Oxidoreductase, endoplasmic reticulum oxidoreductin
| 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. | yes | yes: 18 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | yes | yes: 8, no: 4 |
| NetGPI | no | yes: 0, no: 12 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005789 | endoplasmic reticulum membrane | 4 | 13 |
| GO:0016020 | membrane | 2 | 13 |
| GO:0031090 | organelle membrane | 3 | 13 |
| GO:0110165 | cellular anatomical entity | 1 | 13 |
Related structures:
AlphaFold database: A0A3S7WU69
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006457 | protein folding | 2 | 13 |
| GO:0009987 | cellular process | 1 | 13 |
| GO:0034975 | protein folding in endoplasmic reticulum | 3 | 13 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000166 | nucleotide binding | 3 | 13 |
| GO:0003824 | catalytic activity | 1 | 13 |
| GO:0005488 | binding | 1 | 13 |
| GO:0015035 | protein-disulfide reductase activity | 3 | 13 |
| GO:0015036 | disulfide oxidoreductase activity | 4 | 13 |
| GO:0016491 | oxidoreductase activity | 2 | 13 |
| GO:0016667 | oxidoreductase activity, acting on a sulfur group of donors | 3 | 13 |
| GO:0016670 | oxidoreductase activity, acting on a sulfur group of donors, oxygen as acceptor | 4 | 13 |
| GO:0016972 | thiol oxidase activity | 5 | 13 |
| GO:0036094 | small molecule binding | 2 | 13 |
| GO:0043167 | ion binding | 2 | 13 |
| GO:0043168 | anion binding | 3 | 13 |
| GO:0050660 | flavin adenine dinucleotide binding | 4 | 13 |
| GO:0071949 | FAD binding | 5 | 13 |
| GO:0097159 | organic cyclic compound binding | 2 | 13 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 13 |
| GO:1901265 | nucleoside phosphate binding | 3 | 13 |
| GO:1901363 | heterocyclic compound binding | 2 | 13 |
| GO:0003756 | protein disulfide isomerase activity | 3 | 1 |
| GO:0016853 | isomerase activity | 2 | 1 |
| GO:0016860 | intramolecular oxidoreductase activity | 3 | 1 |
| GO:0016864 | intramolecular oxidoreductase activity, transposing S-S bonds | 4 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 200 | 204 | PF00656 | 0.233 |
| CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.319 |
| CLV_PCSK_PC1ET2_1 | 263 | 265 | PF00082 | 0.393 |
| CLV_PCSK_SKI1_1 | 144 | 148 | PF00082 | 0.369 |
| CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.403 |
| CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.344 |
| CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.345 |
| CLV_PCSK_SKI1_1 | 45 | 49 | PF00082 | 0.600 |
| CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.476 |
| CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.327 |
| DEG_APCC_DBOX_1 | 212 | 220 | PF00400 | 0.425 |
| DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.567 |
| DEG_ODPH_VHL_1 | 265 | 277 | PF01847 | 0.369 |
| DEG_SCF_FBW7_1 | 135 | 141 | PF00400 | 0.447 |
| DOC_CKS1_1 | 135 | 140 | PF01111 | 0.425 |
| DOC_CYCLIN_RxL_1 | 210 | 217 | PF00134 | 0.431 |
| DOC_CYCLIN_RxL_1 | 408 | 416 | PF00134 | 0.367 |
| DOC_CYCLIN_yClb5_NLxxxL_5 | 404 | 413 | PF00134 | 0.345 |
| DOC_MAPK_DCC_7 | 144 | 152 | PF00069 | 0.369 |
| DOC_MAPK_HePTP_8 | 8 | 20 | PF00069 | 0.579 |
| DOC_MAPK_MEF2A_6 | 11 | 20 | PF00069 | 0.529 |
| DOC_MAPK_MEF2A_6 | 3 | 10 | PF00069 | 0.499 |
| DOC_MAPK_MEF2A_6 | 30 | 39 | PF00069 | 0.604 |
| DOC_PP1_RVXF_1 | 409 | 416 | PF00149 | 0.425 |
| DOC_PP1_SILK_1 | 209 | 214 | PF00149 | 0.447 |
| DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.437 |
| DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.470 |
| DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.533 |
| DOC_USP7_UBL2_3 | 375 | 379 | PF12436 | 0.425 |
| DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.402 |
| DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.311 |
| DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.491 |
| DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.324 |
| DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.560 |
| DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.376 |
| LIG_14-3-3_CanoR_1 | 395 | 399 | PF00244 | 0.453 |
| LIG_14-3-3_CanoR_1 | 78 | 82 | PF00244 | 0.443 |
| LIG_APCC_ABBA_1 | 265 | 270 | PF00400 | 0.415 |
| LIG_BRCT_BRCA1_1 | 288 | 292 | PF00533 | 0.369 |
| LIG_BRCT_BRCA1_1 | 329 | 333 | PF00533 | 0.291 |
| LIG_BRCT_BRCA1_1 | 81 | 85 | PF00533 | 0.347 |
| LIG_deltaCOP1_diTrp_1 | 153 | 158 | PF00928 | 0.345 |
| LIG_eIF4E_1 | 98 | 104 | PF01652 | 0.327 |
| LIG_FHA_1 | 109 | 115 | PF00498 | 0.425 |
| LIG_FHA_1 | 292 | 298 | PF00498 | 0.433 |
| LIG_FHA_1 | 376 | 382 | PF00498 | 0.310 |
| LIG_FHA_1 | 48 | 54 | PF00498 | 0.561 |
| LIG_FHA_1 | 67 | 73 | PF00498 | 0.378 |
| LIG_FHA_2 | 104 | 110 | PF00498 | 0.385 |
| LIG_FHA_2 | 203 | 209 | PF00498 | 0.463 |
| LIG_FHA_2 | 307 | 313 | PF00498 | 0.327 |
| LIG_FHA_2 | 330 | 336 | PF00498 | 0.311 |
| LIG_FHA_2 | 49 | 55 | PF00498 | 0.560 |
| LIG_LIR_Apic_2 | 178 | 183 | PF02991 | 0.325 |
| LIG_LIR_Apic_2 | 229 | 235 | PF02991 | 0.425 |
| LIG_LIR_Gen_1 | 166 | 174 | PF02991 | 0.312 |
| LIG_LIR_Nem_3 | 166 | 170 | PF02991 | 0.312 |
| LIG_LIR_Nem_3 | 82 | 88 | PF02991 | 0.330 |
| LIG_MLH1_MIPbox_1 | 81 | 85 | PF16413 | 0.393 |
| LIG_NRBOX | 211 | 217 | PF00104 | 0.393 |
| LIG_Pex14_1 | 189 | 193 | PF04695 | 0.298 |
| LIG_SH2_CRK | 180 | 184 | PF00017 | 0.327 |
| LIG_SH2_CRK | 247 | 251 | PF00017 | 0.429 |
| LIG_SH2_NCK_1 | 247 | 251 | PF00017 | 0.447 |
| LIG_SH2_PTP2 | 167 | 170 | PF00017 | 0.311 |
| LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.306 |
| LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.350 |
| LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.514 |
| LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.371 |
| LIG_SH3_3 | 143 | 149 | PF00018 | 0.449 |
| LIG_SUMO_SIM_anti_2 | 15 | 21 | PF11976 | 0.573 |
| LIG_SUMO_SIM_anti_2 | 208 | 214 | PF11976 | 0.425 |
| LIG_SUMO_SIM_anti_2 | 401 | 408 | PF11976 | 0.302 |
| LIG_SUMO_SIM_anti_2 | 71 | 77 | PF11976 | 0.395 |
| LIG_SxIP_EBH_1 | 343 | 354 | PF03271 | 0.447 |
| LIG_TRAF2_1 | 205 | 208 | PF00917 | 0.408 |
| MOD_CDC14_SPxK_1 | 239 | 242 | PF00782 | 0.333 |
| MOD_CDK_SPK_2 | 25 | 30 | PF00069 | 0.477 |
| MOD_CDK_SPxK_1 | 236 | 242 | PF00069 | 0.333 |
| MOD_CDK_SPxxK_3 | 79 | 86 | PF00069 | 0.376 |
| MOD_CK1_1 | 291 | 297 | PF00069 | 0.330 |
| MOD_CK1_1 | 425 | 431 | PF00069 | 0.543 |
| MOD_CK2_1 | 103 | 109 | PF00069 | 0.385 |
| MOD_CK2_1 | 118 | 124 | PF00069 | 0.419 |
| MOD_CK2_1 | 169 | 175 | PF00069 | 0.425 |
| MOD_CK2_1 | 202 | 208 | PF00069 | 0.373 |
| MOD_CK2_1 | 329 | 335 | PF00069 | 0.313 |
| MOD_CK2_1 | 58 | 64 | PF00069 | 0.491 |
| MOD_CMANNOS | 155 | 158 | PF00535 | 0.345 |
| MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.234 |
| MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.327 |
| MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.298 |
| MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.433 |
| MOD_GSK3_1 | 130 | 137 | PF00069 | 0.330 |
| MOD_GSK3_1 | 138 | 145 | PF00069 | 0.424 |
| MOD_GSK3_1 | 207 | 214 | PF00069 | 0.354 |
| MOD_GSK3_1 | 25 | 32 | PF00069 | 0.615 |
| MOD_GSK3_1 | 291 | 298 | PF00069 | 0.376 |
| MOD_GSK3_1 | 394 | 401 | PF00069 | 0.438 |
| MOD_GSK3_1 | 99 | 106 | PF00069 | 0.378 |
| MOD_N-GLC_1 | 250 | 255 | PF02516 | 0.326 |
| MOD_N-GLC_1 | 356 | 361 | PF02516 | 0.294 |
| MOD_N-GLC_1 | 48 | 53 | PF02516 | 0.485 |
| MOD_N-GLC_2 | 110 | 112 | PF02516 | 0.345 |
| MOD_NEK2_1 | 103 | 108 | PF00069 | 0.393 |
| MOD_NEK2_1 | 219 | 224 | PF00069 | 0.298 |
| MOD_NEK2_1 | 286 | 291 | PF00069 | 0.340 |
| MOD_NEK2_1 | 322 | 327 | PF00069 | 0.319 |
| MOD_NEK2_1 | 356 | 361 | PF00069 | 0.425 |
| MOD_NEK2_1 | 413 | 418 | PF00069 | 0.328 |
| MOD_NEK2_1 | 48 | 53 | PF00069 | 0.610 |
| MOD_NEK2_2 | 250 | 255 | PF00069 | 0.425 |
| MOD_NEK2_2 | 279 | 284 | PF00069 | 0.455 |
| MOD_OFUCOSY | 105 | 112 | PF10250 | 0.367 |
| MOD_PK_1 | 422 | 428 | PF00069 | 0.324 |
| MOD_PKA_2 | 394 | 400 | PF00069 | 0.441 |
| MOD_PKA_2 | 77 | 83 | PF00069 | 0.447 |
| MOD_Plk_1 | 118 | 124 | PF00069 | 0.449 |
| MOD_Plk_1 | 207 | 213 | PF00069 | 0.447 |
| MOD_Plk_1 | 250 | 256 | PF00069 | 0.330 |
| MOD_Plk_1 | 295 | 301 | PF00069 | 0.359 |
| MOD_Plk_1 | 306 | 312 | PF00069 | 0.278 |
| MOD_Plk_1 | 356 | 362 | PF00069 | 0.301 |
| MOD_Plk_1 | 6 | 12 | PF00069 | 0.596 |
| MOD_Plk_2-3 | 118 | 124 | PF00069 | 0.369 |
| MOD_Plk_2-3 | 394 | 400 | PF00069 | 0.447 |
| MOD_Plk_4 | 12 | 18 | PF00069 | 0.583 |
| MOD_Plk_4 | 142 | 148 | PF00069 | 0.431 |
| MOD_Plk_4 | 207 | 213 | PF00069 | 0.403 |
| MOD_Plk_4 | 227 | 233 | PF00069 | 0.116 |
| MOD_Plk_4 | 295 | 301 | PF00069 | 0.390 |
| MOD_Plk_4 | 402 | 408 | PF00069 | 0.345 |
| MOD_Plk_4 | 68 | 74 | PF00069 | 0.448 |
| MOD_Plk_4 | 99 | 105 | PF00069 | 0.407 |
| MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.402 |
| MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.311 |
| MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.492 |
| MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.324 |
| MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.559 |
| MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.376 |
| TRG_DiLeu_BaEn_1 | 402 | 407 | PF01217 | 0.298 |
| TRG_DiLeu_BaLyEn_6 | 323 | 328 | PF01217 | 0.393 |
| TRG_ENDOCYTIC_2 | 167 | 170 | PF00928 | 0.311 |
| TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.338 |
| TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.270 |
| TRG_ER_diArg_1 | 42 | 45 | PF00400 | 0.606 |
| TRG_ER_diArg_1 | 438 | 441 | PF00400 | 0.680 |
| TRG_Pf-PMV_PEXEL_1 | 345 | 350 | PF00026 | 0.393 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1HYQ4 | Leptomonas seymouri | 75% | 100% |
| A0A0S4JAH9 | Bodo saltans | 34% | 92% |
| A0A0S4JHX0 | Bodo saltans | 39% | 89% |
| A0A1X0P0B6 | Trypanosomatidae | 51% | 99% |
| A0A422NE38 | Trypanosoma rangeli | 52% | 97% |
| A4H8T2 | Leishmania braziliensis | 86% | 100% |
| A4HX51 | Leishmania infantum | 100% | 100% |
| A5PJN2 | Bos taurus | 31% | 95% |
| B1H1F9 | Xenopus tropicalis | 29% | 93% |
| B6CVD7 | Sus scrofa | 32% | 95% |
| C9ZVU0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
| E9AQW6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
| O74401 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 95% |
| Q03103 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 79% |
| Q4QEL2 | Leishmania major | 95% | 100% |
| Q6DD71 | Xenopus laevis | 29% | 95% |
| Q75BB5 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 28% | 81% |
| Q7SEY9 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 25% | 66% |
| Q7T3D1 | Danio rerio | 29% | 91% |
| Q7X9I4 | Arabidopsis thaliana | 31% | 94% |
| Q7YTU4 | Caenorhabditis elegans | 28% | 93% |
| Q86YB8 | Homo sapiens | 29% | 95% |
| Q8NIP5 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 27% | 79% |
| Q8R180 | Mus musculus | 31% | 95% |
| Q8R2E9 | Mus musculus | 29% | 95% |
| Q8R4A1 | Rattus norvegicus | 31% | 95% |
| Q96HE7 | Homo sapiens | 31% | 95% |
| Q9C7S7 | Arabidopsis thaliana | 33% | 94% |
| Q9V3A6 | Drosophila melanogaster | 27% | 92% |
| Q9Y7P1 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 78% |
| V5BI75 | Trypanosoma cruzi | 51% | 100% |