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: Q4Q7F1
Term | Name | Level | Count |
---|---|---|---|
GO:0000075 | cell cycle checkpoint signaling | 4 | 2 |
GO:0000076 | DNA replication checkpoint signaling | 6 | 2 |
GO:0000077 | DNA damage checkpoint signaling | 5 | 2 |
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:0007093 | mitotic cell cycle checkpoint signaling | 4 | 2 |
GO:0007165 | signal transduction | 2 | 2 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 2 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0010389 | regulation of G2/M transition of mitotic cell cycle | 7 | 2 |
GO:0010564 | regulation of cell cycle process | 5 | 2 |
GO:0010948 | negative regulation of cell cycle process | 6 | 2 |
GO:0010972 | negative regulation of G2/M transition of mitotic cell cycle | 8 | 2 |
GO:0022402 | cell cycle process | 2 | 2 |
GO:0031570 | DNA integrity checkpoint signaling | 5 | 2 |
GO:0033314 | mitotic DNA replication checkpoint signaling | 6 | 2 |
GO:0033554 | cellular response to stress | 3 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0035556 | intracellular signal transduction | 3 | 2 |
GO:0042770 | signal transduction in response to DNA damage | 4 | 2 |
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:0044774 | mitotic DNA integrity checkpoint signaling | 5 | 2 |
GO:0044818 | mitotic G2/M transition checkpoint | 5 | 2 |
GO:0045786 | negative regulation of cell cycle | 5 | 2 |
GO:0045930 | negative regulation of mitotic cell cycle | 6 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0048519 | negative regulation of biological process | 3 | 2 |
GO:0048523 | negative regulation of cellular process | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0050896 | response to stimulus | 1 | 7 |
GO:0051716 | cellular response to stimulus | 2 | 7 |
GO:0051726 | regulation of cell cycle | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
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:1901987 | regulation of cell cycle phase transition | 6 | 2 |
GO:1901988 | negative regulation of cell cycle phase transition | 7 | 2 |
GO:1901990 | regulation of mitotic cell cycle phase transition | 6 | 2 |
GO:1901991 | negative regulation of mitotic cell cycle phase transition | 7 | 2 |
GO:1902749 | regulation of cell cycle G2/M phase transition | 7 | 2 |
GO:1902750 | negative regulation of cell cycle G2/M phase transition | 8 | 2 |
GO:1903047 | mitotic cell cycle process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003682 | chromatin binding | 2 | 2 |
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 152 | 156 | PF00656 | 0.602 |
CLV_C14_Caspase3-7 | 487 | 491 | PF00656 | 0.641 |
CLV_C14_Caspase3-7 | 508 | 512 | PF00656 | 0.674 |
CLV_C14_Caspase3-7 | 566 | 570 | PF00656 | 0.668 |
CLV_C14_Caspase3-7 | 682 | 686 | PF00656 | 0.580 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.723 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.478 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.751 |
CLV_NRD_NRD_1 | 549 | 551 | PF00675 | 0.697 |
CLV_NRD_NRD_1 | 586 | 588 | PF00675 | 0.721 |
CLV_NRD_NRD_1 | 613 | 615 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 651 | 653 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 708 | 710 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 782 | 784 | PF00675 | 0.733 |
CLV_NRD_NRD_1 | 832 | 834 | PF00675 | 0.735 |
CLV_NRD_NRD_1 | 955 | 957 | PF00675 | 0.729 |
CLV_PCSK_FUR_1 | 706 | 710 | PF00082 | 0.671 |
CLV_PCSK_FUR_1 | 830 | 834 | PF00082 | 0.700 |
CLV_PCSK_KEX2_1 | 226 | 228 | PF00082 | 0.723 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.751 |
CLV_PCSK_KEX2_1 | 551 | 553 | PF00082 | 0.761 |
CLV_PCSK_KEX2_1 | 586 | 588 | PF00082 | 0.719 |
CLV_PCSK_KEX2_1 | 613 | 615 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 708 | 710 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 782 | 784 | PF00082 | 0.733 |
CLV_PCSK_KEX2_1 | 830 | 832 | PF00082 | 0.738 |
CLV_PCSK_KEX2_1 | 955 | 957 | PF00082 | 0.729 |
CLV_PCSK_PC1ET2_1 | 284 | 286 | PF00082 | 0.550 |
CLV_PCSK_PC1ET2_1 | 300 | 302 | PF00082 | 0.598 |
CLV_PCSK_PC1ET2_1 | 339 | 341 | PF00082 | 0.819 |
CLV_PCSK_PC1ET2_1 | 551 | 553 | PF00082 | 0.761 |
CLV_PCSK_PC7_1 | 296 | 302 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 587 | 591 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 613 | 617 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 632 | 636 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 652 | 656 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 956 | 960 | PF00082 | 0.720 |
DEG_APCC_DBOX_1 | 1009 | 1017 | PF00400 | 0.659 |
DEG_APCC_DBOX_1 | 190 | 198 | PF00400 | 0.579 |
DEG_APCC_DBOX_1 | 282 | 290 | PF00400 | 0.652 |
DEG_APCC_DBOX_1 | 378 | 386 | PF00400 | 0.563 |
DEG_APCC_DBOX_1 | 651 | 659 | PF00400 | 0.588 |
DEG_APCC_DBOX_1 | 859 | 867 | PF00400 | 0.619 |
DEG_Kelch_Keap1_1 | 509 | 514 | PF01344 | 0.635 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.656 |
DOC_CKS1_1 | 342 | 347 | PF01111 | 0.626 |
DOC_CKS1_1 | 473 | 478 | PF01111 | 0.576 |
DOC_CKS1_1 | 989 | 994 | PF01111 | 0.631 |
DOC_CYCLIN_RxL_1 | 233 | 244 | PF00134 | 0.569 |
DOC_CYCLIN_RxL_1 | 56 | 67 | PF00134 | 0.619 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 235 | 242 | PF00134 | 0.560 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 277 | 286 | PF00134 | 0.554 |
DOC_MAPK_gen_1 | 235 | 241 | PF00069 | 0.480 |
DOC_MAPK_gen_1 | 283 | 292 | PF00069 | 0.579 |
DOC_MAPK_HePTP_8 | 282 | 294 | PF00069 | 0.575 |
DOC_MAPK_MEF2A_6 | 285 | 294 | PF00069 | 0.579 |
DOC_MAPK_MEF2A_6 | 56 | 64 | PF00069 | 0.507 |
DOC_MAPK_MEF2A_6 | 726 | 735 | PF00069 | 0.576 |
DOC_MAPK_MEF2A_6 | 988 | 997 | PF00069 | 0.612 |
DOC_PP1_RVXF_1 | 234 | 241 | PF00149 | 0.560 |
DOC_PP1_RVXF_1 | 724 | 731 | PF00149 | 0.585 |
DOC_PP2B_LxvP_1 | 132 | 135 | PF13499 | 0.746 |
DOC_PP2B_LxvP_1 | 647 | 650 | PF13499 | 0.710 |
DOC_PP4_FxxP_1 | 527 | 530 | PF00568 | 0.707 |
DOC_USP7_MATH_1 | 1029 | 1033 | PF00917 | 0.788 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.797 |
DOC_USP7_MATH_1 | 530 | 534 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 553 | 557 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 607 | 611 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 813 | 817 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 910 | 914 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 944 | 948 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 974 | 978 | PF00917 | 0.717 |
DOC_USP7_UBL2_3 | 337 | 341 | PF12436 | 0.733 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 353 | 358 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 555 | 560 | PF00397 | 0.788 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 845 | 850 | PF00397 | 0.723 |
DOC_WW_Pin1_4 | 889 | 894 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 940 | 945 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 946 | 951 | PF00397 | 0.790 |
DOC_WW_Pin1_4 | 961 | 966 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 972 | 977 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 988 | 993 | PF00397 | 0.680 |
LIG_14-3-3_CanoR_1 | 18 | 23 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 191 | 195 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 302 | 310 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 340 | 345 | PF00244 | 0.824 |
LIG_14-3-3_CanoR_1 | 434 | 438 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 448 | 453 | PF00244 | 0.721 |
LIG_14-3-3_CanoR_1 | 552 | 562 | PF00244 | 0.740 |
LIG_14-3-3_CanoR_1 | 632 | 640 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 688 | 696 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 714 | 721 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 741 | 751 | PF00244 | 0.755 |
LIG_14-3-3_CanoR_1 | 850 | 859 | PF00244 | 0.801 |
LIG_14-3-3_CanoR_1 | 869 | 878 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 955 | 959 | PF00244 | 0.724 |
LIG_14-3-3_CanoR_1 | 960 | 965 | PF00244 | 0.697 |
LIG_APCC_ABBA_1 | 1038 | 1043 | PF00400 | 0.649 |
LIG_BRCT_BRCA1_1 | 1010 | 1014 | PF00533 | 0.756 |
LIG_BRCT_BRCA1_1 | 255 | 259 | PF00533 | 0.517 |
LIG_BRCT_BRCA1_1 | 692 | 696 | PF00533 | 0.762 |
LIG_EH1_1 | 627 | 635 | PF00400 | 0.689 |
LIG_EVH1_2 | 749 | 753 | PF00568 | 0.790 |
LIG_FHA_1 | 1004 | 1010 | PF00498 | 0.630 |
LIG_FHA_1 | 1016 | 1022 | PF00498 | 0.653 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.530 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.649 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.669 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.567 |
LIG_FHA_1 | 513 | 519 | PF00498 | 0.766 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.600 |
LIG_FHA_1 | 644 | 650 | PF00498 | 0.626 |
LIG_FHA_1 | 722 | 728 | PF00498 | 0.525 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.724 |
LIG_FHA_1 | 846 | 852 | PF00498 | 0.816 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.740 |
LIG_FHA_1 | 871 | 877 | PF00498 | 0.678 |
LIG_FHA_1 | 890 | 896 | PF00498 | 0.468 |
LIG_FHA_2 | 242 | 248 | PF00498 | 0.557 |
LIG_FHA_2 | 617 | 623 | PF00498 | 0.648 |
LIG_FHA_2 | 714 | 720 | PF00498 | 0.680 |
LIG_FHA_2 | 786 | 792 | PF00498 | 0.693 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.594 |
LIG_LIR_Apic_2 | 525 | 530 | PF02991 | 0.708 |
LIG_LIR_Gen_1 | 199 | 207 | PF02991 | 0.598 |
LIG_LIR_Gen_1 | 318 | 329 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 729 | 738 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 771 | 781 | PF02991 | 0.653 |
LIG_LIR_Gen_1 | 97 | 107 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 199 | 203 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 318 | 324 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 621 | 626 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 693 | 699 | PF02991 | 0.648 |
LIG_LIR_Nem_3 | 729 | 733 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 739 | 743 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 879 | 883 | PF02991 | 0.699 |
LIG_LIR_Nem_3 | 97 | 102 | PF02991 | 0.553 |
LIG_LRP6_Inhibitor_1 | 658 | 664 | PF00058 | 0.600 |
LIG_LYPXL_yS_3 | 766 | 769 | PF13949 | 0.665 |
LIG_MYND_1 | 985 | 989 | PF01753 | 0.679 |
LIG_NRBOX | 59 | 65 | PF00104 | 0.509 |
LIG_SH2_CRK | 321 | 325 | PF00017 | 0.558 |
LIG_SH2_CRK | 49 | 53 | PF00017 | 0.517 |
LIG_SH2_CRK | 740 | 744 | PF00017 | 0.724 |
LIG_SH2_NCK_1 | 881 | 885 | PF00017 | 0.588 |
LIG_SH2_PTP2 | 886 | 889 | PF00017 | 0.602 |
LIG_SH2_SRC | 115 | 118 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 112 | 116 | PF00017 | 0.456 |
LIG_SH2_STAP1 | 674 | 678 | PF00017 | 0.680 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 623 | 626 | PF00017 | 0.578 |
LIG_SH2_STAT5 | 638 | 641 | PF00017 | 0.702 |
LIG_SH2_STAT5 | 657 | 660 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 665 | 668 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 761 | 764 | PF00017 | 0.798 |
LIG_SH2_STAT5 | 795 | 798 | PF00017 | 0.681 |
LIG_SH2_STAT5 | 886 | 889 | PF00017 | 0.602 |
LIG_SH3_3 | 1034 | 1040 | PF00018 | 0.840 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.633 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.629 |
LIG_SH3_3 | 470 | 476 | PF00018 | 0.676 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.634 |
LIG_SH3_3 | 744 | 750 | PF00018 | 0.756 |
LIG_SH3_3 | 888 | 894 | PF00018 | 0.752 |
LIG_SH3_3 | 931 | 937 | PF00018 | 0.716 |
LIG_SH3_3 | 979 | 985 | PF00018 | 0.677 |
LIG_SH3_3 | 986 | 992 | PF00018 | 0.667 |
LIG_SUMO_SIM_anti_2 | 358 | 363 | PF11976 | 0.615 |
LIG_SUMO_SIM_anti_2 | 853 | 861 | PF11976 | 0.658 |
LIG_SUMO_SIM_par_1 | 20 | 25 | PF11976 | 0.621 |
LIG_SUMO_SIM_par_1 | 288 | 293 | PF11976 | 0.525 |
LIG_SUMO_SIM_par_1 | 446 | 453 | PF11976 | 0.697 |
LIG_SUMO_SIM_par_1 | 563 | 570 | PF11976 | 0.679 |
LIG_SUMO_SIM_par_1 | 887 | 892 | PF11976 | 0.606 |
LIG_TRAF2_1 | 917 | 920 | PF00917 | 0.584 |
LIG_TRFH_1 | 881 | 885 | PF08558 | 0.588 |
LIG_TYR_ITIM | 738 | 743 | PF00017 | 0.719 |
LIG_TYR_ITIM | 764 | 769 | PF00017 | 0.688 |
LIG_TYR_ITIM | 878 | 883 | PF00017 | 0.702 |
LIG_WW_1 | 758 | 761 | PF00397 | 0.795 |
LIG_WW_2 | 893 | 896 | PF00397 | 0.670 |
LIG_WW_3 | 649 | 653 | PF00397 | 0.710 |
MOD_CDK_SPK_2 | 845 | 850 | PF00069 | 0.723 |
MOD_CDK_SPxxK_3 | 472 | 479 | PF00069 | 0.619 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.569 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.796 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.636 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.614 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.719 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.606 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.763 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.549 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.616 |
MOD_CK1_1 | 404 | 410 | PF00069 | 0.678 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.721 |
MOD_CK1_1 | 509 | 515 | PF00069 | 0.765 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.663 |
MOD_CK1_1 | 690 | 696 | PF00069 | 0.754 |
MOD_CK1_1 | 775 | 781 | PF00069 | 0.630 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.672 |
MOD_CK1_1 | 820 | 826 | PF00069 | 0.763 |
MOD_CK1_1 | 843 | 849 | PF00069 | 0.782 |
MOD_CK1_1 | 938 | 944 | PF00069 | 0.750 |
MOD_CK1_1 | 964 | 970 | PF00069 | 0.748 |
MOD_CK1_1 | 977 | 983 | PF00069 | 0.627 |
MOD_CK2_1 | 1029 | 1035 | PF00069 | 0.720 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.692 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.750 |
MOD_CK2_1 | 517 | 523 | PF00069 | 0.821 |
MOD_CK2_1 | 567 | 573 | PF00069 | 0.767 |
MOD_CK2_1 | 616 | 622 | PF00069 | 0.653 |
MOD_CK2_1 | 713 | 719 | PF00069 | 0.681 |
MOD_CK2_1 | 794 | 800 | PF00069 | 0.654 |
MOD_CK2_1 | 897 | 903 | PF00069 | 0.694 |
MOD_DYRK1A_RPxSP_1 | 988 | 992 | PF00069 | 0.645 |
MOD_GlcNHglycan | 1031 | 1035 | PF01048 | 0.778 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.794 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.704 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.600 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.493 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.777 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.696 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.630 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.515 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.678 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.629 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.651 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.677 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.843 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.786 |
MOD_GlcNHglycan | 691 | 695 | PF01048 | 0.692 |
MOD_GlcNHglycan | 774 | 777 | PF01048 | 0.709 |
MOD_GlcNHglycan | 815 | 818 | PF01048 | 0.646 |
MOD_GlcNHglycan | 820 | 823 | PF01048 | 0.677 |
MOD_GlcNHglycan | 907 | 910 | PF01048 | 0.783 |
MOD_GlcNHglycan | 966 | 969 | PF01048 | 0.710 |
MOD_GlcNHglycan | 976 | 979 | PF01048 | 0.689 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.524 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.670 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.522 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.699 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.707 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.562 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.545 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.542 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.693 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.596 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.608 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.765 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.674 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.808 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.780 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.670 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.644 |
MOD_GSK3_1 | 563 | 570 | PF00069 | 0.752 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.733 |
MOD_GSK3_1 | 813 | 820 | PF00069 | 0.621 |
MOD_GSK3_1 | 839 | 846 | PF00069 | 0.808 |
MOD_GSK3_1 | 920 | 927 | PF00069 | 0.777 |
MOD_GSK3_1 | 940 | 947 | PF00069 | 0.512 |
MOD_GSK3_1 | 960 | 967 | PF00069 | 0.749 |
MOD_N-GLC_1 | 700 | 705 | PF02516 | 0.524 |
MOD_N-GLC_1 | 78 | 83 | PF02516 | 0.590 |
MOD_N-GLC_1 | 921 | 926 | PF02516 | 0.728 |
MOD_N-GLC_1 | 95 | 100 | PF02516 | 0.383 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.758 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.520 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.561 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.775 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.740 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.683 |
MOD_NEK2_1 | 567 | 572 | PF00069 | 0.665 |
MOD_NEK2_1 | 624 | 629 | PF00069 | 0.607 |
MOD_NEK2_1 | 692 | 697 | PF00069 | 0.664 |
MOD_NEK2_1 | 721 | 726 | PF00069 | 0.693 |
MOD_NEK2_1 | 736 | 741 | PF00069 | 0.521 |
MOD_NEK2_1 | 777 | 782 | PF00069 | 0.721 |
MOD_NEK2_1 | 959 | 964 | PF00069 | 0.740 |
MOD_NEK2_2 | 954 | 959 | PF00069 | 0.725 |
MOD_PIKK_1 | 371 | 377 | PF00454 | 0.574 |
MOD_PIKK_1 | 567 | 573 | PF00454 | 0.666 |
MOD_PIKK_1 | 607 | 613 | PF00454 | 0.829 |
MOD_PIKK_1 | 632 | 638 | PF00454 | 0.593 |
MOD_PIKK_1 | 912 | 918 | PF00454 | 0.683 |
MOD_PK_1 | 285 | 291 | PF00069 | 0.659 |
MOD_PK_1 | 808 | 814 | PF00069 | 0.754 |
MOD_PKA_1 | 340 | 346 | PF00069 | 0.707 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.478 |
MOD_PKA_2 | 222 | 228 | PF00069 | 0.587 |
MOD_PKA_2 | 332 | 338 | PF00069 | 0.763 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.575 |
MOD_PKA_2 | 498 | 504 | PF00069 | 0.795 |
MOD_PKA_2 | 553 | 559 | PF00069 | 0.744 |
MOD_PKA_2 | 687 | 693 | PF00069 | 0.574 |
MOD_PKA_2 | 713 | 719 | PF00069 | 0.681 |
MOD_PKA_2 | 817 | 823 | PF00069 | 0.741 |
MOD_PKA_2 | 954 | 960 | PF00069 | 0.724 |
MOD_PKB_1 | 283 | 291 | PF00069 | 0.659 |
MOD_PKB_1 | 552 | 560 | PF00069 | 0.765 |
MOD_PKB_1 | 768 | 776 | PF00069 | 0.716 |
MOD_Plk_1 | 105 | 111 | PF00069 | 0.491 |
MOD_Plk_1 | 313 | 319 | PF00069 | 0.651 |
MOD_Plk_1 | 522 | 528 | PF00069 | 0.761 |
MOD_Plk_1 | 700 | 706 | PF00069 | 0.526 |
MOD_Plk_1 | 770 | 776 | PF00069 | 0.631 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.614 |
MOD_Plk_1 | 95 | 101 | PF00069 | 0.517 |
MOD_Plk_2-3 | 494 | 500 | PF00069 | 0.833 |
MOD_Plk_2-3 | 679 | 685 | PF00069 | 0.610 |
MOD_Plk_2-3 | 785 | 791 | PF00069 | 0.760 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.483 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.579 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.610 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.576 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.659 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.684 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.671 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.537 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.483 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.760 |
MOD_ProDKin_1 | 353 | 359 | PF00069 | 0.539 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.684 |
MOD_ProDKin_1 | 555 | 561 | PF00069 | 0.786 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.557 |
MOD_ProDKin_1 | 845 | 851 | PF00069 | 0.717 |
MOD_ProDKin_1 | 889 | 895 | PF00069 | 0.633 |
MOD_ProDKin_1 | 940 | 946 | PF00069 | 0.750 |
MOD_ProDKin_1 | 961 | 967 | PF00069 | 0.736 |
MOD_ProDKin_1 | 972 | 978 | PF00069 | 0.580 |
MOD_ProDKin_1 | 988 | 994 | PF00069 | 0.674 |
TRG_DiLeu_BaEn_1 | 213 | 218 | PF01217 | 0.509 |
TRG_DiLeu_BaLyEn_6 | 1034 | 1039 | PF01217 | 0.841 |
TRG_DiLeu_BaLyEn_6 | 629 | 634 | PF01217 | 0.595 |
TRG_DiLeu_BaLyEn_6 | 723 | 728 | PF01217 | 0.591 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.558 |
TRG_ENDOCYTIC_2 | 623 | 626 | PF00928 | 0.625 |
TRG_ENDOCYTIC_2 | 740 | 743 | PF00928 | 0.727 |
TRG_ENDOCYTIC_2 | 761 | 764 | PF00928 | 0.714 |
TRG_ENDOCYTIC_2 | 766 | 769 | PF00928 | 0.648 |
TRG_ENDOCYTIC_2 | 774 | 777 | PF00928 | 0.642 |
TRG_ENDOCYTIC_2 | 880 | 883 | PF00928 | 0.620 |
TRG_ENDOCYTIC_2 | 886 | 889 | PF00928 | 0.572 |
TRG_ER_diArg_1 | 226 | 228 | PF00400 | 0.623 |
TRG_ER_diArg_1 | 234 | 236 | PF00400 | 0.403 |
TRG_ER_diArg_1 | 282 | 285 | PF00400 | 0.612 |
TRG_ER_diArg_1 | 294 | 297 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 301 | 303 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 550 | 553 | PF00400 | 0.778 |
TRG_ER_diArg_1 | 613 | 615 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 767 | 770 | PF00400 | 0.665 |
TRG_ER_diArg_1 | 781 | 783 | PF00400 | 0.711 |
TRG_ER_diArg_1 | 830 | 833 | PF00400 | 0.738 |
TRG_ER_diArg_1 | 954 | 956 | PF00400 | 0.734 |
TRG_NLS_Bipartite_1 | 283 | 304 | PF00514 | 0.594 |
TRG_NLS_MonoCore_2 | 550 | 555 | PF00514 | 0.778 |
TRG_NLS_MonoExtC_3 | 549 | 554 | PF00514 | 0.699 |
TRG_NLS_MonoExtN_4 | 297 | 304 | PF00514 | 0.614 |
TRG_NLS_MonoExtN_4 | 337 | 343 | PF00514 | 0.815 |
TRG_NLS_MonoExtN_4 | 550 | 555 | PF00514 | 0.726 |
TRG_Pf-PMV_PEXEL_1 | 632 | 636 | PF00026 | 0.546 |
TRG_Pf-PMV_PEXEL_1 | 652 | 656 | PF00026 | 0.683 |
TRG_Pf-PMV_PEXEL_1 | 709 | 713 | PF00026 | 0.657 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8V0 | Leptomonas seymouri | 43% | 100% |
A0A3Q8IRX6 | Leishmania donovani | 88% | 99% |
A4HI98 | Leishmania braziliensis | 73% | 99% |
A4I5I2 | Leishmania infantum | 89% | 99% |
E9B0S7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |