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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 11 |
GO:0005786 | signal recognition particle, endoplasmic reticulum targeting | 4 | 11 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043228 | non-membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 11 |
GO:0048500 | signal recognition particle | 3 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:1990904 | ribonucleoprotein complex | 2 | 11 |
Related structures:
AlphaFold database: E9B570
Term | Name | Level | Count |
---|---|---|---|
GO:0006605 | protein targeting | 5 | 11 |
GO:0006612 | protein targeting to membrane | 5 | 11 |
GO:0006613 | cotranslational protein targeting to membrane | 6 | 11 |
GO:0006614 | SRP-dependent cotranslational protein targeting to membrane | 7 | 11 |
GO:0006810 | transport | 3 | 11 |
GO:0006886 | intracellular protein transport | 4 | 11 |
GO:0008104 | protein localization | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0015031 | protein transport | 4 | 11 |
GO:0033036 | macromolecule localization | 2 | 11 |
GO:0033365 | protein localization to organelle | 5 | 11 |
GO:0045047 | protein targeting to ER | 6 | 11 |
GO:0045184 | establishment of protein localization | 3 | 11 |
GO:0046907 | intracellular transport | 3 | 11 |
GO:0051179 | localization | 1 | 11 |
GO:0051234 | establishment of localization | 2 | 11 |
GO:0051641 | cellular localization | 2 | 11 |
GO:0051649 | establishment of localization in cell | 3 | 11 |
GO:0051668 | localization within membrane | 3 | 11 |
GO:0070727 | cellular macromolecule localization | 3 | 11 |
GO:0070972 | protein localization to endoplasmic reticulum | 6 | 11 |
GO:0071702 | organic substance transport | 4 | 11 |
GO:0071705 | nitrogen compound transport | 4 | 11 |
GO:0072594 | establishment of protein localization to organelle | 4 | 11 |
GO:0072599 | establishment of protein localization to endoplasmic reticulum | 5 | 11 |
GO:0072657 | protein localization to membrane | 4 | 11 |
GO:0090150 | establishment of protein localization to membrane | 4 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0005047 | signal recognition particle binding | 4 | 11 |
GO:0005048 | signal sequence binding | 4 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0008312 | 7S RNA binding | 5 | 11 |
GO:0030942 | endoplasmic reticulum signal peptide binding | 5 | 11 |
GO:0033218 | amide binding | 2 | 11 |
GO:0042277 | peptide binding | 3 | 11 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 11 |
GO:0044877 | protein-containing complex binding | 2 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 561 | 565 | PF00656 | 0.714 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.209 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.181 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.235 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.257 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.186 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 506 | 508 | PF00675 | 0.241 |
CLV_PCSK_FUR_1 | 384 | 388 | PF00082 | 0.146 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.207 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.257 |
CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.193 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.185 |
CLV_PCSK_KEX2_1 | 506 | 508 | PF00082 | 0.314 |
CLV_PCSK_PC1ET2_1 | 115 | 117 | PF00082 | 0.221 |
CLV_PCSK_PC1ET2_1 | 386 | 388 | PF00082 | 0.146 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.245 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.170 |
CLV_PCSK_SKI1_1 | 542 | 546 | PF00082 | 0.228 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.129 |
CLV_Separin_Metazoa | 400 | 404 | PF03568 | 0.435 |
DEG_SPOP_SBC_1 | 571 | 575 | PF00917 | 0.476 |
DOC_ANK_TNKS_1 | 313 | 320 | PF00023 | 0.476 |
DOC_MAPK_MEF2A_6 | 262 | 271 | PF00069 | 0.346 |
DOC_MAPK_MEF2A_6 | 66 | 73 | PF00069 | 0.425 |
DOC_MAPK_NFAT4_5 | 66 | 74 | PF00069 | 0.515 |
DOC_PP1_RVXF_1 | 117 | 124 | PF00149 | 0.421 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.381 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 556 | 560 | PF00917 | 0.613 |
DOC_USP7_UBL2_3 | 115 | 119 | PF12436 | 0.421 |
DOC_USP7_UBL2_3 | 122 | 126 | PF12436 | 0.421 |
DOC_USP7_UBL2_3 | 51 | 55 | PF12436 | 0.478 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 506 | 511 | PF00397 | 0.528 |
LIG_14-3-3_CanoR_1 | 116 | 122 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 153 | 161 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 172 | 176 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 179 | 189 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 200 | 204 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 35 | 40 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 360 | 368 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 506 | 510 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 568 | 576 | PF00244 | 0.476 |
LIG_Actin_WH2_2 | 326 | 344 | PF00022 | 0.515 |
LIG_APCC_ABBA_1 | 71 | 76 | PF00400 | 0.453 |
LIG_APCC_ABBAyCdc20_2 | 50 | 56 | PF00400 | 0.451 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.485 |
LIG_deltaCOP1_diTrp_1 | 444 | 452 | PF00928 | 0.535 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.456 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.449 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.486 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.435 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.524 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.560 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.494 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.457 |
LIG_FHA_1 | 571 | 577 | PF00498 | 0.750 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.424 |
LIG_FHA_2 | 313 | 319 | PF00498 | 0.355 |
LIG_FHA_2 | 549 | 555 | PF00498 | 0.528 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.346 |
LIG_Integrin_isoDGR_2 | 246 | 248 | PF01839 | 0.236 |
LIG_LIR_Apic_2 | 365 | 371 | PF02991 | 0.389 |
LIG_LIR_Apic_2 | 393 | 398 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 184 | 194 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 323 | 333 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 174 | 178 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 184 | 190 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 23 | 28 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 323 | 328 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 550 | 555 | PF02991 | 0.430 |
LIG_SH2_CRK | 175 | 179 | PF00017 | 0.518 |
LIG_SH2_CRK | 325 | 329 | PF00017 | 0.424 |
LIG_SH2_CRK | 368 | 372 | PF00017 | 0.377 |
LIG_SH2_GRB2like | 301 | 304 | PF00017 | 0.515 |
LIG_SH2_NCK_1 | 368 | 372 | PF00017 | 0.346 |
LIG_SH2_PTP2 | 395 | 398 | PF00017 | 0.389 |
LIG_SH2_STAP1 | 253 | 257 | PF00017 | 0.476 |
LIG_SH2_STAT3 | 203 | 206 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 514 | 517 | PF00017 | 0.435 |
LIG_SH3_3 | 527 | 533 | PF00018 | 0.464 |
LIG_SH3_3 | 537 | 543 | PF00018 | 0.386 |
LIG_SH3_3 | 574 | 580 | PF00018 | 0.511 |
LIG_SUMO_SIM_anti_2 | 397 | 403 | PF11976 | 0.435 |
LIG_SUMO_SIM_anti_2 | 461 | 468 | PF11976 | 0.505 |
LIG_SUMO_SIM_par_1 | 290 | 296 | PF11976 | 0.435 |
LIG_TRAF2_1 | 476 | 479 | PF00917 | 0.493 |
LIG_TRAF2_1 | 518 | 521 | PF00917 | 0.441 |
LIG_TYR_ITSM | 321 | 328 | PF00017 | 0.424 |
LIG_WW_1 | 533 | 536 | PF00397 | 0.421 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.461 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.565 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.467 |
MOD_CK1_1 | 495 | 501 | PF00069 | 0.490 |
MOD_CK1_1 | 570 | 576 | PF00069 | 0.604 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.441 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.464 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.436 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.444 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.457 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.531 |
MOD_CK2_1 | 556 | 562 | PF00069 | 0.661 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.374 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.315 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.349 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.160 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.285 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.285 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.227 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.653 |
MOD_GlcNHglycan | 581 | 584 | PF01048 | 0.595 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.421 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.472 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.435 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.419 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.466 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.445 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.525 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.732 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.376 |
MOD_N-GLC_1 | 117 | 122 | PF02516 | 0.235 |
MOD_N-GLC_1 | 180 | 185 | PF02516 | 0.168 |
MOD_N-GLC_1 | 60 | 65 | PF02516 | 0.249 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.435 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.476 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.421 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.478 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.474 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.305 |
MOD_NEK2_2 | 337 | 342 | PF00069 | 0.515 |
MOD_PIKK_1 | 11 | 17 | PF00454 | 0.427 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.474 |
MOD_PIKK_1 | 238 | 244 | PF00454 | 0.515 |
MOD_PIKK_1 | 390 | 396 | PF00454 | 0.419 |
MOD_PIKK_1 | 520 | 526 | PF00454 | 0.549 |
MOD_PK_1 | 581 | 587 | PF00069 | 0.464 |
MOD_PKA_1 | 92 | 98 | PF00069 | 0.476 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.464 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.511 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.491 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.435 |
MOD_PKA_2 | 505 | 511 | PF00069 | 0.448 |
MOD_PKA_2 | 567 | 573 | PF00069 | 0.489 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.441 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.435 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.478 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.478 |
MOD_Plk_1 | 5 | 11 | PF00069 | 0.326 |
MOD_Plk_1 | 520 | 526 | PF00069 | 0.471 |
MOD_Plk_2-3 | 562 | 568 | PF00069 | 0.593 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.407 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.472 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.362 |
MOD_Plk_4 | 510 | 516 | PF00069 | 0.515 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.533 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.432 |
MOD_ProDKin_1 | 506 | 512 | PF00069 | 0.528 |
MOD_SUMO_for_1 | 139 | 142 | PF00179 | 0.456 |
MOD_SUMO_rev_2 | 157 | 167 | PF00179 | 0.478 |
MOD_SUMO_rev_2 | 268 | 276 | PF00179 | 0.502 |
MOD_SUMO_rev_2 | 44 | 52 | PF00179 | 0.480 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.391 |
TRG_ER_diArg_1 | 113 | 116 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 297 | 299 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 341 | 343 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 351 | 354 | PF00400 | 0.394 |
TRG_NLS_MonoCore_2 | 383 | 388 | PF00514 | 0.398 |
TRG_NLS_MonoExtC_3 | 383 | 389 | PF00514 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 345 | 349 | PF00026 | 0.146 |
TRG_PTS2 | 1 | 43 | PF00400 | 0.263 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IH42 | Leptomonas seymouri | 68% | 99% |
A0A0S4J2Z5 | Bodo saltans | 45% | 100% |
A0A1X0PAR6 | Trypanosomatidae | 48% | 100% |
A0A3S7X839 | Leishmania donovani | 89% | 100% |
A4HAZ6 | Leishmania braziliensis | 82% | 100% |
A4IA56 | Leishmania infantum | 90% | 100% |
C9ZM46 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
Q00004 | Canis lupus familiaris | 25% | 96% |
Q20822 | Caenorhabditis elegans | 20% | 96% |
Q4Q2R5 | Leishmania major | 90% | 100% |
Q8BMA6 | Mus musculus | 25% | 96% |
Q9UHB9 | Homo sapiens | 24% | 96% |
Q9VSS2 | Drosophila melanogaster | 24% | 99% |
V5BV06 | Trypanosoma cruzi | 48% | 100% |