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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9APV3
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 11 |
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016310 | phosphorylation | 5 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0036211 | protein modification process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
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 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004672 | protein kinase activity | 3 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016301 | kinase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 11 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
GO:0004713 | protein tyrosine kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 276 | 280 | PF00656 | 0.775 |
CLV_C14_Caspase3-7 | 43 | 47 | PF00656 | 0.788 |
CLV_C14_Caspase3-7 | 517 | 521 | PF00656 | 0.755 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.813 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.769 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 568 | 570 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 659 | 661 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 777 | 779 | PF00675 | 0.355 |
CLV_PCSK_FUR_1 | 421 | 425 | PF00082 | 0.660 |
CLV_PCSK_FUR_1 | 657 | 661 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.817 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.769 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.729 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 568 | 570 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 659 | 661 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 777 | 779 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 890 | 892 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.651 |
CLV_PCSK_PC1ET2_1 | 362 | 364 | PF00082 | 0.719 |
CLV_PCSK_PC1ET2_1 | 423 | 425 | PF00082 | 0.668 |
CLV_PCSK_PC1ET2_1 | 568 | 570 | PF00082 | 0.518 |
CLV_PCSK_PC1ET2_1 | 890 | 892 | PF00082 | 0.355 |
CLV_PCSK_PC7_1 | 564 | 570 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 45 | 49 | PF00082 | 0.671 |
CLV_PCSK_SKI1_1 | 569 | 573 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 586 | 590 | PF00082 | 0.209 |
CLV_PCSK_SKI1_1 | 597 | 601 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 659 | 663 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 777 | 781 | PF00082 | 0.335 |
CLV_Separin_Metazoa | 631 | 635 | PF03568 | 0.447 |
DEG_COP1_1 | 756 | 763 | PF00400 | 0.335 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.551 |
DEG_SCF_FBW7_1 | 824 | 830 | PF00400 | 0.447 |
DEG_SPOP_SBC_1 | 852 | 856 | PF00917 | 0.457 |
DOC_CDC14_PxL_1 | 652 | 660 | PF14671 | 0.355 |
DOC_CKS1_1 | 824 | 829 | PF01111 | 0.335 |
DOC_MAPK_gen_1 | 719 | 728 | PF00069 | 0.335 |
DOC_MAPK_HePTP_8 | 716 | 728 | PF00069 | 0.335 |
DOC_MAPK_MEF2A_6 | 719 | 728 | PF00069 | 0.335 |
DOC_PP1_RVXF_1 | 397 | 404 | PF00149 | 0.594 |
DOC_PP1_RVXF_1 | 696 | 703 | PF00149 | 0.335 |
DOC_PP2B_LxvP_1 | 849 | 852 | PF13499 | 0.188 |
DOC_PP4_FxxP_1 | 317 | 320 | PF00568 | 0.620 |
DOC_PP4_FxxP_1 | 653 | 656 | PF00568 | 0.355 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.791 |
DOC_USP7_MATH_1 | 514 | 518 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 560 | 564 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 844 | 848 | PF00917 | 0.393 |
DOC_USP7_UBL2_3 | 116 | 120 | PF12436 | 0.724 |
DOC_USP7_UBL2_3 | 562 | 566 | PF12436 | 0.584 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.798 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 770 | 775 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 823 | 828 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.757 |
LIG_14-3-3_CanoR_1 | 104 | 112 | PF00244 | 0.816 |
LIG_14-3-3_CanoR_1 | 136 | 144 | PF00244 | 0.717 |
