A large and apprently artificial collection of diverse kinetoplastid protein kinases. A subfamily has 2TM regions, but the majority is cytoplasmic.
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: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 20 |
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: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 3 |
GO:0016020 | membrane | 2 | 14 |
GO:0110165 | cellular anatomical entity | 1 | 14 |
Related structures:
AlphaFold database: Q4Q920
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 9 |
GO:0006468 | protein phosphorylation | 5 | 16 |
GO:0006793 | phosphorus metabolic process | 3 | 16 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 16 |
GO:0006807 | nitrogen compound metabolic process | 2 | 16 |
GO:0008152 | metabolic process | 1 | 16 |
GO:0009889 | regulation of biosynthetic process | 4 | 9 |
GO:0009987 | cellular process | 1 | 16 |
GO:0010468 | regulation of gene expression | 5 | 9 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 9 |
GO:0016310 | phosphorylation | 5 | 16 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 9 |
GO:0019222 | regulation of metabolic process | 3 | 9 |
GO:0019538 | protein metabolic process | 3 | 16 |
GO:0031323 | regulation of cellular metabolic process | 4 | 9 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 9 |
GO:0036211 | protein modification process | 4 | 16 |
GO:0043170 | macromolecule metabolic process | 3 | 16 |
GO:0043412 | macromolecule modification | 4 | 16 |
GO:0044237 | cellular metabolic process | 2 | 16 |
GO:0044238 | primary metabolic process | 2 | 16 |
GO:0050789 | regulation of biological process | 2 | 9 |
GO:0050794 | regulation of cellular process | 3 | 9 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 9 |
GO:0051252 | regulation of RNA metabolic process | 5 | 9 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 9 |
GO:0065007 | biological regulation | 1 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 16 |
GO:0080090 | regulation of primary metabolic process | 4 | 9 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 16 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 9 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 16 |
GO:0003824 | catalytic activity | 1 | 16 |
GO:0004672 | protein kinase activity | 3 | 16 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 4 |
GO:0005488 | binding | 1 | 16 |
GO:0005524 | ATP binding | 5 | 16 |
GO:0016301 | kinase activity | 4 | 16 |
GO:0016740 | transferase activity | 2 | 16 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 16 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 16 |
GO:0017076 | purine nucleotide binding | 4 | 16 |
GO:0030554 | adenyl nucleotide binding | 5 | 16 |
GO:0032553 | ribonucleotide binding | 3 | 16 |
GO:0032555 | purine ribonucleotide binding | 4 | 16 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 16 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 16 |
GO:0036094 | small molecule binding | 2 | 16 |
GO:0043167 | ion binding | 2 | 16 |
GO:0043168 | anion binding | 3 | 16 |
GO:0097159 | organic cyclic compound binding | 2 | 16 |
GO:0097367 | carbohydrate derivative binding | 2 | 16 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 16 |
GO:1901265 | nucleoside phosphate binding | 3 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 582 | 586 | PF00656 | 0.497 |
CLV_C14_Caspase3-7 | 809 | 813 | PF00656 | 0.531 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.692 |
CLV_NRD_NRD_1 | 704 | 706 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 809 | 811 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 833 | 835 | PF00675 | 0.352 |
CLV_NRD_NRD_1 | 975 | 977 | PF00675 | 0.354 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 704 | 706 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 833 | 835 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 975 | 977 | PF00082 | 0.315 |
CLV_PCSK_PC1ET2_1 | 116 | 118 | PF00082 | 0.453 |
CLV_PCSK_PC1ET2_1 | 259 | 261 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 565 | 569 | PF00082 | 0.652 |
CLV_PCSK_SKI1_1 | 628 | 632 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 668 | 672 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 733 | 737 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 847 | 851 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 864 | 868 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.378 |
DEG_APCC_DBOX_1 | 348 | 356 | PF00400 | 0.711 |
DEG_APCC_DBOX_1 | 472 | 480 | PF00400 | 0.451 |
DEG_APCC_DBOX_1 | 846 | 854 | PF00400 | 0.502 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.740 |
DOC_CDC14_PxL_1 | 20 | 28 | PF14671 | 0.612 |
DOC_CYCLIN_RxL_1 | 114 | 124 | PF00134 | 0.639 |
DOC_CYCLIN_RxL_1 | 728 | 741 | PF00134 | 0.644 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 617 | 626 | PF00134 | 0.317 |
DOC_CYCLIN_yCln2_LP_2 | 2 | 8 | PF00134 | 0.687 |
DOC_MAPK_gen_1 | 115 | 121 | PF00069 | 0.641 |
DOC_MAPK_gen_1 | 345 | 355 | PF00069 | 0.708 |
DOC_MAPK_gen_1 | 48 | 56 | PF00069 | 0.670 |
DOC_MAPK_gen_1 | 704 | 712 | PF00069 | 0.597 |
DOC_MAPK_gen_1 | 728 | 737 | PF00069 | 0.675 |
DOC_MAPK_gen_1 | 810 | 817 | PF00069 | 0.496 |
DOC_MAPK_gen_1 | 833 | 842 | PF00069 | 0.531 |
DOC_MAPK_gen_1 | 864 | 873 | PF00069 | 0.500 |
DOC_MAPK_HePTP_8 | 702 | 714 | PF00069 | 0.666 |
DOC_MAPK_JIP1_4 | 836 | 842 | PF00069 | 0.583 |
DOC_MAPK_MEF2A_6 | 348 | 357 | PF00069 | 0.654 |
DOC_MAPK_MEF2A_6 | 50 | 58 | PF00069 | 0.660 |
DOC_MAPK_MEF2A_6 | 650 | 658 | PF00069 | 0.664 |
DOC_MAPK_MEF2A_6 | 705 | 714 | PF00069 | 0.636 |
DOC_MAPK_MEF2A_6 | 810 | 819 | PF00069 | 0.497 |
DOC_PP1_RVXF_1 | 131 | 137 | PF00149 | 0.667 |
DOC_PP1_RVXF_1 | 16 | 22 | PF00149 | 0.559 |
DOC_PP2B_LxvP_1 | 484 | 487 | PF13499 | 0.402 |
DOC_PP4_FxxP_1 | 21 | 24 | PF00568 | 0.549 |
DOC_PP4_FxxP_1 | 929 | 932 | PF00568 | 0.502 |
DOC_USP7_MATH_1 | 1006 | 1010 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 992 | 996 | PF00917 | 0.623 |
DOC_USP7_UBL2_3 | 141 | 145 | PF12436 | 0.547 |
DOC_USP7_UBL2_3 | 246 | 250 | PF12436 | 0.801 |
DOC_USP7_UBL2_3 | 768 | 772 | PF12436 | 0.500 |
DOC_USP7_UBL2_3 | 87 | 91 | PF12436 | 0.689 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 738 | 743 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 930 | 935 | PF00397 | 0.588 |
LIG_14-3-3_CanoR_1 | 115 | 120 | PF00244 | 0.647 |
LIG_14-3-3_CanoR_1 | 133 | 139 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 420 | 430 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 553 | 561 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 646 | 654 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 733 | 738 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 847 | 856 | PF00244 | 0.505 |
LIG_APCC_ABBA_1 | 815 | 820 | PF00400 | 0.466 |
LIG_BIR_III_2 | 585 | 589 | PF00653 | 0.493 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.727 |
LIG_Clathr_ClatBox_1 | 997 | 1001 | PF01394 | 0.619 |
LIG_deltaCOP1_diTrp_1 | 454 | 459 | PF00928 | 0.441 |
LIG_EVH1_2 | 69 | 73 | PF00568 | 0.580 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.704 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.502 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.399 |
LIG_FHA_1 | 509 | 515 | PF00498 | 0.367 |
LIG_FHA_1 | 518 | 524 | PF00498 | 0.424 |
LIG_FHA_1 | 527 | 533 | PF00498 | 0.319 |
LIG_FHA_1 | 604 | 610 | PF00498 | 0.365 |
LIG_FHA_1 | 612 | 618 | PF00498 | 0.378 |
LIG_FHA_1 | 627 | 633 | PF00498 | 0.353 |
LIG_FHA_1 | 759 | 765 | PF00498 | 0.546 |
LIG_FHA_1 | 825 | 831 | PF00498 | 0.583 |
LIG_FHA_1 | 875 | 881 | PF00498 | 0.516 |
LIG_FHA_1 | 944 | 950 | PF00498 | 0.533 |
LIG_FHA_2 | 1000 | 1006 | PF00498 | 0.677 |
LIG_FHA_2 | 458 | 464 | PF00498 | 0.402 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.660 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.655 |
LIG_GBD_Chelix_1 | 842 | 850 | PF00786 | 0.341 |
LIG_LIR_Apic_2 | 269 | 275 | PF02991 | 0.709 |
LIG_LIR_Apic_2 | 898 | 904 | PF02991 | 0.500 |
LIG_LIR_Apic_2 | 927 | 932 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 204 | 211 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 28 | 39 | PF02991 | 0.568 |
LIG_LIR_Gen_1 | 456 | 466 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 52 | 63 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 629 | 637 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 816 | 826 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 160 | 164 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 204 | 208 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.679 |
LIG_LIR_Nem_3 | 269 | 274 | PF02991 | 0.662 |
LIG_LIR_Nem_3 | 28 | 34 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 397 | 401 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 456 | 462 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 498 | 502 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 52 | 58 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 629 | 634 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 71 | 76 | PF02991 | 0.664 |
LIG_LIR_Nem_3 | 753 | 757 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 816 | 821 | PF02991 | 0.583 |
LIG_NRBOX | 547 | 553 | PF00104 | 0.491 |
LIG_PCNA_yPIPBox_3 | 954 | 965 | PF02747 | 0.564 |
LIG_SH2_CRK | 218 | 222 | PF00017 | 0.697 |
LIG_SH2_CRK | 272 | 276 | PF00017 | 0.616 |
LIG_SH2_CRK | 754 | 758 | PF00017 | 0.591 |
LIG_SH2_NCK_1 | 272 | 276 | PF00017 | 0.616 |
LIG_SH2_SRC | 225 | 228 | PF00017 | 0.658 |
LIG_SH2_SRC | 284 | 287 | PF00017 | 0.658 |
LIG_SH2_SRC | 855 | 858 | PF00017 | 0.515 |
LIG_SH2_STAP1 | 218 | 222 | PF00017 | 0.694 |
LIG_SH2_STAT3 | 775 | 778 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.726 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.590 |
LIG_SH2_STAT5 | 560 | 563 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 775 | 778 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 805 | 808 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 855 | 858 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 951 | 954 | PF00017 | 0.502 |
LIG_SH3_3 | 1008 | 1014 | PF00018 | 0.750 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.352 |
LIG_SH3_3 | 367 | 373 | PF00018 | 0.417 |
LIG_SH3_3 | 38 | 44 | PF00018 | 0.716 |
LIG_SH3_3 | 480 | 486 | PF00018 | 0.444 |
LIG_SUMO_SIM_anti_2 | 170 | 176 | PF11976 | 0.462 |
LIG_SUMO_SIM_anti_2 | 623 | 629 | PF11976 | 0.449 |
LIG_SUMO_SIM_anti_2 | 653 | 658 | PF11976 | 0.553 |
LIG_SUMO_SIM_anti_2 | 790 | 796 | PF11976 | 0.512 |
LIG_SUMO_SIM_par_1 | 162 | 168 | PF11976 | 0.356 |
LIG_SUMO_SIM_par_1 | 193 | 199 | PF11976 | 0.398 |
LIG_SUMO_SIM_par_1 | 623 | 629 | PF11976 | 0.419 |
LIG_TRAF2_1 | 239 | 242 | PF00917 | 0.766 |
LIG_TRAF2_1 | 727 | 730 | PF00917 | 0.653 |
LIG_TRFH_1 | 969 | 973 | PF08558 | 0.467 |
LIG_TYR_ITIM | 216 | 221 | PF00017 | 0.667 |
LIG_TYR_ITIM | 53 | 58 | PF00017 | 0.352 |
LIG_TYR_ITSM | 267 | 274 | PF00017 | 0.643 |
LIG_UBA3_1 | 352 | 356 | PF00899 | 0.661 |
LIG_UBA3_1 | 624 | 628 | PF00899 | 0.390 |
LIG_UBA3_1 | 961 | 967 | PF00899 | 0.359 |
LIG_WRC_WIRS_1 | 158 | 163 | PF05994 | 0.511 |
LIG_WRC_WIRS_1 | 202 | 207 | PF05994 | 0.467 |
MOD_CDK_SPxxK_3 | 738 | 745 | PF00069 | 0.469 |
MOD_CK1_1 | 1015 | 1021 | PF00069 | 0.606 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.465 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.440 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.664 |
MOD_CK1_1 | 633 | 639 | PF00069 | 0.381 |
MOD_CK1_1 | 741 | 747 | PF00069 | 0.366 |
MOD_CK1_1 | 762 | 768 | PF00069 | 0.351 |
MOD_CK1_1 | 782 | 788 | PF00069 | 0.173 |
MOD_CK1_1 | 986 | 992 | PF00069 | 0.412 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.725 |
MOD_CK2_1 | 457 | 463 | PF00069 | 0.484 |
MOD_CK2_1 | 633 | 639 | PF00069 | 0.403 |
MOD_CK2_1 | 723 | 729 | PF00069 | 0.556 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.566 |
MOD_Cter_Amidation | 831 | 834 | PF01082 | 0.396 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.433 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.569 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.304 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.775 |
MOD_GlcNHglycan | 647 | 650 | PF01048 | 0.612 |
MOD_GlcNHglycan | 725 | 728 | PF01048 | 0.659 |
MOD_GlcNHglycan | 77 | 82 | PF01048 | 0.618 |
MOD_GlcNHglycan | 988 | 991 | PF01048 | 0.533 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.601 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.650 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.371 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.662 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.611 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.496 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.604 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.382 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.520 |
MOD_GSK3_1 | 758 | 765 | PF00069 | 0.373 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.597 |
MOD_GSK3_1 | 779 | 786 | PF00069 | 0.467 |
MOD_GSK3_1 | 789 | 796 | PF00069 | 0.467 |
MOD_GSK3_1 | 874 | 881 | PF00069 | 0.361 |
MOD_GSK3_1 | 986 | 993 | PF00069 | 0.433 |
MOD_N-GLC_1 | 517 | 522 | PF02516 | 0.599 |
MOD_N-GLC_1 | 603 | 608 | PF02516 | 0.485 |
MOD_N-GLC_1 | 620 | 625 | PF02516 | 0.350 |
MOD_N-GLC_1 | 813 | 818 | PF02516 | 0.467 |
MOD_N-GLC_1 | 937 | 942 | PF02516 | 0.456 |
MOD_N-GLC_1 | 990 | 995 | PF02516 | 0.412 |
MOD_N-GLC_2 | 130 | 132 | PF02516 | 0.473 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.563 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.378 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.368 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.666 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.592 |
MOD_NEK2_1 | 517 | 522 | PF00069 | 0.529 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.387 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.459 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.479 |
MOD_NEK2_1 | 594 | 599 | PF00069 | 0.601 |
MOD_NEK2_1 | 626 | 631 | PF00069 | 0.357 |
MOD_NEK2_1 | 774 | 779 | PF00069 | 0.406 |
MOD_NEK2_1 | 936 | 941 | PF00069 | 0.344 |
MOD_NEK2_1 | 983 | 988 | PF00069 | 0.275 |
MOD_NEK2_2 | 210 | 215 | PF00069 | 0.707 |
MOD_PIKK_1 | 1013 | 1019 | PF00454 | 0.572 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.668 |
MOD_PIKK_1 | 594 | 600 | PF00454 | 0.658 |
MOD_PIKK_1 | 774 | 780 | PF00454 | 0.359 |
MOD_PKA_1 | 115 | 121 | PF00069 | 0.550 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.615 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.707 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.464 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.668 |
MOD_PKA_2 | 552 | 558 | PF00069 | 0.544 |
MOD_PKA_2 | 645 | 651 | PF00069 | 0.636 |
MOD_PKA_2 | 750 | 756 | PF00069 | 0.353 |
MOD_PKA_2 | 895 | 901 | PF00069 | 0.470 |
MOD_PKB_1 | 115 | 123 | PF00069 | 0.542 |
MOD_PKB_1 | 731 | 739 | PF00069 | 0.550 |
MOD_Plk_1 | 418 | 424 | PF00069 | 0.613 |
MOD_Plk_1 | 425 | 431 | PF00069 | 0.616 |
MOD_Plk_1 | 457 | 463 | PF00069 | 0.546 |
MOD_Plk_1 | 603 | 609 | PF00069 | 0.478 |
MOD_Plk_1 | 620 | 626 | PF00069 | 0.220 |
MOD_Plk_1 | 780 | 786 | PF00069 | 0.353 |
MOD_Plk_1 | 789 | 795 | PF00069 | 0.467 |
MOD_Plk_1 | 813 | 819 | PF00069 | 0.389 |
MOD_Plk_1 | 822 | 828 | PF00069 | 0.396 |
MOD_Plk_1 | 937 | 943 | PF00069 | 0.374 |
MOD_Plk_2-3 | 452 | 458 | PF00069 | 0.603 |
MOD_Plk_4 | 1015 | 1021 | PF00069 | 0.698 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.395 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.655 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.367 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.595 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.514 |
MOD_Plk_4 | 498 | 504 | PF00069 | 0.457 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.530 |
MOD_Plk_4 | 555 | 561 | PF00069 | 0.617 |
MOD_Plk_4 | 620 | 626 | PF00069 | 0.410 |
MOD_Plk_4 | 783 | 789 | PF00069 | 0.463 |
MOD_Plk_4 | 813 | 819 | PF00069 | 0.450 |
MOD_Plk_4 | 838 | 844 | PF00069 | 0.365 |
MOD_Plk_4 | 937 | 943 | PF00069 | 0.344 |
MOD_Plk_4 | 983 | 989 | PF00069 | 0.348 |
MOD_Plk_4 | 993 | 999 | PF00069 | 0.546 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.338 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.655 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.606 |
MOD_ProDKin_1 | 738 | 744 | PF00069 | 0.524 |
MOD_ProDKin_1 | 930 | 936 | PF00069 | 0.475 |
MOD_SUMO_for_1 | 873 | 876 | PF00179 | 0.467 |
MOD_SUMO_for_1 | 998 | 1001 | PF00179 | 0.591 |
MOD_SUMO_rev_2 | 1001 | 1009 | PF00179 | 0.598 |
MOD_SUMO_rev_2 | 262 | 269 | PF00179 | 0.669 |
MOD_SUMO_rev_2 | 40 | 49 | PF00179 | 0.569 |
MOD_SUMO_rev_2 | 80 | 89 | PF00179 | 0.611 |
TRG_DiLeu_BaEn_1 | 426 | 431 | PF01217 | 0.651 |
TRG_DiLeu_BaEn_1 | 88 | 93 | PF01217 | 0.516 |
TRG_DiLeu_BaEn_3 | 729 | 735 | PF01217 | 0.543 |
TRG_DiLeu_BaEn_4 | 563 | 569 | PF01217 | 0.459 |
TRG_DiLeu_BaLyEn_6 | 679 | 684 | PF01217 | 0.434 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.626 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 55 | 58 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 754 | 757 | PF00928 | 0.450 |
TRG_ER_diArg_1 | 114 | 117 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 131 | 134 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.651 |
TRG_ER_diArg_1 | 434 | 436 | PF00400 | 0.609 |
TRG_ER_diArg_1 | 703 | 705 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 975 | 977 | PF00400 | 0.427 |
TRG_NLS_MonoExtC_3 | 139 | 144 | PF00514 | 0.541 |
TRG_Pf-PMV_PEXEL_1 | 326 | 330 | PF00026 | 0.427 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7Q2 | Leptomonas seymouri | 81% | 100% |
A0A0N1HX31 | Leptomonas seymouri | 30% | 100% |
A0A0S4JAS0 | Bodo saltans | 29% | 100% |
A0A0S4JMC0 | Bodo saltans | 29% | 100% |
A0A1X0P3F4 | Trypanosomatidae | 29% | 100% |
A0A1X0P7I2 | Trypanosomatidae | 49% | 100% |
A0A3R7K5X0 | Trypanosoma rangeli | 48% | 100% |
A0A3S7WZY4 | Leishmania donovani | 97% | 100% |
A4HD55 | Leishmania braziliensis | 91% | 100% |
A4I2A5 | Leishmania infantum | 97% | 100% |
C9ZXD7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9AYF2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
Q4Q147 | Leishmania major | 29% | 100% |
V5BJQ6 | Trypanosoma cruzi | 48% | 100% |