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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005778 | peroxisomal membrane | 6 | 2 |
GO:0005829 | cytosol | 2 | 2 |
GO:0016020 | membrane | 2 | 2 |
GO:0031090 | organelle membrane | 3 | 2 |
GO:0031903 | microbody membrane | 5 | 2 |
GO:0042579 | microbody | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0098588 | bounding membrane of organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QF14
Term | Name | Level | Count |
---|---|---|---|
GO:0006605 | protein targeting | 5 | 2 |
GO:0006625 | protein targeting to peroxisome | 5 | 2 |
GO:0006810 | transport | 3 | 2 |
GO:0006886 | intracellular protein transport | 4 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007031 | peroxisome organization | 5 | 2 |
GO:0008104 | protein localization | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015031 | protein transport | 4 | 2 |
GO:0015919 | peroxisomal membrane transport | 5 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0016558 | protein import into peroxisome matrix | 5 | 2 |
GO:0033036 | macromolecule localization | 2 | 2 |
GO:0033365 | protein localization to organelle | 5 | 2 |
GO:0043574 | peroxisomal transport | 4 | 2 |
GO:0044743 | protein transmembrane import into intracellular organelle | 4 | 2 |
GO:0045184 | establishment of protein localization | 3 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0055085 | transmembrane transport | 2 | 2 |
GO:0065002 | intracellular protein transmembrane transport | 4 | 2 |
GO:0070727 | cellular macromolecule localization | 3 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071705 | nitrogen compound transport | 4 | 2 |
GO:0071806 | protein transmembrane transport | 3 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0072594 | establishment of protein localization to organelle | 4 | 2 |
GO:0072662 | protein localization to peroxisome | 6 | 2 |
GO:0072663 | establishment of protein localization to peroxisome | 5 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 12 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 12 |
GO:0016887 | ATP hydrolysis activity | 7 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 522 | 526 | PF00656 | 0.611 |
CLV_C14_Caspase3-7 | 536 | 540 | PF00656 | 0.482 |
CLV_C14_Caspase3-7 | 54 | 58 | PF00656 | 0.493 |
CLV_C14_Caspase3-7 | 747 | 751 | PF00656 | 0.315 |
CLV_C14_Caspase3-7 | 900 | 904 | PF00656 | 0.499 |
CLV_NRD_NRD_1 | 318 | 320 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 838 | 840 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 916 | 918 | PF00675 | 0.649 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 657 | 659 | PF00082 | 0.377 |
CLV_PCSK_KEX2_1 | 680 | 682 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 783 | 785 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 950 | 952 | PF00082 | 0.406 |
CLV_PCSK_PC1ET2_1 | 657 | 659 | PF00082 | 0.364 |
CLV_PCSK_PC1ET2_1 | 680 | 682 | PF00082 | 0.418 |
CLV_PCSK_PC1ET2_1 | 783 | 785 | PF00082 | 0.382 |
CLV_PCSK_PC1ET2_1 | 950 | 952 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.639 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 552 | 556 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 676 | 680 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 694 | 698 | PF00082 | 0.190 |
CLV_PCSK_SKI1_1 | 730 | 734 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 756 | 760 | PF00082 | 0.286 |
CLV_PCSK_SKI1_1 | 835 | 839 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 918 | 922 | PF00082 | 0.546 |
DEG_APCC_KENBOX_2 | 425 | 429 | PF00400 | 0.420 |
DEG_SCF_FBW7_1 | 161 | 168 | PF00400 | 0.565 |
DEG_SCF_FBW7_2 | 408 | 414 | PF00400 | 0.498 |
DOC_CDC14_PxL_1 | 663 | 671 | PF14671 | 0.509 |
DOC_CKS1_1 | 128 | 133 | PF01111 | 0.649 |
DOC_CKS1_1 | 408 | 413 | PF01111 | 0.492 |
DOC_CYCLIN_yCln2_LP_2 | 210 | 216 | PF00134 | 0.491 |
DOC_CYCLIN_yCln2_LP_2 | 804 | 810 | PF00134 | 0.346 |
DOC_MAPK_gen_1 | 342 | 352 | PF00069 | 0.551 |
