Homologous to bacterial FtsH and Eukaryotic AFG3 proteins. Probably involved in mitochondrial protein processing.. Localization: Mitochondrial (by homology)
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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0005745 | m-AAA complex | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0098796 | membrane protein complex | 2 | 2 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 2 |
GO:0098800 | inner mitochondrial membrane protein complex | 3 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1905368 | peptidase complex | 3 | 2 |
Related structures:
AlphaFold database: A4HJ48
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 14 |
GO:0006807 | nitrogen compound metabolic process | 2 | 14 |
GO:0008152 | metabolic process | 1 | 14 |
GO:0019538 | protein metabolic process | 3 | 14 |
GO:0043170 | macromolecule metabolic process | 3 | 14 |
GO:0044238 | primary metabolic process | 2 | 14 |
GO:0071704 | organic substance metabolic process | 2 | 14 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 14 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0016485 | protein processing | 5 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0034982 | mitochondrial protein processing | 6 | 2 |
GO:0043933 | protein-containing complex organization | 4 | 2 |
GO:0051604 | protein maturation | 4 | 2 |
GO:0065003 | protein-containing complex assembly | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 14 |
GO:0003824 | catalytic activity | 1 | 14 |
GO:0004175 | endopeptidase activity | 4 | 14 |
GO:0004176 | ATP-dependent peptidase activity | 2 | 14 |
GO:0004222 | metalloendopeptidase activity | 5 | 14 |
GO:0005488 | binding | 1 | 14 |
GO:0005524 | ATP binding | 5 | 14 |
GO:0008233 | peptidase activity | 3 | 14 |
GO:0008237 | metallopeptidase activity | 4 | 14 |
GO:0016462 | pyrophosphatase activity | 5 | 14 |
GO:0016787 | hydrolase activity | 2 | 14 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 14 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 14 |
GO:0016887 | ATP hydrolysis activity | 7 | 14 |
GO:0017076 | purine nucleotide binding | 4 | 14 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 14 |
GO:0030554 | adenyl nucleotide binding | 5 | 14 |
GO:0032553 | ribonucleotide binding | 3 | 14 |
GO:0032555 | purine ribonucleotide binding | 4 | 14 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 14 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 14 |
GO:0036094 | small molecule binding | 2 | 14 |
GO:0043167 | ion binding | 2 | 14 |
GO:0043168 | anion binding | 3 | 14 |
GO:0097159 | organic cyclic compound binding | 2 | 14 |
GO:0097367 | carbohydrate derivative binding | 2 | 14 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 14 |
GO:0140657 | ATP-dependent activity | 1 | 14 |
GO:1901265 | nucleoside phosphate binding | 3 | 14 |
GO:1901363 | heterocyclic compound binding | 2 | 14 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 260 | 264 | PF00656 | 0.641 |
CLV_C14_Caspase3-7 | 360 | 364 | PF00656 | 0.458 |
CLV_C14_Caspase3-7 | 577 | 581 | PF00656 | 0.460 |
CLV_C14_Caspase3-7 | 606 | 610 | PF00656 | 0.437 |
CLV_C14_Caspase3-7 | 896 | 900 | PF00656 | 0.437 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.709 |
