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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: E9AD03
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 247 | 251 | PF00656 | 0.682 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.474 |
CLV_PCSK_KEX2_1 | 106 | 108 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.474 |
CLV_PCSK_PC1ET2_1 | 106 | 108 | PF00082 | 0.314 |
CLV_PCSK_PC1ET2_1 | 93 | 95 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.347 |
DEG_APCC_DBOX_1 | 93 | 101 | PF00400 | 0.546 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.419 |
DEG_SPOP_SBC_1 | 172 | 176 | PF00917 | 0.681 |
DOC_CYCLIN_RxL_1 | 92 | 99 | PF00134 | 0.590 |
DOC_MAPK_gen_1 | 93 | 102 | PF00069 | 0.548 |
DOC_MAPK_MEF2A_6 | 93 | 102 | PF00069 | 0.598 |
DOC_PP4_FxxP_1 | 116 | 119 | PF00568 | 0.606 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.481 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.723 |
LIG_14-3-3_CanoR_1 | 171 | 181 | PF00244 | 0.603 |
LIG_14-3-3_CanoR_1 | 3 | 11 | PF00244 | 0.459 |
LIG_BIR_III_4 | 269 | 273 | PF00653 | 0.606 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.645 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.627 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.608 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.661 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.692 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.333 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.444 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.551 |
LIG_FHA_2 | 252 | 258 | PF00498 | 0.623 |
LIG_Integrin_RGD_1 | 277 | 279 | PF01839 | 0.431 |
LIG_IRF3_LxIS_1 | 146 | 151 | PF10401 | 0.585 |
LIG_LIR_Gen_1 | 205 | 215 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 257 | 267 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 164 | 168 | PF02991 | 0.592 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 257 | 263 | PF02991 | 0.558 |
LIG_MYND_1 | 285 | 289 | PF01753 | 0.703 |
LIG_SH2_CRK | 165 | 169 | PF00017 | 0.635 |
LIG_SH2_STAP1 | 142 | 146 | PF00017 | 0.511 |
LIG_SH2_STAP1 | 208 | 212 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.546 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.581 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.483 |
LIG_SH3_4 | 284 | 291 | PF00018 | 0.732 |
LIG_SUMO_SIM_anti_2 | 17 | 23 | PF11976 | 0.448 |
LIG_SUMO_SIM_anti_2 | 174 | 184 | PF11976 | 0.620 |
LIG_SUMO_SIM_anti_2 | 96 | 102 | PF11976 | 0.572 |
LIG_SUMO_SIM_par_1 | 143 | 151 | PF11976 | 0.649 |
LIG_SUMO_SIM_par_1 | 225 | 231 | PF11976 | 0.595 |
LIG_SUMO_SIM_par_1 | 78 | 84 | PF11976 | 0.291 |
LIG_UBA3_1 | 211 | 216 | PF00899 | 0.609 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.505 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.656 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.592 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.623 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.441 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.738 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.554 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.676 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.645 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.440 |
MOD_CK2_1 | 293 | 299 | PF00069 | 0.770 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.424 |
MOD_Cter_Amidation | 104 | 107 | PF01082 | 0.476 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.408 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.318 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.545 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.646 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.625 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.348 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.629 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.376 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.589 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.601 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.638 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.575 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.357 |
MOD_PKA_2 | 273 | 279 | PF00069 | 0.640 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.768 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.560 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.647 |
MOD_Plk_2-3 | 253 | 259 | PF00069 | 0.629 |
MOD_Plk_2-3 | 50 | 56 | PF00069 | 0.424 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.366 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.573 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.495 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.719 |
TRG_DiLeu_BaLyEn_6 | 144 | 149 | PF01217 | 0.612 |
TRG_DiLeu_BaLyEn_6 | 222 | 227 | PF01217 | 0.621 |
TRG_DiLeu_BaLyEn_6 | 282 | 287 | PF01217 | 0.602 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.621 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.519 |
TRG_NLS_MonoExtN_4 | 289 | 295 | PF00514 | 0.706 |
TRG_Pf-PMV_PEXEL_1 | 95 | 99 | PF00026 | 0.424 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HX16 | Leptomonas seymouri | 43% | 95% |
A0A1X0NLT3 | Trypanosomatidae | 25% | 91% |
A0A3Q8IE36 | Leishmania donovani | 91% | 100% |
A0A3R7M6X5 | Trypanosoma rangeli | 26% | 93% |
A4HFE5 | Leishmania braziliensis | 74% | 100% |
A4I2L5 | Leishmania infantum | 91% | 100% |
C9ZKW5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 84% |
E9AYS8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |