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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032991 | protein-containing complex | 1 | 10 |
GO:0072546 | EMC complex | 3 | 10 |
GO:0098796 | membrane protein complex | 2 | 10 |
GO:0140534 | endoplasmic reticulum protein-containing complex | 2 | 10 |
GO:0005783 | endoplasmic reticulum | 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 | 1 |
Related structures:
AlphaFold database: E9AL39
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.613 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.180 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.282 |
CLV_PCSK_PC1ET2_1 | 130 | 132 | PF00082 | 0.180 |
CLV_PCSK_PC1ET2_1 | 37 | 39 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.282 |
DOC_CYCLIN_yCln2_LP_2 | 243 | 249 | PF00134 | 0.398 |
DOC_PP1_RVXF_1 | 143 | 150 | PF00149 | 0.398 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.356 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.323 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.352 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.306 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.351 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.398 |
LIG_14-3-3_CanoR_1 | 119 | 127 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 139 | 149 | PF00244 | 0.155 |
LIG_14-3-3_CanoR_1 | 172 | 179 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 190 | 194 | PF00244 | 0.200 |
LIG_14-3-3_CanoR_1 | 195 | 203 | PF00244 | 0.398 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.516 |
LIG_BIR_III_2 | 75 | 79 | PF00653 | 0.282 |
LIG_eIF4E_1 | 242 | 248 | PF01652 | 0.355 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.372 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.353 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.255 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.419 |
LIG_FHA_2 | 204 | 210 | PF00498 | 0.222 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.333 |
LIG_HP1_1 | 246 | 250 | PF01393 | 0.264 |
LIG_LIR_Gen_1 | 93 | 103 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 221 | 226 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 93 | 99 | PF02991 | 0.290 |
LIG_SH2_CRK | 23 | 27 | PF00017 | 0.398 |
LIG_SH2_NCK_1 | 96 | 100 | PF00017 | 0.282 |
LIG_SH2_SRC | 96 | 99 | PF00017 | 0.355 |
LIG_SH2_STAP1 | 15 | 19 | PF00017 | 0.342 |
LIG_SH2_STAT3 | 242 | 245 | PF00017 | 0.282 |
LIG_SH2_STAT3 | 25 | 28 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.355 |
LIG_SH3_1 | 23 | 29 | PF00018 | 0.398 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.398 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.398 |
LIG_SUMO_SIM_par_1 | 177 | 183 | PF11976 | 0.423 |
LIG_SUMO_SIM_par_1 | 246 | 252 | PF11976 | 0.268 |
LIG_TYR_ITIM | 94 | 99 | PF00017 | 0.282 |
MOD_CDK_SPxxK_3 | 123 | 130 | PF00069 | 0.398 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.301 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.377 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.474 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.463 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.180 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.343 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.455 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.428 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.411 |
MOD_CK2_1 | 238 | 244 | PF00069 | 0.364 |
MOD_Cter_Amidation | 35 | 38 | PF01082 | 0.282 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.544 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.447 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.396 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.420 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.296 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.235 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.349 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.426 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.422 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.373 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.264 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.255 |
MOD_N-GLC_2 | 153 | 155 | PF02516 | 0.383 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.453 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.193 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.420 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.323 |
MOD_PIKK_1 | 180 | 186 | PF00454 | 0.369 |
MOD_PKA_1 | 37 | 43 | PF00069 | 0.266 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.317 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.372 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.175 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.266 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.319 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.355 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.180 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.398 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.317 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.398 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.306 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.351 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.398 |
TRG_DiLeu_BaLyEn_6 | 142 | 147 | PF01217 | 0.293 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.282 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7U5 | Leptomonas seymouri | 77% | 100% |
A0A1X0NP88 | Trypanosomatidae | 39% | 95% |
A0A3S7WPT3 | Leishmania donovani | 95% | 100% |
A0A422NDI1 | Trypanosoma rangeli | 45% | 100% |
A4H4X4 | Leishmania braziliensis | 86% | 100% |
A4HT47 | Leishmania infantum | 95% | 100% |
C9ZUT0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 93% |
Q4QIR5 | Leishmania major | 93% | 100% |