CLV_NRD_NRD_1 | 567 | 569 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 615 | 617 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 84 | 86 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 926 | 928 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 970 | 972 | PF00675 | 0.320 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 585 | 587 | PF00082 | 0.226 |
CLV_PCSK_KEX2_1 | 615 | 617 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 746 | 748 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 970 | 972 | PF00082 | 0.320 |
CLV_PCSK_PC1ET2_1 | 585 | 587 | PF00082 | 0.226 |
CLV_PCSK_PC1ET2_1 | 746 | 748 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 489 | 493 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 525 | 529 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 561 | 565 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 743 | 747 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 763 | 767 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 892 | 896 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 955 | 959 | PF00082 | 0.232 |
CLV_PCSK_SKI1_1 | 970 | 974 | PF00082 | 0.260 |
DEG_APCC_DBOX_1 | 13 | 21 | PF00400 | 0.562 |
DEG_APCC_DBOX_1 | 286 | 294 | PF00400 | 0.437 |
DEG_APCC_DBOX_1 | 86 | 94 | PF00400 | 0.561 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.573 |
DEG_SCF_FBW7_1 | 648 | 654 | PF00400 | 0.587 |
DEG_SPOP_SBC_1 | 182 | 186 | PF00917 | 0.660 |
DEG_SPOP_SBC_1 | 949 | 953 | PF00917 | 0.422 |
DOC_CDC14_PxL_1 | 63 | 71 | PF14671 | 0.540 |
DOC_CKS1_1 | 124 | 129 | PF01111 | 0.565 |
DOC_CKS1_1 | 648 | 653 | PF01111 | 0.586 |
DOC_CKS1_1 | 70 | 75 | PF01111 | 0.534 |
DOC_CYCLIN_RxL_1 | 558 | 566 | PF00134 | 0.460 |
DOC_CYCLIN_yCln2_LP_2 | 35 | 41 | PF00134 | 0.552 |
DOC_CYCLIN_yCln2_LP_2 | 956 | 962 | PF00134 | 0.520 |
DOC_MAPK_gen_1 | 460 | 468 | PF00069 | 0.597 |
DOC_MAPK_gen_1 | 568 | 576 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 615 | 622 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 638 | 648 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 809 | 817 | PF00069 | 0.377 |
DOC_MAPK_gen_1 | 84 | 92 | PF00069 | 0.563 |
DOC_MAPK_gen_1 | 895 | 905 | PF00069 | 0.497 |
DOC_MAPK_JIP1_4 | 402 | 408 | PF00069 | 0.381 |
DOC_MAPK_MEF2A_6 | 809 | 817 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 862 | 871 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 898 | 905 | PF00069 | 0.437 |
DOC_PP2B_LxvP_1 | 136 | 139 | PF13499 | 0.579 |
DOC_PP2B_LxvP_1 | 209 | 212 | PF13499 | 0.673 |
DOC_PP2B_LxvP_1 | 35 | 38 | PF13499 | 0.548 |
DOC_PP2B_LxvP_1 | 518 | 521 | PF13499 | 0.426 |
DOC_PP2B_LxvP_1 | 704 | 707 | PF13499 | 0.656 |
DOC_PP4_FxxP_1 | 124 | 127 | PF00568 | 0.574 |
DOC_PP4_FxxP_1 | 29 | 32 | PF00568 | 0.543 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.788 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 543 | 547 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 732 | 736 | PF00917 | 0.809 |
DOC_USP7_MATH_1 | 949 | 953 | PF00917 | 0.386 |
DOC_USP7_UBL2_3 | 458 | 462 | PF12436 | 0.617 |
DOC_USP7_UBL2_3 | 506 | 510 | PF12436 | 0.621 |
DOC_USP7_UBL2_3 | 565 | 569 | PF12436 | 0.497 |
DOC_USP7_UBL2_3 | 991 | 995 | PF12436 | 0.533 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 647 | 652 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.533 |
LIG_14-3-3_CanoR_1 | 1022 | 1030 | PF00244 | 0.714 |
LIG_14-3-3_CanoR_1 | 115 | 121 | PF00244 | 0.758 |
