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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000151 | ubiquitin ligase complex | 3 | 1 |
GO:0000152 | nuclear ubiquitin ligase complex | 3 | 1 |
GO:0005680 | anaphase-promoting complex | 4 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 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: A4H6X4
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:0007088 | regulation of mitotic nuclear division | 6 | 1 |
GO:0007091 | metaphase/anaphase transition of mitotic cell cycle | 5 | 1 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 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:0010564 | regulation of cell cycle process | 5 | 1 |
GO:0010638 | positive regulation of organelle organization | 6 | 1 |
GO:0010965 | regulation of mitotic sister chromatid separation | 6 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0030071 | regulation of mitotic metaphase/anaphase transition | 7 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0031145 | anaphase-promoting complex-dependent catabolic process | 7 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0033043 | regulation of organelle organization | 5 | 1 |
GO:0033044 | regulation of chromosome organization | 6 | 1 |
GO:0033045 | regulation of sister chromatid segregation | 5 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 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:0044770 | cell cycle phase transition | 3 | 1 |
GO:0044772 | mitotic cell cycle phase transition | 4 | 1 |
GO:0044784 | metaphase/anaphase transition of cell cycle | 4 | 1 |
GO:0045787 | positive regulation of cell cycle | 5 | 1 |
GO:0045840 | positive regulation of mitotic nuclear division | 7 | 1 |
GO:0045842 | positive regulation of mitotic metaphase/anaphase transition | 8 | 1 |
GO:0045931 | positive regulation of mitotic cell cycle | 6 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051128 | regulation of cellular component organization | 4 | 1 |
GO:0051130 | positive regulation of cellular component organization | 5 | 1 |
GO:0051301 | cell division | 2 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0051726 | regulation of cell cycle | 4 | 1 |
GO:0051783 | regulation of nuclear division | 6 | 1 |
GO:0051785 | positive regulation of nuclear division | 7 | 1 |
GO:0051983 | regulation of chromosome segregation | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090068 | positive regulation of cell cycle process | 6 | 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 |
GO:1901970 | positive regulation of mitotic sister chromatid separation | 7 | 1 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 1 |
GO:1901989 | positive regulation of cell cycle phase transition | 7 | 1 |
GO:1901990 | regulation of mitotic cell cycle phase transition | 6 | 1 |
GO:1901992 | positive regulation of mitotic cell cycle phase transition | 7 | 1 |
GO:1902099 | regulation of metaphase/anaphase transition of cell cycle | 6 | 1 |
GO:1902101 | positive regulation of metaphase/anaphase transition of cell cycle | 7 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
GO:1905818 | regulation of chromosome separation | 5 | 1 |
GO:1905820 | positive regulation of chromosome separation | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 240 | 244 | PF00656 | 0.580 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 764 | 766 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 928 | 930 | PF00675 | 0.733 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.695 |
CLV_PCSK_KEX2_1 | 599 | 601 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 764 | 766 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 928 | 930 | PF00082 | 0.726 |
CLV_PCSK_PC1ET2_1 | 272 | 274 | PF00082 | 0.695 |
CLV_PCSK_PC1ET2_1 | 599 | 601 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 638 | 642 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 73 | 77 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 765 | 769 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 852 | 856 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.596 |
CLV_Separin_Metazoa | 113 | 117 | PF03568 | 0.614 |
CLV_Separin_Metazoa | 156 | 160 | PF03568 | 0.692 |
DEG_APCC_DBOX_1 | 601 | 609 | PF00400 | 0.449 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.559 |
DEG_SCF_FBW7_1 | 442 | 449 | PF00400 | 0.593 |
DEG_SPOP_SBC_1 | 274 | 278 | PF00917 | 0.684 |
DEG_SPOP_SBC_1 | 283 | 287 | PF00917 | 0.581 |
DEG_SPOP_SBC_1 | 503 | 507 | PF00917 | 0.669 |
DOC_ANK_TNKS_1 | 115 | 122 | PF00023 | 0.490 |
DOC_CDC14_PxL_1 | 25 | 33 | PF14671 | 0.617 |
DOC_CKS1_1 | 548 | 553 | PF01111 | 0.497 |
DOC_CYCLIN_yCln2_LP_2 | 32 | 38 | PF00134 | 0.637 |
DOC_CYCLIN_yCln2_LP_2 | 799 | 805 | PF00134 | 0.478 |
DOC_MAPK_gen_1 | 599 | 605 | PF00069 | 0.466 |
DOC_MAPK_gen_1 | 86 | 95 | PF00069 | 0.532 |
DOC_PP2B_LxvP_1 | 150 | 153 | PF13499 | 0.690 |
DOC_PP2B_LxvP_1 | 234 | 237 | PF13499 | 0.714 |
DOC_PP2B_LxvP_1 | 32 | 35 | PF13499 | 0.553 |
DOC_PP2B_LxvP_1 | 799 | 802 | PF13499 | 0.484 |
DOC_PP2B_LxvP_1 | 880 | 883 | PF13499 | 0.671 |
DOC_USP7_MATH_1 | 1002 | 1006 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 1009 | 1013 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 534 | 538 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 790 | 794 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 812 | 816 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 937 | 941 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 945 | 949 | PF00917 | 0.631 |
DOC_WW_Pin1_4 | 1012 | 1017 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 1026 | 1031 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 442 | 447 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 515 | 520 | PF00397 | 0.778 |
DOC_WW_Pin1_4 | 525 | 530 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 547 | 552 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 753 | 758 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 786 | 791 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 819 | 824 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 828 | 833 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 839 | 844 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 938 | 943 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 995 | 1000 | PF00397 | 0.549 |
LIG_14-3-3_CanoR_1 | 159 | 169 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 273 | 283 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 308 | 317 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 51 | 57 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 602 | 612 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 645 | 651 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 73 | 78 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 811 | 819 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 928 | 932 | PF00244 | 0.588 |
LIG_Actin_WH2_2 | 385 | 401 | PF00022 | 0.496 |
LIG_Actin_WH2_2 | 437 | 455 | PF00022 | 0.591 |
LIG_APCC_ABBAyCdc20_2 | 778 | 784 | PF00400 | 0.465 |
LIG_BRCT_BRCA1_1 | 328 | 332 | PF00533 | 0.678 |
LIG_BRCT_BRCA1_1 | 383 | 387 | PF00533 | 0.549 |
LIG_BRCT_BRCA1_1 | 483 | 487 | PF00533 | 0.511 |
LIG_BRCT_BRCA1_1 | 543 | 547 | PF00533 | 0.490 |
LIG_BRCT_BRCA1_1 | 60 | 64 | PF00533 | 0.650 |
LIG_Clathr_ClatBox_1 | 360 | 364 | PF01394 | 0.589 |
LIG_EVH1_2 | 966 | 970 | PF00568 | 0.685 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.648 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.639 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.514 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.746 |
LIG_FHA_1 | 669 | 675 | PF00498 | 0.385 |
LIG_FHA_1 | 712 | 718 | PF00498 | 0.477 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.590 |
LIG_FHA_1 | 766 | 772 | PF00498 | 0.457 |
LIG_FHA_1 | 928 | 934 | PF00498 | 0.587 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.488 |
LIG_FHA_2 | 596 | 602 | PF00498 | 0.465 |
LIG_FHA_2 | 645 | 651 | PF00498 | 0.456 |
LIG_FHA_2 | 677 | 683 | PF00498 | 0.385 |
LIG_FHA_2 | 874 | 880 | PF00498 | 0.616 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.539 |
LIG_LIR_Gen_1 | 174 | 183 | PF02991 | 0.590 |
LIG_LIR_Gen_1 | 537 | 548 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 572 | 583 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 591 | 597 | PF02991 | 0.242 |
LIG_LIR_Gen_1 | 655 | 665 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 537 | 543 | PF02991 | 0.612 |
LIG_LIR_Nem_3 | 572 | 578 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 582 | 588 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 591 | 595 | PF02991 | 0.235 |
LIG_LIR_Nem_3 | 655 | 660 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 756 | 762 | PF02991 | 0.491 |
LIG_NRBOX | 48 | 54 | PF00104 | 0.480 |
LIG_PCNA_yPIPBox_3 | 619 | 630 | PF02747 | 0.422 |
LIG_Pex14_2 | 543 | 547 | PF04695 | 0.490 |
LIG_PTB_Apo_2 | 591 | 598 | PF02174 | 0.428 |
LIG_PTB_Apo_2 | 770 | 777 | PF02174 | 0.486 |
LIG_PTB_Phospho_1 | 591 | 597 | PF10480 | 0.421 |
LIG_PTB_Phospho_1 | 770 | 776 | PF10480 | 0.482 |
LIG_Rb_LxCxE_1 | 740 | 758 | PF01857 | 0.487 |
LIG_Rb_pABgroove_1 | 584 | 592 | PF01858 | 0.446 |
LIG_SH2_CRK | 575 | 579 | PF00017 | 0.454 |
LIG_SH2_CRK | 592 | 596 | PF00017 | 0.251 |
LIG_SH2_GRB2like | 592 | 595 | PF00017 | 0.410 |
LIG_SH2_PTP2 | 630 | 633 | PF00017 | 0.435 |
LIG_SH2_PTP2 | 664 | 667 | PF00017 | 0.385 |
LIG_SH2_SRC | 590 | 593 | PF00017 | 0.437 |
LIG_SH2_SRC | 664 | 667 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 176 | 180 | PF00017 | 0.583 |
LIG_SH2_STAP1 | 592 | 596 | PF00017 | 0.409 |
LIG_SH2_STAT3 | 561 | 564 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.637 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 585 | 588 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 597 | 600 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 630 | 633 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 664 | 667 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 762 | 765 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 776 | 779 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 782 | 785 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 808 | 811 | PF00017 | 0.486 |
LIG_SH3_3 | 1027 | 1033 | PF00018 | 0.575 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.524 |
LIG_SH3_3 | 467 | 473 | PF00018 | 0.630 |
LIG_SH3_3 | 545 | 551 | PF00018 | 0.352 |
LIG_SH3_3 | 577 | 583 | PF00018 | 0.325 |
LIG_SH3_3 | 716 | 722 | PF00018 | 0.460 |
LIG_SH3_3 | 754 | 760 | PF00018 | 0.511 |
LIG_Sin3_3 | 656 | 663 | PF02671 | 0.385 |
LIG_TYR_ITAM | 572 | 588 | PF00017 | 0.463 |
MOD_CDK_SPxxK_3 | 265 | 272 | PF00069 | 0.566 |
MOD_CDK_SPxxK_3 | 337 | 344 | PF00069 | 0.674 |
MOD_CDK_SPxxK_3 | 355 | 362 | PF00069 | 0.462 |
MOD_CDK_SPxxK_3 | 515 | 522 | PF00069 | 0.555 |
MOD_CK1_1 | 1007 | 1013 | PF00069 | 0.681 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.531 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.617 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.546 |
MOD_CK1_1 | 323 | 329 | PF00069 | 0.720 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.672 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.571 |
MOD_CK1_1 | 753 | 759 | PF00069 | 0.526 |
MOD_CK1_1 | 772 | 778 | PF00069 | 0.343 |
MOD_CK1_1 | 833 | 839 | PF00069 | 0.608 |
MOD_CK1_1 | 927 | 933 | PF00069 | 0.603 |
MOD_CK1_1 | 944 | 950 | PF00069 | 0.592 |
MOD_CK2_1 | 676 | 682 | PF00069 | 0.459 |
MOD_CK2_1 | 811 | 817 | PF00069 | 0.554 |
MOD_CK2_1 | 873 | 879 | PF00069 | 0.607 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.544 |
MOD_GlcNHglycan | 1004 | 1007 | PF01048 | 0.699 |
MOD_GlcNHglycan | 1011 | 1014 | PF01048 | 0.642 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.655 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.662 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.656 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.621 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.819 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.593 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.764 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.488 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.515 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.632 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.577 |
MOD_GlcNHglycan | 478 | 481 | PF01048 | 0.555 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.688 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.694 |
MOD_GlcNHglycan | 792 | 795 | PF01048 | 0.465 |
MOD_GlcNHglycan | 832 | 835 | PF01048 | 0.596 |
MOD_GlcNHglycan | 883 | 886 | PF01048 | 0.695 |
MOD_GlcNHglycan | 887 | 890 | PF01048 | 0.660 |
MOD_GlcNHglycan | 897 | 900 | PF01048 | 0.572 |
MOD_GlcNHglycan | 901 | 904 | PF01048 | 0.542 |
MOD_GlcNHglycan | 934 | 937 | PF01048 | 0.718 |
MOD_GlcNHglycan | 943 | 946 | PF01048 | 0.609 |
MOD_GlcNHglycan | 947 | 950 | PF01048 | 0.566 |
MOD_GSK3_1 | 1007 | 1014 | PF00069 | 0.692 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.531 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.617 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.495 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.640 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.647 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.709 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.683 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.747 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.684 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.568 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.593 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.530 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.707 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.443 |
MOD_GSK3_1 | 747 | 754 | PF00069 | 0.596 |
MOD_GSK3_1 | 765 | 772 | PF00069 | 0.320 |
MOD_GSK3_1 | 786 | 793 | PF00069 | 0.582 |
MOD_GSK3_1 | 881 | 888 | PF00069 | 0.601 |
MOD_GSK3_1 | 893 | 900 | PF00069 | 0.636 |
MOD_GSK3_1 | 937 | 944 | PF00069 | 0.685 |
MOD_GSK3_1 | 954 | 961 | PF00069 | 0.551 |
MOD_N-GLC_1 | 241 | 246 | PF02516 | 0.633 |
MOD_N-GLC_1 | 333 | 338 | PF02516 | 0.744 |
MOD_N-GLC_1 | 622 | 627 | PF02516 | 0.265 |
MOD_N-GLC_1 | 668 | 673 | PF02516 | 0.385 |
MOD_N-GLC_1 | 772 | 777 | PF02516 | 0.500 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.626 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.628 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.668 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.551 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.540 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.549 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.542 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.521 |
MOD_NEK2_1 | 603 | 608 | PF00069 | 0.447 |
MOD_NEK2_1 | 970 | 975 | PF00069 | 0.665 |
MOD_NEK2_2 | 327 | 332 | PF00069 | 0.733 |
MOD_PIKK_1 | 1007 | 1013 | PF00454 | 0.693 |
MOD_PIKK_1 | 552 | 558 | PF00454 | 0.525 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.630 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.643 |
MOD_PKA_2 | 644 | 650 | PF00069 | 0.457 |
MOD_PKA_2 | 812 | 818 | PF00069 | 0.560 |
MOD_PKA_2 | 927 | 933 | PF00069 | 0.705 |
MOD_PKB_1 | 379 | 387 | PF00069 | 0.526 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.617 |
MOD_Plk_1 | 622 | 628 | PF00069 | 0.265 |
MOD_Plk_1 | 772 | 778 | PF00069 | 0.501 |
MOD_Plk_1 | 912 | 918 | PF00069 | 0.590 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.612 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.559 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.502 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.526 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.769 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.548 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.451 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.643 |
MOD_Plk_4 | 608 | 614 | PF00069 | 0.455 |
MOD_ProDKin_1 | 1012 | 1018 | PF00069 | 0.549 |
MOD_ProDKin_1 | 1026 | 1032 | PF00069 | 0.536 |
MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.583 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.685 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.696 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.497 |
MOD_ProDKin_1 | 442 | 448 | PF00069 | 0.587 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.690 |
MOD_ProDKin_1 | 515 | 521 | PF00069 | 0.779 |
MOD_ProDKin_1 | 525 | 531 | PF00069 | 0.564 |
MOD_ProDKin_1 | 547 | 553 | PF00069 | 0.501 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.657 |
MOD_ProDKin_1 | 753 | 759 | PF00069 | 0.662 |
MOD_ProDKin_1 | 786 | 792 | PF00069 | 0.522 |
MOD_ProDKin_1 | 819 | 825 | PF00069 | 0.564 |
MOD_ProDKin_1 | 828 | 834 | PF00069 | 0.662 |
MOD_ProDKin_1 | 839 | 845 | PF00069 | 0.552 |
MOD_ProDKin_1 | 938 | 944 | PF00069 | 0.561 |
MOD_ProDKin_1 | 995 | 1001 | PF00069 | 0.550 |
TRG_DiLeu_BaEn_1 | 437 | 442 | PF01217 | 0.515 |
TRG_DiLeu_BaEn_1 | 471 | 476 | PF01217 | 0.561 |
TRG_DiLeu_BaEn_1 | 541 | 546 | PF01217 | 0.481 |
TRG_DiLeu_BaEn_1 | 655 | 660 | PF01217 | 0.385 |
TRG_DiLeu_BaEn_2 | 382 | 388 | PF01217 | 0.507 |
TRG_DiLeu_BaLyEn_6 | 356 | 361 | PF01217 | 0.497 |
TRG_DiLeu_BaLyEn_6 | 393 | 398 | PF01217 | 0.502 |
TRG_DiLeu_BaLyEn_6 | 48 | 53 | PF01217 | 0.479 |
TRG_DiLeu_BaLyEn_6 | 527 | 532 | PF01217 | 0.551 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.583 |
TRG_ENDOCYTIC_2 | 575 | 578 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 585 | 588 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 592 | 595 | PF00928 | 0.251 |
TRG_ENDOCYTIC_2 | 629 | 632 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 664 | 667 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 698 | 701 | PF00928 | 0.448 |
TRG_ER_diArg_1 | 1033 | 1036 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 378 | 381 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 451 | 454 | PF00400 | 0.654 |
TRG_ER_diArg_1 | 565 | 568 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 577 | 580 | PF00400 | 0.351 |
TRG_ER_diArg_1 | 763 | 765 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 971 | 974 | PF00400 | 0.666 |
TRG_ER_diArg_1 | 991 | 994 | PF00400 | 0.489 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H6L1 | Leishmania donovani | 80% | 100% |
E9AGE8 | Leishmania infantum | 80% | 100% |
E9ANY8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 98% |
Q4QGN2 | Leishmania major | 80% | 100% |