Translation, Elongation factor-1 gamma EF1G
| 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: 3 |
| Pissara et al. | yes | yes: 9 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Pires et al. | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Silverman et al. | no | yes: 5 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Jamdhade et al. | no | yes: 10 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 12 |
| NetGPI | no | yes: 0, no: 12 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005634 | nucleus | 5 | 1 |
| GO:0005737 | cytoplasm | 2 | 1 |
| GO:0043226 | organelle | 2 | 1 |
| GO:0043227 | membrane-bounded organelle | 3 | 1 |
| GO:0043229 | intracellular organelle | 3 | 1 |
| GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HU18
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006414 | translational elongation | 5 | 1 |
| GO:0008152 | metabolic process | 1 | 1 |
| GO:0009058 | biosynthetic process | 2 | 1 |
| GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
| GO:0009987 | cellular process | 1 | 1 |
| GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 1 |
| GO:0043170 | macromolecule metabolic process | 3 | 1 |
| GO:0044237 | cellular metabolic process | 2 | 1 |
| GO:0044249 | cellular biosynthetic process | 3 | 1 |
| GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
| GO:0071704 | organic substance metabolic process | 2 | 1 |
| GO:1901576 | organic substance biosynthetic process | 3 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003676 | nucleic acid binding | 3 | 13 |
| GO:0003746 | translation elongation factor activity | 4 | 13 |
| GO:0005488 | binding | 1 | 13 |
| GO:0008135 | translation factor activity, RNA binding | 3 | 13 |
| GO:0045182 | translation regulator activity | 1 | 13 |
| GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 13 |
| GO:0097159 | organic cyclic compound binding | 2 | 13 |
| GO:1901363 | heterocyclic compound binding | 2 | 13 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 155 | 159 | PF00656 | 0.389 |
| CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.286 |
| CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.286 |
| CLV_PCSK_PC1ET2_1 | 315 | 317 | PF00082 | 0.286 |
| CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.293 |
| CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.286 |
| CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.380 |
| DOC_CYCLIN_yCln2_LP_2 | 54 | 60 | PF00134 | 0.408 |
| DOC_MAPK_gen_1 | 374 | 382 | PF00069 | 0.286 |
| DOC_MAPK_MEF2A_6 | 375 | 384 | PF00069 | 0.286 |
| DOC_PP2B_LxvP_1 | 26 | 29 | PF13499 | 0.462 |
| DOC_PP2B_LxvP_1 | 54 | 57 | PF13499 | 0.390 |
| DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.447 |
| DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.327 |
| DOC_USP7_UBL2_3 | 130 | 134 | PF12436 | 0.466 |
| DOC_USP7_UBL2_3 | 264 | 268 | PF12436 | 0.556 |
| DOC_USP7_UBL2_3 | 275 | 279 | PF12436 | 0.571 |
| DOC_USP7_UBL2_3 | 293 | 297 | PF12436 | 0.648 |
| DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.399 |
| DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.548 |
| DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.357 |
| DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.257 |
| LIG_14-3-3_CanoR_1 | 203 | 207 | PF00244 | 0.305 |
| LIG_14-3-3_CanoR_1 | 238 | 244 | PF00244 | 0.286 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.457 |
| LIG_BIR_III_2 | 302 | 306 | PF00653 | 0.417 |
