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: A4H7Z5
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 | 296 | 300 | PF00656 | 0.349 |
CLV_C14_Caspase3-7 | 49 | 53 | PF00656 | 0.242 |
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.251 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.398 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.236 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.398 |
CLV_PCSK_PC1ET2_1 | 113 | 115 | PF00082 | 0.236 |
DOC_MAPK_gen_1 | 112 | 119 | PF00069 | 0.233 |
DOC_MAPK_gen_1 | 332 | 338 | PF00069 | 0.391 |
DOC_SPAK_OSR1_1 | 31 | 35 | PF12202 | 0.317 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.388 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.304 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.300 |
LIG_14-3-3_CanoR_1 | 112 | 118 | PF00244 | 0.258 |
LIG_14-3-3_CanoR_1 | 235 | 245 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 96 | 102 | PF00244 | 0.365 |
LIG_APCC_ABBA_1 | 62 | 67 | PF00400 | 0.246 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.525 |
LIG_BRCT_BRCA1_1 | 200 | 204 | PF00533 | 0.445 |
LIG_BRCT_BRCA1_1 | 25 | 29 | PF00533 | 0.351 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.403 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.308 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.414 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.478 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.414 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.264 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.402 |
LIG_LIR_Gen_1 | 211 | 220 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 225 | 236 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 26 | 37 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 211 | 215 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 225 | 231 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 26 | 32 | PF02991 | 0.343 |
LIG_PDZ_Class_1 | 341 | 346 | PF00595 | 0.370 |
LIG_SH2_CRK | 115 | 119 | PF00017 | 0.368 |
LIG_SH2_PTP2 | 228 | 231 | PF00017 | 0.431 |
LIG_SH2_SRC | 228 | 231 | PF00017 | 0.431 |
LIG_SH2_SRC | 50 | 53 | PF00017 | 0.246 |
LIG_SH2_STAP1 | 115 | 119 | PF00017 | 0.368 |
LIG_SH2_STAP1 | 206 | 210 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.431 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.458 |
LIG_SUMO_SIM_par_1 | 138 | 145 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 183 | 189 | PF11976 | 0.458 |
LIG_SUMO_SIM_par_1 | 81 | 88 | PF11976 | 0.351 |
LIG_UBA3_1 | 184 | 191 | PF00899 | 0.253 |
LIG_UBA3_1 | 244 | 249 | PF00899 | 0.326 |
LIG_WRC_WIRS_1 | 260 | 265 | PF05994 | 0.468 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.350 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.384 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.400 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.394 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.442 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.427 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.379 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.345 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.264 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.452 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.313 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.377 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.505 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.371 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.557 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.402 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.456 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.477 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.367 |
MOD_N-GLC_1 | 236 | 241 | PF02516 | 0.483 |
MOD_N-GLC_1 | 37 | 42 | PF02516 | 0.420 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.485 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.438 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.377 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.406 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.308 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.160 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.390 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.336 |
MOD_NEK2_2 | 107 | 112 | PF00069 | 0.246 |
MOD_PIKK_1 | 23 | 29 | PF00454 | 0.506 |
MOD_PK_1 | 332 | 338 | PF00069 | 0.493 |
MOD_PKA_1 | 113 | 119 | PF00069 | 0.224 |
MOD_PKA_1 | 332 | 338 | PF00069 | 0.493 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.176 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.317 |
MOD_Plk_1 | 251 | 257 | PF00069 | 0.416 |
MOD_Plk_1 | 273 | 279 | PF00069 | 0.424 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.224 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.313 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.498 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.359 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.311 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.424 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.315 |
MOD_SUMO_rev_2 | 123 | 132 | PF00179 | 0.310 |
MOD_SUMO_rev_2 | 281 | 291 | PF00179 | 0.514 |
MOD_SUMO_rev_2 | 326 | 335 | PF00179 | 0.333 |
MOD_SUMO_rev_2 | 339 | 344 | PF00179 | 0.425 |
MOD_SUMO_rev_2 | 40 | 45 | PF00179 | 0.458 |
TRG_DiLeu_BaEn_2 | 27 | 33 | PF01217 | 0.392 |
TRG_ENDOCYTIC_2 | 115 | 118 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 228 | 231 | PF00928 | 0.431 |
TRG_ER_diArg_1 | 111 | 114 | PF00400 | 0.254 |
TRG_ER_diArg_1 | 291 | 293 | PF00400 | 0.408 |
TRG_Pf-PMV_PEXEL_1 | 292 | 296 | PF00026 | 0.426 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZX3 | Leptomonas seymouri | 73% | 100% |
A0A0S4JKW8 | Bodo saltans | 30% | 87% |
A0A1X0NTY1 | Trypanosomatidae | 47% | 99% |
A0A3Q8IA26 | Leishmania donovani | 87% | 100% |
A0A422NSA5 | Trypanosoma rangeli | 47% | 99% |
A4HWC3 | Leishmania infantum | 87% | 100% |
C9ZNW6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 99% |
E9AQ23 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q3KPT3 | Xenopus laevis | 24% | 89% |
Q4QFF8 | Leishmania major | 86% | 100% |
Q4R571 | Macaca fascicularis | 26% | 89% |
Q53HC9 | Homo sapiens | 26% | 89% |
Q5M8I4 | Xenopus tropicalis | 24% | 89% |
Q5PPK9 | Rattus norvegicus | 25% | 90% |
Q5RE10 | Pongo abelii | 27% | 84% |
Q5XJP1 | Danio rerio | 24% | 89% |
Q6DUZ9 | Gekko japonicus | 26% | 89% |
Q6NPN9 | Arabidopsis thaliana | 25% | 99% |
Q8K0G5 | Mus musculus | 24% | 90% |
Q9U1Q0 | Caenorhabditis elegans | 26% | 96% |
V5BGM5 | Trypanosoma cruzi | 44% | 100% |