A large and apprently artificial collection of diverse kinetoplastid protein kinases. A subfamily has 2TM regions, but the majority is cytoplasmic.
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) | yes | yes: 3 |
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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005929 | cilium | 4 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
Related structures:
AlphaFold database: A4HRQ2
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016310 | phosphorylation | 5 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
GO:0007165 | signal transduction | 2 | 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 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004672 | protein kinase activity | 3 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016301 | kinase activity | 4 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 7 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 190 | 194 | PF00656 | 0.682 |
CLV_C14_Caspase3-7 | 236 | 240 | PF00656 | 0.657 |
CLV_C14_Caspase3-7 | 316 | 320 | PF00656 | 0.771 |
CLV_C14_Caspase3-7 | 402 | 406 | PF00656 | 0.776 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 518 | 520 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 598 | 600 | PF00675 | 0.387 |
CLV_NRD_NRD_1 | 913 | 915 | PF00675 | 0.427 |
CLV_PCSK_FUR_1 | 911 | 915 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.400 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 518 | 520 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 598 | 600 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 623 | 625 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 911 | 913 | PF00082 | 0.423 |
CLV_PCSK_PC1ET2_1 | 219 | 221 | PF00082 | 0.506 |
CLV_PCSK_PC1ET2_1 | 623 | 625 | PF00082 | 0.360 |
CLV_PCSK_PC7_1 | 619 | 625 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 743 | 747 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 764 | 768 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 868 | 872 | PF00082 | 0.299 |
CLV_Separin_Metazoa | 202 | 206 | PF03568 | 0.665 |
DEG_APCC_DBOX_1 | 962 | 970 | PF00400 | 0.727 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.567 |
DEG_SCF_FBW7_2 | 35 | 41 | PF00400 | 0.614 |
DEG_SPOP_SBC_1 | 388 | 392 | PF00917 | 0.780 |
DEG_SPOP_SBC_1 | 544 | 548 | PF00917 | 0.628 |
DOC_CKS1_1 | 35 | 40 | PF01111 | 0.621 |
DOC_CKS1_1 | 385 | 390 | PF01111 | 0.754 |
DOC_MAPK_gen_1 | 764 | 773 | PF00069 | 0.499 |
DOC_MAPK_MEF2A_6 | 159 | 167 | PF00069 | 0.299 |
DOC_MAPK_MEF2A_6 | 467 | 474 | PF00069 | 0.578 |
DOC_MAPK_MEF2A_6 | 710 | 719 | PF00069 | 0.499 |
DOC_MAPK_NFAT4_5 | 467 | 475 | PF00069 | 0.581 |
DOC_PP1_RVXF_1 | 48 | 54 | PF00149 | 0.674 |
DOC_PP1_RVXF_1 | 517 | 524 | PF00149 | 0.550 |
DOC_PP2B_LxvP_1 | 541 | 544 | PF13499 | 0.554 |
DOC_PP2B_LxvP_1 | 840 | 843 | PF13499 | 0.499 |
DOC_PP2B_PxIxI_1 | 805 | 811 | PF00149 | 0.551 |
DOC_PP4_FxxP_1 | 589 | 592 | PF00568 | 0.631 |
DOC_PP4_FxxP_1 | 889 | 892 | PF00568 | 0.499 |
DOC_SPAK_OSR1_1 | 489 | 493 | PF12202 | 0.546 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.813 |
DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 544 | 548 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 648 | 652 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 679 | 683 | PF00917 | 0.662 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.807 |
DOC_WW_Pin1_4 | 566 | 571 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 660 | 665 | PF00397 | 0.759 |
LIG_14-3-3_CanoR_1 | 11 | 18 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 116 | 123 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 22 | 32 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 274 | 283 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 50 | 56 | PF00244 | 0.681 |
