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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 11 |
GO:0005840 | ribosome | 5 | 11 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0043228 | non-membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:1990904 | ribonucleoprotein complex | 2 | 12 |
GO:0000315 | organellar large ribosomal subunit | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005762 | mitochondrial large ribosomal subunit | 3 | 1 |
GO:0015934 | large ribosomal subunit | 4 | 1 |
GO:0044391 | ribosomal subunit | 3 | 1 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003735 | structural constituent of ribosome | 2 | 12 |
GO:0005198 | structural molecule activity | 1 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 150 | 154 | PF00656 | 0.417 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.454 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.245 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.449 |
DOC_CYCLIN_RxL_1 | 2 | 16 | PF00134 | 0.541 |
DOC_CYCLIN_RxL_1 | 272 | 284 | PF00134 | 0.453 |
DOC_MAPK_DCC_7 | 30 | 39 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 163 | 171 | PF00069 | 0.349 |
DOC_MAPK_HePTP_8 | 161 | 173 | PF00069 | 0.328 |
DOC_MAPK_MEF2A_6 | 164 | 173 | PF00069 | 0.318 |
DOC_MAPK_MEF2A_6 | 30 | 39 | PF00069 | 0.407 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.475 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.296 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.392 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.269 |
LIG_14-3-3_CanoR_1 | 139 | 148 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 14 | 19 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 158 | 162 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 195 | 202 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 23 | 33 | PF00244 | 0.406 |
LIG_APCC_ABBA_1 | 120 | 125 | PF00400 | 0.220 |
LIG_BIR_III_2 | 153 | 157 | PF00653 | 0.479 |
LIG_BRCT_BRCA1_1 | 267 | 271 | PF00533 | 0.457 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.414 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.452 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.240 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.441 |
LIG_FHA_2 | 258 | 264 | PF00498 | 0.330 |
LIG_IRF3_LxIS_1 | 277 | 284 | PF10401 | 0.309 |
LIG_LIR_Apic_2 | 178 | 184 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 166 | 173 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 166 | 171 | PF02991 | 0.283 |
LIG_MAD2 | 128 | 136 | PF02301 | 0.220 |
LIG_NRBOX | 276 | 282 | PF00104 | 0.352 |
LIG_PCNA_yPIPBox_3 | 200 | 214 | PF02747 | 0.306 |
LIG_PDZ_Class_2 | 286 | 291 | PF00595 | 0.414 |
LIG_REV1ctd_RIR_1 | 92 | 102 | PF16727 | 0.386 |
LIG_RPA_C_Fungi | 93 | 105 | PF08784 | 0.141 |
LIG_SH2_SRC | 123 | 126 | PF00017 | 0.240 |
LIG_SH2_SRC | 170 | 173 | PF00017 | 0.299 |
LIG_SH2_STAP1 | 235 | 239 | PF00017 | 0.324 |
LIG_SH2_STAP1 | 267 | 271 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.244 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.300 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.394 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.713 |
LIG_SUMO_SIM_par_1 | 279 | 284 | PF11976 | 0.308 |
LIG_WRC_WIRS_1 | 246 | 251 | PF05994 | 0.380 |
LIG_WW_3 | 155 | 159 | PF00397 | 0.472 |
MOD_CDK_SPxK_1 | 132 | 138 | PF00069 | 0.386 |
MOD_CDK_SPxxK_3 | 132 | 139 | PF00069 | 0.386 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.481 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.549 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.300 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.356 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.327 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.446 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.356 |
MOD_GlcNHglycan | 282 | 286 | PF01048 | 0.296 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.269 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.638 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.348 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.458 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.430 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.316 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.251 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.639 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.334 |
MOD_NEK2_2 | 157 | 162 | PF00069 | 0.505 |
MOD_NEK2_2 | 219 | 224 | PF00069 | 0.371 |
MOD_NEK2_2 | 267 | 272 | PF00069 | 0.452 |
MOD_PIKK_1 | 201 | 207 | PF00454 | 0.389 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.398 |
MOD_PK_1 | 14 | 20 | PF00069 | 0.639 |
MOD_PKA_1 | 138 | 144 | PF00069 | 0.300 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.655 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.300 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.398 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.375 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.675 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.300 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.476 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.350 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.551 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.355 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.269 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.296 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.396 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.269 |
MOD_SUMO_rev_2 | 248 | 253 | PF00179 | 0.455 |
TRG_DiLeu_BaEn_1 | 70 | 75 | PF01217 | 0.255 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.270 |
TRG_NES_CRM1_1 | 112 | 125 | PF08389 | 0.252 |
TRG_Pf-PMV_PEXEL_1 | 163 | 167 | PF00026 | 0.319 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IH67 | Leptomonas seymouri | 74% | 100% |
A0A0S4J242 | Bodo saltans | 51% | 100% |
A0A1X0NJC0 | Trypanosomatidae | 65% | 100% |
A0A3S7WPC6 | Leishmania donovani | 94% | 100% |
A0A422NCS2 | Trypanosoma rangeli | 64% | 100% |
A4H4H2 | Leishmania braziliensis | 85% | 100% |
A4HSP7 | Leishmania infantum | 95% | 100% |
C9ZT91 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 98% |
Q3SZ22 | Bos taurus | 26% | 100% |
Q4QJ75 | Leishmania major | 95% | 100% |
Q5RBU2 | Pongo abelii | 27% | 100% |
Q5RK00 | Rattus norvegicus | 27% | 100% |
Q9EQI8 | Mus musculus | 28% | 100% |
Q9H2W6 | Homo sapiens | 28% | 100% |
V5AP90 | Trypanosoma cruzi | 66% | 100% |