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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000785 | chromatin | 2 | 1 |
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HEA7
Term | Name | Level | Count |
---|---|---|---|
GO:0006325 | chromatin organization | 4 | 1 |
GO:0006338 | chromatin remodeling | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 14 |
GO:0003824 | catalytic activity | 1 | 14 |
GO:0004386 | helicase activity | 2 | 9 |
GO:0005488 | binding | 1 | 14 |
GO:0005524 | ATP binding | 5 | 14 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 14 |
GO:0016491 | oxidoreductase activity | 2 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 14 |
GO:0030554 | adenyl nucleotide binding | 5 | 14 |
GO:0032553 | ribonucleotide binding | 3 | 14 |
GO:0032555 | purine ribonucleotide binding | 4 | 14 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 14 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 14 |
GO:0036094 | small molecule binding | 2 | 14 |
GO:0043167 | ion binding | 2 | 14 |
GO:0043168 | anion binding | 3 | 14 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0051213 | dioxygenase activity | 3 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 14 |
GO:0097367 | carbohydrate derivative binding | 2 | 14 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 14 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 14 |
GO:0140657 | ATP-dependent activity | 1 | 14 |
GO:0140658 | ATP-dependent chromatin remodeler activity | 3 | 14 |
GO:1901265 | nucleoside phosphate binding | 3 | 14 |
GO:1901363 | heterocyclic compound binding | 2 | 14 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003682 | chromatin binding | 2 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 1 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
GO:0016887 | ATP hydrolysis activity | 7 | 1 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 1 |
GO:0042393 | histone binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 545 | 549 | PF00656 | 0.420 |
CLV_C14_Caspase3-7 | 712 | 716 | PF00656 | 0.518 |
CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.279 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.258 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.220 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.270 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 640 | 642 | PF00675 | 0.406 |
CLV_PCSK_KEX2_1 | 18 | 20 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 307 | 309 | PF00082 | 0.259 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.239 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.270 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 802 | 804 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 812 | 814 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 882 | 884 | PF00082 | 0.419 |
CLV_PCSK_PC1ET2_1 | 18 | 20 | PF00082 | 0.709 |
CLV_PCSK_PC1ET2_1 | 307 | 309 | PF00082 | 0.256 |
CLV_PCSK_PC1ET2_1 | 312 | 314 | PF00082 | 0.238 |
CLV_PCSK_PC1ET2_1 | 44 | 46 | PF00082 | 0.563 |
CLV_PCSK_PC1ET2_1 | 482 | 484 | PF00082 | 0.457 |
CLV_PCSK_PC1ET2_1 | 802 | 804 | PF00082 | 0.576 |
CLV_PCSK_PC1ET2_1 | 812 | 814 | PF00082 | 0.581 |
CLV_PCSK_PC1ET2_1 | 882 | 884 | PF00082 | 0.365 |
CLV_PCSK_PC7_1 | 308 | 314 | PF00082 | 0.244 |
CLV_PCSK_PC7_1 | 45 | 51 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 172 | 176 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 282 | 286 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 338 | 342 | PF00082 | 0.229 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 681 | 685 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 733 | 737 | PF00082 | 0.545 |
