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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:0016020 | membrane | 2 | 2 |
Related structures:
AlphaFold database: Q4QEY5
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006281 | DNA repair | 5 | 12 |
GO:0006304 | DNA modification | 5 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006950 | response to stress | 2 | 12 |
GO:0006974 | DNA damage response | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009451 | RNA modification | 5 | 2 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0033554 | cellular response to stress | 3 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0035510 | DNA dealkylation | 6 | 2 |
GO:0035511 | obsolete oxidative DNA demethylation | 4 | 2 |
GO:0035513 | oxidative RNA demethylation | 4 | 2 |
GO:0035552 | oxidative single-stranded DNA demethylation | 5 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0044728 | obsolete DNA methylation or demethylation | 6 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0050896 | response to stimulus | 1 | 12 |
GO:0051716 | cellular response to stimulus | 2 | 12 |
GO:0070988 | demethylation | 2 | 2 |
GO:0070989 | oxidative demethylation | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0080111 | DNA demethylation | 3 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 2 |
GO:0005506 | iron ion binding | 6 | 2 |
GO:0008198 | ferrous iron binding | 7 | 2 |
GO:0016491 | oxidoreductase activity | 2 | 12 |
GO:0016705 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen | 3 | 2 |
GO:0016706 | 2-oxoglutarate-dependent dioxygenase activity | 4 | 2 |
GO:0032451 | demethylase activity | 2 | 2 |
GO:0035514 | DNA demethylase activity | 3 | 2 |
GO:0035515 | oxidative RNA demethylase activity | 3 | 2 |
GO:0035516 | oxidative DNA demethylase activity | 4 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043169 | cation binding | 3 | 2 |
GO:0046872 | metal ion binding | 4 | 2 |
GO:0046914 | transition metal ion binding | 5 | 2 |
GO:0051213 | dioxygenase activity | 3 | 12 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 2 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 2 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 109 | 113 | PF00656 | 0.468 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 18 | 20 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.601 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.502 |
CLV_PCSK_PC1ET2_1 | 4 | 6 | PF00082 | 0.407 |
CLV_PCSK_PC1ET2_1 | 44 | 46 | PF00082 | 0.406 |
CLV_PCSK_PC7_1 | 13 | 19 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.211 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 362 | 366 | PF00082 | 0.680 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.480 |
DEG_SCF_FBW7_1 | 304 | 309 | PF00400 | 0.379 |
DEG_SPOP_SBC_1 | 127 | 131 | PF00917 | 0.448 |
DOC_CDC14_PxL_1 | 81 | 89 | PF14671 | 0.305 |
DOC_MAPK_gen_1 | 166 | 175 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 44 | 52 | PF00069 | 0.521 |
DOC_PP2B_LxvP_1 | 280 | 283 | PF13499 | 0.501 |
DOC_PP4_FxxP_1 | 258 | 261 | PF00568 | 0.436 |
DOC_PP4_FxxP_1 | 352 | 355 | PF00568 | 0.497 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.436 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.379 |
LIG_14-3-3_CanoR_1 | 138 | 143 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 157 | 162 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 38 | 46 | PF00244 | 0.438 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.417 |
LIG_BRCT_BRCA1_1 | 230 | 234 | PF00533 | 0.411 |
LIG_EH1_1 | 201 | 209 | PF00400 | 0.440 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.482 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.411 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.444 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.469 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.435 |
LIG_LIR_Apic_2 | 130 | 136 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 156 | 165 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 243 | 250 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 264 | 273 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 307 | 318 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 156 | 161 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 243 | 249 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 264 | 269 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 3 | 9 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 307 | 313 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 324 | 329 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 80 | 84 | PF02991 | 0.350 |
LIG_LYPXL_yS_3 | 188 | 191 | PF13949 | 0.501 |
LIG_PCNA_PIPBox_1 | 195 | 204 | PF02747 | 0.411 |
LIG_SH2_CRK | 133 | 137 | PF00017 | 0.514 |
LIG_SH2_CRK | 246 | 250 | PF00017 | 0.431 |
LIG_SH2_SRC | 110 | 113 | PF00017 | 0.446 |
LIG_SH2_SRC | 133 | 136 | PF00017 | 0.454 |
LIG_SH2_STAP1 | 110 | 114 | PF00017 | 0.375 |
LIG_SH2_STAP1 | 144 | 148 | PF00017 | 0.509 |
LIG_SH2_STAP1 | 246 | 250 | PF00017 | 0.437 |
LIG_SH2_STAT3 | 192 | 195 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.389 |
LIG_SH3_1 | 17 | 23 | PF00018 | 0.610 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.599 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.515 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.524 |
LIG_SUMO_SIM_anti_2 | 171 | 177 | PF11976 | 0.493 |
LIG_TYR_ITIM | 199 | 204 | PF00017 | 0.248 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.352 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.332 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.277 |
MOD_CK2_1 | 308 | 314 | PF00069 | 0.446 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.627 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.308 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.384 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.413 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.411 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.248 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.248 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.663 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.279 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.332 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.266 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.339 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.333 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.691 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.282 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.205 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.403 |
MOD_PIKK_1 | 146 | 152 | PF00454 | 0.252 |
MOD_PIKK_1 | 235 | 241 | PF00454 | 0.391 |
MOD_PKA_1 | 13 | 19 | PF00069 | 0.605 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.574 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.336 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.511 |
MOD_PKB_1 | 155 | 163 | PF00069 | 0.300 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.288 |
MOD_Plk_2-3 | 285 | 291 | PF00069 | 0.295 |
MOD_Plk_2-3 | 37 | 43 | PF00069 | 0.444 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.319 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.276 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.203 |
MOD_SUMO_rev_2 | 37 | 46 | PF00179 | 0.399 |
TRG_DiLeu_BaEn_1 | 42 | 47 | PF01217 | 0.442 |
TRG_DiLeu_LyEn_5 | 42 | 47 | PF01217 | 0.442 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.206 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.391 |
TRG_ER_diArg_1 | 165 | 168 | PF00400 | 0.306 |
TRG_ER_diArg_1 | 17 | 19 | PF00400 | 0.620 |
TRG_ER_diArg_1 | 292 | 295 | PF00400 | 0.324 |
TRG_Pf-PMV_PEXEL_1 | 271 | 275 | PF00026 | 0.342 |
TRG_Pf-PMV_PEXEL_1 | 356 | 360 | PF00026 | 0.534 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAG0 | Leptomonas seymouri | 72% | 86% |
A0A0S4IYK4 | Bodo saltans | 46% | 95% |
A0A1X0PAI9 | Trypanosomatidae | 49% | 100% |
A0A3Q8IAB8 | Leishmania donovani | 95% | 100% |
A0A3R7NC97 | Trypanosoma rangeli | 48% | 90% |
A4H8G0 | Leishmania braziliensis | 83% | 100% |
A4HWT4 | Leishmania infantum | 95% | 100% |
C9ZLP0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AQJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q13686 | Homo sapiens | 29% | 95% |
Q54N08 | Dictyostelium discoideum | 26% | 94% |
Q9SA98 | Arabidopsis thaliana | 28% | 100% |
V5BRD6 | Trypanosoma cruzi | 51% | 98% |