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 | no | 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: Q4QDG5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_SKI1_1 | 38 | 42 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.641 |
DEG_APCC_DBOX_1 | 143 | 151 | PF00400 | 0.563 |
DEG_SPOP_SBC_1 | 507 | 511 | PF00917 | 0.331 |
DOC_MAPK_gen_1 | 133 | 142 | PF00069 | 0.711 |
DOC_MAPK_gen_1 | 38 | 46 | PF00069 | 0.479 |
DOC_MAPK_gen_1 | 534 | 542 | PF00069 | 0.509 |
DOC_MAPK_MEF2A_6 | 144 | 153 | PF00069 | 0.569 |
DOC_MAPK_MEF2A_6 | 534 | 542 | PF00069 | 0.546 |
DOC_PP2B_LxvP_1 | 10 | 13 | PF13499 | 0.576 |
DOC_PP2B_LxvP_1 | 20 | 23 | PF13499 | 0.580 |
DOC_PP4_FxxP_1 | 5 | 8 | PF00568 | 0.577 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.335 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.479 |
LIG_14-3-3_CanoR_1 | 195 | 201 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 27 | 35 | PF00244 | 0.695 |
LIG_14-3-3_CanoR_1 | 428 | 437 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 508 | 513 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 537 | 541 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 91 | 100 | PF00244 | 0.451 |
LIG_EH1_1 | 257 | 265 | PF00400 | 0.522 |
LIG_EH1_1 | 517 | 525 | PF00400 | 0.398 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.431 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.456 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.443 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.494 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.581 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.415 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.332 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.402 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.367 |
LIG_FHA_1 | 537 | 543 | PF00498 | 0.692 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.427 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.521 |
LIG_FHA_2 | 494 | 500 | PF00498 | 0.513 |
LIG_GBD_Chelix_1 | 288 | 296 | PF00786 | 0.450 |
LIG_LIR_Apic_2 | 129 | 134 | PF02991 | 0.647 |
LIG_LIR_Apic_2 | 401 | 406 | PF02991 | 0.446 |
LIG_LIR_Apic_2 | 466 | 470 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 219 | 227 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 228 | 238 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 219 | 223 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 228 | 233 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 280 | 286 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 466 | 472 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 94 | 99 | PF02991 | 0.393 |
LIG_LYPXL_S_1 | 100 | 104 | PF13949 | 0.565 |
LIG_PCNA_yPIPBox_3 | 218 | 231 | PF02747 | 0.351 |
LIG_Pex14_1 | 279 | 283 | PF04695 | 0.605 |
LIG_Pex14_2 | 286 | 290 | PF04695 | 0.416 |
LIG_SH2_CRK | 167 | 171 | PF00017 | 0.435 |
LIG_SH2_CRK | 185 | 189 | PF00017 | 0.465 |
LIG_SH2_GRB2like | 190 | 193 | PF00017 | 0.405 |
LIG_SH2_PTP2 | 131 | 134 | PF00017 | 0.640 |
LIG_SH2_PTP2 | 230 | 233 | PF00017 | 0.480 |
LIG_SH2_PTP2 | 403 | 406 | PF00017 | 0.447 |
LIG_SH2_PTP2 | 467 | 470 | PF00017 | 0.449 |
LIG_SH2_SRC | 530 | 533 | PF00017 | 0.319 |
LIG_SH2_SRC | 99 | 102 | PF00017 | 0.436 |
LIG_SH2_STAP1 | 447 | 451 | PF00017 | 0.448 |
LIG_SH2_STAT3 | 447 | 450 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.640 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 283 | 286 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 500 | 503 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 530 | 533 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.374 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.486 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.576 |
LIG_SUMO_SIM_anti_2 | 393 | 402 | PF11976 | 0.453 |
LIG_SUMO_SIM_par_1 | 148 | 154 | PF11976 | 0.268 |
LIG_TRFH_1 | 98 | 102 | PF08558 | 0.566 |
LIG_TYR_ITIM | 165 | 170 | PF00017 | 0.506 |
LIG_TYR_ITIM | 435 | 440 | PF00017 | 0.372 |
LIG_WRC_WIRS_1 | 217 | 222 | PF05994 | 0.553 |
LIG_WW_2 | 8 | 11 | PF00397 | 0.454 |
MOD_CDK_SPxxK_3 | 31 | 38 | PF00069 | 0.456 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.482 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.509 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.684 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.520 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.677 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.623 |
