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:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 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: E9B591
Term | Name | Level | Count |
---|---|---|---|
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:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016310 | phosphorylation | 5 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
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:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0018105 | peptidyl-serine phosphorylation | 6 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018209 | peptidyl-serine modification | 6 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004672 | protein kinase activity | 3 | 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: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 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 613 | 617 | PF00656 | 0.655 |
CLV_C14_Caspase3-7 | 911 | 915 | PF00656 | 0.599 |
CLV_MEL_PAP_1 | 698 | 704 | PF00089 | 0.738 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.500 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.727 |
CLV_NRD_NRD_1 | 597 | 599 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 671 | 673 | PF00675 | 0.742 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.720 |
CLV_NRD_NRD_1 | 868 | 870 | PF00675 | 0.736 |
CLV_PCSK_FUR_1 | 303 | 307 | PF00082 | 0.589 |
CLV_PCSK_FUR_1 | 480 | 484 | PF00082 | 0.411 |
CLV_PCSK_FUR_1 | 81 | 85 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.727 |
CLV_PCSK_KEX2_1 | 597 | 599 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 671 | 673 | PF00082 | 0.798 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.728 |
CLV_PCSK_KEX2_1 | 868 | 870 | PF00082 | 0.733 |
CLV_PCSK_PC7_1 | 593 | 599 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 251 | 255 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 685 | 689 | PF00082 | 0.679 |
CLV_Separin_Metazoa | 787 | 791 | PF03568 | 0.550 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.722 |
DEG_SCF_FBW7_1 | 461 | 468 | PF00400 | 0.394 |
DEG_SPOP_SBC_1 | 144 | 148 | PF00917 | 0.722 |
DOC_CKS1_1 | 192 | 197 | PF01111 | 0.663 |
DOC_CKS1_1 | 462 | 467 | PF01111 | 0.394 |
DOC_MAPK_gen_1 | 303 | 310 | PF00069 | 0.576 |
DOC_MAPK_gen_1 | 81 | 90 | PF00069 | 0.675 |
DOC_MAPK_MEF2A_6 | 356 | 363 | PF00069 | 0.499 |
DOC_PIKK_1 | 342 | 350 | PF02985 | 0.642 |
DOC_PP1_RVXF_1 | 602 | 609 | PF00149 | 0.549 |
DOC_PP2B_LxvP_1 | 179 | 182 | PF13499 | 0.687 |
DOC_PP2B_LxvP_1 | 666 | 669 | PF13499 | 0.764 |
DOC_PP2B_LxvP_1 | 903 | 906 | PF13499 | 0.551 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.763 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 725 | 729 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 791 | 795 | PF00917 | 0.737 |
DOC_USP7_MATH_1 | 826 | 830 | PF00917 | 0.785 |
DOC_USP7_UBL2_3 | 539 | 543 | PF12436 | 0.411 |
DOC_USP7_UBL2_3 | 922 | 926 | PF12436 | 0.711 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.803 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.394 |
DOC_WW_Pin1_4 | 552 | 557 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 763 | 768 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 834 | 839 | PF00397 | 0.707 |
LIG_14-3-3_CanoR_1 | 116 | 126 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 145 | 149 | PF00244 | 0.759 |
LIG_14-3-3_CanoR_1 | 172 | 182 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 415 | 423 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 502 | 507 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 732 | 738 | PF00244 | 0.830 |
LIG_14-3-3_CanoR_1 | 83 | 89 | PF00244 | 0.735 |
LIG_14-3-3_CanoR_1 | 98 | 102 | PF00244 | 0.745 |
LIG_Actin_WH2_2 | 366 | 381 | PF00022 | 0.411 |
LIG_APCC_ABBAyCdc20_2 | 685 | 691 | PF00400 | 0.549 |
LIG_APCC_ABBAyCdc20_2 | 926 | 932 | PF00400 | 0.510 |
LIG_BIR_III_4 | 620 | 624 | PF00653 | 0.756 |
LIG_BIR_III_4 | 649 | 653 | PF00653 | 0.778 |
LIG_BIR_III_4 | 914 | 918 | PF00653 | 0.566 |
LIG_BRCT_BRCA1_1 | 521 | 525 | PF00533 | 0.411 |
LIG_deltaCOP1_diTrp_1 | 518 | 525 | PF00928 | 0.411 |
LIG_EVH1_1 | 666 | 670 | PF00568 | 0.537 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.625 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.412 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.411 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.387 |
LIG_FHA_1 | 530 | 536 | PF00498 | 0.396 |
LIG_FHA_1 | 728 | 734 | PF00498 | 0.728 |
LIG_FHA_1 | 776 | 782 | PF00498 | 0.786 |
LIG_FHA_1 | 898 | 904 | PF00498 | 0.691 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.469 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.368 |
LIG_FHA_2 | 857 | 863 | PF00498 | 0.733 |
LIG_FHA_2 | 905 | 911 | PF00498 | 0.603 |
LIG_Integrin_RGD_1 | 263 | 265 | PF01839 | 0.563 |
LIG_LIR_Apic_2 | 138 | 142 | PF02991 | 0.517 |
LIG_LIR_Apic_2 | 810 | 816 | PF02991 | 0.696 |
LIG_LIR_Gen_1 | 320 | 330 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 500 | 507 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 518 | 528 | PF02991 | 0.249 |
LIG_LIR_Gen_1 | 581 | 591 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 320 | 325 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 422 | 426 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 500 | 506 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 518 | 524 | PF02991 | 0.249 |
LIG_LIR_Nem_3 | 534 | 540 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 565 | 569 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 581 | 587 | PF02991 | 0.471 |
LIG_MYND_1 | 126 | 130 | PF01753 | 0.757 |
LIG_NRBOX | 519 | 525 | PF00104 | 0.411 |
LIG_Pex14_1 | 521 | 525 | PF04695 | 0.411 |
LIG_Pex14_2 | 318 | 322 | PF04695 | 0.497 |
LIG_RPA_C_Fungi | 301 | 313 | PF08784 | 0.357 |
LIG_SH2_CRK | 426 | 430 | PF00017 | 0.411 |
LIG_SH2_CRK | 503 | 507 | PF00017 | 0.411 |
LIG_SH2_CRK | 584 | 588 | PF00017 | 0.473 |
LIG_SH2_CRK | 813 | 817 | PF00017 | 0.751 |
LIG_SH2_NCK_1 | 503 | 507 | PF00017 | 0.411 |
LIG_SH2_PTP2 | 139 | 142 | PF00017 | 0.519 |
LIG_SH2_STAP1 | 503 | 507 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 584 | 588 | PF00017 | 0.574 |
LIG_SH2_STAT3 | 762 | 765 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.375 |
LIG_SH3_1 | 664 | 670 | PF00018 | 0.543 |
LIG_SH3_1 | 813 | 819 | PF00018 | 0.642 |
LIG_SH3_2 | 667 | 672 | PF14604 | 0.546 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.759 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.702 |
LIG_SH3_3 | 189 | 195 | PF00018 | 0.601 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.543 |
LIG_SH3_3 | 459 | 465 | PF00018 | 0.394 |
LIG_SH3_3 | 599 | 605 | PF00018 | 0.542 |
LIG_SH3_3 | 623 | 629 | PF00018 | 0.699 |
LIG_SH3_3 | 662 | 668 | PF00018 | 0.776 |
LIG_SH3_3 | 813 | 819 | PF00018 | 0.704 |
LIG_SUMO_SIM_anti_2 | 341 | 348 | PF11976 | 0.360 |
LIG_SUMO_SIM_par_1 | 332 | 342 | PF11976 | 0.426 |
LIG_SxIP_EBH_1 | 163 | 176 | PF03271 | 0.661 |
LIG_TRAF2_1 | 18 | 21 | PF00917 | 0.500 |
LIG_TRAF2_1 | 330 | 333 | PF00917 | 0.735 |
LIG_TRAF2_1 | 352 | 355 | PF00917 | 0.593 |
LIG_WW_3 | 489 | 493 | PF00397 | 0.411 |
LIG_WW_3 | 668 | 672 | PF00397 | 0.776 |
MOD_CAAXbox | 933 | 936 | PF01239 | 0.659 |
MOD_CDK_SPxK_1 | 211 | 217 | PF00069 | 0.720 |
MOD_CDK_SPxxK_3 | 145 | 152 | PF00069 | 0.538 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.792 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.647 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.650 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.352 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.512 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.411 |
MOD_CK1_1 | 697 | 703 | PF00069 | 0.776 |
MOD_CK1_1 | 836 | 842 | PF00069 | 0.583 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.737 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.647 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.516 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.371 |
MOD_CK2_1 | 481 | 487 | PF00069 | 0.411 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.598 |
MOD_CK2_1 | 791 | 797 | PF00069 | 0.784 |
MOD_CK2_1 | 801 | 807 | PF00069 | 0.668 |
MOD_CK2_1 | 843 | 849 | PF00069 | 0.723 |
MOD_CK2_1 | 856 | 862 | PF00069 | 0.683 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.766 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.696 |
MOD_GlcNHglycan | 227 | 231 | PF01048 | 0.612 |
MOD_GlcNHglycan | 265 | 270 | PF01048 | 0.810 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.352 |
MOD_GlcNHglycan | 616 | 619 | PF01048 | 0.570 |
MOD_GlcNHglycan | 661 | 664 | PF01048 | 0.816 |
MOD_GlcNHglycan | 703 | 706 | PF01048 | 0.794 |
MOD_GlcNHglycan | 715 | 718 | PF01048 | 0.644 |
MOD_GlcNHglycan | 727 | 730 | PF01048 | 0.711 |
MOD_GlcNHglycan | 740 | 743 | PF01048 | 0.744 |
MOD_GlcNHglycan | 770 | 773 | PF01048 | 0.686 |
MOD_GlcNHglycan | 794 | 797 | PF01048 | 0.782 |
MOD_GlcNHglycan | 809 | 812 | PF01048 | 0.558 |
MOD_GlcNHglycan | 828 | 831 | PF01048 | 0.597 |
MOD_GlcNHglycan | 845 | 848 | PF01048 | 0.717 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.725 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.671 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.777 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.514 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.467 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.411 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.411 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.411 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.411 |
MOD_GSK3_1 | 610 | 617 | PF00069 | 0.592 |
MOD_GSK3_1 | 697 | 704 | PF00069 | 0.795 |
MOD_GSK3_1 | 727 | 734 | PF00069 | 0.830 |
MOD_GSK3_1 | 807 | 814 | PF00069 | 0.759 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.725 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.655 |
MOD_N-GLC_1 | 150 | 155 | PF02516 | 0.812 |
MOD_N-GLC_1 | 157 | 162 | PF02516 | 0.719 |
MOD_N-GLC_1 | 165 | 170 | PF02516 | 0.594 |
MOD_N-GLC_1 | 247 | 252 | PF02516 | 0.747 |
MOD_N-GLC_1 | 342 | 347 | PF02516 | 0.351 |
MOD_N-GLC_1 | 6 | 11 | PF02516 | 0.720 |
MOD_N-GLC_1 | 77 | 82 | PF02516 | 0.773 |
MOD_N-GLC_1 | 807 | 812 | PF02516 | 0.756 |
MOD_N-GLC_1 | 851 | 856 | PF02516 | 0.719 |
MOD_N-GLC_1 | 88 | 93 | PF02516 | 0.642 |
MOD_N-GLC_2 | 877 | 879 | PF02516 | 0.800 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.752 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.584 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.495 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.411 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.411 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.472 |
MOD_NEK2_1 | 614 | 619 | PF00069 | 0.700 |
MOD_NEK2_1 | 738 | 743 | PF00069 | 0.575 |
MOD_NEK2_1 | 843 | 848 | PF00069 | 0.723 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.711 |
MOD_NEK2_2 | 6 | 11 | PF00069 | 0.671 |
MOD_NEK2_2 | 744 | 749 | PF00069 | 0.733 |
MOD_PIKK_1 | 109 | 115 | PF00454 | 0.778 |
MOD_PIKK_1 | 117 | 123 | PF00454 | 0.782 |
MOD_PIKK_1 | 415 | 421 | PF00454 | 0.411 |
MOD_PIKK_1 | 818 | 824 | PF00454 | 0.514 |
MOD_PIKK_1 | 851 | 857 | PF00454 | 0.646 |
MOD_PK_1 | 502 | 508 | PF00069 | 0.411 |
MOD_PK_1 | 550 | 556 | PF00069 | 0.515 |
MOD_PKA_1 | 415 | 421 | PF00069 | 0.411 |
MOD_PKA_1 | 83 | 89 | PF00069 | 0.719 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.757 |
MOD_PKA_2 | 151 | 157 | PF00069 | 0.676 |
MOD_PKA_2 | 415 | 421 | PF00069 | 0.411 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.411 |
MOD_PKA_2 | 497 | 503 | PF00069 | 0.411 |
MOD_PKA_2 | 731 | 737 | PF00069 | 0.832 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.733 |
MOD_PKA_2 | 856 | 862 | PF00069 | 0.685 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.740 |
MOD_PKB_1 | 81 | 89 | PF00069 | 0.670 |
MOD_Plk_1 | 333 | 339 | PF00069 | 0.559 |
MOD_Plk_1 | 342 | 348 | PF00069 | 0.512 |
MOD_Plk_1 | 550 | 556 | PF00069 | 0.515 |
MOD_Plk_1 | 6 | 12 | PF00069 | 0.718 |
MOD_Plk_1 | 610 | 616 | PF00069 | 0.675 |
MOD_Plk_1 | 756 | 762 | PF00069 | 0.729 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.771 |
MOD_Plk_1 | 801 | 807 | PF00069 | 0.766 |
MOD_Plk_1 | 851 | 857 | PF00069 | 0.713 |
MOD_Plk_2-3 | 342 | 348 | PF00069 | 0.356 |
MOD_Plk_2-3 | 904 | 910 | PF00069 | 0.552 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.525 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.356 |
MOD_Plk_4 | 586 | 592 | PF00069 | 0.479 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.741 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.804 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.772 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.679 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.675 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.394 |
MOD_ProDKin_1 | 552 | 558 | PF00069 | 0.491 |
MOD_ProDKin_1 | 763 | 769 | PF00069 | 0.627 |
MOD_ProDKin_1 | 834 | 840 | PF00069 | 0.711 |
MOD_SUMO_for_1 | 361 | 364 | PF00179 | 0.475 |
MOD_SUMO_rev_2 | 364 | 370 | PF00179 | 0.411 |
MOD_SUMO_rev_2 | 656 | 662 | PF00179 | 0.562 |
MOD_SUMO_rev_2 | 914 | 924 | PF00179 | 0.812 |
TRG_DiLeu_BaEn_1 | 342 | 347 | PF01217 | 0.640 |
TRG_DiLeu_BaEn_2 | 564 | 570 | PF01217 | 0.478 |
TRG_DiLeu_BaEn_4 | 20 | 26 | PF01217 | 0.492 |
TRG_DiLeu_BaEn_4 | 332 | 338 | PF01217 | 0.701 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 503 | 506 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 584 | 587 | PF00928 | 0.474 |
TRG_ER_diArg_1 | 302 | 305 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 414 | 417 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 479 | 481 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 59 | 61 | PF00400 | 0.710 |
TRG_ER_diArg_1 | 670 | 672 | PF00400 | 0.787 |
TRG_ER_diArg_1 | 81 | 84 | PF00400 | 0.676 |
TRG_NES_CRM1_1 | 518 | 529 | PF08389 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 560 | 565 | PF00026 | 0.497 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IK71 | Leptomonas seymouri | 50% | 100% |
A0A3Q8IFR1 | Leishmania donovani | 87% | 99% |
A4HB21 | Leishmania braziliensis | 62% | 97% |
A4IA78 | Leishmania infantum | 87% | 99% |
Q4Q2P2 | Leishmania major | 86% | 100% |