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 | 1 |
GO:0005856 | cytoskeleton | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I978
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: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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 6 |
GO:0003824 | catalytic activity | 1 | 6 |
GO:0004672 | protein kinase activity | 3 | 6 |
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 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 102 | 106 | PF00656 | 0.342 |
CLV_C14_Caspase3-7 | 731 | 735 | PF00656 | 0.659 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.381 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 521 | 523 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 533 | 535 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 722 | 724 | PF00675 | 0.666 |
CLV_NRD_NRD_1 | 756 | 758 | PF00675 | 0.704 |
CLV_NRD_NRD_1 | 863 | 865 | PF00675 | 0.583 |
CLV_PCSK_FUR_1 | 313 | 317 | PF00082 | 0.385 |
CLV_PCSK_FUR_1 | 531 | 535 | PF00082 | 0.723 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 521 | 523 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 533 | 535 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 722 | 724 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 756 | 758 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 863 | 865 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 901 | 903 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 953 | 955 | PF00082 | 0.642 |
CLV_PCSK_PC1ET2_1 | 369 | 371 | PF00082 | 0.342 |
CLV_PCSK_PC1ET2_1 | 901 | 903 | PF00082 | 0.572 |
CLV_PCSK_PC1ET2_1 | 953 | 955 | PF00082 | 0.642 |
CLV_PCSK_PC7_1 | 529 | 535 | PF00082 | 0.723 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 922 | 926 | PF00082 | 0.681 |
DEG_SPOP_SBC_1 | 429 | 433 | PF00917 | 0.558 |
DEG_SPOP_SBC_1 | 843 | 847 | PF00917 | 0.588 |
DOC_CKS1_1 | 852 | 857 | PF01111 | 0.603 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 164 | 173 | PF00134 | 0.385 |
DOC_CYCLIN_yCln2_LP_2 | 557 | 563 | PF00134 | 0.667 |
DOC_CYCLIN_yCln2_LP_2 | 912 | 915 | PF00134 | 0.692 |
DOC_MAPK_FxFP_2 | 386 | 389 | PF00069 | 0.518 |
DOC_MAPK_gen_1 | 686 | 694 | PF00069 | 0.557 |
DOC_MAPK_gen_1 | 753 | 763 | PF00069 | 0.705 |
DOC_MAPK_gen_1 | 828 | 836 | PF00069 | 0.669 |
DOC_MAPK_HePTP_8 | 244 | 256 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 192 | 199 | PF00069 | 0.414 |
DOC_MAPK_MEF2A_6 | 247 | 256 | PF00069 | 0.527 |
DOC_PP1_RVXF_1 | 260 | 267 | PF00149 | 0.342 |
DOC_PP2B_LxvP_1 | 299 | 302 | PF13499 | 0.385 |
DOC_PP2B_LxvP_1 | 557 | 560 | PF13499 | 0.654 |
DOC_PP2B_LxvP_1 | 912 | 915 | PF13499 | 0.692 |
DOC_PP4_FxxP_1 | 386 | 389 | PF00568 | 0.518 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 429 | 433 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 470 | 474 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 551 | 555 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 578 | 582 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 585 | 589 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 646 | 650 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 703 | 707 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 741 | 745 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 820 | 824 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 838 | 842 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 844 | 848 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 853 | 857 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 884 | 888 | PF00917 | 0.663 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 547 | 552 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 581 | 586 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 636 | 641 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 642 | 647 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 737 | 742 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 744 | 749 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 802 | 807 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 839 | 844 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 851 | 856 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 941 | 946 | PF00397 | 0.693 |
LIG_14-3-3_CanoR_1 | 147 | 154 | PF00244 | 0.342 |
LIG_14-3-3_CanoR_1 | 155 | 164 | PF00244 | 0.285 |
LIG_14-3-3_CanoR_1 | 508 | 514 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 531 | 541 | PF00244 | 0.717 |
LIG_14-3-3_CanoR_1 | 609 | 616 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 622 | 630 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 709 | 719 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 736 | 741 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 802 | 806 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 863 | 873 | PF00244 | 0.653 |
LIG_14-3-3_CanoR_1 | 886 | 892 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 916 | 926 | PF00244 | 0.686 |
LIG_Actin_WH2_2 | 608 | 624 | PF00022 | 0.615 |
LIG_APCC_ABBA_1 | 794 | 799 | PF00400 | 0.688 |
LIG_BRCT_BRCA1_1 | 231 | 235 | PF00533 | 0.384 |
LIG_BRCT_BRCA1_1 | 90 | 94 | PF00533 | 0.385 |
LIG_deltaCOP1_diTrp_1 | 265 | 269 | PF00928 | 0.385 |
LIG_EVH1_1 | 464 | 468 | PF00568 | 0.591 |
LIG_EVH1_2 | 302 | 306 | PF00568 | 0.385 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.342 |
LIG_FHA_1 | 671 | 677 | PF00498 | 0.648 |
LIG_FHA_1 | 689 | 695 | PF00498 | 0.508 |
LIG_FHA_1 | 852 | 858 | PF00498 | 0.659 |
LIG_FHA_1 | 944 | 950 | PF00498 | 0.678 |
LIG_FHA_2 | 27 | 33 | PF00498 | 0.450 |
LIG_Integrin_isoDGR_2 | 58 | 60 | PF01839 | 0.550 |
LIG_LIR_Apic_2 | 246 | 252 | PF02991 | 0.385 |
LIG_LIR_Apic_2 | 297 | 301 | PF02991 | 0.385 |
LIG_LIR_Apic_2 | 385 | 389 | PF02991 | 0.508 |
LIG_LIR_Apic_2 | 787 | 791 | PF02991 | 0.571 |
LIG_LIR_Apic_2 | 899 | 903 | PF02991 | 0.646 |
LIG_LIR_Gen_1 | 161 | 170 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 352 | 363 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 161 | 165 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 265 | 269 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 352 | 358 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 91 | 97 | PF02991 | 0.385 |
LIG_MYND_1 | 855 | 859 | PF01753 | 0.704 |
LIG_Pex14_2 | 358 | 362 | PF04695 | 0.385 |
LIG_Pex14_2 | 94 | 98 | PF04695 | 0.385 |
LIG_REV1ctd_RIR_1 | 316 | 324 | PF16727 | 0.342 |
LIG_SH2_CRK | 143 | 147 | PF00017 | 0.385 |
LIG_SH2_CRK | 241 | 245 | PF00017 | 0.320 |
LIG_SH2_CRK | 788 | 792 | PF00017 | 0.576 |
LIG_SH2_SRC | 682 | 685 | PF00017 | 0.586 |
LIG_SH2_SRC | 774 | 777 | PF00017 | 0.644 |
LIG_SH2_STAP1 | 260 | 264 | PF00017 | 0.342 |
LIG_SH2_STAP1 | 759 | 763 | PF00017 | 0.658 |
LIG_SH2_STAT3 | 44 | 47 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 861 | 864 | PF00017 | 0.605 |
LIG_SH3_2 | 421 | 426 | PF14604 | 0.662 |
LIG_SH3_2 | 911 | 916 | PF14604 | 0.652 |
LIG_SH3_3 | 278 | 284 | PF00018 | 0.385 |
LIG_SH3_3 | 415 | 421 | PF00018 | 0.636 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.531 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.654 |
LIG_SH3_3 | 462 | 468 | PF00018 | 0.588 |
LIG_SH3_3 | 511 | 517 | PF00018 | 0.700 |
LIG_SH3_3 | 538 | 544 | PF00018 | 0.712 |
LIG_SH3_3 | 770 | 776 | PF00018 | 0.641 |
LIG_SH3_3 | 849 | 855 | PF00018 | 0.654 |
LIG_SH3_3 | 908 | 914 | PF00018 | 0.644 |
LIG_SH3_3 | 935 | 941 | PF00018 | 0.676 |
LIG_SH3_3 | 944 | 950 | PF00018 | 0.641 |
LIG_SUMO_SIM_anti_2 | 182 | 188 | PF11976 | 0.348 |
LIG_SUMO_SIM_anti_2 | 691 | 696 | PF11976 | 0.599 |
LIG_SUMO_SIM_par_1 | 193 | 198 | PF11976 | 0.385 |
LIG_SUMO_SIM_par_1 | 226 | 232 | PF11976 | 0.342 |
LIG_SUMO_SIM_par_1 | 483 | 490 | PF11976 | 0.495 |
LIG_SUMO_SIM_par_1 | 690 | 696 | PF11976 | 0.555 |
LIG_TRAF2_1 | 124 | 127 | PF00917 | 0.385 |
LIG_TYR_ITIM | 160 | 165 | PF00017 | 0.385 |
LIG_TYR_ITIM | 37 | 42 | PF00017 | 0.477 |
LIG_WRC_WIRS_1 | 21 | 26 | PF05994 | 0.443 |
LIG_WRC_WIRS_1 | 355 | 360 | PF05994 | 0.385 |
LIG_WW_3 | 371 | 375 | PF00397 | 0.342 |
LIG_WW_3 | 913 | 917 | PF00397 | 0.692 |
MOD_CDK_SPK_2 | 744 | 749 | PF00069 | 0.669 |
MOD_CDK_SPxxK_3 | 636 | 643 | PF00069 | 0.596 |
MOD_CDK_SPxxK_3 | 851 | 858 | PF00069 | 0.694 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.668 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.615 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.571 |
MOD_CK1_1 | 498 | 504 | PF00069 | 0.601 |
MOD_CK1_1 | 581 | 587 | PF00069 | 0.665 |
MOD_CK1_1 | 651 | 657 | PF00069 | 0.635 |
MOD_CK1_1 | 744 | 750 | PF00069 | 0.703 |
MOD_CK1_1 | 829 | 835 | PF00069 | 0.699 |
MOD_CK1_1 | 842 | 848 | PF00069 | 0.583 |
MOD_CK1_1 | 887 | 893 | PF00069 | 0.605 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.496 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.336 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.342 |
MOD_CK2_1 | 563 | 569 | PF00069 | 0.643 |
MOD_Cter_Amidation | 720 | 723 | PF01082 | 0.644 |
MOD_DYRK1A_RPxSP_1 | 802 | 806 | PF00069 | 0.638 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.415 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.385 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.385 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.671 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.628 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.602 |
MOD_GlcNHglycan | 496 | 500 | PF01048 | 0.528 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.666 |
MOD_GlcNHglycan | 564 | 569 | PF01048 | 0.606 |
MOD_GlcNHglycan | 580 | 583 | PF01048 | 0.535 |
MOD_GlcNHglycan | 587 | 590 | PF01048 | 0.597 |
MOD_GlcNHglycan | 616 | 619 | PF01048 | 0.551 |
MOD_GlcNHglycan | 623 | 626 | PF01048 | 0.542 |
MOD_GlcNHglycan | 666 | 669 | PF01048 | 0.645 |
MOD_GlcNHglycan | 696 | 700 | PF01048 | 0.597 |
MOD_GlcNHglycan | 725 | 728 | PF01048 | 0.687 |
MOD_GlcNHglycan | 846 | 849 | PF01048 | 0.680 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.622 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.385 |
MOD_GlcNHglycan | 955 | 958 | PF01048 | 0.647 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.361 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.484 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.629 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.574 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.603 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.573 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.661 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.665 |
MOD_GSK3_1 | 610 | 617 | PF00069 | 0.618 |
MOD_GSK3_1 | 642 | 649 | PF00069 | 0.702 |
MOD_GSK3_1 | 684 | 691 | PF00069 | 0.665 |
MOD_GSK3_1 | 710 | 717 | PF00069 | 0.639 |
MOD_GSK3_1 | 732 | 739 | PF00069 | 0.652 |
MOD_GSK3_1 | 764 | 771 | PF00069 | 0.634 |
MOD_GSK3_1 | 838 | 845 | PF00069 | 0.651 |
MOD_GSK3_1 | 847 | 854 | PF00069 | 0.590 |
MOD_GSK3_1 | 864 | 871 | PF00069 | 0.539 |
MOD_GSK3_1 | 939 | 946 | PF00069 | 0.674 |
MOD_N-GLC_1 | 389 | 394 | PF02516 | 0.521 |
MOD_N-GLC_1 | 405 | 410 | PF02516 | 0.616 |
MOD_N-GLC_1 | 551 | 556 | PF02516 | 0.701 |
MOD_N-GLC_1 | 646 | 651 | PF02516 | 0.658 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.385 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.371 |
MOD_NEK2_1 | 621 | 626 | PF00069 | 0.654 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.568 |
MOD_NEK2_2 | 327 | 332 | PF00069 | 0.320 |
MOD_NEK2_2 | 409 | 414 | PF00069 | 0.660 |
MOD_PIKK_1 | 714 | 720 | PF00454 | 0.650 |
MOD_PIKK_1 | 829 | 835 | PF00454 | 0.669 |
MOD_PIKK_1 | 865 | 871 | PF00454 | 0.661 |
MOD_PIKK_1 | 884 | 890 | PF00454 | 0.526 |
MOD_PIKK_1 | 917 | 923 | PF00454 | 0.576 |
MOD_PK_1 | 697 | 703 | PF00069 | 0.525 |
MOD_PK_1 | 757 | 763 | PF00069 | 0.657 |
MOD_PKA_1 | 521 | 527 | PF00069 | 0.681 |
MOD_PKA_1 | 533 | 539 | PF00069 | 0.630 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.342 |
MOD_PKA_2 | 327 | 333 | PF00069 | 0.342 |
MOD_PKA_2 | 507 | 513 | PF00069 | 0.659 |
MOD_PKA_2 | 521 | 527 | PF00069 | 0.584 |
MOD_PKA_2 | 532 | 538 | PF00069 | 0.640 |
MOD_PKA_2 | 594 | 600 | PF00069 | 0.660 |
MOD_PKA_2 | 621 | 627 | PF00069 | 0.593 |
MOD_PKA_2 | 801 | 807 | PF00069 | 0.636 |
MOD_PKA_2 | 838 | 844 | PF00069 | 0.651 |
MOD_PKA_2 | 865 | 871 | PF00069 | 0.661 |
MOD_PKA_2 | 915 | 921 | PF00069 | 0.657 |
MOD_PKB_1 | 531 | 539 | PF00069 | 0.718 |
MOD_Plk_1 | 104 | 110 | PF00069 | 0.385 |
MOD_Plk_1 | 396 | 402 | PF00069 | 0.621 |
MOD_Plk_1 | 757 | 763 | PF00069 | 0.657 |
MOD_Plk_1 | 829 | 835 | PF00069 | 0.688 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.385 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.404 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.350 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.393 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.329 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.342 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.385 |
MOD_Plk_4 | 697 | 703 | PF00069 | 0.546 |
MOD_Plk_4 | 868 | 874 | PF00069 | 0.639 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.619 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.560 |
MOD_ProDKin_1 | 547 | 553 | PF00069 | 0.661 |
MOD_ProDKin_1 | 581 | 587 | PF00069 | 0.679 |
MOD_ProDKin_1 | 636 | 642 | PF00069 | 0.624 |
MOD_ProDKin_1 | 737 | 743 | PF00069 | 0.707 |
MOD_ProDKin_1 | 744 | 750 | PF00069 | 0.649 |
MOD_ProDKin_1 | 802 | 808 | PF00069 | 0.664 |
MOD_ProDKin_1 | 839 | 845 | PF00069 | 0.695 |
MOD_ProDKin_1 | 851 | 857 | PF00069 | 0.588 |
MOD_ProDKin_1 | 941 | 947 | PF00069 | 0.693 |
MOD_SUMO_for_1 | 210 | 213 | PF00179 | 0.385 |
MOD_SUMO_for_1 | 425 | 428 | PF00179 | 0.651 |
MOD_SUMO_rev_2 | 136 | 142 | PF00179 | 0.385 |
MOD_SUMO_rev_2 | 203 | 212 | PF00179 | 0.385 |
MOD_SUMO_rev_2 | 232 | 240 | PF00179 | 0.385 |
MOD_SUMO_rev_2 | 392 | 396 | PF00179 | 0.654 |
MOD_SUMO_rev_2 | 639 | 645 | PF00179 | 0.658 |
TRG_DiLeu_BaEn_2 | 350 | 356 | PF01217 | 0.385 |
TRG_DiLeu_BaEn_4 | 393 | 399 | PF01217 | 0.632 |
TRG_DiLeu_BaLyEn_6 | 813 | 818 | PF01217 | 0.627 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.385 |
TRG_ER_diArg_1 | 313 | 316 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 325 | 328 | PF00400 | 0.264 |
TRG_ER_diArg_1 | 531 | 534 | PF00400 | 0.727 |
TRG_ER_diArg_1 | 863 | 866 | PF00400 | 0.657 |
TRG_NES_CRM1_1 | 102 | 117 | PF08389 | 0.342 |
TRG_Pf-PMV_PEXEL_1 | 609 | 614 | PF00026 | 0.614 |
TRG_Pf-PMV_PEXEL_1 | 922 | 927 | PF00026 | 0.651 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X6S4 | Leishmania donovani | 100% | 100% |
A4HLP3 | Leishmania braziliensis | 70% | 100% |
E9B419 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q405 | Leishmania major | 92% | 100% |