA_2 | 315 | 321 | PF00069 | 0.450 |
| MOD_PKA_2 | 447 | 453 | PF00069 | 0.453 |
| MOD_Plk_1 | 204 | 210 | PF00069 | 0.476 |
| MOD_Plk_1 | 229 | 235 | PF00069 | 0.371 |
| MOD_Plk_1 | 28 | 34 | PF00069 | 0.350 |
| MOD_Plk_2-3 | 75 | 81 | PF00069 | 0.396 |
| MOD_Plk_4 | 229 | 235 | PF00069 | 0.450 |
| MOD_Plk_4 | 28 | 34 | PF00069 | 0.499 |
| MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.365 |
| MOD_ProDKin_1 | 358 | 364 | PF00069 | 0.512 |
| MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.406 |
| MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.455 |
| MOD_SUMO_for_1 | 266 | 269 | PF00179 | 0.462 |
| MOD_SUMO_rev_2 | 197 | 202 | PF00179 | 0.450 |
| MOD_SUMO_rev_2 | 405 | 413 | PF00179 | 0.533 |
| TRG_DiLeu_BaEn_4 | 408 | 414 | PF01217 | 0.536 |
| TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.415 |
| TRG_ENDOCYTIC_2 | 245 | 248 | PF00928 | 0.450 |
| TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.450 |
| TRG_ER_diArg_1 | 132 | 134 | PF00400 | 0.329 |
| TRG_ER_diArg_1 | 446 | 449 | PF00400 | 0.307 |
| TRG_NLS_Bipartite_1 | 428 | 450 | PF00514 | 0.586 |
| TRG_NLS_MonoExtC_3 | 445 | 451 | PF00514 | 0.496 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P3G3 | Leptomonas seymouri | 84% | 100% |
| A0A0N1HXL2 | Leptomonas seymouri | 41% | 100% |
| A0A0S4IN16 | Bodo saltans | 75% | 100% |
| A0A0S4JC70 | Bodo saltans | 43% | 100% |
| A0A1X0NGJ6 | Trypanosomatidae | 40% | 100% |
| A0A1X0NZB4 | Trypanosomatidae | 76% | 100% |
| A0A3R7MPN7 | Trypanosoma rangeli | 78% | 100% |
| A0A3S7WXL2 | Leishmania donovani | 45% | 100% |
| A0A3S7X238 | Leishmania donovani | 90% | 100% |
| A0A422NW64 | Trypanosoma rangeli | 41% | 100% |
| A2BLD4 | Hyperthermus butylicus (strain DSM 5456 / JCM 9403 / PLM1-5) | 30% | 100% |
| A3MX72 | Pyrobaculum calidifontis (strain DSM 21063 / JCM 11548 / VA1) | 38% | 100% |
| A4HCP4 | Leishmania braziliensis | 38% | 100% |
| A4I070 | Leishmania infantum | 44% | 100% |
| A4I443 | Leishmania infantum | 90% | 100% |
| A4WL99 | Pyrobaculum arsenaticum (strain DSM 13514 / JCM 11321 / PZ6) | 35% | 100% |
| B6YUH1 | Thermococcus onnurineus (strain NA1) | 45% | 100% |
| C6A032 | Thermococcus sibiricus (strain DSM 12597 / MM 739) | 45% | 100% |
| C9ZKR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 78% | 100% |
| E9ADK8 | Leishmania major | 88% | 100% |
| E9AM73 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
| E9AW33 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 100% |
| O26352 | Methanothermobacter thermautotrophicus (strain ATCC 29096 / DSM 1053 / JCM 10044 / NBRC 100330 / Delta H) | 31% | 100% |
| O59584 | Pyrococcus horikoshii (strain ATCC 700860 / DSM 12428 / JCM 9974 / NBRC 100139 / OT-3) | 45% | 100% |
| O96771 | Encephalitozoon cuniculi (strain GB-M1) | 43% | 100% |
| P17248 | Bos taurus | 54% | 99% |
| P23381 | Homo sapiens | 55% | 100% |
| P23612 | Oryctolagus cuniculus | 55% | 100% |
| P32921 | Mus musculus | 55% | 98% |
| Q09692 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 55% | 100% |
| Q12109 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 48% | 100% |
| Q4JBG7 | Sulfolobus acidocaldarius (strain ATCC 33909 / DSM 639 / JCM 8929 / NBRC 15157 / NCIMB 11770) | 46% | 100% |
| Q4QBE4 | Leishmania major | 43% | 100% |
| Q55DZ8 | Dictyostelium discoideum | 54% | 100% |
| Q58810 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 28% | 100% |
| Q5JEP3 | Thermococcus kodakarensis (strain ATCC BAA-918 / JCM 12380 / KOD1) | 44% | 100% |
| Q5R4J1 | Pongo abelii | 55% | 100% |
| Q5V4J1 | Haloarcula marismortui (strain ATCC 43049 / DSM 3752 / JCM 8966 / VKM B-1809) | 26% | 100% |
| Q6P7B0 | Rattus norvegicus | 55% | 98% |
| Q8TYF7 | Methanopyrus kandleri (strain AV19 / DSM 6324 / JCM 9639 / NBRC 100938) | 30% | 100% |
| Q8U453 | Pyrococcus furiosus (strain ATCC 43587 / DSM 3638 / JCM 8422 / Vc1) | 45% | 100% |
| Q8ZTU5 | Pyrobaculum aerophilum (strain ATCC 51768 / DSM 7523 / JCM 9630 / CIP 104966 / NBRC 100827 / IM2) | 35% | 100% |
| Q976M1 | Sulfurisphaera tokodaii (strain DSM 16993 / JCM 10545 / NBRC 100140 / 7) | 46% | 100% |
| Q97ZX0 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 48% | 100% |
| Q9HN66 | Halobacterium salinarum (strain ATCC 700922 / JCM 11081 / NRC-1) | 35% | 100% |
| Q9SR15 | Arabidopsis thaliana | 57% | 100% |
| Q9UY11 | Pyrococcus abyssi (strain GE5 / Orsay) | 45% | 100% |
| Q9Y924 | Aeropyrum pernix (strain ATCC 700893 / DSM 11879 / JCM 9820 / NBRC 100138 / K1) | 31% | 100% |
| V5B4S5 | Trypanosoma cruzi | 79% | 100% |