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: E9ACV4
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 | 17 | 19 | PF00675 | 0.334 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.312 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.240 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.316 |
CLV_PCSK_PC1ET2_1 | 146 | 148 | PF00082 | 0.240 |
CLV_PCSK_PC1ET2_1 | 402 | 404 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 320 | 324 | PF00082 | 0.240 |
DOC_CKS1_1 | 331 | 336 | PF01111 | 0.306 |
DOC_CYCLIN_RxL_1 | 268 | 278 | PF00134 | 0.227 |
DOC_CYCLIN_RxL_1 | 317 | 326 | PF00134 | 0.289 |
DOC_MAPK_gen_1 | 179 | 189 | PF00069 | 0.240 |
DOC_MAPK_gen_1 | 246 | 255 | PF00069 | 0.195 |
DOC_MAPK_MEF2A_6 | 248 | 257 | PF00069 | 0.197 |
DOC_MAPK_MEF2A_6 | 355 | 364 | PF00069 | 0.227 |
DOC_PP2B_LxvP_1 | 316 | 319 | PF13499 | 0.319 |
DOC_PP4_FxxP_1 | 160 | 163 | PF00568 | 0.319 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.329 |
DOC_USP7_UBL2_3 | 19 | 23 | PF12436 | 0.324 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.289 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.316 |
LIG_14-3-3_CanoR_1 | 18 | 22 | PF00244 | 0.338 |
LIG_14-3-3_CanoR_1 | 351 | 355 | PF00244 | 0.258 |
LIG_14-3-3_CanoR_1 | 36 | 41 | PF00244 | 0.176 |
LIG_14-3-3_CanoR_1 | 462 | 467 | PF00244 | 0.376 |
LIG_APCC_ABBA_1 | 393 | 398 | PF00400 | 0.240 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.387 |
LIG_Clathr_ClatBox_1 | 374 | 378 | PF01394 | 0.240 |
LIG_deltaCOP1_diTrp_1 | 196 | 203 | PF00928 | 0.257 |
LIG_deltaCOP1_diTrp_1 | 91 | 99 | PF00928 | 0.240 |
LIG_eIF4E_1 | 249 | 255 | PF01652 | 0.240 |
LIG_eIF4E_1 | 369 | 375 | PF01652 | 0.234 |
LIG_EVH1_2 | 153 | 157 | PF00568 | 0.240 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.282 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.319 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.264 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.417 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.398 |
LIG_FHA_1 | 470 | 476 | PF00498 | 0.243 |
LIG_FHA_2 | 365 | 371 | PF00498 | 0.299 |
LIG_FHA_2 | 474 | 480 | PF00498 | 0.237 |
LIG_FHA_2 | 71 | 77 | PF00498 | 0.305 |
LIG_HP1_1 | 319 | 323 | PF01393 | 0.240 |
LIG_Integrin_RGD_1 | 477 | 479 | PF01839 | 0.227 |
LIG_IRF3_LxIS_1 | 132 | 138 | PF10401 | 0.257 |
LIG_KLC1_Yacidic_2 | 394 | 398 | PF13176 | 0.417 |
LIG_LIR_Apic_2 | 158 | 163 | PF02991 | 0.227 |
LIG_LIR_Apic_2 | 420 | 424 | PF02991 | 0.240 |
LIG_LIR_Gen_1 | 162 | 169 | PF02991 | 0.240 |
LIG_LIR_Gen_1 | 200 | 210 | PF02991 | 0.319 |
LIG_LIR_LC3C_4 | 401 | 406 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 108 | 114 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 162 | 167 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 169 | 175 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 200 | 206 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 24 | 29 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 267 | 273 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 416 | 421 | PF02991 | 0.240 |
LIG_PTB_Apo_2 | 404 | 411 | PF02174 | 0.316 |
LIG_PTB_Phospho_1 | 404 | 410 | PF10480 | 0.316 |
LIG_Rb_pABgroove_1 | 358 | 366 | PF01858 | 0.439 |
LIG_Rb_pABgroove_1 | 369 | 377 | PF01858 | 0.202 |
LIG_SH2_CRK | 421 | 425 | PF00017 | 0.240 |
LIG_SH2_NCK_1 | 421 | 425 | PF00017 | 0.227 |
LIG_SH2_STAP1 | 106 | 110 | PF00017 | 0.253 |
LIG_SH2_STAP1 | 369 | 373 | PF00017 | 0.312 |
LIG_SH2_STAT3 | 130 | 133 | PF00017 | 0.299 |
LIG_SH2_STAT3 | 280 | 283 | PF00017 | 0.319 |
LIG_SH2_STAT3 | 55 | 58 | PF00017 | 0.237 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.227 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 434 | 437 | PF00017 | 0.250 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.252 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.319 |
LIG_SUMO_SIM_par_1 | 320 | 326 | PF11976 | 0.240 |
LIG_UBA3_1 | 253 | 259 | PF00899 | 0.207 |
MOD_CDK_SPxxK_3 | 330 | 337 | PF00069 | 0.304 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.274 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.270 |
MOD_CK2_1 | 204 | 210 | PF00069 | 0.237 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.316 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.317 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.316 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.227 |
