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 | 7 |
GO:0043226 | organelle | 2 | 7 |
GO:0043227 | membrane-bounded organelle | 3 | 7 |
GO:0043229 | intracellular organelle | 3 | 7 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: E9B0S7
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006259 | DNA metabolic process | 4 | 7 |
GO:0006281 | DNA repair | 5 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0006950 | response to stress | 2 | 7 |
GO:0006974 | DNA damage response | 4 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0033554 | cellular response to stress | 3 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0050896 | response to stimulus | 1 | 7 |
GO:0051716 | cellular response to stimulus | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
GO:0000075 | cell cycle checkpoint signaling | 4 | 1 |
GO:0000076 | DNA replication checkpoint signaling | 6 | 1 |
GO:0000077 | DNA damage checkpoint signaling | 5 | 1 |
GO:0007093 | mitotic cell cycle checkpoint signaling | 4 | 1 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 1 |
GO:0010389 | regulation of G2/M transition of mitotic cell cycle | 7 | 1 |
GO:0010564 | regulation of cell cycle process | 5 | 1 |
GO:0010948 | negative regulation of cell cycle process | 6 | 1 |
GO:0010972 | negative regulation of G2/M transition of mitotic cell cycle | 8 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0031570 | DNA integrity checkpoint signaling | 5 | 1 |
GO:0033314 | mitotic DNA replication checkpoint signaling | 6 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0042770 | signal transduction in response to DNA damage | 4 | 1 |
GO:0044774 | mitotic DNA integrity checkpoint signaling | 5 | 1 |
GO:0044818 | mitotic G2/M transition checkpoint | 5 | 1 |
GO:0045786 | negative regulation of cell cycle | 5 | 1 |
GO:0045930 | negative regulation of mitotic cell cycle | 6 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051726 | regulation of cell cycle | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 1 |
GO:1901988 | negative regulation of cell cycle phase transition | 7 | 1 |
GO:1901990 | regulation of mitotic cell cycle phase transition | 6 | 1 |
GO:1901991 | negative regulation of mitotic cell cycle phase transition | 7 | 1 |
GO:1902749 | regulation of cell cycle G2/M phase transition | 7 | 1 |
GO:1902750 | negative regulation of cell cycle G2/M phase transition | 8 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0003682 | chromatin binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 153 | 157 | PF00656 | 0.578 |
CLV_C14_Caspase3-7 | 510 | 514 | PF00656 | 0.611 |
CLV_C14_Caspase3-7 | 568 | 572 | PF00656 | 0.599 |
CLV_C14_Caspase3-7 | 682 | 686 | PF00656 | 0.533 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.716 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 551 | 553 | PF00675 | 0.669 |
CLV_NRD_NRD_1 | 588 | 590 | PF00675 | 0.644 |
CLV_NRD_NRD_1 | 651 | 653 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 708 | 710 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 782 | 784 | PF00675 | 0.707 |
CLV_NRD_NRD_1 | 830 | 832 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 956 | 958 | PF00675 | 0.628 |
CLV_PCSK_FUR_1 | 333 | 337 | PF00082 | 0.620 |
CLV_PCSK_FUR_1 | 706 | 710 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.755 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.693 |
CLV_PCSK_KEX2_1 | 553 | 555 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 587 | 589 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 708 | 710 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 782 | 784 | PF00082 | 0.707 |
CLV_PCSK_KEX2_1 | 830 | 832 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 956 | 958 | PF00082 | 0.628 |
CLV_PCSK_PC1ET2_1 | 285 | 287 | PF00082 | 0.491 |
CLV_PCSK_PC1ET2_1 | 301 | 303 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 341 | 343 | PF00082 | 0.740 |
CLV_PCSK_PC1ET2_1 | 553 | 555 | PF00082 | 0.671 |
CLV_PCSK_PC7_1 | 297 | 303 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 613 | 617 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 632 | 636 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 652 | 656 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 957 | 961 | PF00082 | 0.618 |
DEG_APCC_DBOX_1 | 1010 | 1018 | PF00400 | 0.568 |
DEG_APCC_DBOX_1 | 191 | 199 | PF00400 | 0.500 |
DEG_APCC_DBOX_1 | 283 | 291 | PF00400 | 0.626 |
DEG_APCC_DBOX_1 | 380 | 388 | PF00400 | 0.495 |
DEG_APCC_DBOX_1 | 651 | 659 | PF00400 | 0.492 |
DEG_APCC_DBOX_1 | 860 | 868 | PF00400 | 0.560 |
DEG_COP1_1 | 69 | 78 | PF00400 | 0.481 |
DEG_Kelch_Keap1_1 | 511 | 516 | PF01344 | 0.584 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.494 |
DEG_SPOP_SBC_1 | 319 | 323 | PF00917 | 0.502 |
DEG_SPOP_SBC_1 | 354 | 358 | PF00917 | 0.531 |
DEG_SPOP_SBC_1 | 78 | 82 | PF00917 | 0.563 |
DEG_SPOP_SBC_1 | 941 | 945 | PF00917 | 0.579 |
DOC_CKS1_1 | 344 | 349 | PF01111 | 0.584 |
DOC_CKS1_1 | 990 | 995 | PF01111 | 0.571 |
DOC_CYCLIN_RxL_1 | 234 | 245 | PF00134 | 0.546 |
DOC_CYCLIN_RxL_1 | 56 | 67 | PF00134 | 0.542 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 236 | 243 | PF00134 | 0.547 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 278 | 287 | PF00134 | 0.489 |
DOC_CYCLIN_yCln2_LP_2 | 895 | 898 | PF00134 | 0.497 |
DOC_MAPK_gen_1 | 236 | 242 | PF00069 | 0.494 |
DOC_MAPK_gen_1 | 284 | 293 | PF00069 | 0.591 |
DOC_MAPK_HePTP_8 | 283 | 295 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 286 | 295 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 56 | 64 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 726 | 735 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 799 | 806 | PF00069 | 0.416 |
DOC_MAPK_MEF2A_6 | 989 | 998 | PF00069 | 0.562 |
DOC_PP1_RVXF_1 | 235 | 242 | PF00149 | 0.545 |
DOC_PP2B_LxvP_1 | 133 | 136 | PF13499 | 0.645 |
DOC_PP2B_LxvP_1 | 647 | 650 | PF13499 | 0.578 |
DOC_PP2B_LxvP_1 | 895 | 898 | PF13499 | 0.497 |
DOC_USP7_MATH_1 | 1030 | 1034 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 471 | 475 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 555 | 559 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 607 | 611 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 717 | 721 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 813 | 817 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 911 | 915 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 941 | 945 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 963 | 967 | PF00917 | 0.613 |
DOC_USP7_UBL2_3 | 339 | 343 | PF12436 | 0.681 |
DOC_USP7_UBL2_3 | 541 | 545 | PF12436 | 0.724 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 355 | 360 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 467 | 472 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 474 | 479 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 529 | 534 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 557 | 562 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 846 | 851 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 925 | 930 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 989 | 994 | PF00397 | 0.637 |
LIG_14-3-3_CanoR_1 | 18 | 23 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 192 | 196 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 34 | 39 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 450 | 455 | PF00244 | 0.646 |
LIG_14-3-3_CanoR_1 | 554 | 564 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 632 | 640 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 688 | 696 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 714 | 721 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 741 | 751 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 851 | 860 | PF00244 | 0.772 |
LIG_14-3-3_CanoR_1 | 870 | 879 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 905 | 915 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 956 | 960 | PF00244 | 0.622 |
LIG_Actin_WH2_2 | 191 | 207 | PF00022 | 0.422 |
LIG_APCC_ABBA_1 | 1039 | 1044 | PF00400 | 0.609 |
LIG_BRCT_BRCA1_1 | 1011 | 1015 | PF00533 | 0.650 |
LIG_BRCT_BRCA1_1 | 692 | 696 | PF00533 | 0.672 |
LIG_BRCT_BRCA1_1 | 96 | 100 | PF00533 | 0.415 |
LIG_EH1_1 | 627 | 635 | PF00400 | 0.575 |
LIG_EVH1_2 | 749 | 753 | PF00568 | 0.705 |
LIG_FHA_1 | 1005 | 1011 | PF00498 | 0.571 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.477 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.365 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.422 |
LIG_FHA_1 | 455 | 461 | PF00498 | 0.627 |
LIG_FHA_1 | 468 | 474 | PF00498 | 0.595 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.527 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.586 |
LIG_FHA_1 | 644 | 650 | PF00498 | 0.582 |
LIG_FHA_1 | 722 | 728 | PF00498 | 0.487 |
LIG_FHA_1 | 737 | 743 | PF00498 | 0.481 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.673 |
LIG_FHA_1 | 847 | 853 | PF00498 | 0.715 |
LIG_FHA_1 | 872 | 878 | PF00498 | 0.610 |
LIG_FHA_1 | 977 | 983 | PF00498 | 0.506 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.513 |
LIG_FHA_2 | 617 | 623 | PF00498 | 0.604 |
LIG_FHA_2 | 67 | 73 | PF00498 | 0.473 |
LIG_FHA_2 | 714 | 720 | PF00498 | 0.605 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.507 |
LIG_GBD_Chelix_1 | 727 | 735 | PF00786 | 0.416 |
LIG_LIR_Gen_1 | 200 | 208 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 423 | 433 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 798 | 809 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 97 | 108 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 200 | 204 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 423 | 428 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 621 | 626 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 739 | 743 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 798 | 804 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 880 | 884 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.546 |
LIG_LRP6_Inhibitor_1 | 658 | 664 | PF00058 | 0.526 |
LIG_LYPXL_yS_3 | 766 | 769 | PF13949 | 0.579 |
LIG_MYND_1 | 894 | 898 | PF01753 | 0.492 |
LIG_MYND_1 | 986 | 990 | PF01753 | 0.614 |
LIG_NRBOX | 59 | 65 | PF00104 | 0.446 |
LIG_Pex14_1 | 92 | 96 | PF04695 | 0.446 |
LIG_RPA_C_Fungi | 298 | 310 | PF08784 | 0.480 |
LIG_SH2_CRK | 49 | 53 | PF00017 | 0.498 |
LIG_SH2_CRK | 740 | 744 | PF00017 | 0.642 |
LIG_SH2_NCK_1 | 882 | 886 | PF00017 | 0.529 |
LIG_SH2_PTP2 | 887 | 890 | PF00017 | 0.552 |
LIG_SH2_SRC | 116 | 119 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 113 | 117 | PF00017 | 0.409 |
LIG_SH2_STAP1 | 674 | 678 | PF00017 | 0.589 |
LIG_SH2_STAP1 | 96 | 100 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 623 | 626 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 638 | 641 | PF00017 | 0.664 |
