Dual-specificity kinase

dual specificity tyrosine-phosphorylation-regulated kinase 2, putative

Leishmania major

957

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: 5 |

NetGPI | no | yes: 0, no: 5 |

Term | Name | Level | Count |
---|---|---|---|

GO:0005737 | cytoplasm | 2 | 2 |

GO:0005856 | cytoskeleton | 5 | 2 |

GO:0043226 | organelle | 2 | 2 |

GO:0043228 | non-membrane-bounded organelle | 3 | 2 |

GO:0043229 | intracellular organelle | 3 | 2 |

GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |

GO:0110165 | cellular anatomical entity | 1 | 2 |

Q4Q405

Sequence

MSA

Disorder

Secondary

Topology

Domains

SignalP

GPI

Phosphorylations

ELMs

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: Q4Q405

Term | Name | Level | Count |
---|---|---|---|

GO:0006468 | protein phosphorylation | 5 | 6 |

GO:0006793 | phosphorus metabolic process | 3 | 6 |

GO:0006796 | phosphate-containing compound metabolic process | 4 | 6 |

GO:0006807 | nitrogen compound metabolic process | 2 | 6 |

GO:0008152 | metabolic process | 1 | 6 |

GO:0009987 | cellular process | 1 | 6 |

GO:0016310 | phosphorylation | 5 | 6 |

GO:0018105 | peptidyl-serine phosphorylation | 6 | 2 |

GO:0018107 | peptidyl-threonine phosphorylation | 6 | 2 |

GO:0018193 | peptidyl-amino acid modification | 5 | 2 |

GO:0018209 | peptidyl-serine modification | 6 | 2 |

GO:0018210 | peptidyl-threonine modification | 6 | 2 |

GO:0019538 | protein metabolic process | 3 | 6 |

GO:0036211 | protein modification process | 4 | 6 |

GO:0043170 | macromolecule metabolic process | 3 | 6 |

GO:0043412 | macromolecule modification | 4 | 6 |

GO:0044237 | cellular metabolic process | 2 | 6 |

GO:0044238 | primary metabolic process | 2 | 6 |

GO:0071704 | organic substance metabolic process | 2 | 6 |

GO:1901564 | organonitrogen compound metabolic process | 3 | 6 |

Term | Name | Level | Count |
---|---|---|---|

GO:0000166 | nucleotide binding | 3 | 6 |

GO:0003824 | catalytic activity | 1 | 6 |

GO:0004672 | protein kinase activity | 3 | 6 |

GO:0004674 | protein serine/threonine kinase activity | 4 | 2 |

GO:0004712 | protein serine/threonine/tyrosine kinase activity | 4 | 6 |

GO:0005488 | binding | 1 | 6 |

GO:0005524 | ATP binding | 5 | 6 |

GO:0016301 | kinase activity | 4 | 6 |

GO:0016740 | transferase activity | 2 | 6 |

GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 6 |

GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 6 |

GO:0017076 | purine nucleotide binding | 4 | 6 |

GO:0030554 | adenyl nucleotide binding | 5 | 6 |

GO:0032553 | ribonucleotide binding | 3 | 6 |

GO:0032555 | purine ribonucleotide binding | 4 | 6 |

