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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 9 |
GO:0032991 | protein-containing complex | 1 | 9 |
GO:0043226 | organelle | 2 | 9 |
GO:0043228 | non-membrane-bounded organelle | 3 | 9 |
GO:0043229 | intracellular organelle | 3 | 9 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:1990904 | ribonucleoprotein complex | 2 | 9 |
Related structures:
AlphaFold database: E9AQ23
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 297 | 301 | PF00656 | 0.376 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.433 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.254 |
DOC_MAPK_gen_1 | 333 | 339 | PF00069 | 0.410 |
DOC_PP1_RVXF_1 | 115 | 121 | PF00149 | 0.411 |
DOC_SPAK_OSR1_1 | 31 | 35 | PF12202 | 0.364 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.414 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.331 |
LIG_14-3-3_CanoR_1 | 14 | 20 | PF00244 | 0.347 |
LIG_14-3-3_CanoR_1 | 236 | 246 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 96 | 102 | PF00244 | 0.407 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.554 |
LIG_BRCT_BRCA1_1 | 257 | 261 | PF00533 | 0.478 |
LIG_BRCT_BRCA1_1 | 91 | 95 | PF00533 | 0.297 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.433 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.332 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.371 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.435 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.450 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.427 |
LIG_LIR_Gen_1 | 114 | 122 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 212 | 221 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 226 | 237 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 258 | 269 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 114 | 118 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 128 | 132 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 212 | 216 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 226 | 232 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 258 | 264 | PF02991 | 0.490 |
LIG_PCNA_yPIPBox_3 | 127 | 141 | PF02747 | 0.405 |
LIG_SH2_CRK | 115 | 119 | PF00017 | 0.458 |
LIG_SH2_PTP2 | 229 | 232 | PF00017 | 0.449 |
LIG_SH2_SRC | 229 | 232 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 115 | 119 | PF00017 | 0.458 |
LIG_SH2_STAP1 | 207 | 211 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 207 | 210 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.449 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.474 |
LIG_SUMO_SIM_par_1 | 138 | 145 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 184 | 190 | PF11976 | 0.482 |
LIG_SUMO_SIM_par_1 | 81 | 88 | PF11976 | 0.382 |
LIG_UBA3_1 | 245 | 250 | PF00899 | 0.406 |
LIG_WRC_WIRS_1 | 261 | 266 | PF05994 | 0.525 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.382 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.505 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.469 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.421 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.410 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.424 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.410 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.425 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.425 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.549 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.539 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.344 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.359 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.450 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.512 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.512 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.472 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.566 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.432 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.460 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.513 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.377 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.281 |
MOD_N-GLC_1 | 111 | 116 | PF02516 | 0.403 |
MOD_N-GLC_1 | 152 | 157 | PF02516 | 0.429 |
MOD_N-GLC_1 | 237 | 242 | PF02516 | 0.509 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.333 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.562 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.474 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.407 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.448 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.428 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.345 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.159 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.427 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.362 |
MOD_PIKK_1 | 23 | 29 | PF00454 | 0.515 |
MOD_PK_1 | 333 | 339 | PF00069 | 0.502 |
MOD_PKA_1 | 191 | 197 | PF00069 | 0.468 |
MOD_PKA_1 | 333 | 339 | PF00069 | 0.502 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.386 |
MOD_Plk_1 | 111 | 117 | PF00069 | 0.440 |
MOD_Plk_1 | 274 | 280 | PF00069 | 0.446 |
MOD_Plk_2-3 | 53 | 59 | PF00069 | 0.498 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.384 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.391 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.337 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.502 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.410 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.376 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.449 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.345 |
MOD_SUMO_rev_2 | 282 | 292 | PF00179 | 0.518 |
MOD_SUMO_rev_2 | 327 | 336 | PF00179 | 0.356 |
MOD_SUMO_rev_2 | 40 | 45 | PF00179 | 0.505 |
MOD_SUMO_rev_2 | 49 | 57 | PF00179 | 0.440 |
MOD_SUMO_rev_2 | 98 | 108 | PF00179 | 0.502 |
TRG_DiLeu_BaEn_2 | 27 | 33 | PF01217 | 0.477 |
TRG_ENDOCYTIC_2 | 115 | 118 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 229 | 232 | PF00928 | 0.449 |
TRG_ER_diArg_1 | 292 | 294 | PF00400 | 0.440 |
TRG_Pf-PMV_PEXEL_1 | 117 | 121 | PF00026 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 293 | 297 | PF00026 | 0.456 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZX3 | Leptomonas seymouri | 74% | 100% |
A0A0S4JKW8 | Bodo saltans | 29% | 87% |
A0A1X0NTY1 | Trypanosomatidae | 48% | 100% |
A0A3Q8IA26 | Leishmania donovani | 96% | 100% |
A0A422NSA5 | Trypanosoma rangeli | 48% | 100% |
A4H7Z5 | Leishmania braziliensis | 87% | 100% |
A4HWC3 | Leishmania infantum | 95% | 100% |
C9ZNW6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
Q3KPT3 | Xenopus laevis | 25% | 90% |
Q4QFF8 | Leishmania major | 95% | 100% |
Q4R571 | Macaca fascicularis | 23% | 90% |
Q53HC9 | Homo sapiens | 23% | 90% |
Q5M8I4 | Xenopus tropicalis | 24% | 90% |
Q5PPK9 | Rattus norvegicus | 24% | 90% |
Q5XJP1 | Danio rerio | 23% | 90% |
Q6DUZ9 | Gekko japonicus | 25% | 90% |
Q6NPN9 | Arabidopsis thaliana | 24% | 99% |
Q8K0G5 | Mus musculus | 24% | 90% |
Q9U1Q0 | Caenorhabditis elegans | 22% | 96% |
V5BGM5 | Trypanosoma cruzi | 45% | 100% |