Nucleic acid binding, Uncharacterized
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | yes | yes: 4 |
Forrest at al. (procyclic) | yes | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 15 |
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. | yes | yes: 12 |
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 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
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 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A0A3S7WZJ4
Term | Name | Level | Count |
---|---|---|---|
GO:0006325 | chromatin organization | 4 | 1 |
GO:0006338 | chromatin remodeling | 5 | 1 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031056 | regulation of histone modification | 7 | 1 |
GO:0031058 | obsolete positive regulation of histone modification | 8 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0031399 | regulation of protein modification process | 6 | 1 |
GO:0031401 | positive regulation of protein modification process | 7 | 1 |
GO:0035065 | regulation of histone acetylation | 8 | 1 |
GO:0035066 | positive regulation of histone acetylation | 9 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051246 | regulation of protein metabolic process | 5 | 1 |
GO:0051247 | positive regulation of protein metabolic process | 6 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1901983 | regulation of protein acetylation | 7 | 1 |
GO:1901985 | positive regulation of protein acetylation | 8 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:2000756 | regulation of peptidyl-lysine acetylation | 8 | 1 |
GO:2000758 | positive regulation of peptidyl-lysine acetylation | 9 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003682 | chromatin binding | 2 | 1 |
GO:0003712 | transcription coregulator activity | 2 | 1 |
GO:0003713 | transcription coactivator activity | 3 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0140110 | transcription regulator activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.447 |
CLV_NRD_NRD_1 | 484 | 486 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 546 | 548 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 554 | 556 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 582 | 584 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 632 | 634 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 655 | 657 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 747 | 749 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 759 | 761 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 843 | 845 | PF00675 | 0.521 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 459 | 461 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 484 | 486 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 554 | 556 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 632 | 634 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 747 | 749 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 843 | 845 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.425 |
CLV_PCSK_PC1ET2_1 | 405 | 407 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 413 | 415 | PF00082 | 0.526 |
CLV_PCSK_PC1ET2_1 | 459 | 461 | PF00082 | 0.515 |
CLV_PCSK_PC1ET2_1 | 96 | 98 | PF00082 | 0.450 |
CLV_PCSK_PC7_1 | 92 | 98 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 709 | 713 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 761 | 765 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 843 | 847 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 849 | 853 | PF00082 | 0.447 |
CLV_PCSK_SKI1_1 | 889 | 893 | PF00082 | 0.566 |
DEG_APCC_DBOX_1 | 245 | 253 | PF00400 | 0.508 |
DEG_APCC_DBOX_1 | 264 | 272 | PF00400 | 0.474 |
DEG_APCC_KENBOX_2 | 679 | 683 | PF00400 | 0.576 |
DOC_CYCLIN_RxL_1 | 262 | 269 | PF00134 | 0.528 |
DOC_CYCLIN_RxL_1 | 517 | 528 | PF00134 | 0.584 |
DOC_MAPK_gen_1 | 278 | 286 | PF00069 | 0.459 |
DOC_MAPK_gen_1 | 405 | 412 | PF00069 | 0.649 |
DOC_MAPK_gen_1 | 458 | 467 | PF00069 | 0.629 |
DOC_MAPK_gen_1 | 632 | 640 | PF00069 | 0.579 |
