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: A0A3Q8IRX6
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 | 571 | 575 | PF00656 | 0.583 |
CLV_C14_Caspase3-7 | 687 | 691 | PF00656 | 0.517 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.680 |
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.664 |
CLV_NRD_NRD_1 | 554 | 556 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 591 | 593 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 656 | 658 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 713 | 715 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 787 | 789 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 837 | 839 | PF00675 | 0.633 |
CLV_NRD_NRD_1 | 961 | 963 | PF00675 | 0.608 |
CLV_PCSK_FUR_1 | 711 | 715 | PF00082 | 0.578 |
CLV_PCSK_FUR_1 | 835 | 839 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.680 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.664 |
CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 590 | 592 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 713 | 715 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 787 | 789 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 835 | 837 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 961 | 963 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 989 | 991 | PF00082 | 0.544 |
CLV_PCSK_PC1ET2_1 | 285 | 287 | PF00082 | 0.461 |
CLV_PCSK_PC1ET2_1 | 301 | 303 | PF00082 | 0.516 |
CLV_PCSK_PC1ET2_1 | 340 | 342 | PF00082 | 0.705 |
CLV_PCSK_PC1ET2_1 | 556 | 558 | PF00082 | 0.645 |
CLV_PCSK_PC1ET2_1 | 989 | 991 | PF00082 | 0.531 |
CLV_PCSK_PC7_1 | 297 | 303 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 618 | 622 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 637 | 641 | PF00082 | 0.680 |
CLV_PCSK_SKI1_1 | 657 | 661 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 962 | 966 | PF00082 | 0.602 |
DEG_APCC_DBOX_1 | 1015 | 1023 | PF00400 | 0.549 |
DEG_APCC_DBOX_1 | 191 | 199 | PF00400 | 0.457 |
DEG_APCC_DBOX_1 | 283 | 291 | PF00400 | 0.531 |
DEG_APCC_DBOX_1 | 383 | 391 | PF00400 | 0.462 |
DEG_APCC_DBOX_1 | 656 | 664 | PF00400 | 0.530 |
DEG_APCC_DBOX_1 | 865 | 873 | PF00400 | 0.535 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.536 |
DEG_SPOP_SBC_1 | 950 | 954 | PF00917 | 0.579 |
DOC_CDC14_PxL_1 | 70 | 78 | PF14671 | 0.485 |
DOC_CKS1_1 | 995 | 1000 | PF01111 | 0.541 |
DOC_CYCLIN_RxL_1 | 234 | 245 | PF00134 | 0.458 |
DOC_CYCLIN_RxL_1 | 56 | 67 | PF00134 | 0.485 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 236 | 243 | PF00134 | 0.451 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 278 | 287 | PF00134 | 0.463 |
DOC_CYCLIN_yCln2_LP_2 | 1044 | 1047 | PF00134 | 0.577 |
DOC_MAPK_DCC_7 | 559 | 569 | PF00069 | 0.573 |
DOC_MAPK_gen_1 | 236 | 242 | PF00069 | 0.401 |
DOC_MAPK_gen_1 | 284 | 293 | PF00069 | 0.494 |
DOC_MAPK_HePTP_8 | 283 | 295 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 286 | 295 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 56 | 64 | PF00069 | 0.406 |
DOC_MAPK_MEF2A_6 | 731 | 740 | PF00069 | 0.513 |
DOC_PP1_RVXF_1 | 235 | 242 | PF00149 | 0.449 |
DOC_PP2B_LxvP_1 | 1044 | 1047 | PF13499 | 0.570 |
DOC_PP2B_LxvP_1 | 133 | 136 | PF13499 | 0.618 |
DOC_PP2B_LxvP_1 | 652 | 655 | PF13499 | 0.589 |
DOC_PP2B_LxvP_1 | 979 | 982 | PF13499 | 0.545 |
DOC_PP4_FxxP_1 | 532 | 535 | PF00568 | 0.633 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 406 | 410 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 535 | 539 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 612 | 616 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 822 | 826 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 902 | 906 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 916 | 920 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 950 | 954 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 968 | 972 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 980 | 984 | PF00917 | 0.617 |