MOD_CK2_1 | 493 | 499 | PF00069 | 0.490 |
MOD_CK2_1 | 78 | 84 | PF00069 | 0.600 |
MOD_DYRK1A_RPxSP_1 | 31 | 35 | PF00069 | 0.475 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.566 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.520 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.511 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.566 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.533 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.767 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.568 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.364 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.498 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.485 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.593 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.547 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.511 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.405 |
MOD_N-GLC_1 | 15 | 20 | PF02516 | 0.484 |
MOD_N-GLC_1 | 196 | 201 | PF02516 | 0.462 |
MOD_N-GLC_1 | 203 | 208 | PF02516 | 0.475 |
MOD_N-GLC_1 | 414 | 419 | PF02516 | 0.654 |
MOD_N-GLC_1 | 459 | 464 | PF02516 | 0.464 |
MOD_N-GLC_1 | 490 | 495 | PF02516 | 0.619 |
MOD_N-GLC_1 | 78 | 83 | PF02516 | 0.585 |
MOD_N-GLC_2 | 360 | 362 | PF02516 | 0.536 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.450 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.736 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.532 |
MOD_NEK2_1 | 39 | 44 | PF00069 | 0.619 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.534 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.457 |
MOD_NEK2_1 | 513 | 518 | PF00069 | 0.393 |
MOD_NEK2_1 | 56 | 61 | PF00069 | 0.360 |
MOD_OFUCOSY | 121 | 127 | PF10250 | 0.593 |
MOD_OFUCOSY | 275 | 281 | PF10250 | 0.536 |
MOD_PIKK_1 | 174 | 180 | PF00454 | 0.543 |
MOD_PIKK_1 | 342 | 348 | PF00454 | 0.571 |
MOD_PIKK_1 | 384 | 390 | PF00454 | 0.551 |
MOD_PIKK_1 | 484 | 490 | PF00454 | 0.502 |
MOD_PIKK_1 | 493 | 499 | PF00454 | 0.593 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.560 |
MOD_PK_1 | 508 | 514 | PF00069 | 0.502 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.608 |
MOD_PKA_2 | 507 | 513 | PF00069 | 0.516 |
MOD_PKA_2 | 533 | 539 | PF00069 | 0.347 |
MOD_Plk_1 | 15 | 21 | PF00069 | 0.484 |
MOD_Plk_1 | 196 | 202 | PF00069 | 0.522 |
MOD_Plk_1 | 225 | 231 | PF00069 | 0.501 |
MOD_Plk_1 | 490 | 496 | PF00069 | 0.675 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.583 |
MOD_Plk_2-3 | 216 | 222 | PF00069 | 0.511 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.455 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.454 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.414 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.530 |
MOD_Plk_4 | 508 | 514 | PF00069 | 0.386 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.603 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.461 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.594 |
MOD_SUMO_for_1 | 134 | 137 | PF00179 | 0.559 |
TRG_DiLeu_BaLyEn_6 | 467 | 472 | PF01217 | 0.472 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.507 |
TRG_ENDOCYTIC_2 | 185 | 188 | PF00928 | 0.528 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.562 |
TRG_ENDOCYTIC_2 | 283 | 286 | PF00928 | 0.346 |
TRG_ENDOCYTIC_2 | 437 | 440 | PF00928 | 0.441 |
TRG_ER_diLys_1 | 544 | 548 | PF00400 | 0.593 |
TRG_NLS_MonoExtN_4 | 23 | 28 | PF00514 | 0.716 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8Y8 | Leptomonas seymouri | 53% | 100% |
A0A0S4ITY9 | Bodo saltans | 25% | 100% |
A0A0S4IXB1 | Bodo saltans | 28% | 100% |
A0A0S4IXU4 | Bodo saltans | 28% | 100% |
A0A1X0NVP9 | Trypanosomatidae | 38% | 100% |
A0A1X0NWC8 | Trypanosomatidae | 35% | 100% |
A0A1X0P6A6 | Trypanosomatidae | 28% | 100% |
A0A3Q8IB78 | Leishmania donovani | 89% | 100% |
A0A3S7WVB2 | Leishmania donovani | 89% | 100% |
A0A422N059 | Trypanosoma rangeli | 37% | 100% |
A4HA16 | Leishmania braziliensis | 71% | 100% |
A4HY78 | Leishmania infantum | 89% | 100% |
A4HY79 | Leishmania infantum | 88% | 100% |
C9ZWF5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D0A5X9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 96% |
E9AS08 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
E9AS09 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4QDG4 | Leishmania major | 94% | 100% |
V5C1U9 | Trypanosoma cruzi | 29% | 100% |