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: A0A3S7X7J0
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_NRD_NRD_1 | 571 | 573 | PF00675 | 0.622 |
CLV_PCSK_KEX2_1 | 500 | 502 | PF00082 | 0.431 |
CLV_PCSK_PC1ET2_1 | 500 | 502 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 500 | 504 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 551 | 555 | PF00082 | 0.473 |
DEG_SPOP_SBC_1 | 140 | 144 | PF00917 | 0.622 |
DEG_SPOP_SBC_1 | 211 | 215 | PF00917 | 0.643 |
DOC_CDC14_PxL_1 | 543 | 551 | PF14671 | 0.490 |
DOC_CKS1_1 | 595 | 600 | PF01111 | 0.605 |
DOC_CYCLIN_RxL_1 | 432 | 440 | PF00134 | 0.484 |
DOC_MAPK_gen_1 | 500 | 507 | PF00069 | 0.481 |
DOC_MAPK_gen_1 | 572 | 580 | PF00069 | 0.515 |
DOC_MAPK_MEF2A_6 | 519 | 528 | PF00069 | 0.403 |
DOC_PP1_RVXF_1 | 458 | 465 | PF00149 | 0.572 |
DOC_PP2B_LxvP_1 | 466 | 469 | PF13499 | 0.611 |
DOC_PP4_FxxP_1 | 229 | 232 | PF00568 | 0.744 |
DOC_PP4_FxxP_1 | 97 | 100 | PF00568 | 0.674 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 474 | 478 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 581 | 585 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.793 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 594 | 599 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 607 | 612 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.711 |
LIG_14-3-3_CanoR_1 | 336 | 343 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 403 | 410 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 501 | 506 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 519 | 523 | PF00244 | 0.486 |
LIG_Actin_WH2_2 | 487 | 505 | PF00022 | 0.420 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.706 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.808 |
LIG_BIR_III_2 | 339 | 343 | PF00653 | 0.436 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.808 |
LIG_BRCT_BRCA1_1 | 346 | 350 | PF00533 | 0.468 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.748 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.592 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.695 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.561 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.429 |
LIG_FHA_1 | 502 | 508 | PF00498 | 0.469 |
LIG_FHA_1 | 548 | 554 | PF00498 | 0.558 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.735 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.800 |
LIG_FHA_2 | 511 | 517 | PF00498 | 0.513 |
LIG_FHA_2 | 536 | 542 | PF00498 | 0.474 |
LIG_FHA_2 | 572 | 578 | PF00498 | 0.543 |
LIG_FHA_2 | 611 | 617 | PF00498 | 0.772 |
LIG_LIR_Apic_2 | 592 | 598 | PF02991 | 0.624 |
LIG_LIR_Nem_3 | 171 | 176 | PF02991 | 0.788 |
LIG_LIR_Nem_3 | 63 | 67 | PF02991 | 0.691 |
LIG_LYPXL_yS_3 | 67 | 70 | PF13949 | 0.681 |
LIG_NRBOX | 461 | 467 | PF00104 | 0.574 |
LIG_Rb_pABgroove_1 | 344 | 352 | PF01858 | 0.462 |
LIG_SH2_CRK | 595 | 599 | PF00017 | 0.608 |
LIG_SH2_CRK | 98 | 102 | PF00017 | 0.712 |
LIG_SH2_SRC | 98 | 101 | PF00017 | 0.711 |
LIG_SH2_STAP1 | 404 | 408 | PF00017 | 0.468 |
LIG_SH2_STAT3 | 96 | 99 | PF00017 | 0.800 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.722 |
LIG_SH3_1 | 601 | 607 | PF00018 | 0.825 |
LIG_SH3_1 | 98 | 104 | PF00018 | 0.789 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.702 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.787 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.610 |
LIG_SH3_3 | 601 | 607 | PF00018 | 0.825 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.737 |
LIG_SUMO_SIM_par_1 | 479 | 484 | PF11976 | 0.442 |
LIG_TRAF2_1 | 513 | 516 | PF00917 | 0.468 |
LIG_WRC_WIRS_1 | 489 | 494 | PF05994 | 0.537 |
MOD_CDK_SPxxK_3 | 594 | 601 | PF00069 | 0.740 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.625 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.682 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.694 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.476 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.519 |
MOD_CK1_1 | 605 | 611 | PF00069 | 0.755 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.789 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.796 |
MOD_CK2_1 | 259 | 265 | PF00069 | 0.533 |
MOD_CK2_1 | 510 | 516 | PF00069 | 0.514 |
MOD_CK2_1 | 571 | 577 | PF00069 | 0.541 |
MOD_CK2_1 | 610 | 616 | PF00069 | 0.773 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.791 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.390 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.625 |
MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.814 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.664 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.713 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.760 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.594 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.399 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.470 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.514 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.747 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.768 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.637 |
MOD_N-GLC_1 | 244 | 249 | PF02516 | 0.751 |
MOD_N-GLC_1 | 30 | 35 | PF02516 | 0.691 |
MOD_N-GLC_1 | 352 | 357 | PF02516 | 0.434 |
MOD_N-GLC_1 | 392 | 397 | PF02516 | 0.570 |
MOD_N-GLC_1 | 79 | 84 | PF02516 | 0.816 |
MOD_N-GLC_2 | 330 | 332 | PF02516 | 0.543 |
MOD_N-GLC_2 | 380 | 382 | PF02516 | 0.438 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.811 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.543 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.434 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.458 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.597 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.550 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.409 |
MOD_NEK2_1 | 571 | 576 | PF00069 | 0.541 |
MOD_PIKK_1 | 454 | 460 | PF00454 | 0.468 |
MOD_PIKK_1 | 79 | 85 | PF00454 | 0.694 |
MOD_PIKK_1 | 86 | 92 | PF00454 | 0.646 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.418 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.458 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.458 |
MOD_PKA_2 | 505 | 511 | PF00069 | 0.472 |
MOD_PKA_2 | 518 | 524 | PF00069 | 0.495 |
MOD_PKA_2 | 571 | 577 | PF00069 | 0.541 |
MOD_Plk_1 | 244 | 250 | PF00069 | 0.713 |
MOD_Plk_1 | 30 | 36 | PF00069 | 0.694 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.461 |
MOD_Plk_1 | 454 | 460 | PF00069 | 0.450 |
MOD_Plk_1 | 515 | 521 | PF00069 | 0.514 |
MOD_Plk_1 | 79 | 85 | PF00069 | 0.641 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.785 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.819 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.471 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.443 |
MOD_Plk_4 | 485 | 491 | PF00069 | 0.419 |
MOD_Plk_4 | 524 | 530 | PF00069 | 0.385 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.702 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.681 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.551 |
MOD_ProDKin_1 | 594 | 600 | PF00069 | 0.720 |
MOD_ProDKin_1 | 607 | 613 | PF00069 | 0.691 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.712 |
MOD_SUMO_rev_2 | 115 | 120 | PF00179 | 0.794 |
MOD_SUMO_rev_2 | 390 | 400 | PF00179 | 0.455 |
MOD_SUMO_rev_2 | 561 | 565 | PF00179 | 0.551 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.681 |
TRG_Pf-PMV_PEXEL_1 | 392 | 396 | PF00026 | 0.455 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5N0 | Leptomonas seymouri | 64% | 99% |
A4H7D3 | Leishmania braziliensis | 82% | 100% |
A4I9M5 | Leishmania infantum | 99% | 100% |
E9B4M4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q3F2 | Leishmania major | 95% | 100% |