LIG_14-3-3_CanoR_1 | 16 | 21 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 171 | 179 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 198 | 202 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 231 | 237 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 42 | 48 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 6 | 12 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 74 | 80 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 834 | 839 | PF00244 | 0.593 |
LIG_Actin_WH2_2 | 655 | 670 | PF00022 | 0.507 |
LIG_Actin_WH2_2 | 911 | 929 | PF00022 | 0.437 |
LIG_APCC_ABBA_1 | 211 | 216 | PF00400 | 0.578 |
LIG_APCC_ABBA_1 | 335 | 340 | PF00400 | 0.373 |
LIG_APCC_ABBAyCdc20_2 | 571 | 577 | PF00400 | 0.426 |
LIG_BIR_III_4 | 580 | 584 | PF00653 | 0.460 |
LIG_BIR_III_4 | 673 | 677 | PF00653 | 0.573 |
LIG_BIR_III_4 | 692 | 696 | PF00653 | 0.604 |
LIG_BRCT_BRCA1_1 | 61 | 65 | PF00533 | 0.548 |
LIG_eIF4E_1 | 415 | 421 | PF01652 | 0.278 |
LIG_EVH1_1 | 69 | 73 | PF00568 | 0.528 |
LIG_FAT_LD_1 | 221 | 229 | PF03623 | 0.564 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.714 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.358 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.277 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.491 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.495 |
LIG_FHA_1 | 648 | 654 | PF00498 | 0.587 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.537 |
LIG_FHA_1 | 710 | 716 | PF00498 | 0.686 |
LIG_FHA_1 | 952 | 958 | PF00498 | 0.426 |
LIG_FHA_1 | 981 | 987 | PF00498 | 0.426 |
LIG_FHA_2 | 1006 | 1012 | PF00498 | 0.426 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.541 |
LIG_FHA_2 | 396 | 402 | PF00498 | 0.442 |
LIG_FHA_2 | 598 | 604 | PF00498 | 0.441 |
LIG_FHA_2 | 668 | 674 | PF00498 | 0.645 |
LIG_FHA_2 | 719 | 725 | PF00498 | 0.744 |
LIG_FHA_2 | 835 | 841 | PF00498 | 0.422 |
LIG_FHA_2 | 891 | 897 | PF00498 | 0.426 |
LIG_Integrin_RGD_1 | 616 | 618 | PF01839 | 0.237 |
LIG_LIR_Apic_2 | 122 | 127 | PF02991 | 0.575 |
LIG_LIR_Apic_2 | 281 | 286 | PF02991 | 0.663 |
LIG_LIR_Apic_2 | 83 | 89 | PF02991 | 0.552 |
LIG_LIR_Apic_2 | 944 | 949 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 1008 | 1016 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 120 | 129 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 167 | 177 | PF02991 | 0.719 |
LIG_LIR_Gen_1 | 313 | 322 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 332 | 342 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 502 | 512 | PF02991 | 0.563 |
LIG_LIR_Gen_1 | 546 | 555 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 77 | 86 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 912 | 922 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 1008 | 1012 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 120 | 124 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 167 | 172 | PF02991 | 0.729 |
LIG_LIR_Nem_3 | 313 | 318 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 332 | 337 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 476 | 481 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 502 | 507 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 546 | 551 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 62 | 68 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 759 | 765 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 77 | 82 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 912 | 918 | PF02991 | 0.590 |
LIG_MYND_1 | 67 | 71 | PF01753 | 0.532 |
LIG_NRBOX | 220 | 226 | PF00104 | 0.616 |
LIG_NRBOX | 600 | 606 | PF00104 | 0.426 |
LIG_PCNA_PIPBox_1 | 994 | 1003 | PF02747 | 0.426 |
LIG_Pex14_1 | 197 | 201 | PF04695 | 0.540 |
LIG_Pex14_1 | 428 | 432 | PF04695 | 0.251 |
LIG_Pex14_2 | 434 | 438 | PF04695 | 0.251 |
LIG_PTB_Apo_2 | 884 | 891 | PF02174 | 0.448 |
LIG_SH2_CRK | 169 | 173 | PF00017 | 0.710 |
LIG_SH2_CRK | 504 | 508 | PF00017 | 0.515 |
LIG_SH2_CRK | 934 | 938 | PF00017 | 0.437 |
LIG_SH2_GRB2like | 331 | 334 | PF00017 | 0.301 |
LIG_SH2_NCK_1 | 169 | 173 | PF00017 | 0.688 |
LIG_SH2_SRC | 1009 | 1012 | PF00017 | 0.477 |
LIG_SH2_SRC | 68 | 71 | PF00017 | 0.534 |
LIG_SH2_SRC | 934 | 937 | PF00017 | 0.477 |
LIG_SH2_STAP1 | 1009 | 1013 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 201 | 205 | PF00017 | 0.581 |
LIG_SH2_STAP1 | 331 | 335 | PF00017 | 0.312 |
LIG_SH2_STAP1 | 415 | 419 | PF00017 | 0.282 |
LIG_SH2_STAP1 | 452 | 456 | PF00017 | 0.679 |
LIG_SH2_STAP1 | 780 | 784 | PF00017 | 0.518 |
LIG_SH2_STAP1 | 881 | 885 | PF00017 | 0.460 |
LIG_SH2_STAP1 | 980 | 984 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 1015 | 1018 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.648 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.656 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 445 | 448 | PF00017 | 0.667 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 552 | 555 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.673 |
LIG_SH2_STAT5 | 884 | 887 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 936 | 939 | PF00017 | 0.453 |
LIG_SH3_3 | 397 | 403 | PF00018 | 0.369 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.542 |
LIG_SH3_3 | 645 | 651 | PF00018 | 0.476 |
LIG_SH3_3 | 942 | 948 | PF00018 | 0.454 |
LIG_SUMO_SIM_anti_2 | 618 | 625 | PF11976 | 0.469 |
LIG_SUMO_SIM_anti_2 | 88 | 94 | PF11976 | 0.561 |
LIG_SUMO_SIM_anti_2 | 982 | 988 | PF11976 | 0.520 |
LIG_SUMO_SIM_par_1 | 294 | 299 | PF11976 | 0.296 |
LIG_SUMO_SIM_par_1 | 401 | 407 | PF11976 | 0.316 |
LIG_SUMO_SIM_par_1 | 982 | 988 | PF11976 | 0.520 |
LIG_TRAF2_1 | 272 | 275 | PF00917 | 0.706 |
LIG_TRAF2_1 | 727 | 730 | PF00917 | 0.778 |
LIG_TRAF2_1 | 909 | 912 | PF00917 | 0.377 |
LIG_TYR_ITIM | 1007 | 1012 | PF00017 | 0.453 |
LIG_TYR_ITIM | 932 | 937 | PF00017 | 0.377 |
LIG_WRC_WIRS_1 | 121 | 126 | PF05994 | 0.576 |
LIG_WRC_WIRS_1 | 76 | 81 | PF05994 | 0.558 |
LIG_WRC_WIRS_1 | 937 | 942 | PF05994 | 0.437 |
MOD_CDK_SPK_2 | 69 | 74 | PF00069 | 0.533 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.655 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.732 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.558 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.627 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.631 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.631 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.766 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.668 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.466 |
MOD_CK1_1 | 709 | 715 | PF00069 | 0.735 |
MOD_CK1_1 | 735 | 741 | PF00069 | 0.686 |
MOD_CK1_1 | 951 | 957 | PF00069 | 0.474 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.556 |
MOD_CK2_1 | 262 | 268 | PF00069 | 0.629 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.486 |
MOD_CK2_1 | 597 | 603 | PF00069 | 0.451 |
MOD_CK2_1 | 718 | 724 | PF00069 | 0.708 |
MOD_CK2_1 | 753 | 759 | PF00069 | 0.720 |
MOD_CK2_1 | 767 | 773 | PF00069 | 0.547 |