DOC_MAPK_gen_1 | 643 | 650 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 747 | 756 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 757 | 766 | PF00069 | 0.407 |
DOC_MAPK_gen_1 | 79 | 87 | PF00069 | 0.403 |
DOC_MAPK_gen_1 | 886 | 894 | PF00069 | 0.448 |
DOC_MAPK_HePTP_8 | 754 | 766 | PF00069 | 0.386 |
DOC_MAPK_MEF2A_6 | 156 | 163 | PF00069 | 0.472 |
DOC_MAPK_MEF2A_6 | 210 | 218 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 278 | 286 | PF00069 | 0.459 |
DOC_MAPK_MEF2A_6 | 747 | 756 | PF00069 | 0.470 |
DOC_MAPK_MEF2A_6 | 757 | 766 | PF00069 | 0.407 |
DOC_PP2B_LxvP_1 | 282 | 285 | PF13499 | 0.475 |
DOC_PP4_FxxP_1 | 33 | 36 | PF00568 | 0.446 |
DOC_PP4_MxPP_1 | 34 | 37 | PF00568 | 0.388 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.419 |
DOC_USP7_MATH_2 | 625 | 631 | PF00917 | 0.652 |
DOC_USP7_UBL2_3 | 434 | 438 | PF12436 | 0.648 |
DOC_USP7_UBL2_3 | 482 | 486 | PF12436 | 0.488 |
DOC_USP7_UBL2_3 | 712 | 716 | PF12436 | 0.482 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 800 | 805 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.433 |
LIG_14-3-3_CanoR_1 | 168 | 175 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 265 | 274 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 341 | 347 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 485 | 494 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 547 | 551 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 820 | 826 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 934 | 942 | PF00244 | 0.422 |
LIG_Actin_WH2_2 | 27 | 42 | PF00022 | 0.398 |
LIG_Actin_WH2_2 | 392 | 407 | PF00022 | 0.601 |
LIG_Actin_WH2_2 | 689 | 707 | PF00022 | 0.448 |
LIG_APCC_ABBA_1 | 764 | 769 | PF00400 | 0.555 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.585 |
LIG_BRCT_BRCA1_1 | 234 | 238 | PF00533 | 0.401 |
LIG_Clathr_ClatBox_1 | 615 | 619 | PF01394 | 0.541 |
LIG_Clathr_ClatBox_1 | 647 | 651 | PF01394 | 0.556 |
LIG_deltaCOP1_diTrp_1 | 327 | 333 | PF00928 | 0.460 |
LIG_eIF4E_1 | 812 | 818 | PF01652 | 0.426 |
LIG_EVH1_2 | 908 | 912 | PF00568 | 0.401 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.604 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.379 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.490 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.410 |
LIG_FHA_1 | 499 | 505 | PF00498 | 0.575 |
LIG_FHA_1 | 626 | 632 | PF00498 | 0.540 |
LIG_FHA_1 | 751 | 757 | PF00498 | 0.451 |
LIG_FHA_1 | 797 | 803 | PF00498 | 0.509 |
LIG_FHA_1 | 923 | 929 | PF00498 | 0.472 |
LIG_FHA_2 | 169 | 175 | PF00498 | 0.509 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.488 |
LIG_FHA_2 | 434 | 440 | PF00498 | 0.679 |
LIG_FHA_2 | 576 | 582 | PF00498 | 0.578 |
LIG_FHA_2 | 605 | 611 | PF00498 | 0.508 |
LIG_FHA_2 | 831 | 837 | PF00498 | 0.428 |
LIG_FHA_2 | 848 | 854 | PF00498 | 0.510 |
LIG_FHA_2 | 927 | 933 | PF00498 | 0.412 |
LIG_LIR_Apic_2 | 32 | 36 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 235 | 245 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 330 | 339 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 768 | 777 | PF02991 | 0.538 |
LIG_LIR_LC3C_4 | 374 | 378 | PF02991 | 0.690 |
LIG_LIR_Nem_3 | 224 | 230 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 235 | 241 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 330 | 336 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 768 | 774 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 876 | 882 | PF02991 | 0.571 |
LIG_NRBOX | 841 | 847 | PF00104 | 0.414 |
LIG_PCNA_yPIPBox_3 | 50 | 59 | PF02747 | 0.571 |
LIG_PDZ_Class_2 | 956 | 961 | PF00595 | 0.503 |
LIG_Pex14_2 | 635 | 639 | PF04695 | 0.519 |
LIG_SH2_CRK | 948 | 952 | PF00017 | 0.430 |
LIG_SH2_GRB2like | 227 | 230 | PF00017 | 0.489 |
LIG_SH2_NCK_1 | 230 | 234 | PF00017 | 0.532 |
LIG_SH2_SRC | 130 | 133 | PF00017 | 0.403 |
LIG_SH2_SRC | 230 | 233 | PF00017 | 0.496 |
LIG_SH2_STAP1 | 109 | 113 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 476 | 480 | PF00017 | 0.516 |
LIG_SH2_STAP1 | 767 | 771 | PF00017 | 0.470 |
LIG_SH2_STAP1 | 931 | 935 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 948 | 952 | PF00017 | 0.189 |
LIG_SH2_STAT3 | 101 | 104 | PF00017 | 0.493 |
LIG_SH2_STAT3 | 186 | 189 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 611 | 614 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 646 | 649 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 703 | 706 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 724 | 727 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 767 | 770 | PF00017 | 0.482 |
LIG_SH3_3 | 619 | 625 | PF00018 | 0.609 |
LIG_SH3_3 | 862 | 868 | PF00018 | 0.757 |
LIG_SUMO_SIM_anti_2 | 316 | 321 | PF11976 | 0.475 |
LIG_SUMO_SIM_anti_2 | 824 | 829 | PF11976 | 0.394 |
LIG_SUMO_SIM_anti_2 | 936 | 944 | PF11976 | 0.475 |
LIG_SUMO_SIM_par_1 | 135 | 143 | PF11976 | 0.543 |
LIG_SUMO_SIM_par_1 | 18 | 27 | PF11976 | 0.560 |
LIG_SUMO_SIM_par_1 | 614 | 620 | PF11976 | 0.543 |
LIG_TRAF2_1 | 255 | 258 | PF00917 | 0.538 |
LIG_TRAF2_1 | 429 | 432 | PF00917 | 0.654 |
LIG_TRAF2_1 | 592 | 595 | PF00917 | 0.606 |
LIG_TRAF2_1 | 607 | 610 | PF00917 | 0.540 |
LIG_TRAF2_1 | 895 | 898 | PF00917 | 0.487 |
LIG_UBA3_1 | 354 | 362 | PF00899 | 0.664 |
LIG_UBA3_1 | 647 | 654 | PF00899 | 0.562 |
LIG_UBA3_1 | 845 | 849 | PF00899 | 0.491 |
LIG_WRC_WIRS_1 | 771 | 776 | PF05994 | 0.586 |
MOD_CDK_SPK_2 | 91 | 96 | PF00069 | 0.433 |
MOD_CDK_SPxK_1 | 91 | 97 | PF00069 | 0.432 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.400 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.542 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.524 |
MOD_CK1_1 | 770 | 776 | PF00069 | 0.559 |
MOD_CK1_1 | 900 | 906 | PF00069 | 0.525 |
MOD_CK1_1 | 927 | 933 | PF00069 | 0.411 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.480 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.490 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.603 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.530 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.501 |
MOD_CK2_1 | 588 | 594 | PF00069 | 0.585 |
MOD_CK2_1 | 604 | 610 | PF00069 | 0.515 |
MOD_CK2_1 | 692 | 698 | PF00069 | 0.572 |
MOD_CK2_1 | 830 | 836 | PF00069 | 0.417 |
MOD_CK2_1 | 847 | 853 | PF00069 | 0.445 |
MOD_CK2_1 | 892 | 898 | PF00069 | 0.496 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.603 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.402 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.589 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.680 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.550 |
MOD_GlcNHglycan | 590 | 593 | PF01048 | 0.668 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.563 |
MOD_GlcNHglycan | 894 | 897 | PF01048 | 0.506 |
MOD_GlcNHglycan | 936 | 939 | PF01048 | 0.428 |
MOD_GlcNHglycan | 943 | 946 | PF01048 | 0.380 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.472 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.496 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.466 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.539 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.654 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.540 |
MOD_GSK3_1 | 724 | 731 | PF00069 | 0.511 |
MOD_GSK3_1 | 786 | 793 | PF00069 | 0.473 |
MOD_GSK3_1 | 796 | 803 | PF00069 | 0.510 |
MOD_GSK3_1 | 920 | 927 | PF00069 | 0.473 |
MOD_N-GLC_1 | 334 | 339 | PF02516 | 0.527 |
MOD_N-GLC_1 | 46 | 51 | PF02516 | 0.629 |
MOD_N-GLC_1 | 461 | 466 | PF02516 | 0.635 |
MOD_N-GLC_1 | 470 | 475 | PF02516 | 0.636 |
MOD_N-GLC_1 | 790 | 795 | PF02516 | 0.587 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.373 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.654 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.545 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.437 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.569 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.626 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.384 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.517 |
