The last domain of this multidomain protein is related to animal Stabilins, known lipoprotein receptors. related to the T. cruzi protein “Enriched in surface-labeled proteome protein 10”. Family has expanded on multiple Kinetoplastid branches, also in free-living species. Localization: Cell surface (by feature)
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: 1, no: 1 |
NetGPI | no | yes: 0, no: 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4HJP1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 458 | 460 | PF00675 | 0.576 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 422 | 424 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.578 |
CLV_PCSK_PC1ET2_1 | 457 | 459 | PF00082 | 0.603 |
CLV_PCSK_PC7_1 | 454 | 460 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 454 | 458 | PF00082 | 0.583 |
DEG_SCF_FBW7_2 | 28 | 35 | PF00400 | 0.446 |
DOC_CKS1_1 | 29 | 34 | PF01111 | 0.581 |
DOC_CKS1_1 | 346 | 351 | PF01111 | 0.550 |
DOC_MAPK_gen_1 | 362 | 372 | PF00069 | 0.471 |
DOC_MAPK_gen_1 | 422 | 432 | PF00069 | 0.756 |
DOC_MAPK_MEF2A_6 | 185 | 192 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 365 | 372 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 423 | 432 | PF00069 | 0.736 |
DOC_MAPK_MEF2A_6 | 440 | 447 | PF00069 | 0.702 |
DOC_MAPK_RevD_3 | 384 | 399 | PF00069 | 0.541 |
DOC_MAPK_RevD_3 | 445 | 459 | PF00069 | 0.796 |
DOC_PP4_FxxP_1 | 29 | 32 | PF00568 | 0.574 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.388 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.413 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.719 |
LIG_14-3-3_CanoR_1 | 306 | 311 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 4 | 9 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 434 | 439 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 448 | 453 | PF00244 | 0.580 |
LIG_Actin_WH2_2 | 435 | 450 | PF00022 | 0.689 |
LIG_APCC_ABBA_1 | 131 | 136 | PF00400 | 0.359 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.805 |
LIG_BIR_III_4 | 275 | 279 | PF00653 | 0.527 |
LIG_BRCT_BRCA1_1 | 11 | 15 | PF00533 | 0.506 |
LIG_BRCT_BRCA1_1 | 327 | 331 | PF00533 | 0.506 |
LIG_BRCT_BRCA1_1 | 4 | 8 | PF00533 | 0.596 |
LIG_DLG_GKlike_1 | 448 | 455 | PF00625 | 0.663 |
LIG_eIF4E_1 | 123 | 129 | PF01652 | 0.543 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.451 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.714 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.542 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.481 |
LIG_LIR_Apic_2 | 343 | 349 | PF02991 | 0.546 |
LIG_LIR_Apic_2 | 35 | 41 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 120 | 131 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 373 | 382 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 67 | 73 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 12 | 17 | PF02991 | 0.705 |
LIG_LIR_Nem_3 | 373 | 377 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 67 | 71 | PF02991 | 0.326 |
LIG_MLH1_MIPbox_1 | 11 | 15 | PF16413 | 0.568 |
LIG_NRBOX | 389 | 395 | PF00104 | 0.375 |
LIG_PCNA_PIPBox_1 | 449 | 458 | PF02747 | 0.789 |
LIG_PCNA_yPIPBox_3 | 448 | 456 | PF02747 | 0.788 |
LIG_SH2_CRK | 346 | 350 | PF00017 | 0.545 |
LIG_SH2_CRK | 38 | 42 | PF00017 | 0.414 |
LIG_SH2_NCK_1 | 134 | 138 | PF00017 | 0.504 |
LIG_SH2_NCK_1 | 346 | 350 | PF00017 | 0.545 |
LIG_SH2_SRC | 134 | 137 | PF00017 | 0.497 |
LIG_SH2_STAP1 | 342 | 346 | PF00017 | 0.547 |
LIG_SH2_STAP1 | 66 | 70 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.645 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.369 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.515 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.439 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.375 |
LIG_Sin3_3 | 374 | 381 | PF02671 | 0.375 |
LIG_SUMO_SIM_anti_2 | 373 | 379 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 138 | 144 | PF11976 | 0.484 |
LIG_SUMO_SIM_par_1 | 69 | 76 | PF11976 | 0.369 |
LIG_WRC_WIRS_1 | 407 | 412 | PF05994 | 0.638 |
MOD_CDK_SPxxK_3 | 412 | 419 | PF00069 | 0.647 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.635 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.461 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.750 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.693 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.645 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.578 |
MOD_GlcNHglycan | 136 | 140 | PF01048 | 0.458 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.635 |
MOD_GlcNHglycan | 208 | 213 | PF01048 | 0.635 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.629 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.435 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.674 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.579 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.507 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.459 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.397 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.679 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.637 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.617 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.631 |
MOD_N-GLC_2 | 59 | 61 | PF02516 | 0.414 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.642 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.470 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.645 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.503 |
MOD_OFUCOSY | 207 | 214 | PF10250 | 0.641 |
MOD_OFUCOSY | 325 | 330 | PF10250 | 0.639 |
MOD_OFUCOSY | 39 | 45 | PF10250 | 0.484 |
MOD_OFUCOSY | 54 | 61 | PF10250 | 0.504 |
MOD_PIKK_1 | 350 | 356 | PF00454 | 0.708 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.562 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.549 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.512 |
MOD_Plk_1 | 172 | 178 | PF00069 | 0.685 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.637 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.501 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.498 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.375 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.724 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.589 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.606 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.646 |
TRG_ENDOCYTIC_2 | 123 | 126 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.698 |
TRG_ER_diArg_1 | 359 | 362 | PF00400 | 0.755 |
TRG_ER_diArg_1 | 397 | 399 | PF00400 | 0.705 |
TRG_ER_diArg_1 | 421 | 423 | PF00400 | 0.702 |
TRG_NES_CRM1_1 | 136 | 146 | PF08389 | 0.436 |
TRG_NES_CRM1_1 | 441 | 453 | PF08389 | 0.595 |
TRG_Pf-PMV_PEXEL_1 | 419 | 424 | PF00026 | 0.815 |
TRG_Pf-PMV_PEXEL_1 | 436 | 441 | PF00026 | 0.489 |
TRG_Pf-PMV_PEXEL_1 | 88 | 92 | PF00026 | 0.656 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A4I712 | Leishmania infantum | 72% | 100% |