| 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: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 19 |
| NetGPI | no | yes: 0, no: 19 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 12 |
| GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: E8NHF3
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005975 | carbohydrate metabolic process | 3 | 20 |
| GO:0008152 | metabolic process | 1 | 20 |
| GO:0044238 | primary metabolic process | 2 | 20 |
| GO:0071704 | organic substance metabolic process | 2 | 20 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 20 |
| GO:0004553 | hydrolase activity, hydrolyzing O-glycosyl compounds | 4 | 20 |
| GO:0016787 | hydrolase activity | 2 | 20 |
| GO:0016798 | hydrolase activity, acting on glycosyl bonds | 3 | 20 |
| GO:0004564 | beta-fructofuranosidase activity | 5 | 17 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.286 |
| CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.333 |
| CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.333 |
| CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.336 |
| CLV_PCSK_PC1ET2_1 | 399 | 401 | PF00082 | 0.336 |
| CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.386 |
| CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.387 |
| CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.485 |
| CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.373 |
| DEG_Nend_Nbox_1 | 1 | 2 | PF02207 | 0.204 |
| DOC_CYCLIN_RxL_1 | 314 | 325 | PF00134 | 0.308 |
| DOC_MAPK_MEF2A_6 | 191 | 199 | PF00069 | 0.325 |
| DOC_MAPK_MEF2A_6 | 434 | 441 | PF00069 | 0.275 |
| DOC_PP2B_LxvP_1 | 313 | 316 | PF13499 | 0.340 |
| DOC_PP4_FxxP_1 | 126 | 129 | PF00568 | 0.340 |
| DOC_PP4_FxxP_1 | 276 | 279 | PF00568 | 0.304 |
| DOC_PP4_MxPP_1 | 330 | 333 | PF00568 | 0.333 |
| DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.428 |
| DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.308 |
| DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.270 |
| DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.386 |
| LIG_14-3-3_CanoR_1 | 256 | 262 | PF00244 | 0.286 |
| LIG_14-3-3_CanoR_1 | 434 | 438 | PF00244 | 0.197 |
| LIG_AP2alpha_2 | 322 | 324 | PF02296 | 0.261 |
| LIG_APCC_ABBA_1 | 428 | 433 | PF00400 | 0.300 |
| LIG_BRCT_BRCA1_1 | 263 | 267 | PF00533 | 0.198 |
| LIG_BRCT_BRCA1_1 | 449 | 453 | PF00533 | 0.373 |
| LIG_Clathr_ClatBox_1 | 189 | 193 | PF01394 | 0.229 |
| LIG_deltaCOP1_diTrp_1 | 19 | 26 | PF00928 | 0.310 |
| LIG_EH_1 | 14 | 18 | PF12763 | 0.323 |
| LIG_eIF4E_1 | 277 | 283 | PF01652 | 0.229 |
| LIG_FHA_1 | 146 | 152 | PF00498 | 0.391 |
| LIG_FHA_1 | 157 | 163 | PF00498 | 0.301 |
| LIG_FHA_1 | 229 | 235 | PF00498 | 0.359 |
| LIG_FHA_1 | 323 | 329 | PF00498 | 0.418 |
| LIG_FHA_1 | 353 | 359 | PF00498 | 0.296 |
| LIG_FHA_1 | 420 | 426 | PF00498 | 0.267 |
| LIG_FHA_2 | 156 | 162 | PF00498 | 0.317 |
| LIG_FHA_2 | 28 | 34 | PF00498 | 0.325 |
| LIG_FHA_2 | 362 | 368 | PF00498 | 0.319 |
| LIG_FHA_2 | 76 | 82 | PF00498 | 0.273 |
| LIG_KLC1_Yacidic_2 | 391 | 395 | PF13176 | 0.479 |
| LIG_LIR_Apic_2 | 275 | 279 | PF02991 | 0.304 |
| LIG_LIR_Apic_2 | 296 | 301 | PF02991 | 0.286 |
| LIG_LIR_Gen_1 | 167 | 175 | PF02991 | 0.340 |
| LIG_LIR_Nem_3 | 135 | 141 | PF02991 | 0.367 |
| LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.340 |
| LIG_LIR_Nem_3 | 23 | 29 | PF02991 | 0.233 |
| LIG_LIR_Nem_3 | 264 | 270 | PF02991 | 0.337 |