MOD_NEK2_1 | 711 | 716 | PF00069 | 0.575 |
MOD_NEK2_1 | 941 | 946 | PF00069 | 0.382 |
MOD_NEK2_2 | 329 | 334 | PF00069 | 0.415 |
MOD_NEK2_2 | 433 | 438 | PF00069 | 0.507 |
MOD_PIKK_1 | 252 | 258 | PF00454 | 0.636 |
MOD_PIKK_1 | 289 | 295 | PF00454 | 0.416 |
MOD_PIKK_1 | 775 | 781 | PF00454 | 0.586 |
MOD_PIKK_1 | 796 | 802 | PF00454 | 0.523 |
MOD_PKA_1 | 486 | 492 | PF00069 | 0.564 |
MOD_PKA_2 | 546 | 552 | PF00069 | 0.559 |
MOD_PKA_2 | 933 | 939 | PF00069 | 0.438 |
MOD_PKB_1 | 166 | 174 | PF00069 | 0.455 |
MOD_PKB_1 | 496 | 504 | PF00069 | 0.574 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.559 |
MOD_Plk_1 | 329 | 335 | PF00069 | 0.405 |
MOD_Plk_1 | 461 | 467 | PF00069 | 0.582 |
MOD_Plk_1 | 476 | 482 | PF00069 | 0.458 |
MOD_Plk_1 | 897 | 903 | PF00069 | 0.492 |
MOD_Plk_2-3 | 604 | 610 | PF00069 | 0.481 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.517 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.402 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.410 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.579 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.434 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.474 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.511 |
MOD_Plk_4 | 546 | 552 | PF00069 | 0.522 |
MOD_Plk_4 | 642 | 648 | PF00069 | 0.523 |
MOD_Plk_4 | 692 | 698 | PF00069 | 0.451 |
MOD_Plk_4 | 699 | 705 | PF00069 | 0.425 |
MOD_Plk_4 | 750 | 756 | PF00069 | 0.450 |
MOD_Plk_4 | 767 | 773 | PF00069 | 0.454 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.587 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.484 |
MOD_ProDKin_1 | 800 | 806 | PF00069 | 0.470 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.432 |
MOD_SUMO_for_1 | 169 | 172 | PF00179 | 0.520 |
MOD_SUMO_for_1 | 399 | 402 | PF00179 | 0.561 |
MOD_SUMO_for_1 | 592 | 595 | PF00179 | 0.527 |
MOD_SUMO_for_1 | 687 | 690 | PF00179 | 0.489 |
MOD_SUMO_for_1 | 915 | 918 | PF00179 | 0.442 |
MOD_SUMO_rev_2 | 222 | 228 | PF00179 | 0.481 |
MOD_SUMO_rev_2 | 401 | 407 | PF00179 | 0.533 |
MOD_SUMO_rev_2 | 427 | 436 | PF00179 | 0.621 |
MOD_SUMO_rev_2 | 598 | 608 | PF00179 | 0.502 |
MOD_SUMO_rev_2 | 636 | 645 | PF00179 | 0.565 |
MOD_SUMO_rev_2 | 651 | 655 | PF00179 | 0.452 |
MOD_SUMO_rev_2 | 872 | 879 | PF00179 | 0.607 |
TRG_AP2beta_CARGO_1 | 330 | 340 | PF09066 | 0.480 |
TRG_AP2beta_CARGO_1 | 876 | 886 | PF09066 | 0.544 |
TRG_DiLeu_BaEn_4 | 499 | 505 | PF01217 | 0.563 |
TRG_DiLeu_BaLyEn_6 | 841 | 846 | PF01217 | 0.407 |
TRG_ENDOCYTIC_2 | 812 | 815 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 948 | 951 | PF00928 | 0.388 |
TRG_ER_diArg_1 | 159 | 162 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 166 | 169 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 281 | 284 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 295 | 297 | PF00400 | 0.424 |
TRG_ER_diArg_1 | 339 | 341 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 483 | 485 | PF00400 | 0.610 |
TRG_ER_diArg_1 | 631 | 633 | PF00400 | 0.565 |
TRG_ER_diArg_1 | 667 | 670 | PF00400 | 0.532 |
TRG_ER_diArg_1 | 719 | 722 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 842 | 844 | PF00400 | 0.523 |
TRG_NES_CRM1_1 | 629 | 642 | PF08389 | 0.580 |
TRG_NLS_MonoExtC_3 | 484 | 490 | PF00514 | 0.440 |
TRG_NLS_MonoExtN_4 | 482 | 489 | PF00514 | 0.446 |
TRG_Pf-PMV_PEXEL_1 | 112 | 116 | PF00026 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 356 | 361 | PF00026 | 0.579 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5M6 | Leptomonas seymouri | 76% | 100% |
A0A0S4J6N5 | Bodo saltans | 51% | 99% |
A0A1X0NYF6 | Trypanosomatidae | 62% | 100% |
A0A3R7KAV4 | Trypanosoma rangeli | 64% | 100% |
A4HEE3 | Leishmania braziliensis | 78% | 100% |
C9ZKE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 100% |
E9AHA1 | Leishmania infantum | 100% | 100% |
E9AXX5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4Q9J7 | Leishmania major | 96% | 100% |
V5AK68 | Trypanosoma cruzi | 61% | 100% |