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: 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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A4HPN6
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 11 |
GO:0006793 | phosphorus metabolic process | 3 | 11 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016310 | phosphorylation | 5 | 11 |
GO:0019538 | protein metabolic process | 3 | 11 |
GO:0036211 | protein modification process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043412 | macromolecule modification | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004672 | protein kinase activity | 3 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0016301 | kinase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 11 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 392 | 396 | PF00656 | 0.617 |
CLV_C14_Caspase3-7 | 637 | 641 | PF00656 | 0.688 |
CLV_C14_Caspase3-7 | 856 | 860 | PF00656 | 0.467 |
CLV_C14_Caspase3-7 | 965 | 969 | PF00656 | 0.738 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 659 | 661 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 683 | 685 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 690 | 692 | PF00675 | 0.440 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.260 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 483 | 485 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 674 | 676 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 682 | 684 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 784 | 786 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 883 | 885 | PF00082 | 0.249 |
CLV_PCSK_PC1ET2_1 | 33 | 35 | PF00082 | 0.289 |
CLV_PCSK_PC1ET2_1 | 483 | 485 | PF00082 | 0.489 |
CLV_PCSK_PC1ET2_1 | 674 | 676 | PF00082 | 0.434 |
CLV_PCSK_PC1ET2_1 | 682 | 684 | PF00082 | 0.417 |
CLV_PCSK_PC1ET2_1 | 784 | 786 | PF00082 | 0.282 |
CLV_PCSK_PC1ET2_1 | 883 | 885 | PF00082 | 0.267 |
CLV_PCSK_PC7_1 | 479 | 485 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 426 | 430 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 530 | 534 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 684 | 688 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 799 | 803 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 816 | 820 | PF00082 | 0.236 |
DEG_APCC_DBOX_1 | 107 | 115 | PF00400 | 0.685 |
DEG_APCC_DBOX_1 | 425 | 433 | PF00400 | 0.607 |
DEG_APCC_DBOX_1 | 504 | 512 | PF00400 | 0.616 |
DOC_CYCLIN_RxL_1 | 421 | 431 | PF00134 | 0.661 |
DOC_CYCLIN_yCln2_LP_2 | 109 | 115 | PF00134 | 0.560 |
DOC_CYCLIN_yCln2_LP_2 | 531 | 537 | PF00134 | 0.562 |
DOC_MAPK_gen_1 | 227 | 236 | PF00069 | 0.643 |
DOC_MAPK_gen_1 | 434 | 442 | PF00069 | 0.612 |
DOC_MAPK_gen_1 | 816 | 825 | PF00069 | 0.436 |
DOC_MAPK_HePTP_8 | 70 | 82 | PF00069 | 0.458 |
DOC_MAPK_MEF2A_6 | 108 | 117 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 73 | 82 | PF00069 | 0.464 |
DOC_MAPK_MEF2A_6 | 762 | 771 | PF00069 | 0.436 |
DOC_PP1_RVXF_1 | 436 | 443 | PF00149 | 0.548 |
DOC_PP2B_LxvP_1 | 109 | 112 | PF13499 | 0.665 |
DOC_PP2B_LxvP_1 | 531 | 534 | PF13499 | 0.557 |
DOC_PP2B_LxvP_1 | 80 | 83 | PF13499 | 0.485 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 552 | 556 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 638 | 642 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.567 |
DOC_USP7_MATH_2 | 895 | 901 | PF00917 | 0.531 |
DOC_USP7_UBL2_3 | 720 | 724 | PF12436 | 0.436 |
DOC_USP7_UBL2_3 | 861 | 865 | PF12436 | 0.531 |
DOC_WW_Pin1_4 | 522 | 527 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 690 | 695 | PF00397 | 0.553 |
LIG_14-3-3_CanoR_1 | 181 | 190 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 326 | 334 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 34 | 44 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 418 | 428 | PF00244 | 0.714 |
