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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 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:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QJE1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006396 | RNA processing | 6 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016070 | RNA metabolic process | 5 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0003723 | RNA binding | 4 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 273 | 277 | PF00656 | 0.621 |
CLV_C14_Caspase3-7 | 322 | 326 | PF00656 | 0.600 |
CLV_C14_Caspase3-7 | 357 | 361 | PF00656 | 0.607 |
CLV_C14_Caspase3-7 | 461 | 465 | PF00656 | 0.627 |
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.706 |
CLV_NRD_NRD_1 | 661 | 663 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 668 | 670 | PF00675 | 0.635 |
CLV_PCSK_FUR_1 | 298 | 302 | PF00082 | 0.626 |
CLV_PCSK_FUR_1 | 658 | 662 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 238 | 240 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 317 | 319 | PF00082 | 0.770 |
CLV_PCSK_KEX2_1 | 660 | 662 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 668 | 670 | PF00082 | 0.638 |
CLV_PCSK_PC1ET2_1 | 186 | 188 | PF00082 | 0.282 |
CLV_PCSK_PC1ET2_1 | 317 | 319 | PF00082 | 0.714 |
CLV_PCSK_PC7_1 | 664 | 670 | PF00082 | 0.719 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 720 | 724 | PF00082 | 0.736 |
CLV_PCSK_SKI1_1 | 826 | 830 | PF00082 | 0.644 |
DEG_APCC_DBOX_1 | 211 | 219 | PF00400 | 0.482 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.485 |
DEG_SCF_FBW7_1 | 779 | 786 | PF00400 | 0.646 |
DEG_SIAH_1 | 519 | 527 | PF03145 | 0.533 |
DEG_SPOP_SBC_1 | 113 | 117 | PF00917 | 0.547 |
DEG_SPOP_SBC_1 | 750 | 754 | PF00917 | 0.667 |
DEG_SPOP_SBC_1 | 810 | 814 | PF00917 | 0.683 |
DOC_CYCLIN_yCln2_LP_2 | 143 | 149 | PF00134 | 0.516 |
DOC_CYCLIN_yCln2_LP_2 | 264 | 270 | PF00134 | 0.629 |
DOC_CYCLIN_yCln2_LP_2 | 450 | 456 | PF00134 | 0.555 |
DOC_CYCLIN_yCln2_LP_2 | 78 | 81 | PF00134 | 0.707 |
DOC_MAPK_gen_1 | 151 | 160 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 238 | 244 | PF00069 | 0.459 |
DOC_MAPK_MEF2A_6 | 674 | 683 | PF00069 | 0.468 |
DOC_MAPK_MEF2A_6 | 826 | 833 | PF00069 | 0.518 |
DOC_PP2B_LxvP_1 | 143 | 146 | PF13499 | 0.528 |
DOC_PP2B_LxvP_1 | 147 | 150 | PF13499 | 0.521 |
DOC_PP2B_LxvP_1 | 152 | 155 | PF13499 | 0.482 |
DOC_PP2B_LxvP_1 | 417 | 420 | PF13499 | 0.563 |
DOC_PP2B_LxvP_1 | 681 | 684 | PF13499 | 0.438 |
DOC_PP2B_LxvP_1 | 78 | 81 | PF13499 | 0.653 |
DOC_PP2B_LxvP_1 | 839 | 842 | PF13499 | 0.605 |
DOC_PP4_FxxP_1 | 203 | 206 | PF00568 | 0.482 |
DOC_PP4_FxxP_1 | 64 | 67 | PF00568 | 0.675 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.780 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 397 | 401 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 460 | 464 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 520 | 524 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 526 | 530 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 554 | 558 | PF00917 | 0.791 |
DOC_USP7_MATH_1 | 582 | 586 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 625 | 629 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 652 | 656 | PF00917 | 0.763 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.790 |
DOC_USP7_MATH_1 | 750 | 754 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 794 | 798 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 809 | 813 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 845 | 849 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 876 | 880 | PF00917 | 0.757 |
DOC_USP7_UBL2_3 | 737 | 741 | PF12436 | 0.735 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.779 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 550 | 555 | PF00397 | 0.597 |
DOC_WW_Pin1_4 | 602 | 607 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 626 | 631 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 637 | 642 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 645 | 650 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 653 | 658 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 667 | 672 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 779 | 784 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 788 | 793 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 841 | 846 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.633 |
LIG_14-3-3_CanoR_1 | 214 | 219 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 427 | 436 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 662 | 672 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 90 | 100 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 922 | 926 | PF00244 | 0.513 |
LIG_BRCT_BRCA1_1 | 923 | 927 | PF00533 | 0.520 |
LIG_Clathr_ClatBox_1 | 891 | 895 | PF01394 | 0.664 |
LIG_CSL_BTD_1 | 242 | 245 | PF09270 | 0.490 |
LIG_deltaCOP1_diTrp_1 | 535 | 541 | PF00928 | 0.445 |
LIG_eIF4E_1 | 905 | 911 | PF01652 | 0.607 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.657 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.502 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.481 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.619 |
LIG_FHA_1 | 712 | 718 | PF00498 | 0.604 |
LIG_FHA_1 | 755 | 761 | PF00498 | 0.710 |
LIG_FHA_1 | 784 | 790 | PF00498 | 0.632 |
LIG_FHA_1 | 879 | 885 | PF00498 | 0.676 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.681 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.533 |
LIG_FHA_2 | 162 | 168 | PF00498 | 0.321 |
LIG_FHA_2 | 177 | 183 | PF00498 | 0.482 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.639 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.734 |
LIG_FHA_2 | 459 | 465 | PF00498 | 0.615 |
LIG_FHA_2 | 683 | 689 | PF00498 | 0.505 |
LIG_GSK3_LRP6_1 | 841 | 846 | PF00069 | 0.578 |
LIG_IBAR_NPY_1 | 452 | 454 | PF08397 | 0.577 |
LIG_LIR_Apic_2 | 116 | 122 | PF02991 | 0.614 |
LIG_LIR_Apic_2 | 201 | 206 | PF02991 | 0.482 |
LIG_LIR_Apic_2 | 62 | 67 | PF02991 | 0.682 |
LIG_LIR_Apic_2 | 68 | 74 | PF02991 | 0.632 |
LIG_LIR_Gen_1 | 26 | 36 | PF02991 | 0.656 |
LIG_LIR_Gen_1 | 445 | 455 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 610 | 621 | PF02991 | 0.641 |
LIG_LIR_Gen_1 | 921 | 927 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 26 | 31 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 445 | 450 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 535 | 541 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 610 | 616 | PF02991 | 0.644 |
LIG_LIR_Nem_3 | 921 | 926 | PF02991 | 0.516 |
LIG_MYND_1 | 76 | 80 | PF01753 | 0.683 |
LIG_NRBOX | 164 | 170 | PF00104 | 0.331 |
LIG_NRBOX | 214 | 220 | PF00104 | 0.482 |
LIG_NRBOX | 497 | 503 | PF00104 | 0.427 |
LIG_PCNA_yPIPBox_3 | 40 | 51 | PF02747 | 0.641 |
LIG_PDZ_Class_2 | 922 | 927 | PF00595 | 0.521 |
LIG_Pex14_1 | 824 | 828 | PF04695 | 0.582 |
LIG_Pex14_2 | 828 | 832 | PF04695 | 0.597 |
LIG_PTB_Apo_2 | 190 | 197 | PF02174 | 0.466 |
LIG_SH2_CRK | 119 | 123 | PF00017 | 0.557 |
LIG_SH2_CRK | 216 | 220 | PF00017 | 0.523 |
LIG_SH2_CRK | 71 | 75 | PF00017 | 0.702 |
LIG_SH2_CRK | 905 | 909 | PF00017 | 0.746 |
LIG_SH2_CRK | 923 | 927 | PF00017 | 0.445 |
LIG_SH2_GRB2like | 83 | 86 | PF00017 | 0.665 |
LIG_SH2_NCK_1 | 119 | 123 | PF00017 | 0.557 |
LIG_SH2_NCK_1 | 454 | 458 | PF00017 | 0.572 |
LIG_SH2_PTP2 | 241 | 244 | PF00017 | 0.414 |
LIG_SH2_SRC | 454 | 457 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 923 | 927 | PF00017 | 0.520 |
LIG_SH2_STAT3 | 35 | 38 | PF00017 | 0.624 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 510 | 513 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 539 | 542 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.814 |
LIG_SH3_2 | 245 | 250 | PF14604 | 0.550 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.737 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.429 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.613 |
LIG_SH3_3 | 627 | 633 | PF00018 | 0.739 |
LIG_SH3_3 | 721 | 727 | PF00018 | 0.728 |
