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:0000315 | organellar large ribosomal subunit | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005762 | mitochondrial large ribosomal subunit | 3 | 2 |
GO:0015934 | large ribosomal subunit | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0044391 | ribosomal subunit | 3 | 2 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:1990904 | ribonucleoprotein complex | 2 | 12 |
GO:0005739 | mitochondrion | 5 | 10 |
GO:0005840 | ribosome | 5 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043228 | non-membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 10 |
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_NRD_NRD_1 | 162 | 164 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.497 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.305 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.486 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.669 |
DEG_SPOP_SBC_1 | 18 | 22 | PF00917 | 0.638 |
DOC_CYCLIN_RxL_1 | 2 | 16 | PF00134 | 0.639 |
DOC_CYCLIN_RxL_1 | 272 | 284 | PF00134 | 0.487 |
DOC_MAPK_DCC_7 | 30 | 39 | PF00069 | 0.499 |
DOC_MAPK_gen_1 | 163 | 171 | PF00069 | 0.366 |
DOC_MAPK_gen_1 | 2 | 12 | PF00069 | 0.637 |
DOC_MAPK_HePTP_8 | 161 | 173 | PF00069 | 0.391 |
DOC_MAPK_MEF2A_6 | 164 | 173 | PF00069 | 0.381 |
DOC_MAPK_MEF2A_6 | 30 | 39 | PF00069 | 0.475 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.443 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.357 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.315 |
LIG_14-3-3_CanoR_1 | 139 | 148 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 14 | 19 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 158 | 162 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 195 | 202 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 23 | 33 | PF00244 | 0.478 |
LIG_APCC_ABBA_1 | 120 | 125 | PF00400 | 0.279 |
LIG_APCC_ABBA_1 | 37 | 42 | PF00400 | 0.384 |
LIG_BIR_III_2 | 153 | 157 | PF00653 | 0.620 |
LIG_BRCT_BRCA1_1 | 21 | 25 | PF00533 | 0.616 |
LIG_BRCT_BRCA1_1 | 267 | 271 | PF00533 | 0.496 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.444 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.463 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.420 |
LIG_FHA_2 | 139 | 145 | PF00498 | 0.303 |
LIG_FHA_2 | 258 | 264 | PF00498 | 0.394 |
LIG_IRF3_LxIS_1 | 277 | 284 | PF10401 | 0.373 |
LIG_LIR_Apic_2 | 178 | 184 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 166 | 173 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 166 | 171 | PF02991 | 0.344 |
LIG_MAD2 | 128 | 136 | PF02301 | 0.279 |
LIG_NRBOX | 276 | 282 | PF00104 | 0.413 |
LIG_PDZ_Class_2 | 286 | 291 | PF00595 | 0.557 |
LIG_REV1ctd_RIR_1 | 92 | 102 | PF16727 | 0.423 |
LIG_SH2_CRK | 3 | 7 | PF00017 | 0.595 |
LIG_SH2_SRC | 123 | 126 | PF00017 | 0.303 |
LIG_SH2_SRC | 170 | 173 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 235 | 239 | PF00017 | 0.347 |
LIG_SH2_STAP1 | 267 | 271 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 3 | 6 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.357 |
LIG_SH3_1 | 3 | 9 | PF00018 | 0.692 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.465 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.694 |
LIG_SUMO_SIM_anti_2 | 101 | 106 | PF11976 | 0.325 |
LIG_SUMO_SIM_par_1 | 279 | 284 | PF11976 | 0.438 |
LIG_WRC_WIRS_1 | 246 | 251 | PF05994 | 0.499 |
LIG_WW_3 | 155 | 159 | PF00397 | 0.521 |
MOD_CDK_SPxK_1 | 132 | 138 | PF00069 | 0.423 |
MOD_CDK_SPxxK_3 | 132 | 139 | PF00069 | 0.423 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.594 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.493 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.360 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.377 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.331 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.440 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.443 |
MOD_GlcNHglycan | 282 | 286 | PF01048 | 0.375 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.314 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.629 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.403 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.423 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.436 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.435 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.379 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.314 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.260 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.617 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.388 |
MOD_NEK2_2 | 157 | 162 | PF00069 | 0.541 |
MOD_NEK2_2 | 219 | 224 | PF00069 | 0.514 |
MOD_NEK2_2 | 267 | 272 | PF00069 | 0.491 |
MOD_PIKK_1 | 201 | 207 | PF00454 | 0.545 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.478 |
MOD_PK_1 | 14 | 20 | PF00069 | 0.694 |
MOD_PKA_1 | 138 | 144 | PF00069 | 0.360 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.613 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.360 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.412 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.430 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.655 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.360 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.521 |
MOD_Plk_1 | 227 | 233 | PF00069 | 0.409 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.713 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.414 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.329 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.357 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.470 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.315 |
MOD_SUMO_rev_2 | 248 | 253 | PF00179 | 0.515 |
TRG_DiLeu_BaEn_1 | 70 | 75 | PF01217 | 0.318 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.335 |
TRG_NES_CRM1_1 | 112 | 125 | PF08389 | 0.315 |
TRG_Pf-PMV_PEXEL_1 | 163 | 167 | PF00026 | 0.381 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IH67 | Leptomonas seymouri | 74% | 100% |
A0A0S4J242 | Bodo saltans | 52% | 100% |
A0A1X0NJC0 | Trypanosomatidae | 65% | 100% |
A0A3S7WPC6 | Leishmania donovani | 98% | 100% |
A0A422NCS2 | Trypanosoma rangeli | 65% | 100% |
A4H4H2 | Leishmania braziliensis | 87% | 100% |
A4HSP7 | Leishmania infantum | 98% | 100% |
C9ZT91 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 98% |
E9AKN2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q3SZ22 | Bos taurus | 26% | 100% |
Q5RBU2 | Pongo abelii | 26% | 100% |
Q5RK00 | Rattus norvegicus | 27% | 100% |
Q9EQI8 | Mus musculus | 28% | 100% |
Q9H2W6 | Homo sapiens | 28% | 100% |
V5AP90 | Trypanosoma cruzi | 66% | 100% |