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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AWH8
Term | Name | Level | Count |
---|---|---|---|
GO:0010921 | regulation of phosphatase activity | 5 | 11 |
GO:0019220 | regulation of phosphate metabolic process | 6 | 11 |
GO:0019222 | regulation of metabolic process | 3 | 11 |
GO:0031323 | regulation of cellular metabolic process | 4 | 11 |
GO:0031399 | regulation of protein modification process | 6 | 11 |
GO:0035303 | regulation of dephosphorylation | 7 | 11 |
GO:0035304 | regulation of protein dephosphorylation | 7 | 11 |
GO:0043666 | regulation of phosphoprotein phosphatase activity | 6 | 11 |
GO:0050789 | regulation of biological process | 2 | 11 |
GO:0050790 | regulation of catalytic activity | 3 | 11 |
GO:0050794 | regulation of cellular process | 3 | 11 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 11 |
GO:0051174 | regulation of phosphorus metabolic process | 5 | 11 |
GO:0051246 | regulation of protein metabolic process | 5 | 11 |
GO:0051336 | regulation of hydrolase activity | 4 | 11 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 11 |
GO:0065007 | biological regulation | 1 | 11 |
GO:0065009 | regulation of molecular function | 2 | 11 |
GO:0080090 | regulation of primary metabolic process | 4 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016491 | oxidoreductase activity | 2 | 1 |
GO:0016667 | oxidoreductase activity, acting on a sulfur group of donors | 3 | 1 |
GO:0016671 | oxidoreductase activity, acting on a sulfur group of donors, disulfide as acceptor | 4 | 1 |
GO:0070191 | methionine-R-sulfoxide reductase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 385 | 389 | PF00656 | 0.478 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.537 |
CLV_PCSK_PC1ET2_1 | 14 | 16 | PF00082 | 0.265 |
CLV_PCSK_PC1ET2_1 | 34 | 36 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 518 | 522 | PF00082 | 0.656 |
DEG_APCC_DBOX_1 | 265 | 273 | PF00400 | 0.427 |
DEG_SPOP_SBC_1 | 233 | 237 | PF00917 | 0.512 |
DOC_CDC14_PxL_1 | 79 | 87 | PF14671 | 0.411 |
DOC_CYCLIN_yCln2_LP_2 | 341 | 347 | PF00134 | 0.478 |
DOC_MAPK_DCC_7 | 466 | 476 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 136 | 145 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 308 | 315 | PF00069 | 0.393 |
DOC_MAPK_MEF2A_6 | 334 | 343 | PF00069 | 0.483 |
DOC_MAPK_MEF2A_6 | 398 | 406 | PF00069 | 0.456 |
DOC_PP1_RVXF_1 | 358 | 364 | PF00149 | 0.489 |
DOC_PP1_RVXF_1 | 69 | 75 | PF00149 | 0.458 |
DOC_PP2B_LxvP_1 | 197 | 200 | PF13499 | 0.577 |
DOC_PP2B_LxvP_1 | 341 | 344 | PF13499 | 0.446 |
DOC_PP4_FxxP_1 | 60 | 63 | PF00568 | 0.445 |
DOC_PP4_FxxP_1 | 80 | 83 | PF00568 | 0.145 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.333 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.281 |
DOC_USP7_UBL2_3 | 246 | 250 | PF12436 | 0.584 |
DOC_USP7_UBL2_3 | 356 | 360 | PF12436 | 0.544 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 300 | 305 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 495 | 500 | PF00397 | 0.454 |
LIG_14-3-3_CanoR_1 | 342 | 352 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 430 | 440 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 94 | 102 | PF00244 | 0.360 |
LIG_14-3-3_CterR_2 | 518 | 522 | PF00244 | 0.377 |
LIG_Actin_WH2_2 | 468 | 483 | PF00022 | 0.397 |
LIG_APCC_ABBA_1 | 212 | 217 | PF00400 | 0.748 |
LIG_APCC_ABBA_1 | 456 | 461 | PF00400 | 0.456 |
LIG_BIR_III_4 | 388 | 392 | PF00653 | 0.478 |
LIG_BRCT_BRCA1_1 | 32 | 36 | PF00533 | 0.515 |
LIG_BRCT_BRCA1_1 | 350 | 354 | PF00533 | 0.478 |
LIG_BRCT_BRCA1_1 | 432 | 436 | PF00533 | 0.552 |
LIG_BRCT_BRCA1_2 | 350 | 356 | PF00533 | 0.478 |
LIG_deltaCOP1_diTrp_1 | 309 | 315 | PF00928 | 0.494 |
LIG_deltaCOP1_diTrp_1 | 362 | 369 | PF00928 | 0.466 |
LIG_deltaCOP1_diTrp_1 | 450 | 459 | PF00928 | 0.446 |
LIG_EH1_1 | 314 | 322 | PF00400 | 0.460 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.507 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.397 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.367 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.522 |
LIG_FHA_1 | 505 | 511 | PF00498 | 0.388 |
LIG_FHA_2 | 107 | 113 | PF00498 | 0.331 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.417 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.389 |
LIG_FHA_2 | 333 | 339 | PF00498 | 0.377 |
LIG_FXI_DFP_1 | 182 | 186 | PF00024 | 0.458 |
LIG_FXI_DFP_1 | 407 | 411 | PF00024 | 0.278 |
LIG_IRF3_LxIS_1 | 281 | 288 | PF10401 | 0.434 |
LIG_LIR_Gen_1 | 309 | 320 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 346 | 357 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 409 | 417 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 434 | 444 | PF02991 | 0.466 |
