Belongs to a poorly known protein family found in basal Eukaryota (also containing A0A0A1U905_ENTIV, A0A0A1U245_ENTIV). Very distantly related to animal prominins.. The first TM segment can equally be a signal peptide, with no change in overall topology. If related to prominins, this massively expanded family could play a role in vesicular processes.
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 9 |
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: 18, no: 1 |
NetGPI | no | yes: 0, no: 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 18 |
GO:0110165 | cellular anatomical entity | 1 | 18 |
Related structures:
AlphaFold database: A4HA16
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 510 | 512 | PF00082 | 0.419 |
CLV_PCSK_PC1ET2_1 | 275 | 277 | PF00082 | 0.523 |
CLV_PCSK_PC1ET2_1 | 510 | 512 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.659 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.646 |
DOC_CKS1_1 | 168 | 173 | PF01111 | 0.371 |
DOC_MAPK_MEF2A_6 | 103 | 112 | PF00069 | 0.587 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.474 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.689 |
LIG_14-3-3_CanoR_1 | 154 | 164 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 467 | 472 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 511 | 521 | PF00244 | 0.725 |
LIG_14-3-3_CanoR_1 | 53 | 62 | PF00244 | 0.464 |
LIG_APCC_ABBA_1 | 317 | 322 | PF00400 | 0.360 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.568 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.383 |
LIG_EH1_1 | 200 | 208 | PF00400 | 0.396 |
LIG_EH1_1 | 216 | 224 | PF00400 | 0.427 |
LIG_EH1_1 | 476 | 484 | PF00400 | 0.380 |
LIG_eIF4E_1 | 242 | 248 | PF01652 | 0.270 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.465 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.474 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.496 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.346 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.423 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.396 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.374 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.802 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.372 |
LIG_FHA_2 | 341 | 347 | PF00498 | 0.345 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.478 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.657 |
LIG_LIR_Apic_2 | 360 | 365 | PF02991 | 0.400 |
LIG_LIR_Apic_2 | 395 | 399 | PF02991 | 0.466 |
LIG_LIR_Apic_2 | 425 | 429 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 187 | 197 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 259 | 265 | PF02991 | 0.234 |
LIG_LIR_Gen_1 | 292 | 302 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 195 | 200 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 239 | 245 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 259 | 264 | PF02991 | 0.197 |
LIG_LIR_Nem_3 | 292 | 298 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 425 | 431 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 56 | 61 | PF02991 | 0.396 |
LIG_LYPXL_S_1 | 427 | 431 | PF13949 | 0.473 |
LIG_LYPXL_S_1 | 62 | 66 | PF13949 | 0.562 |
LIG_LYPXL_yS_3 | 428 | 431 | PF13949 | 0.277 |
LIG_Pex14_1 | 238 | 242 | PF04695 | 0.614 |
LIG_Pex14_2 | 245 | 249 | PF04695 | 0.400 |
LIG_SH2_CRK | 126 | 130 | PF00017 | 0.462 |
LIG_SH2_GRB2like | 149 | 152 | PF00017 | 0.403 |
LIG_SH2_PTP2 | 362 | 365 | PF00017 | 0.401 |
LIG_SH2_PTP2 | 426 | 429 | PF00017 | 0.450 |
LIG_SH2_SRC | 396 | 399 | PF00017 | 0.420 |
LIG_SH2_SRC | 426 | 429 | PF00017 | 0.387 |
LIG_SH2_SRC | 61 | 64 | PF00017 | 0.443 |
LIG_SH2_STAP1 | 189 | 193 | PF00017 | 0.412 |
LIG_SH2_STAP1 | 406 | 410 | PF00017 | 0.466 |
LIG_SH2_STAP1 | 449 | 453 | PF00017 | 0.395 |
LIG_SH2_STAT3 | 406 | 409 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.384 |
LIG_SH3_1 | 396 | 402 | PF00018 | 0.424 |
LIG_SH3_2 | 399 | 404 | PF14604 | 0.381 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.493 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.405 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.424 |
LIG_SUMO_SIM_anti_2 | 352 | 361 | PF11976 | 0.467 |
LIG_SUMO_SIM_anti_2 | 74 | 79 | PF11976 | 0.234 |
LIG_SUMO_SIM_par_1 | 355 | 361 | PF11976 | 0.341 |
LIG_TRAF2_1 | 92 | 95 | PF00917 | 0.561 |
LIG_TRFH_1 | 60 | 64 | PF08558 | 0.479 |
LIG_TYR_ITIM | 124 | 129 | PF00017 | 0.512 |
LIG_TYR_ITIM | 198 | 203 | PF00017 | 0.301 |
LIG_UBA3_1 | 44 | 51 | PF00899 | 0.392 |
LIG_Vh1_VBS_1 | 1 | 19 | PF01044 | 0.415 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.295 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.386 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.386 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.429 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.592 |
MOD_CK1_1 | 512 | 518 | PF00069 | 0.716 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.278 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.357 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.465 |
MOD_CK2_1 | 512 | 518 | PF00069 | 0.710 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.742 |
MOD_Cter_Amidation | 508 | 511 | PF01082 | 0.422 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.671 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.644 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.495 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.638 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.675 |
MOD_GlcNHglycan | 506 | 510 | PF01048 | 0.517 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.519 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.364 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.370 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.522 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.366 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.398 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.396 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.453 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.744 |
MOD_N-GLC_1 | 143 | 148 | PF02516 | 0.576 |
MOD_N-GLC_1 | 150 | 155 | PF02516 | 0.568 |
MOD_N-GLC_1 | 162 | 167 | PF02516 | 0.588 |
MOD_N-GLC_1 | 184 | 189 | PF02516 | 0.625 |
MOD_N-GLC_1 | 340 | 345 | PF02516 | 0.595 |
MOD_N-GLC_1 | 373 | 378 | PF02516 | 0.740 |
MOD_N-GLC_1 | 40 | 45 | PF02516 | 0.672 |
MOD_N-GLC_1 | 418 | 423 | PF02516 | 0.582 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.352 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.463 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.576 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.290 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.474 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.434 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.394 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.394 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.439 |
MOD_OFUCOSY | 233 | 240 | PF10250 | 0.427 |
MOD_PIKK_1 | 307 | 313 | PF00454 | 0.426 |
MOD_PIKK_1 | 376 | 382 | PF00454 | 0.471 |
MOD_PIKK_1 | 405 | 411 | PF00454 | 0.378 |
MOD_PIKK_1 | 53 | 59 | PF00454 | 0.455 |
MOD_PK_1 | 467 | 473 | PF00069 | 0.365 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.351 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.427 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.621 |
MOD_PKA_2 | 466 | 472 | PF00069 | 0.429 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.401 |
MOD_Plk_1 | 150 | 156 | PF00069 | 0.428 |
MOD_Plk_1 | 184 | 190 | PF00069 | 0.423 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.457 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.468 |
MOD_Plk_1 | 449 | 455 | PF00069 | 0.531 |
MOD_Plk_2-3 | 143 | 149 | PF00069 | 0.502 |
MOD_Plk_2-3 | 382 | 388 | PF00069 | 0.387 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.329 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.361 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.309 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.366 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.403 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.428 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.329 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.342 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.528 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.691 |
MOD_SUMO_rev_2 | 90 | 99 | PF00179 | 0.549 |
TRG_DiLeu_BaEn_2 | 331 | 337 | PF01217 | 0.388 |
TRG_DiLeu_BaLyEn_6 | 426 | 431 | PF01217 | 0.382 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 428 | 431 | PF00928 | 0.277 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.327 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8Y8 | Leptomonas seymouri | 54% | 100% |
A0A0S4IXB1 | Bodo saltans | 25% | 100% |
A0A0S4IXU4 | Bodo saltans | 26% | 100% |
A0A1X0NVP9 | Trypanosomatidae | 40% | 100% |
A0A1X0NWC8 | Trypanosomatidae | 36% | 100% |
A0A1X0P6A6 | Trypanosomatidae | 29% | 100% |
A0A3Q8IB78 | Leishmania donovani | 73% | 100% |
A0A3S7WVB2 | Leishmania donovani | 74% | 100% |
A0A422N059 | Trypanosoma rangeli | 37% | 100% |
A4HY78 | Leishmania infantum | 73% | 100% |
A4HY79 | Leishmania infantum | 74% | 100% |
C9ZWF5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 97% |
D0A5X9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 93% |
E9AS08 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
E9AS09 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
Q4QDG4 | Leishmania major | 71% | 100% |
Q4QDG5 | Leishmania major | 71% | 100% |
V5C1U9 | Trypanosoma cruzi | 30% | 100% |