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:0005737 | cytoplasm | 2 | 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: Q4Q2P2
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0007165 | signal transduction | 2 | 2 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016310 | phosphorylation | 5 | 7 |
GO:0018105 | peptidyl-serine phosphorylation | 6 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018209 | peptidyl-serine modification | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004672 | protein kinase activity | 3 | 7 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 3 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016301 | kinase activity | 4 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 7 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 332 | 336 | PF00656 | 0.476 |
CLV_C14_Caspase3-7 | 613 | 617 | PF00656 | 0.543 |
CLV_MEL_PAP_1 | 702 | 708 | PF00089 | 0.649 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.314 |
CLV_NRD_NRD_1 | 479 | 481 | PF00675 | 0.310 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.310 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.310 |
CLV_NRD_NRD_1 | 597 | 599 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 671 | 673 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 872 | 874 | PF00675 | 0.670 |
CLV_PCSK_FUR_1 | 303 | 307 | PF00082 | 0.476 |
CLV_PCSK_FUR_1 | 480 | 484 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 479 | 481 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 597 | 599 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 671 | 673 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 871 | 873 | PF00082 | 0.660 |
CLV_PCSK_KEX2_1 | 890 | 892 | PF00082 | 0.548 |
CLV_PCSK_PC1ET2_1 | 871 | 873 | PF00082 | 0.656 |
CLV_PCSK_PC1ET2_1 | 890 | 892 | PF00082 | 0.547 |
CLV_PCSK_PC7_1 | 593 | 599 | PF00082 | 0.420 |
CLV_PCSK_PC7_1 | 867 | 873 | PF00082 | 0.653 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.310 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.622 |
DEG_SCF_FBW7_1 | 461 | 468 | PF00400 | 0.294 |
DEG_SPOP_SBC_1 | 145 | 149 | PF00917 | 0.647 |
DEG_SPOP_SBC_1 | 151 | 155 | PF00917 | 0.642 |
DOC_CKS1_1 | 212 | 217 | PF01111 | 0.560 |
DOC_CKS1_1 | 462 | 467 | PF01111 | 0.294 |
DOC_CKS1_1 | 688 | 693 | PF01111 | 0.608 |
DOC_CYCLIN_yCln2_LP_2 | 187 | 190 | PF00134 | 0.700 |
DOC_CYCLIN_yCln2_LP_2 | 192 | 198 | PF00134 | 0.574 |
DOC_CYCLIN_yCln2_LP_2 | 820 | 826 | PF00134 | 0.534 |
DOC_MAPK_DCC_7 | 178 | 187 | PF00069 | 0.557 |
DOC_MAPK_gen_1 | 303 | 310 | PF00069 | 0.460 |
DOC_MAPK_HePTP_8 | 175 | 187 | PF00069 | 0.552 |
DOC_MAPK_MEF2A_6 | 178 | 187 | PF00069 | 0.557 |
DOC_MAPK_MEF2A_6 | 356 | 363 | PF00069 | 0.412 |
DOC_PIKK_1 | 342 | 350 | PF02985 | 0.546 |
DOC_PP1_RVXF_1 | 602 | 609 | PF00149 | 0.447 |
DOC_PP2B_LxvP_1 | 187 | 190 | PF13499 | 0.624 |
DOC_PP2B_LxvP_1 | 192 | 195 | PF13499 | 0.659 |
DOC_PP2B_LxvP_1 | 666 | 669 | PF13499 | 0.681 |
DOC_PP2B_LxvP_1 | 820 | 823 | PF13499 | 0.535 |
DOC_PP4_FxxP_1 | 169 | 172 | PF00568 | 0.537 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.383 |
DOC_USP7_MATH_1 | 717 | 721 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 729 | 733 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 787 | 791 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 795 | 799 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 830 | 834 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 893 | 897 | PF00917 | 0.573 |
DOC_USP7_UBL2_3 | 539 | 543 | PF12436 | 0.310 |
DOC_USP7_UBL2_3 | 926 | 930 | PF12436 | 0.592 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 120 | 125 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.294 |
DOC_WW_Pin1_4 | 552 | 557 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 687 | 692 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 789 | 794 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 815 | 820 | PF00397 | 0.642 |
LIG_14-3-3_CanoR_1 | 146 | 150 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 415 | 423 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 502 | 507 | PF00244 | 0.326 |
LIG_14-3-3_CanoR_1 | 736 | 742 | PF00244 | 0.700 |
LIG_14-3-3_CanoR_1 | 794 | 802 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 85 | 90 | PF00244 | 0.630 |
LIG_14-3-3_CanoR_1 | 99 | 103 | PF00244 | 0.639 |
LIG_Actin_WH2_2 | 366 | 381 | PF00022 | 0.310 |
LIG_BIR_III_4 | 620 | 624 | PF00653 | 0.645 |
LIG_BIR_III_4 | 649 | 653 | PF00653 | 0.689 |
LIG_BRCT_BRCA1_1 | 521 | 525 | PF00533 | 0.310 |
LIG_deltaCOP1_diTrp_1 | 518 | 525 | PF00928 | 0.310 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.633 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.310 |
LIG_FHA_1 | 467 | 473 | PF00498 | 0.315 |
LIG_FHA_1 | 530 | 536 | PF00498 | 0.310 |
LIG_FHA_1 | 780 | 786 | PF00498 | 0.669 |
LIG_FHA_1 | 902 | 908 | PF00498 | 0.623 |
LIG_FHA_2 | 861 | 867 | PF00498 | 0.681 |
LIG_LIR_Apic_2 | 167 | 172 | PF02991 | 0.537 |
LIG_LIR_Apic_2 | 763 | 769 | PF02991 | 0.605 |
LIG_LIR_Gen_1 | 320 | 330 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 500 | 507 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 518 | 528 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 581 | 591 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 422 | 426 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 500 | 506 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 518 | 524 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 534 | 540 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 565 | 569 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 581 | 587 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 814 | 820 | PF02991 | 0.696 |
LIG_MYND_1 | 127 | 131 | PF01753 | 0.664 |
LIG_NRBOX | 519 | 525 | PF00104 | 0.310 |
LIG_Pex14_1 | 521 | 525 | PF04695 | 0.310 |
LIG_Pex14_2 | 318 | 322 | PF04695 | 0.435 |
LIG_SH2_CRK | 426 | 430 | PF00017 | 0.310 |
LIG_SH2_CRK | 503 | 507 | PF00017 | 0.310 |
LIG_SH2_CRK | 584 | 588 | PF00017 | 0.376 |
LIG_SH2_CRK | 766 | 770 | PF00017 | 0.550 |
LIG_SH2_CRK | 817 | 821 | PF00017 | 0.645 |
LIG_SH2_GRB2like | 63 | 66 | PF00017 | 0.619 |
LIG_SH2_NCK_1 | 503 | 507 | PF00017 | 0.310 |
LIG_SH2_STAP1 | 503 | 507 | PF00017 | 0.310 |
LIG_SH2_STAP1 | 584 | 588 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 426 | 429 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 766 | 769 | PF00017 | 0.559 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.656 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.468 |
LIG_SH3_3 | 459 | 465 | PF00018 | 0.294 |
LIG_SH3_3 | 599 | 605 | PF00018 | 0.444 |
LIG_SH3_3 | 662 | 668 | PF00018 | 0.682 |
LIG_SH3_3 | 688 | 694 | PF00018 | 0.669 |
LIG_TRAF2_1 | 330 | 333 | PF00917 | 0.612 |
LIG_TRAF2_1 | 352 | 355 | PF00917 | 0.531 |
LIG_WW_3 | 489 | 493 | PF00397 | 0.310 |
LIG_WW_3 | 668 | 672 | PF00397 | 0.672 |
MOD_CDK_SPK_2 | 110 | 115 | PF00069 | 0.644 |
MOD_CDK_SPK_2 | 287 | 292 | PF00069 | 0.614 |
MOD_CDK_SPK_2 | 789 | 794 | PF00069 | 0.737 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.686 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.545 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.642 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.568 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.310 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.383 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.346 |
MOD_CK1_1 | 701 | 707 | PF00069 | 0.674 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.627 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.545 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.445 |
MOD_CK2_1 | 481 | 487 | PF00069 | 0.310 |
MOD_CK2_1 | 795 | 801 | PF00069 | 0.689 |
MOD_CK2_1 | 805 | 811 | PF00069 | 0.562 |
MOD_CK2_1 | 847 | 853 | PF00069 | 0.606 |
MOD_CK2_1 | 860 | 866 | PF00069 | 0.631 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.675 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.499 |
MOD_GlcNHglycan | 266 | 270 | PF01048 | 0.751 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.697 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.310 |
MOD_GlcNHglycan | 636 | 639 | PF01048 | 0.596 |
MOD_GlcNHglycan | 707 | 710 | PF01048 | 0.705 |
MOD_GlcNHglycan | 719 | 722 | PF01048 | 0.573 |
MOD_GlcNHglycan | 731 | 734 | PF01048 | 0.619 |
MOD_GlcNHglycan | 744 | 747 | PF01048 | 0.631 |
MOD_GlcNHglycan | 774 | 777 | PF01048 | 0.574 |
MOD_GlcNHglycan | 798 | 801 | PF01048 | 0.663 |
MOD_GlcNHglycan | 813 | 816 | PF01048 | 0.529 |
MOD_GlcNHglycan | 832 | 835 | PF01048 | 0.516 |
MOD_GlcNHglycan | 849 | 852 | PF01048 | 0.601 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.617 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.698 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.578 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.634 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.554 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.537 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.751 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.445 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.630 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.310 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.310 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.310 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.316 |
MOD_GSK3_1 | 610 | 617 | PF00069 | 0.530 |
MOD_GSK3_1 | 701 | 708 | PF00069 | 0.685 |
MOD_GSK3_1 | 731 | 738 | PF00069 | 0.707 |
MOD_GSK3_1 | 811 | 818 | PF00069 | 0.648 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.626 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.562 |
MOD_N-GLC_1 | 151 | 156 | PF02516 | 0.691 |
MOD_N-GLC_1 | 158 | 163 | PF02516 | 0.623 |
MOD_N-GLC_1 | 247 | 252 | PF02516 | 0.668 |
MOD_N-GLC_1 | 6 | 11 | PF02516 | 0.627 |
MOD_N-GLC_1 | 659 | 664 | PF02516 | 0.678 |
MOD_N-GLC_1 | 78 | 83 | PF02516 | 0.685 |
MOD_N-GLC_1 | 811 | 816 | PF02516 | 0.647 |
MOD_N-GLC_1 | 855 | 860 | PF02516 | 0.604 |
MOD_N-GLC_1 | 89 | 94 | PF02516 | 0.560 |
MOD_N-GLC_2 | 881 | 883 | PF02516 | 0.662 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.664 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.493 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.403 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.339 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.396 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.373 |
MOD_NEK2_1 | 614 | 619 | PF00069 | 0.583 |
MOD_NEK2_1 | 847 | 852 | PF00069 | 0.605 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.611 |
MOD_NEK2_1 | 907 | 912 | PF00069 | 0.636 |
MOD_NEK2_2 | 6 | 11 | PF00069 | 0.595 |
MOD_PIKK_1 | 118 | 124 | PF00454 | 0.679 |
MOD_PIKK_1 | 415 | 421 | PF00454 | 0.310 |
MOD_PIKK_1 | 55 | 61 | PF00454 | 0.619 |
MOD_PIKK_1 | 855 | 861 | PF00454 | 0.579 |
MOD_PK_1 | 502 | 508 | PF00069 | 0.310 |
MOD_PK_1 | 550 | 556 | PF00069 | 0.412 |
MOD_PKA_1 | 415 | 421 | PF00069 | 0.310 |
MOD_PKA_1 | 85 | 91 | PF00069 | 0.613 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.665 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.485 |
MOD_PKA_2 | 415 | 421 | PF00069 | 0.310 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.339 |
MOD_PKA_2 | 497 | 503 | PF00069 | 0.396 |
MOD_PKA_2 | 735 | 741 | PF00069 | 0.704 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.629 |
MOD_PKA_2 | 860 | 866 | PF00069 | 0.633 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.629 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.639 |
MOD_Plk_1 | 550 | 556 | PF00069 | 0.412 |
MOD_Plk_1 | 6 | 12 | PF00069 | 0.627 |
MOD_Plk_1 | 610 | 616 | PF00069 | 0.562 |
MOD_Plk_1 | 760 | 766 | PF00069 | 0.624 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.667 |
MOD_Plk_1 | 805 | 811 | PF00069 | 0.646 |
MOD_Plk_1 | 855 | 861 | PF00069 | 0.602 |
MOD_Plk_1 | 907 | 913 | PF00069 | 0.634 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.553 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.627 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.555 |
MOD_Plk_4 | 586 | 592 | PF00069 | 0.379 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.662 |
MOD_ProDKin_1 | 120 | 126 | PF00069 | 0.639 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.694 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.564 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.590 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.498 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.602 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.294 |
MOD_ProDKin_1 | 552 | 558 | PF00069 | 0.415 |
MOD_ProDKin_1 | 687 | 693 | PF00069 | 0.607 |
MOD_ProDKin_1 | 789 | 795 | PF00069 | 0.589 |
MOD_ProDKin_1 | 815 | 821 | PF00069 | 0.643 |
MOD_SUMO_for_1 | 361 | 364 | PF00179 | 0.377 |
MOD_SUMO_for_1 | 889 | 892 | PF00179 | 0.570 |
MOD_SUMO_rev_2 | 364 | 370 | PF00179 | 0.310 |
MOD_SUMO_rev_2 | 918 | 928 | PF00179 | 0.716 |
TRG_DiLeu_BaEn_1 | 342 | 347 | PF01217 | 0.542 |
TRG_DiLeu_BaEn_2 | 564 | 570 | PF01217 | 0.376 |
TRG_DiLeu_BaEn_4 | 332 | 338 | PF01217 | 0.613 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 503 | 506 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 584 | 587 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 817 | 820 | PF00928 | 0.555 |
TRG_ER_diArg_1 | 302 | 305 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 414 | 417 | PF00400 | 0.310 |
TRG_ER_diArg_1 | 479 | 481 | PF00400 | 0.310 |
TRG_ER_diArg_1 | 60 | 62 | PF00400 | 0.601 |
TRG_ER_diArg_1 | 670 | 672 | PF00400 | 0.674 |
TRG_NES_CRM1_1 | 518 | 529 | PF08389 | 0.310 |
TRG_Pf-PMV_PEXEL_1 | 560 | 565 | PF00026 | 0.396 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IK71 | Leptomonas seymouri | 49% | 100% |
A0A3Q8IFR1 | Leishmania donovani | 90% | 100% |
A4HB21 | Leishmania braziliensis | 62% | 100% |
A4IA78 | Leishmania infantum | 91% | 100% |
E9B591 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |