Aurora kinase

Aurora kinase 3, putative

Leishmania major

1043

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:0005813 | centrosome | 3 | 2 |

GO:0005815 | microtubule organizing center | 2 | 2 |

GO:0005874 | microtubule | 6 | 2 |

GO:0005875 | microtubule associated complex | 2 | 2 |

GO:0005876 | spindle microtubule | 7 | 2 |

GO:0031616 | spindle pole centrosome | 4 | 2 |

GO:0032133 | chromosome passenger complex | 3 | 2 |

GO:0032991 | protein-containing complex | 1 | 2 |

GO:0051233 | spindle midzone | 2 | 2 |

GO:0099080 | supramolecular complex | 2 | 2 |

GO:0099081 | supramolecular polymer | 3 | 2 |

GO:0099512 | supramolecular fiber | 4 | 2 |

GO:0099513 | polymeric cytoskeletal fiber | 5 | 2 |

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

Q4Q8U7

Sequence

MSA

Disorder

Secondary

Topology

Domains

SignalP

GPI

Phosphorylations

ELMs

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: Q4Q8U7

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

GO:0000226 | microtubule cytoskeleton organization | 3 | 2 |

GO:0006468 | protein phosphorylation | 5 | 7 |

GO:0006793 | phosphorus metabolic process | 3 | 7 |

GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |

GO:0006807 | nitrogen compound metabolic process | 2 | 7 |

GO:0006996 | organelle organization | 4 | 2 |

GO:0007010 | cytoskeleton organization | 5 | 2 |

GO:0007017 | microtubule-based process | 2 | 2 |

GO:0007051 | spindle organization | 3 | 2 |

GO:0007052 | mitotic spindle organization | 4 | 2 |

GO:0008152 | metabolic process | 1 | 7 |

GO:0009987 | cellular process | 1 | 7 |

GO:0010564 | regulation of cell cycle process | 5 | 2 |

GO:0016043 | cellular component organization | 3 | 2 |

GO:0016310 | phosphorylation | 5 | 7 |

GO:0019538 | protein metabolic process | 3 | 7 |

GO:0022402 | cell cycle process | 2 | 2 |

GO:0032465 | regulation of cytokinesis | 5 | 2 |

GO:0036211 | protein modification process | 4 | 7 |

GO:0043170 | macromolecule metabolic process | 3 | 7 |

GO:0043412 | macromolecule modification | 4 | 7 |

GO:0044237 | cellular metabolic process | 2 | 7 |

GO:0044238 | primary metabolic process | 2 | 7 |

GO:0050789 | regulation of biological process | 2 | 2 |

GO:0050794 | regulation of cellular process | 3 | 2 |

GO:0051302 | regulation of cell division | 4 | 2 |

GO:0051726 | regulation of cell cycle | 4 | 2 |

GO:0065007 | biological regulation | 1 | 2 |

GO:0071704 | organic substance metabolic process | 2 | 7 |

GO:0071840 | cellular component organization or biogenesis | 2 | 2 |

GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |

GO:1902850 | microtubule cytoskeleton organization involved in mitosis | 4 | 2 |

GO:1903047 | mitotic cell cycle process | 3 | 2 |

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

GO:0000166 | nucleotide binding | 3 | 7 |

GO:0003824 | catalytic activity | 1 | 7 |

GO:0004672 | protein kinase activity | 3 | 7 |

GO:0004674 | protein serine/threonine kinase activity | 4 | 7 |

GO:0005488 | binding | 1 | 7 |

GO:0005524 | ATP binding | 5 | 7 |

GO:0016301 | kinase activity | 4 | 7 |

GO:0016740 | transferase activity | 2 | 7 |

GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 7 |

GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 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:0035173 | histone kinase activity | 4 | 2 |

GO:0035174 | obsolete histone serine kinase activity | 5 | 2 |

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:0140096 | catalytic activity, acting on a protein | 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 | 209 | 213 | PF00656 | 0.745 |

