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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 2 |
GO:0097014 | ciliary plasm | 5 | 2 |
GO:0099568 | cytoplasmic region | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QEE5
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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004672 | protein kinase activity | 3 | 10 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 2 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
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: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 | 171 | 175 | PF00656 | 0.657 |
CLV_C14_Caspase3-7 | 64 | 68 | PF00656 | 0.722 |
CLV_C14_Caspase3-7 | 95 | 99 | PF00656 | 0.665 |
CLV_MEL_PAP_1 | 284 | 290 | PF00089 | 0.510 |
CLV_MEL_PAP_1 | 834 | 840 | PF00089 | 0.191 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.607 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 290 | 292 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 450 | 452 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 588 | 590 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 682 | 684 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.679 |
CLV_NRD_NRD_1 | 870 | 872 | PF00675 | 0.322 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.765 |
CLV_PCSK_FUR_1 | 208 | 212 | PF00082 | 0.721 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 278 | 280 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 588 | 590 | PF00082 | 0.372 |
CLV_PCSK_KEX2_1 | 682 | 684 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.681 |
CLV_PCSK_KEX2_1 | 743 | 745 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 869 | 871 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.625 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.556 |
CLV_PCSK_PC1ET2_1 | 743 | 745 | PF00082 | 0.289 |
CLV_PCSK_PC1ET2_1 | 869 | 871 | PF00082 | 0.330 |
CLV_PCSK_PC7_1 | 274 | 280 | PF00082 | 0.629 |
CLV_PCSK_PC7_1 | 866 | 872 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.742 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 517 | 521 | PF00082 | 0.659 |
CLV_PCSK_SKI1_1 | 631 | 635 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 684 | 688 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 702 | 706 | PF00082 | 0.211 |
CLV_PCSK_SKI1_1 | 719 | 723 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 829 | 833 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 866 | 870 | PF00082 | 0.340 |
CLV_Separin_Metazoa | 794 | 798 | PF03568 | 0.322 |
DEG_APCC_DBOX_1 | 701 | 709 | PF00400 | 0.349 |
DEG_SCF_FBW7_1 | 24 | 30 | PF00400 | 0.546 |
DEG_SPOP_SBC_1 | 190 | 194 | PF00917 | 0.707 |
DOC_CKS1_1 | 24 | 29 | PF01111 | 0.788 |
DOC_CYCLIN_RxL_1 | 572 | 583 | PF00134 | 0.512 |
DOC_MAPK_gen_1 | 256 | 265 | PF00069 | 0.712 |
DOC_MAPK_gen_1 | 631 | 639 | PF00069 | 0.372 |
DOC_MAPK_gen_1 | 687 | 696 | PF00069 | 0.289 |
DOC_MAPK_gen_1 | 719 | 728 | PF00069 | 0.289 |
DOC_MAPK_gen_1 | 850 | 857 | PF00069 | 0.318 |
DOC_MAPK_gen_1 | 869 | 877 | PF00069 | 0.202 |
DOC_MAPK_MEF2A_6 | 259 | 267 | PF00069 | 0.606 |
DOC_MAPK_MEF2A_6 | 850 | 859 | PF00069 | 0.338 |
DOC_PP1_RVXF_1 | 264 | 270 | PF00149 | 0.539 |
DOC_PP4_FxxP_1 | 790 | 793 | PF00568 | 0.275 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 536 | 540 | PF00917 | 0.813 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.585 |
DOC_USP7_MATH_2 | 201 | 207 | PF00917 | 0.611 |
DOC_USP7_UBL2_3 | 213 | 217 | PF12436 | 0.516 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.805 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.782 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 486 | 491 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 504 | 509 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 510 | 515 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 766 | 771 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 784 | 789 | PF00397 | 0.209 |
DOC_WW_Pin1_4 | 893 | 898 | PF00397 | 0.534 |
DOC_WW_Pin1_4 | 900 | 905 | PF00397 | 0.624 |
LIG_14-3-3_CanoR_1 | 291 | 299 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 384 | 389 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 495 | 502 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 517 | 523 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 588 | 593 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 7 | 16 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 870 | 878 | PF00244 | 0.279 |
LIG_APCC_ABBA_1 | 666 | 671 | PF00400 | 0.289 |
LIG_BRCT_BRCA1_1 | 561 | 565 | PF00533 | 0.613 |
LIG_BRCT_BRCA1_1 | 786 | 790 | PF00533 | 0.338 |
LIG_CtBP_PxDLS_1 | 347 | 351 | PF00389 | 0.514 |
LIG_DLG_GKlike_1 | 384 | 392 | PF00625 | 0.617 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.615 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.659 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.443 |
LIG_FHA_1 | 496 | 502 | PF00498 | 0.670 |
LIG_FHA_1 | 522 | 528 | PF00498 | 0.678 |
LIG_FHA_1 | 574 | 580 | PF00498 | 0.625 |
LIG_FHA_1 | 654 | 660 | PF00498 | 0.336 |
LIG_FHA_1 | 699 | 705 | PF00498 | 0.404 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.660 |
LIG_FHA_2 | 292 | 298 | PF00498 | 0.624 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.641 |
LIG_FHA_2 | 598 | 604 | PF00498 | 0.409 |
LIG_FHA_2 | 871 | 877 | PF00498 | 0.267 |
LIG_FHA_2 | 882 | 888 | PF00498 | 0.386 |
LIG_LIR_Apic_2 | 787 | 793 | PF02991 | 0.275 |
LIG_LIR_Gen_1 | 313 | 323 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 294 | 299 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 313 | 319 | PF02991 | 0.656 |
LIG_LIR_Nem_3 | 542 | 546 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 597 | 601 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 667 | 672 | PF02991 | 0.372 |
LIG_LRP6_Inhibitor_1 | 19 | 25 | PF00058 | 0.654 |
LIG_MLH1_MIPbox_1 | 786 | 790 | PF16413 | 0.338 |
LIG_Pex14_2 | 832 | 836 | PF04695 | 0.338 |
LIG_Pex14_2 | 860 | 864 | PF04695 | 0.268 |
LIG_PROFILIN_1 | 477 | 483 | PF00235 | 0.515 |
LIG_PTB_Apo_2 | 440 | 447 | PF02174 | 0.599 |
LIG_PTB_Phospho_1 | 440 | 446 | PF10480 | 0.598 |
LIG_REV1ctd_RIR_1 | 857 | 866 | PF16727 | 0.269 |
LIG_SH2_GRB2like | 441 | 444 | PF00017 | 0.590 |
LIG_SH2_NCK_1 | 441 | 445 | PF00017 | 0.590 |
LIG_SH2_SRC | 710 | 713 | PF00017 | 0.289 |
LIG_SH2_STAP1 | 441 | 445 | PF00017 | 0.590 |
LIG_SH2_STAP1 | 700 | 704 | PF00017 | 0.289 |
LIG_SH2_STAT3 | 652 | 655 | PF00017 | 0.289 |
LIG_SH2_STAT3 | 700 | 703 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 299 | 302 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 446 | 449 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 463 | 466 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 700 | 703 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 710 | 713 | PF00017 | 0.246 |
LIG_SH2_STAT5 | 802 | 805 | PF00017 | 0.338 |
LIG_SH3_1 | 14 | 20 | PF00018 | 0.721 |
LIG_SH3_3 | 14 | 20 | PF00018 | 0.679 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.712 |
LIG_SH3_3 | 342 | 348 | PF00018 | 0.691 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.741 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.626 |
LIG_SH3_3 | 508 | 514 | PF00018 | 0.705 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.665 |
LIG_SH3_3 | 782 | 788 | PF00018 | 0.275 |
LIG_SH3_3 | 891 | 897 | PF00018 | 0.501 |
LIG_SUMO_SIM_anti_2 | 430 | 436 | PF11976 | 0.423 |
LIG_SUMO_SIM_anti_2 | 693 | 699 | PF11976 | 0.289 |
LIG_SUMO_SIM_anti_2 | 873 | 879 | PF11976 | 0.300 |
LIG_SUMO_SIM_par_1 | 197 | 206 | PF11976 | 0.615 |
LIG_SUMO_SIM_par_1 | 42 | 50 | PF11976 | 0.644 |
LIG_TRAF2_1 | 144 | 147 | PF00917 | 0.832 |
LIG_TRAF2_1 | 162 | 165 | PF00917 | 0.496 |
LIG_TRAF2_1 | 769 | 772 | PF00917 | 0.322 |
LIG_TRAF2_1 | 889 | 892 | PF00917 | 0.557 |
LIG_TRFH_1 | 404 | 408 | PF08558 | 0.627 |
LIG_TYR_ITSM | 598 | 605 | PF00017 | 0.372 |
LIG_UBA3_1 | 639 | 646 | PF00899 | 0.289 |
LIG_UBA3_1 | 727 | 735 | PF00899 | 0.313 |
LIG_UBA3_1 | 831 | 840 | PF00899 | 0.312 |
LIG_WRC_WIRS_1 | 519 | 524 | PF05994 | 0.476 |
MOD_CDC14_SPxK_1 | 111 | 114 | PF00782 | 0.505 |
MOD_CDC14_SPxK_1 | 50 | 53 | PF00782 | 0.607 |
MOD_CDK_SPK_2 | 404 | 409 | PF00069 | 0.578 |
MOD_CDK_SPxK_1 | 108 | 114 | PF00069 | 0.510 |
MOD_CDK_SPxK_1 | 47 | 53 | PF00069 | 0.610 |
MOD_CDK_SPxxK_3 | 47 | 54 | PF00069 | 0.643 |
MOD_CDK_SPxxK_3 | 486 | 493 | PF00069 | 0.637 |
MOD_CDK_SPxxK_3 | 510 | 517 | PF00069 | 0.610 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.702 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.547 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.738 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.709 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.492 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.536 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.738 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.625 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.681 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.712 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.625 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.667 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.495 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.613 |
MOD_CK1_1 | 486 | 492 | PF00069 | 0.666 |
MOD_CK1_1 | 526 | 532 | PF00069 | 0.625 |
MOD_CK1_1 | 557 | 563 | PF00069 | 0.583 |
MOD_CK1_1 | 597 | 603 | PF00069 | 0.404 |
MOD_CK1_1 | 677 | 683 | PF00069 | 0.372 |
MOD_CK1_1 | 896 | 902 | PF00069 | 0.585 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.663 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.615 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.607 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.601 |
MOD_CK2_1 | 536 | 542 | PF00069 | 0.685 |
MOD_CK2_1 | 597 | 603 | PF00069 | 0.404 |
MOD_CK2_1 | 766 | 772 | PF00069 | 0.464 |
MOD_CK2_1 | 870 | 876 | PF00069 | 0.260 |
MOD_CK2_1 | 896 | 902 | PF00069 | 0.585 |
MOD_Cter_Amidation | 215 | 218 | PF01082 | 0.642 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.530 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.702 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.615 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.467 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.538 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.557 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.616 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.615 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.626 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.662 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.649 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.598 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.665 |
MOD_GlcNHglycan | 556 | 559 | PF01048 | 0.615 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.698 |
MOD_GlcNHglycan | 728 | 731 | PF01048 | 0.347 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.652 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.668 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.584 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.617 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.614 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.568 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.610 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.814 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.776 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.672 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.596 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.589 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.609 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.582 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.605 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.629 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.745 |
MOD_GSK3_1 | 692 | 699 | PF00069 | 0.293 |
MOD_GSK3_1 | 780 | 787 | PF00069 | 0.275 |
MOD_GSK3_1 | 896 | 903 | PF00069 | 0.591 |
MOD_N-GLC_1 | 359 | 364 | PF02516 | 0.584 |
MOD_N-GLC_1 | 392 | 397 | PF02516 | 0.643 |
MOD_N-GLC_1 | 457 | 462 | PF02516 | 0.573 |
MOD_N-GLC_1 | 565 | 570 | PF02516 | 0.560 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.744 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.701 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.688 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.583 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.584 |
MOD_NEK2_1 | 520 | 525 | PF00069 | 0.651 |
MOD_NEK2_1 | 565 | 570 | PF00069 | 0.545 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.535 |
MOD_NEK2_1 | 639 | 644 | PF00069 | 0.272 |
MOD_NEK2_1 | 692 | 697 | PF00069 | 0.289 |
MOD_NEK2_1 | 739 | 744 | PF00069 | 0.319 |
MOD_NEK2_1 | 780 | 785 | PF00069 | 0.338 |
MOD_PIKK_1 | 119 | 125 | PF00454 | 0.707 |
MOD_PIKK_1 | 217 | 223 | PF00454 | 0.629 |
MOD_PIKK_1 | 30 | 36 | PF00454 | 0.753 |
MOD_PIKK_1 | 388 | 394 | PF00454 | 0.703 |
MOD_PIKK_1 | 461 | 467 | PF00454 | 0.483 |
MOD_PIKK_1 | 603 | 609 | PF00454 | 0.372 |
MOD_PIKK_1 | 896 | 902 | PF00454 | 0.585 |
MOD_PIKK_1 | 9 | 15 | PF00454 | 0.525 |
MOD_PK_1 | 588 | 594 | PF00069 | 0.372 |
MOD_PKA_1 | 217 | 223 | PF00069 | 0.667 |
MOD_PKA_1 | 291 | 297 | PF00069 | 0.584 |
MOD_PKA_1 | 588 | 594 | PF00069 | 0.372 |
MOD_PKA_1 | 870 | 876 | PF00069 | 0.326 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.670 |
MOD_PKA_2 | 331 | 337 | PF00069 | 0.631 |
MOD_PKA_2 | 439 | 445 | PF00069 | 0.559 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.668 |
MOD_PKA_2 | 588 | 594 | PF00069 | 0.428 |
MOD_PKA_2 | 836 | 842 | PF00069 | 0.403 |
MOD_PKA_2 | 870 | 876 | PF00069 | 0.277 |
MOD_Plk_1 | 410 | 416 | PF00069 | 0.564 |
MOD_Plk_1 | 457 | 463 | PF00069 | 0.573 |
MOD_Plk_1 | 565 | 571 | PF00069 | 0.572 |
MOD_Plk_1 | 617 | 623 | PF00069 | 0.384 |
MOD_Plk_2-3 | 141 | 147 | PF00069 | 0.720 |
MOD_Plk_2-3 | 309 | 315 | PF00069 | 0.524 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.693 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.686 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.613 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.482 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.585 |
MOD_Plk_4 | 588 | 594 | PF00069 | 0.420 |
MOD_Plk_4 | 597 | 603 | PF00069 | 0.363 |
MOD_Plk_4 | 647 | 653 | PF00069 | 0.366 |
MOD_Plk_4 | 780 | 786 | PF00069 | 0.272 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.636 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.803 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.692 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.780 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.654 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.575 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.600 |
MOD_ProDKin_1 | 486 | 492 | PF00069 | 0.768 |
MOD_ProDKin_1 | 504 | 510 | PF00069 | 0.536 |
MOD_ProDKin_1 | 766 | 772 | PF00069 | 0.436 |
MOD_ProDKin_1 | 784 | 790 | PF00069 | 0.209 |
MOD_ProDKin_1 | 893 | 899 | PF00069 | 0.545 |
MOD_ProDKin_1 | 900 | 906 | PF00069 | 0.629 |
MOD_SUMO_for_1 | 633 | 636 | PF00179 | 0.372 |
MOD_SUMO_rev_2 | 422 | 431 | PF00179 | 0.594 |
MOD_SUMO_rev_2 | 47 | 55 | PF00179 | 0.692 |
MOD_SUMO_rev_2 | 603 | 612 | PF00179 | 0.289 |
MOD_SUMO_rev_2 | 729 | 737 | PF00179 | 0.289 |
TRG_ENDOCYTIC_2 | 602 | 605 | PF00928 | 0.308 |
TRG_ER_diArg_1 | 207 | 210 | PF00400 | 0.635 |
TRG_ER_diArg_1 | 277 | 279 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 587 | 589 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 681 | 683 | PF00400 | 0.289 |
TRG_NES_CRM1_1 | 317 | 333 | PF08389 | 0.513 |
TRG_NES_CRM1_1 | 567 | 583 | PF08389 | 0.598 |
TRG_NES_CRM1_1 | 807 | 817 | PF08389 | 0.392 |
TRG_NLS_MonoExtN_4 | 866 | 873 | PF00514 | 0.322 |
TRG_Pf-PMV_PEXEL_1 | 888 | 892 | PF00026 | 0.476 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NSX9 | Trypanosomatidae | 43% | 96% |
A0A3R7M724 | Trypanosoma rangeli | 43% | 100% |
A0A3S5H705 | Leishmania donovani | 90% | 100% |
A4HXC3 | Leishmania infantum | 93% | 100% |
C9ZU16 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AI55 | Leishmania braziliensis | 63% | 88% |
E9AR18 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 99% |
V5B639 | Trypanosoma cruzi | 43% | 100% |