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:0005737 | cytoplasm | 2 | 1 |
GO:0005856 | cytoskeleton | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HLP3
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:0018105 | peptidyl-serine phosphorylation | 6 | 1 |
GO:0018107 | peptidyl-threonine phosphorylation | 6 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018209 | peptidyl-serine modification | 6 | 1 |
GO:0018210 | peptidyl-threonine modification | 6 | 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:0004712 | protein serine/threonine/tyrosine kinase activity | 4 | 6 |
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 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 480 | 484 | PF00656 | 0.554 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.371 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 533 | 535 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 729 | 731 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 753 | 755 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 899 | 901 | PF00675 | 0.530 |
CLV_PCSK_FUR_1 | 313 | 317 | PF00082 | 0.385 |
CLV_PCSK_FUR_1 | 531 | 535 | PF00082 | 0.699 |
CLV_PCSK_FUR_1 | 751 | 755 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 533 | 535 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 729 | 731 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 753 | 755 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 899 | 901 | PF00082 | 0.593 |
CLV_PCSK_PC1ET2_1 | 315 | 317 | PF00082 | 0.243 |
CLV_PCSK_PC7_1 | 529 | 535 | PF00082 | 0.707 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 495 | 499 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 913 | 917 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 933 | 937 | PF00082 | 0.579 |
DEG_APCC_DBOX_1 | 753 | 761 | PF00400 | 0.550 |
DOC_CKS1_1 | 941 | 946 | PF01111 | 0.552 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 164 | 173 | PF00134 | 0.385 |
DOC_CYCLIN_yCln2_LP_2 | 557 | 563 | PF00134 | 0.692 |
DOC_CYCLIN_yCln2_LP_2 | 854 | 860 | PF00134 | 0.518 |
DOC_CYCLIN_yCln2_LP_2 | 909 | 912 | PF00134 | 0.656 |
DOC_MAPK_FxFP_2 | 386 | 389 | PF00069 | 0.593 |
DOC_MAPK_gen_1 | 153 | 160 | PF00069 | 0.243 |
DOC_MAPK_gen_1 | 174 | 183 | PF00069 | 0.343 |
DOC_MAPK_gen_1 | 751 | 760 | PF00069 | 0.683 |
DOC_MAPK_HePTP_8 | 173 | 185 | PF00069 | 0.243 |
DOC_MAPK_HePTP_8 | 244 | 256 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 176 | 185 | PF00069 | 0.378 |
DOC_MAPK_MEF2A_6 | 192 | 199 | PF00069 | 0.414 |
DOC_MAPK_MEF2A_6 | 247 | 256 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 836 | 843 | PF00069 | 0.547 |
DOC_PP2B_LxvP_1 | 299 | 302 | PF13499 | 0.385 |
DOC_PP2B_LxvP_1 | 466 | 469 | PF13499 | 0.542 |
DOC_PP2B_LxvP_1 | 557 | 560 | PF13499 | 0.663 |
DOC_PP2B_LxvP_1 | 673 | 676 | PF13499 | 0.549 |
DOC_PP2B_LxvP_1 | 841 | 844 | PF13499 | 0.544 |
DOC_PP2B_LxvP_1 | 854 | 857 | PF13499 | 0.477 |
DOC_PP2B_LxvP_1 | 909 | 912 | PF13499 | 0.656 |
DOC_PP4_FxxP_1 | 386 | 389 | PF00568 | 0.593 |
DOC_PP4_FxxP_1 | 514 | 517 | PF00568 | 0.567 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 551 | 555 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 635 | 639 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 642 | 646 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 724 | 728 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 798 | 802 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 844 | 848 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 850 | 854 | PF00917 | 0.558 |
DOC_USP7_UBL2_3 | 933 | 937 | PF12436 | 0.581 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.243 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.510 |
DOC_WW_Pin1_4 | 581 | 586 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 607 | 612 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 640 | 645 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 734 | 739 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 763 | 768 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 806 | 811 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 835 | 840 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 852 | 857 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 940 | 945 | PF00397 | 0.680 |
LIG_14-3-3_CanoR_1 | 192 | 198 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 487 | 492 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 531 | 541 | PF00244 | 0.695 |
LIG_14-3-3_CanoR_1 | 660 | 669 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 706 | 716 | PF00244 | 0.699 |
LIG_14-3-3_CanoR_1 | 886 | 896 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 918 | 922 | PF00244 | 0.665 |
LIG_Actin_WH2_2 | 588 | 605 | PF00022 | 0.558 |
LIG_APCC_ABBA_1 | 791 | 796 | PF00400 | 0.693 |
LIG_BRCT_BRCA1_1 | 474 | 478 | PF00533 | 0.546 |
LIG_BRCT_BRCA1_1 | 90 | 94 | PF00533 | 0.385 |
LIG_CtBP_PxDLS_1 | 762 | 766 | PF00389 | 0.542 |
LIG_deltaCOP1_diTrp_1 | 265 | 269 | PF00928 | 0.385 |
LIG_EH1_1 | 142 | 150 | PF00400 | 0.243 |
LIG_EVH1_2 | 302 | 306 | PF00568 | 0.385 |
LIG_EVH1_2 | 856 | 860 | PF00568 | 0.510 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.243 |
LIG_FHA_1 | 621 | 627 | PF00498 | 0.605 |
LIG_FHA_1 | 668 | 674 | PF00498 | 0.668 |
LIG_FHA_1 | 684 | 690 | PF00498 | 0.546 |
LIG_FHA_1 | 711 | 717 | PF00498 | 0.569 |
LIG_FHA_1 | 941 | 947 | PF00498 | 0.669 |
LIG_FHA_2 | 27 | 33 | PF00498 | 0.448 |
LIG_FHA_2 | 327 | 333 | PF00498 | 0.243 |
LIG_FHA_2 | 388 | 394 | PF00498 | 0.564 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.530 |
LIG_FHA_2 | 478 | 484 | PF00498 | 0.567 |
LIG_FHA_2 | 627 | 633 | PF00498 | 0.555 |
LIG_Integrin_isoDGR_2 | 524 | 526 | PF01839 | 0.589 |
LIG_LIR_Apic_2 | 246 | 252 | PF02991 | 0.385 |
LIG_LIR_Apic_2 | 297 | 301 | PF02991 | 0.385 |
LIG_LIR_Apic_2 | 384 | 389 | PF02991 | 0.585 |
LIG_LIR_Apic_2 | 784 | 788 | PF02991 | 0.702 |
LIG_LIR_Gen_1 | 161 | 170 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 239 | 249 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 344 | 353 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 354 | 363 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 700 | 708 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 161 | 165 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 239 | 244 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 265 | 269 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 344 | 349 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 352 | 358 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 700 | 704 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 855 | 861 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 91 | 97 | PF02991 | 0.385 |
LIG_MYND_1 | 464 | 468 | PF01753 | 0.555 |
LIG_MYND_1 | 852 | 856 | PF01753 | 0.662 |
LIG_NRP_CendR_1 | 950 | 951 | PF00754 | 0.546 |
LIG_Pex14_2 | 358 | 362 | PF04695 | 0.385 |
LIG_Pex14_2 | 94 | 98 | PF04695 | 0.385 |
LIG_PTB_Apo_2 | 148 | 155 | PF02174 | 0.385 |
LIG_SH2_CRK | 143 | 147 | PF00017 | 0.385 |
LIG_SH2_CRK | 785 | 789 | PF00017 | 0.701 |
LIG_SH2_CRK | 858 | 862 | PF00017 | 0.528 |
LIG_SH2_NCK_1 | 39 | 43 | PF00017 | 0.310 |
LIG_SH2_PTP2 | 241 | 244 | PF00017 | 0.243 |
LIG_SH2_SRC | 241 | 244 | PF00017 | 0.243 |
LIG_SH2_STAP1 | 39 | 43 | PF00017 | 0.310 |
LIG_SH2_STAT3 | 44 | 47 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.444 |
LIG_SH3_1 | 836 | 842 | PF00018 | 0.547 |
LIG_SH3_2 | 422 | 427 | PF14604 | 0.661 |
LIG_SH3_2 | 517 | 522 | PF14604 | 0.562 |
LIG_SH3_3 | 278 | 284 | PF00018 | 0.385 |
LIG_SH3_3 | 419 | 425 | PF00018 | 0.653 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.368 |
LIG_SH3_3 | 514 | 520 | PF00018 | 0.685 |
LIG_SH3_3 | 538 | 544 | PF00018 | 0.696 |