DOC_MAPK_gen_1 | 657 | 668 | PF00069 | 0.367 |
DOC_MAPK_gen_1 | 676 | 686 | PF00069 | 0.390 |
DOC_MAPK_gen_1 | 814 | 823 | PF00069 | 0.329 |
DOC_MAPK_HePTP_8 | 765 | 777 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 333 | 340 | PF00069 | 0.570 |
DOC_MAPK_MEF2A_6 | 661 | 668 | PF00069 | 0.364 |
DOC_MAPK_MEF2A_6 | 737 | 745 | PF00069 | 0.315 |
DOC_MAPK_MEF2A_6 | 768 | 777 | PF00069 | 0.268 |
DOC_MAPK_MEF2A_6 | 917 | 924 | PF00069 | 0.426 |
DOC_MAPK_NFAT4_5 | 661 | 669 | PF00069 | 0.369 |
DOC_PP1_RVXF_1 | 513 | 519 | PF00149 | 0.347 |
DOC_PP1_RVXF_1 | 728 | 734 | PF00149 | 0.268 |
DOC_PP2B_LxvP_1 | 210 | 213 | PF13499 | 0.467 |
DOC_PP2B_LxvP_1 | 821 | 824 | PF13499 | 0.376 |
DOC_PP4_FxxP_1 | 441 | 444 | PF00568 | 0.537 |
DOC_PP4_FxxP_1 | 555 | 558 | PF00568 | 0.479 |
DOC_PP4_FxxP_1 | 686 | 689 | PF00568 | 0.268 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 615 | 619 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 867 | 871 | PF00917 | 0.318 |
DOC_USP7_MATH_1 | 897 | 901 | PF00917 | 0.577 |
DOC_USP7_MATH_2 | 219 | 225 | PF00917 | 0.526 |
DOC_USP7_UBL2_3 | 676 | 680 | PF12436 | 0.465 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 573 | 578 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 737 | 742 | PF00397 | 0.268 |
DOC_WW_Pin1_4 | 898 | 903 | PF00397 | 0.642 |
LIG_14-3-3_CanoR_1 | 123 | 131 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 16 | 23 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 279 | 288 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 312 | 321 | PF00244 | 0.648 |
LIG_14-3-3_CanoR_1 | 373 | 380 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 503 | 507 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 568 | 574 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 768 | 777 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 917 | 923 | PF00244 | 0.594 |
LIG_Actin_WH2_2 | 921 | 937 | PF00022 | 0.362 |
LIG_BIR_III_2 | 525 | 529 | PF00653 | 0.408 |
LIG_BIR_III_2 | 57 | 61 | PF00653 | 0.505 |
LIG_BIR_III_2 | 903 | 907 | PF00653 | 0.490 |
LIG_BIR_III_4 | 761 | 765 | PF00653 | 0.268 |
LIG_CaM_IQ_9 | 392 | 408 | PF13499 | 0.365 |
LIG_CaM_NSCaTE_8 | 276 | 283 | PF13499 | 0.659 |
LIG_Clathr_ClatBox_1 | 774 | 778 | PF01394 | 0.286 |
LIG_EVH1_1 | 86 | 90 | PF00568 | 0.550 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.614 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.603 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.571 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.646 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.545 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.448 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.464 |
LIG_FHA_1 | 582 | 588 | PF00498 | 0.325 |
LIG_FHA_1 | 680 | 686 | PF00498 | 0.429 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.529 |
LIG_FHA_1 | 888 | 894 | PF00498 | 0.626 |
LIG_FHA_2 | 162 | 168 | PF00498 | 0.618 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.758 |
LIG_FHA_2 | 481 | 487 | PF00498 | 0.406 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.632 |
LIG_FHA_2 | 534 | 540 | PF00498 | 0.551 |
LIG_FHA_2 | 586 | 592 | PF00498 | 0.471 |
LIG_FHA_2 | 824 | 830 | PF00498 | 0.363 |
LIG_FHA_2 | 859 | 865 | PF00498 | 0.323 |
LIG_FHA_2 | 937 | 943 | PF00498 | 0.465 |
LIG_GBD_Chelix_1 | 114 | 122 | PF00786 | 0.605 |
LIG_KLC1_Yacidic_2 | 285 | 290 | PF13176 | 0.540 |
LIG_LIR_Gen_1 | 588 | 596 | PF02991 | 0.397 |
LIG_LIR_Gen_1 | 632 | 642 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 179 | 184 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 20 | 26 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 208 | 214 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 215 | 220 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 56 | 62 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 588 | 592 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 632 | 638 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 864 | 868 | PF02991 | 0.437 |
LIG_LYPXL_yS_3 | 261 | 264 | PF13949 | 0.568 |
LIG_LYPXL_yS_3 | 59 | 62 | PF13949 | 0.641 |
LIG_MYND_1 | 667 | 671 | PF01753 | 0.398 |
LIG_NRBOX | 133 | 139 | PF00104 | 0.533 |
LIG_NRBOX | 515 | 521 | PF00104 | 0.264 |
LIG_SH2_CRK | 23 | 27 | PF00017 | 0.514 |
LIG_SH2_CRK | 398 | 402 | PF00017 | 0.426 |
LIG_SH2_CRK | 635 | 639 | PF00017 | 0.468 |
LIG_SH2_CRK | 687 | 691 | PF00017 | 0.315 |
LIG_SH2_GRB2like | 205 | 208 | PF00017 | 0.586 |
LIG_SH2_NCK_1 | 189 | 193 | PF00017 | 0.599 |
LIG_SH2_NCK_1 | 635 | 639 | PF00017 | 0.468 |
LIG_SH2_SRC | 211 | 214 | PF00017 | 0.470 |
LIG_SH2_SRC | 589 | 592 | PF00017 | 0.465 |
LIG_SH2_STAP1 | 205 | 209 | PF00017 | 0.524 |
LIG_SH2_STAP1 | 589 | 593 | PF00017 | 0.476 |
LIG_SH2_STAT3 | 34 | 37 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.729 |
LIG_SH2_STAT5 | 629 | 632 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 721 | 724 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 820 | 823 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 860 | 863 | PF00017 | 0.324 |
LIG_SH3_3 | 240 | 246 | PF00018 | 0.512 |
LIG_SH3_3 | 374 | 380 | PF00018 | 0.553 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.549 |
LIG_SH3_3 | 508 | 514 | PF00018 | 0.634 |
LIG_SH3_3 | 709 | 715 | PF00018 | 0.268 |
LIG_SH3_3 | 81 | 87 | PF00018 | 0.512 |
LIG_SH3_3 | 849 | 855 | PF00018 | 0.477 |
LIG_SH3_CIN85_PxpxPR_1 | 510 | 515 | PF14604 | 0.434 |
LIG_SUMO_SIM_anti_2 | 302 | 309 | PF11976 | 0.678 |
LIG_SUMO_SIM_anti_2 | 366 | 371 | PF11976 | 0.628 |
LIG_SUMO_SIM_anti_2 | 474 | 479 | PF11976 | 0.360 |
LIG_SUMO_SIM_anti_2 | 591 | 597 | PF11976 | 0.386 |
LIG_SUMO_SIM_anti_2 | 612 | 619 | PF11976 | 0.645 |
LIG_SUMO_SIM_par_1 | 591 | 597 | PF11976 | 0.478 |
LIG_SUMO_SIM_par_1 | 773 | 778 | PF11976 | 0.286 |
LIG_TRAF2_1 | 452 | 455 | PF00917 | 0.505 |
LIG_TRAF2_1 | 547 | 550 | PF00917 | 0.508 |
LIG_TRAF2_1 | 826 | 829 | PF00917 | 0.389 |
LIG_TRAF2_1 | 880 | 883 | PF00917 | 0.540 |
LIG_TRAF2_1 | 912 | 915 | PF00917 | 0.701 |
LIG_TYR_ITIM | 209 | 214 | PF00017 | 0.396 |
LIG_TYR_ITIM | 259 | 264 | PF00017 | 0.579 |
LIG_TYR_ITIM | 587 | 592 | PF00017 | 0.465 |
LIG_TYR_ITIM | 818 | 823 | PF00017 | 0.315 |
LIG_UBA3_1 | 831 | 835 | PF00899 | 0.411 |
LIG_WRC_WIRS_1 | 417 | 422 | PF05994 | 0.466 |
MOD_CDK_SPK_2 | 127 | 132 | PF00069 | 0.496 |
MOD_CDK_SPK_2 | 573 | 578 | PF00069 | 0.544 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.544 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.539 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.547 |
MOD_CK1_1 | 576 | 582 | PF00069 | 0.378 |
MOD_CK1_1 | 618 | 624 | PF00069 | 0.474 |
MOD_CK1_1 | 636 | 642 | PF00069 | 0.533 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.516 |
MOD_CK1_1 | 785 | 791 | PF00069 | 0.310 |
MOD_CK2_1 | 591 | 597 | PF00069 | 0.436 |
MOD_CK2_1 | 822 | 828 | PF00069 | 0.364 |
MOD_DYRK1A_RPxSP_1 | 407 | 411 | PF00069 | 0.438 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.569 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.570 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.698 |
MOD_GlcNHglycan | 221 | 226 | PF01048 | 0.575 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.588 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.652 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.614 |
MOD_GlcNHglycan | 344 | 348 | PF01048 | 0.564 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.576 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.691 |
MOD_GlcNHglycan | 789 | 792 | PF01048 | 0.389 |
MOD_GlcNHglycan | 842 | 846 | PF01048 | 0.406 |
MOD_GlcNHglycan | 848 | 852 | PF01048 | 0.363 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.527 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.638 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.601 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.414 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.423 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.349 |
