Nucleic acid binding, mitochondrial RNA binding complex 1 subunit 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:0005739 | mitochondrion | 5 | 1 |
GO:0016020 | membrane | 2 | 1 |
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:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I6F7
Term | Name | Level | Count |
---|---|---|---|
GO:0000959 | mitochondrial RNA metabolic process | 6 | 1 |
GO:0000963 | mitochondrial RNA processing | 6 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009894 | regulation of catabolic process | 4 | 1 |
GO:0009895 | negative regulation of catabolic process | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010467 | gene expression | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
GO:0010628 | positive regulation of gene expression | 6 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016553 | base conversion or substitution editing | 6 | 1 |
GO:0016554 | cytidine to uridine editing | 7 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 1 |
GO:0031329 | regulation of cellular catabolic process | 5 | 1 |
GO:0031330 | negative regulation of cellular catabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043487 | regulation of RNA stability | 3 | 1 |
GO:0043488 | regulation of mRNA stability | 4 | 1 |
GO:0043489 | RNA stabilization | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0048255 | mRNA stabilization | 5 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0051253 | negative regulation of RNA metabolic process | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0061013 | regulation of mRNA catabolic process | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:0140053 | mitochondrial gene expression | 5 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
GO:1902369 | negative regulation of RNA catabolic process | 7 | 1 |
GO:1902373 | negative regulation of mRNA catabolic process | 7 | 1 |
GO:1903311 | regulation of mRNA metabolic process | 6 | 1 |
GO:1903312 | negative regulation of mRNA metabolic process | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0003729 | mRNA binding | 5 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 212 | 216 | PF00656 | 0.764 |
CLV_C14_Caspase3-7 | 289 | 293 | PF00656 | 0.570 |
CLV_C14_Caspase3-7 | 545 | 549 | PF00656 | 0.752 |
CLV_C14_Caspase3-7 | 664 | 668 | PF00656 | 0.318 |
CLV_C14_Caspase3-7 | 782 | 786 | PF00656 | 0.427 |
CLV_NRD_NRD_1 | 1008 | 1010 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 422 | 424 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 580 | 582 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 807 | 809 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 810 | 812 | PF00675 | 0.467 |
CLV_PCSK_FUR_1 | 578 | 582 | PF00082 | 0.427 |
CLV_PCSK_FUR_1 | 808 | 812 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 1008 | 1010 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 474 | 476 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 481 | 483 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 580 | 582 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 747 | 749 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 768 | 770 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 809 | 811 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 818 | 820 | PF00082 | 0.546 |
CLV_PCSK_PC1ET2_1 | 103 | 105 | PF00082 | 0.619 |
CLV_PCSK_PC1ET2_1 | 175 | 177 | PF00082 | 0.712 |
CLV_PCSK_PC1ET2_1 | 329 | 331 | PF00082 | 0.532 |
CLV_PCSK_PC1ET2_1 | 424 | 426 | PF00082 | 0.421 |
CLV_PCSK_PC1ET2_1 | 481 | 483 | PF00082 | 0.469 |
CLV_PCSK_PC1ET2_1 | 69 | 71 | PF00082 | 0.488 |
CLV_PCSK_PC1ET2_1 | 747 | 749 | PF00082 | 0.584 |
CLV_PCSK_PC1ET2_1 | 768 | 770 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 809 | 811 | PF00082 | 0.556 |
CLV_PCSK_PC1ET2_1 | 818 | 820 | PF00082 | 0.664 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 452 | 456 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 858 | 862 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 914 | 918 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 919 | 923 | PF00082 | 0.434 |
CLV_Separin_Metazoa | 449 | 453 | PF03568 | 0.392 |
CLV_Separin_Metazoa | 670 | 674 | PF03568 | 0.450 |
DEG_APCC_DBOX_1 | 11 | 19 | PF00400 | 0.422 |
DEG_APCC_DBOX_1 | 481 | 489 | PF00400 | 0.433 |
DEG_APCC_DBOX_1 | 882 | 890 | PF00400 | 0.518 |
DEG_APCC_DBOX_1 | 918 | 926 | PF00400 | 0.447 |
DEG_APCC_DBOX_1 | 963 | 971 | PF00400 | 0.464 |
DEG_APCC_DBOX_1 | 985 | 993 | PF00400 | 0.509 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.453 |
DEG_SCF_FBW7_2 | 756 | 761 | PF00400 | 0.563 |
DEG_SPOP_SBC_1 | 343 | 347 | PF00917 | 0.623 |
DOC_CDC14_PxL_1 | 71 | 79 | PF14671 | 0.735 |
DOC_CDC14_PxL_1 | 909 | 917 | PF14671 | 0.561 |
DOC_CYCLIN_RxL_1 | 853 | 864 | PF00134 | 0.546 |
DOC_CYCLIN_RxL_1 | 914 | 923 | PF00134 | 0.523 |
DOC_CYCLIN_yClb1_LxF_4 | 434 | 440 | PF00134 | 0.456 |
DOC_CYCLIN_yCln2_LP_2 | 611 | 617 | PF00134 | 0.497 |
DOC_CYCLIN_yCln2_LP_2 | 874 | 880 | PF00134 | 0.566 |
DOC_MAPK_DCC_7 | 609 | 617 | PF00069 | 0.433 |
DOC_MAPK_DCC_7 | 870 | 880 | PF00069 | 0.591 |
DOC_MAPK_gen_1 | 12 | 21 | PF00069 | 0.421 |
DOC_MAPK_gen_1 | 423 | 429 | PF00069 | 0.418 |
DOC_MAPK_gen_1 | 662 | 671 | PF00069 | 0.509 |
DOC_MAPK_gen_1 | 721 | 728 | PF00069 | 0.750 |
DOC_MAPK_gen_1 | 747 | 753 | PF00069 | 0.516 |
DOC_MAPK_gen_1 | 768 | 776 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 808 | 815 | PF00069 | 0.565 |
DOC_MAPK_gen_1 | 924 | 933 | PF00069 | 0.561 |
DOC_MAPK_gen_1 | 981 | 989 | PF00069 | 0.487 |
DOC_MAPK_JIP1_4 | 613 | 619 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 14 | 23 | PF00069 | 0.373 |
DOC_MAPK_MEF2A_6 | 769 | 778 | PF00069 | 0.391 |
DOC_MAPK_MEF2A_6 | 971 | 980 | PF00069 | 0.504 |
DOC_MAPK_RevD_3 | 467 | 482 | PF00069 | 0.454 |
DOC_PP1_RVXF_1 | 423 | 430 | PF00149 | 0.407 |
DOC_PP4_FxxP_1 | 142 | 145 | PF00568 | 0.482 |
DOC_PP4_FxxP_1 | 600 | 603 | PF00568 | 0.437 |
DOC_PP4_FxxP_1 | 623 | 626 | PF00568 | 0.438 |
DOC_USP7_MATH_1 | 209 | 213 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.727 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 534 | 538 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 556 | 560 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 714 | 718 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 752 | 756 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 797 | 801 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 936 | 940 | PF00917 | 0.586 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.552 |
DOC_WW_Pin1_4 | 462 | 467 | PF00397 | 0.545 |
DOC_WW_Pin1_4 | 677 | 682 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 754 | 759 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 817 | 822 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 962 | 967 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 970 | 975 | PF00397 | 0.416 |
LIG_14-3-3_CanoR_1 | 255 | 263 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 26 | 32 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 297 | 301 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 499 | 508 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 51 | 60 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 568 | 574 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 630 | 638 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 639 | 646 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 673 | 682 | PF00244 | 0.552 |
LIG_14-3-3_CanoR_1 | 70 | 74 | PF00244 | 0.670 |
LIG_14-3-3_CanoR_1 | 723 | 729 | PF00244 | 0.700 |
LIG_14-3-3_CanoR_1 | 999 | 1006 | PF00244 | 0.606 |
LIG_Actin_WH2_2 | 242 | 257 | PF00022 | 0.421 |
LIG_Actin_WH2_2 | 659 | 675 | PF00022 | 0.487 |
LIG_BIR_III_2 | 192 | 196 | PF00653 | 0.565 |
LIG_BRCT_BRCA1_1 | 464 | 468 | PF00533 | 0.538 |
LIG_BRCT_BRCA1_1 | 60 | 64 | PF00533 | 0.489 |
LIG_CaM_IQ_9 | 321 | 336 | PF13499 | 0.559 |
LIG_EH1_1 | 281 | 289 | PF00400 | 0.417 |
LIG_EVH1_2 | 624 | 628 | PF00568 | 0.412 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.509 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.540 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.476 |
LIG_FHA_1 | 436 | 442 | PF00498 | 0.469 |
LIG_FHA_1 | 589 | 595 | PF00498 | 0.371 |
LIG_FHA_1 | 627 | 633 | PF00498 | 0.421 |
LIG_FHA_1 | 723 | 729 | PF00498 | 0.692 |
LIG_FHA_1 | 755 | 761 | PF00498 | 0.563 |
LIG_FHA_1 | 935 | 941 | PF00498 | 0.574 |
LIG_FHA_1 | 957 | 963 | PF00498 | 0.556 |
LIG_FHA_1 | 970 | 976 | PF00498 | 0.456 |
LIG_FHA_1 | 995 | 1001 | PF00498 | 0.518 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.755 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.598 |
LIG_FHA_2 | 662 | 668 | PF00498 | 0.490 |
LIG_FHA_2 | 682 | 688 | PF00498 | 0.527 |
LIG_FHA_2 | 703 | 709 | PF00498 | 0.736 |
LIG_FHA_2 | 780 | 786 | PF00498 | 0.416 |
LIG_FHA_2 | 833 | 839 | PF00498 | 0.640 |
LIG_FHA_2 | 949 | 955 | PF00498 | 0.448 |
LIG_FHA_2 | 963 | 969 | PF00498 | 0.427 |
LIG_FHA_2 | 988 | 994 | PF00498 | 0.446 |
LIG_Integrin_RGD_1 | 225 | 227 | PF01839 | 0.587 |
LIG_LIR_Apic_2 | 140 | 145 | PF02991 | 0.488 |
LIG_LIR_Apic_2 | 443 | 447 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 22 | 32 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 39 | 49 | PF02991 | 0.628 |
LIG_LIR_Gen_1 | 465 | 476 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 495 | 505 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 513 | 523 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 591 | 600 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 627 | 632 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 854 | 861 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 957 | 966 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 39 | 44 | PF02991 | 0.706 |
LIG_LIR_Nem_3 | 408 | 413 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 426 | 432 | PF02991 | 0.218 |
LIG_LIR_Nem_3 | 507 | 511 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 513 | 519 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 591 | 596 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 627 | 631 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 785 | 790 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 842 | 848 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 854 | 859 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 957 | 961 | PF02991 | 0.552 |
LIG_Pex14_2 | 43 | 47 | PF04695 | 0.635 |
LIG_SH2_CRK | 158 | 162 | PF00017 | 0.585 |
LIG_SH2_CRK | 410 | 414 | PF00017 | 0.502 |
LIG_SH2_CRK | 491 | 495 | PF00017 | 0.506 |
LIG_SH2_CRK | 871 | 875 | PF00017 | 0.591 |
LIG_SH2_STAP1 | 54 | 58 | PF00017 | 0.488 |
LIG_SH2_STAT3 | 230 | 233 | PF00017 | 0.570 |
LIG_SH2_STAT3 | 303 | 306 | PF00017 | 0.579 |
LIG_SH2_STAT3 | 54 | 57 | PF00017 | 0.493 |
LIG_SH2_STAT3 | 844 | 847 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 622 | 625 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 696 | 699 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 704 | 707 | PF00017 | 0.712 |
LIG_SH3_1 | 239 | 245 | PF00018 | 0.320 |
LIG_SH3_1 | 481 | 487 | PF00018 | 0.554 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.688 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.540 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.538 |
LIG_SH3_3 | 481 | 487 | PF00018 | 0.554 |
LIG_SH3_3 | 612 | 618 | PF00018 | 0.511 |
LIG_SH3_3 | 653 | 659 | PF00018 | 0.521 |
LIG_SH3_3 | 726 | 732 | PF00018 | 0.544 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.693 |
LIG_SUMO_SIM_anti_2 | 256 | 264 | PF11976 | 0.563 |
LIG_SUMO_SIM_anti_2 | 725 | 730 | PF11976 | 0.615 |
LIG_SUMO_SIM_anti_2 | 890 | 896 | PF11976 | 0.525 |
LIG_SUMO_SIM_par_1 | 135 | 141 | PF11976 | 0.753 |
LIG_SUMO_SIM_par_1 | 16 | 22 | PF11976 | 0.367 |
LIG_SUMO_SIM_par_1 | 256 | 264 | PF11976 | 0.615 |
LIG_SUMO_SIM_par_1 | 285 | 293 | PF11976 | 0.400 |
LIG_SUMO_SIM_par_1 | 757 | 765 | PF11976 | 0.526 |
LIG_SUMO_SIM_par_1 | 777 | 782 | PF11976 | 0.205 |
LIG_TRAF2_1 | 115 | 118 | PF00917 | 0.600 |
LIG_TRAF2_1 | 127 | 130 | PF00917 | 0.667 |
LIG_TRAF2_1 | 264 | 267 | PF00917 | 0.468 |
LIG_TRAF2_1 | 369 | 372 | PF00917 | 0.723 |
LIG_TRAF2_1 | 543 | 546 | PF00917 | 0.733 |
LIG_TRAF2_1 | 705 | 708 | PF00917 | 0.744 |
LIG_UBA3_1 | 921 | 927 | PF00899 | 0.558 |
LIG_WRC_WIRS_1 | 139 | 144 | PF05994 | 0.492 |
LIG_WRC_WIRS_1 | 436 | 441 | PF05994 | 0.456 |
LIG_WRC_WIRS_1 | 505 | 510 | PF05994 | 0.420 |
LIG_WRC_WIRS_1 | 955 | 960 | PF05994 | 0.444 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.627 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.469 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.556 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.691 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.465 |
MOD_CK1_1 | 504 | 510 | PF00069 | 0.477 |
MOD_CK1_1 | 554 | 560 | PF00069 | 0.639 |
MOD_CK1_1 | 588 | 594 | PF00069 | 0.361 |
MOD_CK1_1 | 699 | 705 | PF00069 | 0.601 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.626 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.479 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.546 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.679 |
MOD_CK2_1 | 702 | 708 | PF00069 | 0.691 |
MOD_CK2_1 | 709 | 715 | PF00069 | 0.748 |
MOD_CK2_1 | 832 | 838 | PF00069 | 0.657 |
MOD_CK2_1 | 887 | 893 | PF00069 | 0.505 |
MOD_CK2_1 | 917 | 923 | PF00069 | 0.488 |
MOD_CK2_1 | 962 | 968 | PF00069 | 0.529 |
MOD_CK2_1 | 987 | 993 | PF00069 | 0.504 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.465 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.457 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.708 |
MOD_GlcNHglycan | 186 | 190 | PF01048 | 0.779 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.708 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.710 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.733 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.605 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.455 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.356 |
MOD_GlcNHglycan | 556 | 559 | PF01048 | 0.664 |
MOD_GlcNHglycan | 712 | 715 | PF01048 | 0.743 |
MOD_GlcNHglycan | 716 | 719 | PF01048 | 0.736 |
MOD_GlcNHglycan | 798 | 802 | PF01048 | 0.434 |
MOD_GlcNHglycan | 832 | 835 | PF01048 | 0.742 |
MOD_GlcNHglycan | 889 | 892 | PF01048 | 0.406 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.644 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.535 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.528 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.631 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.692 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.528 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.627 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.629 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.482 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.514 |
MOD_GSK3_1 | 696 | 703 | PF00069 | 0.514 |
MOD_GSK3_1 | 710 | 717 | PF00069 | 0.689 |
MOD_GSK3_1 | 988 | 995 | PF00069 | 0.565 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.668 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.775 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.647 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.449 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.717 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.425 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.522 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.675 |
MOD_NEK2_1 | 631 | 636 | PF00069 | 0.494 |
MOD_NEK2_1 | 697 | 702 | PF00069 | 0.594 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.692 |
MOD_NEK2_1 | 915 | 920 | PF00069 | 0.462 |
MOD_NEK2_1 | 987 | 992 | PF00069 | 0.438 |
MOD_OFUCOSY | 90 | 95 | PF10250 | 0.654 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.736 |
MOD_PIKK_1 | 282 | 288 | PF00454 | 0.476 |
MOD_PIKK_1 | 302 | 308 | PF00454 | 0.245 |
MOD_PIKK_1 | 321 | 327 | PF00454 | 0.347 |
MOD_PIKK_1 | 567 | 573 | PF00454 | 0.583 |
MOD_PIKK_1 | 673 | 679 | PF00454 | 0.538 |
MOD_PIKK_1 | 681 | 687 | PF00454 | 0.236 |
MOD_PIKK_1 | 779 | 785 | PF00454 | 0.533 |
MOD_PKA_1 | 176 | 182 | PF00069 | 0.781 |
MOD_PKA_1 | 69 | 75 | PF00069 | 0.689 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.625 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.756 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.443 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.469 |
MOD_PKA_2 | 296 | 302 | PF00069 | 0.459 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.431 |
MOD_PKA_2 | 567 | 573 | PF00069 | 0.531 |
MOD_PKA_2 | 638 | 644 | PF00069 | 0.399 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.664 |
MOD_PKA_2 | 722 | 728 | PF00069 | 0.724 |
MOD_PKA_2 | 830 | 836 | PF00069 | 0.725 |
MOD_PKA_2 | 852 | 858 | PF00069 | 0.400 |
MOD_PKA_2 | 998 | 1004 | PF00069 | 0.595 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.686 |
MOD_Plk_1 | 226 | 232 | PF00069 | 0.607 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.422 |
MOD_Plk_4 | 226 | 232 | PF00069 | 0.589 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.459 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.449 |
MOD_Plk_4 | 435 | 441 | PF00069 | 0.486 |
MOD_Plk_4 | 585 | 591 | PF00069 | 0.404 |
MOD_Plk_4 | 724 | 730 | PF00069 | 0.655 |
MOD_Plk_4 | 936 | 942 | PF00069 | 0.550 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.550 |
MOD_ProDKin_1 | 462 | 468 | PF00069 | 0.538 |
MOD_ProDKin_1 | 677 | 683 | PF00069 | 0.479 |
MOD_ProDKin_1 | 754 | 760 | PF00069 | 0.539 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.647 |
MOD_ProDKin_1 | 817 | 823 | PF00069 | 0.621 |
MOD_ProDKin_1 | 962 | 968 | PF00069 | 0.421 |
MOD_ProDKin_1 | 970 | 976 | PF00069 | 0.409 |
MOD_SUMO_rev_2 | 520 | 530 | PF00179 | 0.496 |
MOD_SUMO_rev_2 | 545 | 552 | PF00179 | 0.751 |
TRG_DiLeu_BaEn_1 | 258 | 263 | PF01217 | 0.561 |
TRG_DiLeu_BaEn_1 | 670 | 675 | PF01217 | 0.506 |
TRG_DiLeu_BaEn_4 | 525 | 531 | PF01217 | 0.587 |
TRG_DiLeu_BaLyEn_6 | 607 | 612 | PF01217 | 0.323 |
TRG_DiLeu_BaLyEn_6 | 755 | 760 | PF01217 | 0.558 |
TRG_DiLeu_LyEn_5 | 670 | 675 | PF01217 | 0.466 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.593 |
TRG_ENDOCYTIC_2 | 238 | 241 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 307 | 310 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 410 | 413 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 436 | 439 | PF00928 | 0.526 |
TRG_ENDOCYTIC_2 | 491 | 494 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 845 | 848 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 871 | 874 | PF00928 | 0.596 |
TRG_ER_diArg_1 | 110 | 112 | PF00400 | 0.669 |
TRG_ER_diArg_1 | 12 | 14 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 158 | 160 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 176 | 178 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 330 | 332 | PF00400 | 0.683 |
TRG_ER_diArg_1 | 474 | 476 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 578 | 581 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 720 | 723 | PF00400 | 0.792 |
TRG_ER_diArg_1 | 730 | 733 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 807 | 810 | PF00400 | 0.490 |
TRG_NES_CRM1_1 | 885 | 896 | PF08389 | 0.396 |
TRG_NLS_Bipartite_1 | 159 | 179 | PF00514 | 0.653 |
TRG_NLS_MonoCore_2 | 174 | 179 | PF00514 | 0.654 |
TRG_NLS_MonoCore_2 | 328 | 333 | PF00514 | 0.585 |
TRG_Pf-PMV_PEXEL_1 | 509 | 513 | PF00026 | 0.432 |
TRG_Pf-PMV_PEXEL_1 | 643 | 647 | PF00026 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 673 | 677 | PF00026 | 0.476 |
TRG_Pf-PMV_PEXEL_1 | 919 | 923 | PF00026 | 0.520 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDG9 | Leptomonas seymouri | 57% | 100% |
A0A1X0NJ60 | Trypanosomatidae | 42% | 100% |
A0A3Q8IF71 | Leishmania donovani | 100% | 100% |
A0A3S5IRN6 | Trypanosoma rangeli | 43% | 100% |
A4HJ42 | Leishmania braziliensis | 79% | 100% |
C9ZN75 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
C9ZWW8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9B1L4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 98% |
Q4Q6K0 | Leishmania major | 93% | 100% |