LIG_14-3-3_CanoR_1 | 74 | 79 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 882 | 890 | PF00244 | 0.502 |
LIG_Actin_WH2_2 | 100 | 118 | PF00022 | 0.620 |
LIG_Actin_WH2_2 | 367 | 383 | PF00022 | 0.723 |
LIG_Actin_WH2_2 | 457 | 475 | PF00022 | 0.566 |
LIG_Actin_WH2_2 | 780 | 797 | PF00022 | 0.499 |
LIG_APCC_ABBA_1 | 715 | 720 | PF00400 | 0.499 |
LIG_BRCT_BRCA1_1 | 100 | 104 | PF00533 | 0.607 |
LIG_BRCT_BRCA1_1 | 195 | 199 | PF00533 | 0.761 |
LIG_BRCT_BRCA1_1 | 486 | 490 | PF00533 | 0.594 |
LIG_BRCT_BRCA1_1 | 533 | 537 | PF00533 | 0.616 |
LIG_BRCT_BRCA1_1 | 585 | 589 | PF00533 | 0.727 |
LIG_BRCT_BRCA1_1 | 92 | 96 | PF00533 | 0.604 |
LIG_CSL_BTD_1 | 35 | 38 | PF09270 | 0.626 |
LIG_eIF4E_1 | 62 | 68 | PF01652 | 0.621 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.670 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.501 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.434 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.338 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.695 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.550 |
LIG_FHA_1 | 675 | 681 | PF00498 | 0.680 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.698 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.675 |
LIG_FHA_2 | 234 | 240 | PF00498 | 0.703 |
LIG_FHA_2 | 247 | 253 | PF00498 | 0.714 |
LIG_FHA_2 | 314 | 320 | PF00498 | 0.722 |
LIG_FHA_2 | 882 | 888 | PF00498 | 0.487 |
LIG_LIR_Apic_2 | 586 | 592 | PF02991 | 0.658 |
LIG_LIR_Apic_2 | 59 | 65 | PF02991 | 0.663 |
LIG_LIR_Apic_2 | 69 | 73 | PF02991 | 0.567 |
LIG_LIR_Apic_2 | 800 | 806 | PF02991 | 0.499 |
LIG_LIR_Apic_2 | 887 | 892 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 319 | 330 | PF02991 | 0.768 |
LIG_LIR_Gen_1 | 466 | 477 | PF02991 | 0.576 |
LIG_LIR_Gen_1 | 512 | 521 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 52 | 61 | PF02991 | 0.645 |
LIG_LIR_Gen_1 | 800 | 809 | PF02991 | 0.499 |
LIG_LIR_Gen_1 | 93 | 104 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 101 | 107 | PF02991 | 0.594 |
LIG_LIR_Nem_3 | 319 | 325 | PF02991 | 0.765 |
LIG_LIR_Nem_3 | 466 | 472 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 487 | 493 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 512 | 516 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 52 | 56 | PF02991 | 0.642 |
LIG_LIR_Nem_3 | 716 | 721 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 887 | 893 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 93 | 99 | PF02991 | 0.577 |
LIG_MAD2 | 424 | 432 | PF02301 | 0.746 |
LIG_MAD2 | 760 | 768 | PF02301 | 0.491 |
LIG_MLH1_MIPbox_1 | 195 | 199 | PF16413 | 0.748 |
LIG_NRBOX | 139 | 145 | PF00104 | 0.383 |
LIG_NRBOX | 549 | 555 | PF00104 | 0.582 |
LIG_PCNA_yPIPBox_3 | 442 | 452 | PF02747 | 0.622 |
LIG_Pex14_1 | 465 | 469 | PF04695 | 0.589 |
LIG_Pex14_2 | 153 | 157 | PF04695 | 0.425 |
LIG_Pex14_2 | 605 | 609 | PF04695 | 0.582 |
LIG_REV1ctd_RIR_1 | 520 | 530 | PF16727 | 0.513 |
LIG_SH2_CRK | 322 | 326 | PF00017 | 0.748 |
LIG_SH2_CRK | 890 | 894 | PF00017 | 0.499 |
LIG_SH2_GRB2like | 62 | 65 | PF00017 | 0.627 |
LIG_SH2_NCK_1 | 191 | 195 | PF00017 | 0.627 |
LIG_SH2_SRC | 191 | 194 | PF00017 | 0.683 |
LIG_SH2_SRC | 62 | 65 | PF00017 | 0.679 |
LIG_SH2_STAP1 | 191 | 195 | PF00017 | 0.620 |
LIG_SH2_STAP1 | 92 | 96 | PF00017 | 0.639 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.750 |
LIG_SH2_STAT5 | 248 | 251 | PF00017 | 0.763 |
LIG_SH2_STAT5 | 594 | 597 | PF00017 | 0.585 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.627 |
LIG_SH2_STAT5 | 626 | 629 | PF00017 | 0.620 |
LIG_SH2_STAT5 | 707 | 710 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 755 | 758 | PF00017 | 0.499 |
LIG_SH3_3 | 564 | 570 | PF00018 | 0.744 |
LIG_SH3_3 | 582 | 588 | PF00018 | 0.671 |
LIG_SH3_3 | 734 | 740 | PF00018 | 0.499 |
LIG_SH3_3 | 807 | 813 | PF00018 | 0.499 |
LIG_SH3_3 | 830 | 836 | PF00018 | 0.499 |
LIG_SUMO_SIM_anti_2 | 145 | 150 | PF11976 | 0.345 |
LIG_SUMO_SIM_anti_2 | 172 | 177 | PF11976 | 0.345 |
LIG_SUMO_SIM_anti_2 | 690 | 696 | PF11976 | 0.499 |
LIG_SUMO_SIM_par_1 | 139 | 145 | PF11976 | 0.377 |
LIG_SUMO_SIM_par_1 | 64 | 69 | PF11976 | 0.584 |
LIG_SUMO_SIM_par_1 | 829 | 834 | PF11976 | 0.499 |
LIG_TRAF2_1 | 17 | 20 | PF00917 | 0.738 |
LIG_TRAF2_1 | 573 | 576 | PF00917 | 0.768 |
LIG_TRAF2_1 | 668 | 671 | PF00917 | 0.680 |
LIG_TYR_ITIM | 888 | 893 | PF00017 | 0.335 |
LIG_WW_1 | 288 | 291 | PF00397 | 0.738 |
MOD_CDK_SPK_2 | 660 | 665 | PF00069 | 0.662 |
MOD_CDK_SPxK_1 | 34 | 40 | PF00069 | 0.488 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.597 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.500 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.626 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.589 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.728 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.552 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.401 |
MOD_CK1_1 | 660 | 666 | PF00069 | 0.637 |
MOD_CK1_1 | 726 | 732 | PF00069 | 0.335 |
MOD_CK1_1 | 751 | 757 | PF00069 | 0.408 |
MOD_CK1_1 | 968 | 974 | PF00069 | 0.625 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.625 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.592 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.453 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.521 |
MOD_CK2_1 | 881 | 887 | PF00069 | 0.319 |
MOD_Cter_Amidation | 421 | 424 | PF01082 | 0.602 |
MOD_Cter_Amidation | 596 | 599 | PF01082 | 0.462 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.552 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.706 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.648 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.726 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.595 |
MOD_GlcNHglycan | 502 | 506 | PF01048 | 0.493 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.466 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.417 |
MOD_GlcNHglycan | 640 | 643 | PF01048 | 0.661 |
MOD_GlcNHglycan | 650 | 653 | PF01048 | 0.543 |
MOD_GlcNHglycan | 659 | 662 | PF01048 | 0.734 |
MOD_GlcNHglycan | 732 | 735 | PF01048 | 0.335 |
MOD_GlcNHglycan | 750 | 753 | PF01048 | 0.335 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.485 |
MOD_GlcNHglycan | 970 | 973 | PF01048 | 0.613 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.489 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.506 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.396 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.646 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.605 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.712 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.812 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.609 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.409 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.492 |
MOD_GSK3_1 | 675 | 682 | PF00069 | 0.612 |
MOD_GSK3_1 | 726 | 733 | PF00069 | 0.335 |
MOD_GSK3_1 | 778 | 785 | PF00069 | 0.335 |
MOD_GSK3_1 | 971 | 978 | PF00069 | 0.628 |
MOD_N-GLC_1 | 20 | 25 | PF02516 | 0.647 |
MOD_N-GLC_1 | 443 | 448 | PF02516 | 0.414 |
MOD_N-GLC_2 | 243 | 245 | PF02516 | 0.657 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.535 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.501 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.412 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.607 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.484 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.378 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.503 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.450 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.460 |
MOD_NEK2_1 | 730 | 735 | PF00069 | 0.335 |
MOD_NEK2_1 | 975 | 980 | PF00069 | 0.682 |
MOD_NEK2_2 | 119 | 124 | PF00069 | 0.534 |
MOD_OFUCOSY | 113 | 119 | PF10250 | 0.612 |
MOD_PIKK_1 | 11 | 17 | PF00454 | 0.582 |
MOD_PIKK_1 | 157 | 163 | PF00454 | 0.493 |
MOD_PIKK_1 | 455 | 461 | PF00454 | 0.501 |
MOD_PIKK_1 | 583 | 589 | PF00454 | 0.700 |
MOD_PIKK_1 | 679 | 685 | PF00454 | 0.491 |
MOD_PK_1 | 897 | 903 | PF00069 | 0.529 |
MOD_PKA_1 | 11 | 17 | PF00069 | 0.556 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.574 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.527 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.729 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.662 |
MOD_PKA_2 | 380 | 386 | PF00069 | 0.787 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.585 |
MOD_PKA_2 | 472 | 478 | PF00069 | 0.507 |
MOD_PKA_2 | 484 | 490 | PF00069 | 0.458 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.592 |
MOD_PKA_2 | 797 | 803 | PF00069 | 0.408 |
MOD_PKA_2 | 881 | 887 | PF00069 | 0.339 |
MOD_PKA_2 | 896 | 902 | PF00069 | 0.477 |
MOD_Plk_1 | 134 | 140 | PF00069 | 0.345 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.667 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.543 |
MOD_Plk_1 | 313 | 319 | PF00069 | 0.634 |
MOD_Plk_1 | 443 | 449 | PF00069 | 0.403 |
MOD_Plk_1 | 897 | 903 | PF00069 | 0.529 |
MOD_Plk_2-3 | 313 | 319 | PF00069 | 0.634 |
MOD_Plk_2-3 | 829 | 835 | PF00069 | 0.335 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.508 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.300 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.527 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.453 |
MOD_Plk_4 | 509 | 515 | PF00069 | 0.418 |
MOD_Plk_4 | 751 | 757 | PF00069 | 0.408 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.574 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.550 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.766 |
MOD_ProDKin_1 | 566 | 572 | PF00069 | 0.668 |
MOD_ProDKin_1 | 660 | 666 | PF00069 | 0.700 |
TRG_DiLeu_BaEn_1 | 345 | 350 | PF01217 | 0.678 |
TRG_DiLeu_BaEn_1 | 741 | 746 | PF01217 | 0.335 |
TRG_DiLeu_BaLyEn_6 | 344 | 349 | PF01217 | 0.675 |
TRG_DiLeu_BaLyEn_6 | 537 | 542 | PF01217 | 0.474 |
TRG_DiLeu_BaLyEn_6 | 567 | 572 | PF01217 | 0.666 |
TRG_DiLeu_BaLyEn_6 | 62 | 67 | PF01217 | 0.478 |
TRG_DiLeu_BaLyEn_6 | 792 | 797 | PF01217 | 0.324 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.669 |
TRG_ENDOCYTIC_2 | 322 | 325 | PF00928 | 0.709 |
TRG_ENDOCYTIC_2 | 849 | 852 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 890 | 893 | PF00928 | 0.335 |
TRG_ER_diArg_1 | 228 | 231 | PF00400 | 0.618 |
TRG_ER_diArg_1 | 518 | 520 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 598 | 600 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 73 | 76 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 911 | 914 | PF00400 | 0.577 |
TRG_NES_CRM1_1 | 506 | 517 | PF08389 | 0.405 |
TRG_Pf-PMV_PEXEL_1 | 274 | 278 | PF00026 | 0.566 |
TRG_Pf-PMV_PEXEL_1 | 685 | 689 | PF00026 | 0.335 |
TRG_Pf-PMV_PEXEL_1 | 76 | 81 | PF00026 | 0.463 |
TRG_Pf-PMV_PEXEL_1 | 764 | 769 | PF00026 | 0.335 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2E5 | Leptomonas seymouri | 57% | 75% |
A0A451EJJ2 | Leishmania donovani | 100% | 69% |
A4H3E7 | Leishmania braziliensis | 78% | 100% |
E9ACD1 | Leishmania major | 93% | 100% |
E9AJL9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |