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: 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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
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: A4H6V1
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:0003824 | catalytic activity | 1 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0003676 | nucleic acid binding | 3 | 3 |
GO:0003746 | translation elongation factor activity | 4 | 3 |
GO:0005488 | binding | 1 | 3 |
GO:0008135 | translation factor activity, RNA binding | 3 | 3 |
GO:0045182 | translation regulator activity | 1 | 3 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 3 |
GO:0097159 | organic cyclic compound binding | 2 | 3 |
GO:1901363 | heterocyclic compound binding | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 118 | 122 | PF00656 | 0.509 |
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.723 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.588 |
CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.723 |
CLV_PCSK_PC1ET2_1 | 155 | 157 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.310 |
DEG_APCC_DBOX_1 | 304 | 312 | PF00400 | 0.560 |
DEG_SCF_FBW7_1 | 276 | 283 | PF00400 | 0.681 |
DOC_CYCLIN_RxL_1 | 233 | 246 | PF00134 | 0.643 |
DOC_CYCLIN_yCln2_LP_2 | 355 | 361 | PF00134 | 0.496 |
DOC_MAPK_gen_1 | 233 | 243 | PF00069 | 0.653 |
DOC_MAPK_gen_1 | 305 | 311 | PF00069 | 0.346 |
DOC_MAPK_gen_1 | 349 | 359 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 352 | 359 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 76 | 84 | PF00069 | 0.628 |
DOC_MAPK_NFAT4_5 | 352 | 360 | PF00069 | 0.519 |
DOC_MIT_MIM_1 | 162 | 172 | PF04212 | 0.431 |
DOC_PP1_RVXF_1 | 128 | 134 | PF00149 | 0.521 |
DOC_PP1_RVXF_1 | 236 | 243 | PF00149 | 0.453 |
DOC_PP1_RVXF_1 | 304 | 311 | PF00149 | 0.358 |
DOC_PP2B_LxvP_1 | 355 | 358 | PF13499 | 0.478 |
DOC_PP4_FxxP_1 | 103 | 106 | PF00568 | 0.438 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.219 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.596 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.644 |
LIG_14-3-3_CanoR_1 | 188 | 198 | PF00244 | 0.695 |
LIG_14-3-3_CanoR_1 | 213 | 218 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 281 | 285 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 349 | 355 | PF00244 | 0.475 |
LIG_Actin_WH2_2 | 157 | 174 | PF00022 | 0.470 |
LIG_deltaCOP1_diTrp_1 | 121 | 126 | PF00928 | 0.373 |
LIG_eIF4E_1 | 13 | 19 | PF01652 | 0.447 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.269 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.274 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.463 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.470 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.400 |
LIG_FHA_2 | 116 | 122 | PF00498 | 0.453 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.329 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.642 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.663 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.464 |
LIG_FHA_2 | 91 | 97 | PF00498 | 0.477 |
LIG_LIR_Gen_1 | 121 | 131 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 121 | 126 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 347 | 351 | PF02991 | 0.510 |
LIG_LRP6_Inhibitor_1 | 367 | 373 | PF00058 | 0.468 |
LIG_Rb_LxCxE_1 | 326 | 347 | PF01857 | 0.562 |
LIG_SH2_CRK | 23 | 27 | PF00017 | 0.480 |
LIG_SH2_CRK | 351 | 355 | PF00017 | 0.554 |
LIG_SH2_STAP1 | 134 | 138 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 13 | 16 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.644 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.320 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.686 |
LIG_SUMO_SIM_anti_2 | 77 | 83 | PF11976 | 0.630 |
LIG_SUMO_SIM_par_1 | 80 | 85 | PF11976 | 0.566 |
LIG_TRAF2_1 | 192 | 195 | PF00917 | 0.594 |
LIG_UBA3_1 | 240 | 245 | PF00899 | 0.640 |
MOD_CDK_SPK_2 | 276 | 281 | PF00069 | 0.644 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.550 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.591 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.632 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.676 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.670 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.400 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.469 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.426 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.511 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.603 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.545 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.478 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.312 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.367 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.531 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.625 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.566 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.548 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.686 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.710 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.521 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.291 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.589 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.553 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.666 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.584 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.549 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.653 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.577 |
MOD_N-GLC_1 | 38 | 43 | PF02516 | 0.330 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.392 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.531 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.487 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.389 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.725 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.509 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.491 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.310 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.534 |
MOD_PIKK_1 | 115 | 121 | PF00454 | 0.524 |
MOD_PIKK_1 | 8 | 14 | PF00454 | 0.441 |
MOD_PK_1 | 213 | 219 | PF00069 | 0.608 |
MOD_PKA_1 | 136 | 142 | PF00069 | 0.464 |
MOD_PKA_1 | 244 | 250 | PF00069 | 0.614 |
MOD_PKA_1 | 265 | 271 | PF00069 | 0.717 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.563 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.643 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.450 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.655 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.499 |
MOD_Plk_1 | 256 | 262 | PF00069 | 0.604 |
MOD_Plk_2-3 | 38 | 44 | PF00069 | 0.433 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.384 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.489 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.420 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.581 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.707 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.704 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.519 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.642 |
MOD_SUMO_rev_2 | 139 | 145 | PF00179 | 0.413 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.523 |
TRG_ER_diArg_1 | 166 | 168 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 224 | 227 | PF00400 | 0.673 |
TRG_ER_diArg_1 | 265 | 267 | PF00400 | 0.723 |
TRG_NLS_Bipartite_1 | 136 | 158 | PF00514 | 0.344 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY02 | Leptomonas seymouri | 67% | 100% |
A0A1X0NNU8 | Trypanosomatidae | 37% | 93% |
A0A3R7MZA1 | Trypanosoma rangeli | 36% | 100% |
A0A3S7WRV8 | Leishmania donovani | 83% | 100% |
C9ZQA1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AGC3 | Leishmania infantum | 83% | 100% |
E9ANW3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4QGQ7 | Leishmania major | 83% | 99% |
V5DE18 | Trypanosoma cruzi | 40% | 100% |