A large and apprently artificial collection of diverse kinetoplastid protein kinases. None of them appear to be TM.
Protein kinase, serine/threonine kinase
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. | yes | 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: A0A3S7X2Q3
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: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 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 444 | 448 | PF00656 | 0.763 |
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.481 |
CLV_NRD_NRD_1 | 353 | 355 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 504 | 506 | PF00675 | 0.711 |
CLV_NRD_NRD_1 | 534 | 536 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 615 | 617 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 671 | 673 | PF00675 | 0.708 |
CLV_NRD_NRD_1 | 811 | 813 | PF00675 | 0.457 |
CLV_PCSK_FUR_1 | 351 | 355 | PF00082 | 0.497 |
CLV_PCSK_FUR_1 | 669 | 673 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 615 | 617 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 671 | 673 | PF00082 | 0.708 |
CLV_PCSK_PC1ET2_1 | 320 | 322 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.271 |
CLV_PCSK_SKI1_1 | 577 | 581 | PF00082 | 0.508 |
DEG_MDM2_SWIB_1 | 579 | 586 | PF02201 | 0.457 |
DEG_SPOP_SBC_1 | 480 | 484 | PF00917 | 0.747 |
DEG_SPOP_SBC_1 | 752 | 756 | PF00917 | 0.634 |
DOC_ANK_TNKS_1 | 634 | 641 | PF00023 | 0.579 |
DOC_CKS1_1 | 103 | 108 | PF01111 | 0.289 |
DOC_MAPK_gen_1 | 158 | 167 | PF00069 | 0.271 |
DOC_MAPK_gen_1 | 306 | 315 | PF00069 | 0.520 |
DOC_MAPK_gen_1 | 327 | 335 | PF00069 | 0.378 |
DOC_MAPK_gen_1 | 781 | 790 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 79 | 90 | PF00069 | 0.272 |
DOC_MAPK_HePTP_8 | 205 | 217 | PF00069 | 0.289 |
DOC_MAPK_MEF2A_6 | 208 | 217 | PF00069 | 0.289 |
DOC_MAPK_MEF2A_6 | 306 | 315 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 391 | 399 | PF00069 | 0.518 |
DOC_PP1_RVXF_1 | 172 | 179 | PF00149 | 0.271 |
DOC_PP1_RVXF_1 | 206 | 212 | PF00149 | 0.289 |
DOC_PP2B_LxvP_1 | 277 | 280 | PF13499 | 0.289 |
DOC_PP4_FxxP_1 | 91 | 94 | PF00568 | 0.271 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.352 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.777 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 676 | 680 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 712 | 716 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 728 | 732 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 751 | 755 | PF00917 | 0.690 |
DOC_USP7_UBL2_3 | 383 | 387 | PF12436 | 0.664 |
DOC_USP7_UBL2_3 | 580 | 584 | PF12436 | 0.375 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.289 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.271 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 584 | 589 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 735 | 740 | PF00397 | 0.735 |
DOC_WW_Pin1_4 | 743 | 748 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 761 | 766 | PF00397 | 0.633 |
LIG_14-3-3_CanoR_1 | 276 | 280 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 295 | 305 | PF00244 | 0.344 |
LIG_14-3-3_CanoR_1 | 309 | 314 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 594 | 602 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 610 | 619 | PF00244 | 0.678 |
LIG_Actin_RPEL_3 | 147 | 166 | PF02755 | 0.404 |
LIG_Actin_WH2_2 | 59 | 75 | PF00022 | 0.314 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.675 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.683 |