CLV_C14_Caspase3-7 | 228 | 232 | PF00656 | 0.685 |

CLV_C14_Caspase3-7 | 376 | 380 | PF00656 | 0.509 |

CLV_C14_Caspase3-7 | 607 | 611 | PF00656 | 0.511 |

CLV_C14_Caspase3-7 | 659 | 663 | PF00656 | 0.512 |

CLV_NRD_NRD_1 | 1013 | 1015 | PF00675 | 0.739 |

CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.670 |

CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.811 |

CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.500 |

CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.342 |

CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.346 |

CLV_NRD_NRD_1 | 369 | 371 | PF00675 | 0.519 |

CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.413 |

CLV_NRD_NRD_1 | 704 | 706 | PF00675 | 0.662 |

CLV_NRD_NRD_1 | 780 | 782 | PF00675 | 0.820 |

CLV_NRD_NRD_1 | 890 | 892 | PF00675 | 0.710 |

CLV_PCSK_FUR_1 | 1011 | 1015 | PF00082 | 0.547 |

CLV_PCSK_KEX2_1 | 1013 | 1015 | PF00082 | 0.811 |

CLV_PCSK_KEX2_1 | 1024 | 1026 | PF00082 | 0.632 |

CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.637 |

CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.811 |

CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.500 |

CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.342 |

CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.346 |

CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.519 |

CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.413 |

CLV_PCSK_KEX2_1 | 517 | 519 | PF00082 | 0.428 |

CLV_PCSK_KEX2_1 | 704 | 706 | PF00082 | 0.662 |

CLV_PCSK_KEX2_1 | 780 | 782 | PF00082 | 0.783 |

CLV_PCSK_KEX2_1 | 889 | 891 | PF00082 | 0.719 |

CLV_PCSK_PC1ET2_1 | 1024 | 1026 | PF00082 | 0.740 |

CLV_PCSK_PC1ET2_1 | 517 | 519 | PF00082 | 0.509 |

CLV_PCSK_PC7_1 | 885 | 891 | PF00082 | 0.724 |

CLV_PCSK_SKI1_1 | 1031 | 1035 | PF00082 | 0.716 |

CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.509 |

CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.432 |

CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.387 |

CLV_PCSK_SKI1_1 | 541 | 545 | PF00082 | 0.463 |

CLV_PCSK_SKI1_1 | 704 | 708 | PF00082 | 0.539 |

CLV_PCSK_SKI1_1 | 959 | 963 | PF00082 | 0.717 |

DEG_SCF_FBW7_1 | 4 | 10 | PF00400 | 0.505 |

DEG_SCF_FBW7_1 | 695 | 702 | PF00400 | 0.665 |

DEG_SCF_FBW7_1 | 906 | 911 | PF00400 | 0.607 |

DEG_SPOP_SBC_1 | 1006 | 1010 | PF00917 | 0.726 |

DEG_SPOP_SBC_1 | 689 | 693 | PF00917 | 0.589 |

DEG_SPOP_SBC_1 | 7 | 11 | PF00917 | 0.500 |

DEG_SPOP_SBC_1 | 774 | 778 | PF00917 | 0.698 |

DEG_SPOP_SBC_1 | 809 | 813 | PF00917 | 0.723 |

DEG_SPOP_SBC_1 | 932 | 936 | PF00917 | 0.709 |

