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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005739 | mitochondrion | 5 | 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: A4H8B0
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006281 | DNA repair | 5 | 12 |
GO:0006298 | mismatch repair | 6 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006950 | response to stress | 2 | 12 |
GO:0006974 | DNA damage response | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0033554 | cellular response to stress | 3 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0050896 | response to stimulus | 1 | 12 |
GO:0051716 | cellular response to stimulus | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0032042 | mitochondrial DNA metabolic process | 5 | 1 |
GO:0043504 | mitochondrial DNA repair | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003690 | double-stranded DNA binding | 5 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0030983 | mismatched DNA binding | 6 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 12 |
GO:0140299 | small molecule sensor activity | 1 | 12 |
GO:0140612 | DNA damage sensor activity | 2 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:0140664 | ATP-dependent DNA damage sensor activity | 3 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 682 | 686 | PF00656 | 0.549 |
CLV_C14_Caspase3-7 | 974 | 978 | PF00656 | 0.377 |
CLV_MEL_PAP_1 | 73 | 79 | PF00089 | 0.313 |
CLV_MEL_PAP_1 | 765 | 771 | PF00089 | 0.256 |
CLV_NRD_NRD_1 | 1000 | 1002 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.259 |
CLV_NRD_NRD_1 | 601 | 603 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.264 |
CLV_NRD_NRD_1 | 882 | 884 | PF00675 | 0.306 |
CLV_PCSK_KEX2_1 | 1000 | 1002 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.259 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.264 |
CLV_PCSK_KEX2_1 | 882 | 884 | PF00082 | 0.357 |
CLV_PCSK_PC1ET2_1 | 3 | 5 | PF00082 | 0.548 |
CLV_PCSK_PC7_1 | 71 | 77 | PF00082 | 0.264 |
CLV_PCSK_SKI1_1 | 1000 | 1004 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 602 | 606 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 783 | 787 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 882 | 886 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 920 | 924 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 954 | 958 | PF00082 | 0.286 |
CLV_Separin_Metazoa | 687 | 691 | PF03568 | 0.502 |
DEG_APCC_DBOX_1 | 230 | 238 | PF00400 | 0.562 |
DEG_APCC_DBOX_1 | 417 | 425 | PF00400 | 0.557 |
DEG_APCC_DBOX_1 | 992 | 1000 | PF00400 | 0.405 |
DEG_SCF_FBW7_1 | 429 | 434 | PF00400 | 0.557 |
DEG_SPOP_SBC_1 | 730 | 734 | PF00917 | 0.614 |
DOC_CDC14_PxL_1 | 843 | 851 | PF14671 | 0.557 |
DOC_CKS1_1 | 648 | 653 | PF01111 | 0.477 |
DOC_CYCLIN_RxL_1 | 228 | 235 | PF00134 | 0.452 |
DOC_CYCLIN_RxL_1 | 242 | 250 | PF00134 | 0.462 |
DOC_CYCLIN_RxL_1 | 600 | 611 | PF00134 | 0.538 |
DOC_CYCLIN_yCln2_LP_2 | 895 | 901 | PF00134 | 0.513 |
DOC_MAPK_gen_1 | 229 | 238 | PF00069 | 0.558 |
DOC_MAPK_gen_1 | 3 | 13 | PF00069 | 0.369 |
DOC_MAPK_gen_1 | 75 | 82 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 882 | 889 | PF00069 | 0.538 |
DOC_MAPK_HePTP_8 | 43 | 55 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 229 | 238 | PF00069 | 0.553 |
DOC_MAPK_MEF2A_6 | 454 | 461 | PF00069 | 0.405 |
DOC_MAPK_MEF2A_6 | 46 | 55 | PF00069 | 0.493 |
DOC_PIKK_1 | 466 | 473 | PF02985 | 0.535 |
DOC_PP1_RVXF_1 | 243 | 250 | PF00149 | 0.510 |
DOC_PP1_RVXF_1 | 60 | 66 | PF00149 | 0.477 |
DOC_PP2B_LxvP_1 | 398 | 401 | PF13499 | 0.482 |
DOC_PP2B_LxvP_1 | 441 | 444 | PF13499 | 0.533 |
DOC_PP2B_LxvP_1 | 605 | 608 | PF13499 | 0.464 |
DOC_PP2B_LxvP_1 | 622 | 625 | PF13499 | 0.464 |
DOC_PP2B_LxvP_1 | 844 | 847 | PF13499 | 0.557 |
