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 | yes | yes: 9, no: 1 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: E9B139
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 109 | 113 | PF00656 | 0.371 |
CLV_C14_Caspase3-7 | 259 | 263 | PF00656 | 0.390 |
CLV_C14_Caspase3-7 | 274 | 278 | PF00656 | 0.522 |
CLV_MEL_PAP_1 | 196 | 202 | PF00089 | 0.509 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.391 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.613 |
CLV_PCSK_PC1ET2_1 | 319 | 321 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.534 |
DEG_APCC_DBOX_1 | 292 | 300 | PF00400 | 0.258 |
DOC_AGCK_PIF_1 | 143 | 148 | PF00069 | 0.281 |
DOC_CKS1_1 | 286 | 291 | PF01111 | 0.357 |
DOC_CYCLIN_RxL_1 | 289 | 298 | PF00134 | 0.250 |
DOC_MAPK_gen_1 | 172 | 181 | PF00069 | 0.397 |
DOC_MAPK_gen_1 | 292 | 299 | PF00069 | 0.268 |
DOC_MAPK_gen_1 | 319 | 325 | PF00069 | 0.634 |
DOC_MAPK_gen_1 | 9 | 19 | PF00069 | 0.440 |
DOC_MAPK_MEF2A_6 | 172 | 181 | PF00069 | 0.406 |
DOC_MAPK_MEF2A_6 | 292 | 301 | PF00069 | 0.260 |
DOC_PP4_FxxP_1 | 165 | 168 | PF00568 | 0.286 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.328 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.348 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.247 |
DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.538 |
LIG_14-3-3_CanoR_1 | 100 | 107 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 134 | 143 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 144 | 149 | PF00244 | 0.229 |
LIG_CtBP_PxDLS_1 | 82 | 86 | PF00389 | 0.403 |
LIG_eIF4E_1 | 217 | 223 | PF01652 | 0.350 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.457 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.470 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.569 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.422 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.287 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.314 |
LIG_IRF3_LxIS_1 | 291 | 298 | PF10401 | 0.329 |
LIG_LIR_Apic_2 | 162 | 168 | PF02991 | 0.305 |
LIG_LIR_Apic_2 | 58 | 63 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 298 | 308 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 355 | 363 | PF02991 | 0.695 |
LIG_LIR_Nem_3 | 141 | 146 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 298 | 303 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 355 | 360 | PF02991 | 0.668 |
LIG_NRBOX | 290 | 296 | PF00104 | 0.344 |
LIG_Pex14_2 | 145 | 149 | PF04695 | 0.342 |
LIG_Pex14_2 | 233 | 237 | PF04695 | 0.245 |
LIG_Pex14_2 | 52 | 56 | PF04695 | 0.420 |
LIG_Pex3_1 | 291 | 302 | PF04882 | 0.291 |
LIG_PTB_Apo_2 | 93 | 100 | PF02174 | 0.366 |
LIG_PTB_Phospho_1 | 93 | 99 | PF10480 | 0.361 |
LIG_SH2_CRK | 235 | 239 | PF00017 | 0.337 |
LIG_SH2_CRK | 357 | 361 | PF00017 | 0.731 |
LIG_SH2_CRK | 60 | 64 | PF00017 | 0.304 |
LIG_SH2_GRB2like | 94 | 97 | PF00017 | 0.361 |
LIG_SH2_SRC | 94 | 97 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.680 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.361 |
LIG_SH3_1 | 174 | 180 | PF00018 | 0.351 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.350 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.280 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.525 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.640 |
LIG_SH3_3 | 38 | 44 | PF00018 | 0.447 |
LIG_SUMO_SIM_anti_2 | 21 | 27 | PF11976 | 0.534 |
LIG_SUMO_SIM_anti_2 | 72 | 78 | PF11976 | 0.271 |
LIG_SUMO_SIM_par_1 | 293 | 298 | PF11976 | 0.401 |
LIG_WRC_WIRS_1 | 145 | 150 | PF05994 | 0.291 |
MOD_CDK_SPxK_1 | 138 | 144 | PF00069 | 0.328 |
MOD_CDK_SPxxK_3 | 285 | 292 | PF00069 | 0.411 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.283 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.588 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.440 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.367 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.397 |
MOD_Cter_Amidation | 317 | 320 | PF01082 | 0.439 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.620 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.628 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.541 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.587 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.781 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.420 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.651 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.482 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.478 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.474 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.410 |
MOD_N-GLC_1 | 269 | 274 | PF02516 | 0.706 |
MOD_N-GLC_1 | 95 | 100 | PF02516 | 0.469 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.463 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.324 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.377 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.317 |
MOD_PIKK_1 | 282 | 288 | PF00454 | 0.488 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.330 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.422 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.402 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.312 |
MOD_Plk_1 | 95 | 101 | PF00069 | 0.270 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.338 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.403 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.501 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.502 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.390 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.444 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.247 |
MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.410 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.531 |
MOD_SUMO_rev_2 | 201 | 210 | PF00179 | 0.461 |
TRG_DiLeu_BaEn_1 | 72 | 77 | PF01217 | 0.286 |
TRG_DiLeu_BaLyEn_6 | 290 | 295 | PF01217 | 0.446 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.608 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.633 |
TRG_ER_diArg_1 | 133 | 136 | PF00400 | 0.395 |
TRG_ER_diArg_1 | 291 | 293 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 350 | 352 | PF00400 | 0.621 |
TRG_ER_diArg_1 | 9 | 11 | PF00400 | 0.519 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVT9 | Leptomonas seymouri | 47% | 97% |
A0A1X0P1M4 | Trypanosomatidae | 33% | 94% |
A0A3S7X3V1 | Leishmania donovani | 89% | 100% |
A0A422NM26 | Trypanosoma rangeli | 33% | 96% |
A4HIK0 | Leishmania braziliensis | 69% | 100% |
A4I5U4 | Leishmania infantum | 89% | 100% |
C9ZR64 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
Q4Q727 | Leishmania major | 88% | 100% |
V5DNY7 | Trypanosoma cruzi | 33% | 88% |