| LIG_BRCT_BRCA1_1 | 209 | 213 | PF00533 | 0.366 |
| LIG_CtBP_PxDLS_1 | 226 | 231 | PF00389 | 0.366 |
| LIG_deltaCOP1_diTrp_1 | 147 | 152 | PF00928 | 0.347 |
| LIG_deltaCOP1_diTrp_1 | 190 | 198 | PF00928 | 0.307 |
| LIG_EH1_1 | 377 | 385 | PF00400 | 0.286 |
| LIG_EVH1_2 | 305 | 309 | PF00568 | 0.286 |
| LIG_FHA_1 | 195 | 201 | PF00498 | 0.286 |
| LIG_FHA_1 | 247 | 253 | PF00498 | 0.368 |
| LIG_FHA_1 | 321 | 327 | PF00498 | 0.288 |
| LIG_FHA_1 | 357 | 363 | PF00498 | 0.302 |
| LIG_FHA_1 | 430 | 436 | PF00498 | 0.329 |
| LIG_FHA_1 | 49 | 55 | PF00498 | 0.556 |
| LIG_FHA_2 | 137 | 143 | PF00498 | 0.391 |
| LIG_FHA_2 | 179 | 185 | PF00498 | 0.402 |
| LIG_FHA_2 | 203 | 209 | PF00498 | 0.286 |
| LIG_LIR_Gen_1 | 147 | 157 | PF02991 | 0.347 |
| LIG_LIR_Gen_1 | 337 | 347 | PF02991 | 0.415 |
| LIG_LIR_Gen_1 | 417 | 426 | PF02991 | 0.373 |
| LIG_LIR_Nem_3 | 147 | 152 | PF02991 | 0.349 |
| LIG_LIR_Nem_3 | 167 | 172 | PF02991 | 0.154 |
| LIG_LIR_Nem_3 | 19 | 25 | PF02991 | 0.474 |
| LIG_LIR_Nem_3 | 337 | 343 | PF02991 | 0.298 |
| LIG_LIR_Nem_3 | 394 | 398 | PF02991 | 0.360 |
| LIG_LIR_Nem_3 | 417 | 421 | PF02991 | 0.368 |
| LIG_LIR_Nem_3 | 51 | 55 | PF02991 | 0.449 |
| LIG_LYPXL_SIV_4 | 73 | 81 | PF13949 | 0.366 |
| LIG_Pex14_1 | 256 | 260 | PF04695 | 0.511 |
| LIG_Pex14_2 | 213 | 217 | PF04695 | 0.286 |
| LIG_SH2_CRK | 240 | 244 | PF00017 | 0.299 |
| LIG_SH2_CRK | 52 | 56 | PF00017 | 0.399 |
| LIG_SH2_GRB2like | 318 | 321 | PF00017 | 0.286 |
| LIG_SH2_GRB2like | 74 | 77 | PF00017 | 0.366 |
| LIG_SH2_NCK_1 | 74 | 78 | PF00017 | 0.366 |
| LIG_SH2_SRC | 27 | 30 | PF00017 | 0.458 |
| LIG_SH2_SRC | 74 | 77 | PF00017 | 0.366 |
| LIG_SH2_STAP1 | 340 | 344 | PF00017 | 0.293 |
| LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.366 |
| LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.366 |
| LIG_SH2_STAT5 | 27 | 30 | PF00017 | 0.458 |
| LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.286 |
| LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.286 |
| LIG_SH2_STAT5 | 434 | 437 | PF00017 | 0.324 |
| LIG_SH3_3 | 323 | 329 | PF00018 | 0.286 |
| LIG_SH3_3 | 437 | 443 | PF00018 | 0.357 |
| LIG_SH3_3 | 54 | 60 | PF00018 | 0.486 |
| LIG_SUMO_SIM_anti_2 | 249 | 254 | PF11976 | 0.368 |
| LIG_TRAF2_1 | 181 | 184 | PF00917 | 0.417 |
| LIG_TRAF2_1 | 292 | 295 | PF00917 | 0.684 |
| LIG_UBA3_1 | 121 | 130 | PF00899 | 0.417 |
| LIG_WRC_WIRS_1 | 166 | 171 | PF05994 | 0.303 |
| LIG_WRC_WIRS_1 | 392 | 397 | PF05994 | 0.303 |
| MOD_CDC14_SPxK_1 | 33 | 36 | PF00782 | 0.470 |
| MOD_CDK_SPK_2 | 30 | 35 | PF00069 | 0.463 |
| MOD_CDK_SPxK_1 | 30 | 36 | PF00069 | 0.465 |
| MOD_CDK_SPxxK_3 | 97 | 104 | PF00069 | 0.305 |
| MOD_CK1_1 | 107 | 113 | PF00069 | 0.366 |
| MOD_CK1_1 | 30 | 36 | PF00069 | 0.706 |
| MOD_CK2_1 | 136 | 142 | PF00069 | 0.374 |
| MOD_CK2_1 | 178 | 184 | PF00069 | 0.346 |
| MOD_CK2_1 | 288 | 294 | PF00069 | 0.574 |
| MOD_GlcNHglycan | 129 | 133 | PF01048 | 0.403 |
| MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.334 |
| MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.478 |
| MOD_GlcNHglycan | 287 | 293 | PF01048 | 0.745 |
| MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.756 |
| MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.438 |
| MOD_GSK3_1 | 12 | 19 | PF00069 | 0.541 |
| MOD_GSK3_1 | 136 | 143 | PF00069 | 0.493 |
| MOD_GSK3_1 | 174 | 181 | PF00069 | 0.450 |
| MOD_GSK3_1 | 316 | 323 | PF00069 | 0.286 |
| MOD_GSK3_1 | 334 | 341 | PF00069 | 0.286 |
| MOD_N-GLC_1 | 89 | 94 | PF02516 | 0.305 |
| MOD_N-GLC_1 | 97 | 102 | PF02516 | 0.305 |
| MOD_NEK2_1 | 115 | 120 | PF00069 | 0.409 |
| MOD_NEK2_1 | 141 | 146 | PF00069 | 0.389 |
| MOD_NEK2_1 | 165 | 170 | PF00069 | 0.498 |
| MOD_NEK2_1 | 182 | 187 | PF00069 | 0.261 |
| MOD_NEK2_1 | 239 | 244 | PF00069 | 0.286 |
| MOD_PIKK_1 | 141 | 147 | PF00454 | 0.343 |
| MOD_PIKK_1 | 27 | 33 | PF00454 | 0.458 |
| MOD_PKA_2 | 202 | 208 | PF00069 | 0.286 |
| MOD_Plk_1 | 141 | 147 | PF00069 | 0.423 |
| MOD_Plk_1 | 182 | 188 | PF00069 | 0.417 |
| MOD_Plk_1 | 207 | 213 | PF00069 | 0.366 |
| MOD_Plk_2-3 | 202 | 208 | PF00069 | 0.286 |
| MOD_Plk_4 | 239 | 245 | PF00069 | 0.286 |
| MOD_Plk_4 | 305 | 311 | PF00069 | 0.402 |
| MOD_Plk_4 | 391 | 397 | PF00069 | 0.324 |
| MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.393 |
| MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.550 |
| MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.357 |
| MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.257 |
| MOD_SUMO_for_1 | 274 | 277 | PF00179 | 0.598 |
| MOD_SUMO_for_1 | 292 | 295 | PF00179 | 0.701 |
| MOD_SUMO_rev_2 | 271 | 280 | PF00179 | 0.729 |
| MOD_SUMO_rev_2 | 288 | 298 | PF00179 | 0.588 |
| MOD_SUMO_rev_2 | 414 | 424 | PF00179 | 0.495 |
| MOD_SUMO_rev_2 | 78 | 83 | PF00179 | 0.303 |
| TRG_DiLeu_BaEn_2 | 193 | 199 | PF01217 | 0.286 |
| TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.299 |
| TRG_ENDOCYTIC_2 | 340 | 343 | PF00928 | 0.286 |
| TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.447 |
| TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.366 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1HSJ4 | Leptomonas seymouri | 80% | 100% |
| A0A1X0NID9 | Trypanosomatidae | 69% | 100% |
| A0A3Q8I8H5 | Leishmania donovani | 100% | 100% |
| A0A3R7LEF5 | Trypanosoma rangeli | 60% | 100% |
| A0A3S7WQR4 | Leishmania donovani | 100% | 100% |
| A2Q127 | Equus caballus | 32% | 100% |
| A4H5S5 | Leishmania braziliensis | 91% | 100% |
| A4HU19 | Leishmania infantum | 100% | 100% |
| D0A9I7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 66% | 97% |
| D0A9K2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 69% | 100% |
| E9AMU9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
| O04487 | Arabidopsis thaliana | 36% | 100% |
| P12261 | Artemia salina | 29% | 100% |
| P26641 | Homo sapiens | 32% | 100% |
| P26642 | Xenopus laevis | 31% | 100% |
| P29547 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% |
| P29694 | Oryctolagus cuniculus | 32% | 100% |
| P34715 | Trypanosoma cruzi | 65% | 100% |
| P36008 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
| P40921 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% |
| P54412 | Caenorhabditis elegans | 30% | 100% |
| Q29387 | Sus scrofa | 32% | 100% |
| Q3SZV3 | Bos taurus | 31% | 100% |
| Q4R7H5 | Macaca fascicularis | 32% | 100% |
| Q5Z627 | Oryza sativa subsp. japonica | 36% | 100% |
| Q66NE0 | Leishmania major | 98% | 100% |
| Q68FR6 | Rattus norvegicus | 32% | 100% |
| Q6PE25 | Danio rerio | 32% | 100% |
| Q6YW46 | Oryza sativa subsp. japonica | 36% | 100% |
| Q90YC0 | Carassius auratus | 33% | 100% |
| Q91375 | Xenopus laevis | 31% | 100% |
| Q9D8N0 | Mus musculus | 33% | 100% |
| Q9FUM1 | Prunus avium | 33% | 100% |
| Q9FVT2 | Arabidopsis thaliana | 36% | 100% |
| Q9NJH0 | Drosophila melanogaster | 30% | 100% |
| Q9ZRI7 | Oryza sativa subsp. japonica | 36% | 100% |