MOD_Cter_Amidation | 289 | 292 | PF01082 | 0.279 |
MOD_GlcNHglycan | 325 | 330 | PF01048 | 0.261 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.247 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.316 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.309 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.277 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.327 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.316 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.315 |
MOD_N-GLC_1 | 355 | 360 | PF02516 | 0.252 |
MOD_N-GLC_1 | 469 | 474 | PF02516 | 0.372 |
MOD_N-GLC_1 | 483 | 488 | PF02516 | 0.302 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.264 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.289 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.202 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.304 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.388 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.247 |
MOD_NEK2_1 | 483 | 488 | PF00069 | 0.452 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.319 |
MOD_NEK2_2 | 350 | 355 | PF00069 | 0.227 |
MOD_PIKK_1 | 124 | 130 | PF00454 | 0.257 |
MOD_PIKK_1 | 355 | 361 | PF00454 | 0.234 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.318 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.240 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.254 |
MOD_PKB_1 | 246 | 254 | PF00069 | 0.289 |
MOD_Plk_1 | 124 | 130 | PF00069 | 0.257 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.240 |
MOD_Plk_1 | 355 | 361 | PF00069 | 0.281 |
MOD_Plk_1 | 364 | 370 | PF00069 | 0.342 |
MOD_Plk_1 | 435 | 441 | PF00069 | 0.320 |
MOD_Plk_1 | 483 | 489 | PF00069 | 0.346 |
MOD_Plk_2-3 | 365 | 371 | PF00069 | 0.247 |
MOD_Plk_2-3 | 436 | 442 | PF00069 | 0.316 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.214 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.240 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.372 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.249 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.408 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.289 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.313 |
TRG_DiLeu_BaLyEn_6 | 358 | 363 | PF01217 | 0.266 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 434 | 437 | PF00928 | 0.257 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.319 |
TRG_ER_diArg_1 | 245 | 248 | PF00400 | 0.319 |
TRG_ER_diArg_1 | 291 | 293 | PF00400 | 0.312 |
TRG_NES_CRM1_1 | 128 | 139 | PF08389 | 0.240 |
TRG_NES_CRM1_1 | 426 | 441 | PF08389 | 0.365 |
TRG_Pf-PMV_PEXEL_1 | 320 | 325 | PF00026 | 0.289 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8F7 | Leptomonas seymouri | 81% | 100% |
A0A1X0NFY9 | Trypanosomatidae | 24% | 100% |
A0A1X0NTL0 | Trypanosomatidae | 24% | 77% |
A0A1X0NTM3 | Trypanosomatidae | 22% | 77% |
A0A1X0NY19 | Trypanosomatidae | 25% | 77% |
A0A1X0P322 | Trypanosomatidae | 24% | 77% |
A0A1X0P5Y7 | Trypanosomatidae | 25% | 76% |
A0A3Q8IB13 | Leishmania donovani | 49% | 89% |
A0A3Q8IFU7 | Leishmania donovani | 52% | 93% |
A0A3S5H595 | Leishmania donovani | 23% | 76% |
A0A3S5H7I4 | Leishmania donovani | 95% | 100% |
A0A3S7WXQ4 | Leishmania donovani | 52% | 95% |
A0A3S7WXS2 | Leishmania donovani | 52% | 93% |
A1STJ9 | Psychromonas ingrahamii (strain 37) | 33% | 90% |
A2R0E0 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 26% | 91% |
A2X5P7 | Oryza sativa subsp. indica | 25% | 85% |
A2YZ01 | Oryza sativa subsp. indica | 23% | 82% |
A4H3V1 | Leishmania braziliensis | 25% | 76% |
A4HCV9 | Leishmania braziliensis | 50% | 90% |
A4HCW0 | Leishmania braziliensis | 51% | 100% |
A4HG14 | Leishmania braziliensis | 85% | 100% |
A4HS26 | Leishmania infantum | 23% | 76% |
A4I0D9 | Leishmania infantum | 50% | 89% |
A4I0E0 | Leishmania infantum | 51% | 95% |
A4I336 | Leishmania infantum | 95% | 100% |
A4IAW1 | Leishmania infantum | 26% | 70% |
A5ABL2 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 26% | 95% |
A5DHM6 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 23% | 95% |
A5EZZ8 | Vibrio cholerae serotype O1 (strain ATCC 39541 / Classical Ogawa 395 / O395) | 30% | 90% |