GO:0032559 | adenyl ribonucleotide binding | 5 | 6 |

GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 6 |

GO:0036094 | small molecule binding | 2 | 6 |

GO:0043167 | ion binding | 2 | 6 |

GO:0043168 | anion binding | 3 | 6 |

GO:0097159 | organic cyclic compound binding | 2 | 6 |

GO:0097367 | carbohydrate derivative binding | 2 | 6 |

GO:0140096 | catalytic activity, acting on a protein | 2 | 6 |

GO:1901265 | nucleoside phosphate binding | 3 | 6 |

GO:1901363 | heterocyclic compound binding | 2 | 6 |

Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|

CLV_C14_Caspase3-7 | 102 | 106 | PF00656 | 0.452 |

CLV_C14_Caspase3-7 | 730 | 734 | PF00656 | 0.760 |

CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.530 |

CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.522 |

CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.608 |

CLV_NRD_NRD_1 | 401 | 403 | PF00675 | 0.597 |

CLV_NRD_NRD_1 | 520 | 522 | PF00675 | 0.737 |

CLV_NRD_NRD_1 | 532 | 534 | PF00675 | 0.827 |

CLV_NRD_NRD_1 | 721 | 723 | PF00675 | 0.778 |

CLV_NRD_NRD_1 | 755 | 757 | PF00675 | 0.849 |

CLV_PCSK_FUR_1 | 313 | 317 | PF00082 | 0.530 |

CLV_PCSK_FUR_1 | 530 | 534 | PF00082 | 0.832 |

CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.530 |

CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.452 |

CLV_PCSK_KEX2_1 | 520 | 522 | PF00082 | 0.737 |

CLV_PCSK_KEX2_1 | 532 | 534 | PF00082 | 0.827 |

CLV_PCSK_KEX2_1 | 721 | 723 | PF00082 | 0.778 |

CLV_PCSK_KEX2_1 | 755 | 757 | PF00082 | 0.849 |

CLV_PCSK_KEX2_1 | 952 | 954 | PF00082 | 0.777 |

CLV_PCSK_PC1ET2_1 | 369 | 371 | PF00082 | 0.452 |

CLV_PCSK_PC1ET2_1 | 952 | 954 | PF00082 | 0.777 |

CLV_PCSK_PC7_1 | 528 | 534 | PF00082 | 0.840 |

CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.436 |

CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.530 |

CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.530 |

CLV_PCSK_SKI1_1 | 921 | 925 | PF00082 | 0.825 |

DEG_SCF_FBW7_1 | 420 | 426 | PF00400 | 0.591 |

DEG_SPOP_SBC_1 | 800 | 804 | PF00917 | 0.618 |

DOC_CKS1_1 | 420 | 425 | PF01111 | 0.588 |

DOC_CYCLIN_yClb5_NLxxxL_5 | 164 | 173 | PF00134 | 0.530 |

DOC_CYCLIN_yCln2_LP_2 | 556 | 562 | PF00134 | 0.794 |

DOC_CYCLIN_yCln2_LP_2 | 911 | 914 | PF00134 | 0.841 |

DOC_MAPK_FxFP_2 | 386 | 389 | PF00069 | 0.672 |

DOC_MAPK_gen_1 | 752 | 762 | PF00069 | 0.850 |

DOC_MAPK_gen_1 | 827 | 835 | PF00069 | 0.779 |

DOC_MAPK_HePTP_8 | 244 | 256 | PF00069 | 0.530 |

DOC_MAPK_MEF2A_6 | 192 | 199 | PF00069 | 0.530 |

DOC_MAPK_MEF2A_6 | 247 | 256 | PF00069 | 0.530 |

DOC_PP1_RVXF_1 | 260 | 267 | PF00149 | 0.452 |

DOC_PP2B_LxvP_1 | 299 | 302 | PF13499 | 0.369 |

DOC_PP2B_LxvP_1 | 556 | 559 | PF13499 | 0.758 |

DOC_PP2B_LxvP_1 | 911 | 914 | PF13499 | 0.841 |

DOC_PP4_FxxP_1 | 386 | 389 | PF00568 | 0.672 |

DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.535 |

DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.764 |

DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.789 |

DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.725 |

DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.593 |

DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.666 |

DOC_USP7_MATH_1 | 550 | 554 | PF00917 | 0.831 |

DOC_USP7_MATH_1 | 562 | 566 | PF00917 | 0.630 |

DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.709 |

DOC_USP7_MATH_1 | 647 | 651 | PF00917 | 0.784 |

DOC_USP7_MATH_1 | 702 | 706 | PF00917 | 0.740 |

DOC_USP7_MATH_1 | 726 | 730 | PF00917 | 0.764 |

DOC_USP7_MATH_1 | 740 | 744 | PF00917 | 0.706 |

DOC_USP7_MATH_1 | 800 | 804 | PF00917 | 0.718 |

DOC_USP7_MATH_1 | 819 | 823 | PF00917 | 0.656 |

DOC_USP7_MATH_1 | 837 | 841 | PF00917 | 0.596 |

DOC_USP7_MATH_1 | 846 | 850 | PF00917 | 0.738 |

DOC_USP7_MATH_1 | 852 | 856 | PF00917 | 0.639 |

DOC_USP7_MATH_1 | 883 | 887 | PF00917 | 0.753 |

DOC_USP7_MATH_1 | 919 | 923 | PF00917 | 0.656 |

DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.610 |

DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.799 |

DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.685 |

DOC_WW_Pin1_4 | 546 | 551 | PF00397 | 0.759 |

DOC_WW_Pin1_4 | 580 | 585 | PF00397 | 0.820 |

DOC_WW_Pin1_4 | 613 | 618 | PF00397 | 0.634 |

DOC_WW_Pin1_4 | 736 | 741 | PF00397 | 0.851 |

DOC_WW_Pin1_4 | 743 | 748 | PF00397 | 0.748 |

DOC_WW_Pin1_4 | 801 | 806 | PF00397 | 0.776 |

DOC_WW_Pin1_4 | 838 | 843 | PF00397 | 0.846 |

DOC_WW_Pin1_4 | 850 | 855 | PF00397 | 0.650 |

DOC_WW_Pin1_4 | 940 | 945 | PF00397 | 0.831 |

LIG_14-3-3_CanoR_1 | 147 | 154 | PF00244 | 0.452 |

LIG_14-3-3_CanoR_1 | 155 | 164 | PF00244 | 0.351 |

LIG_14-3-3_CanoR_1 | 192 | 198 | PF00244 | 0.375 |

LIG_14-3-3_CanoR_1 | 507 | 513 | PF00244 | 0.747 |

LIG_14-3-3_CanoR_1 | 530 | 540 | PF00244 | 0.826 |

LIG_14-3-3_CanoR_1 | 608 | 617 | PF00244 | 0.739 |

LIG_14-3-3_CanoR_1 | 621 | 629 | PF00244 | 0.587 |

LIG_14-3-3_CanoR_1 | 708 | 718 | PF00244 | 0.825 |

LIG_14-3-3_CanoR_1 | 735 | 740 | PF00244 | 0.735 |

LIG_14-3-3_CanoR_1 | 801 | 805 | PF00244 | 0.725 |

LIG_14-3-3_CanoR_1 | 863 | 872 | PF00244 | 0.737 |

LIG_14-3-3_CanoR_1 | 915 | 919 | PF00244 | 0.829 |

LIG_Actin_WH2_2 | 607 | 623 | PF00022 | 0.743 |

LIG_AP2alpha_2 | 692 | 694 | PF02296 | 0.585 |

LIG_APCC_ABBA_1 | 793 | 798 | PF00400 | 0.819 |

LIG_BRCT_BRCA1_1 | 231 | 235 | PF00533 | 0.452 |

LIG_BRCT_BRCA1_1 | 706 | 710 | PF00533 | 0.613 |

LIG_BRCT_BRCA1_1 | 90 | 94 | PF00533 | 0.530 |

LIG_deltaCOP1_diTrp_1 | 265 | 269 | PF00928 | 0.530 |

LIG_EVH1_2 | 302 | 306 | PF00568 | 0.369 |

LIG_FHA_1 | 180 | 186 | PF00498 | 0.452 |

LIG_FHA_1 | 622 | 628 | PF00498 | 0.705 |

LIG_FHA_1 | 670 | 676 | PF00498 | 0.643 |

LIG_FHA_1 | 767 | 773 | PF00498 | 0.601 |

LIG_FHA_1 | 851 | 857 | PF00498 | 0.778 |

LIG_FHA_1 | 943 | 949 | PF00498 | 0.786 |

LIG_FHA_2 | 27 | 33 | PF00498 | 0.595 |

LIG_FHA_2 | 388 | 394 | PF00498 | 0.572 |

LIG_Integrin_isoDGR_2 | 58 | 60 | PF01839 | 0.650 |

LIG_LIR_Apic_2 | 246 | 252 | PF02991 | 0.530 |

LIG_LIR_Apic_2 | 297 | 301 | PF02991 | 0.501 |

LIG_LIR_Apic_2 | 385 | 389 | PF02991 | 0.659 |

LIG_LIR_Apic_2 | 786 | 790 | PF02991 | 0.752 |

LIG_LIR_Apic_2 | 898 | 902 | PF02991 | 0.761 |

LIG_LIR_Gen_1 | 161 | 170 | PF02991 | 0.530 |

LIG_LIR_Gen_1 | 305 | 312 | PF02991 | 0.427 |

LIG_LIR_Gen_1 | 352 | 363 | PF02991 | 0.487 |

LIG_LIR_Nem_3 | 161 | 165 | PF02991 | 0.530 |

LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.333 |

LIG_LIR_Nem_3 | 265 | 269 | PF02991 | 0.374 |

LIG_LIR_Nem_3 | 305 | 309 | PF02991 | 0.427 |

LIG_LIR_Nem_3 | 352 | 358 | PF02991 | 0.487 |

LIG_LIR_Nem_3 | 91 | 97 | PF02991 | 0.413 |

LIG_MYND_1 | 854 | 858 | PF01753 | 0.845 |

LIG_Pex14_2 | 358 | 362 | PF04695 | 0.394 |

LIG_Pex14_2 | 94 | 98 | PF04695 | 0.407 |

LIG_REV1ctd_RIR_1 | 316 | 324 | PF16727 | 0.452 |

LIG_SH2_CRK | 143 | 147 | PF00017 | 0.530 |

LIG_SH2_CRK | 241 | 245 | PF00017 | 0.413 |

LIG_SH2_CRK | 787 | 791 | PF00017 | 0.747 |

LIG_SH2_SRC | 555 | 558 | PF00017 | 0.611 |

LIG_SH2_SRC | 681 | 684 | PF00017 | 0.703 |

LIG_SH2_SRC | 773 | 776 | PF00017 | 0.759 |

LIG_SH2_STAP1 | 260 | 264 | PF00017 | 0.452 |

LIG_SH2_STAP1 | 758 | 762 | PF00017 | 0.775 |

LIG_SH2_STAT3 | 44 | 47 | PF00017 | 0.584 |

LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.378 |

LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.369 |

LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.506 |

LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.771 |

LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.594 |

LIG_SH3_2 | 420 | 425 | PF14604 | 0.783 |

LIG_SH3_2 | 910 | 915 | PF14604 | 0.765 |

LIG_SH3_3 | 278 | 284 | PF00018 | 0.530 |

LIG_SH3_3 | 417 | 423 | PF00018 | 0.761 |

LIG_SH3_3 | 431 | 437 | PF00018 | 0.577 |

LIG_SH3_3 | 454 | 460 | PF00018 | 0.695 |

LIG_SH3_3 | 461 | 467 | PF00018 | 0.595 |

LIG_SH3_3 | 510 | 516 | PF00018 | 0.857 |

LIG_SH3_3 | 537 | 543 | PF00018 | 0.826 |

