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: A4HI98
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 | 1043 | 1047 | PF00656 | 0.548 |
CLV_C14_Caspase3-7 | 1059 | 1063 | PF00656 | 0.519 |
CLV_C14_Caspase3-7 | 370 | 374 | PF00656 | 0.388 |
CLV_C14_Caspase3-7 | 464 | 468 | PF00656 | 0.518 |
CLV_C14_Caspase3-7 | 507 | 511 | PF00656 | 0.584 |
CLV_C14_Caspase3-7 | 518 | 522 | PF00656 | 0.607 |
CLV_C14_Caspase3-7 | 578 | 582 | PF00656 | 0.631 |
CLV_C14_Caspase3-7 | 591 | 595 | PF00656 | 0.623 |
CLV_C14_Caspase3-7 | 694 | 698 | PF00656 | 0.499 |
CLV_C14_Caspase3-7 | 800 | 804 | PF00656 | 0.543 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.769 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.746 |
CLV_NRD_NRD_1 | 560 | 562 | PF00675 | 0.651 |
CLV_NRD_NRD_1 | 663 | 665 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 720 | 722 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 798 | 800 | PF00675 | 0.679 |
CLV_NRD_NRD_1 | 842 | 844 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 968 | 970 | PF00675 | 0.618 |
CLV_PCSK_FUR_1 | 347 | 351 | PF00082 | 0.669 |
CLV_PCSK_FUR_1 | 718 | 722 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.769 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.746 |
CLV_PCSK_KEX2_1 | 562 | 564 | PF00082 | 0.659 |
CLV_PCSK_KEX2_1 | 720 | 722 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 798 | 800 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 842 | 844 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 968 | 970 | PF00082 | 0.618 |
CLV_PCSK_PC1ET2_1 | 293 | 295 | PF00082 | 0.433 |
CLV_PCSK_PC1ET2_1 | 349 | 351 | PF00082 | 0.715 |
CLV_PCSK_PC1ET2_1 | 562 | 564 | PF00082 | 0.659 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 466 | 470 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 644 | 648 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 664 | 668 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 969 | 973 | PF00082 | 0.611 |
DEG_APCC_DBOX_1 | 1022 | 1030 | PF00400 | 0.521 |
DEG_APCC_DBOX_1 | 199 | 207 | PF00400 | 0.463 |
DEG_APCC_DBOX_1 | 291 | 299 | PF00400 | 0.513 |
DEG_APCC_DBOX_1 | 388 | 396 | PF00400 | 0.427 |
DEG_APCC_DBOX_1 | 663 | 671 | PF00400 | 0.477 |
DEG_APCC_DBOX_1 | 872 | 880 | PF00400 | 0.489 |
DEG_COP1_1 | 705 | 714 | PF00400 | 0.471 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.492 |
DEG_SPOP_SBC_1 | 402 | 406 | PF00917 | 0.420 |
DEG_SPOP_SBC_1 | 86 | 90 | PF00917 | 0.602 |
DOC_CKS1_1 | 960 | 965 | PF01111 | 0.553 |
DOC_CYCLIN_RxL_1 | 241 | 253 | PF00134 | 0.455 |
DOC_CYCLIN_RxL_1 | 56 | 67 | PF00134 | 0.467 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 245 | 251 | PF00134 | 0.443 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 286 | 295 | PF00134 | 0.433 |
DOC_CYCLIN_yCln2_LP_2 | 952 | 955 | PF00134 | 0.536 |
DOC_MAPK_MEF2A_6 | 1001 | 1010 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 56 | 64 | PF00069 | 0.384 |
DOC_MAPK_MEF2A_6 | 738 | 747 | PF00069 | 0.487 |
DOC_PP1_RVXF_1 | 243 | 250 | PF00149 | 0.451 |
DOC_PP1_RVXF_1 | 840 | 847 | PF00149 | 0.519 |
DOC_PP2B_LxvP_1 | 133 | 136 | PF13499 | 0.618 |
DOC_PP2B_LxvP_1 | 168 | 171 | PF13499 | 0.504 |
DOC_PP2B_LxvP_1 | 659 | 662 | PF13499 | 0.586 |
DOC_PP2B_LxvP_1 | 952 | 955 | PF13499 | 0.536 |
DOC_PP4_FxxP_1 | 951 | 954 | PF00568 | 0.600 |
DOC_USP7_MATH_1 | 1039 | 1043 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 474 | 478 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 485 | 489 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 564 | 568 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 619 | 623 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 729 | 733 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 825 | 829 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 923 | 927 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 975 | 979 | PF00917 | 0.546 |
DOC_USP7_UBL2_3 | 550 | 554 | PF12436 | 0.618 |
DOC_WW_Pin1_4 | 1001 | 1006 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.369 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 534 | 539 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 565 | 570 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 858 | 863 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 937 | 942 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 953 | 958 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 959 | 964 | PF00397 | 0.706 |
LIG_14-3-3_CanoR_1 | 118 | 124 | PF00244 | 0.293 |
LIG_14-3-3_CanoR_1 | 151 | 156 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 172 | 180 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 18 | 23 | PF00244 | 0.401 |
LIG_14-3-3_CanoR_1 | 200 | 204 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 235 | 243 | PF00244 | 0.359 |
LIG_14-3-3_CanoR_1 | 350 | 356 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 458 | 463 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 471 | 481 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 563 | 569 | PF00244 | 0.670 |
LIG_14-3-3_CanoR_1 | 644 | 652 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 700 | 708 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 726 | 733 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 74 | 84 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 753 | 763 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 863 | 872 | PF00244 | 0.735 |
LIG_14-3-3_CanoR_1 | 882 | 891 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 968 | 972 | PF00244 | 0.613 |
LIG_Actin_WH2_2 | 199 | 215 | PF00022 | 0.338 |
LIG_Actin_WH2_2 | 282 | 298 | PF00022 | 0.346 |
LIG_Actin_WH2_2 | 327 | 342 | PF00022 | 0.506 |
LIG_BRCT_BRCA1_1 | 1023 | 1027 | PF00533 | 0.601 |
LIG_BRCT_BRCA1_1 | 704 | 708 | PF00533 | 0.629 |
LIG_EH1_1 | 639 | 647 | PF00400 | 0.569 |
LIG_EVH1_2 | 761 | 765 | PF00568 | 0.666 |
LIG_EVH1_2 | 770 | 774 | PF00568 | 0.585 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.425 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.570 |
LIG_FHA_1 | 523 | 529 | PF00498 | 0.680 |
LIG_FHA_1 | 656 | 662 | PF00498 | 0.640 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.637 |
LIG_FHA_1 | 803 | 809 | PF00498 | 0.514 |
LIG_FHA_1 | 859 | 865 | PF00498 | 0.683 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.681 |
LIG_FHA_1 | 884 | 890 | PF00498 | 0.526 |
LIG_FHA_2 | 1041 | 1047 | PF00498 | 0.646 |
LIG_FHA_2 | 251 | 257 | PF00498 | 0.458 |
LIG_FHA_2 | 448 | 454 | PF00498 | 0.496 |
LIG_FHA_2 | 589 | 595 | PF00498 | 0.547 |
LIG_FHA_2 | 629 | 635 | PF00498 | 0.654 |
LIG_FHA_2 | 726 | 732 | PF00498 | 0.573 |
LIG_FHA_2 | 798 | 804 | PF00498 | 0.783 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.450 |
LIG_LIR_Gen_1 | 208 | 216 | PF02991 | 0.584 |
LIG_LIR_Gen_1 | 309 | 319 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 366 | 377 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 431 | 437 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 98 | 108 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 208 | 212 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 309 | 315 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 431 | 436 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 633 | 638 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 705 | 711 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 751 | 755 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 892 | 896 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 98 | 103 | PF02991 | 0.498 |
LIG_LRP6_Inhibitor_1 | 670 | 676 | PF00058 | 0.488 |
LIG_LYPXL_yS_3 | 778 | 781 | PF13949 | 0.546 |
LIG_MYND_1 | 950 | 954 | PF01753 | 0.531 |
LIG_NRBOX | 59 | 65 | PF00104 | 0.376 |
LIG_SH2_CRK | 49 | 53 | PF00017 | 0.402 |
LIG_SH2_CRK | 752 | 756 | PF00017 | 0.583 |
LIG_SH2_NCK_1 | 894 | 898 | PF00017 | 0.445 |
LIG_SH2_PTP2 | 899 | 902 | PF00017 | 0.460 |
LIG_SH2_STAP1 | 113 | 117 | PF00017 | 0.391 |
LIG_SH2_STAP1 | 686 | 690 | PF00017 | 0.673 |
LIG_SH2_STAT3 | 773 | 776 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 635 | 638 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 650 | 653 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 669 | 672 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 677 | 680 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 773 | 776 | PF00017 | 0.690 |
LIG_SH2_STAT5 | 899 | 902 | PF00017 | 0.460 |
LIG_SH3_3 | 1047 | 1053 | PF00018 | 0.719 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.464 |
LIG_SH3_3 | 566 | 572 | PF00018 | 0.595 |
LIG_SH3_3 | 609 | 615 | PF00018 | 0.615 |
LIG_SH3_3 | 756 | 762 | PF00018 | 0.625 |
LIG_SH3_3 | 901 | 907 | PF00018 | 0.605 |
LIG_SH3_3 | 944 | 950 | PF00018 | 0.605 |
LIG_SH3_3 | 951 | 957 | PF00018 | 0.614 |
LIG_SH3_3 | 990 | 996 | PF00018 | 0.614 |
LIG_SUMO_SIM_par_1 | 20 | 25 | PF11976 | 0.483 |
LIG_SUMO_SIM_par_1 | 575 | 582 | PF11976 | 0.619 |
LIG_TRFH_1 | 894 | 898 | PF08558 | 0.445 |
LIG_TRFH_1 | 951 | 955 | PF08558 | 0.538 |
LIG_TYR_ITIM | 750 | 755 | PF00017 | 0.586 |
LIG_TYR_ITIM | 891 | 896 | PF00017 | 0.530 |
LIG_UBA3_1 | 203 | 207 | PF00899 | 0.303 |
LIG_WRC_WIRS_1 | 135 | 140 | PF05994 | 0.485 |
LIG_WW_1 | 770 | 773 | PF00397 | 0.680 |
LIG_WW_3 | 661 | 665 | PF00397 | 0.583 |
MOD_CDC14_SPxK_1 | 416 | 419 | PF00782 | 0.499 |
MOD_CDK_SPK_2 | 858 | 863 | PF00069 | 0.600 |
MOD_CDK_SPxK_1 | 413 | 419 | PF00069 | 0.503 |
MOD_CDK_SPxxK_3 | 534 | 541 | PF00069 | 0.682 |
MOD_CK1_1 | 1042 | 1048 | PF00069 | 0.572 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.470 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.714 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.609 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.489 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.652 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.546 |
MOD_CK1_1 | 475 | 481 | PF00069 | 0.594 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.564 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.655 |
MOD_CK1_1 | 529 | 535 | PF00069 | 0.592 |
MOD_CK1_1 | 702 | 708 | PF00069 | 0.620 |
MOD_CK1_1 | 823 | 829 | PF00069 | 0.577 |
MOD_CK1_1 | 856 | 862 | PF00069 | 0.676 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.497 |
MOD_CK1_1 | 977 | 983 | PF00069 | 0.669 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.591 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.576 |
MOD_CK2_1 | 528 | 534 | PF00069 | 0.728 |
MOD_CK2_1 | 579 | 585 | PF00069 | 0.693 |
MOD_CK2_1 | 628 | 634 | PF00069 | 0.592 |
MOD_CK2_1 | 725 | 731 | PF00069 | 0.575 |
MOD_CK2_1 | 806 | 812 | PF00069 | 0.558 |
MOD_Cter_Amidation | 233 | 236 | PF01082 | 0.561 |
MOD_GlcNHglycan | 1029 | 1032 | PF01048 | 0.529 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.709 |
MOD_GlcNHglycan | 163 | 167 | PF01048 | 0.551 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.685 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.408 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.628 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.387 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.464 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.521 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.527 |