LIG_SH3_3 | 835 | 841 | PF00018 | 0.697 |
LIG_SH3_3 | 854 | 860 | PF00018 | 0.668 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.558 |
LIG_SUMO_SIM_anti_2 | 163 | 171 | PF11976 | 0.411 |
LIG_SUMO_SIM_anti_2 | 677 | 683 | PF11976 | 0.556 |
LIG_TRAF2_1 | 179 | 182 | PF00917 | 0.502 |
LIG_TRAF2_1 | 284 | 287 | PF00917 | 0.649 |
LIG_TYR_ITIM | 537 | 542 | PF00017 | 0.473 |
LIG_UBA3_1 | 821 | 826 | PF00899 | 0.507 |
LIG_WW_1 | 80 | 83 | PF00397 | 0.798 |
MOD_CDK_SPK_2 | 653 | 658 | PF00069 | 0.666 |
MOD_CDK_SPK_2 | 85 | 90 | PF00069 | 0.548 |
MOD_CDK_SPxxK_3 | 653 | 660 | PF00069 | 0.689 |
MOD_CDK_SPxxK_3 | 667 | 674 | PF00069 | 0.597 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.700 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.540 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.624 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.637 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.723 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.608 |
MOD_CK1_1 | 557 | 563 | PF00069 | 0.811 |
MOD_CK1_1 | 585 | 591 | PF00069 | 0.671 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.579 |
MOD_CK1_1 | 602 | 608 | PF00069 | 0.525 |
MOD_CK1_1 | 640 | 646 | PF00069 | 0.636 |
MOD_CK1_1 | 648 | 654 | PF00069 | 0.676 |
MOD_CK1_1 | 749 | 755 | PF00069 | 0.707 |
MOD_CK1_1 | 790 | 796 | PF00069 | 0.775 |
MOD_CK1_1 | 797 | 803 | PF00069 | 0.700 |
MOD_CK1_1 | 812 | 818 | PF00069 | 0.542 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.677 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.599 |
MOD_CK2_1 | 176 | 182 | PF00069 | 0.482 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.658 |
MOD_CK2_1 | 352 | 358 | PF00069 | 0.788 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.594 |
MOD_CK2_1 | 396 | 402 | PF00069 | 0.731 |
MOD_CK2_1 | 667 | 673 | PF00069 | 0.588 |
MOD_CK2_1 | 682 | 688 | PF00069 | 0.503 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.682 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.627 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.513 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.716 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.749 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.669 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.840 |
MOD_GlcNHglycan | 347 | 350 | PF01048 | 0.560 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.695 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.803 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.747 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.533 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.597 |
MOD_GlcNHglycan | 555 | 559 | PF01048 | 0.719 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.700 |
MOD_GlcNHglycan | 588 | 591 | PF01048 | 0.646 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.586 |
MOD_GlcNHglycan | 650 | 653 | PF01048 | 0.691 |
MOD_GlcNHglycan | 748 | 751 | PF01048 | 0.667 |
MOD_GlcNHglycan | 792 | 795 | PF01048 | 0.689 |
MOD_GlcNHglycan | 796 | 799 | PF01048 | 0.727 |
MOD_GlcNHglycan | 814 | 817 | PF01048 | 0.536 |
MOD_GlcNHglycan | 847 | 850 | PF01048 | 0.745 |
MOD_GlcNHglycan | 911 | 914 | PF01048 | 0.528 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.696 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.709 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.732 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.615 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.684 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.647 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.756 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.688 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.677 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.817 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.648 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.685 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.717 |
MOD_GSK3_1 | 636 | 643 | PF00069 | 0.779 |
MOD_GSK3_1 | 648 | 655 | PF00069 | 0.655 |
MOD_GSK3_1 | 663 | 670 | PF00069 | 0.538 |
MOD_GSK3_1 | 746 | 753 | PF00069 | 0.651 |
MOD_GSK3_1 | 779 | 786 | PF00069 | 0.672 |
MOD_GSK3_1 | 790 | 797 | PF00069 | 0.583 |
MOD_GSK3_1 | 805 | 812 | PF00069 | 0.804 |
MOD_GSK3_1 | 841 | 848 | PF00069 | 0.663 |
MOD_LATS_1 | 304 | 310 | PF00433 | 0.679 |
MOD_N-GLC_1 | 330 | 335 | PF02516 | 0.639 |
MOD_N-GLC_1 | 548 | 553 | PF02516 | 0.515 |
MOD_N-GLC_1 | 566 | 571 | PF02516 | 0.641 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.430 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.482 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.594 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.545 |
MOD_NEK2_1 | 751 | 756 | PF00069 | 0.667 |
MOD_NEK2_2 | 764 | 769 | PF00069 | 0.607 |
MOD_PIKK_1 | 226 | 232 | PF00454 | 0.619 |
MOD_PIKK_1 | 386 | 392 | PF00454 | 0.737 |
MOD_PIKK_1 | 663 | 669 | PF00454 | 0.607 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.701 |
MOD_PIKK_1 | 703 | 709 | PF00454 | 0.661 |
MOD_PIKK_1 | 895 | 901 | PF00454 | 0.678 |
MOD_PKA_1 | 366 | 372 | PF00069 | 0.625 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.568 |
MOD_PKA_2 | 663 | 669 | PF00069 | 0.668 |
MOD_PKA_2 | 921 | 927 | PF00069 | 0.523 |
MOD_PKB_1 | 151 | 159 | PF00069 | 0.430 |
MOD_PKB_1 | 212 | 220 | PF00069 | 0.482 |
MOD_PKB_1 | 332 | 340 | PF00069 | 0.672 |
MOD_Plk_1 | 160 | 166 | PF00069 | 0.422 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.650 |
MOD_Plk_1 | 876 | 882 | PF00069 | 0.601 |
MOD_Plk_2-3 | 161 | 167 | PF00069 | 0.412 |
MOD_Plk_2-3 | 458 | 464 | PF00069 | 0.525 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.412 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.482 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.613 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.430 |
MOD_Plk_4 | 59 | 65 | PF00069 | 0.496 |
MOD_Plk_4 | 682 | 688 | PF00069 | 0.509 |
MOD_Plk_4 | 860 | 866 | PF00069 | 0.658 |
MOD_Plk_4 | 887 | 893 | PF00069 | 0.645 |
MOD_Plk_4 | 921 | 927 | PF00069 | 0.523 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.779 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.599 |
MOD_ProDKin_1 | 392 | 398 | PF00069 | 0.675 |
MOD_ProDKin_1 | 550 | 556 | PF00069 | 0.606 |
MOD_ProDKin_1 | 602 | 608 | PF00069 | 0.548 |
MOD_ProDKin_1 | 626 | 632 | PF00069 | 0.732 |
MOD_ProDKin_1 | 637 | 643 | PF00069 | 0.641 |
MOD_ProDKin_1 | 645 | 651 | PF00069 | 0.707 |
MOD_ProDKin_1 | 653 | 659 | PF00069 | 0.636 |
MOD_ProDKin_1 | 667 | 673 | PF00069 | 0.601 |
MOD_ProDKin_1 | 779 | 785 | PF00069 | 0.664 |
MOD_ProDKin_1 | 788 | 794 | PF00069 | 0.771 |
MOD_ProDKin_1 | 841 | 847 | PF00069 | 0.696 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.628 |
MOD_SUMO_for_1 | 185 | 188 | PF00179 | 0.482 |
MOD_SUMO_rev_2 | 359 | 369 | PF00179 | 0.588 |
MOD_SUMO_rev_2 | 45 | 53 | PF00179 | 0.634 |
TRG_DiLeu_BaEn_1 | 161 | 166 | PF01217 | 0.415 |
TRG_DiLeu_BaLyEn_6 | 74 | 79 | PF01217 | 0.696 |
TRG_DiLeu_BaLyEn_6 | 906 | 911 | PF01217 | 0.576 |
TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.519 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.594 |
TRG_ENDOCYTIC_2 | 539 | 542 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 613 | 616 | PF00928 | 0.628 |
TRG_ENDOCYTIC_2 | 923 | 926 | PF00928 | 0.510 |
TRG_ER_diArg_1 | 150 | 153 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 298 | 301 | PF00400 | 0.621 |
TRG_ER_diArg_1 | 414 | 417 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 657 | 660 | PF00400 | 0.694 |
TRG_ER_diArg_1 | 661 | 664 | PF00400 | 0.691 |
TRG_ER_diArg_1 | 717 | 720 | PF00400 | 0.584 |
TRG_NES_CRM1_1 | 492 | 503 | PF08389 | 0.503 |
TRG_Pf-PMV_PEXEL_1 | 473 | 478 | PF00026 | 0.478 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAE1 | Leptomonas seymouri | 41% | 98% |
A0A3S7WP43 | Leishmania donovani | 91% | 95% |
A4HD48 | Leishmania braziliensis | 73% | 94% |
A4HSI3 | Leishmania infantum | 91% | 95% |
E9AKG7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |