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:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ASD1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 269 | 273 | PF00656 | 0.279 |
CLV_C14_Caspase3-7 | 31 | 35 | PF00656 | 0.714 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 155 | 157 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.491 |
CLV_PCSK_FUR_1 | 118 | 122 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.288 |
CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 174 | 176 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.520 |
CLV_PCSK_PC1ET2_1 | 100 | 102 | PF00082 | 0.501 |
CLV_PCSK_PC1ET2_1 | 276 | 278 | PF00082 | 0.524 |
CLV_PCSK_PC1ET2_1 | 306 | 308 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.386 |
DEG_APCC_DBOX_1 | 290 | 298 | PF00400 | 0.362 |
DEG_APCC_DBOX_1 | 357 | 365 | PF00400 | 0.381 |
DOC_MAPK_gen_1 | 120 | 130 | PF00069 | 0.564 |
DOC_MAPK_gen_1 | 174 | 181 | PF00069 | 0.414 |
DOC_MAPK_gen_1 | 305 | 311 | PF00069 | 0.413 |
DOC_MAPK_gen_1 | 314 | 323 | PF00069 | 0.413 |
DOC_MAPK_gen_1 | 355 | 363 | PF00069 | 0.482 |
DOC_MAPK_HePTP_8 | 311 | 323 | PF00069 | 0.167 |
DOC_MAPK_MEF2A_6 | 174 | 181 | PF00069 | 0.391 |
DOC_MAPK_MEF2A_6 | 314 | 323 | PF00069 | 0.167 |
DOC_PP1_RVXF_1 | 326 | 333 | PF00149 | 0.347 |
DOC_USP7_UBL2_3 | 123 | 127 | PF12436 | 0.449 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.627 |
LIG_14-3-3_CanoR_1 | 101 | 109 | PF00244 | 0.346 |
LIG_14-3-3_CanoR_1 | 146 | 154 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 310 | 316 | PF00244 | 0.299 |
LIG_14-3-3_CanoR_1 | 51 | 58 | PF00244 | 0.593 |
LIG_Actin_WH2_2 | 345 | 360 | PF00022 | 0.309 |
LIG_AP2alpha_2 | 300 | 302 | PF02296 | 0.413 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.626 |
LIG_BRCT_BRCA1_1 | 298 | 302 | PF00533 | 0.467 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.413 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.351 |
LIG_FHA_1 | 344 | 350 | PF00498 | 0.355 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.502 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.395 |
LIG_FHA_2 | 102 | 108 | PF00498 | 0.446 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.520 |
LIG_FHA_2 | 41 | 47 | PF00498 | 0.409 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.504 |
LIG_GBD_Chelix_1 | 353 | 361 | PF00786 | 0.361 |
LIG_LIR_Gen_1 | 43 | 53 | PF02991 | 0.424 |
LIG_LIR_Gen_1 | 73 | 83 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 313 | 319 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 43 | 48 | PF02991 | 0.411 |
LIG_PCNA_PIPBox_1 | 252 | 261 | PF02747 | 0.476 |
LIG_RPA_C_Fungi | 207 | 219 | PF08784 | 0.469 |
LIG_SH2_NCK_1 | 204 | 208 | PF00017 | 0.548 |
LIG_SH2_SRC | 204 | 207 | PF00017 | 0.421 |
LIG_SH2_STAP1 | 204 | 208 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.474 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.739 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.431 |
LIG_SH3_3 | 316 | 322 | PF00018 | 0.210 |
LIG_SUMO_SIM_anti_2 | 90 | 97 | PF11976 | 0.445 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.620 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.579 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.386 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.427 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.467 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.626 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.518 |
MOD_Cter_Amidation | 140 | 143 | PF01082 | 0.467 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.643 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.618 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.628 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.602 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.565 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.306 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.266 |
MOD_N-GLC_1 | 240 | 245 | PF02516 | 0.662 |
MOD_N-GLC_1 | 25 | 30 | PF02516 | 0.742 |
MOD_N-GLC_1 | 343 | 348 | PF02516 | 0.307 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.285 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.358 |
MOD_NEK2_2 | 286 | 291 | PF00069 | 0.362 |
MOD_OFUCOSY | 66 | 72 | PF10250 | 0.392 |
MOD_PIKK_1 | 38 | 44 | PF00454 | 0.402 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.405 |
MOD_PKA_1 | 305 | 311 | PF00069 | 0.328 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.416 |
MOD_Plk_1 | 240 | 246 | PF00069 | 0.626 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.338 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.570 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.423 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.280 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.391 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.366 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.625 |
MOD_SUMO_for_1 | 147 | 150 | PF00179 | 0.497 |
MOD_SUMO_for_1 | 217 | 220 | PF00179 | 0.434 |
MOD_SUMO_rev_2 | 124 | 128 | PF00179 | 0.443 |
MOD_SUMO_rev_2 | 2 | 8 | PF00179 | 0.610 |
TRG_DiLeu_BaEn_1 | 325 | 330 | PF01217 | 0.337 |
TRG_DiLeu_BaEn_4 | 125 | 131 | PF01217 | 0.486 |
TRG_DiLeu_BaLyEn_6 | 288 | 293 | PF01217 | 0.337 |
TRG_DiLeu_LyEn_5 | 325 | 330 | PF01217 | 0.292 |
TRG_ER_diArg_1 | 118 | 121 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 154 | 156 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 174 | 176 | PF00400 | 0.273 |
TRG_ER_diArg_1 | 274 | 277 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 354 | 356 | PF00400 | 0.337 |
TRG_ER_FFAT_1 | 201 | 209 | PF00635 | 0.385 |
TRG_NES_CRM1_1 | 150 | 162 | PF08389 | 0.480 |
TRG_NLS_MonoExtC_3 | 274 | 279 | PF00514 | 0.354 |
TRG_Pf-PMV_PEXEL_1 | 101 | 105 | PF00026 | 0.478 |
TRG_Pf-PMV_PEXEL_1 | 113 | 117 | PF00026 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 355 | 359 | PF00026 | 0.494 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I208 | Leptomonas seymouri | 63% | 99% |
A0A0S4JLL2 | Bodo saltans | 42% | 94% |
A0A1X0P8K7 | Trypanosomatidae | 47% | 100% |
A0A3S5IQV7 | Trypanosoma rangeli | 48% | 100% |
A0A3S7XA96 | Leishmania donovani | 91% | 100% |
A4HNM0 | Leishmania braziliensis | 79% | 100% |
A4ICX4 | Leishmania infantum | 90% | 100% |
D0A2H5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 89% |
Q4Q265 | Leishmania major | 89% | 100% |
V5BQK6 | Trypanosoma cruzi | 44% | 100% |