DOC_CKS1_1 | 4 | 9 | PF01111 | 0.504 |

DOC_CKS1_1 | 872 | 877 | PF01111 | 0.698 |

DOC_CYCLIN_RxL_1 | 538 | 548 | PF00134 | 0.463 |

DOC_CYCLIN_yCln2_LP_2 | 240 | 246 | PF00134 | 0.583 |

DOC_MAPK_gen_1 | 1024 | 1032 | PF00069 | 0.660 |

DOC_MAPK_gen_1 | 288 | 294 | PF00069 | 0.539 |

DOC_MAPK_gen_1 | 313 | 321 | PF00069 | 0.380 |

DOC_MAPK_HePTP_8 | 1022 | 1034 | PF00069 | 0.662 |

DOC_MAPK_MEF2A_6 | 1025 | 1034 | PF00069 | 0.751 |

DOC_MAPK_MEF2A_6 | 315 | 323 | PF00069 | 0.411 |

DOC_MAPK_MEF2A_6 | 608 | 616 | PF00069 | 0.560 |

DOC_PP1_RVXF_1 | 1029 | 1035 | PF00149 | 0.701 |

DOC_PP4_FxxP_1 | 182 | 185 | PF00568 | 0.698 |

DOC_PP4_FxxP_1 | 193 | 196 | PF00568 | 0.703 |

DOC_PP4_FxxP_1 | 246 | 249 | PF00568 | 0.683 |

DOC_USP7_MATH_1 | 1006 | 1010 | PF00917 | 0.815 |

DOC_USP7_MATH_1 | 1026 | 1030 | PF00917 | 0.470 |

DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.726 |

DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.556 |

DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.708 |

DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.701 |

DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.742 |

DOC_USP7_MATH_1 | 549 | 553 | PF00917 | 0.509 |

DOC_USP7_MATH_1 | 573 | 577 | PF00917 | 0.670 |

DOC_USP7_MATH_1 | 583 | 587 | PF00917 | 0.749 |

DOC_USP7_MATH_1 | 589 | 593 | PF00917 | 0.574 |

DOC_USP7_MATH_1 | 604 | 608 | PF00917 | 0.566 |

DOC_USP7_MATH_1 | 689 | 693 | PF00917 | 0.699 |

DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.724 |

DOC_USP7_MATH_1 | 726 | 730 | PF00917 | 0.712 |

DOC_USP7_MATH_1 | 738 | 742 | PF00917 | 0.679 |

DOC_USP7_MATH_1 | 774 | 778 | PF00917 | 0.730 |

DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.647 |

DOC_USP7_MATH_1 | 836 | 840 | PF00917 | 0.673 |

DOC_USP7_MATH_1 | 908 | 912 | PF00917 | 0.759 |

DOC_USP7_MATH_1 | 923 | 927 | PF00917 | 0.646 |

DOC_USP7_MATH_1 | 945 | 949 | PF00917 | 0.754 |

DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.774 |

DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.727 |

DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.706 |

DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.711 |

DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.665 |

DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.796 |

DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.755 |

DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.727 |

DOC_WW_Pin1_4 | 525 | 530 | PF00397 | 0.416 |

DOC_WW_Pin1_4 | 568 | 573 | PF00397 | 0.606 |

DOC_WW_Pin1_4 | 664 | 669 | PF00397 | 0.717 |