LIG_14-3-3_CanoR_1 | 438 | 443 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 484 | 493 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 505 | 509 | PF00244 | 0.712 |
LIG_14-3-3_CanoR_1 | 921 | 929 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 964 | 972 | PF00244 | 0.675 |
LIG_APCC_ABBA_1 | 469 | 474 | PF00400 | 0.704 |
LIG_APCC_ABBA_1 | 932 | 937 | PF00400 | 0.603 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.653 |
LIG_BRCT_BRCA1_1 | 728 | 732 | PF00533 | 0.492 |
LIG_BRCT_BRCA1_1 | 972 | 976 | PF00533 | 0.725 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.372 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.592 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.631 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.648 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.636 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.597 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.582 |
LIG_FHA_1 | 526 | 532 | PF00498 | 0.574 |
LIG_FHA_1 | 711 | 717 | PF00498 | 0.492 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.617 |
LIG_FHA_1 | 764 | 770 | PF00498 | 0.444 |
LIG_FHA_1 | 837 | 843 | PF00498 | 0.478 |
LIG_FHA_1 | 924 | 930 | PF00498 | 0.477 |
LIG_FHA_2 | 183 | 189 | PF00498 | 0.610 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.615 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.536 |
LIG_FHA_2 | 314 | 320 | PF00498 | 0.671 |
LIG_FHA_2 | 776 | 782 | PF00498 | 0.531 |
LIG_LIR_Apic_2 | 849 | 855 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 161 | 171 | PF02991 | 0.629 |
LIG_LIR_Gen_1 | 17 | 25 | PF02991 | 0.662 |
LIG_LIR_Gen_1 | 185 | 195 | PF02991 | 0.545 |
LIG_LIR_Gen_1 | 312 | 322 | PF02991 | 0.629 |
LIG_LIR_Gen_1 | 468 | 476 | PF02991 | 0.526 |
LIG_LIR_Gen_1 | 487 | 496 | PF02991 | 0.682 |
LIG_LIR_Gen_1 | 66 | 74 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 161 | 167 | PF02991 | 0.652 |
LIG_LIR_Nem_3 | 17 | 22 | PF02991 | 0.678 |
LIG_LIR_Nem_3 | 185 | 190 | PF02991 | 0.612 |
LIG_LIR_Nem_3 | 395 | 401 | PF02991 | 0.607 |
LIG_LIR_Nem_3 | 41 | 47 | PF02991 | 0.701 |
LIG_LIR_Nem_3 | 412 | 416 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 468 | 472 | PF02991 | 0.612 |
LIG_LIR_Nem_3 | 487 | 493 | PF02991 | 0.691 |
LIG_LIR_Nem_3 | 62 | 67 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 685 | 690 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 885 | 890 | PF02991 | 0.373 |
LIG_NRBOX | 155 | 161 | PF00104 | 0.193 |
LIG_PCNA_PIPBox_1 | 377 | 386 | PF02747 | 0.590 |
LIG_PCNA_yPIPBox_3 | 776 | 790 | PF02747 | 0.492 |
LIG_PTB_Apo_2 | 463 | 470 | PF02174 | 0.606 |
LIG_SH2_CRK | 164 | 168 | PF00017 | 0.568 |
LIG_SH2_CRK | 44 | 48 | PF00017 | 0.555 |
LIG_SH2_CRK | 490 | 494 | PF00017 | 0.582 |
LIG_SH2_NCK_1 | 187 | 191 | PF00017 | 0.606 |
LIG_SH2_SRC | 13 | 16 | PF00017 | 0.573 |
LIG_SH2_STAP1 | 31 | 35 | PF00017 | 0.551 |
LIG_SH2_STAP1 | 74 | 78 | PF00017 | 0.546 |
LIG_SH2_STAT3 | 403 | 406 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.652 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.737 |
LIG_SH2_STAT5 | 631 | 634 | PF00017 | 0.589 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 757 | 760 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 807 | 810 | PF00017 | 0.445 |
LIG_SH3_3 | 541 | 547 | PF00018 | 0.592 |
LIG_SUMO_SIM_anti_2 | 127 | 132 | PF11976 | 0.435 |
LIG_SUMO_SIM_anti_2 | 149 | 155 | PF11976 | 0.404 |
LIG_SUMO_SIM_anti_2 | 267 | 273 | PF11976 | 0.578 |
LIG_SUMO_SIM_anti_2 | 559 | 565 | PF11976 | 0.574 |
LIG_SUMO_SIM_anti_2 | 742 | 747 | PF11976 | 0.377 |
LIG_SUMO_SIM_par_1 | 111 | 116 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 266 | 273 | PF11976 | 0.519 |
LIG_SUMO_SIM_par_1 | 340 | 345 | PF11976 | 0.667 |
LIG_SUMO_SIM_par_1 | 346 | 351 | PF11976 | 0.623 |
LIG_SUMO_SIM_par_1 | 561 | 567 | PF11976 | 0.532 |
LIG_SUMO_SIM_par_1 | 609 | 615 | PF11976 | 0.639 |
LIG_SUMO_SIM_par_1 | 925 | 931 | PF11976 | 0.527 |
LIG_TRAF2_1 | 211 | 214 | PF00917 | 0.603 |
LIG_TRAF2_1 | 599 | 602 | PF00917 | 0.522 |
LIG_TRAF2_1 | 676 | 679 | PF00917 | 0.577 |
LIG_TRAF2_1 | 894 | 897 | PF00917 | 0.482 |
LIG_TRAF2_1 | 952 | 955 | PF00917 | 0.749 |
LIG_TYR_ITIM | 162 | 167 | PF00017 | 0.654 |
LIG_TYR_ITIM | 42 | 47 | PF00017 | 0.357 |
LIG_TYR_ITSM | 183 | 190 | PF00017 | 0.410 |
LIG_UBA3_1 | 159 | 168 | PF00899 | 0.559 |
LIG_UBA3_1 | 532 | 538 | PF00899 | 0.615 |
LIG_UBA3_1 | 561 | 568 | PF00899 | 0.445 |
LIG_WRC_WIRS_1 | 380 | 385 | PF05994 | 0.509 |
LIG_WRC_WIRS_1 | 439 | 444 | PF05994 | 0.435 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.373 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.547 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.598 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.611 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.438 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.598 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.579 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.500 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.523 |
MOD_CK1_1 | 615 | 621 | PF00069 | 0.375 |
MOD_CK1_1 | 693 | 699 | PF00069 | 0.314 |
MOD_CK1_1 | 714 | 720 | PF00069 | 0.271 |
MOD_CK1_1 | 900 | 906 | PF00069 | 0.404 |
MOD_CK1_1 | 962 | 968 | PF00069 | 0.574 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.524 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.636 |
MOD_CK2_1 | 313 | 319 | PF00069 | 0.604 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.516 |
MOD_CK2_1 | 860 | 866 | PF00069 | 0.404 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.450 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.534 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.589 |
MOD_GlcNHglycan | 412 | 416 | PF01048 | 0.547 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.531 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.596 |
MOD_GlcNHglycan | 513 | 516 | PF01048 | 0.413 |
MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.528 |
MOD_GlcNHglycan | 728 | 731 | PF01048 | 0.376 |
MOD_GlcNHglycan | 862 | 865 | PF01048 | 0.335 |
MOD_GlcNHglycan | 884 | 887 | PF01048 | 0.418 |
MOD_GlcNHglycan | 901 | 905 | PF01048 | 0.393 |
MOD_GlcNHglycan | 961 | 964 | PF01048 | 0.519 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.590 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.629 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.549 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.569 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.519 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.328 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.556 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.617 |
MOD_GSK3_1 | 710 | 717 | PF00069 | 0.289 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.297 |
MOD_GSK3_1 | 830 | 837 | PF00069 | 0.274 |
MOD_GSK3_1 | 860 | 867 | PF00069 | 0.418 |
MOD_GSK3_1 | 916 | 923 | PF00069 | 0.311 |
MOD_GSK3_1 | 959 | 966 | PF00069 | 0.614 |
MOD_N-GLC_1 | 465 | 470 | PF02516 | 0.510 |
MOD_N-GLC_1 | 574 | 579 | PF02516 | 0.439 |
MOD_N-GLC_2 | 194 | 196 | PF02516 | 0.438 |
MOD_N-GLC_2 | 668 | 670 | PF02516 | 0.382 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.431 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.358 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.515 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.437 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.543 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.566 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.531 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.579 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.468 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.486 |
MOD_NEK2_1 | 455 | 460 | PF00069 | 0.539 |
MOD_NEK2_1 | 589 | 594 | PF00069 | 0.355 |