DOC_SPAK_OSR1_1 | 248 | 252 | PF12202 | 0.543 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 485 | 489 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 698 | 702 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 704 | 708 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 709 | 713 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 730 | 734 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 822 | 826 | PF00917 | 0.477 |
DOC_USP7_MATH_2 | 147 | 153 | PF00917 | 0.358 |
DOC_USP7_MATH_2 | 86 | 92 | PF00917 | 0.464 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.464 |
DOC_WW_Pin1_4 | 561 | 566 | PF00397 | 0.464 |
DOC_WW_Pin1_4 | 615 | 620 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 647 | 652 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 735 | 740 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 933 | 938 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 948 | 953 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 954 | 959 | PF00397 | 0.452 |
LIG_14-3-3_CanoR_1 | 231 | 237 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 290 | 296 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 508 | 513 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 559 | 565 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 666 | 670 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 819 | 827 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 861 | 867 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 882 | 888 | PF00244 | 0.471 |
LIG_14-3-3_CterR_2 | 1000 | 1005 | PF00244 | 0.664 |
LIG_Actin_WH2_1 | 494 | 510 | PF00022 | 0.377 |
LIG_Actin_WH2_2 | 543 | 561 | PF00022 | 0.557 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.583 |
LIG_BRCT_BRCA1_1 | 128 | 132 | PF00533 | 0.527 |
LIG_BRCT_BRCA1_1 | 201 | 205 | PF00533 | 0.506 |
LIG_BRCT_BRCA1_1 | 944 | 948 | PF00533 | 0.474 |
LIG_Clathr_ClatBox_1 | 853 | 857 | PF01394 | 0.452 |
LIG_CtBP_PxDLS_1 | 777 | 783 | PF00389 | 0.452 |
LIG_eIF4E_1 | 140 | 146 | PF01652 | 0.513 |
LIG_eIF4E_1 | 717 | 723 | PF01652 | 0.507 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.490 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.591 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.534 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.573 |
LIG_FHA_1 | 546 | 552 | PF00498 | 0.448 |
LIG_FHA_1 | 561 | 567 | PF00498 | 0.510 |
LIG_FHA_1 | 616 | 622 | PF00498 | 0.473 |
LIG_FHA_1 | 648 | 654 | PF00498 | 0.464 |
LIG_FHA_1 | 790 | 796 | PF00498 | 0.513 |
LIG_FHA_1 | 838 | 844 | PF00498 | 0.462 |
LIG_FHA_1 | 884 | 890 | PF00498 | 0.455 |
LIG_FHA_2 | 165 | 171 | PF00498 | 0.692 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.331 |
LIG_FHA_2 | 562 | 568 | PF00498 | 0.496 |
LIG_FHA_2 | 680 | 686 | PF00498 | 0.559 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.525 |
LIG_IRF3_LxIS_1 | 739 | 745 | PF10401 | 0.304 |
LIG_LIR_Apic_2 | 346 | 351 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 202 | 211 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 301 | 311 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 499 | 507 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 792 | 799 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 814 | 822 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 88 | 97 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 890 | 900 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 301 | 306 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 355 | 361 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 499 | 503 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 611 | 615 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 792 | 796 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 88 | 92 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 890 | 895 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 923 | 929 | PF02991 | 0.477 |
LIG_MAD2 | 842 | 850 | PF02301 | 0.557 |
LIG_MYND_3 | 607 | 611 | PF01753 | 0.464 |
