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 |
Related structures:
AlphaFold database: A4I1Q1
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 18 |
GO:0016787 | hydrolase activity | 2 | 18 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 18 |
GO:0016791 | phosphatase activity | 5 | 18 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 18 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 111 | 115 | PF00656 | 0.559 |
CLV_C14_Caspase3-7 | 345 | 349 | PF00656 | 0.373 |
CLV_Separin_Metazoa | 326 | 330 | PF03568 | 0.395 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.739 |
DEG_SCF_FBW7_1 | 76 | 81 | PF00400 | 0.521 |
DEG_SPOP_SBC_1 | 39 | 43 | PF00917 | 0.710 |
DOC_CDC14_PxL_1 | 328 | 336 | PF14671 | 0.352 |
DOC_CYCLIN_yCln2_LP_2 | 171 | 177 | PF00134 | 0.541 |
DOC_MAPK_gen_1 | 179 | 188 | PF00069 | 0.298 |
DOC_MAPK_gen_1 | 260 | 269 | PF00069 | 0.441 |
DOC_MAPK_MEF2A_6 | 179 | 188 | PF00069 | 0.301 |
DOC_MAPK_MEF2A_6 | 202 | 211 | PF00069 | 0.260 |
DOC_MAPK_MEF2A_6 | 213 | 221 | PF00069 | 0.243 |
DOC_MAPK_NFAT4_5 | 181 | 189 | PF00069 | 0.291 |
DOC_MAPK_RevD_3 | 168 | 182 | PF00069 | 0.371 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.241 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.650 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.338 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.527 |
LIG_APCC_ABBA_1 | 267 | 272 | PF00400 | 0.318 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.541 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.438 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.280 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.351 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.795 |
LIG_FHA_2 | 247 | 253 | PF00498 | 0.470 |
LIG_FHA_2 | 340 | 346 | PF00498 | 0.354 |
LIG_LIR_Apic_2 | 248 | 253 | PF02991 | 0.278 |
LIG_LIR_Gen_1 | 341 | 352 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 12 | 18 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 341 | 347 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 348 | 353 | PF02991 | 0.311 |
LIG_MYND_1 | 168 | 172 | PF01753 | 0.457 |
LIG_REV1ctd_RIR_1 | 12 | 20 | PF16727 | 0.516 |
LIG_SH2_CRK | 350 | 354 | PF00017 | 0.285 |
LIG_SH2_GRB2like | 197 | 200 | PF00017 | 0.228 |
LIG_SH2_STAP1 | 203 | 207 | PF00017 | 0.362 |
LIG_SH2_STAT3 | 305 | 308 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 305 | 308 | PF00017 | 0.267 |
LIG_SH3_2 | 49 | 54 | PF14604 | 0.549 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.338 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.646 |
LIG_SUMO_SIM_anti_2 | 284 | 289 | PF11976 | 0.234 |
LIG_SUMO_SIM_anti_2 | 293 | 299 | PF11976 | 0.225 |
LIG_SUMO_SIM_par_1 | 184 | 191 | PF11976 | 0.307 |
LIG_SUMO_SIM_par_1 | 207 | 212 | PF11976 | 0.430 |
LIG_UBA3_1 | 254 | 260 | PF00899 | 0.352 |
MOD_CDC14_SPxK_1 | 51 | 54 | PF00782 | 0.550 |
MOD_CDK_SPxK_1 | 48 | 54 | PF00069 | 0.549 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.669 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.627 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.250 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.655 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.636 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.579 |
MOD_CK2_1 | 319 | 325 | PF00069 | 0.356 |
MOD_GlcNHglycan | 109 | 113 | PF01048 | 0.641 |
MOD_GlcNHglycan | 114 | 118 | PF01048 | 0.608 |
MOD_GlcNHglycan | 163 | 167 | PF01048 | 0.507 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.820 |
MOD_GlcNHglycan | 361 | 365 | PF01048 | 0.554 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.637 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.750 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.641 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.501 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.309 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.274 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.416 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.638 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.605 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.619 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.632 |
MOD_N-GLC_1 | 157 | 162 | PF02516 | 0.403 |
MOD_N-GLC_1 | 7 | 12 | PF02516 | 0.741 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.317 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.308 |
MOD_PIKK_1 | 21 | 27 | PF00454 | 0.570 |
MOD_PIKK_1 | 81 | 87 | PF00454 | 0.536 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.370 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.556 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.774 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.305 |
MOD_Plk_1 | 283 | 289 | PF00069 | 0.284 |
MOD_Plk_2-3 | 339 | 345 | PF00069 | 0.404 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.512 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.391 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.316 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.305 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.263 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.309 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.328 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.553 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.449 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.338 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.680 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.653 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.611 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.695 |
TRG_DiLeu_BaEn_1 | 326 | 331 | PF01217 | 0.292 |
TRG_DiLeu_LyEn_5 | 326 | 331 | PF01217 | 0.302 |
TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.319 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.320 |
TRG_ER_diArg_1 | 137 | 140 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 148 | 151 | PF00400 | 0.344 |
TRG_Pf-PMV_PEXEL_1 | 290 | 294 | PF00026 | 0.323 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PG96 | Leptomonas seymouri | 68% | 100% |
A0A0S4IJH3 | Bodo saltans | 46% | 100% |
A0A0S4IMS1 | Bodo saltans | 65% | 100% |
A0A0S4JCX0 | Bodo saltans | 46% | 100% |
A0A1X0NYI7 | Trypanosomatidae | 45% | 91% |
A0A3Q8IDG4 | Leishmania donovani | 100% | 100% |
A0A3S7WZH2 | Leishmania donovani | 52% | 100% |
A0A422P4K3 | Trypanosoma rangeli | 40% | 89% |
A4HEA5 | Leishmania braziliensis | 88% | 100% |
A4HEM1 | Leishmania braziliensis | 50% | 100% |
A4I1V3 | Leishmania infantum | 51% | 100% |
A4ICB8 | Leishmania infantum | 27% | 100% |
C9ZKA3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 87% |
E9AXT5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
E9AXZ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 100% |
Q4Q9H6 | Leishmania major | 51% | 100% |
Q4Q9N6 | Leishmania major | 96% | 100% |
V5BAV0 | Trypanosoma cruzi | 24% | 100% |