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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q9W4
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 7 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009056 | catabolic process | 2 | 7 |
GO:0009057 | macromolecule catabolic process | 4 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044248 | cellular catabolic process | 3 | 7 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 7 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 7 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
GO:1901575 | organic substance catabolic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0019899 | enzyme binding | 3 | 2 |
GO:0031625 | ubiquitin protein ligase binding | 5 | 2 |
GO:0032182 | ubiquitin-like protein binding | 3 | 2 |
GO:0043130 | ubiquitin binding | 4 | 2 |
GO:0044389 | ubiquitin-like protein ligase binding | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 202 | 206 | PF00656 | 0.673 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 568 | 570 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.494 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 371 | 373 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 568 | 570 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.493 |
CLV_PCSK_PC1ET2_1 | 222 | 224 | PF00082 | 0.565 |
CLV_PCSK_PC1ET2_1 | 568 | 570 | PF00082 | 0.484 |
CLV_PCSK_PC1ET2_1 | 75 | 77 | PF00082 | 0.473 |
CLV_PCSK_PC7_1 | 211 | 217 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 392 | 396 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 524 | 528 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 541 | 545 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 608 | 612 | PF00082 | 0.583 |
DEG_APCC_DBOX_1 | 290 | 298 | PF00400 | 0.480 |
DEG_SPOP_SBC_1 | 270 | 274 | PF00917 | 0.617 |
DOC_MAPK_gen_1 | 360 | 370 | PF00069 | 0.612 |
DOC_MAPK_gen_1 | 568 | 574 | PF00069 | 0.527 |
DOC_MAPK_gen_1 | 79 | 88 | PF00069 | 0.509 |
DOC_MAPK_MEF2A_6 | 382 | 391 | PF00069 | 0.473 |
DOC_MAPK_RevD_3 | 356 | 372 | PF00069 | 0.533 |
DOC_PP1_RVXF_1 | 282 | 288 | PF00149 | 0.457 |
DOC_PP2B_PxIxI_1 | 447 | 453 | PF00149 | 0.515 |
DOC_PP4_FxxP_1 | 51 | 54 | PF00568 | 0.410 |
DOC_PP4_FxxP_1 | 535 | 538 | PF00568 | 0.492 |
DOC_PP4_MxPP_1 | 552 | 555 | PF00568 | 0.484 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.689 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 457 | 462 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 472 | 477 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 534 | 539 | PF00397 | 0.490 |
LIG_14-3-3_CanoR_1 | 105 | 114 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 30 | 39 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 524 | 530 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 561 | 567 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 569 | 575 | PF00244 | 0.461 |
LIG_Actin_WH2_2 | 137 | 154 | PF00022 | 0.424 |
LIG_Actin_WH2_2 | 357 | 373 | PF00022 | 0.550 |
LIG_BRCT_BRCA1_1 | 145 | 149 | PF00533 | 0.628 |
LIG_BRCT_BRCA1_1 | 248 | 252 | PF00533 | 0.557 |
LIG_BRCT_BRCA1_1 | 4 | 8 | PF00533 | 0.440 |
LIG_BRCT_BRCA1_1 | 570 | 574 | PF00533 | 0.493 |
LIG_BRCT_BRCA1_1 | 93 | 97 | PF00533 | 0.514 |
LIG_Clathr_ClatBox_1 | 294 | 298 | PF01394 | 0.410 |
LIG_EH_1 | 37 | 41 | PF12763 | 0.406 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.647 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.541 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.438 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.510 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.609 |
LIG_FHA_1 | 492 | 498 | PF00498 | 0.524 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.393 |
LIG_FHA_2 | 500 | 506 | PF00498 | 0.570 |
LIG_FHA_2 | 517 | 523 | PF00498 | 0.500 |
LIG_FHA_2 | 575 | 581 | PF00498 | 0.511 |
LIG_FHA_2 | 591 | 597 | PF00498 | 0.374 |
LIG_LIR_Apic_2 | 49 | 54 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 249 | 260 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 527 | 535 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 580 | 588 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 84 | 93 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 150 | 156 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 249 | 255 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 347 | 353 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 523 | 529 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 580 | 584 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 84 | 88 | PF02991 | 0.473 |
LIG_NRBOX | 583 | 589 | PF00104 | 0.506 |
LIG_Pex14_1 | 525 | 529 | PF04695 | 0.416 |
LIG_Pex14_2 | 149 | 153 | PF04695 | 0.408 |
LIG_Rb_pABgroove_1 | 320 | 328 | PF01858 | 0.599 |
LIG_SH2_CRK | 319 | 323 | PF00017 | 0.550 |
LIG_SH2_CRK | 617 | 621 | PF00017 | 0.555 |
LIG_SH2_NCK_1 | 326 | 330 | PF00017 | 0.512 |
LIG_SH2_PTP2 | 529 | 532 | PF00017 | 0.419 |
LIG_SH2_SRC | 326 | 329 | PF00017 | 0.599 |
LIG_SH2_STAP1 | 173 | 177 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 241 | 245 | PF00017 | 0.525 |
LIG_SH2_STAP1 | 319 | 323 | PF00017 | 0.599 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 529 | 532 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 563 | 566 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 586 | 589 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 599 | 602 | PF00017 | 0.459 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.451 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.463 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.521 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.490 |
LIG_SH3_3 | 547 | 553 | PF00018 | 0.536 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.538 |
LIG_SUMO_SIM_anti_2 | 41 | 47 | PF11976 | 0.417 |
