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: Q4Q2R5
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 | 0.736 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.245 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.260 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.294 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.218 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 40 | 42 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 506 | 508 | PF00675 | 0.636 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.232 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.260 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.218 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.221 |
CLV_PCSK_KEX2_1 | 40 | 42 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 506 | 508 | PF00082 | 0.670 |
CLV_PCSK_PC1ET2_1 | 115 | 117 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.261 |
CLV_PCSK_SKI1_1 | 162 | 166 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.196 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.195 |
CLV_PCSK_SKI1_1 | 542 | 546 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.127 |
CLV_PCSK_SKI1_1 | 572 | 576 | PF00082 | 0.648 |
CLV_Separin_Metazoa | 400 | 404 | PF03568 | 0.473 |
DEG_SPOP_SBC_1 | 366 | 370 | PF00917 | 0.544 |
DOC_ANK_TNKS_1 | 313 | 320 | PF00023 | 0.563 |
DOC_CYCLIN_RxL_1 | 340 | 349 | PF00134 | 0.464 |
DOC_CYCLIN_RxL_1 | 35 | 48 | PF00134 | 0.523 |
DOC_MAPK_MEF2A_6 | 66 | 73 | PF00069 | 0.463 |
DOC_MAPK_NFAT4_5 | 66 | 74 | PF00069 | 0.539 |
DOC_PP1_RVXF_1 | 117 | 124 | PF00149 | 0.459 |
DOC_PP1_RVXF_1 | 436 | 442 | PF00149 | 0.396 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 495 | 499 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 556 | 560 | PF00917 | 0.633 |
DOC_USP7_UBL2_3 | 115 | 119 | PF12436 | 0.459 |
DOC_USP7_UBL2_3 | 122 | 126 | PF12436 | 0.459 |
DOC_USP7_UBL2_3 | 51 | 55 | PF12436 | 0.511 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.467 |
DOC_WW_Pin1_4 | 506 | 511 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.505 |
LIG_14-3-3_CanoR_1 | 116 | 122 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 153 | 161 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 179 | 189 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 200 | 204 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 239 | 245 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 342 | 346 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 35 | 40 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 41 | 46 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 506 | 510 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 96 | 103 | PF00244 | 0.396 |
LIG_Actin_WH2_2 | 326 | 344 | PF00022 | 0.539 |
LIG_APCC_ABBA_1 | 71 | 76 | PF00400 | 0.490 |
LIG_APCC_ABBAyCdc20_2 | 50 | 56 | PF00400 | 0.488 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.518 |
LIG_BRCT_BRCA1_1 | 351 | 355 | PF00533 | 0.438 |
LIG_BRCT_BRCA1_1 | 370 | 374 | PF00533 | 0.567 |
LIG_deltaCOP1_diTrp_1 | 444 | 452 | PF00928 | 0.539 |
LIG_deltaCOP1_diTrp_1 | 593 | 598 | PF00928 | 0.589 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.518 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.569 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.473 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.526 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.522 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.629 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.593 |
LIG_FHA_1 | 571 | 577 | PF00498 | 0.754 |
LIG_FHA_1 | 6 | 12 | PF00498 | 0.470 |
LIG_FHA_2 | 549 | 555 | PF00498 | 0.459 |
LIG_Integrin_isoDGR_2 | 246 | 248 | PF01839 | 0.273 |
LIG_LIR_Apic_2 | 393 | 398 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 173 | 181 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 184 | 194 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 323 | 333 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 184 | 190 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 23 | 28 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 323 | 328 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 550 | 555 | PF02991 | 0.541 |
LIG_SH2_CRK | 175 | 179 | PF00017 | 0.539 |
LIG_SH2_CRK | 325 | 329 | PF00017 | 0.479 |
LIG_SH2_GRB2like | 301 | 304 | PF00017 | 0.539 |
LIG_SH2_PTP2 | 395 | 398 | PF00017 | 0.424 |
LIG_SH2_STAP1 | 253 | 257 | PF00017 | 0.563 |
LIG_SH2_STAP1 | 351 | 355 | PF00017 | 0.438 |
LIG_SH2_STAT3 | 203 | 206 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 514 | 517 | PF00017 | 0.559 |
LIG_SH3_1 | 537 | 543 | PF00018 | 0.408 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.479 |
LIG_SH3_3 | 527 | 533 | PF00018 | 0.591 |
LIG_SH3_3 | 537 | 543 | PF00018 | 0.437 |
LIG_SUMO_SIM_anti_2 | 397 | 403 | PF11976 | 0.473 |
LIG_SUMO_SIM_anti_2 | 461 | 468 | PF11976 | 0.532 |
LIG_SUMO_SIM_par_1 | 290 | 296 | PF11976 | 0.473 |
