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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A0A3Q8IEB1
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 10 |
GO:0006793 | phosphorus metabolic process | 3 | 10 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016310 | phosphorylation | 5 | 10 |
GO:0019538 | protein metabolic process | 3 | 10 |
GO:0036211 | protein modification process | 4 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043412 | macromolecule modification | 4 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 10 |
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0010941 | regulation of cell death | 4 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0042981 | regulation of apoptotic process | 6 | 1 |
GO:0043067 | regulation of programmed cell death | 5 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 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:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004672 | protein kinase activity | 3 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0008270 | zinc ion binding | 6 | 9 |
GO:0016301 | kinase activity | 4 | 10 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 10 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0043169 | cation binding | 3 | 9 |
GO:0046872 | metal ion binding | 4 | 9 |
GO:0046914 | transition metal ion binding | 5 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 609 | 613 | PF00656 | 0.534 |
CLV_NRD_NRD_1 | 535 | 537 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 572 | 574 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 661 | 663 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 790 | 792 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 844 | 846 | PF00675 | 0.419 |
CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.694 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.403 |
CLV_PCSK_PC1ET2_1 | 7 | 9 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.244 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 507 | 511 | PF00082 | 0.731 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 640 | 644 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 792 | 796 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 969 | 973 | PF00082 | 0.419 |
DEG_APCC_DBOX_1 | 637 | 645 | PF00400 | 0.590 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.452 |
DEG_SPOP_SBC_1 | 488 | 492 | PF00917 | 0.544 |
DOC_ANK_TNKS_1 | 7 | 14 | PF00023 | 0.419 |
DOC_CKS1_1 | 270 | 275 | PF01111 | 0.307 |
DOC_CYCLIN_RxL_1 | 457 | 465 | PF00134 | 0.688 |
DOC_CYCLIN_RxL_1 | 636 | 646 | PF00134 | 0.578 |
DOC_MAPK_gen_1 | 102 | 112 | PF00069 | 0.604 |
DOC_MAPK_gen_1 | 236 | 245 | PF00069 | 0.307 |
DOC_MAPK_gen_1 | 24 | 34 | PF00069 | 0.381 |
DOC_MAPK_gen_1 | 48 | 56 | PF00069 | 0.320 |
DOC_MAPK_gen_1 | 636 | 644 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 662 | 672 | PF00069 | 0.478 |
DOC_MAPK_MEF2A_6 | 48 | 56 | PF00069 | 0.311 |
DOC_PP1_RVXF_1 | 458 | 465 | PF00149 | 0.691 |
DOC_PP1_RVXF_1 | 977 | 983 | PF00149 | 0.522 |
DOC_PP2B_LxvP_1 | 514 | 517 | PF13499 | 0.679 |
DOC_PP2B_LxvP_1 | 550 | 553 | PF13499 | 0.470 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 135 | 139 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.326 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 471 | 475 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 655 | 659 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 722 | 726 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 728 | 732 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 865 | 869 | PF00917 | 0.419 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.612 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.307 |
DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.306 |
DOC_WW_Pin1_4 | 366 | 371 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 448 | 453 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.816 |
DOC_WW_Pin1_4 | 600 | 605 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 610 | 615 | PF00397 | 0.423 |
DOC_WW_Pin1_4 | 720 | 725 | PF00397 | 0.790 |
DOC_WW_Pin1_4 | 792 | 797 | PF00397 | 0.508 |
LIG_14-3-3_CanoR_1 | 24 | 34 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 266 | 274 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 425 | 433 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 478 | 482 | PF00244 | 0.788 |
LIG_14-3-3_CanoR_1 | 729 | 733 | PF00244 | 0.729 |
LIG_14-3-3_CanoR_1 | 979 | 983 | PF00244 | 0.482 |
LIG_APCC_ABBAyCdc20_2 | 231 | 237 | PF00400 | 0.368 |
LIG_BIR_III_2 | 793 | 797 | PF00653 | 0.445 |
LIG_BIR_III_4 | 815 | 819 | PF00653 | 0.362 |
LIG_BRCT_BRCA1_1 | 505 | 509 | PF00533 | 0.634 |
LIG_Clathr_ClatBox_1 | 641 | 645 | PF01394 | 0.611 |
LIG_eIF4E_1 | 64 | 70 | PF01652 | 0.307 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.625 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.377 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.654 |
LIG_FHA_1 | 580 | 586 | PF00498 | 0.487 |
LIG_FHA_1 | 588 | 594 | PF00498 | 0.456 |
LIG_FHA_1 | 793 | 799 | PF00498 | 0.502 |
LIG_FHA_1 | 889 | 895 | PF00498 | 0.376 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.307 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.425 |
LIG_FHA_2 | 671 | 677 | PF00498 | 0.521 |
LIG_FHA_2 | 956 | 962 | PF00498 | 0.368 |
LIG_GBD_Chelix_1 | 176 | 184 | PF00786 | 0.419 |
LIG_GBD_Chelix_1 | 337 | 345 | PF00786 | 0.425 |
LIG_GSK3_LRP6_1 | 720 | 725 | PF00069 | 0.570 |
LIG_LIR_Apic_2 | 272 | 278 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 506 | 517 | PF02991 | 0.651 |
LIG_LIR_Gen_1 | 63 | 71 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 756 | 765 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 821 | 829 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 246 | 251 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 506 | 512 | PF02991 | 0.658 |
LIG_LIR_Nem_3 | 63 | 67 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 756 | 760 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 821 | 825 | PF02991 | 0.457 |
LIG_LRP6_Inhibitor_1 | 867 | 873 | PF00058 | 0.307 |
LIG_LRP6_Inhibitor_1 | 913 | 919 | PF00058 | 0.419 |
LIG_MAD2 | 51 | 59 | PF02301 | 0.368 |
LIG_NRBOX | 298 | 304 | PF00104 | 0.419 |
LIG_NRBOX | 336 | 342 | PF00104 | 0.333 |
LIG_PCNA_yPIPBox_3 | 187 | 198 | PF02747 | 0.422 |
LIG_Pex14_2 | 67 | 71 | PF04695 | 0.307 |
LIG_PTB_Apo_2 | 114 | 121 | PF02174 | 0.488 |
LIG_SH2_CRK | 248 | 252 | PF00017 | 0.425 |
LIG_SH2_CRK | 822 | 826 | PF00017 | 0.455 |
LIG_SH2_NCK_1 | 526 | 530 | PF00017 | 0.546 |
LIG_SH2_NCK_1 | 822 | 826 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 30 | 34 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 333 | 337 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 904 | 907 | PF00017 | 0.307 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.322 |
LIG_SH3_3 | 482 | 488 | PF00018 | 0.629 |
LIG_SH3_3 | 661 | 667 | PF00018 | 0.635 |
LIG_SH3_3 | 718 | 724 | PF00018 | 0.740 |
LIG_SUMO_SIM_par_1 | 296 | 301 | PF11976 | 0.307 |
LIG_SUMO_SIM_par_1 | 584 | 591 | PF11976 | 0.414 |
LIG_SUMO_SIM_par_1 | 606 | 613 | PF11976 | 0.434 |
LIG_TRAF2_1 | 197 | 200 | PF00917 | 0.362 |
LIG_TRAF2_1 | 38 | 41 | PF00917 | 0.399 |
LIG_TRFH_1 | 274 | 278 | PF08558 | 0.368 |
LIG_UBA3_1 | 378 | 386 | PF00899 | 0.682 |
MOD_CDK_SPK_2 | 792 | 797 | PF00069 | 0.508 |
MOD_CDK_SPxxK_3 | 792 | 799 | PF00069 | 0.504 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.558 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.425 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.714 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.720 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.730 |
MOD_CK1_1 | 524 | 530 | PF00069 | 0.711 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.419 |
MOD_CK1_1 | 665 | 671 | PF00069 | 0.560 |
MOD_CK1_1 | 690 | 696 | PF00069 | 0.414 |
MOD_CK1_1 | 701 | 707 | PF00069 | 0.657 |
MOD_CK1_1 | 978 | 984 | PF00069 | 0.512 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.632 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.472 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.307 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.419 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.489 |
MOD_CK2_1 | 519 | 525 | PF00069 | 0.630 |
MOD_CK2_1 | 670 | 676 | PF00069 | 0.563 |
MOD_CK2_1 | 682 | 688 | PF00069 | 0.421 |
MOD_CK2_1 | 865 | 871 | PF00069 | 0.333 |
MOD_CK2_1 | 894 | 900 | PF00069 | 0.388 |
MOD_Cter_Amidation | 533 | 536 | PF01082 | 0.581 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.665 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.495 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.423 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.717 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.688 |
MOD_GlcNHglycan | 537 | 541 | PF01048 | 0.707 |
MOD_GlcNHglycan | 620 | 623 | PF01048 | 0.427 |
MOD_GlcNHglycan | 657 | 660 | PF01048 | 0.750 |
MOD_GlcNHglycan | 688 | 692 | PF01048 | 0.384 |
MOD_GlcNHglycan | 710 | 713 | PF01048 | 0.677 |
MOD_GlcNHglycan | 780 | 783 | PF01048 | 0.427 |
MOD_GlcNHglycan | 815 | 819 | PF01048 | 0.362 |
MOD_GlcNHglycan | 838 | 841 | PF01048 | 0.419 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.774 |
MOD_GlcNHglycan | 896 | 899 | PF01048 | 0.372 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.641 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.714 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.594 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.376 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.432 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.307 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.503 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.686 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.632 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.552 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.742 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.754 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.707 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.574 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.621 |
MOD_GSK3_1 | 618 | 625 | PF00069 | 0.418 |
MOD_GSK3_1 | 697 | 704 | PF00069 | 0.730 |
MOD_GSK3_1 | 708 | 715 | PF00069 | 0.685 |
MOD_N-GLC_1 | 431 | 436 | PF02516 | 0.744 |
MOD_N-GLC_1 | 471 | 476 | PF02516 | 0.725 |
MOD_N-GLC_1 | 579 | 584 | PF02516 | 0.531 |
MOD_N-GLC_1 | 708 | 713 | PF02516 | 0.632 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.577 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.468 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.333 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.307 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.713 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.627 |
MOD_NEK2_1 | 462 | 467 | PF00069 | 0.763 |
MOD_NEK2_1 | 587 | 592 | PF00069 | 0.523 |
MOD_NEK2_1 | 768 | 773 | PF00069 | 0.512 |
MOD_NEK2_1 | 881 | 886 | PF00069 | 0.307 |
MOD_NEK2_1 | 926 | 931 | PF00069 | 0.311 |
MOD_PK_1 | 361 | 367 | PF00069 | 0.569 |
MOD_PK_1 | 57 | 63 | PF00069 | 0.419 |
MOD_PKA_1 | 662 | 668 | PF00069 | 0.553 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.425 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.307 |
MOD_PKA_2 | 424 | 430 | PF00069 | 0.657 |
MOD_PKA_2 | 477 | 483 | PF00069 | 0.788 |
MOD_PKA_2 | 622 | 628 | PF00069 | 0.410 |
MOD_PKA_2 | 665 | 671 | PF00069 | 0.521 |
MOD_PKA_2 | 682 | 688 | PF00069 | 0.273 |
MOD_PKA_2 | 715 | 721 | PF00069 | 0.742 |
MOD_PKA_2 | 728 | 734 | PF00069 | 0.760 |
MOD_PKA_2 | 978 | 984 | PF00069 | 0.481 |
MOD_PKB_1 | 419 | 427 | PF00069 | 0.679 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.698 |
MOD_Plk_1 | 524 | 530 | PF00069 | 0.711 |
MOD_Plk_2-3 | 301 | 307 | PF00069 | 0.307 |
MOD_Plk_2-3 | 744 | 750 | PF00069 | 0.563 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.687 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.691 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.307 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.376 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.297 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.268 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.679 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.689 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.503 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.325 |
MOD_Plk_4 | 722 | 728 | PF00069 | 0.677 |
MOD_Plk_4 | 753 | 759 | PF00069 | 0.444 |
MOD_Plk_4 | 978 | 984 | PF00069 | 0.461 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.307 |
MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.306 |
MOD_ProDKin_1 | 366 | 372 | PF00069 | 0.543 |
MOD_ProDKin_1 | 448 | 454 | PF00069 | 0.721 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.815 |
MOD_ProDKin_1 | 600 | 606 | PF00069 | 0.435 |
MOD_ProDKin_1 | 610 | 616 | PF00069 | 0.416 |
MOD_ProDKin_1 | 720 | 726 | PF00069 | 0.790 |
MOD_ProDKin_1 | 792 | 798 | PF00069 | 0.503 |
MOD_SUMO_rev_2 | 246 | 251 | PF00179 | 0.307 |
TRG_DiLeu_BaEn_1 | 49 | 54 | PF01217 | 0.307 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 822 | 825 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 946 | 949 | PF00928 | 0.307 |
TRG_ER_diArg_1 | 76 | 78 | PF00400 | 0.362 |
TRG_ER_diArg_1 | 796 | 799 | PF00400 | 0.500 |
TRG_NES_CRM1_1 | 291 | 301 | PF08389 | 0.419 |
TRG_NLS_MonoExtC_3 | 6 | 12 | PF00514 | 0.419 |
TRG_NLS_MonoExtN_4 | 842 | 849 | PF00514 | 0.419 |
TRG_Pf-PMV_PEXEL_1 | 280 | 284 | PF00026 | 0.307 |
TRG_Pf-PMV_PEXEL_1 | 496 | 501 | PF00026 | 0.736 |
TRG_Pf-PMV_PEXEL_1 | 772 | 776 | PF00026 | 0.431 |
TRG_Pf-PMV_PEXEL_1 | 8 | 12 | PF00026 | 0.419 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFF2 | Leptomonas seymouri | 72% | 99% |
A0A1X0P1U2 | Trypanosomatidae | 45% | 100% |
A0A422N709 | Trypanosoma rangeli | 48% | 100% |
A4HIE5 | Leishmania braziliensis | 85% | 99% |
A4I5P2 | Leishmania infantum | 100% | 100% |
E9B0Y6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q9NE58 | Leishmania major | 95% | 99% |
V5DCX1 | Trypanosoma cruzi | 47% | 100% |