DOC_USP7_UBL2_3 | 338 | 342 | PF12436 | 0.653 |
DOC_USP7_UBL2_3 | 480 | 484 | PF12436 | 0.564 |
DOC_WW_Pin1_4 | 138 | 143 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.395 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 470 | 475 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 560 | 565 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 851 | 856 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 895 | 900 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 946 | 951 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 994 | 999 | PF00397 | 0.595 |
LIG_14-3-3_CanoR_1 | 192 | 196 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 303 | 311 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 341 | 346 | PF00244 | 0.810 |
LIG_14-3-3_CanoR_1 | 453 | 458 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 637 | 645 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 693 | 701 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 719 | 726 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 746 | 756 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 875 | 884 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 910 | 920 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 961 | 965 | PF00244 | 0.605 |
LIG_BRCT_BRCA1_1 | 1016 | 1020 | PF00533 | 0.610 |
LIG_BRCT_BRCA1_1 | 256 | 260 | PF00533 | 0.444 |
LIG_BRCT_BRCA1_1 | 525 | 529 | PF00533 | 0.552 |
LIG_BRCT_BRCA1_1 | 697 | 701 | PF00533 | 0.649 |
LIG_BRCT_BRCA1_1 | 96 | 100 | PF00533 | 0.402 |
LIG_EH1_1 | 632 | 640 | PF00400 | 0.574 |
LIG_EVH1_2 | 754 | 758 | PF00568 | 0.669 |
LIG_FHA_1 | 1010 | 1016 | PF00498 | 0.514 |
LIG_FHA_1 | 1022 | 1028 | PF00498 | 0.557 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.595 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.587 |
LIG_FHA_1 | 518 | 524 | PF00498 | 0.659 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.545 |
LIG_FHA_1 | 649 | 655 | PF00498 | 0.644 |
LIG_FHA_1 | 852 | 858 | PF00498 | 0.749 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.690 |
LIG_FHA_1 | 877 | 883 | PF00498 | 0.571 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.466 |
LIG_FHA_2 | 622 | 628 | PF00498 | 0.601 |
LIG_FHA_2 | 719 | 725 | PF00498 | 0.574 |
LIG_FHA_2 | 791 | 797 | PF00498 | 0.657 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.501 |
LIG_LIR_Apic_2 | 530 | 535 | PF02991 | 0.629 |
LIG_LIR_Gen_1 | 200 | 208 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 426 | 436 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 526 | 535 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 776 | 786 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 97 | 108 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 200 | 204 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 426 | 431 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 526 | 532 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 626 | 631 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 698 | 704 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 744 | 748 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 885 | 889 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.520 |
LIG_LRP6_Inhibitor_1 | 663 | 669 | PF00058 | 0.491 |
LIG_LYPXL_yS_3 | 771 | 774 | PF13949 | 0.560 |
LIG_MYND_1 | 991 | 995 | PF01753 | 0.577 |
LIG_NRBOX | 59 | 65 | PF00104 | 0.406 |
LIG_RPA_C_Fungi | 298 | 310 | PF08784 | 0.473 |
LIG_SH2_CRK | 49 | 53 | PF00017 | 0.432 |
LIG_SH2_CRK | 745 | 749 | PF00017 | 0.601 |
LIG_SH2_GRB2like | 116 | 119 | PF00017 | 0.311 |
LIG_SH2_NCK_1 | 887 | 891 | PF00017 | 0.499 |
LIG_SH2_PTP2 | 892 | 895 | PF00017 | 0.525 |
LIG_SH2_SRC | 116 | 119 | PF00017 | 0.399 |
LIG_SH2_STAP1 | 679 | 683 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 628 | 631 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 643 | 646 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 662 | 665 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 670 | 673 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 766 | 769 | PF00017 | 0.771 |
LIG_SH2_STAT5 | 800 | 803 | PF00017 | 0.655 |
LIG_SH2_STAT5 | 892 | 895 | PF00017 | 0.525 |
LIG_SH3_1 | 555 | 561 | PF00018 | 0.581 |
LIG_SH3_3 | 1040 | 1046 | PF00018 | 0.715 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.508 |
LIG_SH3_3 | 475 | 481 | PF00018 | 0.616 |
LIG_SH3_3 | 555 | 561 | PF00018 | 0.629 |
LIG_SH3_3 | 68 | 74 | PF00018 | 0.521 |
LIG_SH3_3 | 749 | 755 | PF00018 | 0.633 |
LIG_SH3_3 | 894 | 900 | PF00018 | 0.618 |
LIG_SH3_3 | 937 | 943 | PF00018 | 0.608 |
LIG_SH3_3 | 974 | 980 | PF00018 | 0.623 |
LIG_SH3_3 | 992 | 998 | PF00018 | 0.564 |
LIG_SH3_4 | 480 | 487 | PF00018 | 0.567 |
LIG_SUMO_SIM_anti_2 | 361 | 368 | PF11976 | 0.537 |
LIG_SUMO_SIM_anti_2 | 860 | 867 | PF11976 | 0.554 |
LIG_SUMO_SIM_par_1 | 20 | 26 | PF11976 | 0.497 |
LIG_SUMO_SIM_par_1 | 453 | 458 | PF11976 | 0.606 |
LIG_SUMO_SIM_par_1 | 568 | 575 | PF11976 | 0.593 |
LIG_SUMO_SIM_par_1 | 893 | 898 | PF11976 | 0.521 |
LIG_TRFH_1 | 887 | 891 | PF08558 | 0.499 |
LIG_TYR_ITIM | 743 | 748 | PF00017 | 0.601 |
LIG_TYR_ITIM | 769 | 774 | PF00017 | 0.581 |
LIG_TYR_ITIM | 884 | 889 | PF00017 | 0.587 |
LIG_WW_1 | 763 | 766 | PF00397 | 0.641 |
LIG_WW_2 | 899 | 902 | PF00397 | 0.588 |
LIG_WW_2 | 977 | 980 | PF00397 | 0.538 |
LIG_WW_3 | 654 | 658 | PF00397 | 0.586 |
MOD_CDC14_SPxK_1 | 477 | 480 | PF00782 | 0.554 |
MOD_CDK_SPK_2 | 851 | 856 | PF00069 | 0.625 |
MOD_CDK_SPxK_1 | 474 | 480 | PF00069 | 0.551 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.453 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.796 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.558 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.621 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.482 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.653 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.548 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.554 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.578 |
MOD_CK1_1 | 458 | 464 | PF00069 | 0.569 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.611 |
MOD_CK1_1 | 483 | 489 | PF00069 | 0.604 |
MOD_CK1_1 | 514 | 520 | PF00069 | 0.672 |
MOD_CK1_1 | 695 | 701 | PF00069 | 0.641 |
MOD_CK1_1 | 825 | 831 | PF00069 | 0.657 |
MOD_CK1_1 | 849 | 855 | PF00069 | 0.712 |
MOD_CK1_1 | 944 | 950 | PF00069 | 0.638 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.486 |
MOD_CK1_1 | 970 | 976 | PF00069 | 0.666 |
MOD_CK1_1 | 983 | 989 | PF00069 | 0.548 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.604 |
MOD_CK2_1 | 499 | 505 | PF00069 | 0.660 |
MOD_CK2_1 | 522 | 528 | PF00069 | 0.685 |
MOD_CK2_1 | 572 | 578 | PF00069 | 0.656 |
MOD_CK2_1 | 621 | 627 | PF00069 | 0.601 |
MOD_CK2_1 | 718 | 724 | PF00069 | 0.577 |
MOD_CK2_1 | 799 | 805 | PF00069 | 0.559 |
MOD_CK2_1 | 903 | 909 | PF00069 | 0.601 |
MOD_Cter_Amidation | 155 | 158 | PF01082 | 0.510 |
MOD_Cter_Amidation | 225 | 228 | PF01082 | 0.570 |
MOD_DYRK1A_RPxSP_1 | 994 | 998 | PF00069 | 0.541 |
