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: 10, no: 0 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: E9B092
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 237 | 241 | PF00656 | 0.320 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 327 | 329 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.306 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.725 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.672 |
DEG_APCC_DBOX_1 | 327 | 335 | PF00400 | 0.713 |
DEG_SPOP_SBC_1 | 118 | 122 | PF00917 | 0.537 |
DEG_SPOP_SBC_1 | 233 | 237 | PF00917 | 0.534 |
DOC_CYCLIN_RxL_1 | 3 | 11 | PF00134 | 0.575 |
DOC_MAPK_DCC_7 | 275 | 283 | PF00069 | 0.438 |
DOC_MAPK_gen_1 | 275 | 283 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 277 | 285 | PF00069 | 0.454 |
DOC_PP1_RVXF_1 | 132 | 139 | PF00149 | 0.319 |
DOC_PP4_FxxP_1 | 360 | 363 | PF00568 | 0.767 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.354 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.520 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 160 | 165 | PF00397 | 0.342 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.480 |
LIG_14-3-3_CanoR_1 | 207 | 216 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 328 | 336 | PF00244 | 0.683 |
LIG_14-3-3_CanoR_1 | 339 | 345 | PF00244 | 0.691 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.684 |
LIG_BRCT_BRCA1_1 | 173 | 177 | PF00533 | 0.247 |
LIG_BRCT_BRCA1_1 | 299 | 303 | PF00533 | 0.402 |
LIG_BRCT_BRCA1_1 | 356 | 360 | PF00533 | 0.674 |
LIG_BRCT_BRCA1_1 | 64 | 68 | PF00533 | 0.437 |
LIG_deltaCOP1_diTrp_1 | 46 | 52 | PF00928 | 0.390 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.369 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.224 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.475 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.452 |
LIG_FHA_2 | 198 | 204 | PF00498 | 0.422 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.382 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.413 |
LIG_LIR_Apic_2 | 102 | 106 | PF02991 | 0.373 |
LIG_LIR_Apic_2 | 357 | 363 | PF02991 | 0.746 |
LIG_LIR_Gen_1 | 291 | 299 | PF02991 | 0.284 |
LIG_LIR_Gen_1 | 300 | 311 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 66 | 77 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 291 | 295 | PF02991 | 0.284 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.385 |
LIG_Pex14_1 | 135 | 139 | PF04695 | 0.339 |
LIG_Pex14_1 | 47 | 51 | PF04695 | 0.263 |
LIG_Pex14_1 | 64 | 68 | PF04695 | 0.421 |
LIG_Pex14_2 | 138 | 142 | PF04695 | 0.259 |
LIG_SH2_CRK | 185 | 189 | PF00017 | 0.388 |
LIG_SH2_SRC | 267 | 270 | PF00017 | 0.407 |
LIG_SH2_STAP1 | 131 | 135 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 209 | 213 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 349 | 352 | PF00017 | 0.647 |
LIG_SH3_1 | 348 | 354 | PF00018 | 0.641 |
LIG_SH3_2 | 351 | 356 | PF14604 | 0.700 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.444 |
LIG_SH3_3 | 348 | 354 | PF00018 | 0.637 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.753 |
LIG_SUMO_SIM_anti_2 | 15 | 21 | PF11976 | 0.571 |
LIG_TYR_ITIM | 183 | 188 | PF00017 | 0.370 |
LIG_UBA3_1 | 284 | 290 | PF00899 | 0.478 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.499 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.507 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.546 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.400 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.377 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.345 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.451 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.683 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.546 |
MOD_GlcNHglycan | 219 | 223 | PF01048 | 0.577 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.672 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.625 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.537 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.555 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.449 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.400 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.362 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.304 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.435 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.480 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.417 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.342 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.744 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.560 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.660 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.280 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.363 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.577 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.486 |
MOD_N-GLC_1 | 197 | 202 | PF02516 | 0.543 |
MOD_N-GLC_1 | 247 | 252 | PF02516 | 0.645 |
MOD_N-GLC_1 | 297 | 302 | PF02516 | 0.402 |
MOD_N-GLC_1 | 314 | 319 | PF02516 | 0.503 |
MOD_N-GLC_1 | 329 | 334 | PF02516 | 0.510 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.533 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.369 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.342 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.400 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.501 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.487 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.660 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.673 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.374 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.581 |
MOD_NEK2_2 | 129 | 134 | PF00069 | 0.322 |
MOD_NEK2_2 | 64 | 69 | PF00069 | 0.331 |
MOD_PIKK_1 | 108 | 114 | PF00454 | 0.523 |
MOD_PIKK_1 | 137 | 143 | PF00454 | 0.262 |
MOD_PIKK_1 | 154 | 160 | PF00454 | 0.366 |
MOD_PKB_1 | 338 | 346 | PF00069 | 0.721 |
MOD_Plk_1 | 297 | 303 | PF00069 | 0.402 |
MOD_Plk_1 | 329 | 335 | PF00069 | 0.710 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.400 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.241 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.402 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.719 |
MOD_Plk_4 | 64 | 70 | PF00069 | 0.378 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.387 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.562 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.412 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.552 |
MOD_ProDKin_1 | 160 | 166 | PF00069 | 0.338 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.480 |
TRG_DiLeu_BaEn_1 | 179 | 184 | PF01217 | 0.317 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 349 | 352 | PF00928 | 0.713 |
TRG_ER_diArg_1 | 3 | 6 | PF00400 | 0.671 |
TRG_ER_diArg_1 | 326 | 328 | PF00400 | 0.709 |
TRG_ER_diArg_1 | 338 | 340 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 366 | 369 | PF00400 | 0.781 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3M3 | Leptomonas seymouri | 49% | 99% |
A0A1X0NQJ6 | Trypanosomatidae | 36% | 100% |
A0A3S7X1V5 | Leishmania donovani | 87% | 100% |
A0A422MSP0 | Trypanosoma rangeli | 35% | 100% |
A4HGX2 | Leishmania braziliensis | 69% | 100% |
A4I402 | Leishmania infantum | 88% | 100% |
D0A972 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
Q4Q7Z3 | Leishmania major | 83% | 99% |
V5AWR0 | Trypanosoma cruzi | 34% | 100% |