LIG_SUMO_SIM_par_1 | 41 | 47 | PF11976 | 0.417 |
LIG_SUMO_SIM_par_1 | 447 | 453 | PF11976 | 0.609 |
LIG_SxIP_EBH_1 | 19 | 32 | PF03271 | 0.414 |
LIG_TYR_ITSM | 525 | 532 | PF00017 | 0.413 |
LIG_UBA3_1 | 251 | 259 | PF00899 | 0.580 |
LIG_WRC_WIRS_1 | 305 | 310 | PF05994 | 0.408 |
MOD_CDC14_SPxK_1 | 53 | 56 | PF00782 | 0.408 |
MOD_CDK_SPxK_1 | 50 | 56 | PF00069 | 0.414 |
MOD_CDK_SPxxK_3 | 224 | 231 | PF00069 | 0.646 |
MOD_CDK_SPxxK_3 | 50 | 57 | PF00069 | 0.453 |
MOD_CDK_SPxxK_3 | 534 | 541 | PF00069 | 0.490 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.647 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.513 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.604 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.599 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.671 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.440 |
MOD_CK2_1 | 570 | 576 | PF00069 | 0.481 |
MOD_CK2_1 | 591 | 597 | PF00069 | 0.487 |
MOD_Cter_Amidation | 255 | 258 | PF01082 | 0.390 |
MOD_DYRK1A_RPxSP_1 | 107 | 111 | PF00069 | 0.461 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.605 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.506 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.708 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.729 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.549 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.476 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.423 |
MOD_GlcNHglycan | 505 | 509 | PF01048 | 0.572 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.676 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.534 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.507 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.566 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.387 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.466 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.628 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.682 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.583 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.420 |
MOD_GSK3_1 | 511 | 518 | PF00069 | 0.524 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.423 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.480 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.503 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.485 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.511 |
MOD_LATS_1 | 509 | 515 | PF00433 | 0.598 |
MOD_N-GLC_1 | 199 | 204 | PF02516 | 0.570 |
MOD_N-GLC_2 | 244 | 246 | PF02516 | 0.530 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.463 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.441 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.469 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.472 |
MOD_NEK2_1 | 574 | 579 | PF00069 | 0.433 |
MOD_NEK2_2 | 46 | 51 | PF00069 | 0.465 |
MOD_NEK2_2 | 58 | 63 | PF00069 | 0.429 |
MOD_OFUCOSY | 10 | 16 | PF10250 | 0.419 |
MOD_OFUCOSY | 121 | 128 | PF10250 | 0.417 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.510 |
MOD_PIKK_1 | 187 | 193 | PF00454 | 0.435 |
MOD_PIKK_1 | 271 | 277 | PF00454 | 0.612 |
MOD_PIKK_1 | 289 | 295 | PF00454 | 0.375 |
MOD_PIKK_1 | 586 | 592 | PF00454 | 0.452 |
MOD_PKA_1 | 56 | 62 | PF00069 | 0.427 |
MOD_PKA_1 | 568 | 574 | PF00069 | 0.495 |
MOD_PKA_1 | 608 | 614 | PF00069 | 0.374 |
MOD_PKA_1 | 81 | 87 | PF00069 | 0.470 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.543 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.717 |
MOD_PKA_2 | 545 | 551 | PF00069 | 0.467 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.495 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.549 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.459 |
MOD_Plk_1 | 399 | 405 | PF00069 | 0.412 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.615 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.458 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.464 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.410 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.628 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.586 |
MOD_Plk_4 | 525 | 531 | PF00069 | 0.416 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.470 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.596 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.487 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.414 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.581 |
MOD_ProDKin_1 | 457 | 463 | PF00069 | 0.446 |
MOD_ProDKin_1 | 472 | 478 | PF00069 | 0.469 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.452 |
MOD_ProDKin_1 | 534 | 540 | PF00069 | 0.485 |
MOD_SUMO_for_1 | 221 | 224 | PF00179 | 0.507 |
TRG_DiLeu_BaLyEn_6 | 24 | 29 | PF01217 | 0.435 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.550 |
TRG_ENDOCYTIC_2 | 529 | 532 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 617 | 620 | PF00928 | 0.443 |
TRG_ER_diArg_1 | 215 | 217 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 370 | 372 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 62 | 65 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 76 | 79 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 95 | 97 | PF00400 | 0.485 |
TRG_NES_CRM1_1 | 385 | 400 | PF08389 | 0.444 |
TRG_NES_CRM1_1 | 576 | 590 | PF08389 | 0.445 |
TRG_NLS_MonoExtC_3 | 74 | 79 | PF00514 | 0.468 |
TRG_NLS_MonoExtN_4 | 567 | 572 | PF00514 | 0.533 |
TRG_NLS_MonoExtN_4 | 72 | 79 | PF00514 | 0.467 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4H2 | Leptomonas seymouri | 72% | 100% |
A0A3S7WZ51 | Leishmania donovani | 96% | 100% |
A4HE71 | Leishmania braziliensis | 88% | 100% |
C9ZK00 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9AXK7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 99% |