Appears to be a family of secreted proteins, probably ER-localized, like its homologs in other Eukaryotes.. Seems to carry a putative KDEL-like signal on its C-terminus.. Localization: Secreted (by homology)
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 1 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 20 |
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. | yes | yes: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 10, no: 1 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005788 | endoplasmic reticulum lumen | 5 | 10 |
GO:0031974 | membrane-enclosed lumen | 2 | 10 |
GO:0043233 | organelle lumen | 3 | 10 |
GO:0070013 | intracellular organelle lumen | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8IS34
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034976 | response to endoplasmic reticulum stress | 4 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003756 | protein disulfide isomerase activity | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0016853 | isomerase activity | 2 | 12 |
GO:0016860 | intramolecular oxidoreductase activity | 3 | 12 |
GO:0016864 | intramolecular oxidoreductase activity, transposing S-S bonds | 4 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 278 | 282 | PF00656 | 0.555 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.492 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.341 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.499 |
CLV_PCSK_PC1ET2_1 | 216 | 218 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.659 |
CLV_PCSK_SKI1_1 | 331 | 335 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.375 |
DEG_APCC_DBOX_1 | 2 | 10 | PF00400 | 0.692 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.706 |
DOC_MAPK_gen_1 | 140 | 148 | PF00069 | 0.571 |
DOC_MAPK_gen_1 | 243 | 252 | PF00069 | 0.526 |
DOC_MAPK_gen_1 | 270 | 279 | PF00069 | 0.437 |
DOC_MAPK_HePTP_8 | 267 | 279 | PF00069 | 0.470 |
DOC_MAPK_MEF2A_6 | 270 | 279 | PF00069 | 0.382 |
DOC_MAPK_MEF2A_6 | 89 | 96 | PF00069 | 0.443 |
DOC_PP1_RVXF_1 | 243 | 250 | PF00149 | 0.478 |
DOC_PP2B_LxvP_1 | 292 | 295 | PF13499 | 0.493 |
DOC_PP4_FxxP_1 | 377 | 380 | PF00568 | 0.408 |
DOC_PP4_FxxP_1 | 43 | 46 | PF00568 | 0.443 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.747 |
DOC_USP7_UBL2_3 | 128 | 132 | PF12436 | 0.571 |
DOC_USP7_UBL2_3 | 334 | 338 | PF12436 | 0.623 |
DOC_USP7_UBL2_3 | 451 | 455 | PF12436 | 0.518 |
DOC_USP7_UBL2_3 | 85 | 89 | PF12436 | 0.452 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.477 |
LIG_14-3-3_CanoR_1 | 217 | 227 | PF00244 | 0.498 |
LIG_BIR_III_2 | 344 | 348 | PF00653 | 0.617 |
LIG_EH1_1 | 7 | 15 | PF00400 | 0.626 |
LIG_eIF4E_1 | 271 | 277 | PF01652 | 0.528 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.651 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.465 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.461 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.408 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.408 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.555 |
LIG_FHA_2 | 410 | 416 | PF00498 | 0.493 |
LIG_FHA_2 | 444 | 450 | PF00498 | 0.475 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.555 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.439 |
LIG_GBD_Chelix_1 | 165 | 173 | PF00786 | 0.560 |
LIG_LIR_Apic_2 | 105 | 109 | PF02991 | 0.493 |
LIG_LIR_Apic_2 | 428 | 433 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 28 | 38 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 4 | 13 | PF02991 | 0.684 |
LIG_LIR_Nem_3 | 225 | 230 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 233 | 238 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 28 | 33 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 283 | 288 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 297 | 303 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 315 | 320 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 362 | 366 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 4 | 8 | PF02991 | 0.691 |
LIG_LIR_Nem_3 | 424 | 429 | PF02991 | 0.416 |
LIG_OCRL_FandH_1 | 306 | 318 | PF00620 | 0.438 |
LIG_PDZ_Class_3 | 472 | 477 | PF00595 | 0.790 |
LIG_Pex14_2 | 303 | 307 | PF04695 | 0.438 |
LIG_Pex14_2 | 377 | 381 | PF04695 | 0.400 |
LIG_Pex14_2 | 43 | 47 | PF04695 | 0.427 |
LIG_SH2_CRK | 106 | 110 | PF00017 | 0.528 |
LIG_SH2_CRK | 285 | 289 | PF00017 | 0.572 |
LIG_SH2_CRK | 317 | 321 | PF00017 | 0.341 |
LIG_SH2_NCK_1 | 317 | 321 | PF00017 | 0.341 |
LIG_SH2_NCK_1 | 392 | 396 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 392 | 396 | PF00017 | 0.465 |
LIG_SH2_STAT3 | 271 | 274 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.555 |
LIG_SUMO_SIM_anti_2 | 37 | 42 | PF11976 | 0.466 |
LIG_SUMO_SIM_par_1 | 263 | 269 | PF11976 | 0.477 |
LIG_TRAF2_1 | 472 | 475 | PF00917 | 0.793 |
LIG_TRAF2_1 | 77 | 80 | PF00917 | 0.477 |
LIG_WRC_WIRS_1 | 276 | 281 | PF05994 | 0.470 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.522 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.484 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.439 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.524 |
MOD_CK1_1 | 456 | 462 | PF00069 | 0.644 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.763 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.488 |
MOD_CK2_1 | 469 | 475 | PF00069 | 0.838 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.545 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.511 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.491 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.680 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.528 |
MOD_GlcNHglycan | 422 | 426 | PF01048 | 0.455 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.705 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.764 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.788 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.515 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.515 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.435 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.735 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.523 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.722 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.430 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.451 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.459 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.383 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.620 |
MOD_PIKK_1 | 168 | 174 | PF00454 | 0.590 |
MOD_PIKK_1 | 270 | 276 | PF00454 | 0.505 |
MOD_PIKK_1 | 367 | 373 | PF00454 | 0.477 |
MOD_PKA_1 | 140 | 146 | PF00069 | 0.549 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.505 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.559 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.512 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.604 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.423 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.527 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.397 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.614 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.461 |
MOD_Plk_4 | 36 | 42 | PF00069 | 0.460 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.422 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.424 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.647 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.477 |
MOD_SUMO_for_1 | 139 | 142 | PF00179 | 0.540 |
MOD_SUMO_for_1 | 333 | 336 | PF00179 | 0.630 |
MOD_SUMO_rev_2 | 296 | 301 | PF00179 | 0.431 |
MOD_SUMO_rev_2 | 330 | 340 | PF00179 | 0.563 |
MOD_SUMO_rev_2 | 448 | 453 | PF00179 | 0.443 |
TRG_DiLeu_BaEn_4 | 134 | 140 | PF01217 | 0.525 |
TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.519 |
TRG_ENDOCYTIC_2 | 317 | 320 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 392 | 395 | PF00928 | 0.465 |
TRG_NES_CRM1_1 | 167 | 180 | PF08389 | 0.576 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P805 | Leptomonas seymouri | 67% | 100% |
A0A0S4KL52 | Bodo saltans | 40% | 100% |
A0A1X0NMX9 | Trypanosomatidae | 46% | 99% |
A0A3R7L858 | Trypanosoma rangeli | 44% | 99% |
A3KPF5 | Arabidopsis thaliana | 25% | 89% |
A4HQL6 | Leishmania braziliensis | 77% | 99% |
A4ICD5 | Leishmania infantum | 99% | 100% |
D0A3S0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 96% |
D3Z6P0 | Mus musculus | 31% | 91% |
D4B2L8 | Arthroderma benhamiae (strain ATCC MYA-4681 / CBS 112371) | 34% | 91% |
E9AUD1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 99% |
P04785 | Rattus norvegicus | 30% | 94% |
P05307 | Bos taurus | 30% | 94% |
P07237 | Homo sapiens | 30% | 94% |
P08003 | Mus musculus | 32% | 75% |
P09102 | Gallus gallus | 30% | 93% |
P09103 | Mus musculus | 31% | 94% |
P11598 | Rattus norvegicus | 32% | 94% |
P12865 | Trypanosoma brucei brucei | 37% | 96% |
P13667 | Homo sapiens | 33% | 74% |
P17967 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 91% |
P21195 | Oryctolagus cuniculus | 30% | 94% |
P27773 | Mus musculus | 32% | 94% |
P29828 | Medicago sativa | 32% | 93% |
P30101 | Homo sapiens | 32% | 94% |
P32474 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 92% |
P34329 | Caenorhabditis elegans | 32% | 77% |
P38657 | Bos taurus | 33% | 94% |
P38658 | Schistosoma mansoni | 30% | 99% |
P38659 | Rattus norvegicus | 31% | 74% |
P52588 | Zea mays | 33% | 93% |
P52589 | Triticum aestivum | 33% | 93% |
P54399 | Drosophila melanogaster | 32% | 96% |
P55059 | Humicola insolens | 35% | 94% |
P80284 | Hordeum vulgare | 33% | 93% |
Q00002 | Alternaria alternata | 27% | 100% |
Q00248 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 34% | 93% |
Q0JD42 | Oryza sativa subsp. japonica | 23% | 100% |
Q10057 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 97% |
Q12730 | Aspergillus niger | 32% | 93% |
Q13087 | Homo sapiens | 32% | 91% |
Q17770 | Caenorhabditis elegans | 31% | 97% |
Q17967 | Caenorhabditis elegans | 31% | 98% |
Q29RV1 | Bos taurus | 33% | 74% |
Q2HWU2 | Macaca fuscata fuscata | 30% | 94% |
Q43116 | Ricinus communis | 31% | 96% |
Q4Q059 | Leishmania major | 94% | 100% |
Q4VIT4 | Chlorocebus aethiops | 32% | 94% |
Q53LQ0 | Oryza sativa subsp. japonica | 33% | 93% |
Q54EN4 | Dictyostelium discoideum | 30% | 93% |
Q5R5B6 | Pongo abelii | 30% | 94% |
Q5RCH2 | Pongo abelii | 32% | 91% |
Q5RDG4 | Pongo abelii | 32% | 94% |
Q5WA72 | Oryza sativa subsp. japonica | 25% | 89% |
Q5XI02 | Rattus norvegicus | 21% | 81% |
Q66GQ3 | Arabidopsis thaliana | 27% | 89% |
Q67IX6 | Oryza sativa subsp. japonica | 30% | 85% |
Q69ST6 | Oryza sativa subsp. japonica | 29% | 88% |
Q7XRB5 | Oryza sativa subsp. japonica | 30% | 92% |
Q8JG64 | Gallus gallus | 32% | 94% |
Q8N807 | Homo sapiens | 21% | 82% |
Q8R4U2 | Cricetulus griseus | 30% | 94% |
Q8VX13 | Arabidopsis thaliana | 30% | 82% |
Q95LM0 | Macaca fascicularis | 20% | 82% |
Q9DAN1 | Mus musculus | 21% | 81% |
Q9FF55 | Arabidopsis thaliana | 29% | 80% |
Q9SRG3 | Arabidopsis thaliana | 32% | 94% |
Q9XF61 | Datisca glomerata | 29% | 94% |
Q9XI01 | Arabidopsis thaliana | 32% | 95% |
V5BHP7 | Trypanosoma cruzi | 43% | 100% |