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: A4HCW0
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_C14_Caspase3-7 | 327 | 331 | PF00656 | 0.285 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.302 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.302 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.184 |
CLV_PCSK_PC1ET2_1 | 373 | 375 | PF00082 | 0.305 |
CLV_PCSK_PC1ET2_1 | 44 | 46 | PF00082 | 0.184 |
CLV_PCSK_SKI1_1 | 144 | 148 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.188 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.233 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.180 |
DEG_SPOP_SBC_1 | 22 | 26 | PF00917 | 0.189 |
DOC_MAPK_MEF2A_6 | 408 | 415 | PF00069 | 0.250 |
DOC_PP1_RVXF_1 | 196 | 203 | PF00149 | 0.242 |
DOC_PP2B_LxvP_1 | 286 | 289 | PF13499 | 0.309 |
DOC_PP4_FxxP_1 | 125 | 128 | PF00568 | 0.309 |
DOC_PP4_FxxP_1 | 248 | 251 | PF00568 | 0.264 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.352 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.217 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.184 |
DOC_USP7_UBL2_3 | 207 | 211 | PF12436 | 0.184 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.415 |
LIG_14-3-3_CanoR_1 | 313 | 321 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 436 | 441 | PF00244 | 0.359 |
LIG_Actin_WH2_2 | 297 | 315 | PF00022 | 0.313 |
LIG_APCC_ABBA_1 | 402 | 407 | PF00400 | 0.272 |
LIG_BRCT_BRCA1_1 | 423 | 427 | PF00533 | 0.313 |
LIG_FHA_1 | 145 | 151 | PF00498 | 0.436 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.271 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.284 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.224 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.273 |
LIG_FHA_2 | 336 | 342 | PF00498 | 0.304 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.295 |
LIG_KLC1_Yacidic_2 | 365 | 369 | PF13176 | 0.388 |
LIG_LIR_Apic_2 | 247 | 251 | PF02991 | 0.264 |
LIG_LIR_Gen_1 | 13 | 22 | PF02991 | 0.231 |
LIG_LIR_Gen_1 | 166 | 174 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 13 | 17 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 134 | 140 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 187 | 191 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 238 | 242 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 71 | 77 | PF02991 | 0.270 |
LIG_NRBOX | 149 | 155 | PF00104 | 0.322 |
LIG_PTB_Apo_2 | 375 | 382 | PF02174 | 0.305 |
LIG_PTB_Phospho_1 | 375 | 381 | PF10480 | 0.305 |
LIG_SH2_NCK_1 | 294 | 298 | PF00017 | 0.242 |
LIG_SH2_SRC | 18 | 21 | PF00017 | 0.224 |
LIG_SH2_SRC | 367 | 370 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 23 | 27 | PF00017 | 0.317 |
LIG_SH2_STAP1 | 340 | 344 | PF00017 | 0.302 |
LIG_SH2_STAT3 | 249 | 252 | PF00017 | 0.309 |
LIG_SH2_STAT3 | 95 | 98 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 367 | 370 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.261 |
LIG_SH3_1 | 85 | 91 | PF00018 | 0.184 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.333 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.271 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.233 |
LIG_TRAF2_1 | 305 | 308 | PF00917 | 0.256 |
LIG_WW_1 | 119 | 122 | PF00397 | 0.322 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.319 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.303 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.305 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.305 |
MOD_CK2_1 | 406 | 412 | PF00069 | 0.336 |