LIG_NRBOX | 420 | 426 | PF00104 | 0.464 |
LIG_NRBOX | 534 | 540 | PF00104 | 0.557 |
LIG_NRBOX | 875 | 881 | PF00104 | 0.463 |
LIG_PCNA_yPIPBox_3 | 465 | 474 | PF02747 | 0.381 |
LIG_SH2_CRK | 303 | 307 | PF00017 | 0.432 |
LIG_SH2_CRK | 358 | 362 | PF00017 | 0.483 |
LIG_SH2_CRK | 612 | 616 | PF00017 | 0.477 |
LIG_SH2_CRK | 648 | 652 | PF00017 | 0.538 |
LIG_SH2_CRK | 892 | 896 | PF00017 | 0.513 |
LIG_SH2_NCK_1 | 264 | 268 | PF00017 | 0.454 |
LIG_SH2_PTP2 | 717 | 720 | PF00017 | 0.381 |
LIG_SH2_SRC | 264 | 267 | PF00017 | 0.491 |
LIG_SH2_SRC | 333 | 336 | PF00017 | 0.544 |
LIG_SH2_STAP1 | 303 | 307 | PF00017 | 0.378 |
LIG_SH2_STAT3 | 899 | 902 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 717 | 720 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 760 | 763 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 817 | 820 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 878 | 881 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 892 | 895 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 899 | 902 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 950 | 953 | PF00017 | 0.377 |
LIG_SH3_3 | 720 | 726 | PF00018 | 0.517 |
LIG_SH3_3 | 733 | 739 | PF00018 | 0.631 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.528 |
LIG_SH3_3 | 844 | 850 | PF00018 | 0.557 |
LIG_SUMO_SIM_anti_2 | 235 | 240 | PF11976 | 0.403 |
LIG_SUMO_SIM_anti_2 | 268 | 273 | PF11976 | 0.433 |
LIG_SUMO_SIM_anti_2 | 707 | 712 | PF11976 | 0.544 |
LIG_SUMO_SIM_anti_2 | 852 | 858 | PF11976 | 0.469 |
LIG_SUMO_SIM_par_1 | 235 | 240 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 268 | 273 | PF11976 | 0.364 |
LIG_SUMO_SIM_par_1 | 41 | 48 | PF11976 | 0.538 |
LIG_SUMO_SIM_par_1 | 737 | 743 | PF11976 | 0.564 |
LIG_TRAF2_1 | 114 | 117 | PF00917 | 0.477 |
LIG_TRAF2_1 | 168 | 171 | PF00917 | 0.768 |
LIG_TRAF2_1 | 453 | 456 | PF00917 | 0.538 |
LIG_TYR_ITIM | 610 | 615 | PF00017 | 0.477 |
LIG_UBA3_1 | 580 | 585 | PF00899 | 0.557 |
LIG_WRC_WIRS_1 | 238 | 243 | PF05994 | 0.374 |
LIG_WRC_WIRS_1 | 790 | 795 | PF05994 | 0.513 |
MOD_CDK_SPxK_1 | 948 | 954 | PF00069 | 0.377 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.464 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.607 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.569 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.380 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.476 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.588 |
MOD_CK1_1 | 732 | 738 | PF00069 | 0.616 |
MOD_CK1_1 | 932 | 938 | PF00069 | 0.530 |
MOD_CK1_1 | 980 | 986 | PF00069 | 0.506 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.694 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.352 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.656 |
MOD_CK2_1 | 561 | 567 | PF00069 | 0.463 |
MOD_CK2_1 | 822 | 828 | PF00069 | 0.452 |
MOD_CK2_1 | 912 | 918 | PF00069 | 0.473 |
MOD_CK2_1 | 933 | 939 | PF00069 | 0.377 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.282 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.266 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.541 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.613 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.561 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.490 |
MOD_GlcNHglycan | 508 | 511 | PF01048 | 0.306 |
MOD_GlcNHglycan | 783 | 786 | PF01048 | 0.252 |
MOD_GlcNHglycan | 982 | 985 | PF01048 | 0.289 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.475 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.520 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.555 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.630 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.454 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.525 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.744 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.461 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.549 |
MOD_GSK3_1 | 557 | 564 | PF00069 | 0.529 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.433 |
MOD_GSK3_1 | 637 | 644 | PF00069 | 0.452 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.452 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.464 |
MOD_GSK3_1 | 730 | 737 | PF00069 | 0.623 |
MOD_GSK3_1 | 828 | 835 | PF00069 | 0.502 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.491 |
MOD_GSK3_1 | 883 | 890 | PF00069 | 0.469 |
MOD_GSK3_1 | 929 | 936 | PF00069 | 0.483 |
MOD_GSK3_1 | 942 | 949 | PF00069 | 0.454 |
MOD_GSK3_1 | 973 | 980 | PF00069 | 0.513 |
MOD_LATS_1 | 639 | 645 | PF00433 | 0.494 |
MOD_N-GLC_1 | 217 | 222 | PF02516 | 0.473 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.538 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.464 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.464 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.321 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.477 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.557 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.538 |
MOD_NEK2_1 | 557 | 562 | PF00069 | 0.456 |
MOD_NEK2_1 | 637 | 642 | PF00069 | 0.382 |
MOD_NEK2_1 | 731 | 736 | PF00069 | 0.425 |
MOD_NEK2_1 | 742 | 747 | PF00069 | 0.230 |
MOD_NEK2_1 | 789 | 794 | PF00069 | 0.496 |
MOD_NEK2_1 | 837 | 842 | PF00069 | 0.462 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.461 |
MOD_NEK2_1 | 887 | 892 | PF00069 | 0.379 |
MOD_NEK2_1 | 946 | 951 | PF00069 | 0.473 |
MOD_PIKK_1 | 134 | 140 | PF00454 | 0.538 |
MOD_PIKK_1 | 240 | 246 | PF00454 | 0.449 |
MOD_PIKK_1 | 258 | 264 | PF00454 | 0.488 |
MOD_PIKK_1 | 285 | 291 | PF00454 | 0.592 |
MOD_PIKK_1 | 709 | 715 | PF00454 | 0.486 |
MOD_PIKK_1 | 742 | 748 | PF00454 | 0.266 |
MOD_PK_1 | 326 | 332 | PF00069 | 0.557 |
MOD_PK_1 | 508 | 514 | PF00069 | 0.557 |
MOD_PK_1 | 912 | 918 | PF00069 | 0.377 |
MOD_PKA_1 | 882 | 888 | PF00069 | 0.526 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.464 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.509 |
MOD_PKA_2 | 289 | 295 | PF00069 | 0.519 |
MOD_PKA_2 | 417 | 423 | PF00069 | 0.531 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.557 |
MOD_PKA_2 | 665 | 671 | PF00069 | 0.536 |
MOD_PKA_2 | 679 | 685 | PF00069 | 0.545 |
MOD_PKA_2 | 860 | 866 | PF00069 | 0.469 |
MOD_PKA_2 | 882 | 888 | PF00069 | 0.515 |
MOD_PKA_2 | 980 | 986 | PF00069 | 0.493 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.754 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.501 |
MOD_Plk_1 | 425 | 431 | PF00069 | 0.465 |
MOD_Plk_1 | 446 | 452 | PF00069 | 0.556 |
MOD_Plk_1 | 838 | 844 | PF00069 | 0.458 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.464 |
MOD_Plk_1 | 920 | 926 | PF00069 | 0.557 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.469 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.422 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.463 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.351 |
MOD_Plk_4 | 417 | 423 | PF00069 | 0.454 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.490 |
MOD_Plk_4 | 508 | 514 | PF00069 | 0.552 |
MOD_Plk_4 | 789 | 795 | PF00069 | 0.538 |
MOD_Plk_4 | 822 | 828 | PF00069 | 0.452 |
MOD_Plk_4 | 829 | 835 | PF00069 | 0.452 |
MOD_Plk_4 | 849 | 855 | PF00069 | 0.321 |
MOD_Plk_4 | 883 | 889 | PF00069 | 0.453 |
MOD_Plk_4 | 942 | 948 | PF00069 | 0.528 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.613 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.634 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.321 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.669 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.530 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.464 |
MOD_ProDKin_1 | 561 | 567 | PF00069 | 0.464 |