A8W7I5 | Meyerozyma guilliermondii | 23% | 95% |
B6DXP5 | Leymus chinensis | 25% | 82% |
B6DZC8 | Triticum aestivum | 25% | 82% |
B6DZD0 | Triticum urartu | 24% | 82% |
B6DZD1 | Aegilops speltoides | 24% | 82% |
B6DZD2 | Aegilops tauschii | 25% | 82% |
D2IGW7 | Bromus pictus | 24% | 81% |
E1ABX2 | Aspergillus ficuum | 26% | 91% |
E8NHF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 93% |
E8NHF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 100% |
E9AK13 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 77% |
E9AWA3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 100% |
E9AZE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
F8DVG5 | Zymomonas mobilis subsp. mobilis (strain ATCC 10988 / DSM 424 / LMG 404 / NCIMB 8938 / NRRL B-806 / ZM1) | 37% | 96% |
H2DF87 | Rosa hybrid cultivar | 25% | 83% |
H2DF88 | Rosa hybrid cultivar | 24% | 76% |
K0E681 | Aspergillus rugulosus | 24% | 96% |
O07003 | Bacillus subtilis (strain 168) | 26% | 95% |
O24509 | Phaseolus vulgaris | 27% | 75% |
O33833 | Thermotoga maritima (strain ATCC 43589 / DSM 3109 / JCM 10099 / NBRC 100826 / MSB8) | 32% | 100% |
O42878 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 96% |
O59852 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 84% |
O74641 | Aspergillus niger | 26% | 95% |
O74642 | Aspergillus niger | 26% | 95% |
O94220 | Aspergillus ficuum | 27% | 95% |
P05656 | Bacillus subtilis (strain 168) | 29% | 72% |
P07819 | Bacillus subtilis (strain 168) | 35% | 100% |
P0DJA7 | Zymomonas mobilis subsp. mobilis (strain ATCC 31821 / ZM4 / CP4) | 37% | 96% |
P10594 | Saccharomyces cerevisiae | 22% | 92% |
P10596 | Saccharomyces cerevisiae | 25% | 92% |
P13394 | Vibrio alginolyticus | 28% | 100% |
P13522 | Streptococcus mutans serotype c (strain ATCC 700610 / UA159) | 27% | 100% |
P16553 | Escherichia coli | 48% | 100% |
P24133 | Schwanniomyces occidentalis | 27% | 92% |
P26792 | Daucus carota | 25% | 83% |
P27217 | Klebsiella pneumoniae | 32% | 100% |
P29000 | Solanum lycopersicum | 24% | 77% |
P29001 | Vigna radiata var. radiata | 26% | 75% |
P37075 | Salmonella typhimurium | 32% | 100% |
P40714 | Escherichia coli | 46% | 100% |
P40912 | Wickerhamomyces anomalus | 25% | 89% |
P43471 | Pediococcus pentosaceus | 25% | 98% |
P49174 | Zea mays | 27% | 83% |
P49175 | Zea mays | 25% | 73% |
P80065 | Daucus carota | 24% | 74% |
P92916 | Allium cepa | 26% | 80% |
P93761 | Capsicum annuum | 25% | 76% |
P94469 | Geobacillus stearothermophilus | 26% | 100% |
Q01IS7 | Oryza sativa subsp. indica | 26% | 82% |
Q01IS8 | Oryza sativa subsp. indica | 23% | 83% |
Q04937 | Lactococcus lactis subsp. lactis | 26% | 100% |
Q05936 | Staphylococcus xylosus | 30% | 99% |
Q0E0P0 | Oryza sativa subsp. japonica | 25% | 85% |
Q0J360 | Oryza sativa subsp. japonica | 26% | 82% |
Q0JDC5 | Oryza sativa subsp. japonica | 26% | 82% |
Q0JDC6 | Oryza sativa subsp. japonica | 23% | 83% |
Q1PEF8 | Arabidopsis thaliana | 24% | 83% |
Q2UXF7 | Triticum aestivum | 26% | 82% |
Q39041 | Arabidopsis thaliana | 27% | 74% |
Q39692 | Daucus carota | 27% | 83% |
Q39693 | Daucus carota | 25% | 84% |
Q43089 | Pisum sativum | 24% | 88% |
Q43348 | Arabidopsis thaliana | 26% | 75% |
Q43857 | Vicia faba | 23% | 76% |
Q43866 | Arabidopsis thaliana | 24% | 84% |
Q4QB75 | Leishmania major | 52% | 95% |
Q4QB76 | Leishmania major | 50% | 89% |
Q56660 | Vibrio cholerae | 30% | 90% |
Q56UD0 | Oryza sativa subsp. japonica | 27% | 82% |
Q56UD1 | Oryza sativa subsp. japonica | 24% | 90% |
Q5FC15 | Asparagus officinalis | 24% | 80% |
Q5JJV0 | Oryza sativa subsp. japonica | 23% | 83% |
Q67XZ3 | Arabidopsis thaliana | 27% | 82% |
Q6BJW6 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 24% | 92% |
Q70AT7 | Hordeum vulgare | 24% | 82% |
Q70XE6 | Beta vulgaris | 27% | 81% |
Q76HP6 | Aspergillus niger | 26% | 91% |
Q84LA1 | Triticum aestivum | 24% | 82% |
Q84PN8 | Triticum aestivum | 24% | 82% |
Q8W413 | Arabidopsis thaliana | 27% | 83% |
Q8W4S6 | Arabidopsis thaliana | 27% | 89% |
Q96TU3 | Aspergillus awamori | 25% | 91% |
Q9FSV7 | Festuca arundinacea | 26% | 75% |
Q9KLT6 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 30% | 89% |
Q9LIB9 | Arabidopsis thaliana | 28% | 85% |
Q9XTP3 | Leishmania major | 23% | 76% |