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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4H6M7
Term | Name | Level | Count |
---|---|---|---|
GO:0005975 | carbohydrate metabolic process | 3 | 1 |
GO:0006066 | alcohol metabolic process | 3 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 3 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 3 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009987 | cellular process | 1 | 3 |
GO:0016311 | dephosphorylation | 5 | 3 |
GO:0019637 | organophosphate metabolic process | 3 | 3 |
GO:0019751 | polyol metabolic process | 4 | 1 |
GO:0019932 | second-messenger-mediated signaling | 4 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0043647 | inositol phosphate metabolic process | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0044262 | obsolete cellular carbohydrate metabolic process | 3 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0044282 | small molecule catabolic process | 3 | 1 |
GO:0046164 | alcohol catabolic process | 4 | 1 |
GO:0046174 | polyol catabolic process | 5 | 1 |
GO:0046434 | organophosphate catabolic process | 4 | 1 |
GO:0046838 | obsolete phosphorylated carbohydrate dephosphorylation | 4 | 1 |
GO:0046855 | obsolete inositol phosphate dephosphorylation | 5 | 1 |
GO:0048016 | inositol phosphate-mediated signaling | 5 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071545 | inositol phosphate catabolic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:1901615 | organic hydroxy compound metabolic process | 3 | 1 |
GO:1901616 | organic hydroxy compound catabolic process | 4 | 1 |
GO:0006629 | lipid metabolic process | 3 | 2 |
GO:0006644 | phospholipid metabolic process | 4 | 2 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 2 |
GO:0030258 | lipid modification | 4 | 2 |
GO:0044255 | cellular lipid metabolic process | 3 | 2 |
GO:0046486 | glycerolipid metabolic process | 4 | 2 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 2 |
GO:0046839 | phospholipid dephosphorylation | 5 | 2 |
GO:0046856 | phosphatidylinositol dephosphorylation | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004445 | inositol-polyphosphate 5-phosphatase activity | 8 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 11 |
GO:0016791 | phosphatase activity | 5 | 11 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 11 |
GO:0046030 | inositol trisphosphate phosphatase activity | 7 | 11 |
GO:0052658 | inositol-1,4,5-trisphosphate 5-phosphatase activity | 8 | 9 |
GO:0052659 | inositol-1,3,4,5-tetrakisphosphate 5-phosphatase activity | 8 | 9 |
GO:0052743 | inositol tetrakisphosphate phosphatase activity | 7 | 9 |
GO:0052745 | inositol phosphate phosphatase activity | 6 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 431 | 435 | PF00656 | 0.572 |
CLV_MEL_PAP_1 | 143 | 149 | PF00089 | 0.250 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.350 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.769 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 233 | 235 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.769 |
CLV_PCSK_PC1ET2_1 | 233 | 235 | PF00082 | 0.515 |
CLV_PCSK_PC7_1 | 229 | 235 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 166 | 170 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.462 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.586 |
DEG_SPOP_SBC_1 | 10 | 14 | PF00917 | 0.544 |
DOC_AGCK_PIF_3 | 464 | 467 | PF00069 | 0.457 |
DOC_CYCLIN_RxL_1 | 25 | 35 | PF00134 | 0.505 |
DOC_CYCLIN_yCln2_LP_2 | 197 | 203 | PF00134 | 0.361 |
DOC_MAPK_gen_1 | 135 | 145 | PF00069 | 0.470 |
DOC_MAPK_MEF2A_6 | 137 | 145 | PF00069 | 0.437 |
DOC_MAPK_NFAT4_5 | 138 | 146 | PF00069 | 0.375 |
DOC_PP1_RVXF_1 | 26 | 33 | PF00149 | 0.505 |
DOC_PP1_RVXF_1 | 394 | 400 | PF00149 | 0.311 |
DOC_PP2B_LxvP_1 | 100 | 103 | PF13499 | 0.514 |
DOC_PP2B_LxvP_1 | 358 | 361 | PF13499 | 0.521 |
DOC_PP4_FxxP_1 | 245 | 248 | PF00568 | 0.421 |
DOC_PP4_FxxP_1 | 88 | 91 | PF00568 | 0.561 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.447 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.417 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.372 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.592 |
LIG_14-3-3_CanoR_1 | 28 | 33 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 355 | 361 | PF00244 | 0.658 |
LIG_APCC_ABBA_1 | 157 | 162 | PF00400 | 0.327 |
LIG_APCC_ABBA_1 | 201 | 206 | PF00400 | 0.302 |
LIG_BRCT_BRCA1_1 | 126 | 130 | PF00533 | 0.467 |
LIG_BRCT_BRCA1_1 | 143 | 147 | PF00533 | 0.228 |
LIG_BRCT_BRCA1_1 | 84 | 88 | PF00533 | 0.439 |
LIG_deltaCOP1_diTrp_1 | 239 | 245 | PF00928 | 0.368 |
LIG_eIF4E_1 | 450 | 456 | PF01652 | 0.420 |
LIG_eIF4E_1 | 63 | 69 | PF01652 | 0.450 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.718 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.689 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.806 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.571 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.431 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.583 |
LIG_FHA_2 | 456 | 462 | PF00498 | 0.513 |
LIG_FHA_2 | 62 | 68 | PF00498 | 0.559 |
LIG_LIR_Apic_2 | 243 | 248 | PF02991 | 0.423 |
LIG_LIR_Apic_2 | 85 | 91 | PF02991 | 0.554 |
LIG_LIR_Gen_1 | 239 | 248 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 461 | 467 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 77 | 88 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 106 | 110 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 239 | 245 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 287 | 291 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 445 | 450 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 461 | 467 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 77 | 83 | PF02991 | 0.508 |
LIG_PDZ_Class_2 | 462 | 467 | PF00595 | 0.305 |
LIG_Pex14_2 | 241 | 245 | PF04695 | 0.378 |
LIG_Rb_LxCxE_1 | 231 | 253 | PF01857 | 0.438 |
LIG_SH2_NCK_1 | 450 | 454 | PF00017 | 0.559 |
LIG_SH2_PTP2 | 107 | 110 | PF00017 | 0.506 |
LIG_SH2_SRC | 107 | 110 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.725 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.516 |
LIG_SH3_3 | 351 | 357 | PF00018 | 0.783 |
LIG_SH3_3 | 358 | 364 | PF00018 | 0.707 |
LIG_SUMO_SIM_anti_2 | 268 | 274 | PF11976 | 0.411 |
LIG_SUMO_SIM_anti_2 | 452 | 459 | PF11976 | 0.505 |
LIG_SUMO_SIM_par_1 | 192 | 199 | PF11976 | 0.390 |
LIG_SUMO_SIM_par_1 | 339 | 345 | PF11976 | 0.488 |
LIG_TRAF2_1 | 342 | 345 | PF00917 | 0.489 |
LIG_WW_2 | 361 | 364 | PF00397 | 0.467 |
MOD_CDC14_SPxK_1 | 379 | 382 | PF00782 | 0.573 |
MOD_CDK_SPK_2 | 87 | 92 | PF00069 | 0.565 |
MOD_CDK_SPxK_1 | 376 | 382 | PF00069 | 0.586 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.725 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.432 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.588 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.683 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.355 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.523 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.367 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.488 |
MOD_Cter_Amidation | 177 | 180 | PF01082 | 0.397 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.378 |
MOD_GlcNHglycan | 190 | 194 | PF01048 | 0.480 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.656 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.639 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.590 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.647 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.550 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.565 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.737 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.443 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.803 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.608 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.570 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.572 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.699 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.424 |
MOD_N-GLC_1 | 35 | 40 | PF02516 | 0.700 |
MOD_N-GLC_1 | 59 | 64 | PF02516 | 0.522 |
MOD_N-GLC_2 | 153 | 155 | PF02516 | 0.428 |
MOD_N-GLC_2 | 384 | 386 | PF02516 | 0.459 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.502 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.320 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.472 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.630 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.775 |
MOD_OFUCOSY | 441 | 446 | PF10250 | 0.415 |
MOD_PIKK_1 | 247 | 253 | PF00454 | 0.591 |
MOD_PIKK_1 | 312 | 318 | PF00454 | 0.489 |
MOD_PIKK_1 | 321 | 327 | PF00454 | 0.489 |
MOD_PIKK_1 | 416 | 422 | PF00454 | 0.579 |
MOD_PKA_1 | 28 | 34 | PF00069 | 0.651 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.545 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.596 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.710 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.468 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.488 |
MOD_Plk_1 | 59 | 65 | PF00069 | 0.464 |
MOD_Plk_2-3 | 243 | 249 | PF00069 | 0.300 |
MOD_Plk_2-3 | 339 | 345 | PF00069 | 0.488 |
MOD_Plk_2-3 | 67 | 73 | PF00069 | 0.431 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.391 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.581 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.417 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.375 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.518 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.586 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.586 |
MOD_SUMO_rev_2 | 206 | 216 | PF00179 | 0.413 |
MOD_SUMO_rev_2 | 218 | 224 | PF00179 | 0.342 |
TRG_DiLeu_BaEn_1 | 261 | 266 | PF01217 | 0.334 |
TRG_ENDOCYTIC_2 | 107 | 110 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 288 | 291 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 450 | 453 | PF00928 | 0.450 |
TRG_ER_diArg_1 | 16 | 19 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 179 | 182 | PF00400 | 0.419 |
TRG_ER_diArg_1 | 254 | 257 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 28 | 30 | PF00400 | 0.695 |
TRG_ER_diArg_1 | 352 | 355 | PF00400 | 0.653 |
TRG_NLS_MonoExtN_4 | 230 | 237 | PF00514 | 0.506 |
TRG_Pf-PMV_PEXEL_1 | 214 | 218 | PF00026 | 0.293 |
TRG_Pf-PMV_PEXEL_1 | 28 | 33 | PF00026 | 0.505 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2E4 | Leptomonas seymouri | 53% | 70% |
A0A1X0NVI9 | Trypanosomatidae | 37% | 80% |
A0A3S5H6J4 | Leishmania donovani | 75% | 68% |
A0A422NRL6 | Trypanosoma rangeli | 39% | 81% |
A4HV10 | Leishmania infantum | 75% | 68% |
D0A7D8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 83% |
E9ANP5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 68% |
Q4QGX8 | Leishmania major | 73% | 100% |
V5DT49 | Trypanosoma cruzi | 41% | 100% |