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: A0A3S7XAY1
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 | 0.389 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.754 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.482 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.754 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.348 |
CLV_PCSK_PC1ET2_1 | 204 | 206 | PF00082 | 0.570 |
CLV_PCSK_PC1ET2_1 | 92 | 94 | PF00082 | 0.449 |
CLV_PCSK_PC7_1 | 200 | 206 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 53 | 57 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.473 |
DEG_APCC_DBOX_1 | 296 | 304 | PF00400 | 0.557 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.742 |
DOC_CKS1_1 | 387 | 392 | PF01111 | 0.374 |
DOC_MAPK_gen_1 | 258 | 267 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 270 | 278 | PF00069 | 0.391 |
DOC_MAPK_MEF2A_6 | 380 | 387 | PF00069 | 0.335 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.377 |
DOC_USP7_UBL2_3 | 49 | 53 | PF12436 | 0.600 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.409 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.363 |
LIG_14-3-3_CanoR_1 | 142 | 150 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 270 | 275 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 384 | 388 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 5 | 12 | PF00244 | 0.763 |
LIG_Actin_WH2_2 | 239 | 257 | PF00022 | 0.533 |
LIG_AP2alpha_1 | 155 | 159 | PF02296 | 0.353 |
LIG_APCC_ABBA_1 | 172 | 177 | PF00400 | 0.422 |
LIG_APCC_ABBA_1 | 367 | 372 | PF00400 | 0.551 |
LIG_CSL_BTD_1 | 387 | 390 | PF09270 | 0.409 |
LIG_DLG_GKlike_1 | 270 | 277 | PF00625 | 0.376 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.546 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.414 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.687 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.378 |
LIG_FHA_2 | 20 | 26 | PF00498 | 0.736 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.397 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.486 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.569 |
LIG_LIR_Apic_2 | 228 | 232 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 126 | 135 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 203 | 213 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 234 | 243 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 289 | 296 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 379 | 390 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 424 | 435 | PF02991 | 0.441 |
LIG_LIR_LC3C_4 | 63 | 67 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 109 | 115 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 234 | 239 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 289 | 293 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 379 | 385 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 386 | 391 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 424 | 430 | PF02991 | 0.402 |
LIG_PCNA_PIPBox_1 | 275 | 284 | PF02747 | 0.420 |
LIG_PCNA_yPIPBox_3 | 270 | 282 | PF02747 | 0.408 |
LIG_Pex14_2 | 155 | 159 | PF04695 | 0.357 |
LIG_Pex14_2 | 171 | 175 | PF04695 | 0.338 |
LIG_Pex14_2 | 338 | 342 | PF04695 | 0.390 |
LIG_Rb_pABgroove_1 | 276 | 284 | PF01858 | 0.356 |
LIG_SH2_CRK | 236 | 240 | PF00017 | 0.444 |
LIG_SH2_CRK | 391 | 395 | PF00017 | 0.537 |
LIG_SH2_GRB2like | 206 | 209 | PF00017 | 0.450 |
LIG_SH2_NCK_1 | 346 | 350 | PF00017 | 0.448 |
LIG_SH2_PTP2 | 229 | 232 | PF00017 | 0.622 |
LIG_SH2_PTP2 | 382 | 385 | PF00017 | 0.354 |
LIG_SH2_SRC | 164 | 167 | PF00017 | 0.644 |
LIG_SH2_SRC | 236 | 239 | PF00017 | 0.502 |
LIG_SH2_STAP1 | 374 | 378 | PF00017 | 0.489 |
LIG_SH2_STAP1 | 94 | 98 | PF00017 | 0.364 |
LIG_SH2_STAT3 | 433 | 436 | PF00017 | 0.606 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.617 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.612 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.197 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.222 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.328 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.496 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.609 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.377 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.328 |
LIG_SUMO_SIM_anti_2 | 63 | 69 | PF11976 | 0.385 |
LIG_TRAF2_1 | 321 | 324 | PF00917 | 0.465 |
LIG_TRAF2_1 | 434 | 437 | PF00917 | 0.662 |
LIG_TRAF2_2 | 312 | 317 | PF00917 | 0.685 |
LIG_TYR_ITSM | 387 | 394 | PF00017 | 0.491 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.687 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.647 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.754 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.517 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.569 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.743 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.319 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.729 |
MOD_GlcNHglycan | 95 | 99 | PF01048 | 0.404 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.448 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.697 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.521 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.448 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.566 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.432 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.372 |
MOD_N-GLC_1 | 195 | 200 | PF02516 | 0.471 |
MOD_N-GLC_1 | 270 | 275 | PF02516 | 0.377 |
MOD_N-GLC_1 | 303 | 308 | PF02516 | 0.536 |
MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.587 |
MOD_N-GLC_1 | 376 | 381 | PF02516 | 0.593 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.566 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.516 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.514 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.465 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.384 |
MOD_NEK2_2 | 398 | 403 | PF00069 | 0.464 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.638 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.415 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.371 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.376 |
MOD_Plk_1 | 303 | 309 | PF00069 | 0.580 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.405 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.560 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.489 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.435 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.365 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.402 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.605 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.370 |
MOD_SUMO_rev_2 | 406 | 413 | PF00179 | 0.512 |
MOD_SUMO_rev_2 | 45 | 55 | PF00179 | 0.585 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.361 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 391 | 394 | PF00928 | 0.429 |
TRG_ER_diArg_1 | 191 | 193 | PF00400 | 0.430 |
TRG_NES_CRM1_1 | 264 | 275 | PF08389 | 0.418 |
TRG_Pf-PMV_PEXEL_1 | 297 | 301 | PF00026 | 0.557 |
TRG_Pf-PMV_PEXEL_1 | 414 | 418 | PF00026 | 0.467 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKN6 | Leptomonas seymouri | 76% | 97% |
A0A0S4JT27 | Bodo saltans | 51% | 100% |
A0A1X0P7L7 | Trypanosomatidae | 59% | 92% |
A0A422NCB6 | Trypanosoma rangeli | 59% | 97% |
A4HPB3 | Leishmania braziliensis | 81% | 100% |
A4ICF3 | Leishmania infantum | 100% | 100% |
D0A3C2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 100% |
E9AT24 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q1H4 | Leishmania major | 96% | 100% |
V5BCK5 | Trypanosoma cruzi | 62% | 98% |