A large and apprently artificial collection of diverse kinetoplastid protein kinases. None of them appear to be TM.
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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9ALM1
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:0007165 | signal transduction | 2 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 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:0004674 | protein serine/threonine kinase activity | 4 | 9 |
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 444 | 448 | PF00656 | 0.785 |
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 504 | 506 | PF00675 | 0.772 |
CLV_NRD_NRD_1 | 534 | 536 | PF00675 | 0.734 |
CLV_NRD_NRD_1 | 615 | 617 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 671 | 673 | PF00675 | 0.759 |
CLV_NRD_NRD_1 | 742 | 744 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 811 | 813 | PF00675 | 0.585 |
CLV_PCSK_FUR_1 | 351 | 355 | PF00082 | 0.539 |
CLV_PCSK_FUR_1 | 669 | 673 | PF00082 | 0.746 |
CLV_PCSK_FUR_1 | 740 | 744 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.747 |
CLV_PCSK_KEX2_1 | 615 | 617 | PF00082 | 0.668 |
CLV_PCSK_KEX2_1 | 671 | 673 | PF00082 | 0.759 |
CLV_PCSK_KEX2_1 | 742 | 744 | PF00082 | 0.773 |
CLV_PCSK_PC1ET2_1 | 320 | 322 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.335 |
DEG_MDM2_SWIB_1 | 579 | 586 | PF02201 | 0.494 |
DEG_SPOP_SBC_1 | 480 | 484 | PF00917 | 0.766 |
DEG_SPOP_SBC_1 | 752 | 756 | PF00917 | 0.772 |
DOC_CKS1_1 | 103 | 108 | PF01111 | 0.355 |
DOC_MAPK_gen_1 | 158 | 167 | PF00069 | 0.335 |
DOC_MAPK_gen_1 | 306 | 315 | PF00069 | 0.560 |
DOC_MAPK_gen_1 | 327 | 335 | PF00069 | 0.486 |
DOC_MAPK_gen_1 | 781 | 790 | PF00069 | 0.512 |
DOC_MAPK_gen_1 | 79 | 90 | PF00069 | 0.337 |
DOC_MAPK_HePTP_8 | 205 | 217 | PF00069 | 0.355 |
DOC_MAPK_MEF2A_6 | 208 | 217 | PF00069 | 0.347 |
DOC_MAPK_MEF2A_6 | 306 | 315 | PF00069 | 0.560 |
DOC_MAPK_MEF2A_6 | 391 | 399 | PF00069 | 0.591 |
DOC_PP1_RVXF_1 | 172 | 179 | PF00149 | 0.335 |
DOC_PP1_RVXF_1 | 206 | 212 | PF00149 | 0.355 |
DOC_PP2B_LxvP_1 | 277 | 280 | PF13499 | 0.342 |
DOC_PP4_FxxP_1 | 91 | 94 | PF00568 | 0.335 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.789 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 610 | 614 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 624 | 628 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 638 | 642 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 676 | 680 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 712 | 716 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 751 | 755 | PF00917 | 0.731 |
DOC_USP7_UBL2_3 | 383 | 387 | PF12436 | 0.696 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.355 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.335 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 584 | 589 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 606 | 611 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 760 | 765 | PF00397 | 0.619 |
LIG_14-3-3_CanoR_1 | 276 | 280 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 295 | 305 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 309 | 314 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 594 | 602 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 615 | 620 | PF00244 | 0.690 |
LIG_14-3-3_CanoR_1 | 742 | 748 | PF00244 | 0.479 |
LIG_Actin_RPEL_3 | 147 | 166 | PF02755 | 0.447 |
LIG_Actin_WH2_2 | 59 | 75 | PF00022 | 0.378 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.728 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.734 |
LIG_BRCT_BRCA1_1 | 771 | 775 | PF00533 | 0.562 |
LIG_deltaCOP1_diTrp_1 | 580 | 589 | PF00928 | 0.298 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.567 |
LIG_FHA_1 | 734 | 740 | PF00498 | 0.502 |
LIG_FHA_1 | 753 | 759 | PF00498 | 0.747 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.335 |
LIG_FHA_2 | 387 | 393 | PF00498 | 0.592 |
LIG_FHA_2 | 431 | 437 | PF00498 | 0.705 |
LIG_FHA_2 | 539 | 545 | PF00498 | 0.537 |
LIG_FHA_2 | 654 | 660 | PF00498 | 0.770 |
LIG_GBD_Chelix_1 | 798 | 806 | PF00786 | 0.426 |
LIG_LIR_Apic_2 | 196 | 202 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 107 | 116 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 120 | 126 | PF02991 | 0.317 |
LIG_LIR_Gen_1 | 570 | 581 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 58 | 67 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 598 | 604 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 120 | 125 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 46 | 50 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 570 | 576 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 580 | 586 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 587 | 592 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 598 | 603 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 772 | 778 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 789 | 793 | PF02991 | 0.432 |
LIG_MAD2 | 154 | 162 | PF02301 | 0.447 |
LIG_MLH1_MIPbox_1 | 771 | 775 | PF16413 | 0.562 |
LIG_NRBOX | 223 | 229 | PF00104 | 0.355 |
LIG_NRBOX | 801 | 807 | PF00104 | 0.549 |
LIG_OCRL_FandH_1 | 774 | 786 | PF00620 | 0.628 |
LIG_PCNA_yPIPBox_3 | 761 | 774 | PF02747 | 0.588 |
LIG_Pex14_2 | 579 | 583 | PF04695 | 0.442 |
LIG_REV1ctd_RIR_1 | 773 | 781 | PF16727 | 0.621 |
LIG_SH2_CRK | 122 | 126 | PF00017 | 0.408 |
LIG_SH2_CRK | 225 | 229 | PF00017 | 0.335 |
LIG_SH2_CRK | 251 | 255 | PF00017 | 0.355 |
LIG_SH2_CRK | 344 | 348 | PF00017 | 0.357 |
LIG_SH2_CRK | 573 | 577 | PF00017 | 0.427 |
LIG_SH2_NCK_1 | 100 | 104 | PF00017 | 0.335 |
LIG_SH2_NCK_1 | 199 | 203 | PF00017 | 0.335 |
LIG_SH2_NCK_1 | 251 | 255 | PF00017 | 0.447 |
LIG_SH2_PTP2 | 61 | 64 | PF00017 | 0.447 |
LIG_SH2_SRC | 115 | 118 | PF00017 | 0.340 |
LIG_SH2_SRC | 122 | 125 | PF00017 | 0.342 |
LIG_SH2_SRC | 485 | 488 | PF00017 | 0.698 |
LIG_SH2_STAP1 | 122 | 126 | PF00017 | 0.355 |
LIG_SH2_STAP1 | 298 | 302 | PF00017 | 0.629 |
LIG_SH2_STAT3 | 124 | 127 | PF00017 | 0.402 |
LIG_SH2_STAT3 | 138 | 141 | PF00017 | 0.249 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.237 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 425 | 428 | PF00017 | 0.380 |
LIG_SH2_STAT5 | 540 | 543 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 700 | 703 | PF00017 | 0.746 |
LIG_SH2_STAT5 | 774 | 777 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 786 | 789 | PF00017 | 0.245 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.709 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.330 |
LIG_SH3_3 | 582 | 588 | PF00018 | 0.477 |
LIG_SH3_3 | 719 | 725 | PF00018 | 0.524 |
LIG_SH3_3 | 762 | 768 | PF00018 | 0.636 |
LIG_SUMO_SIM_anti_2 | 801 | 808 | PF11976 | 0.524 |
LIG_SUMO_SIM_anti_2 | 84 | 89 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 267 | 272 | PF11976 | 0.339 |
LIG_SUMO_SIM_par_1 | 404 | 413 | PF11976 | 0.648 |
LIG_SUMO_SIM_par_1 | 767 | 772 | PF11976 | 0.533 |
LIG_SUMO_SIM_par_1 | 801 | 808 | PF11976 | 0.442 |
LIG_TRAF2_1 | 541 | 544 | PF00917 | 0.546 |
LIG_TYR_ITIM | 223 | 228 | PF00017 | 0.335 |
LIG_TYR_ITIM | 342 | 347 | PF00017 | 0.354 |
LIG_UBA3_1 | 242 | 250 | PF00899 | 0.335 |
LIG_WRC_WIRS_1 | 460 | 465 | PF05994 | 0.742 |
LIG_WRC_WIRS_1 | 576 | 581 | PF05994 | 0.482 |
MOD_CDC14_SPxK_1 | 587 | 590 | PF00782 | 0.544 |
MOD_CDK_SPxK_1 | 584 | 590 | PF00069 | 0.539 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.378 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.471 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.185 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.569 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.643 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.620 |
MOD_CK1_1 | 479 | 485 | PF00069 | 0.653 |
MOD_CK1_1 | 606 | 612 | PF00069 | 0.644 |
MOD_CK1_1 | 620 | 626 | PF00069 | 0.534 |
MOD_CK1_1 | 641 | 647 | PF00069 | 0.780 |
MOD_CK1_1 | 679 | 685 | PF00069 | 0.704 |
MOD_CK1_1 | 689 | 695 | PF00069 | 0.568 |
MOD_CK1_1 | 717 | 723 | PF00069 | 0.737 |
MOD_CK1_1 | 733 | 739 | PF00069 | 0.748 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.467 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.498 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.678 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.590 |
MOD_CK2_1 | 538 | 544 | PF00069 | 0.550 |
MOD_CK2_1 | 592 | 598 | PF00069 | 0.487 |
MOD_CK2_1 | 728 | 734 | PF00069 | 0.745 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.769 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.355 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.644 |
MOD_GlcNHglycan | 447 | 451 | PF01048 | 0.742 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.704 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.627 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.541 |
MOD_GlcNHglycan | 622 | 625 | PF01048 | 0.713 |
MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.725 |
MOD_GlcNHglycan | 635 | 638 | PF01048 | 0.768 |
MOD_GlcNHglycan | 640 | 643 | PF01048 | 0.789 |
MOD_GlcNHglycan | 681 | 684 | PF01048 | 0.751 |
MOD_GlcNHglycan | 714 | 717 | PF01048 | 0.699 |
MOD_GlcNHglycan | 719 | 722 | PF01048 | 0.710 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.447 |
MOD_GlcNHglycan | 730 | 733 | PF01048 | 0.669 |
MOD_GlcNHglycan | 749 | 752 | PF01048 | 0.543 |
MOD_GlcNHglycan | 755 | 758 | PF01048 | 0.737 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.335 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.305 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.473 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.401 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.641 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.662 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.575 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.758 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.689 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.448 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.714 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.546 |
MOD_GSK3_1 | 620 | 627 | PF00069 | 0.645 |
MOD_GSK3_1 | 686 | 693 | PF00069 | 0.598 |
MOD_GSK3_1 | 728 | 735 | PF00069 | 0.689 |
MOD_GSK3_1 | 743 | 750 | PF00069 | 0.588 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.480 |
MOD_N-GLC_1 | 522 | 527 | PF02516 | 0.698 |
MOD_N-GLC_1 | 610 | 615 | PF02516 | 0.665 |
MOD_N-GLC_2 | 95 | 97 | PF02516 | 0.335 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.415 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.309 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.239 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.377 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.511 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.475 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.584 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.633 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.581 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.681 |
MOD_NEK2_1 | 592 | 597 | PF00069 | 0.477 |
MOD_NEK2_1 | 688 | 693 | PF00069 | 0.768 |
MOD_NEK2_2 | 298 | 303 | PF00069 | 0.503 |
MOD_NEK2_2 | 459 | 464 | PF00069 | 0.742 |
MOD_PIKK_1 | 397 | 403 | PF00454 | 0.581 |
MOD_PIKK_1 | 515 | 521 | PF00454 | 0.742 |
MOD_PIKK_1 | 653 | 659 | PF00454 | 0.599 |
MOD_PIKK_1 | 690 | 696 | PF00454 | 0.749 |
MOD_PK_1 | 309 | 315 | PF00069 | 0.536 |
MOD_PK_1 | 529 | 535 | PF00069 | 0.663 |
MOD_PKA_1 | 615 | 621 | PF00069 | 0.664 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.447 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.335 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.448 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.447 |
MOD_PKA_2 | 463 | 469 | PF00069 | 0.729 |
MOD_PKA_2 | 593 | 599 | PF00069 | 0.484 |
MOD_PKA_2 | 615 | 621 | PF00069 | 0.682 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.355 |
MOD_Plk_1 | 441 | 447 | PF00069 | 0.772 |
MOD_Plk_1 | 733 | 739 | PF00069 | 0.682 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.501 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.406 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.484 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.738 |
MOD_Plk_4 | 769 | 775 | PF00069 | 0.502 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.355 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.335 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.578 |
MOD_ProDKin_1 | 584 | 590 | PF00069 | 0.485 |
MOD_ProDKin_1 | 606 | 612 | PF00069 | 0.559 |
MOD_ProDKin_1 | 760 | 766 | PF00069 | 0.616 |
MOD_SUMO_for_1 | 160 | 163 | PF00179 | 0.335 |
MOD_SUMO_rev_2 | 74 | 81 | PF00179 | 0.385 |
MOD_SUMO_rev_2 | 783 | 793 | PF00179 | 0.564 |
TRG_DiLeu_BaEn_2 | 542 | 548 | PF01217 | 0.522 |
TRG_DiLeu_BaEn_3 | 543 | 549 | PF01217 | 0.542 |
TRG_DiLeu_BaLyEn_6 | 237 | 242 | PF01217 | 0.447 |
TRG_DiLeu_BaLyEn_6 | 587 | 592 | PF01217 | 0.477 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 573 | 576 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.447 |
TRG_ER_diArg_1 | 351 | 354 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 503 | 505 | PF00400 | 0.752 |
TRG_ER_diArg_1 | 669 | 672 | PF00400 | 0.762 |
TRG_NES_CRM1_1 | 355 | 369 | PF08389 | 0.602 |
TRG_NLS_MonoExtN_4 | 245 | 251 | PF00514 | 0.408 |
TRG_NLS_MonoExtN_4 | 49 | 55 | PF00514 | 0.408 |
TRG_Pf-PMV_PEXEL_1 | 137 | 141 | PF00026 | 0.363 |
TRG_Pf-PMV_PEXEL_1 | 158 | 163 | PF00026 | 0.335 |
TRG_Pf-PMV_PEXEL_1 | 262 | 266 | PF00026 | 0.335 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I379 | Leptomonas seymouri | 70% | 99% |
A0A1X0P022 | Trypanosomatidae | 61% | 100% |
A0A3R7MPF2 | Trypanosoma rangeli | 61% | 100% |
A0A3S7X2Q3 | Leishmania donovani | 95% | 100% |
A4HHK1 | Leishmania braziliensis | 86% | 100% |
A4I4Q9 | Leishmania infantum | 95% | 100% |
C9ZLF2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9AE64 | Leishmania major | 96% | 100% |
V5BL06 | Trypanosoma cruzi | 58% | 100% |