LIG_LIR_LC3C_4 | 115 | 119 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 309 | 315 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 330 | 336 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 346 | 352 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 433 | 439 | PF02991 | 0.444 |
LIG_MLH1_MIPbox_1 | 433 | 437 | PF16413 | 0.446 |
LIG_Pex14_1 | 365 | 369 | PF04695 | 0.431 |
LIG_Pex14_1 | 74 | 78 | PF04695 | 0.266 |
LIG_Pex14_2 | 406 | 410 | PF04695 | 0.456 |
LIG_Pex14_2 | 436 | 440 | PF04695 | 0.456 |
LIG_REV1ctd_RIR_1 | 242 | 250 | PF16727 | 0.557 |
LIG_SH2_CRK | 202 | 206 | PF00017 | 0.687 |
LIG_SH2_STAP1 | 18 | 22 | PF00017 | 0.393 |
LIG_SH2_STAP1 | 202 | 206 | PF00017 | 0.687 |
LIG_SH2_STAT3 | 78 | 81 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.279 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.446 |
LIG_SUMO_SIM_anti_2 | 149 | 155 | PF11976 | 0.331 |
LIG_SUMO_SIM_par_1 | 141 | 146 | PF11976 | 0.337 |
LIG_SUMO_SIM_par_1 | 149 | 155 | PF11976 | 0.252 |
LIG_SUMO_SIM_par_1 | 298 | 303 | PF11976 | 0.397 |
LIG_SUMO_SIM_par_1 | 506 | 511 | PF11976 | 0.383 |
LIG_SxIP_EBH_1 | 235 | 246 | PF03271 | 0.567 |
LIG_SxIP_EBH_1 | 93 | 104 | PF03271 | 0.167 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.381 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.441 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.226 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.433 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.416 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.329 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.145 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.619 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.445 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.350 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.381 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.430 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.456 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.506 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.437 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.309 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.674 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.531 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.474 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.387 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.476 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.429 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.523 |
MOD_N-GLC_1 | 146 | 151 | PF02516 | 0.411 |
MOD_N-GLC_2 | 368 | 370 | PF02516 | 0.287 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.428 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.355 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.439 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.364 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.473 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.316 |
MOD_NEK2_2 | 348 | 353 | PF00069 | 0.287 |
MOD_PIKK_1 | 271 | 277 | PF00454 | 0.403 |
MOD_PK_1 | 298 | 304 | PF00069 | 0.357 |
MOD_Plk_1 | 398 | 404 | PF00069 | 0.276 |
MOD_Plk_2-3 | 332 | 338 | PF00069 | 0.297 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.319 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.411 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.599 |
MOD_Plk_4 | 504 | 510 | PF00069 | 0.444 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.557 |
MOD_ProDKin_1 | 300 | 306 | PF00069 | 0.460 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.415 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.414 |
MOD_ProDKin_1 | 495 | 501 | PF00069 | 0.449 |
MOD_SUMO_for_1 | 245 | 248 | PF00179 | 0.564 |
MOD_SUMO_rev_2 | 276 | 281 | PF00179 | 0.512 |
MOD_SUMO_rev_2 | 326 | 336 | PF00179 | 0.402 |
MOD_SUMO_rev_2 | 355 | 361 | PF00179 | 0.421 |
MOD_SUMO_rev_2 | 487 | 497 | PF00179 | 0.561 |
TRG_DiLeu_BaEn_1 | 332 | 337 | PF01217 | 0.537 |
TRG_DiLeu_BaEn_1 | 375 | 380 | PF01217 | 0.232 |
TRG_ENDOCYTIC_2 | 18 | 21 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.684 |
TRG_ENDOCYTIC_2 | 407 | 410 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 429 | 432 | PF00928 | 0.331 |
TRG_NES_CRM1_1 | 170 | 184 | PF08389 | 0.200 |
TRG_Pf-PMV_PEXEL_1 | 15 | 19 | PF00026 | 0.354 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5N3 | Leptomonas seymouri | 68% | 100% |
A0A0S4JL71 | Bodo saltans | 35% | 100% |
A0A1X0NWX3 | Trypanosomatidae | 43% | 97% |
A0A3S7WY26 | Leishmania donovani | 93% | 100% |
A0A422NJH6 | Trypanosoma rangeli | 44% | 94% |
A4HD30 | Leishmania braziliensis | 83% | 100% |
A4I0L7 | Leishmania infantum | 93% | 100% |
C9ZNQ7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 91% |
Q4QAZ2 | Leishmania major | 94% | 100% |
V5BB88 | Trypanosoma cruzi | 46% | 95% |