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:0005778 | peroxisomal membrane | 6 | 2 |
GO:0016020 | membrane | 2 | 2 |
GO:0031090 | organelle membrane | 3 | 2 |
GO:0031903 | microbody membrane | 5 | 2 |
GO:0042579 | microbody | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0098588 | bounding membrane of organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QI32
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016043 | cellular component organization | 3 | 11 |
GO:0016559 | peroxisome fission | 6 | 11 |
GO:0032535 | regulation of cellular component size | 4 | 2 |
GO:0044375 | regulation of peroxisome size | 5 | 2 |
GO:0048285 | organelle fission | 5 | 11 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065008 | regulation of biological quality | 2 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
GO:0090066 | regulation of anatomical structure size | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.330 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.328 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.185 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.341 |
DEG_APCC_DBOX_1 | 170 | 178 | PF00400 | 0.413 |
DEG_APCC_DBOX_1 | 38 | 46 | PF00400 | 0.344 |
DEG_MDM2_SWIB_1 | 269 | 276 | PF02201 | 0.328 |
DOC_CYCLIN_RxL_1 | 133 | 143 | PF00134 | 0.413 |
DOC_CYCLIN_RxL_1 | 26 | 35 | PF00134 | 0.328 |
DOC_MAPK_DCC_7 | 171 | 179 | PF00069 | 0.385 |
DOC_MAPK_gen_1 | 73 | 81 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 106 | 115 | PF00069 | 0.353 |
DOC_MAPK_MEF2A_6 | 171 | 179 | PF00069 | 0.328 |
DOC_MAPK_MEF2A_6 | 280 | 289 | PF00069 | 0.328 |
DOC_PP1_RVXF_1 | 134 | 141 | PF00149 | 0.449 |
DOC_PP1_RVXF_1 | 51 | 57 | PF00149 | 0.449 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.398 |
DOC_USP7_MATH_2 | 67 | 73 | PF00917 | 0.444 |
DOC_USP7_UBL2_3 | 222 | 226 | PF12436 | 0.428 |
DOC_USP7_UBL2_3 | 237 | 241 | PF12436 | 0.145 |
LIG_14-3-3_CanoR_1 | 315 | 320 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 99 | 105 | PF00244 | 0.328 |
LIG_BRCT_BRCA1_1 | 57 | 61 | PF00533 | 0.413 |
LIG_EH_1 | 17 | 21 | PF12763 | 0.608 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.354 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.317 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.478 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.468 |
LIG_FHA_2 | 248 | 254 | PF00498 | 0.476 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.436 |
LIG_GBD_Chelix_1 | 121 | 129 | PF00786 | 0.363 |
LIG_LIR_Gen_1 | 209 | 217 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 259 | 269 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 270 | 281 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 284 | 292 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 69 | 79 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 96 | 105 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 109 | 115 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 215 | 220 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 259 | 264 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 270 | 276 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 284 | 289 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 40 | 46 | PF02991 | 0.243 |
LIG_NRBOX | 28 | 34 | PF00104 | 0.363 |
LIG_PCNA_PIPBox_1 | 87 | 96 | PF02747 | 0.449 |
LIG_Pex14_1 | 120 | 124 | PF04695 | 0.344 |
LIG_Pex14_2 | 140 | 144 | PF04695 | 0.359 |
LIG_Pex14_2 | 269 | 273 | PF04695 | 0.331 |
LIG_Pex14_2 | 93 | 97 | PF04695 | 0.344 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.449 |
LIG_SH2_CRK | 261 | 265 | PF00017 | 0.349 |
LIG_SH2_NCK_1 | 217 | 221 | PF00017 | 0.328 |
LIG_SH2_PTP2 | 112 | 115 | PF00017 | 0.340 |
LIG_SH2_SRC | 112 | 115 | PF00017 | 0.321 |
LIG_SH2_SRC | 257 | 260 | PF00017 | 0.457 |
LIG_SH2_SRC | 65 | 68 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 261 | 265 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.271 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.344 |
LIG_SUMO_SIM_par_1 | 175 | 180 | PF11976 | 0.359 |
LIG_TRAF2_1 | 231 | 234 | PF00917 | 0.478 |
LIG_TYR_ITIM | 110 | 115 | PF00017 | 0.340 |
LIG_WRC_WIRS_1 | 141 | 146 | PF05994 | 0.359 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.340 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.328 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.396 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.473 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.376 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.355 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.330 |
MOD_GlcNHglycan | 194 | 198 | PF01048 | 0.470 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.466 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.164 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.437 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.326 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.355 |
MOD_N-GLC_1 | 247 | 252 | PF02516 | 0.483 |
MOD_N-GLC_1 | 69 | 74 | PF02516 | 0.398 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.328 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.391 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.226 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.351 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.344 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.344 |
MOD_NEK2_2 | 309 | 314 | PF00069 | 0.328 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.344 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.385 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.328 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.449 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.328 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.361 |
MOD_SUMO_rev_2 | 229 | 236 | PF00179 | 0.449 |
TRG_AP2beta_CARGO_1 | 284 | 293 | PF09066 | 0.449 |
TRG_DiLeu_BaEn_1 | 278 | 283 | PF01217 | 0.328 |
TRG_DiLeu_BaEn_2 | 145 | 151 | PF01217 | 0.344 |
TRG_DiLeu_BaLyEn_6 | 161 | 166 | PF01217 | 0.413 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 217 | 220 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.320 |
TRG_ER_diArg_1 | 223 | 225 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 50 | 53 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 85 | 87 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 98 | 101 | PF00400 | 0.328 |
TRG_Pf-PMV_PEXEL_1 | 30 | 34 | PF00026 | 0.357 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHS3 | Leptomonas seymouri | 82% | 100% |
A0A0S4JT81 | Bodo saltans | 46% | 84% |
A0A1X0NNH2 | Trypanosomatidae | 68% | 100% |
A0A3S5H6A5 | Leishmania donovani | 97% | 100% |
A0A422NE20 | Trypanosoma rangeli | 66% | 100% |
A4H5I0 | Leishmania braziliensis | 92% | 85% |
A4HTS1 | Leishmania infantum | 97% | 100% |
D0A980 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 100% |
E9AMK4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
V5B2S3 | Trypanosoma cruzi | 65% | 100% |