MOD_CK2_1 | 815 | 821 | PF00069 | 0.453 |
MOD_CK2_1 | 836 | 842 | PF00069 | 0.426 |
MOD_CK2_1 | 890 | 896 | PF00069 | 0.426 |
MOD_Cter_Amidation | 613 | 616 | PF01082 | 0.277 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.416 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.375 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.405 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.397 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.350 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.425 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.590 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.261 |
MOD_GlcNHglycan | 677 | 680 | PF01048 | 0.538 |
MOD_GlcNHglycan | 698 | 701 | PF01048 | 0.530 |
MOD_GlcNHglycan | 733 | 737 | PF01048 | 0.595 |
MOD_GlcNHglycan | 749 | 752 | PF01048 | 0.443 |
MOD_GlcNHglycan | 755 | 758 | PF01048 | 0.460 |
MOD_GlcNHglycan | 876 | 879 | PF01048 | 0.226 |
MOD_GSK3_1 | 1017 | 1024 | PF00069 | 0.604 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.675 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.610 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.613 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.736 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.592 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.656 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.349 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.705 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.641 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.548 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.571 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.615 |
MOD_GSK3_1 | 675 | 682 | PF00069 | 0.647 |
MOD_GSK3_1 | 706 | 713 | PF00069 | 0.672 |
MOD_GSK3_1 | 714 | 721 | PF00069 | 0.712 |
MOD_GSK3_1 | 747 | 754 | PF00069 | 0.696 |
MOD_GSK3_1 | 832 | 839 | PF00069 | 0.548 |
MOD_GSK3_1 | 897 | 904 | PF00069 | 0.432 |
MOD_GSK3_1 | 916 | 923 | PF00069 | 0.378 |
MOD_N-GLC_1 | 251 | 256 | PF02516 | 0.427 |
MOD_N-GLC_1 | 888 | 893 | PF02516 | 0.326 |
MOD_N-GLC_2 | 786 | 788 | PF02516 | 0.271 |
MOD_N-GLC_2 | 798 | 800 | PF02516 | 0.203 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.605 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.602 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.644 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.204 |
MOD_NEK2_1 | 406 | 411 | PF00069 | 0.444 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.383 |
MOD_NEK2_1 | 622 | 627 | PF00069 | 0.431 |
MOD_NEK2_1 | 714 | 719 | PF00069 | 0.680 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.647 |
MOD_NEK2_1 | 867 | 872 | PF00069 | 0.443 |
MOD_NEK2_1 | 890 | 895 | PF00069 | 0.497 |
MOD_PIKK_1 | 215 | 221 | PF00454 | 0.618 |
MOD_PIKK_1 | 351 | 357 | PF00454 | 0.355 |
MOD_PIKK_1 | 372 | 378 | PF00454 | 0.432 |
MOD_PIKK_1 | 440 | 446 | PF00454 | 0.517 |
MOD_PIKK_1 | 603 | 609 | PF00454 | 0.437 |
MOD_PIKK_1 | 714 | 720 | PF00454 | 0.749 |
MOD_PK_1 | 16 | 22 | PF00069 | 0.556 |
MOD_PKA_1 | 230 | 236 | PF00069 | 0.572 |
MOD_PKA_2 | 1018 | 1024 | PF00069 | 0.561 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.628 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.550 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.706 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.624 |
MOD_PKA_2 | 230 | 236 | PF00069 | 0.610 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.717 |