DOC_WW_Pin1_4 | 691 | 696 | PF00397 | 0.794 |

DOC_WW_Pin1_4 | 732 | 737 | PF00397 | 0.681 |

DOC_WW_Pin1_4 | 786 | 791 | PF00397 | 0.837 |

DOC_WW_Pin1_4 | 794 | 799 | PF00397 | 0.716 |

DOC_WW_Pin1_4 | 812 | 817 | PF00397 | 0.525 |

DOC_WW_Pin1_4 | 871 | 876 | PF00397 | 0.840 |

DOC_WW_Pin1_4 | 904 | 909 | PF00397 | 0.699 |

LIG_14-3-3_CanoR_1 | 115 | 119 | PF00244 | 0.686 |

LIG_14-3-3_CanoR_1 | 227 | 231 | PF00244 | 0.736 |

LIG_14-3-3_CanoR_1 | 278 | 282 | PF00244 | 0.760 |

LIG_14-3-3_CanoR_1 | 288 | 293 | PF00244 | 0.428 |

LIG_14-3-3_CanoR_1 | 422 | 427 | PF00244 | 0.406 |

LIG_14-3-3_CanoR_1 | 483 | 492 | PF00244 | 0.392 |

LIG_14-3-3_CanoR_1 | 551 | 558 | PF00244 | 0.373 |

LIG_14-3-3_CanoR_1 | 814 | 820 | PF00244 | 0.823 |

LIG_14-3-3_CanoR_1 | 909 | 918 | PF00244 | 0.633 |

LIG_14-3-3_CanoR_1 | 964 | 970 | PF00244 | 0.617 |

LIG_14-3-3_CanoR_1 | 985 | 993 | PF00244 | 0.702 |

LIG_Actin_WH2_2 | 417 | 434 | PF00022 | 0.416 |

LIG_APCC_ABBA_1 | 323 | 328 | PF00400 | 0.416 |

LIG_BIR_III_4 | 231 | 235 | PF00653 | 0.685 |

LIG_BRCT_BRCA1_1 | 110 | 114 | PF00533 | 0.657 |

LIG_BRCT_BRCA1_1 | 290 | 294 | PF00533 | 0.312 |

LIG_BRCT_BRCA1_1 | 620 | 624 | PF00533 | 0.773 |

LIG_BRCT_BRCA1_1 | 762 | 766 | PF00533 | 0.700 |

LIG_BRCT_BRCA1_1 | 841 | 845 | PF00533 | 0.800 |

LIG_BRCT_BRCA1_1 | 935 | 939 | PF00533 | 0.530 |

LIG_Clathr_ClatBox_1 | 543 | 547 | PF01394 | 0.509 |

LIG_deltaCOP1_diTrp_1 | 490 | 499 | PF00928 | 0.509 |

LIG_FHA_1 | 1017 | 1023 | PF00498 | 0.748 |

LIG_FHA_1 | 153 | 159 | PF00498 | 0.514 |

LIG_FHA_1 | 336 | 342 | PF00498 | 0.421 |

LIG_FHA_1 | 437 | 443 | PF00498 | 0.411 |

LIG_FHA_1 | 569 | 575 | PF00498 | 0.605 |

LIG_FHA_1 | 621 | 627 | PF00498 | 0.773 |

LIG_FHA_1 | 73 | 79 | PF00498 | 0.803 |

LIG_FHA_1 | 797 | 803 | PF00498 | 0.706 |

LIG_FHA_1 | 960 | 966 | PF00498 | 0.764 |

LIG_FHA_1 | 981 | 987 | PF00498 | 0.694 |

LIG_FHA_1 | 988 | 994 | PF00498 | 0.624 |

LIG_FHA_2 | 1034 | 1040 | PF00498 | 0.727 |

LIG_FHA_2 | 226 | 232 | PF00498 | 0.731 |

LIG_FHA_2 | 799 | 805 | PF00498 | 0.710 |

LIG_FHA_2 | 893 | 899 | PF00498 | 0.714 |

LIG_GBD_Chelix_1 | 33 | 41 | PF00786 | 0.395 |

LIG_Integrin_RGD_1 | 896 | 898 | PF01839 | 0.726 |

LIG_LIR_Apic_2 | 191 | 196 | PF02991 | 0.725 |

LIG_LIR_Apic_2 | 471 | 477 | PF02991 | 0.416 |

LIG_LIR_Nem_3 | 184 | 189 | PF02991 | 0.693 |

LIG_LIR_Nem_3 | 291 | 297 | PF02991 | 0.313 |

LIG_LIR_Nem_3 | 741 | 745 | PF02991 | 0.719 |

LIG_LIR_Nem_3 | 763 | 769 | PF02991 | 0.705 |

LIG_LIR_Nem_3 | 877 | 881 | PF02991 | 0.615 |

LIG_MLH1_MIPbox_1 | 110 | 114 | PF16413 | 0.756 |

LIG_Pex14_1 | 290 | 294 | PF04695 | 0.312 |

LIG_Pex14_2 | 110 | 114 | PF04695 | 0.756 |

LIG_Pex14_2 | 182 | 186 | PF04695 | 0.687 |

LIG_PTAP_UEV_1 | 248 | 253 | PF05743 | 0.651 |

LIG_PTB_Apo_2 | 324 | 331 | PF02174 | 0.416 |

LIG_PTB_Apo_2 | 849 | 856 | PF02174 | 0.508 |

LIG_PTB_Phospho_1 | 324 | 330 | PF10480 | 0.416 |

LIG_PTB_Phospho_1 | 849 | 855 | PF10480 | 0.505 |

LIG_REV1ctd_RIR_1 | 111 | 119 | PF16727 | 0.769 |

LIG_SH2_CRK | 878 | 882 | PF00017 | 0.698 |

LIG_SH2_NCK_1 | 377 | 381 | PF00017 | 0.430 |

LIG_SH2_NCK_1 | 43 | 47 | PF00017 | 0.572 |

LIG_SH2_NCK_1 | 474 | 478 | PF00017 | 0.416 |

LIG_SH2_SRC | 377 | 380 | PF00017 | 0.509 |

LIG_SH2_SRC | 43 | 46 | PF00017 | 0.661 |

LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.710 |

LIG_SH2_STAT5 | 855 | 858 | PF00017 | 0.677 |

LIG_SH3_3 | 217 | 223 | PF00018 | 0.660 |

LIG_SH3_3 | 246 | 252 | PF00018 | 0.653 |

LIG_SH3_3 | 609 | 615 | PF00018 | 0.591 |

LIG_Sin3_3 | 91 | 98 | PF02671 | 0.700 |

LIG_SUMO_SIM_anti_2 | 68 | 73 | PF11976 | 0.462 |

LIG_SUMO_SIM_par_1 | 265 | 270 | PF11976 | 0.539 |

LIG_SUMO_SIM_par_1 | 98 | 103 | PF11976 | 0.637 |

LIG_SUMO_SIM_par_1 | 988 | 995 | PF11976 | 0.704 |

LIG_TRAF2_1 | 770 | 773 | PF00917 | 0.726 |

LIG_TYR_ITIM | 41 | 46 | PF00017 | 0.570 |

LIG_WRC_WIRS_1 | 739 | 744 | PF05994 | 0.808 |

LIG_WW_3 | 275 | 279 | PF00397 | 0.530 |

MOD_CDK_SPK_2 | 904 | 909 | PF00069 | 0.657 |

MOD_CDK_SPxK_1 | 272 | 278 | PF00069 | 0.764 |

MOD_CDK_SPxxK_3 | 272 | 279 | PF00069 | 0.710 |

MOD_CDK_SPxxK_3 | 664 | 671 | PF00069 | 0.686 |

MOD_CK1_1 | 1009 | 1015 | PF00069 | 0.591 |

MOD_CK1_1 | 213 | 219 | PF00069 | 0.819 |

MOD_CK1_1 | 306 | 312 | PF00069 | 0.509 |

MOD_CK1_1 | 486 | 492 | PF00069 | 0.391 |

MOD_CK1_1 | 553 | 559 | PF00069 | 0.465 |

MOD_CK1_1 | 584 | 590 | PF00069 | 0.722 |

MOD_CK1_1 | 622 | 628 | PF00069 | 0.778 |

MOD_CK1_1 | 644 | 650 | PF00069 | 0.795 |

MOD_CK1_1 | 684 | 690 | PF00069 | 0.805 |

MOD_CK1_1 | 729 | 735 | PF00069 | 0.718 |

MOD_CK1_1 | 761 | 767 | PF00069 | 0.761 |

MOD_CK1_1 | 794 | 800 | PF00069 | 0.698 |

MOD_CK1_1 | 803 | 809 | PF00069 | 0.648 |

MOD_CK1_1 | 839 | 845 | PF00069 | 0.706 |

MOD_CK1_1 | 847 | 853 | PF00069 | 0.695 |

MOD_CK1_1 | 892 | 898 | PF00069 | 0.730 |

MOD_CK1_1 | 904 | 910 | PF00069 | 0.652 |

MOD_CK1_1 | 913 | 919 | PF00069 | 0.712 |

MOD_CK1_1 | 926 | 932 | PF00069 | 0.698 |

MOD_CK1_1 | 933 | 939 | PF00069 | 0.655 |

MOD_CK1_1 | 948 | 954 | PF00069 | 0.589 |

MOD_CK1_1 | 989 | 995 | PF00069 | 0.693 |

MOD_CK2_1 | 114 | 120 | PF00069 | 0.752 |

MOD_CK2_1 | 142 | 148 | PF00069 | 0.556 |

MOD_CK2_1 | 164 | 170 | PF00069 | 0.711 |

MOD_CK2_1 | 767 | 773 | PF00069 | 0.720 |

MOD_Cter_Amidation | 297 | 300 | PF01082 | 0.411 |

MOD_Cter_Amidation | 778 | 781 | PF01082 | 0.761 |

MOD_DYRK1A_RPxSP_1 | 279 | 283 | PF00069 | 0.705 |

MOD_GlcNHglycan | 1016 | 1019 | PF01048 | 0.619 |

MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.790 |

MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.714 |

MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.458 |

MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.479 |

MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.468 |

MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.390 |

MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.421 |

MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.509 |

MOD_GlcNHglycan | 575 | 578 | PF01048 | 0.711 |

MOD_GlcNHglycan | 583 | 586 | PF01048 | 0.629 |

MOD_GlcNHglycan | 591 | 594 | PF01048 | 0.665 |

MOD_GlcNHglycan | 756 | 759 | PF01048 | 0.763 |

MOD_GlcNHglycan | 760 | 763 | PF01048 | 0.752 |

MOD_GlcNHglycan | 777 | 780 | PF01048 | 0.671 |

MOD_GlcNHglycan | 804 | 808 | PF01048 | 0.690 |

MOD_GlcNHglycan | 820 | 823 | PF01048 | 0.733 |

MOD_GlcNHglycan | 833 | 836 | PF01048 | 0.614 |

MOD_GlcNHglycan | 841 | 844 | PF01048 | 0.634 |

MOD_GlcNHglycan | 885 | 888 | PF01048 | 0.712 |

MOD_GlcNHglycan | 912 | 915 | PF01048 | 0.656 |

MOD_GlcNHglycan | 971 | 974 | PF01048 | 0.654 |

MOD_GlcNHglycan | 999 | 1002 | PF01048 | 0.601 |

MOD_GSK3_1 | 1005 | 1012 | PF00069 | 0.670 |

MOD_GSK3_1 | 1035 | 1042 | PF00069 | 0.616 |

MOD_GSK3_1 | 158 | 165 | PF00069 | 0.695 |

MOD_GSK3_1 | 17 | 24 | PF00069 | 0.645 |

MOD_GSK3_1 | 247 | 254 | PF00069 | 0.654 |

MOD_GSK3_1 | 279 | 286 | PF00069 | 0.676 |

MOD_GSK3_1 | 3 | 10 | PF00069 | 0.679 |

MOD_GSK3_1 | 431 | 438 | PF00069 | 0.229 |

MOD_GSK3_1 | 535 | 542 | PF00069 | 0.402 |

MOD_GSK3_1 | 549 | 556 | PF00069 | 0.447 |

MOD_GSK3_1 | 614 | 621 | PF00069 | 0.779 |

MOD_GSK3_1 | 684 | 691 | PF00069 | 0.733 |

MOD_GSK3_1 | 695 | 702 | PF00069 | 0.651 |

MOD_GSK3_1 | 726 | 733 | PF00069 | 0.721 |

MOD_GSK3_1 | 754 | 761 | PF00069 | 0.721 |

MOD_GSK3_1 | 782 | 789 | PF00069 | 0.849 |

MOD_GSK3_1 | 794 | 801 | PF00069 | 0.611 |

MOD_GSK3_1 | 805 | 812 | PF00069 | 0.714 |

MOD_GSK3_1 | 814 | 821 | PF00069 | 0.498 |

MOD_GSK3_1 | 879 | 886 | PF00069 | 0.806 |

MOD_GSK3_1 | 897 | 904 | PF00069 | 0.704 |

MOD_GSK3_1 | 913 | 920 | PF00069 | 0.711 |

MOD_GSK3_1 | 926 | 933 | PF00069 | 0.609 |

MOD_GSK3_1 | 965 | 972 | PF00069 | 0.767 |

MOD_GSK3_1 | 985 | 992 | PF00069 | 0.653 |

MOD_N-GLC_1 | 791 | 796 | PF02516 | 0.819 |

MOD_NEK2_1 | 108 | 113 | PF00069 | 0.762 |

MOD_NEK2_1 | 114 | 119 | PF00069 | 0.681 |

MOD_NEK2_1 | 164 | 169 | PF00069 | 0.554 |

MOD_NEK2_1 | 225 | 230 | PF00069 | 0.724 |

MOD_NEK2_1 | 519 | 524 | PF00069 | 0.386 |

MOD_NEK2_1 | 532 | 537 | PF00069 | 0.411 |

MOD_NEK2_1 | 539 | 544 | PF00069 | 0.183 |

MOD_NEK2_1 | 578 | 583 | PF00069 | 0.665 |

MOD_NEK2_1 | 620 | 625 | PF00069 | 0.673 |

MOD_NEK2_1 | 688 | 693 | PF00069 | 0.774 |

MOD_NEK2_1 | 730 | 735 | PF00069 | 0.800 |

MOD_NEK2_1 | 760 | 765 | PF00069 | 0.699 |

MOD_NEK2_1 | 805 | 810 | PF00069 | 0.742 |

MOD_NEK2_1 | 831 | 836 | PF00069 | 0.806 |

MOD_NEK2_1 | 841 | 846 | PF00069 | 0.636 |

MOD_NEK2_1 | 930 | 935 | PF00069 | 0.737 |

MOD_NEK2_1 | 969 | 974 | PF00069 | 0.585 |

MOD_NEK2_1 | 986 | 991 | PF00069 | 0.621 |

MOD_NEK2_2 | 1026 | 1031 | PF00069 | 0.608 |

MOD_NEK2_2 | 290 | 295 | PF00069 | 0.553 |

MOD_NEK2_2 | 561 | 566 | PF00069 | 0.351 |

MOD_NEK2_2 | 945 | 950 | PF00069 | 0.640 |

MOD_OFUCOSY | 481 | 487 | PF10250 | 0.398 |

MOD_PIKK_1 | 108 | 114 | PF00454 | 0.761 |

MOD_PIKK_1 | 22 | 28 | PF00454 | 0.658 |

MOD_PIKK_1 | 855 | 861 | PF00454 | 0.729 |

MOD_PKA_1 | 159 | 165 | PF00069 | 0.653 |

MOD_PKA_1 | 288 | 294 | PF00069 | 0.611 |

MOD_PKA_1 | 704 | 710 | PF00069 | 0.536 |

MOD_PKA_1 | 780 | 786 | PF00069 | 0.776 |

MOD_PKA_1 | 889 | 895 | PF00069 | 0.709 |

MOD_PKA_2 | 108 | 114 | PF00069 | 0.634 |

MOD_PKA_2 | 158 | 164 | PF00069 | 0.656 |

MOD_PKA_2 | 21 | 27 | PF00069 | 0.752 |

MOD_PKA_2 | 226 | 232 | PF00069 | 0.731 |

MOD_PKA_2 | 270 | 276 | PF00069 | 0.774 |

MOD_PKA_2 | 277 | 283 | PF00069 | 0.721 |

MOD_PKA_2 | 288 | 294 | PF00069 | 0.366 |

MOD_PKA_2 | 431 | 437 | PF00069 | 0.350 |

MOD_PKA_2 | 550 | 556 | PF00069 | 0.411 |

MOD_PKA_2 | 644 | 650 | PF00069 | 0.772 |

MOD_PKA_2 | 704 | 710 | PF00069 | 0.723 |

MOD_PKA_2 | 72 | 78 | PF00069 | 0.699 |

MOD_PKA_2 | 780 | 786 | PF00069 | 0.776 |

MOD_PKA_2 | 82 | 88 | PF00069 | 0.594 |

MOD_PKA_2 | 889 | 895 | PF00069 | 0.709 |

MOD_PKA_2 | 908 | 914 | PF00069 | 0.486 |

MOD_PKB_1 | 1014 | 1022 | PF00069 | 0.549 |

MOD_Plk_1 | 1026 | 1032 | PF00069 | 0.749 |

MOD_Plk_1 | 604 | 610 | PF00069 | 0.559 |

MOD_Plk_1 | 791 | 797 | PF00069 | 0.547 |

MOD_Plk_1 | 897 | 903 | PF00069 | 0.816 |

MOD_Plk_1 | 923 | 929 | PF00069 | 0.799 |

MOD_Plk_2-3 | 1035 | 1041 | PF00069 | 0.689 |

MOD_Plk_2-3 | 120 | 126 | PF00069 | 0.805 |

MOD_Plk_2-3 | 917 | 923 | PF00069 | 0.658 |

MOD_Plk_4 | 114 | 120 | PF00069 | 0.672 |

MOD_Plk_4 | 256 | 262 | PF00069 | 0.667 |

MOD_Plk_4 | 290 | 296 | PF00069 | 0.522 |

MOD_Plk_4 | 306 | 312 | PF00069 | 0.401 |

MOD_Plk_4 | 535 | 541 | PF00069 | 0.411 |

MOD_Plk_4 | 761 | 767 | PF00069 | 0.753 |

MOD_Plk_4 | 805 | 811 | PF00069 | 0.714 |

MOD_Plk_4 | 836 | 842 | PF00069 | 0.762 |

MOD_Plk_4 | 935 | 941 | PF00069 | 0.745 |

MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.771 |

MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.728 |

MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.710 |

MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.707 |

MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.661 |

MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.798 |

MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.751 |

MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.727 |

MOD_ProDKin_1 | 525 | 531 | PF00069 | 0.416 |

MOD_ProDKin_1 | 568 | 574 | PF00069 | 0.604 |

MOD_ProDKin_1 | 664 | 670 | PF00069 | 0.713 |

MOD_ProDKin_1 | 691 | 697 | PF00069 | 0.795 |

MOD_ProDKin_1 | 732 | 738 | PF00069 | 0.675 |

MOD_ProDKin_1 | 786 | 792 | PF00069 | 0.838 |

MOD_ProDKin_1 | 794 | 800 | PF00069 | 0.716 |

MOD_ProDKin_1 | 812 | 818 | PF00069 | 0.524 |

MOD_ProDKin_1 | 871 | 877 | PF00069 | 0.839 |

MOD_ProDKin_1 | 904 | 910 | PF00069 | 0.694 |

TRG_DiLeu_BaLyEn_6 | 240 | 245 | PF01217 | 0.533 |

TRG_DiLeu_BaLyEn_6 | 263 | 268 | PF01217 | 0.652 |

TRG_DiLeu_BaLyEn_6 | 515 | 520 | PF01217 | 0.229 |

TRG_ENDOCYTIC_2 | 362 | 365 | PF00928 | 0.411 |

TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.356 |

TRG_ENDOCYTIC_2 | 43 | 46 | PF00928 | 0.563 |

TRG_ENDOCYTIC_2 | 878 | 881 | PF00928 | 0.702 |

TRG_ER_diArg_1 | 1011 | 1014 | PF00400 | 0.763 |

TRG_ER_diArg_1 | 158 | 160 | PF00400 | 0.675 |

TRG_ER_diArg_1 | 277 | 279 | PF00400 | 0.602 |

TRG_ER_diArg_1 | 288 | 290 | PF00400 | 0.581 |

TRG_ER_diArg_1 | 299 | 301 | PF00400 | 0.342 |

TRG_ER_diArg_1 | 431 | 433 | PF00400 | 0.369 |

TRG_ER_diArg_1 | 455 | 458 | PF00400 | 0.463 |

TRG_ER_diArg_1 | 704 | 706 | PF00400 | 0.541 |

TRG_ER_diArg_1 | 780 | 782 | PF00400 | 0.773 |

TRG_ER_diArg_1 | 889 | 891 | PF00400 | 0.719 |

TRG_Pf-PMV_PEXEL_1 | 412 | 416 | PF00026 | 0.509 |

TRG_Pf-PMV_PEXEL_1 | 457 | 461 | PF00026 | 0.463 |

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

A0A0N0P7Y5 | Leptomonas seymouri | 30% | 93% |

A0A3S7X078 | Leishmania donovani | 88% | 100% |

A4HF89 | Leishmania braziliensis | 62% | 81% |

A4I2H1 | Leishmania infantum | 88% | 100% |

E9AYM5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |