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:0000922 | spindle pole | 2 | 1 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005813 | centrosome | 3 | 1 |
GO:0005815 | microtubule organizing center | 2 | 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: A4HCF9
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: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 |
GO:0000278 | mitotic cell cycle | 3 | 1 |
GO:0007049 | cell cycle | 2 | 1 |
GO:0010564 | regulation of cell cycle process | 5 | 1 |
GO:0032465 | regulation of cytokinesis | 5 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051302 | regulation of cell division | 4 | 1 |
GO:0051726 | regulation of cell cycle | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 6 |
GO:0003824 | catalytic activity | 1 | 6 |
GO:0004672 | protein kinase activity | 3 | 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 | 245 | 249 | PF00656 | 0.506 |
CLV_C14_Caspase3-7 | 261 | 265 | PF00656 | 0.393 |
CLV_C14_Caspase3-7 | 517 | 521 | PF00656 | 0.644 |
CLV_C14_Caspase3-7 | 533 | 537 | PF00656 | 0.516 |
CLV_C14_Caspase3-7 | 805 | 809 | PF00656 | 0.662 |
CLV_C14_Caspase3-7 | 904 | 908 | PF00656 | 0.534 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 533 | 535 | PF00675 | 0.619 |
CLV_NRD_NRD_1 | 539 | 541 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 698 | 700 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 711 | 713 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 735 | 737 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 851 | 853 | PF00675 | 0.663 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 539 | 541 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 698 | 700 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 734 | 736 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 851 | 853 | PF00082 | 0.663 |
CLV_PCSK_PC1ET2_1 | 191 | 193 | PF00082 | 0.536 |
CLV_PCSK_PC1ET2_1 | 52 | 54 | PF00082 | 0.453 |
CLV_PCSK_PC7_1 | 48 | 54 | PF00082 | 0.439 |
CLV_PCSK_PC7_1 | 847 | 853 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 493 | 497 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 943 | 947 | PF00082 | 0.487 |
CLV_Separin_Metazoa | 344 | 348 | PF03568 | 0.385 |
CLV_Separin_Metazoa | 695 | 699 | PF03568 | 0.503 |
DEG_APCC_DBOX_1 | 393 | 401 | PF00400 | 0.385 |
DEG_SPOP_SBC_1 | 202 | 206 | PF00917 | 0.545 |
DOC_CKS1_1 | 673 | 678 | PF01111 | 0.525 |
DOC_CYCLIN_RxL_1 | 275 | 282 | PF00134 | 0.243 |
DOC_CYCLIN_yCln2_LP_2 | 840 | 846 | PF00134 | 0.681 |
DOC_MAPK_DCC_7 | 394 | 402 | PF00069 | 0.385 |
DOC_MAPK_gen_1 | 896 | 905 | PF00069 | 0.635 |
DOC_MAPK_MEF2A_6 | 394 | 402 | PF00069 | 0.385 |
DOC_MAPK_MEF2A_6 | 837 | 846 | PF00069 | 0.654 |
DOC_MAPK_NFAT4_5 | 837 | 845 | PF00069 | 0.540 |
DOC_PP2B_LxvP_1 | 840 | 843 | PF13499 | 0.683 |
DOC_PP2B_LxvP_1 | 880 | 883 | PF13499 | 0.531 |
DOC_PP4_FxxP_1 | 173 | 176 | PF00568 | 0.507 |
DOC_PP4_FxxP_1 | 324 | 327 | PF00568 | 0.243 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 495 | 499 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 574 | 578 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 724 | 728 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 738 | 742 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 836 | 840 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 853 | 857 | PF00917 | 0.503 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 518 | 523 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 545 | 550 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 580 | 585 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 664 | 669 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 672 | 677 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 687 | 692 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 890 | 895 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 929 | 934 | PF00397 | 0.493 |
LIG_14-3-3_CanoR_1 | 121 | 127 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 132 | 139 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 192 | 197 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 338 | 342 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 37 | 46 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 466 | 471 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 493 | 501 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 555 | 563 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 70 | 76 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 887 | 891 | PF00244 | 0.541 |
LIG_BRCT_BRCA1_1 | 320 | 324 | PF00533 | 0.385 |
LIG_BRCT_BRCA1_1 | 680 | 684 | PF00533 | 0.546 |
LIG_CaM_IQ_9 | 616 | 632 | PF13499 | 0.443 |
LIG_deltaCOP1_diTrp_1 | 57 | 62 | PF00928 | 0.470 |
LIG_eIF4E_1 | 95 | 101 | PF01652 | 0.435 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.576 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.554 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.422 |
LIG_FHA_1 | 494 | 500 | PF00498 | 0.521 |
LIG_FHA_1 | 634 | 640 | PF00498 | 0.672 |
LIG_FHA_1 | 672 | 678 | PF00498 | 0.537 |
LIG_FHA_1 | 817 | 823 | PF00498 | 0.698 |
LIG_FHA_1 | 877 | 883 | PF00498 | 0.530 |
LIG_FHA_1 | 930 | 936 | PF00498 | 0.540 |
LIG_FHA_1 | 940 | 946 | PF00498 | 0.509 |
LIG_FHA_2 | 136 | 142 | PF00498 | 0.674 |
LIG_FHA_2 | 432 | 438 | PF00498 | 0.533 |
LIG_FHA_2 | 512 | 518 | PF00498 | 0.680 |
LIG_FHA_2 | 825 | 831 | PF00498 | 0.638 |
LIG_FHA_2 | 902 | 908 | PF00498 | 0.538 |
LIG_GBD_Chelix_1 | 400 | 408 | PF00786 | 0.385 |
LIG_IRF3_LxIS_1 | 310 | 317 | PF10401 | 0.243 |
LIG_LIR_Apic_2 | 172 | 176 | PF02991 | 0.505 |
LIG_LIR_Apic_2 | 321 | 327 | PF02991 | 0.272 |
LIG_LIR_Gen_1 | 498 | 507 | PF02991 | 0.667 |
LIG_LIR_Gen_1 | 768 | 775 | PF02991 | 0.553 |
LIG_LIR_Gen_1 | 92 | 101 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 938 | 947 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 349 | 354 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 498 | 504 | PF02991 | 0.667 |
LIG_MYND_1 | 602 | 606 | PF01753 | 0.640 |
LIG_PCNA_yPIPBox_3 | 12 | 24 | PF02747 | 0.478 |
LIG_PDZ_Class_2 | 942 | 947 | PF00595 | 0.487 |
LIG_SH2_CRK | 156 | 160 | PF00017 | 0.529 |
LIG_SH2_CRK | 623 | 627 | PF00017 | 0.444 |
LIG_SH2_SRC | 934 | 937 | PF00017 | 0.600 |
LIG_SH2_STAP1 | 50 | 54 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 934 | 937 | PF00017 | 0.600 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.308 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.385 |
LIG_SH3_3 | 516 | 522 | PF00018 | 0.598 |
LIG_SH3_3 | 543 | 549 | PF00018 | 0.670 |
LIG_SH3_3 | 670 | 676 | PF00018 | 0.579 |
LIG_SH3_3 | 715 | 721 | PF00018 | 0.538 |
LIG_SH3_3 | 859 | 865 | PF00018 | 0.652 |
LIG_SUMO_SIM_par_1 | 669 | 675 | PF11976 | 0.658 |
LIG_TRAF2_1 | 412 | 415 | PF00917 | 0.385 |
LIG_TRAF2_1 | 651 | 654 | PF00917 | 0.508 |
LIG_UBA3_1 | 100 | 108 | PF00899 | 0.450 |
LIG_WRC_WIRS_1 | 170 | 175 | PF05994 | 0.506 |
LIG_WRC_WIRS_1 | 504 | 509 | PF05994 | 0.671 |
MOD_CDC14_SPxK_1 | 893 | 896 | PF00782 | 0.530 |
MOD_CDK_SPK_2 | 186 | 191 | PF00069 | 0.525 |
MOD_CDK_SPK_2 | 687 | 692 | PF00069 | 0.661 |
MOD_CDK_SPxK_1 | 186 | 192 | PF00069 | 0.526 |
MOD_CDK_SPxK_1 | 890 | 896 | PF00069 | 0.538 |
MOD_CDK_SPxxK_3 | 409 | 416 | PF00069 | 0.385 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.553 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.615 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.785 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.525 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.395 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.564 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.752 |
MOD_CK1_1 | 564 | 570 | PF00069 | 0.581 |
MOD_CK1_1 | 578 | 584 | PF00069 | 0.519 |
MOD_CK1_1 | 727 | 733 | PF00069 | 0.690 |
MOD_CK1_1 | 788 | 794 | PF00069 | 0.672 |
MOD_CK1_1 | 802 | 808 | PF00069 | 0.535 |
MOD_CK1_1 | 825 | 831 | PF00069 | 0.690 |
MOD_CK1_1 | 871 | 877 | PF00069 | 0.680 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.385 |
MOD_CK2_1 | 431 | 437 | PF00069 | 0.537 |
MOD_CK2_1 | 824 | 830 | PF00069 | 0.634 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.574 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.599 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.729 |
MOD_GlcNHglycan | 220 | 224 | PF01048 | 0.645 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.464 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.364 |
MOD_GlcNHglycan | 508 | 511 | PF01048 | 0.673 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.623 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.633 |
MOD_GlcNHglycan | 653 | 658 | PF01048 | 0.538 |
MOD_GlcNHglycan | 680 | 683 | PF01048 | 0.658 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.494 |
MOD_GlcNHglycan | 731 | 734 | PF01048 | 0.653 |
MOD_GlcNHglycan | 740 | 743 | PF01048 | 0.582 |
MOD_GlcNHglycan | 824 | 827 | PF01048 | 0.544 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.642 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.447 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.447 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.531 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.583 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.592 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.790 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.517 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.527 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.698 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.608 |
MOD_GSK3_1 | 574 | 581 | PF00069 | 0.568 |
MOD_GSK3_1 | 584 | 591 | PF00069 | 0.604 |
MOD_GSK3_1 | 640 | 647 | PF00069 | 0.452 |
MOD_GSK3_1 | 671 | 678 | PF00069 | 0.666 |
MOD_GSK3_1 | 738 | 745 | PF00069 | 0.597 |
MOD_GSK3_1 | 759 | 766 | PF00069 | 0.664 |
MOD_GSK3_1 | 781 | 788 | PF00069 | 0.544 |
MOD_GSK3_1 | 868 | 875 | PF00069 | 0.565 |
MOD_GSK3_1 | 882 | 889 | PF00069 | 0.550 |
MOD_N-GLC_1 | 104 | 109 | PF02516 | 0.332 |
MOD_N-GLC_1 | 831 | 836 | PF02516 | 0.552 |
MOD_N-GLC_1 | 872 | 877 | PF02516 | 0.659 |
MOD_N-GLC_1 | 939 | 944 | PF02516 | 0.454 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.383 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.395 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.614 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.484 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.495 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.199 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.361 |
MOD_NEK2_1 | 538 | 543 | PF00069 | 0.584 |
MOD_NEK2_1 | 562 | 567 | PF00069 | 0.579 |
MOD_NEK2_1 | 579 | 584 | PF00069 | 0.600 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.333 |
MOD_NEK2_1 | 886 | 891 | PF00069 | 0.685 |
MOD_NEK2_2 | 378 | 383 | PF00069 | 0.385 |
MOD_NEK2_2 | 495 | 500 | PF00069 | 0.520 |
MOD_NEK2_2 | 542 | 547 | PF00069 | 0.551 |
MOD_NEK2_2 | 836 | 841 | PF00069 | 0.686 |
MOD_PIKK_1 | 124 | 130 | PF00454 | 0.373 |
MOD_PIKK_1 | 640 | 646 | PF00454 | 0.592 |
MOD_PIKK_1 | 724 | 730 | PF00454 | 0.706 |
MOD_PK_1 | 466 | 472 | PF00069 | 0.545 |
MOD_PKA_1 | 191 | 197 | PF00069 | 0.540 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.430 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.602 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.492 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.199 |
MOD_PKA_2 | 390 | 396 | PF00069 | 0.385 |
MOD_PKA_2 | 538 | 544 | PF00069 | 0.693 |
MOD_PKA_2 | 816 | 822 | PF00069 | 0.554 |
MOD_PKA_2 | 836 | 842 | PF00069 | 0.507 |
MOD_PKA_2 | 886 | 892 | PF00069 | 0.559 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.542 |
MOD_Plk_1 | 799 | 805 | PF00069 | 0.670 |
MOD_Plk_1 | 872 | 878 | PF00069 | 0.653 |
MOD_Plk_2-3 | 901 | 907 | PF00069 | 0.541 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.579 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.508 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.414 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.470 |
MOD_Plk_4 | 466 | 472 | PF00069 | 0.665 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.746 |
MOD_Plk_4 | 575 | 581 | PF00069 | 0.553 |
MOD_Plk_4 | 706 | 712 | PF00069 | 0.516 |
MOD_Plk_4 | 799 | 805 | PF00069 | 0.670 |
MOD_Plk_4 | 872 | 878 | PF00069 | 0.569 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.531 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.555 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.385 |
MOD_ProDKin_1 | 518 | 524 | PF00069 | 0.579 |
MOD_ProDKin_1 | 545 | 551 | PF00069 | 0.567 |
MOD_ProDKin_1 | 580 | 586 | PF00069 | 0.673 |
MOD_ProDKin_1 | 664 | 670 | PF00069 | 0.554 |
MOD_ProDKin_1 | 672 | 678 | PF00069 | 0.549 |
MOD_ProDKin_1 | 687 | 693 | PF00069 | 0.627 |
MOD_ProDKin_1 | 890 | 896 | PF00069 | 0.538 |
MOD_ProDKin_1 | 929 | 935 | PF00069 | 0.490 |
MOD_SUMO_for_1 | 651 | 654 | PF00179 | 0.595 |
TRG_DiLeu_BaEn_1 | 635 | 640 | PF01217 | 0.595 |
TRG_DiLeu_BaLyEn_6 | 404 | 409 | PF01217 | 0.385 |
TRG_ENDOCYTIC_2 | 366 | 369 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 623 | 626 | PF00928 | 0.584 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.415 |
TRG_ER_diArg_1 | 120 | 122 | PF00400 | 0.351 |
TRG_ER_diArg_1 | 32 | 35 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 371 | 374 | PF00400 | 0.366 |
TRG_ER_diArg_1 | 538 | 540 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 626 | 629 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 697 | 699 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 734 | 736 | PF00400 | 0.681 |
TRG_ER_diArg_1 | 851 | 853 | PF00400 | 0.641 |
TRG_ER_diArg_1 | 896 | 899 | PF00400 | 0.637 |
TRG_Pf-PMV_PEXEL_1 | 278 | 282 | PF00026 | 0.385 |
TRG_Pf-PMV_PEXEL_1 | 53 | 57 | PF00026 | 0.495 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IBH5 | Leishmania donovani | 62% | 100% |
A4HZY8 | Leishmania infantum | 62% | 96% |
E9AVU9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 59% | 100% |
Q4QBN0 | Leishmania major | 61% | 98% |