MOD_GlcNHglycan | 1037 | 1041 | PF01048 | 0.683 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.762 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.630 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.535 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.507 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.764 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.626 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.528 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.472 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.629 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.579 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.639 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.682 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.707 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.577 |
MOD_GlcNHglycan | 610 | 613 | PF01048 | 0.578 |
MOD_GlcNHglycan | 696 | 700 | PF01048 | 0.618 |
MOD_GlcNHglycan | 779 | 782 | PF01048 | 0.586 |
MOD_GlcNHglycan | 825 | 828 | PF01048 | 0.654 |
MOD_GlcNHglycan | 913 | 916 | PF01048 | 0.651 |
MOD_GlcNHglycan | 972 | 975 | PF01048 | 0.614 |
MOD_GlcNHglycan | 982 | 985 | PF01048 | 0.588 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.447 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.581 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.619 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.619 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.486 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.454 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.447 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.630 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.628 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.623 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.537 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.656 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.592 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.607 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.709 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.628 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.552 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.709 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.596 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.629 |
MOD_GSK3_1 | 845 | 852 | PF00069 | 0.692 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.443 |
MOD_GSK3_1 | 926 | 933 | PF00069 | 0.661 |
MOD_GSK3_1 | 946 | 953 | PF00069 | 0.492 |
MOD_GSK3_1 | 966 | 973 | PF00069 | 0.675 |
MOD_N-GLC_1 | 927 | 932 | PF02516 | 0.627 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.657 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.524 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.433 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.468 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.651 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.623 |
MOD_NEK2_1 | 572 | 577 | PF00069 | 0.601 |
MOD_NEK2_1 | 629 | 634 | PF00069 | 0.528 |
MOD_NEK2_1 | 697 | 702 | PF00069 | 0.576 |
MOD_NEK2_1 | 732 | 737 | PF00069 | 0.543 |
MOD_NEK2_1 | 741 | 746 | PF00069 | 0.461 |
MOD_NEK2_1 | 903 | 908 | PF00069 | 0.531 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.479 |
MOD_NEK2_1 | 955 | 960 | PF00069 | 0.608 |
MOD_NEK2_1 | 967 | 972 | PF00069 | 0.622 |
MOD_NEK2_2 | 309 | 314 | PF00069 | 0.485 |
MOD_NEK2_2 | 960 | 965 | PF00069 | 0.605 |
MOD_PIKK_1 | 376 | 382 | PF00454 | 0.477 |
MOD_PIKK_1 | 398 | 404 | PF00454 | 0.507 |
MOD_PIKK_1 | 415 | 421 | PF00454 | 0.480 |
MOD_PIKK_1 | 572 | 578 | PF00454 | 0.591 |
MOD_PIKK_1 | 612 | 618 | PF00454 | 0.713 |
MOD_PIKK_1 | 637 | 643 | PF00454 | 0.515 |
MOD_PIKK_1 | 918 | 924 | PF00454 | 0.696 |
MOD_PK_1 | 286 | 292 | PF00069 | 0.539 |
MOD_PK_1 | 813 | 819 | PF00069 | 0.642 |
MOD_PKA_1 | 334 | 340 | PF00069 | 0.653 |
MOD_PKA_1 | 341 | 347 | PF00069 | 0.626 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.764 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.384 |