MOD_GSK3_1 | 621 | 628 | PF00069 | 0.453 |
MOD_GSK3_1 | 629 | 636 | PF00069 | 0.392 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.639 |
MOD_GSK3_1 | 893 | 900 | PF00069 | 0.571 |
MOD_GSK3_1 | 949 | 956 | PF00069 | 0.511 |
MOD_N-GLC_1 | 328 | 333 | PF02516 | 0.474 |
MOD_N-GLC_1 | 42 | 47 | PF02516 | 0.693 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.518 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.651 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.662 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.718 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.474 |
MOD_NEK2_1 | 560 | 565 | PF00069 | 0.519 |
MOD_NEK2_1 | 637 | 642 | PF00069 | 0.446 |
MOD_NEK2_1 | 858 | 863 | PF00069 | 0.336 |
MOD_NEK2_1 | 893 | 898 | PF00069 | 0.620 |
MOD_NEK2_1 | 953 | 958 | PF00069 | 0.546 |
MOD_PIKK_1 | 190 | 196 | PF00454 | 0.619 |
MOD_PIKK_1 | 768 | 774 | PF00454 | 0.402 |
MOD_PKA_1 | 319 | 325 | PF00069 | 0.482 |
MOD_PKA_1 | 679 | 685 | PF00069 | 0.449 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.662 |
MOD_PKA_2 | 372 | 378 | PF00069 | 0.608 |
MOD_PKA_2 | 502 | 508 | PF00069 | 0.643 |
MOD_PKA_2 | 533 | 539 | PF00069 | 0.560 |
MOD_PKA_2 | 607 | 613 | PF00069 | 0.509 |
MOD_Plk_1 | 118 | 124 | PF00069 | 0.525 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.620 |
MOD_Plk_1 | 847 | 853 | PF00069 | 0.475 |
MOD_Plk_2-3 | 591 | 597 | PF00069 | 0.458 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.538 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.502 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.646 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.418 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.530 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.519 |
MOD_Plk_4 | 569 | 575 | PF00069 | 0.483 |
MOD_Plk_4 | 591 | 597 | PF00069 | 0.370 |
MOD_Plk_4 | 621 | 627 | PF00069 | 0.357 |
MOD_Plk_4 | 633 | 639 | PF00069 | 0.485 |
MOD_Plk_4 | 692 | 698 | PF00069 | 0.315 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.511 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.651 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.565 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.550 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.567 |
MOD_ProDKin_1 | 573 | 579 | PF00069 | 0.567 |
MOD_ProDKin_1 | 737 | 743 | PF00069 | 0.268 |
MOD_ProDKin_1 | 898 | 904 | PF00069 | 0.645 |
MOD_SUMO_for_1 | 656 | 659 | PF00179 | 0.356 |
MOD_SUMO_rev_2 | 914 | 920 | PF00179 | 0.610 |
TRG_DiLeu_BaEn_2 | 853 | 859 | PF01217 | 0.482 |
TRG_DiLeu_BaLyEn_6 | 512 | 517 | PF01217 | 0.306 |
TRG_DiLeu_BaLyEn_6 | 555 | 560 | PF01217 | 0.498 |
TRG_DiLeu_BaLyEn_6 | 727 | 732 | PF01217 | 0.268 |
TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.522 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 589 | 592 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.641 |
TRG_ENDOCYTIC_2 | 635 | 638 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.660 |
TRG_ENDOCYTIC_2 | 820 | 823 | PF00928 | 0.380 |
TRG_ENDOCYTIC_2 | 946 | 949 | PF00928 | 0.426 |
TRG_ER_diArg_1 | 405 | 407 | PF00400 | 0.403 |
TRG_ER_diArg_1 | 928 | 931 | PF00400 | 0.384 |
TRG_NES_CRM1_1 | 659 | 672 | PF08389 | 0.517 |
TRG_NLS_MonoExtN_4 | 676 | 683 | PF00514 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 16 | 20 | PF00026 | 0.588 |
TRG_Pf-PMV_PEXEL_1 | 658 | 662 | PF00026 | 0.372 |
TRG_Pf-PMV_PEXEL_1 | 730 | 734 | PF00026 | 0.268 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7Z4 | Leptomonas seymouri | 67% | 99% |
A0A1X0NZ72 | Trypanosomatidae | 41% | 100% |
A0A3S5H6W4 | Leishmania donovani | 94% | 100% |
A0A422NAC8 | Trypanosoma rangeli | 47% | 100% |
A4H8D3 | Leishmania braziliensis | 81% | 100% |
A4HFM9 | Leishmania braziliensis | 36% | 100% |
A4HWQ5 | Leishmania infantum | 94% | 100% |
C9ZPS5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 98% |
E9AQG2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5ARC8 | Trypanosoma cruzi | 43% | 100% |