| 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 | 13 |
| GO:0110165 | cellular anatomical entity | 1 | 13 |
Related structures:
AlphaFold database: A0A3Q8IFU7
| 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:0004564 | beta-fructofuranosidase activity | 5 | 18 |
| GO:0016787 | hydrolase activity | 2 | 20 |
| GO:0016798 | hydrolase activity, acting on glycosyl bonds | 3 | 20 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.316 |
| CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.316 |
| CLV_PCSK_KEX2_1 | 440 | 442 | PF00082 | 0.320 |
| CLV_PCSK_PC1ET2_1 | 440 | 442 | PF00082 | 0.320 |
| CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.349 |
| CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.350 |
| CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.192 |
| CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.280 |
| CLV_PCSK_SKI1_1 | 441 | 445 | PF00082 | 0.339 |
| DEG_COP1_1 | 381 | 390 | PF00400 | 0.335 |
| DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.514 |
| DOC_CDC14_PxL_1 | 384 | 392 | PF14671 | 0.325 |
| DOC_CKS1_1 | 293 | 298 | PF01111 | 0.203 |
| DOC_CKS1_1 | 379 | 384 | PF01111 | 0.534 |
| DOC_MAPK_MEF2A_6 | 261 | 268 | PF00069 | 0.298 |
| DOC_MAPK_MEF2A_6 | 475 | 482 | PF00069 | 0.261 |
| DOC_MAPK_NFAT4_5 | 261 | 269 | PF00069 | 0.240 |
| DOC_PP1_RVXF_1 | 263 | 270 | PF00149 | 0.255 |
| DOC_PP2B_LxvP_1 | 353 | 356 | PF13499 | 0.323 |
| DOC_PP4_FxxP_1 | 192 | 195 | PF00568 | 0.323 |
| DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.496 |
| DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.385 |
| DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.221 |
| DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.349 |
| DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.543 |
| LIG_14-3-3_CanoR_1 | 503 | 508 | PF00244 | 0.393 |
| LIG_APCC_ABBA_1 | 469 | 474 | PF00400 | 0.285 |
| LIG_BRCT_BRCA1_1 | 490 | 494 | PF00533 | 0.339 |
| LIG_deltaCOP1_diTrp_1 | 85 | 92 | PF00928 | 0.294 |
| LIG_DLG_GKlike_1 | 357 | 365 | PF00625 | 0.240 |
| LIG_EH_1 | 80 | 84 | PF12763 | 0.297 |
| LIG_FHA_1 | 212 | 218 | PF00498 | 0.375 |
| LIG_FHA_1 | 223 | 229 | PF00498 | 0.286 |
| LIG_FHA_1 | 363 | 369 | PF00498 | 0.308 |
| LIG_FHA_1 | 387 | 393 | PF00498 | 0.314 |
| LIG_FHA_1 | 461 | 467 | PF00498 | 0.250 |
| LIG_FHA_2 | 142 | 148 | PF00498 | 0.255 |
| LIG_FHA_2 | 403 | 409 | PF00498 | 0.317 |
| LIG_FHA_2 | 94 | 100 | PF00498 | 0.326 |
| LIG_KLC1_Yacidic_2 | 432 | 436 | PF13176 | 0.428 |
| LIG_LIR_Gen_1 | 233 | 241 | PF02991 | 0.323 |
| LIG_LIR_Nem_3 | 201 | 207 | PF02991 | 0.350 |
| LIG_LIR_Nem_3 | 233 | 239 | PF02991 | 0.323 |
| LIG_LIR_Nem_3 | 254 | 258 | PF02991 | 0.266 |
| LIG_LIR_Nem_3 | 305 | 309 | PF02991 | 0.326 |
| LIG_NRBOX | 216 | 222 | PF00104 | 0.349 |
| LIG_Pex14_1 | 48 | 52 | PF04695 | 0.348 |
| LIG_Pex14_2 | 83 | 87 | PF04695 | 0.257 |
| LIG_PTB_Apo_2 | 128 | 135 | PF02174 | 0.276 |
| LIG_PTB_Apo_2 | 442 | 449 | PF02174 | 0.320 |
| LIG_PTB_Apo_2 | 68 | 75 | PF02174 | 0.255 |
| LIG_PTB_Phospho_1 | 128 | 134 | PF10480 | 0.276 |
| LIG_PTB_Phospho_1 | 442 | 448 | PF10480 | 0.320 |
| LIG_PTB_Phospho_1 | 68 | 74 | PF10480 | 0.255 |
| LIG_SH2_GRB2like | 69 | 72 | PF00017 | 0.255 |
| LIG_SH2_NCK_1 | 361 | 365 | PF00017 | 0.255 |
| LIG_SH2_SRC | 434 | 437 | PF00017 | 0.339 |
| LIG_SH2_STAP1 | 407 | 411 | PF00017 | 0.329 |
| LIG_SH2_STAT3 | 162 | 165 | PF00017 | 0.302 |
| LIG_SH2_STAT3 | 316 | 319 | PF00017 | 0.323 |
| LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.323 |
| LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.347 |
| LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.229 |
| LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.349 |
| LIG_SH2_STAT5 | 434 | 437 | PF00017 | 0.428 |
| LIG_SH3_2 | 296 | 301 | PF14604 | 0.203 |
| LIG_SH3_3 | 179 | 185 | PF00018 | 0.323 |
| LIG_SH3_3 | 293 | 299 | PF00018 | 0.289 |
| LIG_SUMO_SIM_par_1 | 388 | 393 | PF11976 | 0.269 |
| LIG_TRAF2_1 | 25 | 28 | PF00917 | 0.364 |
| LIG_WRC_WIRS_1 | 54 | 59 | PF05994 | 0.219 |
| LIG_WW_1 | 186 | 189 | PF00397 | 0.349 |
| MOD_CK1_1 | 123 | 129 | PF00069 | 0.278 |
| MOD_CK1_1 | 277 | 283 | PF00069 | 0.202 |
| MOD_CK2_1 | 141 | 147 | PF00069 | 0.255 |
| MOD_CK2_1 | 21 | 27 | PF00069 | 0.486 |
| MOD_CK2_1 | 357 | 363 | PF00069 | 0.242 |
| MOD_CK2_1 | 402 | 408 | PF00069 | 0.317 |
| MOD_CK2_1 | 415 | 421 | PF00069 | 0.172 |
| MOD_CK2_1 | 426 | 432 | PF00069 | 0.320 |
| MOD_CK2_1 | 473 | 479 | PF00069 | 0.330 |
| MOD_Cter_Amidation | 272 | 275 | PF01082 | 0.255 |
| MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.312 |
| MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.461 |
| MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.300 |
| MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.369 |
| MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.503 |
| MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.342 |
| MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.319 |
| MOD_GSK3_1 | 143 | 150 | PF00069 | 0.235 |
| MOD_GSK3_1 | 2 | 9 | PF00069 | 0.523 |
| MOD_GSK3_1 | 337 | 344 | PF00069 | 0.328 |
| MOD_GSK3_1 | 347 | 354 | PF00069 | 0.340 |
| MOD_GSK3_1 | 451 | 458 | PF00069 | 0.323 |
| MOD_GSK3_1 | 503 | 510 | PF00069 | 0.301 |
| MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.329 |
| MOD_N-GLC_1 | 393 | 398 | PF02516 | 0.255 |
| MOD_N-GLC_1 | 402 | 407 | PF02516 | 0.225 |
| MOD_N-GLC_1 | 507 | 512 | PF02516 | 0.381 |
| MOD_NEK2_1 | 122 | 127 | PF00069 | 0.323 |
| MOD_NEK2_1 | 415 | 420 | PF00069 | 0.371 |
| MOD_NEK2_1 | 521 | 526 | PF00069 | 0.475 |
| MOD_PK_1 | 39 | 45 | PF00069 | 0.292 |
| MOD_PK_1 | 503 | 509 | PF00069 | 0.293 |
| MOD_PKA_1 | 274 | 280 | PF00069 | 0.255 |
| MOD_PKA_2 | 474 | 480 | PF00069 | 0.285 |
| MOD_Plk_1 | 277 | 283 | PF00069 | 0.409 |
| MOD_Plk_1 | 33 | 39 | PF00069 | 0.360 |
| MOD_Plk_1 | 357 | 363 | PF00069 | 0.258 |
| MOD_Plk_1 | 402 | 408 | PF00069 | 0.367 |
| MOD_Plk_1 | 473 | 479 | PF00069 | 0.320 |
| MOD_Plk_1 | 485 | 491 | PF00069 | 0.320 |
| MOD_Plk_2-3 | 474 | 480 | PF00069 | 0.320 |
| MOD_Plk_4 | 157 | 163 | PF00069 | 0.276 |
| MOD_Plk_4 | 317 | 323 | PF00069 | 0.395 |
| MOD_Plk_4 | 386 | 392 | PF00069 | 0.260 |
| MOD_Plk_4 | 514 | 520 | PF00069 | 0.394 |
| MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.221 |
| MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.349 |
| MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.547 |
| MOD_SUMO_for_1 | 20 | 23 | PF00179 | 0.479 |