LIG_SH2_STAT5 | 657 | 660 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 665 | 668 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 761 | 764 | PF00017 | 0.673 |
LIG_SH2_STAT5 | 795 | 798 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 887 | 890 | PF00017 | 0.552 |
LIG_SH3_1 | 932 | 938 | PF00018 | 0.529 |
LIG_SH3_3 | 1035 | 1041 | PF00018 | 0.731 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.504 |
LIG_SH3_3 | 214 | 220 | PF00018 | 0.468 |
LIG_SH3_3 | 341 | 347 | PF00018 | 0.616 |
LIG_SH3_3 | 527 | 533 | PF00018 | 0.539 |
LIG_SH3_3 | 68 | 74 | PF00018 | 0.588 |
LIG_SH3_3 | 744 | 750 | PF00018 | 0.682 |
LIG_SH3_3 | 891 | 897 | PF00018 | 0.656 |
LIG_SH3_3 | 932 | 938 | PF00018 | 0.639 |
LIG_SH3_3 | 987 | 993 | PF00018 | 0.627 |
LIG_SH3_CIN85_PxpxPR_1 | 951 | 956 | PF14604 | 0.522 |
LIG_SUMO_SIM_anti_2 | 360 | 365 | PF11976 | 0.558 |
LIG_SUMO_SIM_anti_2 | 854 | 862 | PF11976 | 0.564 |
LIG_SUMO_SIM_par_1 | 20 | 26 | PF11976 | 0.549 |
LIG_SUMO_SIM_par_1 | 450 | 455 | PF11976 | 0.635 |
LIG_SUMO_SIM_par_1 | 565 | 572 | PF11976 | 0.574 |
LIG_TRFH_1 | 882 | 886 | PF08558 | 0.529 |
LIG_TYR_ITIM | 738 | 743 | PF00017 | 0.632 |
LIG_TYR_ITIM | 764 | 769 | PF00017 | 0.591 |
LIG_TYR_ITIM | 879 | 884 | PF00017 | 0.617 |
LIG_WW_1 | 758 | 761 | PF00397 | 0.685 |
LIG_WW_3 | 649 | 653 | PF00397 | 0.583 |
MOD_CDC14_SPxK_1 | 330 | 333 | PF00782 | 0.535 |
MOD_CDK_SPK_2 | 846 | 851 | PF00069 | 0.634 |
MOD_CDK_SPxK_1 | 327 | 333 | PF00069 | 0.534 |
MOD_CDK_SPxxK_3 | 474 | 481 | PF00069 | 0.586 |
MOD_CDK_SPxxK_3 | 529 | 536 | PF00069 | 0.589 |
MOD_CDK_SPxxK_3 | 925 | 932 | PF00069 | 0.556 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.509 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.713 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.642 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.592 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.658 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.738 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.623 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.592 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.623 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.597 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.679 |
MOD_CK1_1 | 524 | 530 | PF00069 | 0.585 |
MOD_CK1_1 | 532 | 538 | PF00069 | 0.620 |
MOD_CK1_1 | 690 | 696 | PF00069 | 0.671 |
MOD_CK1_1 | 820 | 826 | PF00069 | 0.702 |
MOD_CK1_1 | 844 | 850 | PF00069 | 0.734 |
MOD_CK1_1 | 939 | 945 | PF00069 | 0.678 |
MOD_CK1_1 | 965 | 971 | PF00069 | 0.678 |
MOD_CK1_1 | 978 | 984 | PF00069 | 0.573 |
MOD_CK2_1 | 1030 | 1036 | PF00069 | 0.646 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.600 |
MOD_CK2_1 | 496 | 502 | PF00069 | 0.687 |
MOD_CK2_1 | 519 | 525 | PF00069 | 0.774 |
MOD_CK2_1 | 569 | 575 | PF00069 | 0.678 |
MOD_CK2_1 | 616 | 622 | PF00069 | 0.604 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.460 |
MOD_CK2_1 | 713 | 719 | PF00069 | 0.603 |
MOD_CK2_1 | 794 | 800 | PF00069 | 0.549 |
MOD_CK2_1 | 813 | 819 | PF00069 | 0.597 |
MOD_Cter_Amidation | 225 | 228 | PF01082 | 0.594 |
MOD_DYRK1A_RPxSP_1 | 989 | 993 | PF00069 | 0.577 |
MOD_GlcNHglycan | 1032 | 1035 | PF01048 | 0.672 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.658 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.573 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.807 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.560 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.505 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.615 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.668 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.586 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.742 |
MOD_GlcNHglycan | 513 | 516 | PF01048 | 0.714 |
MOD_GlcNHglycan | 691 | 695 | PF01048 | 0.639 |
MOD_GlcNHglycan | 791 | 794 | PF01048 | 0.573 |
MOD_GlcNHglycan | 815 | 818 | PF01048 | 0.640 |
MOD_GlcNHglycan | 819 | 823 | PF01048 | 0.679 |
MOD_GlcNHglycan | 899 | 902 | PF01048 | 0.638 |
MOD_GlcNHglycan | 908 | 911 | PF01048 | 0.726 |
MOD_GlcNHglycan | 944 | 947 | PF01048 | 0.576 |
MOD_GlcNHglycan | 967 | 970 | PF01048 | 0.623 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.455 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.590 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.432 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.652 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.555 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.507 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.564 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.614 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.577 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.675 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.593 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.623 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.742 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.634 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.569 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.676 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.656 |
MOD_GSK3_1 | 713 | 720 | PF00069 | 0.756 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.665 |
MOD_GSK3_1 | 813 | 820 | PF00069 | 0.622 |
MOD_GSK3_1 | 840 | 847 | PF00069 | 0.701 |
MOD_GSK3_1 | 921 | 928 | PF00069 | 0.707 |
MOD_GSK3_1 | 936 | 943 | PF00069 | 0.578 |
MOD_GSK3_1 | 945 | 952 | PF00069 | 0.647 |
MOD_GSK3_1 | 961 | 968 | PF00069 | 0.686 |
MOD_N-GLC_1 | 256 | 261 | PF02516 | 0.485 |
MOD_N-GLC_1 | 539 | 544 | PF02516 | 0.550 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.673 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.369 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.488 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.536 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.675 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.657 |
MOD_NEK2_1 | 480 | 485 | PF00069 | 0.607 |
MOD_NEK2_1 | 569 | 574 | PF00069 | 0.587 |
MOD_NEK2_1 | 624 | 629 | PF00069 | 0.534 |
MOD_NEK2_1 | 692 | 697 | PF00069 | 0.588 |
MOD_NEK2_1 | 721 | 726 | PF00069 | 0.660 |
MOD_NEK2_1 | 727 | 732 | PF00069 | 0.567 |
MOD_NEK2_1 | 777 | 782 | PF00069 | 0.548 |
MOD_NEK2_1 | 962 | 967 | PF00069 | 0.641 |
MOD_NEK2_2 | 955 | 960 | PF00069 | 0.622 |
MOD_NEK2_2 | 96 | 101 | PF00069 | 0.343 |
MOD_PIKK_1 | 373 | 379 | PF00454 | 0.499 |
MOD_PIKK_1 | 395 | 401 | PF00454 | 0.503 |
MOD_PIKK_1 | 569 | 575 | PF00454 | 0.591 |
MOD_PIKK_1 | 607 | 613 | PF00454 | 0.722 |
MOD_PIKK_1 | 632 | 638 | PF00454 | 0.489 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.536 |
MOD_PK_1 | 286 | 292 | PF00069 | 0.576 |
MOD_PK_1 | 808 | 814 | PF00069 | 0.650 |
MOD_PKA_1 | 588 | 594 | PF00069 | 0.588 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.624 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.410 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.478 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.727 |
MOD_PKA_2 | 480 | 486 | PF00069 | 0.533 |
MOD_PKA_2 | 500 | 506 | PF00069 | 0.741 |
MOD_PKA_2 | 555 | 561 | PF00069 | 0.705 |
MOD_PKA_2 | 588 | 594 | PF00069 | 0.593 |
MOD_PKA_2 | 687 | 693 | PF00069 | 0.571 |
MOD_PKA_2 | 713 | 719 | PF00069 | 0.603 |
MOD_PKA_2 | 817 | 823 | PF00069 | 0.675 |
MOD_PKA_2 | 955 | 961 | PF00069 | 0.621 |
MOD_PKB_1 | 284 | 292 | PF00069 | 0.577 |
MOD_PKB_1 | 32 | 40 | PF00069 | 0.439 |
MOD_PKB_1 | 554 | 562 | PF00069 | 0.688 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.437 |
MOD_Plk_1 | 256 | 262 | PF00069 | 0.439 |
MOD_Plk_1 | 524 | 530 | PF00069 | 0.682 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.605 |
MOD_Plk_2-3 | 496 | 502 | PF00069 | 0.743 |
MOD_Plk_2-3 | 66 | 72 | PF00069 | 0.418 |
MOD_Plk_2-3 | 679 | 685 | PF00069 | 0.613 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.498 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.497 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.403 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.550 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.520 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.484 |
MOD_Plk_4 | 565 | 571 | PF00069 | 0.572 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.474 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.592 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.547 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.511 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.541 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.678 |
MOD_ProDKin_1 | 355 | 361 | PF00069 | 0.513 |
MOD_ProDKin_1 | 467 | 473 | PF00069 | 0.705 |
MOD_ProDKin_1 | 474 | 480 | PF00069 | 0.609 |
MOD_ProDKin_1 | 529 | 535 | PF00069 | 0.577 |
MOD_ProDKin_1 | 557 | 563 | PF00069 | 0.723 |
MOD_ProDKin_1 | 846 | 852 | PF00069 | 0.650 |
MOD_ProDKin_1 | 925 | 931 | PF00069 | 0.690 |
MOD_ProDKin_1 | 989 | 995 | PF00069 | 0.633 |
MOD_SUMO_rev_2 | 535 | 542 | PF00179 | 0.608 |
TRG_DiLeu_BaEn_1 | 66 | 71 | PF01217 | 0.496 |
TRG_DiLeu_BaEn_2 | 213 | 219 | PF01217 | 0.462 |
TRG_DiLeu_BaLyEn_6 | 1035 | 1040 | PF01217 | 0.732 |
TRG_DiLeu_BaLyEn_6 | 629 | 634 | PF01217 | 0.495 |
TRG_DiLeu_BaLyEn_6 | 891 | 896 | PF01217 | 0.480 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 623 | 626 | PF00928 | 0.548 |
TRG_ENDOCYTIC_2 | 740 | 743 | PF00928 | 0.653 |
TRG_ENDOCYTIC_2 | 761 | 764 | PF00928 | 0.637 |
TRG_ENDOCYTIC_2 | 766 | 769 | PF00928 | 0.565 |
TRG_ENDOCYTIC_2 | 881 | 884 | PF00928 | 0.556 |
TRG_ENDOCYTIC_2 | 887 | 890 | PF00928 | 0.524 |
TRG_ER_diArg_1 | 235 | 237 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 283 | 286 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 302 | 304 | PF00400 | 0.405 |
TRG_ER_diArg_1 | 333 | 336 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 552 | 555 | PF00400 | 0.702 |
TRG_ER_diArg_1 | 587 | 589 | PF00400 | 0.601 |
TRG_ER_diArg_1 | 767 | 770 | PF00400 | 0.550 |
TRG_ER_diArg_1 | 781 | 783 | PF00400 | 0.664 |
TRG_ER_diArg_1 | 830 | 833 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 955 | 957 | PF00400 | 0.629 |
TRG_NLS_Bipartite_1 | 284 | 305 | PF00514 | 0.535 |
TRG_NLS_MonoCore_2 | 552 | 557 | PF00514 | 0.701 |
TRG_NLS_MonoExtC_3 | 340 | 345 | PF00514 | 0.532 |
TRG_NLS_MonoExtC_3 | 551 | 556 | PF00514 | 0.699 |
TRG_NLS_MonoExtN_4 | 339 | 345 | PF00514 | 0.730 |
TRG_NLS_MonoExtN_4 | 552 | 557 | PF00514 | 0.714 |
TRG_Pf-PMV_PEXEL_1 | 632 | 636 | PF00026 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 652 | 656 | PF00026 | 0.581 |
TRG_Pf-PMV_PEXEL_1 | 709 | 713 | PF00026 | 0.584 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8V0 | Leptomonas seymouri | 42% | 100% |
A0A3Q8IRX6 | Leishmania donovani | 86% | 100% |
A4HI98 | Leishmania braziliensis | 72% | 100% |
A4I5I2 | Leishmania infantum | 87% | 100% |
Q4Q7F1 | Leishmania major | 86% | 100% |