Protein kinase, kinase Uncharacterized
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:0005737 | cytoplasm | 2 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HXC3
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 |
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 | 172 | 176 | PF00656 | 0.781 |
CLV_C14_Caspase3-7 | 64 | 68 | PF00656 | 0.725 |
CLV_MEL_PAP_1 | 285 | 291 | PF00089 | 0.432 |
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.767 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.788 |
CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 291 | 293 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 451 | 453 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.634 |
CLV_NRD_NRD_1 | 591 | 593 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 685 | 687 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.704 |
CLV_NRD_NRD_1 | 873 | 875 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.667 |
CLV_PCSK_FUR_1 | 209 | 213 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.774 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.793 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 451 | 453 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 591 | 593 | PF00082 | 0.402 |
CLV_PCSK_KEX2_1 | 685 | 687 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.707 |
CLV_PCSK_KEX2_1 | 746 | 748 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 872 | 874 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.648 |
CLV_PCSK_PC1ET2_1 | 746 | 748 | PF00082 | 0.269 |
CLV_PCSK_PC1ET2_1 | 872 | 874 | PF00082 | 0.294 |
CLV_PCSK_PC7_1 | 275 | 281 | PF00082 | 0.581 |
CLV_PCSK_PC7_1 | 869 | 875 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.780 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 634 | 638 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 644 | 648 | PF00082 | 0.222 |
CLV_PCSK_SKI1_1 | 687 | 691 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 705 | 709 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 722 | 726 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 832 | 836 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 873 | 877 | PF00082 | 0.314 |
CLV_Separin_Metazoa | 797 | 801 | PF03568 | 0.383 |
DEG_APCC_DBOX_1 | 704 | 712 | PF00400 | 0.312 |
DEG_SCF_FBW7_1 | 81 | 86 | PF00400 | 0.551 |
DEG_SPOP_SBC_1 | 191 | 195 | PF00917 | 0.657 |
DOC_CYCLIN_RxL_1 | 517 | 527 | PF00134 | 0.578 |
DOC_CYCLIN_RxL_1 | 575 | 586 | PF00134 | 0.467 |
DOC_MAPK_gen_1 | 257 | 266 | PF00069 | 0.630 |
DOC_MAPK_gen_1 | 380 | 389 | PF00069 | 0.723 |
DOC_MAPK_gen_1 | 634 | 642 | PF00069 | 0.331 |
DOC_MAPK_gen_1 | 690 | 699 | PF00069 | 0.302 |
DOC_MAPK_gen_1 | 722 | 731 | PF00069 | 0.269 |
DOC_MAPK_gen_1 | 853 | 860 | PF00069 | 0.403 |
DOC_MAPK_gen_1 | 872 | 880 | PF00069 | 0.205 |
DOC_MAPK_MEF2A_6 | 260 | 268 | PF00069 | 0.595 |
DOC_MAPK_MEF2A_6 | 853 | 862 | PF00069 | 0.304 |
DOC_PP1_RVXF_1 | 265 | 271 | PF00149 | 0.486 |
DOC_PP4_FxxP_1 | 793 | 796 | PF00568 | 0.307 |
DOC_USP7_MATH_1 | 108 | 112 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 539 | 543 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 557 | 561 | PF00917 | 0.500 |
DOC_USP7_MATH_2 | 202 | 208 | PF00917 | 0.573 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.776 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 489 | 494 | PF00397 | 0.783 |
DOC_WW_Pin1_4 | 507 | 512 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 513 | 518 | PF00397 | 0.759 |
DOC_WW_Pin1_4 | 769 | 774 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 787 | 792 | PF00397 | 0.195 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.776 |
DOC_WW_Pin1_4 | 896 | 901 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 903 | 908 | PF00397 | 0.559 |
LIG_14-3-3_CanoR_1 | 292 | 300 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 385 | 390 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 498 | 505 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 591 | 596 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 873 | 881 | PF00244 | 0.285 |
LIG_APCC_ABBA_1 | 669 | 674 | PF00400 | 0.269 |
LIG_BRCT_BRCA1_1 | 564 | 568 | PF00533 | 0.549 |
LIG_BRCT_BRCA1_1 | 789 | 793 | PF00533 | 0.432 |
LIG_DLG_GKlike_1 | 385 | 393 | PF00625 | 0.591 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.576 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.619 |
LIG_FHA_1 | 499 | 505 | PF00498 | 0.707 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.704 |
LIG_FHA_1 | 577 | 583 | PF00498 | 0.552 |
LIG_FHA_1 | 657 | 663 | PF00498 | 0.357 |
LIG_FHA_1 | 702 | 708 | PF00498 | 0.402 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.597 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.624 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.536 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.565 |
LIG_FHA_2 | 601 | 607 | PF00498 | 0.402 |
LIG_FHA_2 | 874 | 880 | PF00498 | 0.249 |
LIG_FHA_2 | 885 | 891 | PF00498 | 0.372 |
LIG_LIR_Apic_2 | 790 | 796 | PF02991 | 0.309 |
LIG_LIR_Gen_1 | 314 | 324 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 295 | 300 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 314 | 320 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 600 | 604 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 670 | 675 | PF02991 | 0.402 |
LIG_LRP6_Inhibitor_1 | 19 | 25 | PF00058 | 0.616 |
LIG_MLH1_MIPbox_1 | 789 | 793 | PF16413 | 0.432 |
LIG_MYND_1 | 349 | 353 | PF01753 | 0.532 |
LIG_Pex14_2 | 835 | 839 | PF04695 | 0.390 |
LIG_Pex14_2 | 863 | 867 | PF04695 | 0.249 |
LIG_PTB_Apo_2 | 441 | 448 | PF02174 | 0.551 |
LIG_PTB_Phospho_1 | 441 | 447 | PF10480 | 0.545 |
LIG_REV1ctd_RIR_1 | 860 | 869 | PF16727 | 0.250 |
LIG_SH2_GRB2like | 442 | 445 | PF00017 | 0.551 |
LIG_SH2_NCK_1 | 442 | 446 | PF00017 | 0.593 |
LIG_SH2_SRC | 713 | 716 | PF00017 | 0.269 |
LIG_SH2_STAP1 | 442 | 446 | PF00017 | 0.544 |
LIG_SH2_STAP1 | 703 | 707 | PF00017 | 0.287 |
LIG_SH2_STAT3 | 655 | 658 | PF00017 | 0.269 |
LIG_SH2_STAT3 | 703 | 706 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 447 | 450 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 703 | 706 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 713 | 716 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 805 | 808 | PF00017 | 0.390 |
LIG_SH3_1 | 14 | 20 | PF00018 | 0.606 |
LIG_SH3_3 | 14 | 20 | PF00018 | 0.608 |
LIG_SH3_3 | 334 | 340 | PF00018 | 0.728 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.729 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.684 |
LIG_SH3_3 | 475 | 481 | PF00018 | 0.582 |
LIG_SH3_3 | 511 | 517 | PF00018 | 0.786 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.628 |
LIG_SH3_3 | 785 | 791 | PF00018 | 0.256 |
LIG_SH3_3 | 894 | 900 | PF00018 | 0.561 |
LIG_SUMO_SIM_anti_2 | 696 | 702 | PF11976 | 0.287 |
LIG_SUMO_SIM_anti_2 | 876 | 882 | PF11976 | 0.276 |
LIG_SUMO_SIM_par_1 | 198 | 207 | PF11976 | 0.575 |
LIG_SUMO_SIM_par_1 | 42 | 50 | PF11976 | 0.614 |
LIG_TRAF2_1 | 145 | 148 | PF00917 | 0.703 |
LIG_TRAF2_1 | 163 | 166 | PF00917 | 0.699 |
LIG_TRAF2_1 | 772 | 775 | PF00917 | 0.290 |
LIG_TRAF2_1 | 892 | 895 | PF00917 | 0.560 |
LIG_TRFH_1 | 405 | 409 | PF08558 | 0.595 |
LIG_TYR_ITSM | 601 | 608 | PF00017 | 0.402 |
LIG_UBA3_1 | 642 | 649 | PF00899 | 0.269 |
LIG_UBA3_1 | 730 | 738 | PF00899 | 0.287 |
LIG_UBA3_1 | 834 | 843 | PF00899 | 0.310 |
MOD_CDC14_SPxK_1 | 50 | 53 | PF00782 | 0.588 |
MOD_CDK_SPK_2 | 405 | 410 | PF00069 | 0.551 |
MOD_CDK_SPxK_1 | 47 | 53 | PF00069 | 0.589 |
MOD_CDK_SPxxK_3 | 47 | 54 | PF00069 | 0.618 |
MOD_CDK_SPxxK_3 | 489 | 496 | PF00069 | 0.606 |
MOD_CDK_SPxxK_3 | 513 | 520 | PF00069 | 0.573 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.700 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.801 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.727 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.739 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.568 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.620 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.757 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.655 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.634 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.590 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.456 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.588 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.650 |
MOD_CK1_1 | 529 | 535 | PF00069 | 0.730 |
MOD_CK1_1 | 560 | 566 | PF00069 | 0.531 |
MOD_CK1_1 | 600 | 606 | PF00069 | 0.360 |
MOD_CK1_1 | 680 | 686 | PF00069 | 0.402 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.587 |
MOD_CK1_1 | 899 | 905 | PF00069 | 0.551 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.784 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.775 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.584 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.554 |
MOD_CK2_1 | 420 | 426 | PF00069 | 0.562 |
MOD_CK2_1 | 539 | 545 | PF00069 | 0.644 |
MOD_CK2_1 | 600 | 606 | PF00069 | 0.347 |
MOD_CK2_1 | 769 | 775 | PF00069 | 0.460 |
MOD_CK2_1 | 873 | 879 | PF00069 | 0.253 |
MOD_CK2_1 | 899 | 905 | PF00069 | 0.697 |
MOD_Cter_Amidation | 216 | 219 | PF01082 | 0.767 |
MOD_DYRK1A_RPxSP_1 | 79 | 83 | PF00069 | 0.558 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.655 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.587 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.585 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.771 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.569 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.601 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.643 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.608 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.652 |
MOD_GlcNHglycan | 505 | 508 | PF01048 | 0.752 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.769 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.617 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.731 |
MOD_GlcNHglycan | 731 | 734 | PF01048 | 0.347 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.646 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.767 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.799 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.722 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.591 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.716 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.732 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.599 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.630 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.626 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.576 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.624 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.715 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.699 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.724 |
MOD_GSK3_1 | 695 | 702 | PF00069 | 0.275 |
MOD_GSK3_1 | 783 | 790 | PF00069 | 0.256 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.655 |
MOD_GSK3_1 | 899 | 906 | PF00069 | 0.728 |
MOD_N-GLC_1 | 360 | 365 | PF02516 | 0.562 |
MOD_N-GLC_1 | 393 | 398 | PF02516 | 0.611 |
MOD_N-GLC_1 | 458 | 463 | PF02516 | 0.547 |
MOD_N-GLC_1 | 568 | 573 | PF02516 | 0.479 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.734 |
MOD_NEK2_1 | 387 | 392 | PF00069 | 0.740 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.626 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.584 |
MOD_NEK2_1 | 523 | 528 | PF00069 | 0.601 |
MOD_NEK2_1 | 568 | 573 | PF00069 | 0.467 |
MOD_NEK2_1 | 576 | 581 | PF00069 | 0.468 |
MOD_NEK2_1 | 642 | 647 | PF00069 | 0.260 |
MOD_NEK2_1 | 695 | 700 | PF00069 | 0.278 |
MOD_NEK2_1 | 742 | 747 | PF00069 | 0.296 |
MOD_NEK2_1 | 783 | 788 | PF00069 | 0.390 |
MOD_PIKK_1 | 119 | 125 | PF00454 | 0.659 |
MOD_PIKK_1 | 218 | 224 | PF00454 | 0.594 |
MOD_PIKK_1 | 30 | 36 | PF00454 | 0.740 |
MOD_PIKK_1 | 389 | 395 | PF00454 | 0.583 |
MOD_PIKK_1 | 606 | 612 | PF00454 | 0.331 |
MOD_PIKK_1 | 899 | 905 | PF00454 | 0.697 |
MOD_PK_1 | 591 | 597 | PF00069 | 0.402 |
MOD_PKA_1 | 218 | 224 | PF00069 | 0.765 |
MOD_PKA_1 | 292 | 298 | PF00069 | 0.524 |
MOD_PKA_1 | 591 | 597 | PF00069 | 0.402 |
MOD_PKA_1 | 873 | 879 | PF00069 | 0.290 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.774 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.481 |
MOD_PKA_2 | 591 | 597 | PF00069 | 0.421 |
MOD_PKA_2 | 839 | 845 | PF00069 | 0.304 |
MOD_PKA_2 | 868 | 874 | PF00069 | 0.279 |
MOD_PKB_1 | 383 | 391 | PF00069 | 0.538 |
MOD_Plk_1 | 411 | 417 | PF00069 | 0.676 |
MOD_Plk_1 | 458 | 464 | PF00069 | 0.553 |
MOD_Plk_1 | 568 | 574 | PF00069 | 0.487 |
MOD_Plk_1 | 620 | 626 | PF00069 | 0.390 |
MOD_Plk_2-3 | 132 | 138 | PF00069 | 0.628 |
MOD_Plk_2-3 | 142 | 148 | PF00069 | 0.699 |
MOD_Plk_2-3 | 175 | 181 | PF00069 | 0.666 |
MOD_Plk_2-3 | 310 | 316 | PF00069 | 0.415 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.674 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.714 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.583 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.471 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.735 |
MOD_Plk_4 | 591 | 597 | PF00069 | 0.399 |
MOD_Plk_4 | 600 | 606 | PF00069 | 0.317 |
MOD_Plk_4 | 650 | 656 | PF00069 | 0.402 |
MOD_Plk_4 | 783 | 789 | PF00069 | 0.253 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.731 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.715 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.776 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.662 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.623 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.617 |
MOD_ProDKin_1 | 489 | 495 | PF00069 | 0.779 |
MOD_ProDKin_1 | 507 | 513 | PF00069 | 0.629 |
MOD_ProDKin_1 | 769 | 775 | PF00069 | 0.421 |
MOD_ProDKin_1 | 787 | 793 | PF00069 | 0.195 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.775 |
MOD_ProDKin_1 | 896 | 902 | PF00069 | 0.508 |
MOD_ProDKin_1 | 903 | 909 | PF00069 | 0.563 |
MOD_SUMO_for_1 | 636 | 639 | PF00179 | 0.331 |
MOD_SUMO_rev_2 | 423 | 432 | PF00179 | 0.664 |
MOD_SUMO_rev_2 | 47 | 55 | PF00179 | 0.659 |
MOD_SUMO_rev_2 | 606 | 615 | PF00179 | 0.269 |
MOD_SUMO_rev_2 | 732 | 740 | PF00179 | 0.269 |
TRG_ENDOCYTIC_2 | 605 | 608 | PF00928 | 0.269 |
TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.551 |
TRG_ER_diArg_1 | 208 | 211 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 278 | 280 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 590 | 592 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 684 | 686 | PF00400 | 0.269 |
TRG_NES_CRM1_1 | 318 | 334 | PF08389 | 0.425 |
TRG_NES_CRM1_1 | 570 | 586 | PF08389 | 0.529 |
TRG_NES_CRM1_1 | 810 | 820 | PF08389 | 0.333 |
TRG_NLS_MonoExtN_4 | 869 | 876 | PF00514 | 0.290 |
TRG_Pf-PMV_PEXEL_1 | 891 | 895 | PF00026 | 0.535 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5H5 | Leptomonas seymouri | 51% | 69% |
A0A1X0NSX9 | Trypanosomatidae | 43% | 96% |
A0A3R7M724 | Trypanosoma rangeli | 44% | 100% |
A0A3S5H705 | Leishmania donovani | 97% | 100% |
C9ZU16 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AI55 | Leishmania braziliensis | 64% | 100% |
E9AR18 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 99% |
Q4QEE5 | Leishmania major | 93% | 100% |
V5B639 | Trypanosoma cruzi | 44% | 100% |