DEG_APCC_DBOX_1 | 949 | 957 | PF00400 | 0.461 |
DEG_COP1_1 | 414 | 424 | PF00400 | 0.375 |
DEG_SPOP_SBC_1 | 27 | 31 | PF00917 | 0.728 |
DEG_SPOP_SBC_1 | 701 | 705 | PF00917 | 0.490 |
DOC_CKS1_1 | 120 | 125 | PF01111 | 0.326 |
DOC_CKS1_1 | 297 | 302 | PF01111 | 0.429 |
DOC_CKS1_1 | 86 | 91 | PF01111 | 0.511 |
DOC_CYCLIN_RxL_1 | 41 | 48 | PF00134 | 0.682 |
DOC_MAPK_DCC_7 | 950 | 958 | PF00069 | 0.460 |
DOC_MAPK_FxFP_2 | 366 | 369 | PF00069 | 0.420 |
DOC_MAPK_gen_1 | 289 | 297 | PF00069 | 0.429 |
DOC_MAPK_gen_1 | 307 | 318 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 399 | 409 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 618 | 627 | PF00069 | 0.250 |
DOC_MAPK_MEF2A_6 | 265 | 272 | PF00069 | 0.441 |
DOC_MAPK_MEF2A_6 | 311 | 320 | PF00069 | 0.522 |
DOC_MAPK_MEF2A_6 | 400 | 409 | PF00069 | 0.440 |
DOC_MAPK_NFAT4_5 | 402 | 410 | PF00069 | 0.422 |
DOC_MAPK_RevD_3 | 36 | 50 | PF00069 | 0.604 |
DOC_PP1_RVXF_1 | 517 | 524 | PF00149 | 0.453 |
DOC_PP2B_LxvP_1 | 38 | 41 | PF13499 | 0.634 |
DOC_PP2B_LxvP_1 | 407 | 410 | PF13499 | 0.420 |
DOC_PP4_FxxP_1 | 366 | 369 | PF00568 | 0.420 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 566 | 570 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 701 | 705 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 714 | 718 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 881 | 885 | PF00917 | 0.462 |
DOC_USP7_UBL2_3 | 690 | 694 | PF12436 | 0.502 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.393 |
DOC_WW_Pin1_4 | 296 | 301 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 669 | 674 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 697 | 702 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 761 | 766 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.602 |
LIG_14-3-3_CanoR_1 | 101 | 107 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 313 | 319 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 338 | 346 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 540 | 545 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 674 | 680 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 813 | 818 | PF00244 | 0.383 |
LIG_Actin_WH2_2 | 158 | 174 | PF00022 | 0.517 |
LIG_Actin_WH2_2 | 728 | 746 | PF00022 | 0.327 |
LIG_APCC_ABBAyCdc20_2 | 733 | 739 | PF00400 | 0.300 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.511 |
LIG_BIR_III_4 | 858 | 862 | PF00653 | 0.383 |
LIG_BIR_III_4 | 917 | 921 | PF00653 | 0.494 |
LIG_BRCT_BRCA1_1 | 567 | 571 | PF00533 | 0.420 |
LIG_BRCT_BRCA1_1 | 843 | 847 | PF00533 | 0.336 |
LIG_Clathr_ClatBox_1 | 302 | 306 | PF01394 | 0.444 |
LIG_Clathr_ClatBox_1 | 735 | 739 | PF01394 | 0.329 |
LIG_deltaCOP1_diTrp_1 | 359 | 366 | PF00928 | 0.420 |
LIG_DLG_GKlike_1 | 540 | 547 | PF00625 | 0.483 |
LIG_eIF4E_1 | 424 | 430 | PF01652 | 0.438 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.441 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.445 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.429 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.507 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.473 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.420 |
LIG_FHA_1 | 589 | 595 | PF00498 | 0.429 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.497 |
LIG_FHA_1 | 615 | 621 | PF00498 | 0.408 |
LIG_FHA_1 | 670 | 676 | PF00498 | 0.665 |
LIG_FHA_1 | 921 | 927 | PF00498 | 0.551 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.517 |
LIG_FHA_2 | 526 | 532 | PF00498 | 0.524 |
LIG_FHA_2 | 585 | 591 | PF00498 | 0.437 |
LIG_FHA_2 | 628 | 634 | PF00498 | 0.369 |
LIG_FHA_2 | 663 | 669 | PF00498 | 0.764 |
LIG_FHA_2 | 674 | 680 | PF00498 | 0.536 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.640 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.510 |
LIG_FHA_2 | 909 | 915 | PF00498 | 0.525 |
LIG_LIR_Apic_2 | 117 | 123 | PF02991 | 0.415 |
LIG_LIR_Apic_2 | 365 | 369 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 147 | 157 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 359 | 369 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 423 | 432 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 543 | 548 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 568 | 579 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 844 | 855 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 147 | 153 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 365 | 371 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 423 | 427 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 543 | 547 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 568 | 574 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 844 | 850 | PF02991 | 0.322 |
LIG_LYPXL_S_1 | 367 | 371 | PF13949 | 0.241 |
LIG_LYPXL_yS_3 | 368 | 371 | PF13949 | 0.483 |
LIG_MYND_1 | 91 | 95 | PF01753 | 0.510 |
LIG_NRBOX | 428 | 434 | PF00104 | 0.444 |
LIG_NRBOX | 59 | 65 | PF00104 | 0.457 |
LIG_PCNA_yPIPBox_3 | 419 | 433 | PF02747 | 0.530 |
LIG_PCNA_yPIPBox_3 | 610 | 623 | PF02747 | 0.502 |
LIG_Pex14_2 | 135 | 139 | PF04695 | 0.286 |
LIG_Pex14_2 | 153 | 157 | PF04695 | 0.482 |
LIG_Pex14_2 | 366 | 370 | PF04695 | 0.505 |
LIG_Pex14_2 | 595 | 599 | PF04695 | 0.483 |
LIG_REV1ctd_RIR_1 | 154 | 164 | PF16727 | 0.359 |
LIG_SH2_NCK_1 | 563 | 567 | PF00017 | 0.444 |
LIG_SH2_NCK_1 | 921 | 925 | PF00017 | 0.483 |
LIG_SH2_PTP2 | 395 | 398 | PF00017 | 0.483 |
LIG_SH2_PTP2 | 424 | 427 | PF00017 | 0.375 |
LIG_SH2_SRC | 375 | 378 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 395 | 398 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 424 | 427 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 505 | 508 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 644 | 647 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 854 | 857 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 887 | 890 | PF00017 | 0.295 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.640 |
LIG_SH3_3 | 294 | 300 | PF00018 | 0.441 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.548 |
LIG_SH3_3 | 376 | 382 | PF00018 | 0.503 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.469 |
LIG_SH3_3 | 775 | 781 | PF00018 | 0.381 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.682 |
LIG_SUMO_SIM_anti_2 | 527 | 534 | PF11976 | 0.430 |
LIG_SUMO_SIM_anti_2 | 53 | 64 | PF11976 | 0.599 |
LIG_SUMO_SIM_par_1 | 316 | 322 | PF11976 | 0.432 |
LIG_SUMO_SIM_par_1 | 428 | 434 | PF11976 | 0.573 |
LIG_SUMO_SIM_par_1 | 527 | 534 | PF11976 | 0.494 |
LIG_SUMO_SIM_par_1 | 55 | 66 | PF11976 | 0.504 |
LIG_SUMO_SIM_par_1 | 590 | 596 | PF11976 | 0.450 |
LIG_SUMO_SIM_par_1 | 954 | 960 | PF11976 | 0.456 |
LIG_TRAF2_1 | 437 | 440 | PF00917 | 0.444 |
LIG_TRAF2_1 | 630 | 633 | PF00917 | 0.302 |
LIG_TRAF2_1 | 969 | 972 | PF00917 | 0.496 |
LIG_TYR_ITIM | 393 | 398 | PF00017 | 0.335 |
LIG_UBA3_1 | 302 | 307 | PF00899 | 0.280 |
LIG_UBA3_1 | 509 | 514 | PF00899 | 0.393 |
LIG_WRC_WIRS_1 | 363 | 368 | PF05994 | 0.323 |
LIG_WW_3 | 409 | 413 | PF00397 | 0.305 |
LIG_WW_3 | 803 | 807 | PF00397 | 0.456 |
MOD_CDC14_SPxK_1 | 764 | 767 | PF00782 | 0.578 |
MOD_CDK_SPK_2 | 669 | 674 | PF00069 | 0.464 |
MOD_CDK_SPxK_1 | 761 | 767 | PF00069 | 0.623 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.568 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.286 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.319 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.393 |
MOD_CK1_1 | 524 | 530 | PF00069 | 0.306 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.562 |
MOD_CK1_1 | 700 | 706 | PF00069 | 0.697 |
MOD_CK1_1 | 717 | 723 | PF00069 | 0.650 |
MOD_CK1_1 | 898 | 904 | PF00069 | 0.501 |
MOD_CK1_1 | 939 | 945 | PF00069 | 0.550 |
MOD_CK2_1 | 627 | 633 | PF00069 | 0.347 |
MOD_CK2_1 | 707 | 713 | PF00069 | 0.762 |
MOD_CK2_1 | 954 | 960 | PF00069 | 0.586 |
MOD_Cter_Amidation | 800 | 803 | PF01082 | 0.332 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.633 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.377 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.292 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.194 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.336 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.717 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.280 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.275 |
MOD_GlcNHglycan | 498 | 502 | PF01048 | 0.336 |
MOD_GlcNHglycan | 719 | 722 | PF01048 | 0.690 |
MOD_GlcNHglycan | 725 | 728 | PF01048 | 0.569 |
MOD_GlcNHglycan | 745 | 748 | PF01048 | 0.398 |
MOD_GlcNHglycan | 806 | 809 | PF01048 | 0.490 |
MOD_GlcNHglycan | 858 | 862 | PF01048 | 0.628 |
MOD_GlcNHglycan | 902 | 905 | PF01048 | 0.612 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.647 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.293 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.293 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.686 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.321 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.349 |
MOD_GSK3_1 | 584 | 591 | PF00069 | 0.284 |
MOD_GSK3_1 | 669 | 676 | PF00069 | 0.634 |
MOD_GSK3_1 | 697 | 704 | PF00069 | 0.709 |
MOD_GSK3_1 | 715 | 722 | PF00069 | 0.756 |
MOD_GSK3_1 | 837 | 844 | PF00069 | 0.303 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.654 |
MOD_GSK3_1 | 895 | 902 | PF00069 | 0.444 |
MOD_N-GLC_1 | 257 | 262 | PF02516 | 0.183 |
MOD_N-GLC_1 | 473 | 478 | PF02516 | 0.406 |
MOD_N-GLC_1 | 524 | 529 | PF02516 | 0.246 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.611 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.415 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.249 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.292 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.264 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.388 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.255 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.319 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.280 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.650 |
MOD_NEK2_1 | 743 | 748 | PF00069 | 0.398 |
MOD_NEK2_1 | 786 | 791 | PF00069 | 0.357 |
MOD_NEK2_1 | 837 | 842 | PF00069 | 0.332 |
MOD_NEK2_1 | 857 | 862 | PF00069 | 0.442 |
MOD_NEK2_1 | 896 | 901 | PF00069 | 0.476 |
MOD_NEK2_2 | 191 | 196 | PF00069 | 0.414 |
MOD_NEK2_2 | 566 | 571 | PF00069 | 0.335 |
