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 | no | yes: 1, no: 1 |
NetGPI | no | yes: 0, no: 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I712
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 287 | 291 | PF00656 | 0.340 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 458 | 460 | PF00675 | 0.584 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.589 |
CLV_PCSK_PC1ET2_1 | 435 | 437 | PF00082 | 0.452 |
CLV_PCSK_PC1ET2_1 | 457 | 459 | PF00082 | 0.601 |
CLV_PCSK_PC7_1 | 453 | 459 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.586 |
DEG_SCF_FBW7_1 | 28 | 35 | PF00400 | 0.395 |
DOC_CKS1_1 | 29 | 34 | PF01111 | 0.587 |
DOC_CKS1_1 | 346 | 351 | PF01111 | 0.526 |
DOC_CYCLIN_yCln2_LP_2 | 382 | 388 | PF00134 | 0.287 |
DOC_MAPK_gen_1 | 434 | 445 | PF00069 | 0.718 |
DOC_MAPK_MEF2A_6 | 185 | 192 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 438 | 447 | PF00069 | 0.730 |
DOC_MAPK_RevD_3 | 385 | 399 | PF00069 | 0.453 |
DOC_MAPK_RevD_3 | 445 | 459 | PF00069 | 0.803 |
DOC_PP1_RVXF_1 | 114 | 120 | PF00149 | 0.326 |
DOC_PP2B_LxvP_1 | 382 | 385 | PF13499 | 0.287 |
DOC_PP4_FxxP_1 | 29 | 32 | PF00568 | 0.583 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.326 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.497 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.430 |
LIG_14-3-3_CanoR_1 | 120 | 129 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 306 | 311 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 58 | 66 | PF00244 | 0.351 |
LIG_Actin_WH2_2 | 170 | 187 | PF00022 | 0.320 |
LIG_APCC_ABBA_1 | 131 | 136 | PF00400 | 0.476 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.467 |
LIG_BIR_III_4 | 275 | 279 | PF00653 | 0.510 |
LIG_BRCT_BRCA1_1 | 327 | 331 | PF00533 | 0.493 |
LIG_eIF4E_1 | 123 | 129 | PF01652 | 0.543 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.490 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.269 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.355 |
LIG_LIR_Apic_2 | 343 | 349 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 122 | 131 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 373 | 382 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 408 | 418 | PF02991 | 0.645 |
LIG_LIR_Nem_3 | 11 | 17 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 373 | 377 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 408 | 413 | PF02991 | 0.645 |
LIG_LIR_Nem_3 | 417 | 421 | PF02991 | 0.618 |
LIG_PCNA_PIPBox_1 | 449 | 458 | PF02747 | 0.796 |
LIG_PCNA_yPIPBox_3 | 448 | 456 | PF02747 | 0.796 |
LIG_SH2_CRK | 346 | 350 | PF00017 | 0.522 |
LIG_SH2_NCK_1 | 134 | 138 | PF00017 | 0.493 |
LIG_SH2_NCK_1 | 346 | 350 | PF00017 | 0.522 |
LIG_SH2_SRC | 134 | 137 | PF00017 | 0.483 |
LIG_SH2_STAP1 | 342 | 346 | PF00017 | 0.534 |
LIG_SH2_STAP1 | 6 | 10 | PF00017 | 0.377 |
LIG_SH2_STAP1 | 66 | 70 | PF00017 | 0.488 |
LIG_SH2_STAT3 | 21 | 24 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 8 | 11 | PF00017 | 0.505 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.513 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.325 |
LIG_SUMO_SIM_anti_2 | 373 | 379 | PF11976 | 0.387 |
LIG_SUMO_SIM_anti_2 | 67 | 72 | PF11976 | 0.294 |
LIG_SUMO_SIM_par_1 | 139 | 144 | PF11976 | 0.466 |
LIG_SUMO_SIM_par_1 | 69 | 75 | PF11976 | 0.483 |
LIG_UBA3_1 | 442 | 448 | PF00899 | 0.531 |
LIG_WRC_WIRS_1 | 76 | 81 | PF05994 | 0.393 |
LIG_WW_1 | 366 | 369 | PF00397 | 0.481 |
LIG_WW_3 | 266 | 270 | PF00397 | 0.447 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.441 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.631 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.730 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.658 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.469 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.403 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.389 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.607 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.625 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.616 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.414 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.381 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.657 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.331 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.473 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.664 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.341 |
MOD_N-GLC_1 | 241 | 246 | PF02516 | 0.362 |
MOD_N-GLC_1 | 259 | 264 | PF02516 | 0.393 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.446 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.623 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.452 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.611 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.375 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.669 |
MOD_NEK2_2 | 194 | 199 | PF00069 | 0.407 |
MOD_NEK2_2 | 72 | 77 | PF00069 | 0.354 |
MOD_OFUCOSY | 207 | 214 | PF10250 | 0.640 |
MOD_OFUCOSY | 325 | 330 | PF10250 | 0.610 |
MOD_OFUCOSY | 39 | 45 | PF10250 | 0.654 |
MOD_OFUCOSY | 54 | 61 | PF10250 | 0.424 |
MOD_PIKK_1 | 30 | 36 | PF00454 | 0.482 |
MOD_PIKK_1 | 350 | 356 | PF00454 | 0.661 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.342 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.623 |
MOD_PKA_2 | 361 | 367 | PF00069 | 0.487 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.432 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.587 |
MOD_Plk_1 | 172 | 178 | PF00069 | 0.646 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.611 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.474 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.618 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.639 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.469 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.335 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.735 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.527 |
TRG_ENDOCYTIC_2 | 123 | 126 | PF00928 | 0.722 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.404 |
TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.685 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.462 |
TRG_ER_diArg_1 | 359 | 362 | PF00400 | 0.743 |
TRG_ER_diArg_1 | 397 | 399 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 434 | 437 | PF00400 | 0.621 |
TRG_ER_diArg_1 | 452 | 454 | PF00400 | 0.483 |
TRG_NLS_MonoExtC_3 | 433 | 438 | PF00514 | 0.554 |
TRG_Pf-PMV_PEXEL_1 | 419 | 424 | PF00026 | 0.745 |
TRG_Pf-PMV_PEXEL_1 | 88 | 92 | PF00026 | 0.653 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A4HJP1 | Leishmania braziliensis | 72% | 100% |