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: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 20 |
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005975 | carbohydrate metabolic process | 3 | 12 |
GO:0006091 | generation of precursor metabolites and energy | 3 | 12 |
GO:0006098 | pentose-phosphate shunt | 5 | 11 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006739 | NADP metabolic process | 7 | 12 |
GO:0006740 | NADPH regeneration | 4 | 12 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009117 | nucleotide metabolic process | 5 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0019362 | pyridine nucleotide metabolic process | 5 | 12 |
GO:0019637 | organophosphate metabolic process | 3 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044281 | small molecule metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0046496 | nicotinamide nucleotide metabolic process | 6 | 12 |
GO:0051156 | glucose 6-phosphate metabolic process | 4 | 12 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0072524 | pyridine-containing compound metabolic process | 4 | 12 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:0009051 | pentose-phosphate shunt, oxidative branch | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 12 |
GO:0017057 | 6-phosphogluconolactonase activity | 5 | 12 |
GO:0052689 | carboxylic ester hydrolase activity | 4 | 12 |
GO:0016853 | isomerase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.277 |
CLV_PCSK_KEX2_1 | 109 | 111 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.484 |
CLV_PCSK_PC1ET2_1 | 50 | 52 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.366 |
DOC_CYCLIN_RxL_1 | 90 | 98 | PF00134 | 0.476 |
DOC_MAPK_gen_1 | 247 | 257 | PF00069 | 0.468 |
DOC_MAPK_gen_1 | 32 | 41 | PF00069 | 0.444 |
DOC_MAPK_HePTP_8 | 29 | 41 | PF00069 | 0.277 |
DOC_MAPK_MEF2A_6 | 151 | 160 | PF00069 | 0.277 |
DOC_MAPK_MEF2A_6 | 250 | 257 | PF00069 | 0.329 |
DOC_MAPK_MEF2A_6 | 32 | 41 | PF00069 | 0.383 |
DOC_PP4_FxxP_1 | 190 | 193 | PF00568 | 0.376 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.355 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.346 |
LIG_14-3-3_CanoR_1 | 201 | 205 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 229 | 239 | PF00244 | 0.277 |
LIG_14-3-3_CanoR_1 | 250 | 256 | PF00244 | 0.504 |
LIG_BRCT_BRCA1_1 | 186 | 190 | PF00533 | 0.390 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.355 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.364 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.416 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.425 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.450 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.436 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.417 |
LIG_LIR_Apic_2 | 187 | 193 | PF02991 | 0.378 |
LIG_PCNA_yPIPBox_3 | 222 | 232 | PF02747 | 0.476 |
LIG_PDZ_Class_2 | 262 | 267 | PF00595 | 0.547 |
LIG_SH2_STAP1 | 133 | 137 | PF00017 | 0.390 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.382 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.504 |
LIG_SUMO_SIM_anti_2 | 157 | 162 | PF11976 | 0.357 |
LIG_SUMO_SIM_anti_2 | 252 | 258 | PF11976 | 0.323 |
LIG_SUMO_SIM_anti_2 | 60 | 65 | PF11976 | 0.471 |
LIG_SUMO_SIM_par_1 | 101 | 108 | PF11976 | 0.412 |
LIG_SUMO_SIM_par_1 | 180 | 189 | PF11976 | 0.482 |
LIG_SUMO_SIM_par_1 | 252 | 258 | PF11976 | 0.323 |
LIG_SUMO_SIM_par_1 | 39 | 44 | PF11976 | 0.476 |
LIG_TRAF2_1 | 180 | 183 | PF00917 | 0.277 |
LIG_UBA3_1 | 137 | 144 | PF00899 | 0.373 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.638 |
MOD_CDK_SPK_2 | 193 | 198 | PF00069 | 0.351 |
MOD_CDK_SPK_2 | 45 | 50 | PF00069 | 0.355 |
MOD_CDK_SPxK_1 | 45 | 51 | PF00069 | 0.476 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.473 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.461 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.397 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.450 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.436 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.335 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.313 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.330 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.420 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.293 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.441 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.409 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.382 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.391 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.348 |
MOD_N-GLC_1 | 146 | 151 | PF02516 | 0.482 |
MOD_N-GLC_1 | 86 | 91 | PF02516 | 0.504 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.488 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.401 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.513 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.355 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.535 |
MOD_Plk_1 | 12 | 18 | PF00069 | 0.450 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.401 |
MOD_Plk_1 | 86 | 92 | PF00069 | 0.504 |
MOD_Plk_2-3 | 103 | 109 | PF00069 | 0.277 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.355 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.393 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.413 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.435 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.355 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.346 |
MOD_SUMO_rev_2 | 132 | 138 | PF00179 | 0.511 |
TRG_DiLeu_BaLyEn_6 | 74 | 79 | PF01217 | 0.409 |
TRG_ENDOCYTIC_2 | 53 | 56 | PF00928 | 0.355 |
TRG_Pf-PMV_PEXEL_1 | 244 | 248 | PF00026 | 0.413 |
TRG_Pf-PMV_PEXEL_1 | 50 | 54 | PF00026 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 77 | 81 | PF00026 | 0.409 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9Y4 | Leptomonas seymouri | 68% | 98% |
A0A0S4J8H1 | Bodo saltans | 37% | 100% |
A0A1X0NX24 | Trypanosomatidae | 46% | 100% |
A0A3Q8IG46 | Leishmania donovani | 83% | 100% |
A0A3R7NAW7 | Trypanosoma rangeli | 47% | 100% |
A2XI04 | Oryza sativa subsp. indica | 25% | 90% |
A2YNH4 | Oryza sativa subsp. indica | 25% | 95% |
A2YXS5 | Oryza sativa subsp. indica | 27% | 82% |
A2Z3C4 | Oryza sativa subsp. indica | 29% | 82% |
A6ZT71 | Saccharomyces cerevisiae (strain YJM789) | 27% | 100% |
B3LSS7 | Saccharomyces cerevisiae (strain RM11-1a) | 27% | 100% |
B5VK90 | Saccharomyces cerevisiae (strain AWRI1631) | 27% | 100% |
D0A7E6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9AHB9 | Leishmania infantum | 83% | 100% |
E9AYQ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
O18229 | Caenorhabditis elegans | 29% | 99% |
O51240 | Borreliella burgdorferi (strain ATCC 35210 / DSM 4680 / CIP 102532 / B31) | 23% | 100% |
O74455 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 100% |
O83490 | Treponema pallidum (strain Nichols) | 31% | 100% |
O84189 | Chlamydia trachomatis (strain D/UW-3/Cx) | 27% | 100% |
O95336 | Homo sapiens | 28% | 100% |
P37262 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 85% |
P38858 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 100% |
P46016 | Nostoc sp. (strain PCC 7120 / SAG 25.82 / UTEX 2576) | 30% | 100% |
P50278 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 83% |
P53315 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 100% |
P63339 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 31% | 100% |
P74618 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 31% | 100% |
P85971 | Rattus norvegicus | 31% | 100% |
P9WQP4 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 31% | 100% |
P9WQP5 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 31% | 100% |
Q2TBQ8 | Bos taurus | 29% | 100% |
Q49700 | Mycobacterium leprae (strain TN) | 27% | 100% |
Q4Q8S1 | Leishmania major | 84% | 100% |
Q57039 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 28% | 100% |
Q69NG5 | Oryza sativa subsp. japonica | 29% | 82% |
Q6Z4H0 | Oryza sativa subsp. japonica | 25% | 95% |
Q6Z9C3 | Oryza sativa subsp. japonica | 27% | 82% |
Q75IV7 | Oryza sativa subsp. japonica | 25% | 90% |
Q84WW2 | Arabidopsis thaliana | 28% | 82% |
Q87EG7 | Xylella fastidiosa (strain Temecula1 / ATCC 700964) | 28% | 100% |
Q8LG70 | Arabidopsis thaliana | 29% | 100% |
Q989A3 | Mesorhizobium japonicum (strain LMG 29417 / CECT 9101 / MAFF 303099) | 27% | 100% |
Q9CQ60 | Mus musculus | 30% | 100% |
Q9EV79 | Pseudomonas putida | 25% | 100% |
Q9LMX8 | Arabidopsis thaliana | 25% | 100% |
Q9PEG5 | Xylella fastidiosa (strain 9a5c) | 29% | 100% |
Q9VZ64 | Drosophila melanogaster | 28% | 100% |
Q9X2N2 | Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) | 28% | 100% |
Q9Z3S1 | Rhizobium meliloti (strain 1021) | 24% | 100% |
Q9Z8U5 | Chlamydia pneumoniae | 27% | 100% |
Q9ZKB1 | Helicobacter pylori (strain J99 / ATCC 700824) | 26% | 100% |
V5D050 | Trypanosoma cruzi | 45% | 100% |