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: A4HIE5
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 | 124 | 128 | PF00656 | 0.523 |
CLV_C14_Caspase3-7 | 520 | 524 | PF00656 | 0.430 |
CLV_C14_Caspase3-7 | 607 | 611 | PF00656 | 0.536 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 533 | 535 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 570 | 572 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 659 | 661 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 838 | 840 | PF00675 | 0.411 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 533 | 535 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 7 | 9 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.667 |
CLV_PCSK_SKI1_1 | 571 | 575 | PF00082 | 0.557 |
CLV_PCSK_SKI1_1 | 786 | 790 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 963 | 967 | PF00082 | 0.411 |
DEG_APCC_DBOX_1 | 429 | 437 | PF00400 | 0.541 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.467 |
DEG_SPOP_SBC_1 | 353 | 357 | PF00917 | 0.336 |
DOC_ANK_TNKS_1 | 7 | 14 | PF00023 | 0.411 |
DOC_CKS1_1 | 270 | 275 | PF01111 | 0.296 |
DOC_MAPK_gen_1 | 236 | 245 | PF00069 | 0.296 |
DOC_MAPK_gen_1 | 24 | 34 | PF00069 | 0.365 |
DOC_MAPK_gen_1 | 48 | 56 | PF00069 | 0.303 |
DOC_MAPK_gen_1 | 660 | 670 | PF00069 | 0.473 |
DOC_MAPK_MEF2A_6 | 48 | 56 | PF00069 | 0.300 |
DOC_MAPK_MEF2A_6 | 713 | 722 | PF00069 | 0.239 |
DOC_PP2B_LxvP_1 | 512 | 515 | PF13499 | 0.646 |
DOC_PP2B_LxvP_1 | 548 | 551 | PF13499 | 0.465 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.296 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 515 | 519 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 653 | 657 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 859 | 863 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.573 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.296 |
DOC_WW_Pin1_4 | 366 | 371 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 580 | 585 | PF00397 | 0.383 |
DOC_WW_Pin1_4 | 598 | 603 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 608 | 613 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 714 | 719 | PF00397 | 0.393 |
DOC_WW_Pin1_4 | 786 | 791 | PF00397 | 0.411 |
LIG_14-3-3_CanoR_1 | 24 | 34 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 266 | 274 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 352 | 362 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 425 | 433 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 476 | 480 | PF00244 | 0.687 |
LIG_14-3-3_CanoR_1 | 723 | 727 | PF00244 | 0.393 |
LIG_APCC_ABBAyCdc20_2 | 231 | 237 | PF00400 | 0.357 |
LIG_BIR_III_4 | 809 | 813 | PF00653 | 0.296 |
LIG_BRCT_BRCA1_1 | 503 | 507 | PF00533 | 0.568 |
LIG_eIF4E_1 | 64 | 70 | PF01652 | 0.296 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.262 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.692 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.211 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.357 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.667 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.512 |
LIG_FHA_1 | 580 | 586 | PF00498 | 0.501 |
LIG_FHA_1 | 649 | 655 | PF00498 | 0.804 |
LIG_FHA_1 | 709 | 715 | PF00498 | 0.439 |
LIG_FHA_1 | 787 | 793 | PF00498 | 0.411 |
LIG_FHA_1 | 883 | 889 | PF00498 | 0.365 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.612 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.296 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.460 |
LIG_FHA_2 | 468 | 474 | PF00498 | 0.500 |
LIG_FHA_2 | 669 | 675 | PF00498 | 0.411 |
LIG_FHA_2 | 950 | 956 | PF00498 | 0.357 |
LIG_GBD_Chelix_1 | 176 | 184 | PF00786 | 0.411 |
LIG_GBD_Chelix_1 | 337 | 345 | PF00786 | 0.393 |
LIG_LIR_Apic_2 | 272 | 278 | PF02991 | 0.296 |
LIG_LIR_Gen_1 | 504 | 515 | PF02991 | 0.599 |
LIG_LIR_Gen_1 | 63 | 71 | PF02991 | 0.296 |
LIG_LIR_Gen_1 | 750 | 759 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 815 | 823 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 246 | 251 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 444 | 448 | PF02991 | 0.703 |
LIG_LIR_Nem_3 | 483 | 488 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 504 | 510 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 63 | 67 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 750 | 754 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 815 | 819 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 939 | 943 | PF02991 | 0.243 |
LIG_LRP6_Inhibitor_1 | 861 | 867 | PF00058 | 0.296 |
LIG_LRP6_Inhibitor_1 | 907 | 913 | PF00058 | 0.411 |
LIG_MAD2 | 51 | 59 | PF02301 | 0.357 |
LIG_NRBOX | 298 | 304 | PF00104 | 0.411 |
LIG_NRBOX | 336 | 342 | PF00104 | 0.321 |
LIG_PCNA_TLS_4 | 621 | 628 | PF02747 | 0.288 |
LIG_PCNA_yPIPBox_3 | 187 | 200 | PF02747 | 0.414 |
LIG_Pex14_2 | 111 | 115 | PF04695 | 0.486 |
LIG_Pex14_2 | 67 | 71 | PF04695 | 0.296 |
LIG_PTB_Apo_2 | 478 | 485 | PF02174 | 0.505 |
LIG_SH2_CRK | 248 | 252 | PF00017 | 0.393 |
LIG_SH2_CRK | 816 | 820 | PF00017 | 0.411 |
LIG_SH2_NCK_1 | 816 | 820 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 286 | 290 | PF00017 | 0.203 |
LIG_SH2_STAP1 | 30 | 34 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 333 | 337 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.247 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 898 | 901 | PF00017 | 0.296 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.296 |
LIG_SH3_3 | 449 | 455 | PF00018 | 0.510 |
LIG_SH3_3 | 659 | 665 | PF00018 | 0.614 |
LIG_SH3_3 | 712 | 718 | PF00018 | 0.415 |
LIG_SUMO_SIM_par_1 | 296 | 301 | PF11976 | 0.296 |
LIG_SUMO_SIM_par_1 | 582 | 589 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 604 | 611 | PF11976 | 0.435 |
LIG_TRAF2_1 | 38 | 41 | PF00917 | 0.375 |
LIG_TRFH_1 | 274 | 278 | PF08558 | 0.357 |
LIG_UBA3_1 | 378 | 386 | PF00899 | 0.665 |
LIG_WRC_WIRS_1 | 112 | 117 | PF05994 | 0.482 |
MOD_CDK_SPK_2 | 786 | 791 | PF00069 | 0.411 |
MOD_CDK_SPxxK_3 | 786 | 793 | PF00069 | 0.411 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.510 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.652 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.393 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.482 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.677 |
MOD_CK1_1 | 446 | 452 | PF00069 | 0.581 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.704 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.680 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.623 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.411 |
MOD_CK1_1 | 663 | 669 | PF00069 | 0.547 |
MOD_CK1_1 | 688 | 694 | PF00069 | 0.303 |
MOD_CK1_1 | 695 | 701 | PF00069 | 0.307 |
MOD_CK1_1 | 724 | 730 | PF00069 | 0.211 |
MOD_CK1_1 | 972 | 978 | PF00069 | 0.482 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.641 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.468 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.296 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.407 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.460 |
MOD_CK2_1 | 653 | 659 | PF00069 | 0.586 |
MOD_CK2_1 | 668 | 674 | PF00069 | 0.452 |
MOD_CK2_1 | 680 | 686 | PF00069 | 0.337 |
MOD_CK2_1 | 859 | 865 | PF00069 | 0.321 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.411 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.689 |
MOD_GlcNHglycan | 535 | 539 | PF01048 | 0.696 |
MOD_GlcNHglycan | 618 | 621 | PF01048 | 0.410 |
MOD_GlcNHglycan | 655 | 658 | PF01048 | 0.747 |
MOD_GlcNHglycan | 686 | 690 | PF01048 | 0.302 |
MOD_GlcNHglycan | 774 | 777 | PF01048 | 0.361 |
MOD_GlcNHglycan | 809 | 813 | PF01048 | 0.296 |
MOD_GlcNHglycan | 832 | 835 | PF01048 | 0.411 |
MOD_GlcNHglycan | 878 | 881 | PF01048 | 0.326 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.755 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.636 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.682 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.782 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.591 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.365 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.211 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.460 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.296 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.284 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.469 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.594 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.677 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.700 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.686 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.495 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.592 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.388 |
MOD_GSK3_1 | 616 | 623 | PF00069 | 0.389 |
MOD_GSK3_1 | 648 | 655 | PF00069 | 0.602 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.439 |
MOD_GSK3_1 | 696 | 703 | PF00069 | 0.391 |
MOD_GSK3_1 | 714 | 721 | PF00069 | 0.421 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.586 |
MOD_N-GLC_1 | 431 | 436 | PF02516 | 0.695 |
MOD_N-GLC_1 | 480 | 485 | PF02516 | 0.722 |
MOD_N-GLC_1 | 488 | 493 | PF02516 | 0.580 |
MOD_N-GLC_1 | 577 | 582 | PF02516 | 0.543 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.623 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.455 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.344 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.296 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.656 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.632 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.722 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.726 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.532 |
MOD_NEK2_1 | 700 | 705 | PF00069 | 0.300 |
MOD_NEK2_1 | 722 | 727 | PF00069 | 0.393 |
MOD_NEK2_1 | 762 | 767 | PF00069 | 0.411 |
MOD_NEK2_1 | 875 | 880 | PF00069 | 0.296 |
MOD_NEK2_1 | 920 | 925 | PF00069 | 0.300 |
MOD_NEK2_2 | 718 | 723 | PF00069 | 0.211 |
MOD_OFUCOSY | 401 | 407 | PF10250 | 0.474 |
MOD_PIKK_1 | 11 | 17 | PF00454 | 0.211 |
MOD_PIKK_1 | 209 | 215 | PF00454 | 0.211 |
MOD_PIKK_1 | 524 | 530 | PF00454 | 0.582 |
MOD_PK_1 | 361 | 367 | PF00069 | 0.524 |
MOD_PK_1 | 57 | 63 | PF00069 | 0.411 |
MOD_PKA_1 | 163 | 169 | PF00069 | 0.489 |
MOD_PKA_1 | 660 | 666 | PF00069 | 0.547 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.489 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.393 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.296 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.211 |
MOD_PKA_2 | 424 | 430 | PF00069 | 0.619 |
MOD_PKA_2 | 475 | 481 | PF00069 | 0.688 |
MOD_PKA_2 | 663 | 669 | PF00069 | 0.520 |
MOD_PKA_2 | 680 | 686 | PF00069 | 0.195 |
MOD_PKA_2 | 722 | 728 | PF00069 | 0.441 |
MOD_Plk_1 | 2 | 8 | PF00069 | 0.247 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.669 |
MOD_Plk_1 | 480 | 486 | PF00069 | 0.582 |
MOD_Plk_1 | 522 | 528 | PF00069 | 0.623 |
MOD_Plk_2-3 | 301 | 307 | PF00069 | 0.296 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.659 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.679 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.296 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.361 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.409 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.254 |
MOD_Plk_4 | 374 | 380 | PF00069 | 0.655 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.660 |
MOD_Plk_4 | 480 | 486 | PF00069 | 0.543 |
MOD_Plk_4 | 543 | 549 | PF00069 | 0.461 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.307 |
MOD_Plk_4 | 747 | 753 | PF00069 | 0.357 |
MOD_Plk_4 | 972 | 978 | PF00069 | 0.447 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.296 |
MOD_ProDKin_1 | 366 | 372 | PF00069 | 0.524 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.651 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.513 |
MOD_ProDKin_1 | 580 | 586 | PF00069 | 0.381 |
MOD_ProDKin_1 | 598 | 604 | PF00069 | 0.500 |
MOD_ProDKin_1 | 608 | 614 | PF00069 | 0.405 |
MOD_ProDKin_1 | 714 | 720 | PF00069 | 0.393 |
MOD_ProDKin_1 | 786 | 792 | PF00069 | 0.411 |
MOD_SUMO_for_1 | 784 | 787 | PF00179 | 0.292 |
MOD_SUMO_rev_2 | 246 | 251 | PF00179 | 0.296 |
MOD_SUMO_rev_2 | 655 | 663 | PF00179 | 0.610 |
MOD_SUMO_rev_2 | 890 | 895 | PF00179 | 0.292 |
TRG_DiLeu_BaEn_1 | 49 | 54 | PF01217 | 0.296 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 816 | 819 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 940 | 943 | PF00928 | 0.296 |
TRG_ER_diArg_1 | 790 | 793 | PF00400 | 0.411 |
TRG_NES_CRM1_1 | 291 | 301 | PF08389 | 0.387 |
TRG_NLS_MonoExtC_3 | 6 | 12 | PF00514 | 0.411 |
TRG_NLS_MonoExtN_4 | 836 | 843 | PF00514 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 280 | 284 | PF00026 | 0.296 |
TRG_Pf-PMV_PEXEL_1 | 766 | 770 | PF00026 | 0.357 |
TRG_Pf-PMV_PEXEL_1 | 8 | 12 | PF00026 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 886 | 890 | PF00026 | 0.211 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFF2 | Leptomonas seymouri | 70% | 99% |
A0A1X0P1U2 | Trypanosomatidae | 45% | 100% |
A0A3Q8IEB1 | Leishmania donovani | 85% | 99% |
A0A422N709 | Trypanosoma rangeli | 48% | 100% |
A4I5P2 | Leishmania infantum | 85% | 99% |
E9B0Y6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 99% |
Q9NE58 | Leishmania major | 84% | 99% |
V5DCX1 | Trypanosoma cruzi | 46% | 100% |