MOD_NEK2_2 | 881 | 886 | PF00069 | 0.448 |
MOD_OFUCOSY | 885 | 890 | PF10250 | 0.438 |
MOD_PIKK_1 | 473 | 479 | PF00454 | 0.614 |
MOD_PIKK_1 | 63 | 69 | PF00454 | 0.653 |
MOD_PKA_1 | 338 | 344 | PF00069 | 0.276 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.401 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.508 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.299 |
MOD_PKA_2 | 398 | 404 | PF00069 | 0.246 |
MOD_PKA_2 | 662 | 668 | PF00069 | 0.704 |
MOD_PKA_2 | 673 | 679 | PF00069 | 0.411 |
MOD_PKA_2 | 708 | 714 | PF00069 | 0.579 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.499 |
MOD_PKA_2 | 743 | 749 | PF00069 | 0.527 |
MOD_PKA_2 | 867 | 873 | PF00069 | 0.503 |
MOD_PKB_1 | 280 | 288 | PF00069 | 0.256 |
MOD_PKB_1 | 661 | 669 | PF00069 | 0.503 |
MOD_Plk_1 | 58 | 64 | PF00069 | 0.380 |
MOD_Plk_1 | 75 | 81 | PF00069 | 0.487 |
MOD_Plk_1 | 939 | 945 | PF00069 | 0.694 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.340 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.335 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.330 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.394 |
MOD_Plk_4 | 505 | 511 | PF00069 | 0.299 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.380 |
MOD_Plk_4 | 588 | 594 | PF00069 | 0.259 |
MOD_Plk_4 | 703 | 709 | PF00069 | 0.572 |
MOD_Plk_4 | 954 | 960 | PF00069 | 0.664 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.392 |
MOD_ProDKin_1 | 296 | 302 | PF00069 | 0.259 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.292 |
MOD_ProDKin_1 | 669 | 675 | PF00069 | 0.508 |
MOD_ProDKin_1 | 697 | 703 | PF00069 | 0.468 |
MOD_ProDKin_1 | 761 | 767 | PF00069 | 0.623 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.623 |
MOD_SUMO_rev_2 | 875 | 881 | PF00179 | 0.433 |
TRG_DiLeu_BaEn_1 | 359 | 364 | PF01217 | 0.259 |
TRG_DiLeu_BaEn_1 | 59 | 64 | PF01217 | 0.454 |
TRG_DiLeu_BaEn_2 | 200 | 206 | PF01217 | 0.385 |
TRG_DiLeu_BaLyEn_6 | 42 | 47 | PF01217 | 0.596 |
TRG_DiLeu_BaLyEn_6 | 462 | 467 | PF01217 | 0.354 |
TRG_DiLeu_BaLyEn_6 | 781 | 786 | PF01217 | 0.402 |
TRG_DiLeu_BaLyEn_6 | 860 | 865 | PF01217 | 0.505 |
TRG_ENDOCYTIC_2 | 368 | 371 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 395 | 398 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 424 | 427 | PF00928 | 0.251 |
TRG_ENDOCYTIC_2 | 544 | 547 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 854 | 857 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 871 | 874 | PF00928 | 0.386 |
TRG_ER_diArg_1 | 279 | 282 | PF00400 | 0.280 |
TRG_ER_diArg_1 | 310 | 313 | PF00400 | 0.265 |
TRG_ER_diArg_1 | 398 | 400 | PF00400 | 0.316 |
TRG_ER_diArg_1 | 661 | 664 | PF00400 | 0.522 |
TRG_NES_CRM1_1 | 169 | 185 | PF08389 | 0.330 |
TRG_NLS_MonoExtN_4 | 308 | 315 | PF00514 | 0.280 |
TRG_Pf-PMV_PEXEL_1 | 465 | 469 | PF00026 | 0.366 |
TRG_Pf-PMV_PEXEL_1 | 853 | 858 | PF00026 | 0.453 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE28 | Leptomonas seymouri | 69% | 96% |
A0A0S4JP66 | Bodo saltans | 43% | 87% |
A0A1X0NY53 | Trypanosomatidae | 55% | 99% |
A0A3S7WZF4 | Leishmania donovani | 84% | 93% |
A0A422P4R6 | Trypanosoma rangeli | 57% | 100% |
A4HGB7 | Leishmania braziliensis | 24% | 100% |
A4I1Q3 | Leishmania infantum | 84% | 93% |
C9ZKA7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AXT7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 93% |
E9AZN8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
Q4Q9N4 | Leishmania major | 83% | 100% |
V5DIY2 | Trypanosoma cruzi | 57% | 100% |