LIG_14-3-3_CanoR_1 | 18 | 22 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 199 | 207 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 424 | 430 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 597 | 602 | PF00244 | 0.355 |
LIG_14-3-3_CanoR_1 | 784 | 793 | PF00244 | 0.335 |
LIG_14-3-3_CanoR_1 | 843 | 852 | PF00244 | 0.295 |
LIG_14-3-3_CanoR_1 | 853 | 858 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 891 | 898 | PF00244 | 0.447 |
LIG_AP2alpha_2 | 439 | 441 | PF02296 | 0.648 |
LIG_BRCT_BRCA1_1 | 703 | 707 | PF00533 | 0.335 |
LIG_EH1_1 | 462 | 470 | PF00400 | 0.410 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.627 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.823 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.609 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.739 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.693 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.621 |
LIG_FHA_1 | 58 | 64 | PF00498 | 0.752 |
LIG_FHA_1 | 628 | 634 | PF00498 | 0.333 |
LIG_FHA_1 | 660 | 666 | PF00498 | 0.381 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.720 |
LIG_FHA_1 | 748 | 754 | PF00498 | 0.335 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.630 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.724 |
LIG_FHA_2 | 359 | 365 | PF00498 | 0.597 |
LIG_FHA_2 | 38 | 44 | PF00498 | 0.795 |
LIG_FHA_2 | 441 | 447 | PF00498 | 0.524 |
LIG_FHA_2 | 546 | 552 | PF00498 | 0.488 |
LIG_FHA_2 | 634 | 640 | PF00498 | 0.447 |
LIG_FHA_2 | 757 | 763 | PF00498 | 0.335 |
LIG_FHA_2 | 876 | 882 | PF00498 | 0.261 |
LIG_FHA_2 | 891 | 897 | PF00498 | 0.451 |
LIG_LIR_Apic_2 | 650 | 656 | PF02991 | 0.355 |
LIG_LIR_Apic_2 | 718 | 724 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 20 | 28 | PF02991 | 0.608 |
LIG_LIR_Gen_1 | 367 | 378 | PF02991 | 0.720 |
LIG_LIR_Gen_1 | 388 | 397 | PF02991 | 0.581 |
LIG_LIR_Gen_1 | 400 | 408 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 856 | 867 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 873 | 884 | PF02991 | 0.239 |
LIG_LIR_Nem_3 | 20 | 24 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 219 | 224 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 367 | 373 | PF02991 | 0.624 |
LIG_LIR_Nem_3 | 388 | 394 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 400 | 406 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 448 | 454 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 639 | 643 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 650 | 655 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 819 | 825 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 856 | 862 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 873 | 879 | PF02991 | 0.271 |
LIG_MAD2 | 766 | 774 | PF02301 | 0.335 |
LIG_NRBOX | 597 | 603 | PF00104 | 0.447 |
LIG_PDZ_Class_2 | 903 | 908 | PF00595 | 0.617 |
LIG_Pex14_2 | 441 | 445 | PF04695 | 0.638 |
LIG_SH2_CRK | 221 | 225 | PF00017 | 0.627 |
LIG_SH2_CRK | 574 | 578 | PF00017 | 0.447 |
LIG_SH2_CRK | 825 | 829 | PF00017 | 0.335 |
LIG_SH2_CRK | 859 | 863 | PF00017 | 0.335 |
LIG_SH2_GRB2like | 789 | 792 | PF00017 | 0.447 |
LIG_SH2_NCK_1 | 370 | 374 | PF00017 | 0.714 |
LIG_SH2_NCK_1 | 463 | 467 | PF00017 | 0.511 |
LIG_SH2_NCK_1 | 54 | 58 | PF00017 | 0.700 |
LIG_SH2_NCK_1 | 825 | 829 | PF00017 | 0.331 |
LIG_SH2_SRC | 370 | 373 | PF00017 | 0.685 |
LIG_SH2_SRC | 463 | 466 | PF00017 | 0.391 |
LIG_SH2_SRC | 638 | 641 | PF00017 | 0.335 |
LIG_SH2_SRC | 671 | 674 | PF00017 | 0.335 |
LIG_SH2_SRC | 797 | 800 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 21 | 25 | PF00017 | 0.633 |
LIG_SH2_STAP1 | 391 | 395 | PF00017 | 0.661 |
LIG_SH2_STAP1 | 499 | 503 | PF00017 | 0.770 |
LIG_SH2_STAP1 | 692 | 696 | PF00017 | 0.447 |
LIG_SH2_STAT3 | 481 | 484 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 652 | 655 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 671 | 674 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 715 | 718 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 769 | 772 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 789 | 792 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 822 | 825 | PF00017 | 0.339 |
LIG_SH3_1 | 278 | 284 | PF00018 | 0.792 |
LIG_SH3_1 | 449 | 455 | PF00018 | 0.606 |
LIG_SH3_3 | 278 | 284 | PF00018 | 0.792 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.595 |
LIG_SH3_3 | 384 | 390 | PF00018 | 0.580 |
LIG_SH3_3 | 449 | 455 | PF00018 | 0.606 |
LIG_SH3_4 | 566 | 573 | PF00018 | 0.438 |
LIG_SUMO_SIM_anti_2 | 624 | 631 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 392 | 398 | PF11976 | 0.546 |
LIG_TRAF2_1 | 408 | 411 | PF00917 | 0.555 |
LIG_TYR_ITIM | 572 | 577 | PF00017 | 0.476 |
LIG_TYR_ITSM | 217 | 224 | PF00017 | 0.728 |
LIG_UBA3_1 | 465 | 471 | PF00899 | 0.442 |
LIG_UBA3_1 | 598 | 606 | PF00899 | 0.324 |
LIG_WRC_WIRS_1 | 429 | 434 | PF05994 | 0.523 |
LIG_WRC_WIRS_1 | 876 | 881 | PF05994 | 0.190 |
LIG_WW_3 | 850 | 854 | PF00397 | 0.480 |
MOD_CDK_SPxxK_3 | 770 | 777 | PF00069 | 0.447 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.773 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.664 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.714 |
MOD_CK1_1 | 839 | 845 | PF00069 | 0.405 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.757 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.669 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.712 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.783 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.622 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.519 |
MOD_CK2_1 | 545 | 551 | PF00069 | 0.522 |
MOD_CK2_1 | 589 | 595 | PF00069 | 0.335 |
MOD_CK2_1 | 756 | 762 | PF00069 | 0.321 |
MOD_CK2_1 | 875 | 881 | PF00069 | 0.246 |
MOD_CK2_1 | 890 | 896 | PF00069 | 0.431 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.605 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.578 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.741 |
MOD_GlcNHglycan | 372 | 376 | PF01048 | 0.669 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.670 |
MOD_GlcNHglycan | 846 | 849 | PF01048 | 0.188 |
MOD_GlcNHglycan | 893 | 896 | PF01048 | 0.480 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.507 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.675 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.701 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.561 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.744 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.784 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.734 |
MOD_GSK3_1 | 667 | 674 | PF00069 | 0.447 |
MOD_GSK3_1 | 702 | 709 | PF00069 | 0.335 |
MOD_GSK3_1 | 711 | 718 | PF00069 | 0.335 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.702 |
MOD_GSK3_1 | 823 | 830 | PF00069 | 0.442 |
MOD_GSK3_1 | 835 | 842 | PF00069 | 0.447 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.644 |
MOD_GSK3_1 | 853 | 860 | PF00069 | 0.426 |
MOD_LATS_1 | 888 | 894 | PF00433 | 0.447 |
MOD_N-GLC_1 | 268 | 273 | PF02516 | 0.776 |
MOD_N-GLC_1 | 37 | 42 | PF02516 | 0.755 |
MOD_N-GLC_1 | 582 | 587 | PF02516 | 0.335 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.662 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.655 |
MOD_NEK2_1 | 633 | 638 | PF00069 | 0.410 |
MOD_NEK2_1 | 651 | 656 | PF00069 | 0.150 |
MOD_NEK2_1 | 688 | 693 | PF00069 | 0.335 |
MOD_NEK2_1 | 702 | 707 | PF00069 | 0.335 |
MOD_PIKK_1 | 104 | 110 | PF00454 | 0.790 |
MOD_PIKK_1 | 142 | 148 | PF00454 | 0.716 |
MOD_PIKK_1 | 190 | 196 | PF00454 | 0.801 |
MOD_PIKK_1 | 223 | 229 | PF00454 | 0.630 |
MOD_PK_1 | 11 | 17 | PF00069 | 0.683 |
MOD_PKA_1 | 659 | 665 | PF00069 | 0.434 |
MOD_PKA_1 | 890 | 896 | PF00069 | 0.447 |
MOD_PKA_1 | 9 | 15 | PF00069 | 0.637 |
MOD_PKA_2 | 135 | 141 | PF00069 | 0.674 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.614 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.679 |
MOD_PKA_2 | 633 | 639 | PF00069 | 0.447 |
MOD_PKA_2 | 659 | 665 | PF00069 | 0.434 |
MOD_PKA_2 | 783 | 789 | PF00069 | 0.335 |
MOD_PKA_2 | 852 | 858 | PF00069 | 0.279 |
MOD_PKA_2 | 890 | 896 | PF00069 | 0.447 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.637 |
MOD_PKB_1 | 657 | 665 | PF00069 | 0.447 |
MOD_PKB_1 | 9 | 17 | PF00069 | 0.687 |
MOD_Plk_1 | 138 | 144 | PF00069 | 0.556 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.739 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.680 |
MOD_Plk_1 | 589 | 595 | PF00069 | 0.335 |
MOD_Plk_2-3 | 165 | 171 | PF00069 | 0.773 |
MOD_Plk_2-3 | 491 | 497 | PF00069 | 0.711 |
MOD_Plk_2-3 | 875 | 881 | PF00069 | 0.289 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.453 |
MOD_Plk_4 | 597 | 603 | PF00069 | 0.334 |
MOD_Plk_4 | 633 | 639 | PF00069 | 0.398 |
MOD_Plk_4 | 667 | 673 | PF00069 | 0.447 |
MOD_Plk_4 | 711 | 717 | PF00069 | 0.335 |
MOD_Plk_4 | 857 | 863 | PF00069 | 0.360 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.798 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.580 |
MOD_ProDKin_1 | 770 | 776 | PF00069 | 0.447 |
MOD_ProDKin_1 | 823 | 829 | PF00069 | 0.335 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.756 |
MOD_SUMO_for_1 | 682 | 685 | PF00179 | 0.335 |
MOD_SUMO_rev_2 | 271 | 280 | PF00179 | 0.782 |
MOD_SUMO_rev_2 | 41 | 47 | PF00179 | 0.770 |
MOD_SUMO_rev_2 | 446 | 451 | PF00179 | 0.495 |
MOD_SUMO_rev_2 | 646 | 651 | PF00179 | 0.402 |
TRG_DiLeu_BaEn_1 | 624 | 629 | PF01217 | 0.335 |
TRG_DiLeu_BaEn_2 | 684 | 690 | PF01217 | 0.335 |
TRG_DiLeu_BaEn_3 | 874 | 880 | PF01217 | 0.402 |
TRG_DiLeu_BaEn_4 | 819 | 825 | PF01217 | 0.447 |
TRG_DiLeu_BaLyEn_6 | 594 | 599 | PF01217 | 0.335 |
TRG_DiLeu_BaLyEn_6 | 612 | 617 | PF01217 | 0.335 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.593 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.623 |
TRG_ENDOCYTIC_2 | 238 | 241 | PF00928 | 0.596 |
TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.708 |
TRG_ENDOCYTIC_2 | 391 | 394 | PF00928 | 0.669 |
TRG_ENDOCYTIC_2 | 463 | 466 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 574 | 577 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 652 | 655 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 825 | 828 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 859 | 862 | PF00928 | 0.335 |
TRG_ER_diArg_1 | 253 | 255 | PF00400 | 0.702 |
TRG_ER_diArg_1 | 412 | 415 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 656 | 659 | PF00400 | 0.336 |
TRG_ER_diArg_1 | 776 | 778 | PF00400 | 0.355 |
TRG_ER_diArg_1 | 9 | 11 | PF00400 | 0.653 |
TRG_NES_CRM1_1 | 667 | 681 | PF08389 | 0.335 |
TRG_NES_CRM1_1 | 875 | 887 | PF08389 | 0.447 |
TRG_NLS_MonoExtN_4 | 112 | 119 | PF00514 | 0.634 |
TRG_NLS_MonoExtN_4 | 566 | 572 | PF00514 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 334 | 339 | PF00026 | 0.645 |
TRG_Pf-PMV_PEXEL_1 | 417 | 422 | PF00026 | 0.558 |
TRG_Pf-PMV_PEXEL_1 | 435 | 439 | PF00026 | 0.493 |
TRG_Pf-PMV_PEXEL_1 | 659 | 664 | PF00026 | 0.350 |
TRG_Pf-PMV_PEXEL_1 | 778 | 782 | PF00026 | 0.355 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4G9 | Leptomonas seymouri | 73% | 88% |
A0A1X0NNI0 | Trypanosomatidae | 51% | 100% |
A0A3Q8IIF0 | Leishmania donovani | 92% | 87% |
A0A422MWR8 | Trypanosoma rangeli | 47% | 100% |
A4H7R1 | Leishmania braziliensis | 78% | 100% |
A4HW49 | Leishmania infantum | 92% | 100% |
C9ZSX0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
Q4QFM8 | Leishmania major | 92% | 100% |
V5AZ01 | Trypanosoma cruzi | 48% | 100% |