| MOD_SUMO_rev_2 | 260 | 267 | PF00179 | 0.238 |
| TRG_DiLeu_BaEn_1 | 262 | 267 | PF01217 | 0.240 |
| TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.350 |
| TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.440 |
| TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.323 |
| TRG_ENDOCYTIC_2 | 80 | 83 | PF00928 | 0.323 |
| TRG_ER_diArg_1 | 281 | 284 | PF00400 | 0.322 |
| TRG_ER_diArg_1 | 328 | 330 | PF00400 | 0.316 |
| TRG_NES_CRM1_1 | 460 | 474 | PF08389 | 0.393 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P8F7 | Leptomonas seymouri | 52% | 100% |
| A0A0N1PBT6 | Leptomonas seymouri | 27% | 82% |
| A0A1X0NFY9 | Trypanosomatidae | 26% | 100% |
| A0A1X0NTL0 | Trypanosomatidae | 24% | 83% |
| A0A1X0NTM3 | Trypanosomatidae | 25% | 83% |
| A0A1X0NY19 | Trypanosomatidae | 28% | 83% |
| A0A1X0P322 | Trypanosomatidae | 25% | 84% |
| A0A1X0P5Y7 | Trypanosomatidae | 26% | 82% |
| A0A3Q8IB13 | Leishmania donovani | 80% | 95% |
| A0A3S5H595 | Leishmania donovani | 27% | 82% |
| A0A3S5H7I4 | Leishmania donovani | 52% | 100% |
| A0A3S7WXQ4 | Leishmania donovani | 86% | 100% |
| A0A3S7WXS2 | Leishmania donovani | 100% | 100% |
| A1STJ9 | Psychromonas ingrahamii (strain 37) | 33% | 97% |
| A2R0E0 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 25% | 98% |
| A2X5P7 | Oryza sativa subsp. indica | 27% | 91% |
| A2YZ01 | Oryza sativa subsp. indica | 30% | 88% |
| A4H3V1 | Leishmania braziliensis | 28% | 82% |
| A4HCV9 | Leishmania braziliensis | 69% | 99% |
| A4HCW0 | Leishmania braziliensis | 78% | 99% |
| A4HG14 | Leishmania braziliensis | 50% | 98% |
| A4HS26 | Leishmania infantum | 27% | 82% |
| A4I0D9 | Leishmania infantum | 80% | 99% |
| A4I0E0 | Leishmania infantum | 86% | 100% |
| A4I336 | Leishmania infantum | 51% | 98% |
| A4IAW1 | Leishmania infantum | 27% | 75% |
| A5ABL2 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 26% | 100% |
| A5DHM6 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 26% | 100% |
| A5EZZ8 | Vibrio cholerae serotype O1 (strain ATCC 39541 / Classical Ogawa 395 / O395) | 32% | 97% |
| A8W7I5 | Meyerozyma guilliermondii | 26% | 100% |
| B6DXP5 | Leymus chinensis | 26% | 88% |
| B6DZC8 | Triticum aestivum | 25% | 88% |
| B6DZD0 | Triticum urartu | 25% | 88% |
| B6DZD1 | Aegilops speltoides | 25% | 89% |
| B6DZD2 | Aegilops tauschii | 25% | 88% |
| D2IGW7 | Bromus pictus | 25% | 88% |
| E1ABX2 | Aspergillus ficuum | 26% | 98% |
| E8NHF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 99% |
| E8NHF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 99% |
| E9ACV4 | Leishmania major | 52% | 98% |
| E9AK13 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
| E9AWA3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
| E9AZE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 97% |
| F8DVG5 | Zymomonas mobilis subsp. mobilis (strain ATCC 10988 / DSM 424 / LMG 404 / NCIMB 8938 / NRRL B-806 / ZM1) | 39% | 100% |
| H2DF87 | Rosa hybrid cultivar | 28% | 90% |
| H2DF88 | Rosa hybrid cultivar | 26% | 82% |
| K0E681 | Aspergillus rugulosus | 26% | 100% |
| O07003 | Bacillus subtilis (strain 168) | 26% | 100% |
| O33833 | Thermotoga maritima (strain ATCC 43589 / DSM 3109 / JCM 10099 / NBRC 100826 / MSB8) | 32% | 100% |
| O42878 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 100% |
| O59852 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 91% |
| O74641 | Aspergillus niger | 26% | 100% |
| O74642 | Aspergillus niger | 26% | 100% |
| O94220 | Aspergillus ficuum | 26% | 100% |
| P00724 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 99% |
| P05656 | Bacillus subtilis (strain 168) | 28% | 78% |
| P07819 | Bacillus subtilis (strain 168) | 35% | 100% |
| P0DJA7 | Zymomonas mobilis subsp. mobilis (strain ATCC 31821 / ZM4 / CP4) | 41% | 100% |
| P10594 | Saccharomyces cerevisiae | 24% | 99% |
| P10596 | Saccharomyces cerevisiae | 24% | 99% |
| P13394 | Vibrio alginolyticus | 30% | 100% |
| P13522 | Streptococcus mutans serotype c (strain ATCC 700610 / UA159) | 29% | 100% |
| P16553 | Escherichia coli | 46% | 100% |
| P24133 | Schwanniomyces occidentalis | 24% | 99% |
| P26792 | Daucus carota | 24% | 89% |
| P27217 | Klebsiella pneumoniae | 35% | 100% |
| P28999 | Kluyveromyces marxianus | 25% | 95% |
| P29000 | Solanum lycopersicum | 26% | 83% |
| P29001 | Vigna radiata var. radiata | 26% | 81% |
| P37075 | Salmonella typhimurium | 36% | 100% |
| P40714 | Escherichia coli | 47% | 100% |
| P40912 | Wickerhamomyces anomalus | 24% | 96% |
| P43471 | Pediococcus pentosaceus | 27% | 100% |
| P49174 | Zea mays | 26% | 89% |
| P49175 | Zea mays | 26% | 79% |
| P80065 | Daucus carota | 26% | 80% |
| P92916 | Allium cepa | 24% | 86% |
| P93761 | Capsicum annuum | 25% | 82% |
| P94469 | Geobacillus stearothermophilus | 27% | 100% |
| Q01IS7 | Oryza sativa subsp. indica | 25% | 88% |
| Q01IS8 | Oryza sativa subsp. indica | 25% | 90% |
| Q04937 | Lactococcus lactis subsp. lactis | 28% | 100% |
| Q05936 | Staphylococcus xylosus | 30% | 100% |
| Q0E0P0 | Oryza sativa subsp. japonica | 27% | 91% |
| Q0J360 | Oryza sativa subsp. japonica | 25% | 88% |
| Q0JDC5 | Oryza sativa subsp. japonica | 25% | 88% |
| Q0JDC6 | Oryza sativa subsp. japonica | 25% | 90% |
| Q1PEF8 | Arabidopsis thaliana | 26% | 89% |
| Q2UXF7 | Triticum aestivum | 29% | 88% |
| Q39692 | Daucus carota | 30% | 89% |
| Q39693 | Daucus carota | 30% | 90% |
| Q43089 | Pisum sativum | 25% | 95% |
| Q43348 | Arabidopsis thaliana | 27% | 81% |
| Q43857 | Vicia faba | 24% | 82% |
| Q43866 | Arabidopsis thaliana | 26% | 90% |
| Q4QB75 | Leishmania major | 84% | 100% |
| Q4QB76 | Leishmania major | 78% | 99% |
| Q56660 | Vibrio cholerae | 31% | 97% |
| Q56UD0 | Oryza sativa subsp. japonica | 28% | 88% |
| Q56UD1 | Oryza sativa subsp. japonica | 24% | 97% |
| Q5FC15 | Asparagus officinalis | 25% | 86% |
| Q5JJV0 | Oryza sativa subsp. japonica | 27% | 89% |
| Q67XZ3 | Arabidopsis thaliana | 28% | 89% |
| Q70AT7 | Hordeum vulgare | 26% | 88% |
| Q70XE6 | Beta vulgaris | 27% | 87% |
| Q76HP6 | Aspergillus niger | 26% | 98% |
| Q84LA1 | Triticum aestivum | 25% | 88% |
| Q84PN8 | Triticum aestivum | 25% | 88% |
| Q8W413 | Arabidopsis thaliana | 28% | 89% |
| Q8W4S6 | Arabidopsis thaliana | 24% | 96% |
| Q96TU3 | Aspergillus awamori | 25% | 98% |
| Q9FSV7 | Festuca arundinacea | 24% | 81% |
| Q9KLT6 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 30% | 96% |
| Q9LIB9 | Arabidopsis thaliana | 23% | 92% |
| Q9XTP3 | Leishmania major | 26% | 82% |