LIG_BRCT_BRCA1_1 | 771 | 775 | PF00533 | 0.486 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.573 |
LIG_FHA_1 | 619 | 625 | PF00498 | 0.729 |
LIG_FHA_1 | 753 | 759 | PF00498 | 0.711 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.271 |
LIG_FHA_2 | 387 | 393 | PF00498 | 0.527 |
LIG_FHA_2 | 431 | 437 | PF00498 | 0.694 |
LIG_FHA_2 | 539 | 545 | PF00498 | 0.491 |
LIG_GBD_Chelix_1 | 798 | 806 | PF00786 | 0.404 |
LIG_LIR_Apic_2 | 196 | 202 | PF02991 | 0.271 |
LIG_LIR_Gen_1 | 107 | 116 | PF02991 | 0.271 |
LIG_LIR_Gen_1 | 120 | 126 | PF02991 | 0.271 |
LIG_LIR_Gen_1 | 570 | 581 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 58 | 67 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 598 | 604 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 120 | 125 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 46 | 50 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 570 | 576 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 587 | 592 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 772 | 778 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 789 | 793 | PF02991 | 0.334 |
LIG_MAD2 | 154 | 162 | PF02301 | 0.404 |
LIG_MLH1_MIPbox_1 | 771 | 775 | PF16413 | 0.486 |
LIG_NRBOX | 223 | 229 | PF00104 | 0.289 |
LIG_NRBOX | 801 | 807 | PF00104 | 0.443 |
LIG_OCRL_FandH_1 | 774 | 786 | PF00620 | 0.498 |
LIG_PCNA_yPIPBox_3 | 767 | 781 | PF02747 | 0.570 |
LIG_Pex14_2 | 579 | 583 | PF04695 | 0.402 |
LIG_REV1ctd_RIR_1 | 773 | 781 | PF16727 | 0.483 |
LIG_SH2_CRK | 122 | 126 | PF00017 | 0.349 |
LIG_SH2_CRK | 225 | 229 | PF00017 | 0.271 |
LIG_SH2_CRK | 251 | 255 | PF00017 | 0.289 |
LIG_SH2_CRK | 344 | 348 | PF00017 | 0.294 |
LIG_SH2_CRK | 573 | 577 | PF00017 | 0.367 |
LIG_SH2_NCK_1 | 100 | 104 | PF00017 | 0.271 |
LIG_SH2_NCK_1 | 199 | 203 | PF00017 | 0.271 |
LIG_SH2_NCK_1 | 251 | 255 | PF00017 | 0.404 |
LIG_SH2_PTP2 | 61 | 64 | PF00017 | 0.404 |
LIG_SH2_SRC | 115 | 118 | PF00017 | 0.289 |
LIG_SH2_SRC | 122 | 125 | PF00017 | 0.289 |
LIG_SH2_SRC | 251 | 254 | PF00017 | 0.311 |
LIG_SH2_SRC | 485 | 488 | PF00017 | 0.572 |
LIG_SH2_STAP1 | 122 | 126 | PF00017 | 0.289 |
LIG_SH2_STAP1 | 298 | 302 | PF00017 | 0.493 |
LIG_SH2_STAT3 | 124 | 127 | PF00017 | 0.341 |
LIG_SH2_STAT3 | 138 | 141 | PF00017 | 0.204 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.278 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.225 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.278 |
LIG_SH2_STAT5 | 540 | 543 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 700 | 703 | PF00017 | 0.707 |
LIG_SH2_STAT5 | 774 | 777 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 786 | 789 | PF00017 | 0.395 |
LIG_SH3_1 | 23 | 29 | PF00018 | 0.473 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.667 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.271 |
LIG_SH3_3 | 582 | 588 | PF00018 | 0.453 |
LIG_SH3_3 | 736 | 742 | PF00018 | 0.789 |
LIG_SH3_3 | 762 | 768 | PF00018 | 0.694 |
LIG_SUMO_SIM_anti_2 | 801 | 809 | PF11976 | 0.518 |
LIG_SUMO_SIM_anti_2 | 84 | 89 | PF11976 | 0.404 |
LIG_SUMO_SIM_par_1 | 267 | 272 | PF11976 | 0.274 |
LIG_SUMO_SIM_par_1 | 404 | 413 | PF11976 | 0.629 |
LIG_SUMO_SIM_par_1 | 767 | 772 | PF11976 | 0.602 |
LIG_SUMO_SIM_par_1 | 801 | 809 | PF11976 | 0.411 |
LIG_TRAF2_1 | 541 | 544 | PF00917 | 0.508 |
LIG_TYR_ITIM | 223 | 228 | PF00017 | 0.271 |
LIG_TYR_ITIM | 342 | 347 | PF00017 | 0.291 |
LIG_UBA3_1 | 242 | 250 | PF00899 | 0.271 |
LIG_WRC_WIRS_1 | 460 | 465 | PF05994 | 0.691 |