| LIG_NRBOX | 150 | 156 | PF00104 | 0.386 |
| LIG_Pex14_1 | 257 | 261 | PF04695 | 0.286 |
| LIG_Pex14_2 | 17 | 21 | PF04695 | 0.270 |
| LIG_PTB_Apo_2 | 401 | 408 | PF02174 | 0.336 |
| LIG_PTB_Apo_2 | 62 | 69 | PF02174 | 0.298 |
| LIG_PTB_Phospho_1 | 401 | 407 | PF10480 | 0.336 |
| LIG_PTB_Phospho_1 | 62 | 68 | PF10480 | 0.298 |
| LIG_RPA_C_Fungi | 210 | 222 | PF08784 | 0.286 |
| LIG_SH2_SRC | 393 | 396 | PF00017 | 0.451 |
| LIG_SH2_STAP1 | 366 | 370 | PF00017 | 0.333 |
| LIG_SH2_STAT3 | 200 | 203 | PF00017 | 0.286 |
| LIG_SH2_STAT3 | 277 | 280 | PF00017 | 0.340 |
| LIG_SH2_STAT3 | 96 | 99 | PF00017 | 0.319 |
| LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.364 |
| LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.386 |
| LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.472 |
| LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.340 |
| LIG_SH3_3 | 113 | 119 | PF00018 | 0.340 |
| LIG_SUMO_SIM_anti_2 | 353 | 362 | PF11976 | 0.261 |
| LIG_SUMO_SIM_par_1 | 353 | 362 | PF11976 | 0.287 |
| LIG_WRC_WIRS_1 | 258 | 263 | PF05994 | 0.286 |
| LIG_WW_1 | 120 | 123 | PF00397 | 0.386 |
| MOD_CDK_SPK_2 | 238 | 243 | PF00069 | 0.261 |
| MOD_CK1_1 | 228 | 234 | PF00069 | 0.274 |
| MOD_CK1_1 | 57 | 63 | PF00069 | 0.293 |
| MOD_CK2_1 | 232 | 238 | PF00069 | 0.277 |
| MOD_CK2_1 | 361 | 367 | PF00069 | 0.333 |
| MOD_CK2_1 | 374 | 380 | PF00069 | 0.336 |
| MOD_CK2_1 | 385 | 391 | PF00069 | 0.336 |
| MOD_CK2_1 | 432 | 438 | PF00069 | 0.336 |
| MOD_CK2_1 | 75 | 81 | PF00069 | 0.273 |
| MOD_Cter_Amidation | 286 | 289 | PF01082 | 0.298 |
| MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.286 |
| MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.264 |
| MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.409 |
| MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.308 |
| MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.373 |
| MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.336 |
| MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.329 |
| MOD_GSK3_1 | 221 | 228 | PF00069 | 0.321 |
| MOD_GSK3_1 | 238 | 245 | PF00069 | 0.282 |
| MOD_GSK3_1 | 257 | 264 | PF00069 | 0.202 |
| MOD_GSK3_1 | 297 | 304 | PF00069 | 0.336 |
| MOD_GSK3_1 | 307 | 314 | PF00069 | 0.348 |
| MOD_GSK3_1 | 410 | 417 | PF00069 | 0.336 |
| MOD_GSK3_1 | 462 | 469 | PF00069 | 0.317 |
| MOD_N-GLC_1 | 225 | 230 | PF02516 | 0.270 |
| MOD_N-GLC_1 | 466 | 471 | PF02516 | 0.423 |
| MOD_NEK2_1 | 221 | 226 | PF00069 | 0.261 |
| MOD_NEK2_1 | 261 | 266 | PF00069 | 0.308 |
| MOD_NEK2_1 | 324 | 329 | PF00069 | 0.361 |
| MOD_NEK2_1 | 374 | 379 | PF00069 | 0.359 |
| MOD_NEK2_1 | 480 | 485 | PF00069 | 0.550 |
| MOD_NEK2_1 | 56 | 61 | PF00069 | 0.340 |
| MOD_PIKK_1 | 232 | 238 | PF00454 | 0.198 |
| MOD_PIKK_1 | 261 | 267 | PF00454 | 0.286 |
| MOD_PK_1 | 462 | 468 | PF00069 | 0.308 |
| MOD_PKA_2 | 433 | 439 | PF00069 | 0.300 |
| MOD_PKB_1 | 213 | 221 | PF00069 | 0.308 |
| MOD_Plk_1 | 225 | 231 | PF00069 | 0.286 |
| MOD_Plk_1 | 361 | 367 | PF00069 | 0.363 |
| MOD_Plk_1 | 432 | 438 | PF00069 | 0.336 |
| MOD_Plk_1 | 444 | 450 | PF00069 | 0.336 |
| MOD_Plk_2-3 | 433 | 439 | PF00069 | 0.336 |
| MOD_Plk_4 | 225 | 231 | PF00069 | 0.286 |
| MOD_Plk_4 | 278 | 284 | PF00069 | 0.423 |
| MOD_Plk_4 | 473 | 479 | PF00069 | 0.410 |
| MOD_Plk_4 | 91 | 97 | PF00069 | 0.298 |
| MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.308 |
| MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.270 |
| MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.386 |
| TRG_DiLeu_BaLyEn_6 | 286 | 291 | PF01217 | 0.272 |
| TRG_ENDOCYTIC_2 | 123 | 126 | PF00928 | 0.367 |
| TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.340 |
| TRG_ENDOCYTIC_2 | 8 | 11 | PF00928 | 0.340 |
| TRG_ER_diArg_1 | 212 | 215 | PF00400 | 0.339 |
| TRG_ER_diArg_1 | 288 | 290 | PF00400 | 0.333 |
| TRG_NES_CRM1_1 | 419 | 433 | PF08389 | 0.438 |
| TRG_Pf-PMV_PEXEL_1 | 149 | 153 | PF00026 | 0.211 |
| TRG_Pf-PMV_PEXEL_1 | 317 | 322 | PF00026 | 0.308 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P8F7 | Leptomonas seymouri | 50% | 99% |
| A0A0N1PBT6 | Leptomonas seymouri | 26% | 75% |
| A0A1X0NFY9 | Trypanosomatidae | 24% | 100% |
| A0A1X0NTL0 | Trypanosomatidae | 24% | 77% |
| A0A1X0NTM3 | Trypanosomatidae | 25% | 77% |
| A0A1X0NY19 | Trypanosomatidae | 24% | 77% |
| A0A1X0P322 | Trypanosomatidae | 23% | 77% |
| A0A1X0P5Y7 | Trypanosomatidae | 24% | 76% |
| A0A3Q8IB13 | Leishmania donovani | 94% | 88% |
| A0A3Q8IFU7 | Leishmania donovani | 76% | 92% |
| A0A3S5H595 | Leishmania donovani | 25% | 76% |
| A0A3S5H7I4 | Leishmania donovani | 50% | 99% |
| A0A3S7WXQ4 | Leishmania donovani | 67% | 95% |
| A0A3S7WXS2 | Leishmania donovani | 75% | 92% |
| A1STJ9 | Psychromonas ingrahamii (strain 37) | 34% | 89% |
| A2R0E0 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 26% | 91% |
| A2X5P7 | Oryza sativa subsp. indica | 26% | 84% |
| A2YZ01 | Oryza sativa subsp. indica | 23% | 82% |
| A4H3V1 | Leishmania braziliensis | 26% | 76% |
| A4HCV9 | Leishmania braziliensis | 83% | 100% |
| A4HCW0 | Leishmania braziliensis | 65% | 94% |
| A4HG14 | Leishmania braziliensis | 49% | 100% |
| A4HS26 | Leishmania infantum | 25% | 76% |
| A4I0D9 | Leishmania infantum | 94% | 88% |
| A4I0E0 | Leishmania infantum | 67% | 95% |
| A4I336 | Leishmania infantum | 50% | 99% |
| A4IAW1 | Leishmania infantum | 26% | 69% |
| A5ABL2 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 25% | 94% |
| A5DHM6 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 25% | 95% |
| A5EZZ8 | Vibrio cholerae serotype O1 (strain ATCC 39541 / Classical Ogawa 395 / O395) | 32% | 89% |
| A8W7I5 | Meyerozyma guilliermondii | 25% | 95% |
| B6DXP5 | Leymus chinensis | 25% | 81% |
| B6DZC8 | Triticum aestivum | 24% | 82% |
| B6DZD0 | Triticum urartu | 25% | 81% |
| B6DZD1 | Aegilops speltoides | 25% | 82% |
| B6DZD2 | Aegilops tauschii | 25% | 82% |
| D2IGW7 | Bromus pictus | 25% | 81% |
| E1ABX2 | Aspergillus ficuum | 27% | 91% |
| E8NHF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 100% | 100% |
| E9ACV4 | Leishmania major | 50% | 100% |
| E9AK13 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 76% |
| E9AWA3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 100% |
| E9AZE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 100% |
| F8DVG5 | Zymomonas mobilis subsp. mobilis (strain ATCC 10988 / DSM 424 / LMG 404 / NCIMB 8938 / NRRL B-806 / ZM1) | 38% | 95% |
| H2DF87 | Rosa hybrid cultivar | 26% | 83% |
| H2DF88 | Rosa hybrid cultivar | 24% | 76% |
| K0E681 | Aspergillus rugulosus | 26% | 96% |
| O07003 | Bacillus subtilis (strain 168) | 25% | 94% |
| O24509 | Phaseolus vulgaris | 26% | 75% |
| O33833 | Thermotoga maritima (strain ATCC 43589 / DSM 3109 / JCM 10099 / NBRC 100826 / MSB8) | 31% | 100% |
| O42878 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 96% |
| O59852 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 84% |
| O74641 | Aspergillus niger | 26% | 94% |
| O74642 | Aspergillus niger | 25% | 94% |
| O94220 | Aspergillus ficuum | 26% | 94% |
| P00724 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 91% |
| P05656 | Bacillus subtilis (strain 168) | 29% | 72% |
| P07819 | Bacillus subtilis (strain 168) | 36% | 100% |
| P0DJA7 | Zymomonas mobilis subsp. mobilis (strain ATCC 31821 / ZM4 / CP4) | 38% | 95% |
| P10594 | Saccharomyces cerevisiae | 28% | 91% |
| P10596 | Saccharomyces cerevisiae | 25% | 91% |
| P13394 | Vibrio alginolyticus | 29% | 100% |
| P13522 | Streptococcus mutans serotype c (strain ATCC 700610 / UA159) | 26% | 100% |
| P16553 | Escherichia coli | 44% | 100% |
| P24133 | Schwanniomyces occidentalis | 21% | 91% |
| P26792 | Daucus carota | 24% | 82% |
| P27217 | Klebsiella pneumoniae | 34% | 100% |
| P28999 | Kluyveromyces marxianus | 26% | 88% |
| P29000 | Solanum lycopersicum | 24% | 76% |
| P29001 | Vigna radiata var. radiata | 25% | 75% |
| P37075 | Salmonella typhimurium | 34% | 100% |
| P40714 | Escherichia coli | 46% | 100% |
| P40912 | Wickerhamomyces anomalus | 23% | 88% |
| P43471 | Pediococcus pentosaceus | 24% | 97% |
| P49174 | Zea mays | 25% | 82% |
| P49175 | Zea mays | 26% | 73% |
| P80065 | Daucus carota | 25% | 74% |
| P92916 | Allium cepa | 23% | 79% |
| P93761 | Capsicum annuum | 25% | 76% |
| P94469 | Geobacillus stearothermophilus | 25% | 100% |
| Q01IS7 | Oryza sativa subsp. indica | 24% | 81% |
| Q01IS8 | Oryza sativa subsp. indica | 25% | 83% |
| Q04937 | Lactococcus lactis subsp. lactis | 24% | 100% |
| Q05936 | Staphylococcus xylosus | 30% | 98% |
| Q0E0P0 | Oryza sativa subsp. japonica | 26% | 84% |
| Q0J360 | Oryza sativa subsp. japonica | 23% | 82% |
| Q0JDC5 | Oryza sativa subsp. japonica | 24% | 81% |
| Q0JDC6 | Oryza sativa subsp. japonica | 25% | 83% |
| Q1PEF8 | Arabidopsis thaliana | 26% | 82% |
| Q2UXF7 | Triticum aestivum | 25% | 81% |
| Q39041 | Arabidopsis thaliana | 26% | 73% |
| Q39692 | Daucus carota | 27% | 82% |
| Q39693 | Daucus carota | 27% | 83% |
| Q43089 | Pisum sativum | 23% | 88% |
| Q43348 | Arabidopsis thaliana | 27% | 75% |
| Q43857 | Vicia faba | 24% | 76% |
| Q43866 | Arabidopsis thaliana | 26% | 83% |
| Q4QB75 | Leishmania major | 66% | 100% |
| Q4QB76 | Leishmania major | 93% | 100% |
| Q56660 | Vibrio cholerae | 33% | 89% |
| Q56UD0 | Oryza sativa subsp. japonica | 25% | 82% |
| Q56UD1 | Oryza sativa subsp. japonica | 24% | 90% |
| Q5FC15 | Asparagus officinalis | 26% | 80% |
| Q5JJV0 | Oryza sativa subsp. japonica | 24% | 82% |
| Q67XZ3 | Arabidopsis thaliana | 26% | 82% |
| Q6BJW6 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 27% | 91% |
| Q70AT7 | Hordeum vulgare | 25% | 81% |
| Q70XE6 | Beta vulgaris | 26% | 80% |
| Q76HP6 | Aspergillus niger | 27% | 91% |
| Q84LA1 | Triticum aestivum | 25% | 82% |
| Q84PN8 | Triticum aestivum | 25% | 81% |
| Q8W413 | Arabidopsis thaliana | 25% | 82% |
| Q8W4S6 | Arabidopsis thaliana | 24% | 88% |
| Q96TU3 | Aspergillus awamori | 25% | 91% |
| Q9FSV7 | Festuca arundinacea | 24% | 74% |
| Q9KLT6 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 32% | 89% |
| Q9LIB9 | Arabidopsis thaliana | 23% | 85% |
| Q9XTP3 | Leishmania major | 25% | 76% |
| Q9Y746 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 22% | 80% |