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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: A4H918
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 205 | 209 | PF00656 | 0.574 |
CLV_MEL_PAP_1 | 197 | 203 | PF00089 | 0.391 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.465 |
CLV_PCSK_FUR_1 | 364 | 368 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.435 |
CLV_PCSK_PC1ET2_1 | 322 | 324 | PF00082 | 0.441 |
CLV_PCSK_PC1ET2_1 | 357 | 359 | PF00082 | 0.399 |
CLV_PCSK_PC1ET2_1 | 90 | 92 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 45 | 49 | PF00082 | 0.239 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.625 |
DOC_CKS1_1 | 30 | 35 | PF01111 | 0.392 |
DOC_CYCLIN_RxL_1 | 332 | 345 | PF00134 | 0.494 |
DOC_CYCLIN_RxL_1 | 42 | 52 | PF00134 | 0.239 |
DOC_CYCLIN_yCln2_LP_2 | 130 | 136 | PF00134 | 0.331 |
DOC_CYCLIN_yCln2_LP_2 | 231 | 237 | PF00134 | 0.410 |
DOC_CYCLIN_yCln2_LP_2 | 47 | 53 | PF00134 | 0.401 |
DOC_MAPK_gen_1 | 212 | 222 | PF00069 | 0.536 |
DOC_MAPK_gen_1 | 332 | 342 | PF00069 | 0.595 |
DOC_MAPK_MEF2A_6 | 212 | 220 | PF00069 | 0.546 |
DOC_PP1_RVXF_1 | 198 | 204 | PF00149 | 0.595 |
DOC_PP1_RVXF_1 | 301 | 307 | PF00149 | 0.606 |
DOC_PP1_RVXF_1 | 82 | 89 | PF00149 | 0.544 |
DOC_PP2B_LxvP_1 | 130 | 133 | PF13499 | 0.341 |
DOC_PP2B_LxvP_1 | 239 | 242 | PF13499 | 0.425 |
DOC_PP2B_LxvP_1 | 47 | 50 | PF13499 | 0.357 |
DOC_PP4_FxxP_1 | 246 | 249 | PF00568 | 0.354 |
DOC_PP4_FxxP_1 | 279 | 282 | PF00568 | 0.623 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.640 |
DOC_USP7_UBL2_3 | 355 | 359 | PF12436 | 0.654 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.401 |
LIG_14-3-3_CanoR_1 | 103 | 109 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 367 | 373 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 45 | 50 | PF00244 | 0.221 |
LIG_Actin_WH2_2 | 251 | 267 | PF00022 | 0.402 |
LIG_APCC_ABBA_1 | 340 | 345 | PF00400 | 0.628 |
LIG_APCC_ABBA_1 | 51 | 56 | PF00400 | 0.399 |
LIG_APCC_ABBAyCdc20_2 | 339 | 345 | PF00400 | 0.575 |
LIG_Clathr_ClatBox_1 | 175 | 179 | PF01394 | 0.410 |
LIG_EVH1_2 | 242 | 246 | PF00568 | 0.285 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.548 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.352 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.355 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.660 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.607 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.651 |
LIG_FHA_2 | 395 | 401 | PF00498 | 0.643 |
LIG_GBD_Chelix_1 | 216 | 224 | PF00786 | 0.184 |
LIG_IRF3_LxIS_1 | 148 | 155 | PF10401 | 0.257 |
LIG_LIR_Gen_1 | 189 | 197 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 102 | 108 | PF02991 | 0.611 |
LIG_LIR_Nem_3 | 189 | 194 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 42 | 47 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 48 | 54 | PF02991 | 0.352 |
LIG_NRBOX | 332 | 338 | PF00104 | 0.548 |
LIG_PCNA_yPIPBox_3 | 200 | 211 | PF02747 | 0.543 |
LIG_RPA_C_Insects | 86 | 101 | PF08784 | 0.439 |
LIG_SH2_NCK_1 | 370 | 374 | PF00017 | 0.396 |
LIG_SH2_NCK_1 | 404 | 408 | PF00017 | 0.455 |
LIG_SH2_PTP2 | 250 | 253 | PF00017 | 0.197 |
LIG_SH2_STAP1 | 23 | 27 | PF00017 | 0.284 |
LIG_SH2_STAP1 | 327 | 331 | PF00017 | 0.491 |
LIG_SH2_STAT3 | 54 | 57 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.535 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.546 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.435 |
LIG_SUMO_SIM_par_1 | 150 | 155 | PF11976 | 0.474 |
LIG_TRAF2_1 | 397 | 400 | PF00917 | 0.652 |
LIG_WRC_WIRS_1 | 105 | 110 | PF05994 | 0.398 |
LIG_WRC_WIRS_1 | 13 | 18 | PF05994 | 0.197 |
LIG_WRC_WIRS_1 | 137 | 142 | PF05994 | 0.464 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.497 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.336 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.627 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.332 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.551 |
MOD_CK1_1 | 378 | 384 | PF00069 | 0.630 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.755 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.637 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.749 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.383 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.427 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.407 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.726 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.508 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.369 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.322 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.405 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.344 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.622 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.645 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.553 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.269 |
MOD_N-GLC_1 | 269 | 274 | PF02516 | 0.420 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.421 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.493 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.512 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.309 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.490 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.518 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.360 |
MOD_NEK2_2 | 186 | 191 | PF00069 | 0.357 |
MOD_NEK2_2 | 263 | 268 | PF00069 | 0.197 |
MOD_PIKK_1 | 317 | 323 | PF00454 | 0.484 |
MOD_PIKK_1 | 378 | 384 | PF00454 | 0.613 |
MOD_PIKK_1 | 395 | 401 | PF00454 | 0.587 |
MOD_Plk_1 | 375 | 381 | PF00069 | 0.405 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.357 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.302 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.405 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.309 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.417 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.225 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.516 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.495 |
TRG_DiLeu_BaLyEn_6 | 332 | 337 | PF01217 | 0.425 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.415 |
TRG_ER_diArg_1 | 364 | 367 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 385 | 387 | PF00400 | 0.653 |
TRG_NLS_MonoCore_2 | 356 | 361 | PF00514 | 0.519 |
TRG_NLS_MonoExtN_4 | 355 | 362 | PF00514 | 0.518 |
TRG_Pf-PMV_PEXEL_1 | 315 | 319 | PF00026 | 0.588 |
TRG_Pf-PMV_PEXEL_1 | 323 | 328 | PF00026 | 0.526 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3N4 | Leptomonas seymouri | 61% | 94% |
A0A0S4KHH7 | Bodo saltans | 37% | 90% |
A0A1X0NTB3 | Trypanosomatidae | 44% | 100% |
A0A3S7WUI4 | Leishmania donovani | 84% | 100% |
A4HXF0 | Leishmania infantum | 84% | 100% |
C9ZP21 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9AR45 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4QEB8 | Leishmania major | 83% | 100% |
V5BFE7 | Trypanosoma cruzi | 47% | 100% |