MOD_GlcNHglycan | 490 | 493 | PF01048 | 0.643 |
MOD_GlcNHglycan | 703 | 707 | PF01048 | 0.585 |
MOD_GlcNHglycan | 712 | 715 | PF01048 | 0.493 |
MOD_GlcNHglycan | 827 | 830 | PF01048 | 0.614 |
MOD_GlcNHglycan | 918 | 921 | PF01048 | 0.640 |
MOD_GlcNHglycan | 979 | 982 | PF01048 | 0.614 |
MOD_GlcNHglycan | 989 | 992 | PF01048 | 0.613 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.445 |
MOD_GSK3_1 | 1035 | 1042 | PF00069 | 0.540 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.577 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.393 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.694 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.597 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.446 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.444 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.624 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.660 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.725 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.517 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.608 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.629 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.572 |
MOD_GSK3_1 | 504 | 511 | PF00069 | 0.719 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.649 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.615 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.736 |
MOD_GSK3_1 | 619 | 626 | PF00069 | 0.602 |
MOD_GSK3_1 | 725 | 732 | PF00069 | 0.728 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.609 |
MOD_GSK3_1 | 797 | 804 | PF00069 | 0.659 |
MOD_GSK3_1 | 825 | 832 | PF00069 | 0.598 |
MOD_GSK3_1 | 852 | 859 | PF00069 | 0.652 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.446 |
MOD_GSK3_1 | 923 | 930 | PF00069 | 0.760 |
MOD_GSK3_1 | 973 | 980 | PF00069 | 0.665 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.384 |
MOD_N-GLC_1 | 413 | 418 | PF02516 | 0.499 |
MOD_N-GLC_1 | 526 | 531 | PF02516 | 0.570 |
MOD_N-GLC_1 | 806 | 811 | PF02516 | 0.479 |
MOD_N-GLC_1 | 934 | 939 | PF02516 | 0.627 |
MOD_N-GLC_1 | 95 | 100 | PF02516 | 0.387 |
MOD_N-GLC_2 | 230 | 232 | PF02516 | 0.478 |
MOD_NEK2_1 | 1027 | 1032 | PF00069 | 0.434 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.534 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.418 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.436 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.710 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.550 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.358 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.482 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.492 |
MOD_NEK2_1 | 579 | 584 | PF00069 | 0.611 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.506 |
MOD_NEK2_1 | 704 | 709 | PF00069 | 0.550 |
MOD_NEK2_1 | 739 | 744 | PF00069 | 0.517 |
MOD_NEK2_1 | 748 | 753 | PF00069 | 0.435 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.468 |
MOD_NEK2_1 | 927 | 932 | PF00069 | 0.732 |
MOD_NEK2_1 | 974 | 979 | PF00069 | 0.633 |
MOD_NEK2_2 | 967 | 972 | PF00069 | 0.616 |
MOD_OFUCOSY | 232 | 238 | PF10250 | 0.444 |
MOD_PIKK_1 | 381 | 387 | PF00454 | 0.452 |
MOD_PIKK_1 | 579 | 585 | PF00454 | 0.611 |
MOD_PIKK_1 | 619 | 625 | PF00454 | 0.696 |
MOD_PIKK_1 | 644 | 650 | PF00454 | 0.500 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.517 |
MOD_PK_1 | 151 | 157 | PF00069 | 0.517 |
MOD_PK_1 | 294 | 300 | PF00069 | 0.521 |
MOD_PK_1 | 820 | 826 | PF00069 | 0.622 |
MOD_PKA_1 | 343 | 349 | PF00069 | 0.642 |
MOD_PKA_1 | 350 | 356 | PF00069 | 0.640 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.591 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.549 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.382 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.454 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.800 |
MOD_PKA_2 | 508 | 514 | PF00069 | 0.678 |
MOD_PKA_2 | 564 | 570 | PF00069 | 0.676 |
MOD_PKA_2 | 699 | 705 | PF00069 | 0.509 |
MOD_PKA_2 | 725 | 731 | PF00069 | 0.575 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.468 |
MOD_PKA_2 | 797 | 803 | PF00069 | 0.649 |
MOD_PKA_2 | 967 | 973 | PF00069 | 0.616 |
MOD_PKB_1 | 292 | 300 | PF00069 | 0.523 |
MOD_PKB_1 | 780 | 788 | PF00069 | 0.590 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.440 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.516 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.384 |
MOD_Plk_1 | 515 | 521 | PF00069 | 0.566 |
MOD_Plk_1 | 522 | 528 | PF00069 | 0.605 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.518 |
MOD_Plk_1 | 95 | 101 | PF00069 | 0.463 |
MOD_Plk_2-3 | 373 | 379 | PF00069 | 0.378 |
MOD_Plk_2-3 | 504 | 510 | PF00069 | 0.706 |
MOD_Plk_2-3 | 515 | 521 | PF00069 | 0.585 |
MOD_Plk_2-3 | 691 | 697 | PF00069 | 0.577 |
MOD_Plk_2-3 | 797 | 803 | PF00069 | 0.784 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.534 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.494 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.582 |
MOD_Plk_4 | 575 | 581 | PF00069 | 0.622 |
MOD_Plk_4 | 623 | 629 | PF00069 | 0.594 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.392 |
MOD_Plk_4 | 704 | 710 | PF00069 | 0.468 |
MOD_ProDKin_1 | 1001 | 1007 | PF00069 | 0.565 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.453 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.376 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.505 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.666 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.503 |
MOD_ProDKin_1 | 534 | 540 | PF00069 | 0.643 |
MOD_ProDKin_1 | 565 | 571 | PF00069 | 0.728 |
MOD_ProDKin_1 | 858 | 864 | PF00069 | 0.594 |
MOD_ProDKin_1 | 937 | 943 | PF00069 | 0.644 |
MOD_ProDKin_1 | 953 | 959 | PF00069 | 0.629 |
MOD_SUMO_rev_2 | 219 | 226 | PF00179 | 0.407 |
MOD_SUMO_rev_2 | 461 | 470 | PF00179 | 0.518 |
TRG_DiLeu_BaLyEn_6 | 1047 | 1052 | PF01217 | 0.719 |
TRG_DiLeu_BaLyEn_6 | 641 | 646 | PF01217 | 0.491 |
TRG_DiLeu_BaLyEn_6 | 735 | 740 | PF01217 | 0.497 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 635 | 638 | PF00928 | 0.552 |
TRG_ENDOCYTIC_2 | 752 | 755 | PF00928 | 0.589 |
TRG_ENDOCYTIC_2 | 778 | 781 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 893 | 896 | PF00928 | 0.478 |
TRG_ENDOCYTIC_2 | 899 | 902 | PF00928 | 0.433 |
TRG_ER_diArg_1 | 291 | 294 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 779 | 782 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 842 | 845 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 967 | 969 | PF00400 | 0.627 |
TRG_NLS_MonoExtC_3 | 291 | 296 | PF00514 | 0.343 |
TRG_NLS_MonoExtC_3 | 560 | 565 | PF00514 | 0.656 |
TRG_NLS_MonoExtN_4 | 292 | 297 | PF00514 | 0.367 |
TRG_NLS_MonoExtN_4 | 347 | 353 | PF00514 | 0.709 |
TRG_NLS_MonoExtN_4 | 561 | 566 | PF00514 | 0.674 |
TRG_Pf-PMV_PEXEL_1 | 213 | 217 | PF00026 | 0.390 |
TRG_Pf-PMV_PEXEL_1 | 296 | 300 | PF00026 | 0.369 |
TRG_Pf-PMV_PEXEL_1 | 644 | 648 | PF00026 | 0.492 |
TRG_Pf-PMV_PEXEL_1 | 664 | 668 | PF00026 | 0.341 |
TRG_Pf-PMV_PEXEL_1 | 721 | 725 | PF00026 | 0.565 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8V0 | Leptomonas seymouri | 42% | 100% |
A0A3Q8IRX6 | Leishmania donovani | 72% | 100% |
A4I5I2 | Leishmania infantum | 73% | 100% |
E9B0S7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
Q4Q7F1 | Leishmania major | 73% | 99% |