| 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: 5 |
| 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. | yes | 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:0005777 | peroxisome | 6 | 12 |
| GO:0005840 | ribosome | 5 | 12 |
| GO:0032991 | protein-containing complex | 1 | 12 |
| GO:0042579 | microbody | 5 | 12 |
| GO:0043226 | organelle | 2 | 12 |
| GO:0043227 | membrane-bounded organelle | 3 | 12 |
| GO:0043228 | non-membrane-bounded organelle | 3 | 12 |
| GO:0043229 | intracellular organelle | 3 | 12 |
| GO:0043231 | intracellular membrane-bounded organelle | 4 | 12 |
| GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 12 |
| GO:0110165 | cellular anatomical entity | 1 | 12 |
| GO:1990904 | ribonucleoprotein complex | 2 | 12 |
| GO:0005737 | cytoplasm | 2 | 1 |
| GO:0005782 | peroxisomal matrix | 6 | 1 |
| GO:0005829 | cytosol | 2 | 1 |
| GO:0020015 | glycosome | 7 | 1 |
| GO:0031907 | microbody lumen | 5 | 1 |
| GO:0031974 | membrane-enclosed lumen | 2 | 1 |
| GO:0043233 | organelle lumen | 3 | 1 |
| GO:0070013 | intracellular organelle lumen | 4 | 1 |
Related structures:
AlphaFold database: A0A3Q8IF18
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006605 | protein targeting | 5 | 12 |
| GO:0006625 | protein targeting to peroxisome | 5 | 12 |
| GO:0006810 | transport | 3 | 12 |
| GO:0006886 | intracellular protein transport | 4 | 12 |
| GO:0006996 | organelle organization | 4 | 12 |
| GO:0007031 | peroxisome organization | 5 | 12 |
| GO:0008104 | protein localization | 4 | 12 |
| GO:0009987 | cellular process | 1 | 12 |
| GO:0015031 | protein transport | 4 | 12 |
| GO:0015919 | peroxisomal membrane transport | 5 | 12 |
| GO:0016043 | cellular component organization | 3 | 12 |
| GO:0016558 | protein import into peroxisome matrix | 5 | 12 |
| GO:0033036 | macromolecule localization | 2 | 12 |
| GO:0033365 | protein localization to organelle | 5 | 12 |
| GO:0043574 | peroxisomal transport | 4 | 12 |
| GO:0044743 | protein transmembrane import into intracellular organelle | 4 | 12 |
| GO:0045184 | establishment of protein localization | 3 | 12 |
| GO:0046907 | intracellular transport | 3 | 12 |
| GO:0051179 | localization | 1 | 12 |
| GO:0051234 | establishment of localization | 2 | 12 |
| GO:0051641 | cellular localization | 2 | 12 |
| GO:0051649 | establishment of localization in cell | 3 | 12 |
| GO:0055085 | transmembrane transport | 2 | 12 |
| GO:0065002 | intracellular protein transmembrane transport | 4 | 12 |
| GO:0070727 | cellular macromolecule localization | 3 | 12 |
| GO:0071702 | organic substance transport | 4 | 12 |
| GO:0071705 | nitrogen compound transport | 4 | 12 |
| GO:0071806 | protein transmembrane transport | 3 | 12 |
| GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
| GO:0072594 | establishment of protein localization to organelle | 4 | 12 |
| GO:0072662 | protein localization to peroxisome | 6 | 12 |
| GO:0072663 | establishment of protein localization to peroxisome | 5 | 12 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000268 | peroxisome targeting sequence binding | 5 | 12 |
| GO:0005048 | signal sequence binding | 4 | 12 |
| GO:0005053 | peroxisome matrix targeting signal-2 binding | 6 | 12 |
| GO:0005488 | binding | 1 | 12 |
| GO:0033218 | amide binding | 2 | 12 |
| GO:0042277 | peptide binding | 3 | 12 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.468 |
| CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.361 |
| CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.210 |
| CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.490 |
| CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.361 |
| CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.210 |
| CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.389 |
| DEG_APCC_DBOX_1 | 191 | 199 | PF00400 | 0.387 |
| DOC_CKS1_1 | 62 | 67 | PF01111 | 0.244 |
| DOC_CYCLIN_yClb5_NLxxxL_5 | 89 | 98 | PF00134 | 0.313 |
| DOC_MAPK_JIP1_4 | 21 | 27 | PF00069 | 0.321 |
| DOC_PP1_RVXF_1 | 248 | 255 | PF00149 | 0.421 |
| DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.356 |
| DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.468 |
| DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.484 |
| DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.350 |
| DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.510 |
| DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.453 |
| DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.334 |
| DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.603 |
| DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.531 |
| DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.461 |
| DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.457 |
| DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.408 |
| DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.383 |
| DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.703 |
| DOC_WW_Pin1_4 | 51 | 56 | PF00397 | 0.420 |
| DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.346 |
| LIG_14-3-3_CanoR_1 | 251 | 261 | PF00244 | 0.503 |
| LIG_BRCT_BRCA1_1 | 206 | 210 | PF00533 | 0.477 |
| LIG_BRCT_BRCA1_1 | 29 | 33 | PF00533 | 0.446 |
| LIG_BRCT_BRCA1_1 | 314 | 318 | PF00533 | 0.416 |
| LIG_BRCT_BRCA1_2 | 206 | 212 | PF00533 | 0.477 |
| LIG_CtBP_PxDLS_1 | 55 | 59 | PF00389 | 0.382 |
| LIG_deltaCOP1_diTrp_1 | 179 | 185 | PF00928 | 0.410 |
| LIG_FHA_1 | 21 | 27 | PF00498 | 0.370 |
| LIG_FHA_1 | 224 | 230 | PF00498 | 0.424 |
| LIG_FHA_1 | 324 | 330 | PF00498 | 0.494 |
| LIG_FHA_1 | 346 | 352 | PF00498 | 0.599 |
| LIG_FHA_2 | 150 | 156 | PF00498 | 0.339 |
| LIG_IRF3_LxIS_1 | 22 | 28 | PF10401 | 0.267 |
| LIG_LIR_Nem_3 | 155 | 160 | PF02991 | 0.489 |
| LIG_LIR_Nem_3 | 30 | 36 | PF02991 | 0.473 |
| LIG_LIR_Nem_3 | 315 | 321 | PF02991 | 0.401 |
| LIG_MAD2 | 349 | 357 | PF02301 | 0.675 |
| LIG_MLH1_MIPbox_1 | 314 | 318 | PF16413 | 0.416 |
| LIG_NRP_CendR_1 | 370 | 373 | PF00754 | 0.709 |
| LIG_PCNA_PIPBox_1 | 150 | 159 | PF02747 | 0.332 |
| LIG_Pex14_2 | 69 | 73 | PF04695 | 0.297 |
| LIG_SH2_CRK | 141 | 145 | PF00017 | 0.355 |
| LIG_SH2_NCK_1 | 161 | 165 | PF00017 | 0.514 |
| LIG_SH2_SRC | 287 | 290 | PF00017 | 0.370 |
| LIG_SH2_STAP1 | 130 | 134 | PF00017 | 0.380 |
| LIG_SH2_STAP1 | 267 | 271 | PF00017 | 0.410 |
| LIG_SH2_STAT5 | 42 | 45 | PF00017 | 0.316 |
| LIG_SH3_1 | 16 | 22 | PF00018 | 0.363 |
| LIG_SH3_3 | 16 | 22 | PF00018 | 0.388 |
| LIG_SH3_3 | 232 | 238 | PF00018 | 0.378 |
| LIG_SH3_3 | 276 | 282 | PF00018 | 0.367 |
| LIG_SH3_3 | 324 | 330 | PF00018 | 0.416 |
| LIG_SH3_3 | 333 | 339 | PF00018 | 0.438 |
| LIG_SH3_3 | 340 | 346 | PF00018 | 0.533 |
| LIG_SH3_3 | 354 | 360 | PF00018 | 0.566 |
| LIG_SH3_3 | 366 | 372 | PF00018 | 0.652 |
| LIG_SUMO_SIM_anti_2 | 54 | 60 | PF11976 | 0.425 |
| LIG_SUMO_SIM_par_1 | 204 | 209 | PF11976 | 0.410 |
| LIG_TRAF2_1 | 152 | 155 | PF00917 | 0.421 |
| LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.436 |
| LIG_WW_3 | 339 | 343 | PF00397 | 0.434 |
| MOD_CDC14_SPxK_1 | 189 | 192 | PF00782 | 0.502 |
| MOD_CDK_SPK_2 | 368 | 373 | PF00069 | 0.710 |
| MOD_CDK_SPxK_1 | 186 | 192 | PF00069 | 0.507 |
| MOD_CK1_1 | 133 | 139 | PF00069 | 0.323 |
| MOD_CK1_1 | 14 | 20 | PF00069 | 0.378 |
| MOD_CK1_1 | 149 | 155 | PF00069 | 0.341 |
| MOD_CK1_1 | 169 | 175 | PF00069 | 0.451 |
| MOD_CK1_1 | 193 | 199 | PF00069 | 0.264 |
| MOD_CK1_1 | 255 | 261 | PF00069 | 0.392 |
| MOD_CK1_1 | 328 | 334 | PF00069 | 0.602 |
| MOD_CK1_1 | 54 | 60 | PF00069 | 0.488 |
| MOD_CK2_1 | 149 | 155 | PF00069 | 0.342 |
| MOD_CMANNOS | 182 | 185 | PF00535 | 0.210 |
| MOD_Cter_Amidation | 123 | 126 | PF01082 | 0.465 |
| MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.498 |
| MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.385 |
| MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.465 |
| MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.220 |
| MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.299 |
| MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.236 |
| MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.351 |
| MOD_GlcNHglycan | 313 | 317 | PF01048 | 0.348 |
| MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.314 |
| MOD_GSK3_1 | 130 | 137 | PF00069 | 0.311 |
| MOD_GSK3_1 | 162 | 169 | PF00069 | 0.484 |
| MOD_GSK3_1 | 174 | 181 | PF00069 | 0.371 |
| MOD_GSK3_1 | 186 | 193 | PF00069 | 0.372 |
| MOD_GSK3_1 | 253 | 260 | PF00069 | 0.469 |
| MOD_GSK3_1 | 308 | 315 | PF00069 | 0.380 |
| MOD_GSK3_1 | 364 | 371 | PF00069 | 0.713 |
| MOD_N-GLC_1 | 186 | 191 | PF02516 | 0.378 |
| MOD_NEK2_1 | 25 | 30 | PF00069 | 0.341 |
| MOD_NEK2_1 | 254 | 259 | PF00069 | 0.449 |
| MOD_NEK2_1 | 261 | 266 | PF00069 | 0.427 |
| MOD_NEK2_1 | 297 | 302 | PF00069 | 0.355 |
| MOD_NEK2_1 | 317 | 322 | PF00069 | 0.407 |
| MOD_NEK2_1 | 363 | 368 | PF00069 | 0.582 |
| MOD_NEK2_1 | 94 | 99 | PF00069 | 0.482 |
| MOD_NEK2_2 | 11 | 16 | PF00069 | 0.398 |
| MOD_NEK2_2 | 134 | 139 | PF00069 | 0.308 |
| MOD_PIKK_1 | 193 | 199 | PF00454 | 0.301 |
| MOD_PIKK_1 | 20 | 26 | PF00454 | 0.356 |
| MOD_PIKK_1 | 27 | 33 | PF00454 | 0.335 |
| MOD_PIKK_1 | 297 | 303 | PF00454 | 0.457 |
| MOD_PIKK_1 | 328 | 334 | PF00454 | 0.602 |
| MOD_PKA_1 | 125 | 131 | PF00069 | 0.430 |
| MOD_PKA_2 | 125 | 131 | PF00069 | 0.371 |
| MOD_PKA_2 | 252 | 258 | PF00069 | 0.514 |
| MOD_PKB_1 | 251 | 259 | PF00069 | 0.534 |
| MOD_Plk_1 | 114 | 120 | PF00069 | 0.446 |
| MOD_Plk_1 | 134 | 140 | PF00069 | 0.184 |
| MOD_Plk_1 | 146 | 152 | PF00069 | 0.416 |
| MOD_Plk_1 | 223 | 229 | PF00069 | 0.421 |
| MOD_Plk_4 | 125 | 131 | PF00069 | 0.344 |
| MOD_Plk_4 | 146 | 152 | PF00069 | 0.426 |
| MOD_Plk_4 | 169 | 175 | PF00069 | 0.421 |
| MOD_Plk_4 | 257 | 263 | PF00069 | 0.533 |
| MOD_Plk_4 | 54 | 60 | PF00069 | 0.433 |
| MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.461 |
| MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.462 |
| MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.408 |
| MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.393 |
| MOD_ProDKin_1 | 51 | 57 | PF00069 | 0.419 |
| MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.345 |
| MOD_SUMO_for_1 | 144 | 147 | PF00179 | 0.506 |
| TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.417 |
| TRG_ER_diArg_1 | 233 | 235 | PF00400 | 0.364 |
| TRG_ER_diArg_1 | 250 | 253 | PF00400 | 0.435 |
| TRG_ER_diArg_1 | 344 | 347 | PF00400 | 0.520 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1IHN2 | Leptomonas seymouri | 25% | 71% |
| A0A0N1IM97 | Leptomonas seymouri | 85% | 100% |
| A0A0S4JHX6 | Bodo saltans | 52% | 92% |
| A0A1X0P138 | Trypanosomatidae | 64% | 100% |
| A0A1X0P551 | Trypanosomatidae | 23% | 84% |
| A0A3Q8IGC4 | Leishmania donovani | 26% | 71% |
| A0A422NRU1 | Trypanosoma rangeli | 67% | 100% |
| A4HDT7 | Leishmania braziliensis | 26% | 71% |
| A4HH81 | Leishmania braziliensis | 90% | 100% |
| A4I135 | Leishmania infantum | 26% | 71% |
| A4I4C7 | Leishmania infantum | 99% | 100% |
| B4GT01 | Drosophila persimilis | 26% | 89% |
| B4HWV6 | Drosophila sechellia | 27% | 89% |
| B4P116 | Drosophila yakuba | 27% | 89% |
| B4Q9T6 | Drosophila simulans | 27% | 89% |
| B8M0Q1 | Talaromyces stipitatus (strain ATCC 10500 / CBS 375.48 / QM 6759 / NRRL 1006) | 26% | 81% |
| C9ZL39 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 64% | 100% |
| C9ZYU6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 84% |
| D1ZEB4 | Sordaria macrospora (strain ATCC MYA-333 / DSM 997 / K(L3346) / K-hell) | 23% | 81% |
| E9AM04 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
| E9AX72 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 71% |
| O00628 | Homo sapiens | 33% | 100% |
| O14021 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 87% |
| O22212 | Arabidopsis thaliana | 26% | 67% |
| O59894 | Komagataella pastoris | 29% | 99% |
| O94244 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 87% |
| P39108 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 99% |
| P49177 | Arabidopsis thaliana | 24% | 99% |
| P78798 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
| P93397 | Nicotiana tabacum | 24% | 99% |
| P93398 | Nicotiana tabacum | 24% | 99% |
| P93563 | Solanum tuberosum | 24% | 99% |
| P97865 | Mus musculus | 34% | 100% |
| Q17963 | Caenorhabditis elegans | 25% | 99% |
| Q24572 | Drosophila melanogaster | 27% | 87% |
| Q29KQ0 | Drosophila pseudoobscura pseudoobscura | 26% | 89% |
| Q2UA71 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 23% | 86% |
| Q40507 | Nicotiana tabacum | 25% | 99% |
| Q4I7L0 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 23% | 86% |
| Q4P9P9 | Ustilago maydis (strain 521 / FGSC 9021) | 27% | 82% |
| Q4QAA4 | Leishmania major | 26% | 71% |
| Q4VQ66 | Leishmania major | 96% | 100% |
| Q4WEI5 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 24% | 86% |
| Q54WA3 | Dictyostelium discoideum | 35% | 100% |
| Q5E9I7 | Bos taurus | 25% | 100% |
| Q5RBZ2 | Pongo abelii | 27% | 100% |
| Q6BK34 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 22% | 90% |
| Q6C7Q4 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 23% | 83% |
| Q6NPN9 | Arabidopsis thaliana | 22% | 100% |
| Q6NX08 | Danio rerio | 27% | 88% |
| Q6P315 | Xenopus tropicalis | 29% | 88% |
| Q75C99 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 23% | 88% |
| Q7RY30 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 24% | 82% |
| Q7S7N3 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 21% | 84% |
| Q7ZTY4 | Danio rerio | 28% | 88% |
| Q8AVH1 | Xenopus laevis | 29% | 88% |
| Q8H594 | Oryza sativa subsp. japonica | 25% | 86% |
| Q8R537 | Cricetulus griseus | 34% | 100% |
| Q9BQA1 | Homo sapiens | 27% | 100% |
| Q9VKQ3 | Drosophila melanogaster | 27% | 89% |
| Q9XF57 | Arabidopsis thaliana | 37% | 100% |
| V5BQ16 | Trypanosoma cruzi | 64% | 100% |