A conserved signal-anchored protein family of obscure function also found in plants and bacteria.. Some of the Leishmaniid proteins might have 3 TM segments instead of 1
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: A0A3S7XC13
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 245 | 249 | PF00656 | 0.525 |
CLV_NRD_NRD_1 | 127 | 129 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.266 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.202 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.236 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.236 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.295 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.451 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.237 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.236 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.236 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.441 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.309 |
CLV_PCSK_PC1ET2_1 | 268 | 270 | PF00082 | 0.350 |
CLV_PCSK_PC1ET2_1 | 450 | 452 | PF00082 | 0.415 |
CLV_PCSK_PC1ET2_1 | 455 | 457 | PF00082 | 0.470 |
CLV_PCSK_PC7_1 | 123 | 129 | PF00082 | 0.458 |
CLV_PCSK_PC7_1 | 451 | 457 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 432 | 436 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 451 | 455 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 56 | 60 | PF00082 | 0.521 |
DEG_APCC_DBOX_1 | 412 | 420 | PF00400 | 0.540 |
DEG_APCC_KENBOX_2 | 477 | 481 | PF00400 | 0.594 |
DEG_COP1_1 | 398 | 407 | PF00400 | 0.494 |
DOC_CKS1_1 | 354 | 359 | PF01111 | 0.543 |
DOC_CYCLIN_RxL_1 | 429 | 438 | PF00134 | 0.560 |
DOC_CYCLIN_RxL_1 | 53 | 64 | PF00134 | 0.309 |
DOC_CYCLIN_yCln2_LP_2 | 59 | 62 | PF00134 | 0.337 |
DOC_MAPK_DCC_7 | 284 | 292 | PF00069 | 0.539 |
DOC_MAPK_gen_1 | 210 | 220 | PF00069 | 0.539 |
DOC_MAPK_gen_1 | 413 | 421 | PF00069 | 0.487 |
DOC_MAPK_gen_1 | 422 | 430 | PF00069 | 0.542 |
DOC_MAPK_MEF2A_6 | 284 | 292 | PF00069 | 0.471 |
DOC_MAPK_MEF2A_6 | 413 | 421 | PF00069 | 0.482 |
DOC_MAPK_RevD_3 | 295 | 308 | PF00069 | 0.606 |
DOC_MAPK_RevD_3 | 442 | 456 | PF00069 | 0.584 |
DOC_PP1_RVXF_1 | 44 | 50 | PF00149 | 0.323 |
DOC_PP2B_LxvP_1 | 58 | 61 | PF13499 | 0.346 |
DOC_PP2B_PxIxI_1 | 184 | 190 | PF00149 | 0.539 |
DOC_PP4_FxxP_1 | 292 | 295 | PF00568 | 0.494 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.406 |
DOC_USP7_UBL2_3 | 276 | 280 | PF12436 | 0.563 |
DOC_USP7_UBL2_3 | 450 | 454 | PF12436 | 0.621 |
DOC_USP7_UBL2_3 | 455 | 459 | PF12436 | 0.671 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.356 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.602 |
LIG_14-3-3_CanoR_1 | 269 | 273 | PF00244 | 0.498 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.354 |
LIG_BRCT_BRCA1_1 | 1 | 5 | PF00533 | 0.364 |
LIG_CaM_IQ_9 | 140 | 156 | PF13499 | 0.539 |
LIG_eIF4E_1 | 411 | 417 | PF01652 | 0.539 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.330 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.568 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.535 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.523 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.558 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.529 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.267 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.279 |
LIG_GBD_Chelix_1 | 386 | 394 | PF00786 | 0.384 |
LIG_LIR_Apic_2 | 37 | 42 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 217 | 228 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 383 | 390 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 479 | 488 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 8 | 19 | PF02991 | 0.167 |
LIG_LIR_Gen_1 | 89 | 100 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.172 |
LIG_LIR_Nem_3 | 217 | 223 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 314 | 319 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 343 | 348 | PF02991 | 0.644 |
LIG_LIR_Nem_3 | 383 | 387 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 406 | 411 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 8 | 14 | PF02991 | 0.162 |
LIG_LIR_Nem_3 | 89 | 95 | PF02991 | 0.332 |
LIG_MLH1_MIPbox_1 | 1 | 5 | PF16413 | 0.354 |
LIG_NRBOX | 385 | 391 | PF00104 | 0.574 |
LIG_Pex14_1 | 158 | 162 | PF04695 | 0.447 |
LIG_Pex14_1 | 384 | 388 | PF04695 | 0.502 |
LIG_REV1ctd_RIR_1 | 29 | 35 | PF16727 | 0.338 |
LIG_RPA_C_Fungi | 160 | 172 | PF08784 | 0.416 |
LIG_SH2_CRK | 39 | 43 | PF00017 | 0.403 |
LIG_SH2_PTP2 | 92 | 95 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 388 | 391 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 482 | 485 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.367 |
LIG_SH3_2 | 471 | 476 | PF14604 | 0.546 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.375 |
LIG_SH3_3 | 348 | 354 | PF00018 | 0.713 |
LIG_SH3_3 | 468 | 474 | PF00018 | 0.411 |
LIG_SUMO_SIM_anti_2 | 177 | 182 | PF11976 | 0.273 |
LIG_SUMO_SIM_anti_2 | 441 | 448 | PF11976 | 0.477 |
LIG_SUMO_SIM_par_1 | 185 | 191 | PF11976 | 0.277 |
LIG_SUMO_SIM_par_1 | 287 | 293 | PF11976 | 0.288 |
LIG_SUMO_SIM_par_1 | 494 | 500 | PF11976 | 0.357 |
LIG_SUMO_SIM_par_1 | 82 | 90 | PF11976 | 0.554 |
LIG_WRC_WIRS_1 | 313 | 318 | PF05994 | 0.367 |
MOD_CDK_SPxK_1 | 32 | 38 | PF00069 | 0.449 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.442 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.616 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.518 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.409 |
MOD_CMANNOS | 342 | 345 | PF00535 | 0.648 |
MOD_Cter_Amidation | 266 | 269 | PF01082 | 0.347 |
MOD_DYRK1A_RPxSP_1 | 353 | 357 | PF00069 | 0.428 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.435 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.607 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.465 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.550 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.554 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.532 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.428 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.379 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.427 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.347 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.519 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.398 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.368 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.511 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.182 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.508 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.367 |
MOD_NEK2_2 | 114 | 119 | PF00069 | 0.410 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.479 |
MOD_PKA_1 | 268 | 274 | PF00069 | 0.347 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.446 |
MOD_PKA_2 | 268 | 274 | PF00069 | 0.411 |
MOD_PKA_2 | 349 | 355 | PF00069 | 0.462 |
MOD_PKB_1 | 212 | 220 | PF00069 | 0.347 |
MOD_Plk_1 | 274 | 280 | PF00069 | 0.225 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.427 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.348 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.305 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.539 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.492 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.474 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.478 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.189 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.438 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.504 |
MOD_SUMO_rev_2 | 142 | 149 | PF00179 | 0.409 |
TRG_DiLeu_BaEn_1 | 479 | 484 | PF01217 | 0.447 |
TRG_DiLeu_BaEn_2 | 134 | 140 | PF01217 | 0.544 |
TRG_DiLeu_BaLyEn_6 | 390 | 395 | PF01217 | 0.488 |
TRG_ENDOCYTIC_2 | 482 | 485 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 55 | 58 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.367 |
TRG_ER_diArg_1 | 126 | 128 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 163 | 166 | PF00400 | 0.273 |
TRG_ER_diArg_1 | 212 | 215 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 234 | 236 | PF00400 | 0.273 |
TRG_ER_diArg_1 | 242 | 244 | PF00400 | 0.273 |
TRG_ER_diArg_1 | 32 | 34 | PF00400 | 0.450 |
TRG_Pf-PMV_PEXEL_1 | 508 | 512 | PF00026 | 0.462 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDN0 | Leptomonas seymouri | 73% | 100% |
A0A0S4J7E4 | Bodo saltans | 36% | 100% |
A0A1X0P0I4 | Trypanosomatidae | 43% | 100% |
A0A3R7R7J3 | Trypanosoma rangeli | 43% | 100% |
A4HQ77 | Leishmania braziliensis | 87% | 100% |
A4IDX5 | Leishmania infantum | 99% | 100% |
D0A437 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9ATZ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q0K0 | Leishmania major | 92% | 100% |
V5B3M2 | Trypanosoma cruzi | 42% | 100% |