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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005777 | peroxisome | 6 | 1 |
GO:0020015 | glycosome | 7 | 1 |
GO:0042579 | microbody | 5 | 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 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: E9AU67
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016559 | peroxisome fission | 6 | 1 |
GO:0048285 | organelle fission | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 263 | 267 | PF00656 | 0.633 |
CLV_MEL_PAP_1 | 178 | 184 | PF00089 | 0.526 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.299 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.298 |
CLV_PCSK_PC1ET2_1 | 255 | 257 | PF00082 | 0.392 |
CLV_PCSK_PC1ET2_1 | 56 | 58 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 56 | 60 | PF00082 | 0.203 |
DEG_APCC_DBOX_1 | 230 | 238 | PF00400 | 0.535 |
DOC_CYCLIN_RxL_1 | 139 | 147 | PF00134 | 0.286 |
DOC_MAPK_DCC_7 | 231 | 239 | PF00069 | 0.528 |
DOC_MAPK_HePTP_8 | 186 | 198 | PF00069 | 0.364 |
DOC_MAPK_MEF2A_6 | 189 | 198 | PF00069 | 0.362 |
DOC_MAPK_MEF2A_6 | 26 | 33 | PF00069 | 0.500 |
DOC_PP1_RVXF_1 | 121 | 127 | PF00149 | 0.386 |
DOC_PP4_FxxP_1 | 74 | 77 | PF00568 | 0.551 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.664 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.787 |
LIG_14-3-3_CanoR_1 | 10 | 15 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 139 | 145 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 156 | 161 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 173 | 179 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 76 | 82 | PF00244 | 0.502 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.715 |
LIG_BRCT_BRCA1_1 | 136 | 140 | PF00533 | 0.290 |
LIG_BRCT_BRCA1_2 | 136 | 142 | PF00533 | 0.285 |
LIG_deltaCOP1_diTrp_1 | 95 | 101 | PF00928 | 0.331 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.288 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.338 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.658 |
LIG_LIR_Apic_2 | 105 | 111 | PF02991 | 0.210 |
LIG_LIR_Gen_1 | 193 | 202 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 95 | 104 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 105 | 110 | PF02991 | 0.212 |
LIG_LIR_Nem_3 | 135 | 141 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 193 | 198 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 95 | 100 | PF02991 | 0.383 |
LIG_PCNA_yPIPBox_3 | 3 | 15 | PF02747 | 0.499 |
LIG_Pex14_1 | 200 | 204 | PF04695 | 0.298 |
LIG_Pex14_1 | 97 | 101 | PF04695 | 0.364 |
LIG_Pex14_2 | 136 | 140 | PF04695 | 0.378 |
LIG_REV1ctd_RIR_1 | 104 | 110 | PF16727 | 0.325 |
LIG_REV1ctd_RIR_1 | 138 | 146 | PF16727 | 0.266 |
LIG_REV1ctd_RIR_1 | 56 | 64 | PF16727 | 0.412 |
LIG_SH2_STAP1 | 48 | 52 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 120 | 123 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.600 |
LIG_SUMO_SIM_anti_2 | 209 | 214 | PF11976 | 0.160 |
LIG_SUMO_SIM_anti_2 | 37 | 43 | PF11976 | 0.468 |
LIG_SUMO_SIM_par_1 | 17 | 23 | PF11976 | 0.566 |
LIG_TRFH_1 | 232 | 236 | PF08558 | 0.617 |
LIG_UBA3_1 | 220 | 228 | PF00899 | 0.240 |
LIG_UBA3_1 | 233 | 241 | PF00899 | 0.574 |
MOD_CDK_SPK_2 | 166 | 171 | PF00069 | 0.416 |
MOD_CDK_SPxxK_3 | 166 | 173 | PF00069 | 0.430 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.636 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.508 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.647 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.577 |
MOD_CMANNOS | 224 | 227 | PF00535 | 0.411 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.570 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.288 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.496 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.236 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.257 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.251 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.683 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.736 |
MOD_N-GLC_1 | 206 | 211 | PF02516 | 0.454 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.629 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.365 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.255 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.348 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.332 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.503 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.484 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.413 |
MOD_PIKK_1 | 260 | 266 | PF00454 | 0.622 |
MOD_PIKK_1 | 79 | 85 | PF00454 | 0.507 |
MOD_PKA_1 | 156 | 162 | PF00069 | 0.217 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.334 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.356 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.345 |
MOD_Plk_1 | 206 | 212 | PF00069 | 0.251 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.623 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.294 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.230 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.481 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.599 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.401 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.619 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.786 |
MOD_SUMO_for_1 | 240 | 243 | PF00179 | 0.557 |
MOD_SUMO_rev_2 | 49 | 58 | PF00179 | 0.416 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.278 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.284 |
TRG_ER_diArg_1 | 55 | 58 | PF00400 | 0.592 |
TRG_Pf-PMV_PEXEL_1 | 162 | 166 | PF00026 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 189 | 193 | PF00026 | 0.467 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDG3 | Leptomonas seymouri | 59% | 100% |
A0A0S4JRR1 | Bodo saltans | 31% | 100% |
A0A1X0NLN6 | Trypanosomatidae | 38% | 100% |
A0A3Q8ILX5 | Leishmania donovani | 88% | 100% |
A0A422N9F2 | Trypanosoma rangeli | 37% | 100% |
A4HQF0 | Leishmania braziliensis | 75% | 100% |
A4IC87 | Leishmania infantum | 88% | 100% |
D0A3T7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
Q4Q0C7 | Leishmania major | 88% | 100% |
V5D8S7 | Trypanosoma cruzi | 37% | 100% |