MOD_PKA_2 | 377 | 383 | PF00069 | 0.363 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.572 |
MOD_PKA_2 | 502 | 508 | PF00069 | 0.515 |
MOD_PKA_2 | 782 | 788 | PF00069 | 0.511 |
MOD_PKA_2 | 897 | 903 | PF00069 | 0.437 |
MOD_PKB_1 | 14 | 22 | PF00069 | 0.559 |
MOD_PKB_1 | 834 | 842 | PF00069 | 0.477 |
MOD_Plk_1 | 597 | 603 | PF00069 | 0.460 |
MOD_Plk_1 | 710 | 716 | PF00069 | 0.664 |
MOD_Plk_1 | 815 | 821 | PF00069 | 0.422 |
MOD_Plk_2-3 | 1005 | 1011 | PF00069 | 0.426 |
MOD_Plk_2-3 | 724 | 730 | PF00069 | 0.638 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.669 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.719 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.556 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.672 |
MOD_Plk_4 | 523 | 529 | PF00069 | 0.460 |
MOD_Plk_4 | 710 | 716 | PF00069 | 0.697 |
MOD_Plk_4 | 867 | 873 | PF00069 | 0.460 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.623 |
MOD_Plk_4 | 941 | 947 | PF00069 | 0.477 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.574 |
MOD_ProDKin_1 | 647 | 653 | PF00069 | 0.546 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.536 |
MOD_SUMO_for_1 | 1002 | 1005 | PF00179 | 0.477 |
MOD_SUMO_for_1 | 487 | 490 | PF00179 | 0.519 |
MOD_SUMO_for_1 | 719 | 722 | PF00179 | 0.688 |
MOD_SUMO_rev_2 | 249 | 257 | PF00179 | 0.589 |
MOD_SUMO_rev_2 | 274 | 280 | PF00179 | 0.716 |
MOD_SUMO_rev_2 | 340 | 344 | PF00179 | 0.334 |
MOD_SUMO_rev_2 | 738 | 748 | PF00179 | 0.719 |
MOD_SUMO_rev_2 | 992 | 997 | PF00179 | 0.520 |
TRG_DiLeu_BaEn_2 | 492 | 498 | PF01217 | 0.484 |
TRG_DiLeu_BaLyEn_6 | 71 | 76 | PF01217 | 0.541 |
TRG_ENDOCYTIC_2 | 1009 | 1012 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 169 | 172 | PF00928 | 0.706 |
TRG_ENDOCYTIC_2 | 334 | 337 | PF00928 | 0.267 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 504 | 507 | PF00928 | 0.549 |
TRG_ENDOCYTIC_2 | 552 | 555 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 934 | 937 | PF00928 | 0.426 |
TRG_ER_diArg_1 | 14 | 17 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 230 | 232 | PF00400 | 0.712 |
TRG_ER_diArg_1 | 39 | 42 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 558 | 561 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 84 | 86 | PF00400 | 0.574 |
TRG_ER_diLys_1 | 1026 | 1030 | PF00400 | 0.676 |
TRG_NES_CRM1_1 | 550 | 562 | PF08389 | 0.426 |
TRG_NLS_MonoExtC_3 | 409 | 414 | PF00514 | 0.301 |
TRG_NLS_MonoExtN_4 | 565 | 572 | PF00514 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 146 | 151 | PF00026 | 0.318 |
TRG_Pf-PMV_PEXEL_1 | 561 | 566 | PF00026 | 0.260 |
TRG_Pf-PMV_PEXEL_1 | 763 | 768 | PF00026 | 0.403 |
TRG_Pf-PMV_PEXEL_1 | 774 | 778 | PF00026 | 0.310 |
TRG_Pf-PMV_PEXEL_1 | 836 | 840 | PF00026 | 0.320 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PGD9 | Leptomonas seymouri | 67% | 100% |
A0A0S4JTL4 | Bodo saltans | 57% | 100% |
A0A1X0NJP5 | Trypanosomatidae | 59% | 100% |
A0A3Q8ICE7 | Leishmania donovani | 83% | 100% |
A0A3Q8IFG3 | Leishmania donovani | 31% | 100% |
A0A422NQX8 | Trypanosoma rangeli | 62% | 100% |
A4I6G4 | Leishmania infantum | 84% | 100% |
A4I809 | Leishmania infantum | 31% | 100% |
C9ZN81 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 100% |
E9B1M1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4Q5D1 | Leishmania major | 31% | 100% |
Q4Q6J3 | Leishmania major | 82% | 99% |