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: 3 |
NetGPI | no | yes: 0, no: 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9APS8
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 4 |
GO:0006793 | phosphorus metabolic process | 3 | 4 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 4 |
GO:0006807 | nitrogen compound metabolic process | 2 | 4 |
GO:0008152 | metabolic process | 1 | 4 |
GO:0009987 | cellular process | 1 | 4 |
GO:0016310 | phosphorylation | 5 | 4 |
GO:0019538 | protein metabolic process | 3 | 4 |
GO:0036211 | protein modification process | 4 | 4 |
GO:0043170 | macromolecule metabolic process | 3 | 4 |
GO:0043412 | macromolecule modification | 4 | 4 |
GO:0044237 | cellular metabolic process | 2 | 4 |
GO:0044238 | primary metabolic process | 2 | 4 |
GO:0071704 | organic substance metabolic process | 2 | 4 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 4 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0018105 | peptidyl-serine phosphorylation | 6 | 1 |
GO:0018107 | peptidyl-threonine phosphorylation | 6 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018209 | peptidyl-serine modification | 6 | 1 |
GO:0018210 | peptidyl-threonine modification | 6 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 1 |
GO:0045893 | positive regulation of DNA-templated transcription | 7 | 1 |
GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 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:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0051254 | positive regulation of RNA metabolic process | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1902680 | positive regulation of RNA biosynthetic process | 7 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:1903508 | positive regulation of nucleic acid-templated transcription | 8 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 4 |
GO:0003824 | catalytic activity | 1 | 4 |
GO:0004672 | protein kinase activity | 3 | 4 |
GO:0005488 | binding | 1 | 4 |
GO:0005524 | ATP binding | 5 | 4 |
GO:0016301 | kinase activity | 4 | 4 |
GO:0016740 | transferase activity | 2 | 4 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 4 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 4 |
GO:0017076 | purine nucleotide binding | 4 | 4 |
GO:0030554 | adenyl nucleotide binding | 5 | 4 |
GO:0032553 | ribonucleotide binding | 3 | 4 |
GO:0032555 | purine ribonucleotide binding | 4 | 4 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 4 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 4 |
GO:0036094 | small molecule binding | 2 | 4 |
GO:0043167 | ion binding | 2 | 4 |
GO:0043168 | anion binding | 3 | 4 |
GO:0097159 | organic cyclic compound binding | 2 | 4 |
GO:0097367 | carbohydrate derivative binding | 2 | 4 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 4 |
GO:1901265 | nucleoside phosphate binding | 3 | 4 |
GO:1901363 | heterocyclic compound binding | 2 | 4 |
GO:0003712 | transcription coregulator activity | 2 | 1 |
GO:0003713 | transcription coactivator activity | 3 | 1 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
GO:0140110 | transcription regulator activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 269 | 273 | PF00656 | 0.590 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.794 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.714 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.631 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.708 |
CLV_NRD_NRD_1 | 441 | 443 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 527 | 529 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 565 | 567 | PF00675 | 0.358 |
CLV_NRD_NRD_1 | 937 | 939 | PF00675 | 0.397 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.798 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 317 | 319 | PF00082 | 0.708 |
CLV_PCSK_KEX2_1 | 810 | 812 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 939 | 941 | PF00082 | 0.410 |
