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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4HFP3
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 8 |
GO:0004722 | protein serine/threonine phosphatase activity | 4 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0016787 | hydrolase activity | 2 | 8 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 8 |
GO:0016791 | phosphatase activity | 5 | 8 |
GO:0017018 | myosin phosphatase activity | 5 | 8 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043169 | cation binding | 3 | 8 |
GO:0046872 | metal ion binding | 4 | 8 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 184 | 188 | PF00656 | 0.609 |
CLV_C14_Caspase3-7 | 212 | 216 | PF00656 | 0.332 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.530 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.417 |
DEG_APCC_DBOX_1 | 335 | 343 | PF00400 | 0.456 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.613 |
DOC_CYCLIN_yCln2_LP_2 | 248 | 254 | PF00134 | 0.451 |
DOC_MAPK_MEF2A_6 | 263 | 272 | PF00069 | 0.427 |
DOC_MAPK_MEF2A_6 | 385 | 393 | PF00069 | 0.398 |
DOC_PP1_RVXF_1 | 1 | 8 | PF00149 | 0.510 |
DOC_PP1_RVXF_1 | 9 | 16 | PF00149 | 0.340 |
DOC_PP2B_LxvP_1 | 268 | 271 | PF13499 | 0.408 |
DOC_PP4_FxxP_1 | 415 | 418 | PF00568 | 0.544 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.407 |
DOC_USP7_UBL2_3 | 125 | 129 | PF12436 | 0.336 |
DOC_USP7_UBL2_3 | 259 | 263 | PF12436 | 0.310 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.372 |
LIG_14-3-3_CanoR_1 | 18 | 24 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 194 | 201 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 207 | 217 | PF00244 | 0.447 |
LIG_APCC_ABBA_1 | 298 | 303 | PF00400 | 0.403 |
LIG_Clathr_ClatBox_1 | 269 | 273 | PF01394 | 0.407 |
LIG_EH1_1 | 291 | 299 | PF00400 | 0.330 |
LIG_eIF4E_1 | 75 | 81 | PF01652 | 0.445 |
LIG_FAT_LD_1 | 339 | 347 | PF03623 | 0.285 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.375 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.461 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.307 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.383 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.379 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.440 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.431 |
LIG_FHA_2 | 335 | 341 | PF00498 | 0.536 |
LIG_IRF3_LxIS_1 | 136 | 141 | PF10401 | 0.340 |
LIG_LIR_Apic_2 | 412 | 418 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 283 | 294 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 34 | 45 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 126 | 131 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 283 | 289 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 296 | 302 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 325 | 329 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 87 | 92 | PF02991 | 0.395 |
LIG_NRBOX | 334 | 340 | PF00104 | 0.470 |
LIG_SH2_CRK | 128 | 132 | PF00017 | 0.288 |
LIG_SH2_GRB2like | 96 | 99 | PF00017 | 0.285 |
LIG_SH2_STAP1 | 329 | 333 | PF00017 | 0.398 |
LIG_SH2_STAP1 | 64 | 68 | PF00017 | 0.338 |
LIG_SH2_STAT3 | 250 | 253 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 75 | 78 | PF00017 | 0.434 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.482 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.393 |
LIG_SUMO_SIM_anti_2 | 276 | 283 | PF11976 | 0.340 |
LIG_SUMO_SIM_par_1 | 107 | 114 | PF11976 | 0.300 |
LIG_SUMO_SIM_par_1 | 129 | 134 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 387 | 394 | PF11976 | 0.395 |
LIG_TRAF2_1 | 118 | 121 | PF00917 | 0.511 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.540 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.585 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.429 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.641 |
MOD_CK2_1 | 406 | 412 | PF00069 | 0.595 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.280 |
MOD_Cter_Amidation | 9 | 12 | PF01082 | 0.479 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.455 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.595 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.761 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.459 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.479 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.318 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.394 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.528 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.420 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.364 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.377 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.425 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.389 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.378 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.632 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.368 |
MOD_NEK2_1 | 391 | 396 | PF00069 | 0.393 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.272 |
MOD_NEK2_2 | 85 | 90 | PF00069 | 0.413 |
MOD_PKA_1 | 11 | 17 | PF00069 | 0.361 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.380 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.326 |
MOD_PKB_1 | 236 | 244 | PF00069 | 0.288 |
MOD_Plk_1 | 171 | 177 | PF00069 | 0.644 |
MOD_Plk_1 | 225 | 231 | PF00069 | 0.305 |
MOD_Plk_1 | 355 | 361 | PF00069 | 0.305 |
MOD_Plk_1 | 387 | 393 | PF00069 | 0.330 |
MOD_Plk_1 | 411 | 417 | PF00069 | 0.399 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.376 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.271 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.371 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.538 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.330 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.391 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.448 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.366 |
TRG_DiLeu_BaLyEn_6 | 264 | 269 | PF01217 | 0.427 |
TRG_DiLeu_BaLyEn_6 | 87 | 92 | PF01217 | 0.399 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.425 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 236 | 239 | PF00400 | 0.283 |
TRG_Pf-PMV_PEXEL_1 | 304 | 308 | PF00026 | 0.294 |
TRG_Pf-PMV_PEXEL_1 | 336 | 340 | PF00026 | 0.460 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC93 | Leptomonas seymouri | 60% | 100% |
A0A0S4JF75 | Bodo saltans | 29% | 81% |
A0A3S7X0P0 | Leishmania donovani | 78% | 100% |
A4I2R9 | Leishmania infantum | 78% | 100% |
E9AD96 | Leishmania major | 76% | 100% |
E9AZ21 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |