A protein kinase likely belonging to the STE20 kinase family. The TM segments are a kinetoplastid innovation, but the kinase is otherwise conservative.
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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A0A3S7WQE5
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 10 |
GO:0006793 | phosphorus metabolic process | 3 | 10 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016310 | phosphorylation | 5 | 10 |
GO:0019538 | protein metabolic process | 3 | 10 |
GO:0036211 | protein modification process | 4 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043412 | macromolecule modification | 4 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 10 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006163 | purine nucleotide metabolic process | 5 | 1 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 1 |
GO:0006171 | cAMP biosynthetic process | 8 | 1 |
GO:0006182 | cGMP biosynthetic process | 8 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009117 | nucleotide metabolic process | 5 | 1 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 1 |
GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 1 |
GO:0009165 | nucleotide biosynthetic process | 6 | 1 |
GO:0009187 | cyclic nucleotide metabolic process | 6 | 1 |
GO:0009190 | cyclic nucleotide biosynthetic process | 7 | 1 |
GO:0009259 | ribonucleotide metabolic process | 5 | 1 |
GO:0009260 | ribonucleotide biosynthetic process | 6 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0019637 | organophosphate metabolic process | 3 | 1 |
GO:0019693 | ribose phosphate metabolic process | 4 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0044281 | small molecule metabolic process | 2 | 1 |
GO:0046058 | cAMP metabolic process | 7 | 1 |
GO:0046068 | cGMP metabolic process | 7 | 1 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0052652 | cyclic purine nucleotide metabolic process | 6 | 1 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 1 |
GO:0072521 | purine-containing compound metabolic process | 4 | 1 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 1 |
GO:0090407 | organophosphate biosynthetic process | 4 | 1 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 1 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 1 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004672 | protein kinase activity | 3 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0016301 | kinase activity | 4 | 10 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 10 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 299 | 301 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.616 |
CLV_NRD_NRD_1 | 615 | 617 | PF00675 | 0.322 |
CLV_NRD_NRD_1 | 736 | 738 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 830 | 832 | PF00675 | 0.342 |
CLV_PCSK_FUR_1 | 613 | 617 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 474 | 476 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 613 | 615 | PF00082 | 0.324 |
CLV_PCSK_KEX2_1 | 736 | 738 | PF00082 | 0.356 |
CLV_PCSK_KEX2_1 | 805 | 807 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 830 | 832 | PF00082 | 0.342 |
CLV_PCSK_PC1ET2_1 | 298 | 300 | PF00082 | 0.525 |
CLV_PCSK_PC1ET2_1 | 805 | 807 | PF00082 | 0.334 |
CLV_PCSK_PC1ET2_1 | 830 | 832 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.568 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 600 | 604 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 736 | 740 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 802 | 806 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 814 | 818 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 832 | 836 | PF00082 | 0.229 |
CLV_Separin_Metazoa | 314 | 318 | PF03568 | 0.753 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.811 |
DEG_SCF_FBW7_1 | 522 | 528 | PF00400 | 0.758 |
DEG_SCF_FBW7_1 | 556 | 562 | PF00400 | 0.701 |
DEG_SPOP_SBC_1 | 39 | 43 | PF00917 | 0.688 |
DEG_SPOP_SBC_1 | 446 | 450 | PF00917 | 0.798 |
DEG_SPOP_SBC_1 | 847 | 851 | PF00917 | 0.703 |
DOC_ANK_TNKS_1 | 694 | 701 | PF00023 | 0.606 |
DOC_CDC14_PxL_1 | 423 | 431 | PF14671 | 0.730 |
DOC_CDC14_PxL_1 | 45 | 53 | PF14671 | 0.498 |
DOC_CKS1_1 | 12 | 17 | PF01111 | 0.669 |
DOC_CKS1_1 | 440 | 445 | PF01111 | 0.758 |
DOC_CKS1_1 | 522 | 527 | PF01111 | 0.758 |
DOC_CKS1_1 | 556 | 561 | PF01111 | 0.710 |
DOC_CKS1_1 | 808 | 813 | PF01111 | 0.558 |
DOC_CYCLIN_yCln2_LP_2 | 547 | 553 | PF00134 | 0.680 |
DOC_MAPK_gen_1 | 298 | 307 | PF00069 | 0.673 |
DOC_MAPK_gen_1 | 340 | 348 | PF00069 | 0.683 |
DOC_MAPK_gen_1 | 614 | 625 | PF00069 | 0.522 |
DOC_MAPK_gen_1 | 813 | 821 | PF00069 | 0.554 |
DOC_MAPK_HePTP_8 | 297 | 309 | PF00069 | 0.711 |
DOC_MAPK_MEF2A_6 | 298 | 306 | PF00069 | 0.676 |
DOC_MAPK_MEF2A_6 | 582 | 590 | PF00069 | 0.534 |
DOC_MAPK_MEF2A_6 | 813 | 821 | PF00069 | 0.594 |
DOC_MAPK_MEF2A_6 | 95 | 103 | PF00069 | 0.361 |
DOC_PP1_RVXF_1 | 276 | 283 | PF00149 | 0.677 |
DOC_PP2B_LxvP_1 | 46 | 49 | PF13499 | 0.498 |
DOC_PP2B_LxvP_1 | 838 | 841 | PF13499 | 0.558 |
DOC_PP4_FxxP_1 | 239 | 242 | PF00568 | 0.817 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.819 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.798 |
DOC_USP7_MATH_1 | 540 | 544 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 677 | 681 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 741 | 745 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 847 | 851 | PF00917 | 0.712 |
DOC_USP7_UBL2_3 | 835 | 839 | PF12436 | 0.596 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.764 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.827 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.747 |
DOC_WW_Pin1_4 | 521 | 526 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 541 | 546 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 555 | 560 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 746 | 751 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 807 | 812 | PF00397 | 0.558 |
LIG_14-3-3_CanoR_1 | 277 | 283 | PF00244 | 0.828 |
LIG_14-3-3_CanoR_1 | 352 | 358 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 36 | 46 | PF00244 | 0.710 |
LIG_14-3-3_CanoR_1 | 474 | 482 | PF00244 | 0.790 |
LIG_14-3-3_CanoR_1 | 587 | 597 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 642 | 652 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 736 | 746 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 74 | 79 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 831 | 838 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 95 | 99 | PF00244 | 0.406 |
LIG_Actin_WH2_2 | 648 | 664 | PF00022 | 0.618 |
LIG_AP2alpha_1 | 378 | 382 | PF02296 | 0.746 |
LIG_APCC_ABBA_1 | 346 | 351 | PF00400 | 0.674 |
LIG_APCC_ABBAyCdc20_2 | 707 | 713 | PF00400 | 0.596 |
LIG_BRCT_BRCA1_1 | 146 | 150 | PF00533 | 0.753 |
LIG_BRCT_BRCA1_1 | 278 | 282 | PF00533 | 0.770 |
LIG_BRCT_BRCA1_1 | 326 | 330 | PF00533 | 0.689 |
LIG_BRCT_BRCA1_1 | 542 | 546 | PF00533 | 0.757 |
LIG_CSL_BTD_1 | 246 | 249 | PF09270 | 0.808 |
LIG_deltaCOP1_diTrp_1 | 767 | 771 | PF00928 | 0.519 |
LIG_EH1_1 | 55 | 63 | PF00400 | 0.499 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.780 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.722 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.658 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.704 |
LIG_FHA_1 | 518 | 524 | PF00498 | 0.799 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.301 |
LIG_FHA_1 | 644 | 650 | PF00498 | 0.543 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.402 |
LIG_FHA_1 | 737 | 743 | PF00498 | 0.567 |
LIG_FHA_1 | 778 | 784 | PF00498 | 0.596 |
LIG_FHA_2 | 12 | 18 | PF00498 | 0.682 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.729 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.750 |
LIG_FHA_2 | 405 | 411 | PF00498 | 0.707 |
LIG_FHA_2 | 426 | 432 | PF00498 | 0.764 |
LIG_FHA_2 | 474 | 480 | PF00498 | 0.812 |
LIG_FHA_2 | 492 | 498 | PF00498 | 0.735 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.744 |
LIG_FHA_2 | 505 | 511 | PF00498 | 0.766 |
LIG_FHA_2 | 556 | 562 | PF00498 | 0.706 |
LIG_FHA_2 | 624 | 630 | PF00498 | 0.559 |
LIG_FHA_2 | 756 | 762 | PF00498 | 0.623 |
LIG_FHA_2 | 822 | 828 | PF00498 | 0.562 |
LIG_FHA_2 | 831 | 837 | PF00498 | 0.494 |
LIG_GBD_Chelix_1 | 302 | 310 | PF00786 | 0.552 |
LIG_Integrin_RGD_1 | 606 | 608 | PF01839 | 0.406 |
LIG_IRF3_LxIS_1 | 106 | 113 | PF10401 | 0.440 |
LIG_IRF3_LxIS_1 | 585 | 591 | PF10401 | 0.606 |
LIG_LIR_Apic_2 | 749 | 755 | PF02991 | 0.519 |
LIG_LIR_Gen_1 | 113 | 121 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 356 | 364 | PF02991 | 0.699 |
LIG_LIR_Gen_1 | 42 | 51 | PF02991 | 0.571 |
LIG_LIR_Gen_1 | 453 | 462 | PF02991 | 0.771 |
LIG_LIR_Gen_1 | 558 | 564 | PF02991 | 0.669 |
LIG_LIR_Gen_1 | 593 | 604 | PF02991 | 0.579 |
LIG_LIR_Gen_1 | 70 | 79 | PF02991 | 0.489 |
LIG_LIR_Gen_1 | 97 | 108 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 113 | 117 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 147 | 152 | PF02991 | 0.727 |
LIG_LIR_Nem_3 | 171 | 175 | PF02991 | 0.680 |
LIG_LIR_Nem_3 | 308 | 312 | PF02991 | 0.699 |
LIG_LIR_Nem_3 | 356 | 360 | PF02991 | 0.644 |
LIG_LIR_Nem_3 | 42 | 48 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 431 | 437 | PF02991 | 0.717 |
LIG_LIR_Nem_3 | 453 | 457 | PF02991 | 0.777 |
LIG_LIR_Nem_3 | 558 | 563 | PF02991 | 0.693 |
LIG_LIR_Nem_3 | 593 | 599 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 70 | 75 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 791 | 795 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.398 |
LIG_MLH1_MIPbox_1 | 146 | 150 | PF16413 | 0.724 |
LIG_PCNA_TLS_4 | 814 | 821 | PF02747 | 0.596 |
LIG_PDZ_Class_3 | 849 | 854 | PF00595 | 0.780 |
LIG_Pex14_1 | 168 | 172 | PF04695 | 0.700 |
LIG_Pex14_1 | 357 | 361 | PF04695 | 0.736 |
LIG_Pex14_2 | 378 | 382 | PF04695 | 0.722 |
LIG_Rb_LxCxE_1 | 818 | 836 | PF01857 | 0.461 |
LIG_SH2_CRK | 96 | 100 | PF00017 | 0.498 |
LIG_SH2_GRB2like | 63 | 66 | PF00017 | 0.570 |
LIG_SH2_PTP2 | 437 | 440 | PF00017 | 0.722 |
LIG_SH2_PTP2 | 63 | 66 | PF00017 | 0.570 |
LIG_SH2_SRC | 24 | 27 | PF00017 | 0.759 |
LIG_SH2_SRC | 63 | 66 | PF00017 | 0.570 |
LIG_SH2_SRC | 826 | 829 | PF00017 | 0.547 |
LIG_SH2_STAP1 | 349 | 353 | PF00017 | 0.703 |
LIG_SH2_STAP1 | 560 | 564 | PF00017 | 0.693 |
LIG_SH2_STAP1 | 785 | 789 | PF00017 | 0.608 |
LIG_SH2_STAP1 | 96 | 100 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 393 | 396 | PF00017 | 0.745 |
LIG_SH2_STAT5 | 399 | 402 | PF00017 | 0.728 |
LIG_SH2_STAT5 | 434 | 437 | PF00017 | 0.718 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 651 | 654 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 667 | 670 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 793 | 796 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 842 | 845 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.412 |
LIG_SH3_3 | 519 | 525 | PF00018 | 0.792 |
LIG_SH3_3 | 539 | 545 | PF00018 | 0.792 |
LIG_SH3_3 | 553 | 559 | PF00018 | 0.677 |
LIG_SH3_3 | 716 | 722 | PF00018 | 0.558 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.489 |
LIG_SUMO_SIM_anti_2 | 102 | 107 | PF11976 | 0.492 |
LIG_SUMO_SIM_anti_2 | 636 | 641 | PF11976 | 0.561 |
LIG_SUMO_SIM_par_1 | 130 | 135 | PF11976 | 0.728 |
LIG_SUMO_SIM_par_1 | 303 | 308 | PF11976 | 0.710 |
LIG_SUMO_SIM_par_1 | 344 | 351 | PF11976 | 0.718 |
LIG_TYR_ITIM | 310 | 315 | PF00017 | 0.634 |
LIG_TYR_ITIM | 61 | 66 | PF00017 | 0.569 |
LIG_WRC_WIRS_1 | 306 | 311 | PF05994 | 0.703 |
LIG_WRC_WIRS_1 | 560 | 565 | PF05994 | 0.548 |
LIG_WRC_WIRS_1 | 651 | 656 | PF05994 | 0.434 |
LIG_WRC_WIRS_1 | 66 | 71 | PF05994 | 0.541 |
LIG_WRC_WIRS_1 | 768 | 773 | PF05994 | 0.376 |
MOD_CDK_SPxK_1 | 807 | 813 | PF00069 | 0.425 |
MOD_CDK_SPxxK_3 | 807 | 814 | PF00069 | 0.484 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.768 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.752 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.652 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.633 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.607 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.714 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.783 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.494 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.665 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.754 |
MOD_CK2_1 | 308 | 314 | PF00069 | 0.668 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.694 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.558 |
MOD_CK2_1 | 425 | 431 | PF00069 | 0.619 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.789 |
MOD_CK2_1 | 555 | 561 | PF00069 | 0.650 |
MOD_CK2_1 | 623 | 629 | PF00069 | 0.440 |
MOD_CK2_1 | 650 | 656 | PF00069 | 0.386 |
MOD_CK2_1 | 741 | 747 | PF00069 | 0.466 |
MOD_CK2_1 | 755 | 761 | PF00069 | 0.346 |
MOD_CK2_1 | 846 | 852 | PF00069 | 0.638 |
MOD_Cter_Amidation | 828 | 831 | PF01082 | 0.294 |
MOD_GlcNHglycan | 171 | 175 | PF01048 | 0.677 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.757 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.485 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.813 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.758 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.600 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.606 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.807 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.748 |
MOD_GlcNHglycan | 723 | 726 | PF01048 | 0.431 |
MOD_GlcNHglycan | 743 | 746 | PF01048 | 0.385 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.637 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.821 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.701 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.655 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.725 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.565 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.649 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.525 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.712 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.727 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.749 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.721 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.590 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.509 |
MOD_GSK3_1 | 732 | 739 | PF00069 | 0.387 |
MOD_GSK3_1 | 751 | 758 | PF00069 | 0.427 |
MOD_N-GLC_2 | 335 | 337 | PF02516 | 0.657 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.325 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.674 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.638 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.681 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.783 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.759 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.434 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.537 |
MOD_NEK2_1 | 676 | 681 | PF00069 | 0.503 |
MOD_NEK2_1 | 732 | 737 | PF00069 | 0.403 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.391 |
MOD_NEK2_2 | 559 | 564 | PF00069 | 0.569 |
MOD_NEK2_2 | 785 | 790 | PF00069 | 0.454 |
MOD_PIKK_1 | 206 | 212 | PF00454 | 0.752 |
MOD_PIKK_1 | 793 | 799 | PF00454 | 0.431 |
MOD_PKA_1 | 474 | 480 | PF00069 | 0.757 |
MOD_PKA_1 | 736 | 742 | PF00069 | 0.431 |
MOD_PKA_1 | 830 | 836 | PF00069 | 0.431 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.649 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.713 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.730 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.724 |
MOD_PKA_2 | 473 | 479 | PF00069 | 0.760 |
MOD_PKA_2 | 643 | 649 | PF00069 | 0.498 |
MOD_PKA_2 | 736 | 742 | PF00069 | 0.431 |
MOD_PKA_2 | 830 | 836 | PF00069 | 0.376 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.486 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.625 |
MOD_Plk_1 | 293 | 299 | PF00069 | 0.710 |
MOD_Plk_1 | 409 | 415 | PF00069 | 0.605 |
MOD_Plk_1 | 464 | 470 | PF00069 | 0.751 |
MOD_Plk_1 | 785 | 791 | PF00069 | 0.454 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.574 |
MOD_Plk_2-3 | 19 | 25 | PF00069 | 0.777 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.676 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.717 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.716 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.597 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.384 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.605 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.596 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.550 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.332 |
MOD_Plk_4 | 559 | 565 | PF00069 | 0.548 |
MOD_Plk_4 | 573 | 579 | PF00069 | 0.434 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.427 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.718 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.806 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.574 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.718 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.657 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.667 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.696 |
MOD_ProDKin_1 | 521 | 527 | PF00069 | 0.715 |
MOD_ProDKin_1 | 541 | 547 | PF00069 | 0.533 |
MOD_ProDKin_1 | 555 | 561 | PF00069 | 0.449 |
MOD_ProDKin_1 | 746 | 752 | PF00069 | 0.379 |
MOD_ProDKin_1 | 807 | 813 | PF00069 | 0.431 |
MOD_SUMO_for_1 | 602 | 605 | PF00179 | 0.440 |
MOD_SUMO_for_1 | 804 | 807 | PF00179 | 0.396 |
MOD_SUMO_rev_2 | 574 | 583 | PF00179 | 0.434 |
MOD_SUMO_rev_2 | 605 | 612 | PF00179 | 0.498 |
MOD_SUMO_rev_2 | 653 | 661 | PF00179 | 0.440 |
TRG_DiLeu_BaEn_1 | 410 | 415 | PF01217 | 0.671 |
TRG_DiLeu_BaEn_2 | 591 | 597 | PF01217 | 0.498 |
TRG_DiLeu_BaEn_2 | 698 | 704 | PF01217 | 0.431 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.578 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.631 |
TRG_ENDOCYTIC_2 | 437 | 440 | PF00928 | 0.659 |
TRG_ENDOCYTIC_2 | 560 | 563 | PF00928 | 0.617 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.564 |
TRG_ENDOCYTIC_2 | 651 | 654 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 792 | 795 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.412 |
TRG_ER_diArg_1 | 117 | 119 | PF00400 | 0.654 |
TRG_ER_diArg_1 | 383 | 385 | PF00400 | 0.713 |
TRG_ER_diArg_1 | 473 | 475 | PF00400 | 0.792 |
TRG_ER_diArg_1 | 612 | 615 | PF00400 | 0.384 |
TRG_NES_CRM1_1 | 128 | 139 | PF08389 | 0.665 |
TRG_NLS_Bipartite_1 | 813 | 834 | PF00514 | 0.425 |
TRG_NLS_MonoExtN_4 | 828 | 834 | PF00514 | 0.425 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5H9 | Leptomonas seymouri | 48% | 98% |
A0A3S5H699 | Leishmania donovani | 100% | 100% |
A4HC47 | Leishmania braziliensis | 85% | 99% |
E9AG93 | Leishmania infantum | 100% | 100% |
E9AMJ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 99% |
Q4QI37 | Leishmania major | 95% | 100% |
Q4QI43 | Leishmania major | 96% | 100% |
V5BPV2 | Trypanosoma cruzi | 26% | 88% |