CLV_PCSK_PC1ET2_1 | 810 | 812 | PF00082 | 0.358 |
CLV_PCSK_PC1ET2_1 | 939 | 941 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 550 | 554 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 574 | 578 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 956 | 960 | PF00082 | 0.515 |
DEG_SCF_FBW7_1 | 176 | 181 | PF00400 | 0.517 |
DEG_SCF_FBW7_1 | 850 | 857 | PF00400 | 0.358 |
DEG_SPOP_SBC_1 | 124 | 128 | PF00917 | 0.634 |
DEG_SPOP_SBC_1 | 35 | 39 | PF00917 | 0.565 |
DEG_SPOP_SBC_1 | 87 | 91 | PF00917 | 0.547 |
DEG_SPOP_SBC_1 | 9 | 13 | PF00917 | 0.688 |
DOC_ANK_TNKS_1 | 872 | 879 | PF00023 | 0.358 |
DOC_CYCLIN_RxL_1 | 426 | 434 | PF00134 | 0.509 |
DOC_CYCLIN_RxL_1 | 571 | 580 | PF00134 | 0.358 |
DOC_CYCLIN_yCln2_LP_2 | 433 | 439 | PF00134 | 0.541 |
DOC_MAPK_gen_1 | 745 | 754 | PF00069 | 0.397 |
DOC_MAPK_HePTP_8 | 481 | 493 | PF00069 | 0.358 |
DOC_MAPK_HePTP_8 | 742 | 754 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 484 | 493 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 534 | 541 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 556 | 564 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 745 | 754 | PF00069 | 0.358 |
DOC_MAPK_NFAT4_5 | 534 | 542 | PF00069 | 0.358 |
DOC_PP1_RVXF_1 | 605 | 612 | PF00149 | 0.358 |
DOC_PP2B_LxvP_1 | 121 | 124 | PF13499 | 0.619 |
DOC_PP2B_LxvP_1 | 41 | 44 | PF13499 | 0.621 |
DOC_PP2B_LxvP_1 | 433 | 436 | PF13499 | 0.522 |
DOC_PP2B_LxvP_1 | 869 | 872 | PF13499 | 0.279 |
DOC_PP4_FxxP_1 | 84 | 87 | PF00568 | 0.631 |
DOC_PP4_FxxP_1 | 951 | 954 | PF00568 | 0.453 |
DOC_PP4_MxPP_1 | 355 | 358 | PF00568 | 0.652 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.811 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 601 | 605 | PF00917 | 0.358 |
DOC_USP7_MATH_1 | 640 | 644 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 687 | 691 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 694 | 698 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 854 | 858 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 957 | 961 | PF00917 | 0.542 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.746 |
DOC_WW_Pin1_4 | 323 | 328 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 371 | 376 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 632 | 637 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 655 | 660 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 746 | 751 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 805 | 810 | PF00397 | 0.375 |
DOC_WW_Pin1_4 | 850 | 855 | PF00397 | 0.358 |
DOC_WW_Pin1_4 | 862 | 867 | PF00397 | 0.263 |
DOC_WW_Pin1_4 | 888 | 893 | PF00397 | 0.335 |
LIG_14-3-3_CanoR_1 | 224 | 233 | PF00244 | 0.705 |
LIG_14-3-3_CanoR_1 | 328 | 335 | PF00244 | 0.672 |
LIG_14-3-3_CanoR_1 | 550 | 555 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 764 | 768 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 938 | 947 | PF00244 | 0.358 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.675 |
LIG_BIR_III_2 | 847 | 851 | PF00653 | 0.358 |
LIG_BIR_III_4 | 446 | 450 | PF00653 | 0.454 |
LIG_BRCT_BRCA1_1 | 383 | 387 | PF00533 | 0.610 |
LIG_BRCT_BRCA1_1 | 864 | 868 | PF00533 | 0.358 |
LIG_Clathr_ClatBox_1 | 576 | 580 | PF01394 | 0.358 |
LIG_deltaCOP1_diTrp_1 | 763 | 770 | PF00928 | 0.358 |
LIG_eIF4E_1 | 426 | 432 | PF01652 | 0.506 |
LIG_EVH1_1 | 282 | 286 | PF00568 | 0.685 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.566 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.582 |
LIG_FHA_1 | 686 | 692 | PF00498 | 0.579 |
LIG_FHA_1 | 757 | 763 | PF00498 | 0.358 |
LIG_FHA_1 | 792 | 798 | PF00498 | 0.358 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.663 |
LIG_FHA_2 | 701 | 707 | PF00498 | 0.612 |
LIG_FHA_2 | 726 | 732 | PF00498 | 0.707 |
LIG_FHA_2 | 758 | 764 | PF00498 | 0.358 |
LIG_LIR_Apic_2 | 279 | 285 | PF02991 | 0.692 |
LIG_LIR_Apic_2 | 744 | 750 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 2 | 10 | PF02991 | 0.675 |
LIG_LIR_Gen_1 | 416 | 426 | PF02991 | 0.627 |
LIG_LIR_Gen_1 | 643 | 651 | PF02991 | 0.553 |
LIG_LIR_Gen_1 | 919 | 929 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.674 |
LIG_LIR_Nem_3 | 416 | 421 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 473 | 477 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 545 | 549 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 555 | 560 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 643 | 647 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 919 | 925 | PF02991 | 0.358 |
LIG_MLH1_MIPbox_1 | 864 | 868 | PF16413 | 0.358 |
LIG_MYND_1 | 850 | 854 | PF01753 | 0.358 |
LIG_MYND_1 | 950 | 954 | PF01753 | 0.358 |
LIG_MYND_1 | 984 | 988 | PF01753 | 0.630 |
LIG_PTAP_UEV_1 | 289 | 294 | PF05743 | 0.560 |
LIG_REV1ctd_RIR_1 | 865 | 871 | PF16727 | 0.358 |
LIG_SH2_CRK | 151 | 155 | PF00017 | 0.656 |
LIG_SH2_CRK | 3 | 7 | PF00017 | 0.667 |
LIG_SH2_CRK | 549 | 553 | PF00017 | 0.358 |
LIG_SH2_CRK | 557 | 561 | PF00017 | 0.295 |
LIG_SH2_CRK | 570 | 574 | PF00017 | 0.518 |
LIG_SH2_CRK | 816 | 820 | PF00017 | 0.311 |
LIG_SH2_CRK | 96 | 100 | PF00017 | 0.697 |
LIG_SH2_NCK_1 | 151 | 155 | PF00017 | 0.528 |
LIG_SH2_NCK_1 | 418 | 422 | PF00017 | 0.492 |
LIG_SH2_NCK_1 | 444 | 448 | PF00017 | 0.465 |
LIG_SH2_NCK_1 | 816 | 820 | PF00017 | 0.321 |
LIG_SH2_NCK_1 | 96 | 100 | PF00017 | 0.697 |
LIG_SH2_SRC | 444 | 447 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 444 | 448 | PF00017 | 0.465 |
LIG_SH2_STAP1 | 758 | 762 | PF00017 | 0.358 |
LIG_SH2_STAT3 | 616 | 619 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 463 | 466 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 499 | 502 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 741 | 744 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 758 | 761 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 792 | 795 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 816 | 819 | PF00017 | 0.369 |
LIG_SH3_1 | 816 | 822 | PF00018 | 0.311 |
LIG_SH3_2 | 779 | 784 | PF14604 | 0.358 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.686 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.672 |
LIG_SH3_3 | 260 | 266 | PF00018 | 0.715 |
LIG_SH3_3 | 277 | 283 | PF00018 | 0.699 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.621 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.561 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.659 |
LIG_SH3_3 | 537 | 543 | PF00018 | 0.358 |
LIG_SH3_3 | 626 | 632 | PF00018 | 0.649 |
LIG_SH3_3 | 696 | 702 | PF00018 | 0.661 |
LIG_SH3_3 | 776 | 782 | PF00018 | 0.358 |
LIG_SH3_3 | 816 | 822 | PF00018 | 0.390 |
LIG_SH3_3 | 960 | 966 | PF00018 | 0.552 |
LIG_SH3_3 | 982 | 988 | PF00018 | 0.805 |
LIG_SH3_5 | 799 | 803 | PF00018 | 0.358 |
LIG_SUMO_SIM_par_1 | 406 | 411 | PF11976 | 0.566 |
LIG_SUMO_SIM_par_1 | 536 | 542 | PF11976 | 0.358 |
LIG_SUMO_SIM_par_1 | 550 | 555 | PF11976 | 0.231 |
LIG_SUMO_SIM_par_1 | 574 | 580 | PF11976 | 0.358 |
LIG_SUMO_SIM_par_1 | 891 | 898 | PF11976 | 0.358 |
LIG_TRAF2_1 | 455 | 458 | PF00917 | 0.446 |
LIG_TRAF2_1 | 703 | 706 | PF00917 | 0.619 |
LIG_TRAF2_1 | 895 | 898 | PF00917 | 0.358 |
LIG_TYR_ITSM | 553 | 560 | PF00017 | 0.358 |
LIG_UBA3_1 | 551 | 556 | PF00899 | 0.358 |
MOD_CDC14_SPxK_1 | 104 | 107 | PF00782 | 0.571 |
MOD_CDC14_SPxK_1 | 808 | 811 | PF00782 | 0.358 |
MOD_CDK_SPK_2 | 323 | 328 | PF00069 | 0.682 |
MOD_CDK_SPK_2 | 805 | 810 | PF00069 | 0.358 |
MOD_CDK_SPxK_1 | 101 | 107 | PF00069 | 0.571 |
MOD_CDK_SPxK_1 | 805 | 811 | PF00069 | 0.358 |
MOD_CDK_SPxxK_3 | 217 | 224 | PF00069 | 0.693 |
MOD_CDK_SPxxK_3 | 371 | 378 | PF00069 | 0.650 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.602 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.696 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.703 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.725 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.574 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.784 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.765 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.797 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.659 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.616 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.599 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.777 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.780 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.358 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.592 |
MOD_CK1_1 | 635 | 641 | PF00069 | 0.750 |
MOD_CK1_1 | 643 | 649 | PF00069 | 0.643 |
MOD_CK1_1 | 820 | 826 | PF00069 | 0.414 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.670 |
MOD_CK2_1 | 413 | 419 | PF00069 | 0.639 |
MOD_CK2_1 | 599 | 605 | PF00069 | 0.358 |
MOD_CK2_1 | 643 | 649 | PF00069 | 0.683 |
MOD_CK2_1 | 700 | 706 | PF00069 | 0.608 |
MOD_CK2_1 | 892 | 898 | PF00069 | 0.518 |
MOD_DYRK1A_RPxSP_1 | 217 | 221 | PF00069 | 0.571 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.606 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.700 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.689 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.643 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.652 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.535 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.690 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.698 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.595 |
MOD_GlcNHglycan | 240 | 244 | PF01048 | 0.613 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.699 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.701 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.639 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.556 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.712 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.533 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.705 |
MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.748 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.593 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.549 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.522 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.599 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.358 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.675 |
MOD_GlcNHglycan | 612 | 615 | PF01048 | 0.358 |
MOD_GlcNHglycan | 651 | 654 | PF01048 | 0.655 |
MOD_GlcNHglycan | 663 | 669 | PF01048 | 0.593 |
MOD_GlcNHglycan | 685 | 688 | PF01048 | 0.595 |
MOD_GlcNHglycan | 696 | 699 | PF01048 | 0.747 |
MOD_GlcNHglycan | 76 | 80 | PF01048 | 0.534 |
MOD_GlcNHglycan | 825 | 828 | PF01048 | 0.494 |
MOD_GlcNHglycan | 856 | 859 | PF01048 | 0.382 |
MOD_GlcNHglycan | 886 | 889 | PF01048 | 0.295 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.574 |
MOD_GlcNHglycan | 966 | 969 | PF01048 | 0.636 |
MOD_GlcNHglycan | 980 | 983 | PF01048 | 0.719 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.804 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.677 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.526 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.539 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.550 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.654 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.635 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.613 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.608 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.620 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.736 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.608 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.567 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.581 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.430 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.604 |