MOD_Cter_Amidation | 205 | 208 | PF01082 | 0.242 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.413 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.313 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.336 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.298 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.318 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.316 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.301 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.202 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.305 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.203 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.213 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.383 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.470 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.309 |
MOD_PIKK_1 | 155 | 161 | PF00454 | 0.202 |
MOD_PK_1 | 436 | 442 | PF00069 | 0.279 |
MOD_PKA_1 | 207 | 213 | PF00069 | 0.242 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.184 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.347 |
MOD_PKA_2 | 407 | 413 | PF00069 | 0.272 |
MOD_Plk_1 | 335 | 341 | PF00069 | 0.370 |
MOD_Plk_1 | 406 | 412 | PF00069 | 0.305 |
MOD_Plk_1 | 418 | 424 | PF00069 | 0.305 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.194 |
MOD_Plk_1 | 454 | 460 | PF00069 | 0.386 |
MOD_Plk_2-3 | 407 | 413 | PF00069 | 0.305 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.381 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.380 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.415 |
MOD_SUMO_rev_2 | 65 | 73 | PF00179 | 0.200 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.309 |
TRG_ER_diArg_1 | 214 | 217 | PF00400 | 0.308 |
TRG_ER_diArg_1 | 261 | 263 | PF00400 | 0.302 |
TRG_NES_CRM1_1 | 393 | 407 | PF08389 | 0.359 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8F7 | Leptomonas seymouri | 54% | 94% |
A0A0N1PBT6 | Leptomonas seymouri | 25% | 71% |
A0A1X0NFY9 | Trypanosomatidae | 26% | 96% |
A0A1X0NTL0 | Trypanosomatidae | 23% | 73% |
A0A1X0NTM3 | Trypanosomatidae | 28% | 73% |
A0A1X0NY19 | Trypanosomatidae | 28% | 73% |
A0A1X0P322 | Trypanosomatidae | 26% | 73% |
A0A1X0P5Y7 | Trypanosomatidae | 26% | 72% |
A0A3Q8IB13 | Leishmania donovani | 66% | 83% |
A0A3Q8IFU7 | Leishmania donovani | 78% | 87% |
A0A3S5H595 | Leishmania donovani | 27% | 72% |
A0A3S5H7I4 | Leishmania donovani | 50% | 94% |
A0A3S7WXQ4 | Leishmania donovani | 83% | 90% |
A0A3S7WXS2 | Leishmania donovani | 78% | 87% |
A1STJ9 | Psychromonas ingrahamii (strain 37) | 34% | 84% |
A2R0E0 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 24% | 86% |
A2X5P7 | Oryza sativa subsp. indica | 27% | 80% |
A2YZ01 | Oryza sativa subsp. indica | 25% | 77% |
A4H3V1 | Leishmania braziliensis | 27% | 72% |
A4HCV9 | Leishmania braziliensis | 68% | 84% |
A4HG14 | Leishmania braziliensis | 50% | 94% |
A4HS26 | Leishmania infantum | 27% | 72% |
A4I0D9 | Leishmania infantum | 65% | 83% |
A4I0E0 | Leishmania infantum | 84% | 90% |
A4I336 | Leishmania infantum | 50% | 94% |
A5ABL2 | Aspergillus niger (strain CBS 513.88 / FGSC A1513) | 24% | 89% |
A5DHM6 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 26% | 89% |
A5EZZ8 | Vibrio cholerae serotype O1 (strain ATCC 39541 / Classical Ogawa 395 / O395) | 32% | 84% |
A8W7I5 | Meyerozyma guilliermondii | 26% | 89% |
B6DXP5 | Leymus chinensis | 27% | 77% |
B6DZC8 | Triticum aestivum | 27% | 77% |
B6DZD0 | Triticum urartu | 28% | 77% |
B6DZD1 | Aegilops speltoides | 28% | 77% |
B6DZD2 | Aegilops tauschii | 28% | 77% |
D2IGW7 | Bromus pictus | 27% | 76% |
E1ABX2 | Aspergillus ficuum | 24% | 86% |
E8NHF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 88% |
E8NHF3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 65% | 95% |
E9ACV4 | Leishmania major | 51% | 100% |
E9AK13 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 72% |
E9AWA3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
E9AZE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 94% |
F8DVG5 | Zymomonas mobilis subsp. mobilis (strain ATCC 10988 / DSM 424 / LMG 404 / NCIMB 8938 / NRRL B-806 / ZM1) | 42% | 90% |
H2DF87 | Rosa hybrid cultivar | 28% | 78% |
H2DF88 | Rosa hybrid cultivar | 26% | 72% |
K0E681 | Aspergillus rugulosus | 25% | 91% |
O07003 | Bacillus subtilis (strain 168) | 26% | 89% |
O24509 | Phaseolus vulgaris | 27% | 71% |
O33833 | Thermotoga maritima (strain ATCC 43589 / DSM 3109 / JCM 10099 / NBRC 100826 / MSB8) | 32% | 100% |
O42878 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 91% |
O59852 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 79% |
O74641 | Aspergillus niger | 25% | 89% |
O74642 | Aspergillus niger | 25% | 89% |
O94220 | Aspergillus ficuum | 25% | 89% |
P00724 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 86% |
P05656 | Bacillus subtilis (strain 168) | 29% | 68% |
P07819 | Bacillus subtilis (strain 168) | 37% | 96% |
P0DJA7 | Zymomonas mobilis subsp. mobilis (strain ATCC 31821 / ZM4 / CP4) | 41% | 90% |
P10594 | Saccharomyces cerevisiae | 23% | 86% |
P10596 | Saccharomyces cerevisiae | 23% | 86% |
P13394 | Vibrio alginolyticus | 31% | 95% |
P13522 | Streptococcus mutans serotype c (strain ATCC 700610 / UA159) | 30% | 96% |
P16553 | Escherichia coli | 48% | 97% |
P24133 | Schwanniomyces occidentalis | 25% | 86% |
P26792 | Daucus carota | 28% | 78% |
P27217 | Klebsiella pneumoniae | 36% | 99% |
P28999 | Kluyveromyces marxianus | 23% | 83% |
P29000 | Solanum lycopersicum | 26% | 72% |
P29001 | Vigna radiata var. radiata | 27% | 71% |
P37075 | Salmonella typhimurium | 35% | 99% |
P40714 | Escherichia coli | 48% | 96% |
P40912 | Wickerhamomyces anomalus | 23% | 84% |
P43471 | Pediococcus pentosaceus | 28% | 92% |
P49174 | Zea mays | 27% | 78% |
P49175 | Zea mays | 26% | 69% |
P80065 | Daucus carota | 26% | 70% |
P92916 | Allium cepa | 25% | 75% |
P93761 | Capsicum annuum | 25% | 72% |
P94469 | Geobacillus stearothermophilus | 27% | 100% |
Q01IS7 | Oryza sativa subsp. indica | 26% | 77% |
Q01IS8 | Oryza sativa subsp. indica | 25% | 78% |
Q04937 | Lactococcus lactis subsp. lactis | 28% | 97% |
Q05936 | Staphylococcus xylosus | 32% | 93% |
Q0E0P0 | Oryza sativa subsp. japonica | 28% | 80% |
Q0J360 | Oryza sativa subsp. japonica | 25% | 77% |
Q0JDC5 | Oryza sativa subsp. japonica | 26% | 77% |
Q0JDC6 | Oryza sativa subsp. japonica | 25% | 78% |
Q1PEF8 | Arabidopsis thaliana | 27% | 78% |
Q2UXF7 | Triticum aestivum | 25% | 77% |
Q39041 | Arabidopsis thaliana | 29% | 69% |
Q39692 | Daucus carota | 29% | 78% |
Q39693 | Daucus carota | 29% | 79% |
Q43089 | Pisum sativum | 25% | 83% |
Q43348 | Arabidopsis thaliana | 26% | 71% |
Q43857 | Vicia faba | 24% | 72% |
Q43866 | Arabidopsis thaliana | 28% | 79% |
Q4QB75 | Leishmania major | 85% | 100% |
Q4QB76 | Leishmania major | 66% | 100% |
Q56660 | Vibrio cholerae | 32% | 84% |
Q56UD0 | Oryza sativa subsp. japonica | 30% | 77% |
Q56UD1 | Oryza sativa subsp. japonica | 25% | 85% |
Q5FC15 | Asparagus officinalis | 26% | 75% |
Q5JJV0 | Oryza sativa subsp. japonica | 28% | 78% |
Q67XZ3 | Arabidopsis thaliana | 28% | 77% |
Q6BJW6 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 24% | 86% |
Q70AT7 | Hordeum vulgare | 28% | 77% |
Q70XE6 | Beta vulgaris | 28% | 76% |
Q76HP6 | Aspergillus niger | 24% | 86% |
Q84LA1 | Triticum aestivum | 28% | 77% |
Q84PN8 | Triticum aestivum | 28% | 77% |
Q8W413 | Arabidopsis thaliana | 28% | 78% |
Q8W4S6 | Arabidopsis thaliana | 26% | 84% |
Q96TU3 | Aspergillus awamori | 23% | 86% |
Q9FSV7 | Festuca arundinacea | 25% | 70% |
Q9KLT6 | Vibrio cholerae serotype O1 (strain ATCC 39315 / El Tor Inaba N16961) | 32% | 84% |
Q9LIB9 | Arabidopsis thaliana | 27% | 80% |
Q9XTP3 | Leishmania major | 26% | 72% |