MOD_ProDKin_1 | 615 | 621 | PF00069 | 0.504 |
MOD_ProDKin_1 | 647 | 653 | PF00069 | 0.477 |
MOD_ProDKin_1 | 735 | 741 | PF00069 | 0.627 |
MOD_ProDKin_1 | 933 | 939 | PF00069 | 0.469 |
MOD_ProDKin_1 | 948 | 954 | PF00069 | 0.453 |
MOD_SUMO_for_1 | 26 | 29 | PF00179 | 0.540 |
MOD_SUMO_rev_2 | 322 | 328 | PF00179 | 0.617 |
TRG_DiLeu_BaEn_1 | 499 | 504 | PF01217 | 0.464 |
TRG_DiLeu_BaEn_2 | 997 | 1003 | PF01217 | 0.620 |
TRG_DiLeu_BaLyEn_6 | 229 | 234 | PF01217 | 0.539 |
TRG_DiLeu_BaLyEn_6 | 530 | 535 | PF01217 | 0.529 |
TRG_DiLeu_BaLyEn_6 | 546 | 551 | PF01217 | 0.558 |
TRG_DiLeu_BaLyEn_6 | 751 | 756 | PF01217 | 0.508 |
TRG_DiLeu_LyEn_5 | 499 | 504 | PF01217 | 0.538 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 612 | 615 | PF00928 | 0.477 |
TRG_ENDOCYTIC_2 | 817 | 820 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 892 | 895 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 926 | 929 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 94 | 97 | PF00928 | 0.457 |
TRG_ER_diArg_1 | 229 | 232 | PF00400 | 0.628 |
TRG_ER_diArg_1 | 437 | 439 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 75 | 77 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 999 | 1001 | PF00400 | 0.509 |
TRG_NLS_MonoExtC_3 | 2 | 8 | PF00514 | 0.578 |
TRG_Pf-PMV_PEXEL_1 | 245 | 250 | PF00026 | 0.524 |
TRG_Pf-PMV_PEXEL_1 | 297 | 301 | PF00026 | 0.498 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7L2 | Leptomonas seymouri | 62% | 99% |
A0A0S4JK96 | Bodo saltans | 34% | 100% |
A0A1X0NU18 | Trypanosomatidae | 45% | 100% |
A0A3Q8IAC6 | Leishmania donovani | 85% | 100% |
A0A422NC23 | Trypanosoma rangeli | 48% | 100% |
A3LU10 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 26% | 98% |
A5DEV6 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 28% | 100% |
A5FQC0 | Dehalococcoides mccartyi (strain ATCC BAA-2100 / JCM 16839 / KCTC 5957 / BAV1) | 25% | 100% |
A8F164 | Rickettsia massiliae (strain Mtu5) | 24% | 100% |
A8GRI6 | Rickettsia rickettsii (strain Sheila Smith) | 24% | 100% |
B0BWY8 | Rickettsia rickettsii (strain Iowa) | 24% | 100% |
B0JFY0 | Microcystis aeruginosa (strain NIES-843 / IAM M-2473) | 27% | 100% |
B2J434 | Nostoc punctiforme (strain ATCC 29133 / PCC 73102) | 27% | 100% |
B3E6P2 | Trichlorobacter lovleyi (strain ATCC BAA-1151 / DSM 17278 / SZ) | 28% | 100% |
B3QPY5 | Chlorobaculum parvum (strain DSM 263 / NCIMB 8327) | 28% | 100% |
B8CX98 | Halothermothrix orenii (strain H 168 / OCM 544 / DSM 9562) | 25% | 100% |
C3PN02 | Rickettsia africae (strain ESF-5) | 24% | 100% |
C9ZXQ8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9AGN0 | Leishmania infantum | 85% | 100% |
E9AQD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
O74502 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 80% |
P0CO92 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 31% | 84% |
P0CO93 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 31% | 84% |
P73769 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 29% | 100% |
Q10YG4 | Trichodesmium erythraeum (strain IMS101) | 27% | 100% |
Q1DQ73 | Coccidioides immitis (strain RS) | 30% | 89% |
Q1H2P1 | Methylobacillus flagellatus (strain KT / ATCC 51484 / DSM 6875) | 29% | 100% |
Q3ZYA0 | Dehalococcoides mccartyi (strain CBDB1) | 25% | 100% |
Q47DJ8 | Dechloromonas aromatica (strain RCB) | 29% | 100% |
Q4QF38 | Leishmania major | 85% | 100% |
Q4UM86 | Rickettsia felis (strain ATCC VR-1525 / URRWXCal2) | 24% | 100% |
Q6CSR1 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 27% | 98% |
Q7UA23 | Parasynechococcus marenigrum (strain WH8102) | 29% | 100% |
Q8PWA7 | Methanosarcina mazei (strain ATCC BAA-159 / DSM 3647 / Goe1 / Go1 / JCM 11833 / OCM 88) | 25% | 100% |
Q92IL9 | Rickettsia conorii (strain ATCC VR-613 / Malish 7) | 24% | 100% |
Q9ZDM9 | Rickettsia prowazekii (strain Madrid E) | 23% | 100% |
V5BK71 | Trypanosoma cruzi | 48% | 100% |