MOD_GSK3_1 | 630 | 637 | PF00069 | 0.804 |
MOD_GSK3_1 | 664 | 671 | PF00069 | 0.718 |
MOD_GSK3_1 | 683 | 690 | PF00069 | 0.569 |
MOD_GSK3_1 | 805 | 812 | PF00069 | 0.340 |
MOD_GSK3_1 | 817 | 824 | PF00069 | 0.417 |
MOD_GSK3_1 | 850 | 857 | PF00069 | 0.414 |
MOD_GSK3_1 | 884 | 891 | PF00069 | 0.502 |
MOD_GSK3_1 | 974 | 981 | PF00069 | 0.734 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.689 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.603 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.694 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.522 |
MOD_NEK2_1 | 544 | 549 | PF00069 | 0.358 |
MOD_NEK2_1 | 562 | 567 | PF00069 | 0.215 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.670 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.576 |
MOD_NEK2_1 | 756 | 761 | PF00069 | 0.358 |
MOD_NEK2_1 | 814 | 819 | PF00069 | 0.451 |
MOD_NEK2_2 | 420 | 425 | PF00069 | 0.489 |
MOD_NEK2_2 | 830 | 835 | PF00069 | 0.231 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.722 |
MOD_PIKK_1 | 373 | 379 | PF00454 | 0.805 |
MOD_PIKK_1 | 408 | 414 | PF00454 | 0.539 |
MOD_PIKK_1 | 499 | 505 | PF00454 | 0.366 |
MOD_PIKK_1 | 668 | 674 | PF00454 | 0.567 |
MOD_PIKK_1 | 809 | 815 | PF00454 | 0.279 |
MOD_PK_1 | 959 | 965 | PF00069 | 0.534 |
MOD_PKA_1 | 198 | 204 | PF00069 | 0.711 |
MOD_PKA_1 | 224 | 230 | PF00069 | 0.575 |
MOD_PKA_1 | 939 | 945 | PF00069 | 0.358 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.702 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.575 |
MOD_PKA_2 | 327 | 333 | PF00069 | 0.673 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.571 |
MOD_PKA_2 | 763 | 769 | PF00069 | 0.358 |
MOD_PKA_2 | 939 | 945 | PF00069 | 0.358 |
MOD_Plk_2-3 | 706 | 712 | PF00069 | 0.546 |
MOD_Plk_4 | 413 | 419 | PF00069 | 0.639 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.513 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.358 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.675 |
MOD_Plk_4 | 792 | 798 | PF00069 | 0.358 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.571 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.654 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.529 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.692 |
MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.664 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.746 |
MOD_ProDKin_1 | 323 | 329 | PF00069 | 0.681 |
MOD_ProDKin_1 | 371 | 377 | PF00069 | 0.650 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.587 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.674 |
MOD_ProDKin_1 | 632 | 638 | PF00069 | 0.665 |
MOD_ProDKin_1 | 655 | 661 | PF00069 | 0.727 |
MOD_ProDKin_1 | 746 | 752 | PF00069 | 0.518 |
MOD_ProDKin_1 | 805 | 811 | PF00069 | 0.375 |
MOD_ProDKin_1 | 850 | 856 | PF00069 | 0.358 |
MOD_ProDKin_1 | 862 | 868 | PF00069 | 0.263 |
MOD_ProDKin_1 | 888 | 894 | PF00069 | 0.414 |
MOD_SUMO_for_1 | 591 | 594 | PF00179 | 0.358 |
TRG_DiLeu_BaEn_1 | 428 | 433 | PF01217 | 0.507 |
TRG_DiLeu_BaLyEn_6 | 547 | 552 | PF01217 | 0.358 |
TRG_DiLeu_BaLyEn_6 | 982 | 987 | PF01217 | 0.539 |
TRG_ENDOCYTIC_2 | 3 | 6 | PF00928 | 0.674 |
TRG_ENDOCYTIC_2 | 418 | 421 | PF00928 | 0.627 |
TRG_ENDOCYTIC_2 | 549 | 552 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 557 | 560 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 570 | 573 | PF00928 | 0.518 |
TRG_ENDOCYTIC_2 | 922 | 925 | PF00928 | 0.358 |
TRG_ER_diArg_1 | 198 | 200 | PF00400 | 0.750 |
TRG_ER_diArg_1 | 223 | 225 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 937 | 940 | PF00400 | 0.358 |
TRG_NLS_MonoExtN_4 | 937 | 942 | PF00514 | 0.358 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H6S1 | Leishmania donovani | 91% | 100% |
Q4QFQ0 | Leishmania major | 91% | 100% |