MOD_NEK2_1 | 823 | 828 | PF00069 | 0.307 |
MOD_NEK2_2 | 284 | 289 | PF00069 | 0.475 |
MOD_NEK2_2 | 583 | 588 | PF00069 | 0.551 |
MOD_PIKK_1 | 371 | 377 | PF00454 | 0.483 |
MOD_PIKK_1 | 386 | 392 | PF00454 | 0.414 |
MOD_PIKK_1 | 393 | 399 | PF00454 | 0.574 |
MOD_PIKK_1 | 693 | 699 | PF00454 | 0.335 |
MOD_PIKK_1 | 823 | 829 | PF00454 | 0.404 |
MOD_PIKK_1 | 95 | 101 | PF00454 | 0.466 |
MOD_PKA_1 | 237 | 243 | PF00069 | 0.426 |
MOD_PKA_1 | 483 | 489 | PF00069 | 0.478 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.522 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.381 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.482 |
MOD_PKA_2 | 504 | 510 | PF00069 | 0.653 |
MOD_PKA_2 | 726 | 732 | PF00069 | 0.349 |
MOD_PKA_2 | 920 | 926 | PF00069 | 0.289 |
MOD_PKA_2 | 963 | 969 | PF00069 | 0.609 |
MOD_PKB_1 | 436 | 444 | PF00069 | 0.603 |
MOD_Plk_1 | 307 | 313 | PF00069 | 0.495 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.556 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.369 |
MOD_Plk_1 | 411 | 417 | PF00069 | 0.507 |
MOD_Plk_1 | 465 | 471 | PF00069 | 0.598 |
MOD_Plk_1 | 763 | 769 | PF00069 | 0.272 |
MOD_Plk_1 | 967 | 973 | PF00069 | 0.659 |
MOD_Plk_2-3 | 775 | 781 | PF00069 | 0.314 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.351 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.235 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.331 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.287 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.605 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.641 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.430 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.385 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.442 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.495 |
MOD_Plk_4 | 504 | 510 | PF00069 | 0.663 |
MOD_Plk_4 | 576 | 582 | PF00069 | 0.538 |
MOD_Plk_4 | 793 | 799 | PF00069 | 0.333 |
MOD_Plk_4 | 923 | 929 | PF00069 | 0.284 |
MOD_Plk_4 | 967 | 973 | PF00069 | 0.616 |
MOD_ProDKin_1 | 522 | 528 | PF00069 | 0.441 |
MOD_ProDKin_1 | 690 | 696 | PF00069 | 0.430 |
MOD_SUMO_for_1 | 537 | 540 | PF00179 | 0.601 |
MOD_SUMO_rev_2 | 441 | 449 | PF00179 | 0.680 |
MOD_SUMO_rev_2 | 477 | 485 | PF00179 | 0.402 |
MOD_SUMO_rev_2 | 612 | 618 | PF00179 | 0.580 |
MOD_SUMO_rev_2 | 671 | 676 | PF00179 | 0.533 |
MOD_SUMO_rev_2 | 856 | 863 | PF00179 | 0.404 |
MOD_SUMO_rev_2 | 954 | 960 | PF00179 | 0.593 |
TRG_AP2beta_CARGO_1 | 17 | 26 | PF09066 | 0.460 |
TRG_DiLeu_BaEn_1 | 66 | 71 | PF01217 | 0.418 |
TRG_DiLeu_BaEn_3 | 213 | 219 | PF01217 | 0.443 |
TRG_DiLeu_BaEn_4 | 601 | 607 | PF01217 | 0.375 |
TRG_DiLeu_BaLyEn_6 | 557 | 562 | PF01217 | 0.589 |
TRG_DiLeu_BaLyEn_6 | 696 | 701 | PF01217 | 0.335 |
TRG_DiLeu_LyEn_5 | 66 | 71 | PF01217 | 0.383 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.679 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.597 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 439 | 442 | PF00928 | 0.571 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.619 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 490 | 493 | PF00928 | 0.622 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.274 |
TRG_ER_diArg_1 | 25 | 27 | PF00400 | 0.306 |
TRG_ER_diArg_1 | 436 | 439 | PF00400 | 0.655 |
TRG_ER_diArg_1 | 787 | 790 | PF00400 | 0.193 |
TRG_Pf-PMV_PEXEL_1 | 26 | 30 | PF00026 | 0.589 |
TRG_Pf-PMV_PEXEL_1 | 426 | 431 | PF00026 | 0.515 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7Q2 | Leptomonas seymouri | 29% | 95% |
A0A0N1HX31 | Leptomonas seymouri | 62% | 100% |
A0A0S4JAS0 | Bodo saltans | 46% | 97% |
A0A0S4JMC0 | Bodo saltans | 46% | 100% |
A0A1X0P3F4 | Trypanosomatidae | 48% | 98% |
A0A3Q8IGC6 | Leishmania donovani | 82% | 100% |
A4ID28 | Leishmania infantum | 82% | 100% |
E9ATF0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4Q147 | Leishmania major | 81% | 100% |