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 |
Related structures:
AlphaFold database: A4HJT1
Term | Name | Level | Count |
---|---|---|---|
GO:0005975 | carbohydrate metabolic process | 3 | 12 |
GO:0006066 | alcohol metabolic process | 3 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009056 | catabolic process | 2 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016311 | dephosphorylation | 5 | 12 |
GO:0019637 | organophosphate metabolic process | 3 | 12 |
GO:0019751 | polyol metabolic process | 4 | 12 |
GO:0043647 | inositol phosphate metabolic process | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044262 | obsolete cellular carbohydrate metabolic process | 3 | 12 |
GO:0044281 | small molecule metabolic process | 2 | 12 |
GO:0044282 | small molecule catabolic process | 3 | 12 |
GO:0046164 | alcohol catabolic process | 4 | 12 |
GO:0046174 | polyol catabolic process | 5 | 12 |
GO:0046434 | organophosphate catabolic process | 4 | 12 |
GO:0046838 | obsolete phosphorylated carbohydrate dephosphorylation | 4 | 12 |
GO:0046855 | obsolete inositol phosphate dephosphorylation | 5 | 12 |
GO:0071545 | inositol phosphate catabolic process | 5 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901575 | organic substance catabolic process | 3 | 12 |
GO:1901615 | organic hydroxy compound metabolic process | 3 | 12 |
GO:1901616 | organic hydroxy compound catabolic process | 4 | 12 |
GO:0006629 | lipid metabolic process | 3 | 1 |
GO:0006644 | phospholipid metabolic process | 4 | 1 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 1 |
GO:0006661 | phosphatidylinositol biosynthetic process | 6 | 1 |
GO:0008610 | lipid biosynthetic process | 4 | 1 |
GO:0008654 | phospholipid biosynthetic process | 5 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 1 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 1 |
GO:0046486 | glycerolipid metabolic process | 4 | 1 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 1 |
GO:0046854 | phosphatidylinositol phosphate biosynthetic process | 7 | 1 |
GO:0090407 | organophosphate biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004441 | inositol-1,4-bisphosphate 1-phosphatase activity | 8 | 6 |
GO:0016312 | inositol bisphosphate phosphatase activity | 7 | 6 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 6 |
GO:0016791 | phosphatase activity | 5 | 6 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 6 |
GO:0052745 | inositol phosphate phosphatase activity | 6 | 6 |
GO:0005488 | binding | 1 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.367 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.211 |
DEG_SCF_FBW7_1 | 241 | 248 | PF00400 | 0.193 |
DEG_SPOP_SBC_1 | 396 | 400 | PF00917 | 0.439 |
DOC_CKS1_1 | 257 | 262 | PF01111 | 0.476 |
DOC_CKS1_1 | 344 | 349 | PF01111 | 0.217 |
DOC_CYCLIN_yCln2_LP_2 | 147 | 153 | PF00134 | 0.193 |
DOC_CYCLIN_yCln2_LP_2 | 257 | 263 | PF00134 | 0.405 |
DOC_CYCLIN_yCln2_LP_2 | 274 | 280 | PF00134 | 0.365 |
DOC_MAPK_DCC_7 | 247 | 255 | PF00069 | 0.326 |
DOC_MAPK_FxFP_2 | 229 | 232 | PF00069 | 0.417 |
DOC_MAPK_gen_1 | 184 | 191 | PF00069 | 0.278 |
DOC_MAPK_gen_1 | 288 | 294 | PF00069 | 0.193 |
DOC_MAPK_MEF2A_6 | 184 | 191 | PF00069 | 0.275 |
DOC_MAPK_MEF2A_6 | 247 | 255 | PF00069 | 0.326 |
DOC_PP1_RVXF_1 | 421 | 428 | PF00149 | 0.410 |
DOC_PP2B_LxvP_1 | 147 | 150 | PF13499 | 0.193 |
DOC_PP4_FxxP_1 | 190 | 193 | PF00568 | 0.247 |
DOC_PP4_FxxP_1 | 229 | 232 | PF00568 | 0.417 |
DOC_PP4_FxxP_1 | 351 | 354 | PF00568 | 0.274 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.318 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.521 |
DOC_USP7_UBL2_3 | 332 | 336 | PF12436 | 0.193 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.209 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.395 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.303 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.328 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.549 |
LIG_14-3-3_CanoR_1 | 108 | 117 | PF00244 | 0.314 |
LIG_14-3-3_CanoR_1 | 15 | 19 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 234 | 241 | PF00244 | 0.223 |
LIG_14-3-3_CanoR_1 | 288 | 293 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 307 | 314 | PF00244 | 0.348 |
LIG_Actin_WH2_2 | 218 | 236 | PF00022 | 0.318 |
LIG_APCC_ABBA_1 | 173 | 178 | PF00400 | 0.369 |
LIG_APCC_ABBA_1 | 187 | 192 | PF00400 | 0.209 |
LIG_APCC_ABBAyCdc20_2 | 186 | 192 | PF00400 | 0.247 |
LIG_BIR_III_4 | 391 | 395 | PF00653 | 0.326 |
LIG_BRCT_BRCA1_1 | 110 | 114 | PF00533 | 0.472 |
LIG_EH1_1 | 22 | 30 | PF00400 | 0.292 |
LIG_eIF4E_1 | 23 | 29 | PF01652 | 0.232 |
LIG_eIF4E_1 | 325 | 331 | PF01652 | 0.417 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.290 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.308 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.392 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.472 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.501 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.191 |
LIG_FHA_2 | 297 | 303 | PF00498 | 0.368 |
LIG_FHA_2 | 308 | 314 | PF00498 | 0.368 |
LIG_FHA_2 | 344 | 350 | PF00498 | 0.368 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.399 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.187 |
LIG_LIR_Apic_2 | 202 | 208 | PF02991 | 0.279 |
LIG_LIR_Apic_2 | 349 | 354 | PF02991 | 0.274 |
LIG_LIR_Gen_1 | 154 | 164 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 264 | 274 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 111 | 117 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 142 | 147 | PF02991 | 0.215 |
LIG_LIR_Nem_3 | 154 | 159 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 264 | 269 | PF02991 | 0.403 |
LIG_LYPXL_yS_3 | 387 | 390 | PF13949 | 0.350 |
LIG_NRBOX | 304 | 310 | PF00104 | 0.326 |
LIG_Pex14_2 | 369 | 373 | PF04695 | 0.193 |
LIG_PTB_Apo_2 | 223 | 230 | PF02174 | 0.274 |
LIG_SH2_CRK | 144 | 148 | PF00017 | 0.417 |
LIG_SH2_CRK | 156 | 160 | PF00017 | 0.193 |
LIG_SH2_CRK | 328 | 332 | PF00017 | 0.417 |
LIG_SH2_PTP2 | 23 | 26 | PF00017 | 0.235 |
LIG_SH2_STAP1 | 151 | 155 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.225 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.318 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.192 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.247 |
LIG_SH3_3 | 341 | 347 | PF00018 | 0.429 |
LIG_SH3_3 | 349 | 355 | PF00018 | 0.408 |
LIG_SUMO_SIM_par_1 | 409 | 414 | PF11976 | 0.453 |
LIG_SUMO_SIM_par_1 | 55 | 61 | PF11976 | 0.339 |
LIG_TYR_ITIM | 385 | 390 | PF00017 | 0.334 |
LIG_UBA3_1 | 25 | 30 | PF00899 | 0.248 |
LIG_UBA3_1 | 330 | 336 | PF00899 | 0.193 |
LIG_WRC_WIRS_1 | 370 | 375 | PF05994 | 0.193 |
MOD_CDK_SPxK_1 | 241 | 247 | PF00069 | 0.193 |
MOD_CDK_SPxxK_3 | 411 | 418 | PF00069 | 0.344 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.281 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.472 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.531 |
MOD_CK2_1 | 296 | 302 | PF00069 | 0.417 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.417 |
MOD_CK2_1 | 396 | 402 | PF00069 | 0.519 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.260 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.547 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.281 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.272 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.473 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.552 |
MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.642 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.405 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.466 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.303 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.249 |
MOD_PIKK_1 | 307 | 313 | PF00454 | 0.395 |
MOD_PKA_1 | 288 | 294 | PF00069 | 0.402 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.316 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.264 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.369 |
MOD_Plk_1 | 36 | 42 | PF00069 | 0.402 |
MOD_Plk_1 | 401 | 407 | PF00069 | 0.313 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.274 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.242 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.259 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.547 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.388 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.343 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.209 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.395 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.303 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.328 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.451 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.653 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.555 |
MOD_SUMO_for_1 | 417 | 420 | PF00179 | 0.250 |
MOD_SUMO_rev_2 | 76 | 81 | PF00179 | 0.193 |
TRG_DiLeu_BaLyEn_6 | 304 | 309 | PF01217 | 0.350 |
TRG_DiLeu_BaLyEn_6 | 385 | 390 | PF01217 | 0.193 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.235 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.334 |
TRG_ER_diArg_1 | 183 | 186 | PF00400 | 0.308 |
TRG_ER_diArg_1 | 423 | 425 | PF00400 | 0.382 |
TRG_Pf-PMV_PEXEL_1 | 108 | 112 | PF00026 | 0.303 |
TRG_Pf-PMV_PEXEL_1 | 307 | 311 | PF00026 | 0.326 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4U3 | Leptomonas seymouri | 56% | 100% |
A0A0S4ISE9 | Bodo saltans | 31% | 88% |
A0A1X0NIY3 | Trypanosomatidae | 39% | 100% |
A0A3R7KA15 | Trypanosoma rangeli | 37% | 100% |
A0A3S5H7Q8 | Leishmania donovani | 76% | 100% |
A4I797 | Leishmania infantum | 76% | 100% |
C9ZWL1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9B292 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
Q4Q5W6 | Leishmania major | 72% | 100% |
V5AS37 | Trypanosoma cruzi | 38% | 100% |