Structural Proteins, leucine-rich repeat
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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 7 |
GO:0042995 | cell projection | 2 | 7 |
GO:0043226 | organelle | 2 | 7 |
GO:0043227 | membrane-bounded organelle | 3 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 7 |
GO:0000151 | ubiquitin ligase complex | 3 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0019005 | SCF ubiquitin ligase complex | 5 | 1 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: A4HTW7
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0031146 | SCF-dependent proteasomal ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 17 | 21 | PF00656 | 0.645 |
CLV_C14_Caspase3-7 | 282 | 286 | PF00656 | 0.436 |
CLV_C14_Caspase3-7 | 721 | 725 | PF00656 | 0.677 |
CLV_C14_Caspase3-7 | 780 | 784 | PF00656 | 0.702 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 522 | 524 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 874 | 876 | PF00675 | 0.737 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.728 |
CLV_PCSK_KEX2_1 | 522 | 524 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 585 | 587 | PF00082 | 0.647 |
CLV_PCSK_KEX2_1 | 874 | 876 | PF00082 | 0.737 |
CLV_PCSK_KEX2_1 | 934 | 936 | PF00082 | 0.770 |
CLV_PCSK_PC1ET2_1 | 585 | 587 | PF00082 | 0.566 |
CLV_PCSK_PC1ET2_1 | 934 | 936 | PF00082 | 0.770 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.781 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 495 | 499 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 611 | 615 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 698 | 702 | PF00082 | 0.732 |
CLV_PCSK_SKI1_1 | 730 | 734 | PF00082 | 0.606 |
CLV_Separin_Metazoa | 519 | 523 | PF03568 | 0.524 |
DEG_APCC_DBOX_1 | 460 | 468 | PF00400 | 0.587 |
DEG_APCC_DBOX_1 | 494 | 502 | PF00400 | 0.604 |
DEG_SIAH_1 | 40 | 48 | PF03145 | 0.576 |
DOC_CDC14_PxL_1 | 288 | 296 | PF14671 | 0.567 |
DOC_CKS1_1 | 830 | 835 | PF01111 | 0.630 |
DOC_CYCLIN_RxL_1 | 319 | 328 | PF00134 | 0.576 |
DOC_CYCLIN_RxL_1 | 446 | 454 | PF00134 | 0.475 |
DOC_CYCLIN_RxL_1 | 734 | 747 | PF00134 | 0.708 |
DOC_CYCLIN_yCln2_LP_2 | 400 | 403 | PF00134 | 0.605 |
DOC_CYCLIN_yCln2_LP_2 | 830 | 836 | PF00134 | 0.766 |
DOC_CYCLIN_yCln2_LP_2 | 869 | 872 | PF00134 | 0.757 |
DOC_MAPK_DCC_7 | 322 | 331 | PF00069 | 0.578 |
DOC_MAPK_DCC_7 | 483 | 492 | PF00069 | 0.601 |
DOC_MAPK_gen_1 | 418 | 427 | PF00069 | 0.578 |
DOC_MAPK_gen_1 | 483 | 492 | PF00069 | 0.540 |
DOC_MAPK_HePTP_8 | 480 | 492 | PF00069 | 0.594 |
DOC_MAPK_MEF2A_6 | 322 | 331 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 483 | 492 | PF00069 | 0.524 |
DOC_PP2B_LxvP_1 | 324 | 327 | PF13499 | 0.449 |
DOC_PP2B_LxvP_1 | 399 | 402 | PF13499 | 0.509 |
DOC_PP2B_LxvP_1 | 488 | 491 | PF13499 | 0.521 |
DOC_PP2B_LxvP_1 | 501 | 504 | PF13499 | 0.527 |
DOC_PP2B_LxvP_1 | 825 | 828 | PF13499 | 0.740 |
DOC_PP2B_LxvP_1 | 869 | 872 | PF13499 | 0.757 |
DOC_PP4_FxxP_1 | 991 | 994 | PF00568 | 0.623 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.284 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.717 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 687 | 691 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 710 | 714 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 761 | 765 | PF00917 | 0.827 |
DOC_USP7_MATH_1 | 853 | 857 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 929 | 933 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 943 | 947 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 948 | 952 | PF00917 | 0.773 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.801 |
DOC_WW_Pin1_4 | 829 | 834 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 859 | 864 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 874 | 879 | PF00397 | 0.842 |
DOC_WW_Pin1_4 | 890 | 895 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 901 | 906 | PF00397 | 0.761 |
LIG_14-3-3_CanoR_1 | 10 | 18 | PF00244 | 0.670 |
LIG_14-3-3_CanoR_1 | 107 | 111 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 191 | 199 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 234 | 243 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 267 | 272 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 406 | 412 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 421 | 426 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 432 | 440 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 495 | 504 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 505 | 511 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 539 | 544 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 603 | 610 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 643 | 650 | PF00244 | 0.347 |
LIG_14-3-3_CanoR_1 | 874 | 878 | PF00244 | 0.731 |
LIG_14-3-3_CanoR_1 | 95 | 104 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 958 | 966 | PF00244 | 0.749 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.776 |
LIG_BIR_III_4 | 848 | 852 | PF00653 | 0.701 |
LIG_BRCT_BRCA1_1 | 167 | 171 | PF00533 | 0.583 |
LIG_BRCT_BRCA1_1 | 269 | 273 | PF00533 | 0.532 |
LIG_BRCT_BRCA1_1 | 541 | 545 | PF00533 | 0.479 |
LIG_BRCT_BRCA1_1 | 801 | 805 | PF00533 | 0.770 |
LIG_BRCT_BRCA1_1 | 855 | 859 | PF00533 | 0.604 |
LIG_BRCT_BRCA1_1 | 945 | 949 | PF00533 | 0.683 |
LIG_FAT_LD_1 | 467 | 475 | PF03623 | 0.512 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.544 |
LIG_FHA_1 | 310 | 316 | PF00498 | 0.472 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.768 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.518 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.569 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.276 |
LIG_FHA_1 | 594 | 600 | PF00498 | 0.537 |
LIG_FHA_1 | 659 | 665 | PF00498 | 0.580 |
LIG_FHA_1 | 822 | 828 | PF00498 | 0.727 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.430 |
LIG_FHA_2 | 542 | 548 | PF00498 | 0.557 |
LIG_FHA_2 | 602 | 608 | PF00498 | 0.581 |
LIG_FHA_2 | 778 | 784 | PF00498 | 0.757 |
LIG_FHA_2 | 875 | 881 | PF00498 | 0.848 |
LIG_GBD_Chelix_1 | 664 | 672 | PF00786 | 0.501 |
LIG_Integrin_isoDGR_2 | 525 | 527 | PF01839 | 0.656 |
LIG_LIR_Apic_2 | 989 | 994 | PF02991 | 0.624 |
LIG_LIR_LC3C_4 | 328 | 331 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 274 | 280 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 553 | 559 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 946 | 952 | PF02991 | 0.700 |
LIG_MAD2 | 449 | 457 | PF02301 | 0.468 |
LIG_NRBOX | 231 | 237 | PF00104 | 0.568 |
LIG_NRBOX | 338 | 344 | PF00104 | 0.579 |
LIG_PCNA_yPIPBox_3 | 183 | 191 | PF02747 | 0.512 |
LIG_Pex14_2 | 269 | 273 | PF04695 | 0.532 |
LIG_Pex14_2 | 991 | 995 | PF04695 | 0.629 |
LIG_SH2_CRK | 277 | 281 | PF00017 | 0.477 |
LIG_SH2_STAT3 | 916 | 919 | PF00017 | 0.728 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 916 | 919 | PF00017 | 0.767 |
LIG_SH3_1 | 875 | 881 | PF00018 | 0.767 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.590 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.753 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.620 |
LIG_SH3_3 | 657 | 663 | PF00018 | 0.603 |
LIG_SH3_3 | 704 | 710 | PF00018 | 0.579 |
LIG_SH3_3 | 830 | 836 | PF00018 | 0.764 |
LIG_SH3_3 | 857 | 863 | PF00018 | 0.695 |
LIG_SH3_3 | 875 | 881 | PF00018 | 0.574 |
LIG_SUMO_SIM_anti_2 | 122 | 129 | PF11976 | 0.705 |
LIG_SUMO_SIM_anti_2 | 395 | 400 | PF11976 | 0.467 |
LIG_SUMO_SIM_anti_2 | 465 | 473 | PF11976 | 0.590 |
LIG_SUMO_SIM_anti_2 | 596 | 601 | PF11976 | 0.542 |
LIG_SUMO_SIM_par_1 | 122 | 129 | PF11976 | 0.663 |
LIG_SUMO_SIM_par_1 | 373 | 378 | PF11976 | 0.566 |
LIG_SUMO_SIM_par_1 | 423 | 428 | PF11976 | 0.443 |
LIG_SUMO_SIM_par_1 | 449 | 454 | PF11976 | 0.587 |
LIG_SUMO_SIM_par_1 | 823 | 829 | PF11976 | 0.733 |
LIG_TRAF2_1 | 920 | 923 | PF00917 | 0.834 |
LIG_TRAF2_1 | 994 | 997 | PF00917 | 0.824 |
LIG_WRC_WIRS_1 | 266 | 271 | PF05994 | 0.476 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.686 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.460 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.476 |
MOD_CK1_1 | 507 | 513 | PF00069 | 0.605 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.534 |
MOD_CK1_1 | 631 | 637 | PF00069 | 0.580 |
MOD_CK1_1 | 713 | 719 | PF00069 | 0.634 |
MOD_CK1_1 | 775 | 781 | PF00069 | 0.736 |
MOD_CK1_1 | 820 | 826 | PF00069 | 0.747 |
MOD_CK1_1 | 829 | 835 | PF00069 | 0.850 |
MOD_CK1_1 | 904 | 910 | PF00069 | 0.775 |
MOD_CK1_1 | 911 | 917 | PF00069 | 0.719 |
MOD_CK1_1 | 960 | 966 | PF00069 | 0.759 |
MOD_CK1_1 | 967 | 973 | PF00069 | 0.646 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.627 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.453 |
MOD_CK2_1 | 541 | 547 | PF00069 | 0.563 |
MOD_CK2_1 | 720 | 726 | PF00069 | 0.596 |
MOD_CK2_1 | 874 | 880 | PF00069 | 0.857 |
MOD_CK2_1 | 917 | 923 | PF00069 | 0.728 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.639 |
MOD_GlcNHglycan | 254 | 258 | PF01048 | 0.604 |
MOD_GlcNHglycan | 376 | 380 | PF01048 | 0.516 |
MOD_GlcNHglycan | 426 | 430 | PF01048 | 0.495 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.505 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.618 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.509 |
MOD_GlcNHglycan | 710 | 713 | PF01048 | 0.639 |
MOD_GlcNHglycan | 746 | 749 | PF01048 | 0.724 |
MOD_GlcNHglycan | 787 | 791 | PF01048 | 0.811 |
MOD_GlcNHglycan | 819 | 822 | PF01048 | 0.706 |
MOD_GlcNHglycan | 910 | 913 | PF01048 | 0.676 |
MOD_GlcNHglycan | 945 | 948 | PF01048 | 0.698 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.653 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.535 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.514 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.681 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.579 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.242 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.522 |
MOD_GSK3_1 | 708 | 715 | PF00069 | 0.749 |
MOD_GSK3_1 | 716 | 723 | PF00069 | 0.511 |
MOD_GSK3_1 | 817 | 824 | PF00069 | 0.642 |
MOD_GSK3_1 | 903 | 910 | PF00069 | 0.777 |
MOD_GSK3_1 | 914 | 921 | PF00069 | 0.739 |
MOD_GSK3_1 | 929 | 936 | PF00069 | 0.548 |
MOD_GSK3_1 | 957 | 964 | PF00069 | 0.787 |
MOD_LATS_1 | 265 | 271 | PF00433 | 0.549 |
MOD_LATS_1 | 573 | 579 | PF00433 | 0.577 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.553 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.541 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.521 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.495 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.591 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.447 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.749 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.565 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.361 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.577 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.440 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.473 |
MOD_NEK2_1 | 777 | 782 | PF00069 | 0.823 |
MOD_NEK2_1 | 933 | 938 | PF00069 | 0.782 |
MOD_NEK2_2 | 929 | 934 | PF00069 | 0.758 |
MOD_PIKK_1 | 165 | 171 | PF00454 | 0.580 |
MOD_PIKK_1 | 234 | 240 | PF00454 | 0.597 |
MOD_PIKK_1 | 316 | 322 | PF00454 | 0.588 |
MOD_PIKK_1 | 504 | 510 | PF00454 | 0.596 |
MOD_PIKK_1 | 559 | 565 | PF00454 | 0.563 |
MOD_PIKK_1 | 611 | 617 | PF00454 | 0.496 |
MOD_PIKK_1 | 914 | 920 | PF00454 | 0.804 |
MOD_PK_1 | 267 | 273 | PF00069 | 0.544 |
MOD_PK_1 | 539 | 545 | PF00069 | 0.559 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.486 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.611 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.577 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.592 |
MOD_PKA_2 | 431 | 437 | PF00069 | 0.579 |
MOD_PKA_2 | 504 | 510 | PF00069 | 0.577 |
MOD_PKA_2 | 538 | 544 | PF00069 | 0.489 |
MOD_PKA_2 | 642 | 648 | PF00069 | 0.356 |
MOD_PKA_2 | 761 | 767 | PF00069 | 0.789 |
MOD_PKA_2 | 873 | 879 | PF00069 | 0.729 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.714 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.480 |
MOD_PKA_2 | 957 | 963 | PF00069 | 0.717 |
MOD_PKA_2 | 964 | 970 | PF00069 | 0.757 |
MOD_Plk_1 | 253 | 259 | PF00069 | 0.523 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.504 |
MOD_Plk_1 | 546 | 552 | PF00069 | 0.451 |
MOD_Plk_1 | 634 | 640 | PF00069 | 0.569 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.507 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.653 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.591 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.429 |
MOD_Plk_4 | 497 | 503 | PF00069 | 0.589 |
MOD_Plk_4 | 546 | 552 | PF00069 | 0.498 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.547 |
MOD_Plk_4 | 772 | 778 | PF00069 | 0.791 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.578 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.798 |
MOD_ProDKin_1 | 829 | 835 | PF00069 | 0.629 |
MOD_ProDKin_1 | 859 | 865 | PF00069 | 0.727 |
MOD_ProDKin_1 | 874 | 880 | PF00069 | 0.842 |
MOD_ProDKin_1 | 890 | 896 | PF00069 | 0.636 |
MOD_ProDKin_1 | 901 | 907 | PF00069 | 0.761 |
MOD_SUMO_for_1 | 70 | 73 | PF00179 | 0.528 |
TRG_DiLeu_BaEn_1 | 122 | 127 | PF01217 | 0.633 |
TRG_DiLeu_BaEn_4 | 122 | 128 | PF01217 | 0.704 |
TRG_DiLeu_BaEn_4 | 535 | 541 | PF01217 | 0.492 |
TRG_DiLeu_BaEn_4 | 73 | 79 | PF01217 | 0.504 |
TRG_DiLeu_BaLyEn_6 | 231 | 236 | PF01217 | 0.564 |
TRG_DiLeu_BaLyEn_6 | 338 | 343 | PF01217 | 0.494 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.561 |
TRG_ER_diArg_1 | 131 | 134 | PF00400 | 0.677 |
TRG_ER_diArg_1 | 521 | 523 | PF00400 | 0.570 |
TRG_ER_diArg_1 | 873 | 875 | PF00400 | 0.738 |
TRG_NES_CRM1_1 | 646 | 658 | PF08389 | 0.535 |
TRG_Pf-PMV_PEXEL_1 | 234 | 238 | PF00026 | 0.462 |
TRG_Pf-PMV_PEXEL_1 | 449 | 454 | PF00026 | 0.522 |
TRG_Pf-PMV_PEXEL_1 | 603 | 607 | PF00026 | 0.583 |
TRG_Pf-PMV_PEXEL_1 | 611 | 615 | PF00026 | 0.451 |
TRG_Pf-PMV_PEXEL_1 | 739 | 744 | PF00026 | 0.707 |
TRG_Pf-PMV_PEXEL_1 | 80 | 84 | PF00026 | 0.544 |
TRG_Pf-PMV_PEXEL_1 | 935 | 939 | PF00026 | 0.761 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WQP1 | Leishmania donovani | 100% | 100% |
A0A422NV64 | Trypanosoma rangeli | 28% | 92% |
A4H5N0 | Leishmania braziliensis | 71% | 98% |
D0A9D1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 95% |
E9AMQ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 99% |
Q4QHX1 | Leishmania major | 92% | 100% |