LIG_TRAF2_1 | 411 | 414 | PF00917 | 0.479 |
LIG_TRAF2_1 | 476 | 479 | PF00917 | 0.523 |
LIG_TRAF2_1 | 518 | 521 | PF00917 | 0.589 |
LIG_TYR_ITSM | 321 | 328 | PF00017 | 0.479 |
LIG_WW_1 | 533 | 536 | PF00397 | 0.487 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.495 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.541 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.480 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.507 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.475 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.459 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.539 |
MOD_CK2_1 | 556 | 562 | PF00069 | 0.684 |
MOD_GlcNHglycan | 142 | 146 | PF01048 | 0.280 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.196 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.339 |
MOD_GlcNHglycan | 434 | 437 | PF01048 | 0.306 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.679 |
MOD_GlcNHglycan | 566 | 571 | PF01048 | 0.709 |
MOD_GlcNHglycan | 582 | 585 | PF01048 | 0.517 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.396 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.459 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.509 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.476 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.448 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.483 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.476 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.672 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.744 |
MOD_N-GLC_1 | 117 | 122 | PF02516 | 0.273 |
MOD_N-GLC_1 | 580 | 585 | PF02516 | 0.750 |
MOD_N-GLC_1 | 60 | 65 | PF02516 | 0.287 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.473 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.563 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.525 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.459 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.511 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.474 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.538 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.366 |
MOD_NEK2_2 | 337 | 342 | PF00069 | 0.539 |
MOD_PIKK_1 | 11 | 17 | PF00454 | 0.478 |
MOD_PIKK_1 | 238 | 244 | PF00454 | 0.515 |
MOD_PIKK_1 | 390 | 396 | PF00454 | 0.457 |
MOD_PIKK_1 | 520 | 526 | PF00454 | 0.679 |
MOD_PKA_1 | 92 | 98 | PF00069 | 0.563 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.396 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.500 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.539 |
MOD_PKA_2 | 238 | 244 | PF00069 | 0.396 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.521 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.473 |
MOD_PKA_2 | 505 | 511 | PF00069 | 0.646 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.507 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.473 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.490 |
MOD_Plk_1 | 358 | 364 | PF00069 | 0.511 |
MOD_Plk_1 | 5 | 11 | PF00069 | 0.387 |
MOD_Plk_1 | 520 | 526 | PF00069 | 0.604 |
MOD_Plk_2-3 | 562 | 568 | PF00069 | 0.687 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.446 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.420 |
MOD_Plk_4 | 510 | 516 | PF00069 | 0.637 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.467 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.502 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.467 |
MOD_ProDKin_1 | 506 | 512 | PF00069 | 0.668 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.505 |
MOD_SUMO_for_1 | 274 | 277 | PF00179 | 0.368 |
MOD_SUMO_for_1 | 91 | 94 | PF00179 | 0.535 |
MOD_SUMO_rev_2 | 157 | 167 | PF00179 | 0.511 |
MOD_SUMO_rev_2 | 268 | 276 | PF00179 | 0.530 |
MOD_SUMO_rev_2 | 44 | 52 | PF00179 | 0.513 |
TRG_DiLeu_BaEn_1 | 413 | 418 | PF01217 | 0.479 |
TRG_DiLeu_BaEn_4 | 413 | 419 | PF01217 | 0.534 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.533 |
TRG_ER_diArg_1 | 113 | 116 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 297 | 299 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 341 | 343 | PF00400 | 0.496 |
TRG_ER_diArg_1 | 353 | 355 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 39 | 41 | PF00400 | 0.506 |
TRG_PTS2 | 1 | 43 | PF00400 | 0.318 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IH42 | Leptomonas seymouri | 68% | 99% |
A0A0S4J2Z5 | Bodo saltans | 44% | 100% |
A0A1X0PAR6 | Trypanosomatidae | 47% | 100% |
A0A3S7X839 | Leishmania donovani | 92% | 100% |
A4HAZ6 | Leishmania braziliensis | 81% | 100% |
A4IA56 | Leishmania infantum | 93% | 100% |
C9ZM46 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9B570 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q00004 | Canis lupus familiaris | 25% | 96% |
Q8BMA6 | Mus musculus | 26% | 96% |
Q9UHB9 | Homo sapiens | 26% | 96% |
Q9VSS2 | Drosophila melanogaster | 23% | 99% |
V5BV06 | Trypanosoma cruzi | 49% | 100% |