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. | yes | yes: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | yes | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005850 | eukaryotic translation initiation factor 2 complex | 2 | 2 |
GO:0005851 | eukaryotic translation initiation factor 2B complex | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0033290 | eukaryotic 48S preinitiation complex | 4 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0043614 | multi-eIF complex | 3 | 2 |
GO:0070993 | translation preinitiation complex | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 2 |
Related structures:
AlphaFold database: E9ACP3
Term | Name | Level | Count |
---|---|---|---|
GO:0006413 | translational initiation | 3 | 2 |
GO:0006950 | response to stress | 2 | 2 |
GO:0007154 | cell communication | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009267 | cellular response to starvation | 4 | 2 |
GO:0009605 | response to external stimulus | 2 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0009991 | response to extracellular stimulus | 3 | 2 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0031667 | response to nutrient levels | 4 | 2 |
GO:0031668 | cellular response to extracellular stimulus | 3 | 2 |
GO:0031669 | cellular response to nutrient levels | 4 | 2 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0042594 | response to starvation | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071496 | cellular response to external stimulus | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0003743 | translation initiation factor activity | 4 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0008135 | translation factor activity, RNA binding | 3 | 11 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 2 |
GO:0043022 | ribosome binding | 4 | 2 |
GO:0044877 | protein-containing complex binding | 2 | 2 |
GO:0045182 | translation regulator activity | 1 | 11 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.529 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.529 |
CLV_PCSK_PC1ET2_1 | 119 | 121 | PF00082 | 0.510 |
CLV_PCSK_PC1ET2_1 | 174 | 176 | PF00082 | 0.399 |
CLV_PCSK_PC1ET2_1 | 397 | 399 | PF00082 | 0.520 |
CLV_PCSK_PC7_1 | 115 | 121 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.725 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.529 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.477 |
DOC_ANK_TNKS_1 | 345 | 352 | PF00023 | 0.599 |
DOC_CKS1_1 | 222 | 227 | PF01111 | 0.584 |
DOC_CYCLIN_RxL_1 | 311 | 324 | PF00134 | 0.584 |
DOC_CYCLIN_RxL_1 | 61 | 70 | PF00134 | 0.622 |
DOC_CYCLIN_yCln2_LP_2 | 68 | 74 | PF00134 | 0.548 |
DOC_MAPK_gen_1 | 208 | 218 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 396 | 404 | PF00069 | 0.520 |
DOC_MAPK_HePTP_8 | 76 | 88 | PF00069 | 0.559 |
DOC_MAPK_MEF2A_6 | 148 | 157 | PF00069 | 0.519 |
DOC_MAPK_MEF2A_6 | 311 | 318 | PF00069 | 0.622 |
DOC_MAPK_MEF2A_6 | 79 | 88 | PF00069 | 0.561 |
DOC_MAPK_NFAT4_5 | 311 | 319 | PF00069 | 0.622 |
DOC_PP1_RVXF_1 | 9 | 15 | PF00149 | 0.480 |
DOC_PP4_FxxP_1 | 72 | 75 | PF00568 | 0.443 |
DOC_USP7_UBL2_3 | 119 | 123 | PF12436 | 0.534 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.623 |
LIG_14-3-3_CanoR_1 | 187 | 193 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 41 | 48 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 56 | 62 | PF00244 | 0.530 |
LIG_Actin_WH2_2 | 295 | 313 | PF00022 | 0.599 |
LIG_Actin_WH2_2 | 388 | 405 | PF00022 | 0.496 |
LIG_APCC_ABBA_1 | 178 | 183 | PF00400 | 0.519 |
LIG_APCC_ABBA_1 | 319 | 324 | PF00400 | 0.599 |
LIG_Clathr_ClatBox_1 | 85 | 89 | PF01394 | 0.463 |
LIG_DLG_GKlike_1 | 188 | 195 | PF00625 | 0.599 |
LIG_FAT_LD_1 | 81 | 89 | PF03623 | 0.590 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.509 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.533 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.522 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.484 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.554 |
LIG_FHA_2 | 222 | 228 | PF00498 | 0.469 |
LIG_LIR_Apic_2 | 70 | 75 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 151 | 160 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 212 | 223 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 320 | 330 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 212 | 218 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 320 | 325 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 44 | 50 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 53 | 57 | PF02991 | 0.529 |
LIG_NRBOX | 80 | 86 | PF00104 | 0.527 |
LIG_Pex14_1 | 277 | 281 | PF04695 | 0.571 |
LIG_RPA_C_Fungi | 183 | 195 | PF08784 | 0.484 |
LIG_SH2_CRK | 48 | 52 | PF00017 | 0.469 |
LIG_SH2_NCK_1 | 181 | 185 | PF00017 | 0.372 |
LIG_SH2_PTP2 | 215 | 218 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.480 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.528 |
LIG_SUMO_SIM_anti_2 | 340 | 345 | PF11976 | 0.391 |
LIG_SUMO_SIM_anti_2 | 82 | 89 | PF11976 | 0.522 |
LIG_SUMO_SIM_par_1 | 82 | 89 | PF11976 | 0.453 |
LIG_TYR_ITIM | 179 | 184 | PF00017 | 0.372 |
LIG_UBA3_1 | 292 | 300 | PF00899 | 0.391 |
LIG_UBA3_1 | 306 | 311 | PF00899 | 0.391 |
LIG_UBA3_1 | 84 | 90 | PF00899 | 0.523 |
LIG_WW_1 | 365 | 368 | PF00397 | 0.372 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.398 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.599 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.697 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.471 |
MOD_CK2_1 | 344 | 350 | PF00069 | 0.439 |
MOD_Cter_Amidation | 172 | 175 | PF01082 | 0.484 |
MOD_Cter_Amidation | 416 | 419 | PF01082 | 0.837 |
MOD_GlcNHglycan | 162 | 166 | PF01048 | 0.372 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.573 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.580 |
MOD_N-GLC_1 | 16 | 21 | PF02516 | 0.466 |
MOD_N-GLC_1 | 160 | 165 | PF02516 | 0.372 |
MOD_N-GLC_1 | 283 | 288 | PF02516 | 0.391 |
MOD_N-GLC_1 | 57 | 62 | PF02516 | 0.571 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.604 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.506 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.410 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.439 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.574 |
MOD_PIKK_1 | 155 | 161 | PF00454 | 0.484 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.500 |
MOD_PKB_1 | 186 | 194 | PF00069 | 0.484 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.452 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.372 |
MOD_Plk_1 | 325 | 331 | PF00069 | 0.445 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.576 |
MOD_Plk_2-3 | 77 | 83 | PF00069 | 0.534 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.521 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.532 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.582 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.553 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.626 |
MOD_SUMO_for_1 | 296 | 299 | PF00179 | 0.283 |
MOD_SUMO_for_1 | 376 | 379 | PF00179 | 0.562 |
MOD_SUMO_rev_2 | 100 | 106 | PF00179 | 0.706 |
MOD_SUMO_rev_2 | 133 | 139 | PF00179 | 0.543 |
MOD_SUMO_rev_2 | 27 | 36 | PF00179 | 0.543 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 215 | 218 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.505 |
TRG_ER_diArg_1 | 186 | 188 | PF00400 | 0.372 |
TRG_ER_diArg_1 | 370 | 373 | PF00400 | 0.388 |
TRG_NES_CRM1_1 | 144 | 159 | PF08389 | 0.484 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P537 | Leptomonas seymouri | 86% | 100% |
A0A1X0P943 | Trypanosomatidae | 62% | 100% |
A0A3S7WNN3 | Leishmania donovani | 99% | 100% |
A0A422NET9 | Trypanosoma rangeli | 60% | 100% |
A4H3R0 | Leishmania braziliensis | 95% | 100% |
A4HRY4 | Leishmania infantum | 99% | 100% |
C9ZKJ3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 100% |
E9AJY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 100% |
P05198 | Homo sapiens | 31% | 100% |
P68101 | Rattus norvegicus | 31% | 100% |
P68102 | Bos taurus | 31% | 100% |
Q5R493 | Pongo abelii | 31% | 100% |
Q5ZLX2 | Gallus gallus | 31% | 100% |
Q6GL89 | Xenopus tropicalis | 32% | 100% |
Q6ZWX6 | Mus musculus | 31% | 100% |
Q7ZTK4 | Xenopus laevis | 33% | 100% |
Q869N9 | Dictyostelium discoideum | 30% | 100% |
Q9SIZ2 | Arabidopsis thaliana | 33% | 100% |
V5BSN3 | Trypanosoma cruzi | 60% | 100% |