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. | yes | 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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000151 | ubiquitin ligase complex | 3 | 2 |
GO:0005634 | nucleus | 5 | 2 |
GO:0005886 | plasma membrane | 3 | 2 |
GO:0005929 | cilium | 4 | 8 |
GO:0016020 | membrane | 2 | 2 |
GO:0019005 | SCF ubiquitin ligase complex | 5 | 2 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0042995 | cell projection | 2 | 8 |
GO:0043226 | organelle | 2 | 8 |
GO:0043227 | membrane-bounded organelle | 3 | 8 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 8 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1990234 | transferase complex | 3 | 2 |
Related structures:
AlphaFold database: Q4Q3F2
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 2 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010498 | proteasomal protein catabolic process | 5 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 2 |
GO:0030163 | protein catabolic process | 4 | 2 |
GO:0031146 | SCF-dependent proteasomal ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 2 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 571 | 573 | PF00675 | 0.621 |
CLV_PCSK_KEX2_1 | 500 | 502 | PF00082 | 0.414 |
CLV_PCSK_PC1ET2_1 | 500 | 502 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 500 | 504 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 551 | 555 | PF00082 | 0.446 |
DOC_CDC14_PxL_1 | 543 | 551 | PF14671 | 0.476 |
DOC_CYCLIN_RxL_1 | 432 | 440 | PF00134 | 0.465 |
DOC_MAPK_gen_1 | 500 | 507 | PF00069 | 0.408 |
DOC_MAPK_gen_1 | 572 | 580 | PF00069 | 0.497 |
DOC_PP1_RVXF_1 | 458 | 465 | PF00149 | 0.469 |
DOC_PP2B_LxvP_1 | 466 | 469 | PF13499 | 0.515 |
DOC_PP4_FxxP_1 | 229 | 232 | PF00568 | 0.634 |
DOC_PP4_FxxP_1 | 97 | 100 | PF00568 | 0.661 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 474 | 478 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.311 |
DOC_USP7_MATH_1 | 581 | 585 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.740 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.679 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 596 | 601 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 609 | 614 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.631 |
LIG_14-3-3_CanoR_1 | 317 | 326 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 336 | 343 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 403 | 410 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 501 | 506 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 519 | 526 | PF00244 | 0.326 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.669 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.686 |
LIG_BIR_III_2 | 339 | 343 | PF00653 | 0.416 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.686 |
LIG_BRCT_BRCA1_1 | 346 | 350 | PF00533 | 0.448 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.813 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.569 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.631 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.457 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.419 |
LIG_FHA_1 | 502 | 508 | PF00498 | 0.456 |
LIG_FHA_1 | 548 | 554 | PF00498 | 0.575 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.691 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.792 |
LIG_FHA_2 | 511 | 517 | PF00498 | 0.438 |
LIG_FHA_2 | 536 | 542 | PF00498 | 0.463 |
LIG_FHA_2 | 572 | 578 | PF00498 | 0.529 |
LIG_FHA_2 | 613 | 619 | PF00498 | 0.747 |
LIG_LIR_Gen_1 | 592 | 600 | PF02991 | 0.691 |
LIG_LIR_Nem_3 | 172 | 176 | PF02991 | 0.692 |
LIG_LIR_Nem_3 | 63 | 67 | PF02991 | 0.668 |
LIG_LYPXL_yS_3 | 67 | 70 | PF13949 | 0.658 |
LIG_NRBOX | 461 | 467 | PF00104 | 0.459 |
LIG_Pex14_2 | 223 | 227 | PF04695 | 0.491 |
LIG_PTB_Apo_2 | 217 | 224 | PF02174 | 0.494 |
LIG_Rb_pABgroove_1 | 344 | 352 | PF01858 | 0.443 |
LIG_SH2_CRK | 98 | 102 | PF00017 | 0.645 |
LIG_SH2_SRC | 98 | 101 | PF00017 | 0.645 |
LIG_SH2_STAP1 | 404 | 408 | PF00017 | 0.451 |
LIG_SH2_STAT3 | 96 | 99 | PF00017 | 0.699 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.659 |
LIG_SH3_1 | 603 | 609 | PF00018 | 0.659 |
LIG_SH3_1 | 98 | 104 | PF00018 | 0.694 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.742 |
LIG_SH3_3 | 168 | 174 | PF00018 | 0.633 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.709 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.719 |
LIG_SH3_3 | 603 | 609 | PF00018 | 0.659 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.735 |
LIG_SUMO_SIM_par_1 | 479 | 484 | PF11976 | 0.360 |
LIG_TRAF2_1 | 513 | 516 | PF00917 | 0.448 |
LIG_WRC_WIRS_1 | 489 | 494 | PF05994 | 0.441 |
MOD_CDK_SPxxK_3 | 596 | 603 | PF00069 | 0.691 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.684 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.679 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.376 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.457 |
MOD_CK1_1 | 607 | 613 | PF00069 | 0.721 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.823 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.789 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.513 |
MOD_CK2_1 | 510 | 516 | PF00069 | 0.464 |
MOD_CK2_1 | 535 | 541 | PF00069 | 0.415 |
MOD_CK2_1 | 571 | 577 | PF00069 | 0.467 |
MOD_CK2_1 | 612 | 618 | PF00069 | 0.744 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.679 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.764 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.378 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.569 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.463 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.710 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.815 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.574 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.762 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.687 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.640 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.613 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.454 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.383 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.450 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.467 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.646 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.660 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.700 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.655 |
MOD_N-GLC_1 | 244 | 249 | PF02516 | 0.663 |
MOD_N-GLC_1 | 30 | 35 | PF02516 | 0.569 |
MOD_N-GLC_1 | 352 | 357 | PF02516 | 0.416 |
MOD_N-GLC_1 | 392 | 397 | PF02516 | 0.469 |
MOD_N-GLC_1 | 535 | 540 | PF02516 | 0.392 |
MOD_N-GLC_1 | 79 | 84 | PF02516 | 0.704 |
MOD_N-GLC_2 | 330 | 332 | PF02516 | 0.440 |
MOD_N-GLC_2 | 380 | 382 | PF02516 | 0.421 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.814 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.661 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.570 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.390 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.352 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.457 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.497 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.514 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.405 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.526 |
MOD_PIKK_1 | 19 | 25 | PF00454 | 0.489 |
MOD_PIKK_1 | 369 | 375 | PF00454 | 0.388 |
MOD_PIKK_1 | 454 | 460 | PF00454 | 0.470 |
MOD_PIKK_1 | 86 | 92 | PF00454 | 0.640 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.443 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.447 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.457 |
MOD_PKA_2 | 505 | 511 | PF00069 | 0.481 |
MOD_PKA_2 | 518 | 524 | PF00069 | 0.489 |
MOD_PKA_2 | 571 | 577 | PF00069 | 0.500 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.665 |
MOD_Plk_1 | 244 | 250 | PF00069 | 0.639 |
MOD_Plk_1 | 30 | 36 | PF00069 | 0.570 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.443 |
MOD_Plk_1 | 454 | 460 | PF00069 | 0.392 |
MOD_Plk_1 | 515 | 521 | PF00069 | 0.473 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.771 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.805 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.451 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.421 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.679 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.709 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.478 |
MOD_ProDKin_1 | 596 | 602 | PF00069 | 0.675 |
MOD_ProDKin_1 | 609 | 615 | PF00069 | 0.653 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.646 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.631 |
MOD_SUMO_rev_2 | 115 | 120 | PF00179 | 0.693 |
MOD_SUMO_rev_2 | 390 | 400 | PF00179 | 0.441 |
MOD_SUMO_rev_2 | 561 | 565 | PF00179 | 0.550 |
TRG_ENDOCYTIC_2 | 595 | 598 | PF00928 | 0.693 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.658 |
TRG_Pf-PMV_PEXEL_1 | 392 | 396 | PF00026 | 0.438 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5N0 | Leptomonas seymouri | 64% | 99% |
A0A3S5ISR4 | Trypanosoma rangeli | 24% | 75% |
A0A3S7X7J0 | Leishmania donovani | 95% | 100% |
A4H7D3 | Leishmania braziliensis | 82% | 100% |
A4I9M5 | Leishmania infantum | 95% | 100% |
E9B4M4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 99% |