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: 7, no: 4 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0020022 | acidocalcisome | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AT24
Term | Name | Level | Count |
---|---|---|---|
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016311 | dephosphorylation | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 2 |
GO:0016791 | phosphatase activity | 5 | 2 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 2 |
GO:0003993 | acid phosphatase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 241 | 245 | PF00656 | 0.329 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.452 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.293 |
CLV_PCSK_PC1ET2_1 | 92 | 94 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.479 |
DEG_APCC_DBOX_1 | 296 | 304 | PF00400 | 0.433 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.736 |
DOC_CKS1_1 | 387 | 392 | PF01111 | 0.334 |
DOC_MAPK_MEF2A_6 | 270 | 278 | PF00069 | 0.368 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.325 |
DOC_USP7_UBL2_3 | 49 | 53 | PF12436 | 0.596 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.355 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.324 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.420 |
LIG_14-3-3_CanoR_1 | 117 | 121 | PF00244 | 0.309 |
LIG_14-3-3_CanoR_1 | 142 | 150 | PF00244 | 0.333 |
LIG_14-3-3_CanoR_1 | 270 | 275 | PF00244 | 0.313 |
LIG_14-3-3_CanoR_1 | 384 | 388 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 420 | 424 | PF00244 | 0.245 |
LIG_14-3-3_CanoR_1 | 5 | 12 | PF00244 | 0.756 |
LIG_Actin_WH2_2 | 239 | 257 | PF00022 | 0.521 |
LIG_APCC_ABBA_1 | 172 | 177 | PF00400 | 0.274 |
LIG_APCC_ABBA_1 | 367 | 372 | PF00400 | 0.435 |
LIG_CSL_BTD_1 | 387 | 390 | PF09270 | 0.369 |
LIG_DLG_GKlike_1 | 270 | 277 | PF00625 | 0.320 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.422 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.511 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.372 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.503 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.667 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.372 |
LIG_FHA_2 | 20 | 26 | PF00498 | 0.699 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.337 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.393 |
LIG_FHA_2 | 432 | 438 | PF00498 | 0.407 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.568 |
LIG_LIR_Gen_1 | 119 | 128 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 203 | 213 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 234 | 243 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 289 | 296 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 379 | 390 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 424 | 435 | PF02991 | 0.386 |
LIG_LIR_LC3C_4 | 63 | 67 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 109 | 115 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 119 | 123 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 234 | 239 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 289 | 293 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 424 | 430 | PF02991 | 0.346 |
LIG_PCNA_PIPBox_1 | 275 | 284 | PF02747 | 0.367 |
LIG_PCNA_yPIPBox_3 | 270 | 282 | PF02747 | 0.373 |
LIG_Pex14_2 | 155 | 159 | PF04695 | 0.308 |
LIG_Pex14_2 | 171 | 175 | PF04695 | 0.274 |
LIG_Pex14_2 | 338 | 342 | PF04695 | 0.337 |
LIG_Rb_pABgroove_1 | 276 | 284 | PF01858 | 0.299 |
LIG_SH2_CRK | 236 | 240 | PF00017 | 0.387 |
LIG_SH2_CRK | 395 | 399 | PF00017 | 0.306 |
LIG_SH2_NCK_1 | 346 | 350 | PF00017 | 0.396 |
LIG_SH2_SRC | 164 | 167 | PF00017 | 0.350 |
LIG_SH2_SRC | 236 | 239 | PF00017 | 0.459 |
LIG_SH2_SRC | 28 | 31 | PF00017 | 0.626 |
LIG_SH2_STAP1 | 94 | 98 | PF00017 | 0.310 |
LIG_SH2_STAT3 | 433 | 436 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.259 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 433 | 436 | PF00017 | 0.415 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.274 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.274 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.329 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.341 |
LIG_SUMO_SIM_anti_2 | 63 | 69 | PF11976 | 0.372 |
LIG_TRAF2_1 | 321 | 324 | PF00917 | 0.382 |
LIG_TRAF2_1 | 434 | 437 | PF00917 | 0.538 |
LIG_TRAF2_2 | 312 | 317 | PF00917 | 0.653 |
LIG_WRC_WIRS_1 | 206 | 211 | PF05994 | 0.356 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.294 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.584 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.730 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.421 |
MOD_CK2_1 | 431 | 437 | PF00069 | 0.387 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.552 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.274 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.229 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.720 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.307 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.671 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.474 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.362 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.616 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.420 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.546 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.318 |
MOD_N-GLC_1 | 128 | 133 | PF02516 | 0.205 |
MOD_N-GLC_1 | 270 | 275 | PF02516 | 0.321 |
MOD_N-GLC_1 | 303 | 308 | PF02516 | 0.477 |
MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.572 |
MOD_N-GLC_1 | 376 | 381 | PF02516 | 0.592 |
MOD_N-GLC_1 | 431 | 436 | PF02516 | 0.348 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.524 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.183 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.502 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.448 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.370 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.329 |
MOD_NEK2_2 | 398 | 403 | PF00069 | 0.378 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.543 |
MOD_PKA_2 | 116 | 122 | PF00069 | 0.388 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.396 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.319 |
MOD_Plk_1 | 108 | 114 | PF00069 | 0.169 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.205 |
MOD_Plk_1 | 24 | 30 | PF00069 | 0.691 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.320 |
MOD_Plk_1 | 303 | 309 | PF00069 | 0.529 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.354 |
MOD_Plk_2-3 | 205 | 211 | PF00069 | 0.257 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.276 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.652 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.452 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.388 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.345 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.306 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.349 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.572 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.331 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.433 |
MOD_SUMO_rev_2 | 406 | 413 | PF00179 | 0.401 |
MOD_SUMO_rev_2 | 45 | 55 | PF00179 | 0.567 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.289 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.337 |
TRG_ER_diArg_1 | 191 | 193 | PF00400 | 0.393 |
TRG_NES_CRM1_1 | 264 | 275 | PF08389 | 0.365 |
TRG_Pf-PMV_PEXEL_1 | 297 | 301 | PF00026 | 0.432 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKN6 | Leptomonas seymouri | 76% | 97% |
A0A0S4JT27 | Bodo saltans | 50% | 100% |
A0A1X0P7L7 | Trypanosomatidae | 59% | 92% |
A0A3S7XAY1 | Leishmania donovani | 91% | 100% |
A0A422NCB6 | Trypanosoma rangeli | 58% | 97% |
A4HPB3 | Leishmania braziliensis | 79% | 100% |
A4ICF3 | Leishmania infantum | 92% | 100% |
D0A3C2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 100% |
Q4Q1H4 | Leishmania major | 91% | 100% |
V5BCK5 | Trypanosoma cruzi | 59% | 98% |