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. | no | 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: 19, no: 1 |
NetGPI | no | yes: 0, no: 20 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 19 |
GO:0110165 | cellular anatomical entity | 1 | 19 |
Related structures:
AlphaFold database: A0A3S7WVB2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.257 |
DEG_APCC_KENBOX_2 | 504 | 508 | PF00400 | 0.486 |
DOC_CKS1_1 | 171 | 176 | PF01111 | 0.308 |
DOC_MAPK_gen_1 | 202 | 211 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 95 | 104 | PF00069 | 0.669 |
DOC_MAPK_MEF2A_6 | 106 | 115 | PF00069 | 0.519 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.425 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 513 | 518 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 521 | 526 | PF00397 | 0.589 |
LIG_14-3-3_CanoR_1 | 157 | 163 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 464 | 471 | PF00244 | 0.257 |
LIG_14-3-3_CanoR_1 | 53 | 62 | PF00244 | 0.404 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.536 |
LIG_EH1_1 | 219 | 227 | PF00400 | 0.486 |
LIG_EH1_1 | 479 | 487 | PF00400 | 0.336 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.405 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.398 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.571 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.448 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.364 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.374 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.376 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.468 |
LIG_FHA_2 | 456 | 462 | PF00498 | 0.449 |
LIG_GBD_Chelix_1 | 250 | 258 | PF00786 | 0.338 |
LIG_LIR_Apic_2 | 363 | 368 | PF02991 | 0.348 |
LIG_LIR_Apic_2 | 398 | 402 | PF02991 | 0.416 |
LIG_LIR_Apic_2 | 428 | 432 | PF02991 | 0.349 |
LIG_LIR_Apic_2 | 91 | 96 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 180 | 189 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 190 | 200 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 297 | 305 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 180 | 185 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 190 | 195 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 242 | 248 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 297 | 301 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 398 | 404 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 428 | 434 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 56 | 61 | PF02991 | 0.338 |
LIG_LYPXL_S_1 | 62 | 66 | PF13949 | 0.515 |
LIG_Pex14_1 | 241 | 245 | PF04695 | 0.452 |
LIG_Pex14_2 | 248 | 252 | PF04695 | 0.356 |
LIG_SH2_CRK | 129 | 133 | PF00017 | 0.408 |
LIG_SH2_CRK | 399 | 403 | PF00017 | 0.295 |
LIG_SH2_GRB2like | 152 | 155 | PF00017 | 0.350 |
LIG_SH2_PTP2 | 192 | 195 | PF00017 | 0.442 |
LIG_SH2_PTP2 | 365 | 368 | PF00017 | 0.350 |
LIG_SH2_PTP2 | 429 | 432 | PF00017 | 0.406 |
LIG_SH2_PTP2 | 93 | 96 | PF00017 | 0.555 |
LIG_SH2_SRC | 61 | 64 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 152 | 155 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.555 |
LIG_SH3_3 | 168 | 174 | PF00018 | 0.435 |
LIG_SH3_3 | 512 | 518 | PF00018 | 0.601 |
LIG_SH3_3 | 519 | 525 | PF00018 | 0.612 |
LIG_SUMO_SIM_anti_2 | 355 | 364 | PF11976 | 0.412 |
LIG_TRFH_1 | 60 | 64 | PF08558 | 0.358 |
LIG_TYR_ITIM | 127 | 132 | PF00017 | 0.467 |
LIG_Vh1_VBS_1 | 1 | 19 | PF01044 | 0.371 |
MOD_CDC14_SPxK_1 | 524 | 527 | PF00782 | 0.583 |
MOD_CDK_SPxK_1 | 521 | 527 | PF00069 | 0.577 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.350 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.381 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.548 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.438 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.437 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.694 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.608 |
