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: 8 |
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:0005929 | cilium | 4 | 7 |
GO:0042995 | cell projection | 2 | 7 |
GO:0043226 | organelle | 2 | 7 |
GO:0043227 | membrane-bounded organelle | 3 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 7 |
GO:0000151 | ubiquitin ligase complex | 3 | 1 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005886 | plasma membrane | 3 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0019005 | SCF ubiquitin ligase complex | 5 | 1 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: E9B4M4
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0031146 | SCF-dependent proteasomal ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 542 | 546 | PF00656 | 0.281 |
CLV_NRD_NRD_1 | 575 | 577 | PF00675 | 0.489 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.389 |
CLV_PCSK_PC1ET2_1 | 504 | 506 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 289 | 293 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 555 | 559 | PF00082 | 0.360 |
DEG_COP1_1 | 542 | 553 | PF00400 | 0.282 |
DEG_ODPH_VHL_1 | 294 | 305 | PF01847 | 0.256 |
DEG_SPOP_SBC_1 | 145 | 149 | PF00917 | 0.565 |
DEG_SPOP_SBC_1 | 215 | 219 | PF00917 | 0.564 |
DOC_CDC14_PxL_1 | 547 | 555 | PF14671 | 0.388 |
DOC_CYCLIN_RxL_1 | 436 | 444 | PF00134 | 0.383 |
DOC_CYCLIN_RxL_1 | 504 | 514 | PF00134 | 0.266 |
DOC_CYCLIN_yCln2_LP_2 | 206 | 212 | PF00134 | 0.518 |
DOC_MAPK_gen_1 | 504 | 511 | PF00069 | 0.374 |
DOC_MAPK_gen_1 | 576 | 584 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 523 | 532 | PF00069 | 0.344 |
DOC_PP1_RVXF_1 | 462 | 469 | PF00149 | 0.445 |
DOC_PP2B_LxvP_1 | 470 | 473 | PF13499 | 0.474 |
DOC_PP4_FxxP_1 | 102 | 105 | PF00568 | 0.582 |
DOC_PP4_FxxP_1 | 233 | 236 | PF00568 | 0.619 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.355 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.338 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 585 | 589 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.665 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 600 | 605 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 613 | 618 | PF00397 | 0.579 |
LIG_14-3-3_CanoR_1 | 321 | 330 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 340 | 347 | PF00244 | 0.287 |
LIG_14-3-3_CanoR_1 | 407 | 414 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 505 | 510 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 523 | 530 | PF00244 | 0.382 |
LIG_Actin_WH2_2 | 496 | 512 | PF00022 | 0.271 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.591 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.667 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.667 |
LIG_BRCT_BRCA1_1 | 350 | 354 | PF00533 | 0.365 |
LIG_FHA_1 | 157 | 163 | PF00498 | 0.671 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.511 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.473 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.363 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.361 |
LIG_FHA_1 | 552 | 558 | PF00498 | 0.487 |
LIG_FHA_1 | 578 | 584 | PF00498 | 0.363 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.641 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.676 |
LIG_FHA_2 | 515 | 521 | PF00498 | 0.474 |
LIG_FHA_2 | 540 | 546 | PF00498 | 0.382 |
LIG_FHA_2 | 576 | 582 | PF00498 | 0.440 |
LIG_LIR_Apic_2 | 76 | 80 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 476 | 487 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 596 | 604 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 176 | 181 | PF02991 | 0.659 |
LIG_LIR_Nem_3 | 476 | 482 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.588 |
LIG_LYPXL_yS_3 | 72 | 75 | PF13949 | 0.590 |
LIG_NRBOX | 465 | 471 | PF00104 | 0.446 |
LIG_Rb_pABgroove_1 | 348 | 356 | PF01858 | 0.361 |
LIG_SH2_CRK | 103 | 107 | PF00017 | 0.625 |
LIG_SH2_CRK | 77 | 81 | PF00017 | 0.476 |
LIG_SH2_SRC | 103 | 106 | PF00017 | 0.624 |
LIG_SH2_STAP1 | 408 | 412 | PF00017 | 0.366 |
LIG_SH2_STAT3 | 101 | 104 | PF00017 | 0.676 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.353 |
LIG_SH3_1 | 103 | 109 | PF00018 | 0.674 |
LIG_SH3_1 | 607 | 613 | PF00018 | 0.660 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.659 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.612 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.728 |
LIG_SH3_3 | 607 | 613 | PF00018 | 0.660 |
LIG_SUMO_SIM_par_1 | 483 | 488 | PF11976 | 0.346 |
LIG_UBA3_1 | 469 | 477 | PF00899 | 0.341 |
MOD_CDK_SPxxK_3 | 600 | 607 | PF00069 | 0.604 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.522 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.567 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.581 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.632 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.570 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.339 |
MOD_CK1_1 | 492 | 498 | PF00069 | 0.392 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.422 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.276 |
MOD_CK1_1 | 611 | 617 | PF00069 | 0.639 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.651 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.673 |
MOD_CK2_1 | 263 | 269 | PF00069 | 0.440 |
MOD_CK2_1 | 514 | 520 | PF00069 | 0.438 |
MOD_CK2_1 | 575 | 581 | PF00069 | 0.436 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.660 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.535 |
MOD_GlcNHglycan | 316 | 320 | PF01048 | 0.313 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.350 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.370 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.527 |
MOD_GlcNHglycan | 595 | 598 | PF01048 | 0.776 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.562 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.614 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.578 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.460 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.287 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.379 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.369 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.380 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.358 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.365 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.407 |
MOD_GSK3_1 | 598 | 605 | PF00069 | 0.589 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.662 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.547 |
MOD_N-GLC_1 | 185 | 190 | PF02516 | 0.492 |
MOD_N-GLC_1 | 248 | 253 | PF02516 | 0.619 |
MOD_N-GLC_1 | 356 | 361 | PF02516 | 0.338 |
MOD_N-GLC_1 | 396 | 401 | PF02516 | 0.487 |
MOD_N-GLC_1 | 473 | 478 | PF02516 | 0.301 |
MOD_N-GLC_1 | 84 | 89 | PF02516 | 0.689 |
MOD_N-GLC_2 | 334 | 336 | PF02516 | 0.429 |
MOD_N-GLC_2 | 384 | 386 | PF02516 | 0.343 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.482 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.402 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.369 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.338 |
MOD_NEK2_1 | 362 | 367 | PF00069 | 0.358 |
MOD_NEK2_1 | 441 | 446 | PF00069 | 0.473 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.502 |
MOD_NEK2_1 | 509 | 514 | PF00069 | 0.366 |
MOD_NEK2_1 | 575 | 580 | PF00069 | 0.436 |
MOD_PIKK_1 | 373 | 379 | PF00454 | 0.319 |
MOD_PIKK_1 | 458 | 464 | PF00454 | 0.370 |
MOD_PIKK_1 | 84 | 90 | PF00454 | 0.612 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.575 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.360 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.366 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.358 |
MOD_PKA_2 | 509 | 515 | PF00069 | 0.363 |
MOD_PKA_2 | 522 | 528 | PF00069 | 0.395 |
MOD_PKA_2 | 575 | 581 | PF00069 | 0.436 |
MOD_Plk_1 | 202 | 208 | PF00069 | 0.584 |
MOD_Plk_1 | 315 | 321 | PF00069 | 0.312 |
MOD_Plk_1 | 390 | 396 | PF00069 | 0.360 |
MOD_Plk_1 | 458 | 464 | PF00069 | 0.352 |
MOD_Plk_1 | 519 | 525 | PF00069 | 0.416 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.579 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.665 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.368 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.344 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.325 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.616 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.585 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.558 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.440 |
MOD_ProDKin_1 | 600 | 606 | PF00069 | 0.584 |
MOD_ProDKin_1 | 613 | 619 | PF00069 | 0.581 |
MOD_SUMO_rev_2 | 120 | 125 | PF00179 | 0.720 |
MOD_SUMO_rev_2 | 394 | 404 | PF00179 | 0.356 |
MOD_SUMO_rev_2 | 565 | 569 | PF00179 | 0.426 |
TRG_ENDOCYTIC_2 | 599 | 602 | PF00928 | 0.564 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.590 |
TRG_Pf-PMV_PEXEL_1 | 396 | 400 | PF00026 | 0.356 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5N0 | Leptomonas seymouri | 63% | 100% |
A0A3S7X7J0 | Leishmania donovani | 92% | 100% |
A4H7D3 | Leishmania braziliensis | 81% | 100% |
A4I9M5 | Leishmania infantum | 92% | 100% |
Q4Q3F2 | Leishmania major | 91% | 99% |