LIG_WRC_WIRS_1 | 576 | 581 | PF05994 | 0.431 |
MOD_CDC14_SPxK_1 | 587 | 590 | PF00782 | 0.510 |
MOD_CDK_SPK_2 | 735 | 740 | PF00069 | 0.598 |
MOD_CDK_SPxK_1 | 584 | 590 | PF00069 | 0.502 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.314 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.349 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.211 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.533 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.621 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.569 |
MOD_CK1_1 | 479 | 485 | PF00069 | 0.587 |
MOD_CK1_1 | 606 | 612 | PF00069 | 0.573 |
MOD_CK1_1 | 620 | 626 | PF00069 | 0.514 |
MOD_CK1_1 | 641 | 647 | PF00069 | 0.751 |
MOD_CK1_1 | 679 | 685 | PF00069 | 0.600 |
MOD_CK1_1 | 717 | 723 | PF00069 | 0.688 |
MOD_CK1_1 | 733 | 739 | PF00069 | 0.759 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.412 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.449 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.537 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.529 |
MOD_CK2_1 | 538 | 544 | PF00069 | 0.502 |
MOD_CK2_1 | 592 | 598 | PF00069 | 0.494 |
MOD_CK2_1 | 728 | 734 | PF00069 | 0.718 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.741 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.289 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.610 |
MOD_GlcNHglycan | 447 | 451 | PF01048 | 0.754 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.655 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.569 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.505 |
MOD_GlcNHglycan | 625 | 629 | PF01048 | 0.659 |
MOD_GlcNHglycan | 635 | 638 | PF01048 | 0.731 |
MOD_GlcNHglycan | 640 | 643 | PF01048 | 0.764 |
MOD_GlcNHglycan | 681 | 684 | PF01048 | 0.635 |
MOD_GlcNHglycan | 714 | 717 | PF01048 | 0.721 |
MOD_GlcNHglycan | 719 | 722 | PF01048 | 0.616 |
MOD_GlcNHglycan | 724 | 727 | PF01048 | 0.627 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.404 |
MOD_GlcNHglycan | 730 | 733 | PF01048 | 0.687 |
MOD_GlcNHglycan | 749 | 752 | PF01048 | 0.527 |
MOD_GlcNHglycan | 755 | 758 | PF01048 | 0.695 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.271 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.473 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.425 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.402 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.596 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.615 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.537 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.744 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.630 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.410 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.664 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.489 |
MOD_GSK3_1 | 620 | 627 | PF00069 | 0.601 |
MOD_GSK3_1 | 728 | 735 | PF00069 | 0.738 |
MOD_GSK3_1 | 743 | 750 | PF00069 | 0.559 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.335 |
MOD_N-GLC_1 | 522 | 527 | PF02516 | 0.592 |
MOD_N-GLC_1 | 610 | 615 | PF02516 | 0.555 |
MOD_N-GLC_1 | 688 | 693 | PF02516 | 0.558 |
MOD_N-GLC_2 | 95 | 97 | PF02516 | 0.271 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.358 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.235 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.241 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.335 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.504 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.452 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.519 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.567 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.526 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.617 |
MOD_NEK2_1 | 592 | 597 | PF00069 | 0.463 |
MOD_NEK2_1 | 603 | 608 | PF00069 | 0.457 |
MOD_NEK2_1 | 688 | 693 | PF00069 | 0.595 |
MOD_NEK2_1 | 806 | 811 | PF00069 | 0.350 |
MOD_NEK2_2 | 298 | 303 | PF00069 | 0.467 |
MOD_NEK2_2 | 459 | 464 | PF00069 | 0.692 |
MOD_PIKK_1 | 397 | 403 | PF00454 | 0.524 |
MOD_PIKK_1 | 515 | 521 | PF00454 | 0.692 |
MOD_PIKK_1 | 604 | 610 | PF00454 | 0.645 |
MOD_PIKK_1 | 690 | 696 | PF00454 | 0.633 |
MOD_PK_1 | 309 | 315 | PF00069 | 0.493 |
MOD_PK_1 | 529 | 535 | PF00069 | 0.575 |
MOD_PKA_1 | 615 | 621 | PF00069 | 0.567 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.404 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.271 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.393 |
MOD_PKA_2 | 38 | 44 | PF00069 | 0.404 |
MOD_PKA_2 | 463 | 469 | PF00069 | 0.685 |
MOD_PKA_2 | 593 | 599 | PF00069 | 0.471 |
MOD_PKA_2 | 615 | 621 | PF00069 | 0.631 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.289 |
MOD_Plk_1 | 441 | 447 | PF00069 | 0.662 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.480 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.358 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.425 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.707 |
MOD_Plk_4 | 806 | 812 | PF00069 | 0.354 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.289 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.271 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.527 |
MOD_ProDKin_1 | 584 | 590 | PF00069 | 0.442 |
MOD_ProDKin_1 | 735 | 741 | PF00069 | 0.735 |
MOD_ProDKin_1 | 743 | 749 | PF00069 | 0.637 |
MOD_ProDKin_1 | 761 | 767 | PF00069 | 0.631 |
MOD_SUMO_for_1 | 160 | 163 | PF00179 | 0.271 |
MOD_SUMO_rev_2 | 74 | 81 | PF00179 | 0.321 |
MOD_SUMO_rev_2 | 783 | 793 | PF00179 | 0.567 |
TRG_DiLeu_BaEn_2 | 542 | 548 | PF01217 | 0.500 |
TRG_DiLeu_BaEn_3 | 543 | 549 | PF01217 | 0.496 |
TRG_DiLeu_BaLyEn_6 | 237 | 242 | PF01217 | 0.404 |
TRG_DiLeu_BaLyEn_6 | 587 | 592 | PF01217 | 0.437 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 122 | 125 | PF00928 | 0.289 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.292 |
TRG_ENDOCYTIC_2 | 573 | 576 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.404 |
TRG_ER_diArg_1 | 351 | 354 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 503 | 505 | PF00400 | 0.689 |
TRG_ER_diArg_1 | 669 | 672 | PF00400 | 0.703 |
TRG_NES_CRM1_1 | 355 | 369 | PF08389 | 0.562 |
TRG_NLS_MonoExtN_4 | 245 | 251 | PF00514 | 0.349 |
TRG_NLS_MonoExtN_4 | 49 | 55 | PF00514 | 0.349 |
TRG_Pf-PMV_PEXEL_1 | 137 | 141 | PF00026 | 0.298 |
TRG_Pf-PMV_PEXEL_1 | 158 | 163 | PF00026 | 0.271 |
TRG_Pf-PMV_PEXEL_1 | 262 | 266 | PF00026 | 0.271 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I379 | Leptomonas seymouri | 70% | 99% |
A0A1X0P022 | Trypanosomatidae | 61% | 100% |
A0A3R7MPF2 | Trypanosoma rangeli | 61% | 100% |
A4HHK1 | Leishmania braziliensis | 86% | 100% |
A4I4Q9 | Leishmania infantum | 100% | 100% |
C9ZLF2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9AE64 | Leishmania major | 97% | 100% |
E9ALM1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
V5BL06 | Trypanosoma cruzi | 59% | 100% |