MOD_GlcNHglycan | 178 | 182 | PF01048 | 0.503 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.594 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.445 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.585 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.569 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.614 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.422 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.302 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.381 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.475 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.354 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.284 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.345 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.507 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.618 |
MOD_N-GLC_1 | 153 | 158 | PF02516 | 0.534 |
MOD_N-GLC_1 | 165 | 170 | PF02516 | 0.553 |
MOD_N-GLC_1 | 187 | 192 | PF02516 | 0.550 |
MOD_N-GLC_1 | 328 | 333 | PF02516 | 0.593 |
MOD_N-GLC_1 | 376 | 381 | PF02516 | 0.681 |
MOD_N-GLC_1 | 40 | 45 | PF02516 | 0.624 |
MOD_N-GLC_1 | 421 | 426 | PF02516 | 0.525 |
MOD_N-GLC_1 | 452 | 457 | PF02516 | 0.665 |
MOD_N-GLC_2 | 322 | 324 | PF02516 | 0.598 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.631 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.388 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.374 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.499 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.396 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.339 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.417 |
MOD_OFUCOSY | 237 | 243 | PF10250 | 0.323 |
MOD_OFUCOSY | 387 | 392 | PF10250 | 0.529 |
MOD_OFUCOSY | 83 | 89 | PF10250 | 0.535 |
MOD_PIKK_1 | 304 | 310 | PF00454 | 0.426 |
MOD_PIKK_1 | 346 | 352 | PF00454 | 0.398 |
MOD_PIKK_1 | 455 | 461 | PF00454 | 0.428 |
MOD_PIKK_1 | 53 | 59 | PF00454 | 0.405 |
MOD_PK_1 | 470 | 476 | PF00069 | 0.309 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.576 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.377 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.383 |
MOD_Plk_1 | 177 | 183 | PF00069 | 0.314 |
MOD_Plk_1 | 187 | 193 | PF00069 | 0.358 |
MOD_Plk_1 | 328 | 334 | PF00069 | 0.379 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.427 |
MOD_Plk_1 | 452 | 458 | PF00069 | 0.489 |
MOD_Plk_2-3 | 146 | 152 | PF00069 | 0.449 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.423 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.355 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.323 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.336 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.441 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.390 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.272 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.394 |
MOD_ProDKin_1 | 513 | 519 | PF00069 | 0.595 |
MOD_ProDKin_1 | 521 | 527 | PF00069 | 0.590 |
MOD_SUMO_for_1 | 96 | 99 | PF00179 | 0.573 |
TRG_DiLeu_BaEn_1 | 385 | 390 | PF01217 | 0.282 |
TRG_DiLeu_BaLyEn_6 | 429 | 434 | PF01217 | 0.342 |
TRG_ENDOCYTIC_2 | 129 | 132 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 192 | 195 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 245 | 248 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.272 |
TRG_Pf-PMV_PEXEL_1 | 27 | 32 | PF00026 | 0.592 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8Y8 | Leptomonas seymouri | 55% | 100% |
A0A0S4ITY9 | Bodo saltans | 25% | 100% |
A0A0S4IXB1 | Bodo saltans | 28% | 100% |
A0A0S4IXU4 | Bodo saltans | 28% | 100% |
A0A1X0NVP9 | Trypanosomatidae | 39% | 100% |
A0A1X0NWC8 | Trypanosomatidae | 37% | 100% |
A0A1X0P6A6 | Trypanosomatidae | 30% | 100% |
A0A3Q8IB78 | Leishmania donovani | 95% | 100% |
A0A422N059 | Trypanosoma rangeli | 38% | 100% |
A4HA16 | Leishmania braziliensis | 74% | 100% |
A4HY78 | Leishmania infantum | 95% | 100% |
A4HY79 | Leishmania infantum | 99% | 100% |
C9ZWF5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 97% |
D0A5X9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 93% |
E9AS08 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
E9AS09 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4QDG4 | Leishmania major | 90% | 100% |
Q4QDG5 | Leishmania major | 89% | 100% |
V5C1U9 | Trypanosoma cruzi | 31% | 100% |