LIG_SH3_3 | 611 | 617 | PF00018 | 0.623 |

LIG_SH3_3 | 769 | 775 | PF00018 | 0.759 |

LIG_SH3_3 | 818 | 824 | PF00018 | 0.631 |

LIG_SH3_3 | 840 | 846 | PF00018 | 0.774 |

LIG_SH3_3 | 907 | 913 | PF00018 | 0.756 |

LIG_SH3_3 | 943 | 949 | PF00018 | 0.720 |

LIG_SUMO_SIM_anti_2 | 182 | 188 | PF11976 | 0.452 |

LIG_SUMO_SIM_par_1 | 13 | 19 | PF11976 | 0.411 |

LIG_SUMO_SIM_par_1 | 193 | 198 | PF11976 | 0.530 |

LIG_SUMO_SIM_par_1 | 226 | 232 | PF11976 | 0.452 |

LIG_SUMO_SIM_par_1 | 622 | 631 | PF11976 | 0.686 |

LIG_SxIP_EBH_1 | 901 | 915 | PF03271 | 0.607 |

LIG_TRAF2_1 | 124 | 127 | PF00917 | 0.530 |

LIG_TYR_ITIM | 160 | 165 | PF00017 | 0.530 |

LIG_TYR_ITIM | 37 | 42 | PF00017 | 0.624 |

LIG_WRC_WIRS_1 | 21 | 26 | PF05994 | 0.551 |

LIG_WRC_WIRS_1 | 355 | 360 | PF05994 | 0.530 |

LIG_WW_3 | 371 | 375 | PF00397 | 0.452 |

LIG_WW_3 | 912 | 916 | PF00397 | 0.842 |

MOD_CDK_SPK_2 | 743 | 748 | PF00069 | 0.786 |

MOD_CDK_SPxK_1 | 419 | 425 | PF00069 | 0.591 |

MOD_CDK_SPxxK_3 | 850 | 857 | PF00069 | 0.840 |

MOD_CK1_1 | 404 | 410 | PF00069 | 0.738 |

MOD_CK1_1 | 499 | 505 | PF00069 | 0.645 |

MOD_CK1_1 | 582 | 588 | PF00069 | 0.813 |

MOD_CK1_1 | 650 | 656 | PF00069 | 0.729 |

MOD_CK1_1 | 743 | 749 | PF00069 | 0.845 |

MOD_CK1_1 | 828 | 834 | PF00069 | 0.831 |

MOD_CK1_1 | 841 | 847 | PF00069 | 0.651 |

MOD_CK2_1 | 13 | 19 | PF00069 | 0.644 |

MOD_CK2_1 | 26 | 32 | PF00069 | 0.387 |

MOD_CK2_1 | 302 | 308 | PF00069 | 0.452 |

MOD_CK2_1 | 345 | 351 | PF00069 | 0.300 |

MOD_CK2_1 | 387 | 393 | PF00069 | 0.521 |

MOD_CK2_1 | 562 | 568 | PF00069 | 0.818 |

MOD_CK2_1 | 748 | 754 | PF00069 | 0.671 |

MOD_Cter_Amidation | 719 | 722 | PF01082 | 0.737 |

MOD_DYRK1A_RPxSP_1 | 801 | 805 | PF00069 | 0.725 |

MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.530 |

MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.530 |

MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.805 |

MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.606 |

MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.728 |

MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.688 |

MOD_GlcNHglycan | 495 | 499 | PF01048 | 0.549 |

MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.799 |

MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.712 |

MOD_GlcNHglycan | 563 | 568 | PF01048 | 0.765 |

MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.689 |

MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.699 |

MOD_GlcNHglycan | 665 | 668 | PF01048 | 0.748 |

MOD_GlcNHglycan | 695 | 699 | PF01048 | 0.776 |

MOD_GlcNHglycan | 718 | 721 | PF01048 | 0.777 |

MOD_GlcNHglycan | 724 | 727 | PF01048 | 0.821 |

MOD_GlcNHglycan | 848 | 851 | PF01048 | 0.834 |

MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.749 |

MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.530 |

MOD_GlcNHglycan | 954 | 957 | PF01048 | 0.758 |

MOD_GSK3_1 | 181 | 188 | PF00069 | 0.452 |

MOD_GSK3_1 | 239 | 246 | PF00069 | 0.452 |

MOD_GSK3_1 | 397 | 404 | PF00069 | 0.726 |

MOD_GSK3_1 | 419 | 426 | PF00069 | 0.617 |

MOD_GSK3_1 | 546 | 553 | PF00069 | 0.761 |

MOD_GSK3_1 | 579 | 586 | PF00069 | 0.793 |

MOD_GSK3_1 | 609 | 616 | PF00069 | 0.758 |

MOD_GSK3_1 | 641 | 648 | PF00069 | 0.841 |

MOD_GSK3_1 | 683 | 690 | PF00069 | 0.709 |

MOD_GSK3_1 | 722 | 729 | PF00069 | 0.680 |

MOD_GSK3_1 | 731 | 738 | PF00069 | 0.755 |

MOD_GSK3_1 | 763 | 770 | PF00069 | 0.752 |

MOD_GSK3_1 | 837 | 844 | PF00069 | 0.771 |

MOD_GSK3_1 | 846 | 853 | PF00069 | 0.665 |

MOD_GSK3_1 | 863 | 870 | PF00069 | 0.541 |

MOD_GSK3_1 | 938 | 945 | PF00069 | 0.796 |

MOD_N-GLC_1 | 404 | 409 | PF02516 | 0.709 |

MOD_N-GLC_1 | 550 | 555 | PF02516 | 0.834 |

MOD_N-GLC_1 | 645 | 650 | PF02516 | 0.770 |

MOD_NEK2_1 | 104 | 109 | PF00069 | 0.530 |

MOD_NEK2_1 | 164 | 169 | PF00069 | 0.335 |

MOD_NEK2_1 | 181 | 186 | PF00069 | 0.416 |

MOD_NEK2_1 | 193 | 198 | PF00069 | 0.375 |

MOD_NEK2_1 | 401 | 406 | PF00069 | 0.659 |

MOD_NEK2_1 | 486 | 491 | PF00069 | 0.576 |

MOD_NEK2_1 | 620 | 625 | PF00069 | 0.825 |

MOD_NEK2_1 | 694 | 699 | PF00069 | 0.615 |

MOD_NEK2_2 | 327 | 332 | PF00069 | 0.413 |

MOD_NEK2_2 | 408 | 413 | PF00069 | 0.787 |

MOD_PIKK_1 | 387 | 393 | PF00454 | 0.621 |

MOD_PIKK_1 | 414 | 420 | PF00454 | 0.639 |

MOD_PIKK_1 | 828 | 834 | PF00454 | 0.777 |

MOD_PIKK_1 | 864 | 870 | PF00454 | 0.756 |

MOD_PIKK_1 | 883 | 889 | PF00454 | 0.510 |

MOD_PK_1 | 345 | 351 | PF00069 | 0.296 |

MOD_PK_1 | 756 | 762 | PF00069 | 0.775 |

MOD_PKA_1 | 520 | 526 | PF00069 | 0.800 |

MOD_PKA_1 | 532 | 538 | PF00069 | 0.823 |

MOD_PKA_2 | 146 | 152 | PF00069 | 0.452 |

MOD_PKA_2 | 327 | 333 | PF00069 | 0.452 |

MOD_PKA_2 | 401 | 407 | PF00069 | 0.747 |

MOD_PKA_2 | 506 | 512 | PF00069 | 0.782 |

MOD_PKA_2 | 520 | 526 | PF00069 | 0.623 |

MOD_PKA_2 | 531 | 537 | PF00069 | 0.815 |

MOD_PKA_2 | 568 | 574 | PF00069 | 0.594 |

MOD_PKA_2 | 593 | 599 | PF00069 | 0.762 |

MOD_PKA_2 | 620 | 626 | PF00069 | 0.714 |

MOD_PKA_2 | 800 | 806 | PF00069 | 0.727 |

MOD_PKA_2 | 837 | 843 | PF00069 | 0.768 |

MOD_PKA_2 | 864 | 870 | PF00069 | 0.756 |

MOD_PKA_2 | 904 | 910 | PF00069 | 0.708 |

MOD_PKA_2 | 914 | 920 | PF00069 | 0.777 |

MOD_PKB_1 | 530 | 538 | PF00069 | 0.826 |

MOD_Plk_1 | 104 | 110 | PF00069 | 0.530 |

MOD_Plk_1 | 396 | 402 | PF00069 | 0.705 |

MOD_Plk_1 | 550 | 556 | PF00069 | 0.648 |

MOD_Plk_1 | 756 | 762 | PF00069 | 0.775 |

MOD_Plk_1 | 828 | 834 | PF00069 | 0.812 |

MOD_Plk_4 | 104 | 110 | PF00069 | 0.530 |

MOD_Plk_4 | 181 | 187 | PF00069 | 0.452 |

MOD_Plk_4 | 195 | 201 | PF00069 | 0.530 |

MOD_Plk_4 | 220 | 226 | PF00069 | 0.468 |

MOD_Plk_4 | 239 | 245 | PF00069 | 0.278 |

MOD_Plk_4 | 302 | 308 | PF00069 | 0.452 |

MOD_Plk_4 | 354 | 360 | PF00069 | 0.530 |

MOD_Plk_4 | 867 | 873 | PF00069 | 0.707 |

MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.614 |

MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.800 |

MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.696 |

MOD_ProDKin_1 | 546 | 552 | PF00069 | 0.761 |

MOD_ProDKin_1 | 580 | 586 | PF00069 | 0.821 |

MOD_ProDKin_1 | 613 | 619 | PF00069 | 0.636 |

MOD_ProDKin_1 | 736 | 742 | PF00069 | 0.853 |

MOD_ProDKin_1 | 743 | 749 | PF00069 | 0.748 |

MOD_ProDKin_1 | 801 | 807 | PF00069 | 0.775 |

MOD_ProDKin_1 | 838 | 844 | PF00069 | 0.849 |

MOD_ProDKin_1 | 850 | 856 | PF00069 | 0.652 |

MOD_ProDKin_1 | 940 | 946 | PF00069 | 0.825 |

MOD_SUMO_for_1 | 210 | 213 | PF00179 | 0.530 |

MOD_SUMO_for_1 | 424 | 427 | PF00179 | 0.770 |

MOD_SUMO_rev_2 | 136 | 142 | PF00179 | 0.530 |

MOD_SUMO_rev_2 | 203 | 212 | PF00179 | 0.530 |

MOD_SUMO_rev_2 | 232 | 240 | PF00179 | 0.530 |

MOD_SUMO_rev_2 | 392 | 396 | PF00179 | 0.795 |

MOD_SUMO_rev_2 | 638 | 644 | PF00179 | 0.697 |

TRG_DiLeu_BaEn_2 | 350 | 356 | PF01217 | 0.530 |

TRG_DiLeu_BaEn_4 | 393 | 399 | PF01217 | 0.732 |

TRG_DiLeu_BaLyEn_6 | 812 | 817 | PF01217 | 0.712 |

TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.530 |

TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.216 |

TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.530 |

TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.491 |

TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.616 |

TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.530 |

TRG_ER_diArg_1 | 313 | 316 | PF00400 | 0.530 |

TRG_ER_diArg_1 | 325 | 328 | PF00400 | 0.199 |

TRG_ER_diArg_1 | 530 | 533 | PF00400 | 0.820 |

TRG_ER_diArg_1 | 706 | 709 | PF00400 | 0.594 |

TRG_ER_diArg_1 | 862 | 865 | PF00400 | 0.757 |

TRG_NES_CRM1_1 | 102 | 117 | PF08389 | 0.452 |

TRG_Pf-PMV_PEXEL_1 | 118 | 122 | PF00026 | 0.333 |

TRG_Pf-PMV_PEXEL_1 | 608 | 613 | PF00026 | 0.740 |

TRG_Pf-PMV_PEXEL_1 | 921 | 926 | PF00026 | 0.772 |

Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|

A0A3S7X6S4 | Leishmania donovani | 92% | 100% |

A4HLP3 | Leishmania braziliensis | 68% | 100% |

A4I978 | Leishmania infantum | 92% | 100% |

E9B419 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |