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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 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: A4HB21
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 6 |
GO:0006793 | phosphorus metabolic process | 3 | 6 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016310 | phosphorylation | 5 | 6 |
GO:0019538 | protein metabolic process | 3 | 6 |
GO:0036211 | protein modification process | 4 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0043412 | macromolecule modification | 4 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 6 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0018105 | peptidyl-serine phosphorylation | 6 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018209 | peptidyl-serine modification | 6 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 6 |
GO:0003824 | catalytic activity | 1 | 6 |
GO:0004672 | protein kinase activity | 3 | 6 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 3 |
GO:0005488 | binding | 1 | 6 |
GO:0005524 | ATP binding | 5 | 6 |
GO:0016301 | kinase activity | 4 | 6 |
GO:0016740 | transferase activity | 2 | 6 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 6 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 6 |
GO:0017076 | purine nucleotide binding | 4 | 6 |
GO:0030554 | adenyl nucleotide binding | 5 | 6 |
GO:0032553 | ribonucleotide binding | 3 | 6 |
GO:0032555 | purine ribonucleotide binding | 4 | 6 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 6 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 6 |
GO:0036094 | small molecule binding | 2 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043168 | anion binding | 3 | 6 |
GO:0097159 | organic cyclic compound binding | 2 | 6 |
GO:0097367 | carbohydrate derivative binding | 2 | 6 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 6 |
GO:1901265 | nucleoside phosphate binding | 3 | 6 |
GO:1901363 | heterocyclic compound binding | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 230 | 234 | PF00656 | 0.588 |
CLV_C14_Caspase3-7 | 597 | 601 | PF00656 | 0.751 |
CLV_C14_Caspase3-7 | 829 | 833 | PF00656 | 0.567 |
CLV_C14_Caspase3-7 | 872 | 876 | PF00656 | 0.551 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.711 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 521 | 523 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 581 | 583 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.845 |
CLV_NRD_NRD_1 | 827 | 829 | PF00675 | 0.677 |
CLV_PCSK_FUR_1 | 254 | 258 | PF00082 | 0.593 |
CLV_PCSK_FUR_1 | 287 | 291 | PF00082 | 0.609 |
CLV_PCSK_FUR_1 | 464 | 468 | PF00082 | 0.529 |
CLV_PCSK_FUR_1 | 825 | 829 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.711 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.620 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 466 | 468 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 581 | 583 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.845 |
CLV_PCSK_KEX2_1 | 827 | 829 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 857 | 859 | PF00082 | 0.599 |
CLV_PCSK_PC1ET2_1 | 857 | 859 | PF00082 | 0.594 |
CLV_PCSK_PC7_1 | 56 | 62 | PF00082 | 0.580 |
CLV_PCSK_PC7_1 | 577 | 583 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.529 |
DEG_APCC_DBOX_1 | 760 | 768 | PF00400 | 0.569 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.850 |
DEG_SCF_FBW7_1 | 672 | 678 | PF00400 | 0.552 |
DOC_CKS1_1 | 672 | 677 | PF01111 | 0.656 |
DOC_MAPK_DCC_7 | 857 | 867 | PF00069 | 0.583 |
DOC_MAPK_gen_1 | 266 | 274 | PF00069 | 0.569 |
DOC_MAPK_gen_1 | 287 | 294 | PF00069 | 0.595 |
DOC_MAPK_JIP1_4 | 268 | 274 | PF00069 | 0.565 |
DOC_MAPK_MEF2A_6 | 340 | 347 | PF00069 | 0.614 |
DOC_MAPK_MEF2A_6 | 703 | 711 | PF00069 | 0.573 |
DOC_MAPK_MEF2A_6 | 858 | 867 | PF00069 | 0.584 |
DOC_PIKK_1 | 326 | 334 | PF02985 | 0.661 |
DOC_PP1_RVXF_1 | 49 | 56 | PF00149 | 0.583 |
DOC_PP1_RVXF_1 | 586 | 593 | PF00149 | 0.653 |
DOC_PP2B_LxvP_1 | 272 | 275 | PF13499 | 0.549 |
DOC_PP4_FxxP_1 | 81 | 84 | PF00568 | 0.585 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.261 |
DOC_USP7_MATH_1 | 675 | 679 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 753 | 757 | PF00917 | 0.783 |
DOC_USP7_MATH_1 | 763 | 767 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 811 | 815 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 818 | 822 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.668 |
DOC_USP7_UBL2_3 | 523 | 527 | PF12436 | 0.529 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.789 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 536 | 541 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 626 | 631 | PF00397 | 0.706 |
DOC_WW_Pin1_4 | 671 | 676 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 739 | 744 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 756 | 761 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 772 | 777 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 892 | 897 | PF00397 | 0.568 |
LIG_14-3-3_CanoR_1 | 196 | 201 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 399 | 407 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 486 | 491 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 703 | 711 | PF00244 | 0.841 |
LIG_14-3-3_CanoR_1 | 761 | 771 | PF00244 | 0.796 |
LIG_14-3-3_CanoR_1 | 85 | 90 | PF00244 | 0.848 |
LIG_14-3-3_CanoR_1 | 870 | 878 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 92 | 96 | PF00244 | 0.621 |
LIG_Actin_WH2_2 | 350 | 365 | PF00022 | 0.529 |
LIG_BIR_III_2 | 627 | 631 | PF00653 | 0.578 |
LIG_BIR_III_4 | 604 | 608 | PF00653 | 0.765 |
LIG_BRCT_BRCA1_1 | 505 | 509 | PF00533 | 0.529 |
LIG_BRCT_BRCA1_1 | 820 | 824 | PF00533 | 0.579 |
LIG_deltaCOP1_diTrp_1 | 502 | 509 | PF00928 | 0.529 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.571 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.298 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.529 |
LIG_FHA_1 | 451 | 457 | PF00498 | 0.454 |
LIG_FHA_1 | 514 | 520 | PF00498 | 0.488 |
LIG_FHA_1 | 699 | 705 | PF00498 | 0.730 |
LIG_FHA_1 | 740 | 746 | PF00498 | 0.717 |
LIG_FHA_1 | 869 | 875 | PF00498 | 0.805 |
LIG_FHA_2 | 305 | 311 | PF00498 | 0.513 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.577 |
LIG_FHA_2 | 839 | 845 | PF00498 | 0.691 |
LIG_FHA_2 | 870 | 876 | PF00498 | 0.563 |
LIG_LIR_Apic_2 | 78 | 84 | PF02991 | 0.585 |
LIG_LIR_Gen_1 | 304 | 311 | PF02991 | 0.614 |
LIG_LIR_Gen_1 | 484 | 491 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 502 | 512 | PF02991 | 0.241 |
LIG_LIR_Gen_1 | 565 | 576 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 28 | 34 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 304 | 309 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 406 | 410 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 484 | 490 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 502 | 508 | PF02991 | 0.241 |
LIG_LIR_Nem_3 | 518 | 524 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 549 | 553 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 565 | 571 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 573 | 579 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 773 | 777 | PF02991 | 0.609 |
LIG_MLH1_MIPbox_1 | 820 | 824 | PF16413 | 0.579 |
LIG_NRBOX | 503 | 509 | PF00104 | 0.529 |
LIG_Pex14_1 | 505 | 509 | PF04695 | 0.529 |
LIG_Pex14_2 | 302 | 306 | PF04695 | 0.614 |
LIG_REV1ctd_RIR_1 | 821 | 832 | PF16727 | 0.574 |
LIG_RPA_C_Fungi | 285 | 297 | PF08784 | 0.377 |
LIG_SH2_CRK | 177 | 181 | PF00017 | 0.594 |
LIG_SH2_CRK | 410 | 414 | PF00017 | 0.529 |
LIG_SH2_CRK | 487 | 491 | PF00017 | 0.529 |
LIG_SH2_CRK | 568 | 572 | PF00017 | 0.583 |
LIG_SH2_NCK_1 | 177 | 181 | PF00017 | 0.594 |
LIG_SH2_NCK_1 | 487 | 491 | PF00017 | 0.529 |
LIG_SH2_STAP1 | 487 | 491 | PF00017 | 0.529 |
LIG_SH2_STAP1 | 568 | 572 | PF00017 | 0.583 |
LIG_SH2_STAP1 | 843 | 847 | PF00017 | 0.565 |
LIG_SH2_STAT3 | 171 | 174 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 455 | 458 | PF00017 | 0.420 |
LIG_SH3_1 | 177 | 183 | PF00018 | 0.587 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.778 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.692 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.592 |
LIG_SH3_3 | 615 | 621 | PF00018 | 0.567 |
LIG_SH3_3 | 669 | 675 | PF00018 | 0.754 |
LIG_SH3_3 | 757 | 763 | PF00018 | 0.563 |
LIG_SH3_3 | 784 | 790 | PF00018 | 0.732 |
LIG_TRAF2_1 | 19 | 22 | PF00917 | 0.529 |
LIG_TRAF2_1 | 314 | 317 | PF00917 | 0.768 |
LIG_TRAF2_1 | 46 | 49 | PF00917 | 0.579 |
LIG_TRAF2_1 | 667 | 670 | PF00917 | 0.571 |
LIG_TYR_ITIM | 574 | 579 | PF00017 | 0.317 |
LIG_WW_3 | 473 | 477 | PF00397 | 0.529 |
MOD_CAAXbox | 904 | 907 | PF01239 | 0.713 |
MOD_CDC14_SPxK_1 | 207 | 210 | PF00782 | 0.585 |
MOD_CDK_SPK_2 | 756 | 761 | PF00069 | 0.775 |
MOD_CDK_SPK_2 | 80 | 85 | PF00069 | 0.585 |
MOD_CDK_SPK_2 | 892 | 897 | PF00069 | 0.568 |
MOD_CDK_SPxK_1 | 204 | 210 | PF00069 | 0.748 |
MOD_CDK_SPxK_1 | 892 | 898 | PF00069 | 0.567 |
MOD_CDK_SPxxK_3 | 204 | 211 | PF00069 | 0.591 |
MOD_CDK_SPxxK_3 | 739 | 746 | PF00069 | 0.547 |
MOD_CDK_SPxxK_3 | 892 | 899 | PF00069 | 0.563 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.682 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.786 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.774 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.682 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.592 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.369 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.529 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.261 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.529 |
MOD_CK1_1 | 756 | 762 | PF00069 | 0.547 |
MOD_CK1_1 | 814 | 820 | PF00069 | 0.594 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.823 |
MOD_CK1_1 | 892 | 898 | PF00069 | 0.567 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.774 |
MOD_CK2_1 | 298 | 304 | PF00069 | 0.642 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.526 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.586 |
MOD_CK2_1 | 465 | 471 | PF00069 | 0.529 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.607 |
MOD_CK2_1 | 762 | 768 | PF00069 | 0.840 |
MOD_CK2_1 | 772 | 778 | PF00069 | 0.654 |
MOD_CK2_1 | 838 | 844 | PF00069 | 0.695 |
MOD_CK2_1 | 897 | 903 | PF00069 | 0.546 |
MOD_DYRK1A_RPxSP_1 | 113 | 117 | PF00069 | 0.573 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.674 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.705 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.565 |
MOD_GlcNHglycan | 260 | 264 | PF01048 | 0.866 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.369 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.594 |
MOD_GlcNHglycan | 600 | 603 | PF01048 | 0.531 |
MOD_GlcNHglycan | 645 | 648 | PF01048 | 0.755 |
MOD_GlcNHglycan | 677 | 680 | PF01048 | 0.643 |
MOD_GlcNHglycan | 698 | 701 | PF01048 | 0.663 |
MOD_GlcNHglycan | 711 | 714 | PF01048 | 0.628 |
MOD_GlcNHglycan | 807 | 811 | PF01048 | 0.749 |
MOD_GlcNHglycan | 813 | 816 | PF01048 | 0.617 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.830 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.806 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.604 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.639 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.393 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.681 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.529 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.529 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.380 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.529 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.597 |
MOD_GSK3_1 | 671 | 678 | PF00069 | 0.639 |
MOD_GSK3_1 | 698 | 705 | PF00069 | 0.831 |
MOD_GSK3_1 | 723 | 730 | PF00069 | 0.575 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.784 |
MOD_GSK3_1 | 814 | 821 | PF00069 | 0.667 |
MOD_GSK3_1 | 857 | 864 | PF00069 | 0.582 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.722 |
MOD_N-GLC_1 | 151 | 156 | PF02516 | 0.749 |
MOD_N-GLC_1 | 159 | 164 | PF02516 | 0.609 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.552 |
MOD_N-GLC_1 | 6 | 11 | PF02516 | 0.824 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.703 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.612 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.529 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.265 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.583 |
MOD_NEK2_1 | 570 | 575 | PF00069 | 0.579 |
MOD_NEK2_1 | 696 | 701 | PF00069 | 0.579 |
MOD_NEK2_2 | 6 | 11 | PF00069 | 0.701 |
MOD_NEK2_2 | 715 | 720 | PF00069 | 0.719 |
MOD_PIKK_1 | 129 | 135 | PF00454 | 0.583 |
MOD_PIKK_1 | 162 | 168 | PF00454 | 0.568 |
MOD_PIKK_1 | 366 | 372 | PF00454 | 0.261 |
MOD_PIKK_1 | 399 | 405 | PF00454 | 0.529 |
MOD_PIKK_1 | 55 | 61 | PF00454 | 0.810 |
MOD_PIKK_1 | 665 | 671 | PF00454 | 0.574 |
MOD_PIKK_1 | 883 | 889 | PF00454 | 0.587 |
MOD_PK_1 | 486 | 492 | PF00069 | 0.529 |
MOD_PK_1 | 534 | 540 | PF00069 | 0.628 |
MOD_PK_1 | 857 | 863 | PF00069 | 0.582 |
MOD_PKA_1 | 399 | 405 | PF00069 | 0.529 |
MOD_PKA_1 | 857 | 863 | PF00069 | 0.589 |
MOD_PKA_1 | 897 | 903 | PF00069 | 0.546 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.569 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.529 |
MOD_PKA_2 | 465 | 471 | PF00069 | 0.529 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.265 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.583 |
MOD_PKA_2 | 702 | 708 | PF00069 | 0.840 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.855 |
MOD_PKA_2 | 857 | 863 | PF00069 | 0.589 |
MOD_PKA_2 | 869 | 875 | PF00069 | 0.500 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.629 |
MOD_PKB_1 | 194 | 202 | PF00069 | 0.575 |
MOD_Plk_1 | 159 | 165 | PF00069 | 0.702 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.569 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.610 |
MOD_Plk_1 | 534 | 540 | PF00069 | 0.628 |
MOD_Plk_1 | 6 | 12 | PF00069 | 0.823 |
MOD_Plk_1 | 727 | 733 | PF00069 | 0.843 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.720 |
MOD_Plk_4 | 570 | 576 | PF00069 | 0.585 |
MOD_Plk_4 | 857 | 863 | PF00069 | 0.582 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.730 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.744 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.738 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.656 |
MOD_ProDKin_1 | 536 | 542 | PF00069 | 0.546 |
MOD_ProDKin_1 | 626 | 632 | PF00069 | 0.704 |
MOD_ProDKin_1 | 671 | 677 | PF00069 | 0.656 |
MOD_ProDKin_1 | 739 | 745 | PF00069 | 0.611 |
MOD_ProDKin_1 | 756 | 762 | PF00069 | 0.721 |
MOD_ProDKin_1 | 772 | 778 | PF00069 | 0.547 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.582 |
MOD_ProDKin_1 | 892 | 898 | PF00069 | 0.567 |
MOD_SUMO_for_1 | 345 | 348 | PF00179 | 0.592 |
MOD_SUMO_rev_2 | 348 | 354 | PF00179 | 0.529 |
TRG_DiLeu_BaEn_1 | 326 | 331 | PF01217 | 0.660 |
TRG_DiLeu_BaEn_2 | 548 | 554 | PF01217 | 0.590 |
TRG_DiLeu_BaEn_4 | 21 | 27 | PF01217 | 0.512 |
TRG_DiLeu_BaEn_4 | 316 | 322 | PF01217 | 0.730 |
TRG_ENDOCYTIC_2 | 410 | 413 | PF00928 | 0.529 |
TRG_ENDOCYTIC_2 | 487 | 490 | PF00928 | 0.529 |
TRG_ENDOCYTIC_2 | 568 | 571 | PF00928 | 0.586 |
TRG_ENDOCYTIC_2 | 576 | 579 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 774 | 777 | PF00928 | 0.599 |
TRG_ER_diArg_1 | 192 | 194 | PF00400 | 0.597 |
TRG_ER_diArg_1 | 254 | 257 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 286 | 289 | PF00400 | 0.604 |
TRG_ER_diArg_1 | 398 | 401 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 463 | 465 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 824 | 827 | PF00400 | 0.576 |
TRG_NES_CRM1_1 | 502 | 513 | PF08389 | 0.529 |
TRG_NES_CRM1_1 | 744 | 758 | PF08389 | 0.546 |
TRG_NLS_MonoExtC_3 | 896 | 901 | PF00514 | 0.544 |
TRG_NLS_MonoExtN_4 | 896 | 902 | PF00514 | 0.545 |
TRG_Pf-PMV_PEXEL_1 | 24 | 28 | PF00026 | 0.591 |
TRG_Pf-PMV_PEXEL_1 | 544 | 549 | PF00026 | 0.613 |
TRG_Pf-PMV_PEXEL_1 | 735 | 739 | PF00026 | 0.571 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IFR1 | Leishmania donovani | 62% | 96% |
A4IA78 | Leishmania infantum | 63% | 96% |
E9B591 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 97% |
Q4Q2P2 | Leishmania major | 62% | 100% |