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. | yes | yes: 3 |
Pissara et al. | no | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | yes | 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 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q66NE0
Term | Name | Level | Count |
---|---|---|---|
GO:0006414 | translational elongation | 5 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009059 | macromolecule biosynthetic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
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 | 106 | 110 | PF00656 | 0.427 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.322 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.322 |
CLV_PCSK_PC1ET2_1 | 266 | 268 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.430 |
DOC_CYCLIN_yCln2_LP_2 | 5 | 11 | PF00134 | 0.429 |
DOC_MAPK_gen_1 | 325 | 333 | PF00069 | 0.322 |
DOC_MAPK_MEF2A_6 | 326 | 335 | PF00069 | 0.322 |
DOC_PP2B_LxvP_1 | 5 | 8 | PF13499 | 0.403 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.470 |
DOC_USP7_UBL2_3 | 215 | 219 | PF12436 | 0.635 |
DOC_USP7_UBL2_3 | 226 | 230 | PF12436 | 0.623 |
DOC_USP7_UBL2_3 | 244 | 248 | PF12436 | 0.707 |
DOC_USP7_UBL2_3 | 81 | 85 | PF12436 | 0.501 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.374 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.384 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.300 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.430 |
LIG_14-3-3_CanoR_1 | 154 | 158 | PF00244 | 0.340 |
LIG_14-3-3_CanoR_1 | 189 | 195 | PF00244 | 0.322 |
LIG_BIR_III_2 | 253 | 257 | PF00653 | 0.454 |
LIG_BIR_III_4 | 287 | 291 | PF00653 | 0.315 |
LIG_BRCT_BRCA1_1 | 160 | 164 | PF00533 | 0.391 |
LIG_CtBP_PxDLS_1 | 177 | 182 | PF00389 | 0.391 |
LIG_deltaCOP1_diTrp_1 | 141 | 149 | PF00928 | 0.322 |
LIG_deltaCOP1_diTrp_1 | 98 | 103 | PF00928 | 0.383 |
LIG_EH1_1 | 328 | 336 | PF00400 | 0.322 |
LIG_EVH1_2 | 256 | 260 | PF00568 | 0.322 |
LIG_FHA_1 | 111 | 117 | PF00498 | 0.384 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.322 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.408 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.322 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.322 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.364 |
LIG_FHA_2 | 130 | 136 | PF00498 | 0.459 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.322 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.466 |
LIG_LIR_Gen_1 | 289 | 298 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 368 | 377 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 98 | 108 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 118 | 123 | PF02991 | 0.197 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 289 | 294 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 345 | 349 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 368 | 372 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 98 | 103 | PF02991 | 0.383 |
LIG_LYPXL_SIV_4 | 24 | 32 | PF13949 | 0.391 |
LIG_Pex14_1 | 207 | 211 | PF04695 | 0.583 |
LIG_Pex14_2 | 164 | 168 | PF04695 | 0.322 |
LIG_SH2_CRK | 191 | 195 | PF00017 | 0.334 |
LIG_SH2_CRK | 3 | 7 | PF00017 | 0.405 |
LIG_SH2_GRB2like | 25 | 28 | PF00017 | 0.391 |
LIG_SH2_GRB2like | 269 | 272 | PF00017 | 0.322 |
LIG_SH2_NCK_1 | 25 | 29 | PF00017 | 0.391 |
LIG_SH2_SRC | 25 | 28 | PF00017 | 0.391 |
LIG_SH2_STAP1 | 291 | 295 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.535 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.322 |
LIG_SH3_3 | 388 | 394 | PF00018 | 0.410 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.515 |
LIG_SUMO_SIM_anti_2 | 200 | 205 | PF11976 | 0.407 |
LIG_TRAF2_1 | 132 | 135 | PF00917 | 0.454 |
LIG_TRAF2_1 | 243 | 246 | PF00917 | 0.737 |
LIG_UBA3_1 | 72 | 81 | PF00899 | 0.483 |
LIG_WRC_WIRS_1 | 117 | 122 | PF05994 | 0.352 |
LIG_WRC_WIRS_1 | 343 | 348 | PF05994 | 0.332 |
MOD_CDK_SPxxK_3 | 48 | 55 | PF00069 | 0.340 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.397 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.421 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.449 |
MOD_Cter_Amidation | 227 | 230 | PF01082 | 0.574 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.463 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.352 |
MOD_GlcNHglycan | 80 | 84 | PF01048 | 0.428 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.458 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.322 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.511 |
MOD_N-GLC_1 | 40 | 45 | PF02516 | 0.375 |
MOD_N-GLC_1 | 48 | 53 | PF02516 | 0.375 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.530 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.437 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.322 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.434 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.421 |
MOD_PIKK_1 | 92 | 98 | PF00454 | 0.412 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.322 |
MOD_Plk_1 | 133 | 139 | PF00069 | 0.454 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.391 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.543 |
MOD_Plk_2-3 | 153 | 159 | PF00069 | 0.322 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.322 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.438 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.352 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.307 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.384 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.300 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.424 |
MOD_SUMO_for_1 | 243 | 246 | PF00179 | 0.754 |
MOD_SUMO_rev_2 | 222 | 231 | PF00179 | 0.779 |
MOD_SUMO_rev_2 | 239 | 249 | PF00179 | 0.646 |
MOD_SUMO_rev_2 | 29 | 34 | PF00179 | 0.332 |
MOD_SUMO_rev_2 | 365 | 375 | PF00179 | 0.535 |
TRG_DiLeu_BaEn_2 | 144 | 150 | PF01217 | 0.349 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 3 | 6 | PF00928 | 0.446 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HSJ4 | Leptomonas seymouri | 79% | 100% |
A0A1X0NID9 | Trypanosomatidae | 68% | 98% |
A0A3Q8I8H5 | Leishmania donovani | 98% | 100% |
A0A3R7LEF5 | Trypanosoma rangeli | 61% | 89% |
A0A3S7WQR4 | Leishmania donovani | 98% | 100% |
A2Q127 | Equus caballus | 32% | 92% |
A4H5S5 | Leishmania braziliensis | 89% | 100% |
A4HU18 | Leishmania infantum | 98% | 89% |
A4HU19 | Leishmania infantum | 98% | 100% |
D0A9I7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 68% | 87% |
D0A9K2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 68% | 100% |
E9AMU9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
O04487 | Arabidopsis thaliana | 36% | 98% |
P12261 | Artemia salina | 29% | 94% |
P26641 | Homo sapiens | 32% | 92% |
P26642 | Xenopus laevis | 30% | 93% |
P29547 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 97% |
P29694 | Oryctolagus cuniculus | 32% | 92% |
P34715 | Trypanosoma cruzi | 65% | 98% |
P36008 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 98% |
P40921 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 99% |
P54412 | Caenorhabditis elegans | 30% | 100% |
Q29387 | Sus scrofa | 32% | 94% |
Q3SZV3 | Bos taurus | 31% | 92% |
Q4R7H5 | Macaca fascicularis | 32% | 92% |
Q5Z627 | Oryza sativa subsp. japonica | 36% | 97% |
Q68FR6 | Rattus norvegicus | 32% | 92% |
Q6PE25 | Danio rerio | 32% | 91% |
Q6YW46 | Oryza sativa subsp. japonica | 37% | 97% |
Q90YC0 | Carassius auratus | 31% | 91% |
Q91375 | Xenopus laevis | 29% | 92% |
Q9D8N0 | Mus musculus | 32% | 92% |
Q9FUM1 | Prunus avium | 33% | 96% |
Q9FVT2 | Arabidopsis thaliana | 36% | 98% |
Q9NJH0 | Drosophila melanogaster | 30% | 94% |
Q9ZRI7 | Oryza sativa subsp. japonica | 36% | 97% |