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: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 6, no: 9 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005795 | Golgi stack | 4 | 2 |
GO:0031984 | organelle subcompartment | 2 | 2 |
GO:0098791 | Golgi apparatus subcompartment | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
GO:0005737 | cytoplasm | 2 | 11 |
Related structures:
AlphaFold database: A4HFN1
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 16 |
GO:0016043 | cellular component organization | 3 | 16 |
GO:0022411 | cellular component disassembly | 4 | 16 |
GO:0032984 | protein-containing complex disassembly | 5 | 16 |
GO:0035494 | SNARE complex disassembly | 6 | 16 |
GO:0043933 | protein-containing complex organization | 4 | 16 |
GO:0071840 | cellular component organization or biogenesis | 2 | 16 |
GO:0006810 | transport | 3 | 13 |
GO:0006891 | intra-Golgi vesicle-mediated transport | 6 | 2 |
GO:0006892 | post-Golgi vesicle-mediated transport | 6 | 2 |
GO:0006893 | Golgi to plasma membrane transport | 5 | 2 |
GO:0008104 | protein localization | 4 | 13 |
GO:0015031 | protein transport | 4 | 13 |
GO:0016192 | vesicle-mediated transport | 4 | 2 |
GO:0033036 | macromolecule localization | 2 | 13 |
GO:0043001 | Golgi to plasma membrane protein transport | 5 | 2 |
GO:0045184 | establishment of protein localization | 3 | 13 |
GO:0048193 | Golgi vesicle transport | 5 | 2 |
GO:0051179 | localization | 1 | 13 |
GO:0051234 | establishment of localization | 2 | 13 |
GO:0051641 | cellular localization | 2 | 13 |
GO:0051668 | localization within membrane | 3 | 2 |
GO:0061951 | establishment of protein localization to plasma membrane | 5 | 2 |
GO:0070727 | cellular macromolecule localization | 3 | 13 |
GO:0071702 | organic substance transport | 4 | 13 |
GO:0071705 | nitrogen compound transport | 4 | 13 |
GO:0072657 | protein localization to membrane | 4 | 2 |
GO:0072659 | protein localization to plasma membrane | 5 | 2 |
GO:0090150 | establishment of protein localization to membrane | 4 | 2 |
GO:0098876 | vesicle-mediated transport to the plasma membrane | 4 | 2 |
GO:1990778 | protein localization to cell periphery | 5 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 16 |
GO:0003824 | catalytic activity | 1 | 16 |
GO:0005488 | binding | 1 | 16 |
GO:0005524 | ATP binding | 5 | 16 |
GO:0016462 | pyrophosphatase activity | 5 | 16 |
GO:0016787 | hydrolase activity | 2 | 16 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 16 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 16 |
GO:0016887 | ATP hydrolysis activity | 7 | 16 |
GO:0017076 | purine nucleotide binding | 4 | 16 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 16 |
GO:0030554 | adenyl nucleotide binding | 5 | 16 |
GO:0032553 | ribonucleotide binding | 3 | 16 |
GO:0032555 | purine ribonucleotide binding | 4 | 16 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 16 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 16 |
GO:0036094 | small molecule binding | 2 | 16 |
GO:0043167 | ion binding | 2 | 16 |
GO:0043168 | anion binding | 3 | 16 |
GO:0097159 | organic cyclic compound binding | 2 | 16 |
GO:0097367 | carbohydrate derivative binding | 2 | 16 |
GO:1901265 | nucleoside phosphate binding | 3 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
GO:0043169 | cation binding | 3 | 13 |
GO:0046872 | metal ion binding | 4 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 101 | 105 | PF00656 | 0.592 |
CLV_C14_Caspase3-7 | 454 | 458 | PF00656 | 0.357 |
CLV_C14_Caspase3-7 | 587 | 591 | PF00656 | 0.501 |
CLV_MEL_PAP_1 | 582 | 588 | PF00089 | 0.496 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.708 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 431 | 433 | PF00675 | 0.290 |
CLV_NRD_NRD_1 | 554 | 556 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 715 | 717 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 844 | 846 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 953 | 955 | PF00675 | 0.426 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.708 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 663 | 665 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 715 | 717 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 844 | 846 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 953 | 955 | PF00082 | 0.319 |
CLV_PCSK_PC1ET2_1 | 235 | 237 | PF00082 | 0.605 |
CLV_PCSK_PC1ET2_1 | 296 | 298 | PF00082 | 0.518 |
CLV_PCSK_PC1ET2_1 | 663 | 665 | PF00082 | 0.543 |
CLV_PCSK_PC7_1 | 190 | 196 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 622 | 626 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 628 | 632 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 660 | 664 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 677 | 681 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 698 | 702 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 731 | 735 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 768 | 772 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 876 | 880 | PF00082 | 0.375 |
DEG_APCC_DBOX_1 | 304 | 312 | PF00400 | 0.406 |
DEG_APCC_DBOX_1 | 461 | 469 | PF00400 | 0.422 |
DEG_APCC_DBOX_1 | 84 | 92 | PF00400 | 0.409 |
DEG_ODPH_VHL_1 | 518 | 529 | PF01847 | 0.423 |
DEG_SPOP_SBC_1 | 819 | 823 | PF00917 | 0.443 |
DOC_CDC14_PxL_1 | 308 | 316 | PF14671 | 0.487 |
DOC_CKS1_1 | 561 | 566 | PF01111 | 0.498 |
DOC_CYCLIN_RxL_1 | 108 | 116 | PF00134 | 0.630 |
DOC_CYCLIN_RxL_1 | 339 | 351 | PF00134 | 0.206 |
DOC_CYCLIN_RxL_1 | 765 | 773 | PF00134 | 0.422 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 341 | 350 | PF00134 | 0.422 |
DOC_MAPK_gen_1 | 208 | 215 | PF00069 | 0.623 |
DOC_MAPK_gen_1 | 412 | 421 | PF00069 | 0.338 |
DOC_MAPK_gen_1 | 460 | 468 | PF00069 | 0.371 |
DOC_MAPK_gen_1 | 483 | 493 | PF00069 | 0.336 |
DOC_MAPK_MEF2A_6 | 208 | 215 | PF00069 | 0.580 |
DOC_MAPK_MEF2A_6 | 412 | 421 | PF00069 | 0.368 |
DOC_MAPK_MEF2A_6 | 462 | 470 | PF00069 | 0.336 |
DOC_MAPK_MEF2A_6 | 486 | 493 | PF00069 | 0.336 |
DOC_MAPK_RevD_3 | 416 | 432 | PF00069 | 0.373 |
DOC_PP1_RVXF_1 | 233 | 240 | PF00149 | 0.581 |
DOC_PP2B_LxvP_1 | 250 | 253 | PF13499 | 0.635 |
DOC_PP4_FxxP_1 | 517 | 520 | PF00568 | 0.525 |
DOC_SPAK_OSR1_1 | 486 | 490 | PF12202 | 0.352 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.401 |
DOC_USP7_MATH_1 | 406 | 410 | PF00917 | 0.206 |
DOC_USP7_MATH_1 | 528 | 532 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 797 | 801 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.541 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.206 |
DOC_WW_Pin1_4 | 560 | 565 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 606 | 611 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 786 | 791 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 910 | 915 | PF00397 | 0.463 |
LIG_14-3-3_CanoR_1 | 179 | 184 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 202 | 207 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 236 | 240 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 355 | 359 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 544 | 550 | PF00244 | 0.351 |
LIG_14-3-3_CanoR_1 | 664 | 672 | PF00244 | 0.323 |
LIG_14-3-3_CanoR_1 | 67 | 76 | PF00244 | 0.709 |
LIG_14-3-3_CanoR_1 | 710 | 717 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 808 | 812 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 838 | 843 | PF00244 | 0.401 |
LIG_14-3-3_CanoR_1 | 85 | 89 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 880 | 886 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 953 | 963 | PF00244 | 0.483 |
LIG_Actin_WH2_2 | 200 | 216 | PF00022 | 0.652 |
LIG_Actin_WH2_2 | 362 | 379 | PF00022 | 0.422 |
LIG_Actin_WH2_2 | 467 | 485 | PF00022 | 0.337 |
LIG_Actin_WH2_2 | 778 | 794 | PF00022 | 0.420 |
LIG_Actin_WH2_2 | 830 | 846 | PF00022 | 0.540 |
LIG_AP2alpha_2 | 273 | 275 | PF02296 | 0.528 |
LIG_APCC_ABBA_1 | 505 | 510 | PF00400 | 0.479 |
LIG_BIR_III_4 | 895 | 899 | PF00653 | 0.403 |
LIG_BRCT_BRCA1_1 | 147 | 151 | PF00533 | 0.529 |
LIG_BRCT_BRCA1_1 | 530 | 534 | PF00533 | 0.476 |
LIG_BRCT_BRCA1_1 | 951 | 955 | PF00533 | 0.582 |
LIG_CaM_IQ_9 | 617 | 633 | PF13499 | 0.326 |
LIG_CtBP_PxDLS_1 | 870 | 874 | PF00389 | 0.444 |
LIG_eIF4E_1 | 554 | 560 | PF01652 | 0.598 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.736 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.641 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.405 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.297 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.337 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.381 |
LIG_FHA_1 | 647 | 653 | PF00498 | 0.507 |
LIG_FHA_1 | 664 | 670 | PF00498 | 0.533 |
LIG_FHA_1 | 678 | 684 | PF00498 | 0.560 |
LIG_FHA_1 | 819 | 825 | PF00498 | 0.469 |
LIG_FHA_1 | 987 | 993 | PF00498 | 0.699 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.721 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.531 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.523 |
LIG_FHA_2 | 521 | 527 | PF00498 | 0.301 |
LIG_FHA_2 | 614 | 620 | PF00498 | 0.479 |
LIG_FHA_2 | 640 | 646 | PF00498 | 0.493 |
LIG_FHA_2 | 897 | 903 | PF00498 | 0.557 |
LIG_GBD_Chelix_1 | 342 | 350 | PF00786 | 0.395 |
LIG_GBD_Chelix_1 | 466 | 474 | PF00786 | 0.330 |
LIG_LIR_Apic_2 | 514 | 520 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 238 | 247 | PF02991 | 0.585 |
LIG_LIR_Gen_1 | 284 | 295 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 423 | 429 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 548 | 554 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 705 | 712 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 748 | 757 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 877 | 886 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 929 | 939 | PF02991 | 0.447 |
LIG_LIR_LC3C_4 | 464 | 468 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 198 | 204 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 238 | 242 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 284 | 290 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 301 | 306 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 378 | 383 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 423 | 428 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 548 | 552 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 705 | 709 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 748 | 753 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 853 | 857 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 872 | 878 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 941 | 946 | PF02991 | 0.531 |
LIG_MAD2 | 137 | 145 | PF02301 | 0.598 |
LIG_MYND_1 | 312 | 316 | PF01753 | 0.563 |
LIG_NRBOX | 766 | 772 | PF00104 | 0.462 |
LIG_PCNA_PIPBox_1 | 244 | 253 | PF02747 | 0.617 |
LIG_PCNA_yPIPBox_3 | 106 | 119 | PF02747 | 0.496 |
LIG_PCNA_yPIPBox_3 | 243 | 251 | PF02747 | 0.612 |
LIG_Pex14_2 | 303 | 307 | PF04695 | 0.504 |
LIG_Pex14_2 | 425 | 429 | PF04695 | 0.395 |
LIG_RPA_C_Fungi | 949 | 961 | PF08784 | 0.308 |
LIG_SH2_CRK | 201 | 205 | PF00017 | 0.613 |
LIG_SH2_CRK | 332 | 336 | PF00017 | 0.416 |
LIG_SH2_CRK | 445 | 449 | PF00017 | 0.290 |
LIG_SH2_CRK | 549 | 553 | PF00017 | 0.499 |
LIG_SH2_CRK | 750 | 754 | PF00017 | 0.383 |
LIG_SH2_SRC | 251 | 254 | PF00017 | 0.542 |
LIG_SH2_SRC | 383 | 386 | PF00017 | 0.326 |
LIG_SH2_STAP1 | 750 | 754 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.688 |
LIG_SH2_STAT5 | 711 | 714 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 920 | 923 | PF00017 | 0.610 |
LIG_SH2_STAT5 | 931 | 934 | PF00017 | 0.582 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.444 |
LIG_SH3_3 | 178 | 184 | PF00018 | 0.673 |
LIG_SH3_3 | 346 | 352 | PF00018 | 0.291 |
LIG_SH3_3 | 824 | 830 | PF00018 | 0.622 |
LIG_SH3_3 | 853 | 859 | PF00018 | 0.474 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.490 |
LIG_SUMO_SIM_anti_2 | 15 | 20 | PF11976 | 0.523 |
LIG_SUMO_SIM_anti_2 | 22 | 27 | PF11976 | 0.492 |
LIG_SUMO_SIM_anti_2 | 353 | 360 | PF11976 | 0.334 |
LIG_SUMO_SIM_anti_2 | 451 | 457 | PF11976 | 0.398 |
LIG_SUMO_SIM_anti_2 | 464 | 469 | PF11976 | 0.315 |
LIG_SUMO_SIM_par_1 | 17 | 22 | PF11976 | 0.672 |
LIG_SUMO_SIM_par_1 | 417 | 424 | PF11976 | 0.313 |
LIG_SUMO_SIM_par_1 | 451 | 457 | PF11976 | 0.308 |
LIG_SUMO_SIM_par_1 | 680 | 686 | PF11976 | 0.518 |
LIG_SUMO_SIM_par_1 | 743 | 749 | PF11976 | 0.414 |
LIG_SUMO_SIM_par_1 | 816 | 823 | PF11976 | 0.403 |
LIG_TRAF2_1 | 196 | 199 | PF00917 | 0.533 |
LIG_TRAF2_1 | 238 | 241 | PF00917 | 0.615 |
LIG_TRAF2_1 | 282 | 285 | PF00917 | 0.507 |
LIG_TRAF2_1 | 389 | 392 | PF00917 | 0.326 |
LIG_TYR_ITIM | 547 | 552 | PF00017 | 0.500 |
LIG_UBA3_1 | 452 | 460 | PF00899 | 0.413 |
LIG_WRC_WIRS_1 | 875 | 880 | PF05994 | 0.504 |
MOD_CDC14_SPxK_1 | 789 | 792 | PF00782 | 0.451 |
MOD_CDC14_SPxK_1 | 913 | 916 | PF00782 | 0.450 |
MOD_CDK_SPxK_1 | 786 | 792 | PF00069 | 0.444 |
MOD_CDK_SPxK_1 | 910 | 916 | PF00069 | 0.463 |
MOD_CDK_SPxxK_3 | 348 | 355 | PF00069 | 0.206 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.474 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.615 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.206 |
MOD_CK1_1 | 398 | 404 | PF00069 | 0.210 |
MOD_CK1_1 | 436 | 442 | PF00069 | 0.368 |
MOD_CK1_1 | 545 | 551 | PF00069 | 0.437 |
MOD_CK1_1 | 602 | 608 | PF00069 | 0.690 |
MOD_CK1_1 | 635 | 641 | PF00069 | 0.629 |
MOD_CK1_1 | 644 | 650 | PF00069 | 0.676 |
MOD_CK1_1 | 675 | 681 | PF00069 | 0.521 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.689 |
MOD_CK1_1 | 807 | 813 | PF00069 | 0.608 |
MOD_CK1_1 | 822 | 828 | PF00069 | 0.423 |
MOD_CK1_1 | 874 | 880 | PF00069 | 0.500 |
MOD_CK1_1 | 903 | 909 | PF00069 | 0.637 |
MOD_CK1_1 | 910 | 916 | PF00069 | 0.567 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.627 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.686 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.561 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.550 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.568 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.433 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.333 |
MOD_CK2_1 | 639 | 645 | PF00069 | 0.567 |
MOD_CK2_1 | 735 | 741 | PF00069 | 0.422 |
MOD_DYRK1A_RPxSP_1 | 348 | 352 | PF00069 | 0.206 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.423 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.655 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.553 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.554 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.506 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.415 |
MOD_GlcNHglycan | 38 | 42 | PF01048 | 0.505 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.346 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.295 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.367 |
MOD_GlcNHglycan | 437 | 442 | PF01048 | 0.315 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.441 |
MOD_GlcNHglycan | 534 | 537 | PF01048 | 0.418 |
MOD_GlcNHglycan | 544 | 547 | PF01048 | 0.399 |
MOD_GlcNHglycan | 573 | 576 | PF01048 | 0.791 |
MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.744 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.523 |
MOD_GlcNHglycan | 645 | 649 | PF01048 | 0.639 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.778 |
MOD_GlcNHglycan | 909 | 912 | PF01048 | 0.644 |
MOD_GlcNHglycan | 956 | 959 | PF01048 | 0.496 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.748 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.613 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.605 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.405 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.471 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.390 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.333 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.405 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.543 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.634 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.554 |
MOD_GSK3_1 | 668 | 675 | PF00069 | 0.362 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.628 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.375 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.498 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.654 |
MOD_GSK3_1 | 807 | 814 | PF00069 | 0.559 |
MOD_GSK3_1 | 818 | 825 | PF00069 | 0.417 |
MOD_GSK3_1 | 896 | 903 | PF00069 | 0.609 |
MOD_LATS_1 | 836 | 842 | PF00433 | 0.388 |
MOD_N-GLC_1 | 216 | 221 | PF02516 | 0.734 |
MOD_N-GLC_1 | 599 | 604 | PF02516 | 0.523 |
MOD_N-GLC_1 | 675 | 680 | PF02516 | 0.635 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.601 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.623 |
MOD_NEK2_1 | 603 | 608 | PF00069 | 0.702 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.417 |
MOD_NEK2_1 | 683 | 688 | PF00069 | 0.453 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.730 |
MOD_NEK2_1 | 818 | 823 | PF00069 | 0.340 |
MOD_NEK2_2 | 520 | 525 | PF00069 | 0.317 |
MOD_NEK2_2 | 763 | 768 | PF00069 | 0.326 |
MOD_NEK2_2 | 80 | 85 | PF00069 | 0.455 |
MOD_NEK2_2 | 859 | 864 | PF00069 | 0.437 |
MOD_PIKK_1 | 102 | 108 | PF00454 | 0.550 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.650 |
MOD_PIKK_1 | 179 | 185 | PF00454 | 0.646 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.688 |
MOD_PIKK_1 | 635 | 641 | PF00454 | 0.601 |
MOD_PK_1 | 202 | 208 | PF00069 | 0.510 |
MOD_PKA_1 | 235 | 241 | PF00069 | 0.463 |
MOD_PKA_1 | 663 | 669 | PF00069 | 0.580 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.440 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.627 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.725 |
MOD_PKA_2 | 235 | 241 | PF00069 | 0.694 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.368 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.574 |
MOD_PKA_2 | 584 | 590 | PF00069 | 0.500 |
MOD_PKA_2 | 663 | 669 | PF00069 | 0.515 |
MOD_PKA_2 | 807 | 813 | PF00069 | 0.601 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.409 |
MOD_PKA_2 | 879 | 885 | PF00069 | 0.367 |
MOD_PKA_2 | 959 | 965 | PF00069 | 0.518 |
MOD_PKB_1 | 430 | 438 | PF00069 | 0.308 |
MOD_Plk_1 | 520 | 526 | PF00069 | 0.526 |
MOD_Plk_1 | 599 | 605 | PF00069 | 0.522 |
MOD_Plk_1 | 632 | 638 | PF00069 | 0.601 |
MOD_Plk_1 | 675 | 681 | PF00069 | 0.471 |
MOD_Plk_1 | 704 | 710 | PF00069 | 0.422 |
MOD_Plk_1 | 882 | 888 | PF00069 | 0.388 |
MOD_Plk_1 | 900 | 906 | PF00069 | 0.559 |
MOD_Plk_2-3 | 901 | 907 | PF00069 | 0.620 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.635 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.409 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.336 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.336 |
MOD_Plk_4 | 448 | 454 | PF00069 | 0.310 |
MOD_Plk_4 | 632 | 638 | PF00069 | 0.530 |
MOD_Plk_4 | 668 | 674 | PF00069 | 0.419 |
MOD_Plk_4 | 797 | 803 | PF00069 | 0.759 |
MOD_Plk_4 | 823 | 829 | PF00069 | 0.486 |
MOD_Plk_4 | 838 | 844 | PF00069 | 0.367 |
MOD_Plk_4 | 926 | 932 | PF00069 | 0.554 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.471 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.545 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.206 |
MOD_ProDKin_1 | 560 | 566 | PF00069 | 0.494 |
MOD_ProDKin_1 | 606 | 612 | PF00069 | 0.688 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.695 |
MOD_ProDKin_1 | 786 | 792 | PF00069 | 0.628 |
MOD_ProDKin_1 | 910 | 916 | PF00069 | 0.463 |
MOD_SUMO_for_1 | 295 | 298 | PF00179 | 0.510 |
MOD_SUMO_for_1 | 630 | 633 | PF00179 | 0.631 |
MOD_SUMO_rev_2 | 228 | 237 | PF00179 | 0.593 |
TRG_AP2beta_CARGO_1 | 423 | 432 | PF09066 | 0.395 |
TRG_DiLeu_BaEn_2 | 501 | 507 | PF01217 | 0.491 |
TRG_DiLeu_BaLyEn_6 | 118 | 123 | PF01217 | 0.594 |
TRG_DiLeu_BaLyEn_6 | 130 | 135 | PF01217 | 0.469 |
TRG_DiLeu_BaLyEn_6 | 160 | 165 | PF01217 | 0.658 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.616 |
TRG_ENDOCYTIC_2 | 445 | 448 | PF00928 | 0.290 |
TRG_ENDOCYTIC_2 | 549 | 552 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 750 | 753 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 772 | 775 | PF00928 | 0.557 |
TRG_ENDOCYTIC_2 | 854 | 857 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 875 | 878 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 931 | 934 | PF00928 | 0.555 |
TRG_ER_diArg_1 | 118 | 120 | PF00400 | 0.711 |
TRG_ER_diArg_1 | 207 | 209 | PF00400 | 0.594 |
TRG_ER_diArg_1 | 303 | 305 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 429 | 432 | PF00400 | 0.291 |
TRG_ER_diArg_1 | 715 | 717 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 843 | 845 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 953 | 955 | PF00400 | 0.325 |
TRG_NLS_MonoExtN_4 | 411 | 416 | PF00514 | 0.206 |
TRG_Pf-PMV_PEXEL_1 | 111 | 115 | PF00026 | 0.584 |
TRG_Pf-PMV_PEXEL_1 | 348 | 353 | PF00026 | 0.342 |
TRG_Pf-PMV_PEXEL_1 | 525 | 530 | PF00026 | 0.541 |
TRG_Pf-PMV_PEXEL_1 | 622 | 626 | PF00026 | 0.351 |
TRG_Pf-PMV_PEXEL_1 | 715 | 719 | PF00026 | 0.353 |
TRG_Pf-PMV_PEXEL_1 | 768 | 773 | PF00026 | 0.409 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6X6 | Leptomonas seymouri | 63% | 98% |
A0A1X0P437 | Trypanosomatidae | 33% | 100% |
A0A3Q8IHJ2 | Leishmania donovani | 79% | 100% |
A0A3Q8IKK0 | Leishmania donovani | 34% | 100% |
A0A422MWC2 | Trypanosoma rangeli | 34% | 100% |
A4HYS3 | Leishmania infantum | 34% | 100% |
A4I2Q9 | Leishmania infantum | 79% | 100% |
D0A5W2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AD85 | Leishmania major | 79% | 99% |
E9AID2 | Leishmania braziliensis | 33% | 100% |
E9AUL9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9AZ09 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4QCW5 | Leishmania major | 33% | 100% |
V5AT58 | Trypanosoma cruzi | 37% | 100% |