LIG_SH3_3 | 592 | 598 | PF00018 | 0.561 |
LIG_SH3_3 | 605 | 611 | PF00018 | 0.576 |
LIG_SH3_3 | 836 | 842 | PF00018 | 0.580 |
LIG_SH3_3 | 846 | 852 | PF00018 | 0.641 |
LIG_SH3_3 | 932 | 938 | PF00018 | 0.690 |
LIG_SH3_3 | 941 | 947 | PF00018 | 0.632 |
LIG_SUMO_SIM_anti_2 | 688 | 693 | PF11976 | 0.619 |
LIG_SUMO_SIM_par_1 | 193 | 198 | PF11976 | 0.385 |
LIG_SUMO_SIM_par_1 | 615 | 623 | PF11976 | 0.600 |
LIG_SUMO_SIM_par_1 | 624 | 630 | PF11976 | 0.598 |
LIG_SUMO_SIM_par_1 | 761 | 766 | PF11976 | 0.545 |
LIG_TRAF2_1 | 124 | 127 | PF00917 | 0.385 |
LIG_TYR_ITIM | 160 | 165 | PF00017 | 0.385 |
LIG_TYR_ITIM | 37 | 42 | PF00017 | 0.467 |
LIG_WRC_WIRS_1 | 355 | 360 | PF05994 | 0.385 |
LIG_WW_2 | 839 | 842 | PF00397 | 0.529 |
LIG_WW_3 | 910 | 914 | PF00397 | 0.664 |
MOD_CDC14_SPxK_1 | 766 | 769 | PF00782 | 0.536 |
MOD_CDK_SPK_2 | 369 | 374 | PF00069 | 0.243 |
MOD_CDK_SPxK_1 | 763 | 769 | PF00069 | 0.543 |
MOD_CDK_SPxxK_3 | 806 | 813 | PF00069 | 0.511 |
MOD_CDK_SPxxK_3 | 852 | 859 | PF00069 | 0.630 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.430 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.250 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.679 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.623 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.568 |
MOD_CK1_1 | 584 | 590 | PF00069 | 0.672 |
MOD_CK1_1 | 615 | 621 | PF00069 | 0.550 |
MOD_CK1_1 | 702 | 708 | PF00069 | 0.565 |
MOD_CK1_1 | 741 | 747 | PF00069 | 0.691 |
MOD_CK1_1 | 832 | 838 | PF00069 | 0.668 |
MOD_CK1_1 | 890 | 896 | PF00069 | 0.580 |
MOD_CK1_1 | 939 | 945 | PF00069 | 0.553 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.501 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.337 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.246 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.251 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.520 |
MOD_CK2_1 | 438 | 444 | PF00069 | 0.533 |
MOD_CK2_1 | 563 | 569 | PF00069 | 0.711 |
MOD_CK2_1 | 635 | 641 | PF00069 | 0.590 |
MOD_CK2_1 | 668 | 674 | PF00069 | 0.548 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.414 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.385 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.385 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.680 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.640 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.627 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.615 |
MOD_GlcNHglycan | 479 | 483 | PF01048 | 0.623 |
MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.539 |
MOD_GlcNHglycan | 564 | 569 | PF01048 | 0.678 |
MOD_GlcNHglycan | 644 | 647 | PF01048 | 0.610 |
MOD_GlcNHglycan | 652 | 655 | PF01048 | 0.603 |
MOD_GlcNHglycan | 663 | 666 | PF01048 | 0.650 |
MOD_GlcNHglycan | 722 | 725 | PF01048 | 0.702 |
MOD_GlcNHglycan | 726 | 729 | PF01048 | 0.665 |
MOD_GlcNHglycan | 743 | 746 | PF01048 | 0.525 |
MOD_GlcNHglycan | 846 | 849 | PF01048 | 0.678 |
MOD_GlcNHglycan | 863 | 866 | PF01048 | 0.489 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.601 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.385 |
MOD_GlcNHglycan | 904 | 907 | PF01048 | 0.537 |
MOD_GlcNHglycan | 927 | 930 | PF01048 | 0.567 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.243 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.243 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.640 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.631 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.515 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.601 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.567 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.580 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.666 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.471 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.642 |
MOD_GSK3_1 | 640 | 647 | PF00069 | 0.730 |
MOD_GSK3_1 | 679 | 686 | PF00069 | 0.678 |
MOD_GSK3_1 | 702 | 709 | PF00069 | 0.617 |
MOD_GSK3_1 | 720 | 727 | PF00069 | 0.622 |
MOD_GSK3_1 | 729 | 736 | PF00069 | 0.660 |
MOD_GSK3_1 | 887 | 894 | PF00069 | 0.538 |
MOD_GSK3_1 | 925 | 932 | PF00069 | 0.630 |
MOD_GSK3_1 | 933 | 940 | PF00069 | 0.670 |
MOD_N-GLC_1 | 406 | 411 | PF02516 | 0.624 |
MOD_N-GLC_1 | 483 | 488 | PF02516 | 0.564 |
MOD_N-GLC_1 | 551 | 556 | PF02516 | 0.706 |
MOD_N-GLC_1 | 661 | 666 | PF02516 | 0.571 |
MOD_N-GLC_1 | 925 | 930 | PF02516 | 0.563 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.385 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.369 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.274 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.589 |
MOD_NEK2_1 | 575 | 580 | PF00069 | 0.566 |
MOD_NEK2_1 | 619 | 624 | PF00069 | 0.693 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.539 |
MOD_NEK2_1 | 861 | 866 | PF00069 | 0.519 |
MOD_NEK2_2 | 410 | 415 | PF00069 | 0.679 |
MOD_PIKK_1 | 365 | 371 | PF00454 | 0.243 |
MOD_PIKK_1 | 387 | 393 | PF00454 | 0.559 |
MOD_PIKK_1 | 416 | 422 | PF00454 | 0.626 |
MOD_PIKK_1 | 711 | 717 | PF00454 | 0.657 |
MOD_PIKK_1 | 768 | 774 | PF00454 | 0.561 |
MOD_PKA_1 | 533 | 539 | PF00069 | 0.601 |
MOD_PKA_1 | 729 | 735 | PF00069 | 0.569 |
MOD_PKA_2 | 532 | 538 | PF00069 | 0.611 |
MOD_PKA_2 | 711 | 717 | PF00069 | 0.584 |
MOD_PKA_2 | 729 | 735 | PF00069 | 0.530 |
MOD_PKA_2 | 917 | 923 | PF00069 | 0.631 |
MOD_PKB_1 | 531 | 539 | PF00069 | 0.693 |
MOD_PKB_1 | 720 | 728 | PF00069 | 0.574 |
MOD_Plk_1 | 104 | 110 | PF00069 | 0.385 |
MOD_Plk_1 | 483 | 489 | PF00069 | 0.566 |
MOD_Plk_1 | 552 | 558 | PF00069 | 0.621 |
MOD_Plk_1 | 699 | 705 | PF00069 | 0.547 |
MOD_Plk_1 | 829 | 835 | PF00069 | 0.674 |
MOD_Plk_1 | 890 | 896 | PF00069 | 0.534 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.412 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.385 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.350 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.378 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.385 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.542 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.512 |
MOD_Plk_4 | 668 | 674 | PF00069 | 0.548 |
MOD_Plk_4 | 891 | 897 | PF00069 | 0.533 |
MOD_Plk_4 | 917 | 923 | PF00069 | 0.552 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.243 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.523 |
MOD_ProDKin_1 | 581 | 587 | PF00069 | 0.679 |
MOD_ProDKin_1 | 607 | 613 | PF00069 | 0.605 |
MOD_ProDKin_1 | 640 | 646 | PF00069 | 0.651 |
MOD_ProDKin_1 | 734 | 740 | PF00069 | 0.706 |
MOD_ProDKin_1 | 763 | 769 | PF00069 | 0.543 |
MOD_ProDKin_1 | 806 | 812 | PF00069 | 0.587 |
MOD_ProDKin_1 | 835 | 841 | PF00069 | 0.686 |
MOD_ProDKin_1 | 852 | 858 | PF00069 | 0.506 |
MOD_ProDKin_1 | 940 | 946 | PF00069 | 0.680 |
MOD_SUMO_for_1 | 210 | 213 | PF00179 | 0.385 |
MOD_SUMO_rev_2 | 136 | 142 | PF00179 | 0.385 |
MOD_SUMO_rev_2 | 203 | 212 | PF00179 | 0.385 |
MOD_SUMO_rev_2 | 232 | 240 | PF00179 | 0.385 |
MOD_SUMO_rev_2 | 26 | 36 | PF00179 | 0.311 |
MOD_SUMO_rev_2 | 392 | 397 | PF00179 | 0.664 |
TRG_DiLeu_BaEn_2 | 350 | 356 | PF01217 | 0.385 |
TRG_DiLeu_BaLyEn_6 | 181 | 186 | PF01217 | 0.243 |
TRG_DiLeu_BaLyEn_6 | 461 | 466 | PF01217 | 0.571 |
TRG_DiLeu_BaLyEn_6 | 944 | 949 | PF01217 | 0.548 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 858 | 861 | PF00928 | 0.531 |
TRG_ER_diArg_1 | 313 | 316 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 531 | 534 | PF00400 | 0.703 |
TRG_Pf-PMV_PEXEL_1 | 380 | 384 | PF00026 | 0.243 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X6S4 | Leishmania donovani | 70% | 99% |
A4I978 | Leishmania infantum | 70% | 99% |
E9B419 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 99% |
Q4Q405 | Leishmania major | 68% | 100% |