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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: E9AU98
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 281 | 285 | PF00656 | 0.512 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.318 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.406 |
CLV_PCSK_FUR_1 | 191 | 195 | PF00082 | 0.320 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.318 |
CLV_PCSK_KEX2_1 | 388 | 390 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.406 |
DOC_CDC14_PxL_1 | 359 | 367 | PF14671 | 0.486 |
DOC_CYCLIN_yCln2_LP_2 | 148 | 154 | PF00134 | 0.313 |
DOC_MAPK_gen_1 | 191 | 198 | PF00069 | 0.631 |
DOC_MAPK_gen_1 | 74 | 82 | PF00069 | 0.643 |
DOC_MAPK_HePTP_8 | 72 | 84 | PF00069 | 0.490 |
DOC_MAPK_MEF2A_6 | 341 | 348 | PF00069 | 0.266 |
DOC_MAPK_MEF2A_6 | 74 | 82 | PF00069 | 0.635 |
DOC_MAPK_RevD_3 | 374 | 389 | PF00069 | 0.357 |
DOC_PP4_FxxP_1 | 142 | 145 | PF00568 | 0.436 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.492 |
LIG_14-3-3_CanoR_1 | 197 | 202 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 23 | 29 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 327 | 336 | PF00244 | 0.711 |
LIG_14-3-3_CanoR_1 | 341 | 345 | PF00244 | 0.232 |
LIG_14-3-3_CanoR_1 | 54 | 64 | PF00244 | 0.272 |
LIG_14-3-3_CanoR_1 | 91 | 97 | PF00244 | 0.645 |
LIG_Actin_WH2_2 | 283 | 298 | PF00022 | 0.500 |
LIG_Actin_WH2_2 | 58 | 76 | PF00022 | 0.365 |
LIG_BRCT_BRCA1_1 | 198 | 202 | PF00533 | 0.357 |
LIG_EH_1 | 180 | 184 | PF12763 | 0.656 |
LIG_EH1_1 | 211 | 219 | PF00400 | 0.313 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.351 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.300 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.384 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.452 |
LIG_FHA_1 | 341 | 347 | PF00498 | 0.433 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.672 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.372 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.669 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.680 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.522 |
LIG_GBD_Chelix_1 | 365 | 373 | PF00786 | 0.483 |
LIG_LIR_Gen_1 | 2 | 12 | PF02991 | 0.665 |
LIG_LIR_Gen_1 | 248 | 257 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 284 | 295 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 106 | 110 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 199 | 204 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.670 |
LIG_LIR_Nem_3 | 20 | 25 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 248 | 252 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 255 | 259 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 273 | 279 | PF02991 | 0.688 |
LIG_LIR_Nem_3 | 284 | 290 | PF02991 | 0.466 |
LIG_NRBOX | 165 | 171 | PF00104 | 0.193 |
LIG_NRBOX | 368 | 374 | PF00104 | 0.324 |
LIG_PDZ_Class_2 | 403 | 408 | PF00595 | 0.635 |
LIG_Pex14_2 | 243 | 247 | PF04695 | 0.302 |
LIG_Pex14_2 | 318 | 322 | PF04695 | 0.313 |
LIG_SH2_NCK_1 | 89 | 93 | PF00017 | 0.666 |
LIG_SH2_PTP2 | 41 | 44 | PF00017 | 0.357 |
LIG_SH2_SRC | 41 | 44 | PF00017 | 0.371 |
LIG_SH2_STAP1 | 137 | 141 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.633 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.480 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.351 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.312 |
LIG_SUMO_SIM_anti_2 | 112 | 117 | PF11976 | 0.316 |
LIG_SUMO_SIM_anti_2 | 205 | 210 | PF11976 | 0.282 |
LIG_SUMO_SIM_anti_2 | 58 | 64 | PF11976 | 0.247 |
LIG_SUMO_SIM_par_1 | 114 | 119 | PF11976 | 0.193 |
LIG_SUMO_SIM_par_1 | 250 | 255 | PF11976 | 0.291 |
LIG_SUMO_SIM_par_1 | 301 | 307 | PF11976 | 0.438 |
LIG_SUMO_SIM_par_1 | 345 | 350 | PF11976 | 0.296 |
LIG_TRAF2_1 | 335 | 338 | PF00917 | 0.523 |
LIG_TYR_ITIM | 263 | 268 | PF00017 | 0.520 |
LIG_TYR_ITIM | 274 | 279 | PF00017 | 0.647 |
LIG_TYR_ITIM | 39 | 44 | PF00017 | 0.434 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.680 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.313 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.639 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.479 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.640 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.647 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.308 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.503 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.420 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.587 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.370 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.320 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.649 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.652 |
MOD_N-GLC_1 | 225 | 230 | PF02516 | 0.589 |
MOD_N-GLC_1 | 56 | 61 | PF02516 | 0.313 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.313 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.452 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.226 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.620 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.303 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.425 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.459 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.665 |
MOD_Plk_1 | 56 | 62 | PF00069 | 0.313 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.552 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.332 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.614 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.294 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.351 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.332 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.334 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.313 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.667 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.488 |
TRG_DiLeu_BaLyEn_6 | 148 | 153 | PF01217 | 0.247 |
TRG_DiLeu_BaLyEn_6 | 264 | 269 | PF01217 | 0.614 |
TRG_DiLeu_BaLyEn_6 | 95 | 100 | PF01217 | 0.687 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.649 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.554 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.644 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.697 |
TRG_ER_diArg_1 | 191 | 194 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 388 | 390 | PF00400 | 0.632 |
TRG_ER_diArg_1 | 73 | 75 | PF00400 | 0.488 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I240 | Leptomonas seymouri | 51% | 100% |
A0A1X0NN35 | Trypanosomatidae | 23% | 100% |
A0A3S7XCE6 | Leishmania donovani | 89% | 100% |
A4HQI5 | Leishmania braziliensis | 73% | 100% |
E9AHZ4 | Leishmania infantum | 89% | 100% |
Q4Q093 | Leishmania major | 89% | 100% |