MOD_PKA_2 | 333 | 339 | PF00069 | 0.705 |
MOD_PKA_2 | 503 | 509 | PF00069 | 0.685 |
MOD_PKA_2 | 692 | 698 | PF00069 | 0.552 |
MOD_PKA_2 | 718 | 724 | PF00069 | 0.577 |
MOD_PKA_2 | 822 | 828 | PF00069 | 0.650 |
MOD_PKA_2 | 960 | 966 | PF00069 | 0.605 |
MOD_PKB_1 | 284 | 292 | PF00069 | 0.540 |
MOD_PKB_1 | 557 | 565 | PF00069 | 0.666 |
MOD_PKB_1 | 773 | 781 | PF00069 | 0.603 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.405 |
MOD_Plk_1 | 314 | 320 | PF00069 | 0.578 |
MOD_Plk_1 | 527 | 533 | PF00069 | 0.656 |
MOD_Plk_1 | 775 | 781 | PF00069 | 0.551 |
MOD_Plk_2-3 | 499 | 505 | PF00069 | 0.710 |
MOD_Plk_2-3 | 528 | 534 | PF00069 | 0.569 |
MOD_Plk_2-3 | 684 | 690 | PF00069 | 0.585 |
MOD_Plk_2-3 | 790 | 796 | PF00069 | 0.657 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.396 |
MOD_Plk_4 | 191 | 197 | PF00069 | 0.457 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.353 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.486 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.489 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.506 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.622 |
MOD_Plk_4 | 568 | 574 | PF00069 | 0.597 |
MOD_Plk_4 | 951 | 957 | PF00069 | 0.557 |
MOD_ProDKin_1 | 138 | 144 | PF00069 | 0.592 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.453 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.402 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.652 |
MOD_ProDKin_1 | 470 | 476 | PF00069 | 0.699 |
MOD_ProDKin_1 | 560 | 566 | PF00069 | 0.718 |
MOD_ProDKin_1 | 851 | 857 | PF00069 | 0.622 |
MOD_ProDKin_1 | 895 | 901 | PF00069 | 0.524 |
MOD_ProDKin_1 | 946 | 952 | PF00069 | 0.628 |
MOD_ProDKin_1 | 994 | 1000 | PF00069 | 0.589 |
TRG_DiLeu_BaEn_1 | 66 | 71 | PF01217 | 0.432 |
TRG_DiLeu_BaEn_4 | 860 | 866 | PF01217 | 0.518 |
TRG_DiLeu_BaLyEn_6 | 1040 | 1045 | PF01217 | 0.716 |
TRG_DiLeu_BaLyEn_6 | 634 | 639 | PF01217 | 0.503 |
TRG_DiLeu_BaLyEn_6 | 728 | 733 | PF01217 | 0.525 |
TRG_DiLeu_LyEn_5 | 214 | 219 | PF01217 | 0.499 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 628 | 631 | PF00928 | 0.580 |
TRG_ENDOCYTIC_2 | 745 | 748 | PF00928 | 0.608 |
TRG_ENDOCYTIC_2 | 766 | 769 | PF00928 | 0.592 |
TRG_ENDOCYTIC_2 | 771 | 774 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 779 | 782 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 886 | 889 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 892 | 895 | PF00928 | 0.504 |
TRG_ER_diArg_1 | 227 | 229 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 235 | 237 | PF00400 | 0.361 |
TRG_ER_diArg_1 | 283 | 286 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 302 | 304 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 555 | 558 | PF00400 | 0.668 |
TRG_ER_diArg_1 | 590 | 592 | PF00400 | 0.597 |
TRG_ER_diArg_1 | 772 | 775 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 786 | 788 | PF00400 | 0.623 |
TRG_ER_diArg_1 | 835 | 838 | PF00400 | 0.641 |
TRG_ER_diArg_1 | 960 | 962 | PF00400 | 0.611 |
TRG_NLS_Bipartite_1 | 284 | 305 | PF00514 | 0.511 |
TRG_NLS_MonoCore_2 | 555 | 560 | PF00514 | 0.672 |
TRG_NLS_MonoExtC_3 | 554 | 559 | PF00514 | 0.646 |
TRG_NLS_MonoExtN_4 | 338 | 344 | PF00514 | 0.699 |
TRG_NLS_MonoExtN_4 | 555 | 560 | PF00514 | 0.663 |
TRG_Pf-PMV_PEXEL_1 | 637 | 641 | PF00026 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 657 | 661 | PF00026 | 0.360 |
TRG_Pf-PMV_PEXEL_1 | 714 | 718 | PF00026 | 0.584 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8V0 | Leptomonas seymouri | 43% | 100% |
A4HI98 | Leishmania braziliensis | 72% | 100% |
A4I5I2 | Leishmania infantum | 99% | 100% |
E9B0S7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 99% |
Q4Q7F1 | Leishmania major | 88% | 99% |