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. | no | 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: A4H8T2
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_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.319 |
CLV_PCSK_PC1ET2_1 | 261 | 263 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.225 |
DEG_APCC_DBOX_1 | 210 | 218 | PF00400 | 0.410 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.395 |
DEG_SCF_FBW7_1 | 133 | 139 | PF00400 | 0.386 |
DOC_CKS1_1 | 133 | 138 | PF01111 | 0.412 |
DOC_CYCLIN_RxL_1 | 208 | 215 | PF00134 | 0.418 |
DOC_CYCLIN_RxL_1 | 406 | 414 | PF00134 | 0.340 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 402 | 411 | PF00134 | 0.316 |
DOC_PP1_RVXF_1 | 407 | 414 | PF00149 | 0.410 |
DOC_PP1_SILK_1 | 207 | 212 | PF00149 | 0.386 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.390 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.306 |
DOC_USP7_UBL2_3 | 373 | 377 | PF12436 | 0.410 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.384 |
DOC_WW_Pin1_4 | 234 | 239 | PF00397 | 0.281 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.310 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.563 |
LIG_14-3-3_CanoR_1 | 31 | 38 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 393 | 397 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 76 | 86 | PF00244 | 0.400 |
LIG_BRCT_BRCA1_1 | 327 | 331 | PF00533 | 0.273 |
LIG_BRCT_BRCA1_1 | 79 | 83 | PF00533 | 0.319 |
LIG_deltaCOP1_diTrp_1 | 151 | 156 | PF00928 | 0.316 |
LIG_eIF4E_1 | 96 | 102 | PF01652 | 0.297 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.410 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.424 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.710 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.289 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.524 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.246 |
LIG_FHA_2 | 102 | 108 | PF00498 | 0.343 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.297 |
LIG_FHA_2 | 328 | 334 | PF00498 | 0.281 |
LIG_LIR_Apic_2 | 176 | 181 | PF02991 | 0.295 |
LIG_LIR_Apic_2 | 227 | 233 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 155 | 163 | PF02991 | 0.179 |
LIG_LIR_Gen_1 | 164 | 172 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 164 | 168 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 80 | 86 | PF02991 | 0.300 |
LIG_MLH1_MIPbox_1 | 79 | 83 | PF16413 | 0.371 |
LIG_NRBOX | 209 | 215 | PF00104 | 0.371 |
LIG_PDZ_Class_3 | 424 | 429 | PF00595 | 0.342 |
LIG_Pex14_1 | 187 | 191 | PF04695 | 0.268 |
LIG_Rb_pABgroove_1 | 315 | 323 | PF01858 | 0.179 |
LIG_SH2_CRK | 178 | 182 | PF00017 | 0.297 |
LIG_SH2_CRK | 245 | 249 | PF00017 | 0.415 |
LIG_SH2_CRK | 277 | 281 | PF00017 | 0.177 |
LIG_SH2_NCK_1 | 245 | 249 | PF00017 | 0.386 |
LIG_SH2_PTP2 | 165 | 168 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 274 | 277 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.344 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.441 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.259 |
LIG_SUMO_SIM_anti_2 | 164 | 170 | PF11976 | 0.219 |
LIG_SUMO_SIM_anti_2 | 206 | 212 | PF11976 | 0.410 |
LIG_SUMO_SIM_anti_2 | 399 | 406 | PF11976 | 0.272 |
LIG_SUMO_SIM_anti_2 | 67 | 75 | PF11976 | 0.369 |
LIG_SxIP_EBH_1 | 341 | 352 | PF03271 | 0.386 |
LIG_TRAF2_1 | 203 | 206 | PF00917 | 0.422 |
LIG_TYR_ITIM | 275 | 280 | PF00017 | 0.186 |
LIG_UBA3_1 | 280 | 286 | PF00899 | 0.219 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.343 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.446 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.283 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.429 |
MOD_CMANNOS | 153 | 156 | PF00535 | 0.316 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.445 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.299 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.268 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.371 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.624 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.420 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.308 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.329 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.317 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.444 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.363 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.586 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.457 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.352 |
MOD_N-GLC_1 | 248 | 253 | PF02516 | 0.296 |
MOD_N-GLC_1 | 354 | 359 | PF02516 | 0.268 |
MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.474 |
MOD_N-GLC_2 | 108 | 110 | PF02516 | 0.316 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.372 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.268 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.574 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.294 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.410 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.317 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.508 |
MOD_NEK2_2 | 248 | 253 | PF00069 | 0.410 |
MOD_NEK2_2 | 26 | 31 | PF00069 | 0.435 |
MOD_OFUCOSY | 103 | 110 | PF10250 | 0.301 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.386 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.400 |
MOD_Plk_1 | 205 | 211 | PF00069 | 0.386 |
MOD_Plk_1 | 248 | 254 | PF00069 | 0.300 |
MOD_Plk_1 | 293 | 299 | PF00069 | 0.339 |
MOD_Plk_1 | 304 | 310 | PF00069 | 0.289 |
MOD_Plk_1 | 354 | 360 | PF00069 | 0.271 |
MOD_Plk_2-3 | 392 | 398 | PF00069 | 0.386 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.231 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.478 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.383 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.115 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.368 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.200 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.322 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.421 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.322 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.398 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.384 |
MOD_ProDKin_1 | 234 | 240 | PF00069 | 0.281 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.310 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.558 |
TRG_DiLeu_BaEn_1 | 164 | 169 | PF01217 | 0.311 |
TRG_DiLeu_BaEn_1 | 400 | 405 | PF01217 | 0.268 |
TRG_DiLeu_BaLyEn_6 | 321 | 326 | PF01217 | 0.371 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.281 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.177 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.241 |
TRG_Pf-PMV_PEXEL_1 | 343 | 348 | PF00026 | 0.371 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYQ4 | Leptomonas seymouri | 73% | 100% |
A0A0S4JAH9 | Bodo saltans | 33% | 89% |
A0A0S4JHX0 | Bodo saltans | 37% | 86% |
A0A1X0P0B6 | Trypanosomatidae | 51% | 96% |
A0A3S7WU69 | Leishmania donovani | 86% | 97% |
A0A422NE38 | Trypanosoma rangeli | 52% | 93% |
A4HX51 | Leishmania infantum | 86% | 97% |
A5PJN2 | Bos taurus | 31% | 92% |
B1H1F9 | Xenopus tropicalis | 31% | 91% |
B6CVD7 | Sus scrofa | 31% | 92% |
C9ZVU0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 97% |
E9AQW6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
O74401 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 92% |
Q03103 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 76% |
Q4QEL2 | Leishmania major | 85% | 100% |
Q6DD71 | Xenopus laevis | 30% | 92% |
Q75BB5 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 26% | 79% |
Q7T3D1 | Danio rerio | 29% | 88% |
Q7X9I4 | Arabidopsis thaliana | 31% | 91% |
Q7YTU4 | Caenorhabditis elegans | 28% | 90% |
Q86YB8 | Homo sapiens | 30% | 92% |
Q8NIP5 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 27% | 76% |
Q8R180 | Mus musculus | 32% | 92% |
Q8R2E9 | Mus musculus | 30% | 92% |
Q8R4A1 | Rattus norvegicus | 31% | 92% |
Q96HE7 | Homo sapiens | 30% | 92% |
Q9C7S7 | Arabidopsis thaliana | 32% | 91% |
Q9V3A6 | Drosophila melanogaster | 28% | 89% |
Q9Y7P1 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 76% |
V5BI75 | Trypanosoma cruzi | 48% | 97% |