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: 10 |
NetGPI | no | yes: 0, no: 10 |
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: A4HP61
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006259 | DNA metabolic process | 4 | 11 |
GO:0006281 | DNA repair | 5 | 11 |
GO:0006298 | mismatch repair | 6 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0006950 | response to stress | 2 | 11 |
GO:0006974 | DNA damage response | 4 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0033554 | cellular response to stress | 3 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0050896 | response to stimulus | 1 | 11 |
GO:0051716 | cellular response to stimulus | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:0032042 | mitochondrial DNA metabolic process | 5 | 1 |
GO:0043504 | mitochondrial DNA repair | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003677 | DNA binding | 4 | 11 |
GO:0003690 | double-stranded DNA binding | 5 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005524 | ATP binding | 5 | 11 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0030554 | adenyl nucleotide binding | 5 | 11 |
GO:0030983 | mismatched DNA binding | 6 | 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:0140097 | catalytic activity, acting on DNA | 3 | 11 |
GO:0140299 | small molecule sensor activity | 1 | 11 |
GO:0140612 | DNA damage sensor activity | 2 | 11 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 11 |
GO:0140657 | ATP-dependent activity | 1 | 11 |
GO:0140664 | ATP-dependent DNA damage sensor activity | 3 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 209 | 213 | PF00656 | 0.538 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.311 |
CLV_NRD_NRD_1 | 608 | 610 | PF00675 | 0.314 |
CLV_NRD_NRD_1 | 903 | 905 | PF00675 | 0.160 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.349 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.217 |
CLV_PCSK_KEX2_1 | 459 | 461 | PF00082 | 0.217 |
CLV_PCSK_KEX2_1 | 563 | 565 | PF00082 | 0.304 |
CLV_PCSK_KEX2_1 | 608 | 610 | PF00082 | 0.314 |
CLV_PCSK_KEX2_1 | 903 | 905 | PF00082 | 0.160 |
CLV_PCSK_PC1ET2_1 | 221 | 223 | PF00082 | 0.583 |
CLV_PCSK_PC1ET2_1 | 459 | 461 | PF00082 | 0.217 |
CLV_PCSK_PC1ET2_1 | 563 | 565 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 527 | 531 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 628 | 632 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 653 | 657 | PF00082 | 0.248 |
CLV_PCSK_SKI1_1 | 673 | 677 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 771 | 775 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 815 | 819 | PF00082 | 0.221 |
CLV_PCSK_SKI1_1 | 86 | 90 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 903 | 907 | PF00082 | 0.268 |
DEG_ODPH_VHL_1 | 172 | 183 | PF01847 | 0.412 |
DEG_SPOP_SBC_1 | 558 | 562 | PF00917 | 0.426 |
DEG_SPOP_SBC_1 | 584 | 588 | PF00917 | 0.511 |
DOC_CKS1_1 | 149 | 154 | PF01111 | 0.417 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 438 | 447 | PF00134 | 0.468 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 506 | 513 | PF00134 | 0.511 |
DOC_CYCLIN_yCln2_LP_2 | 799 | 805 | PF00134 | 0.468 |
DOC_MAPK_DCC_7 | 744 | 754 | PF00069 | 0.224 |
DOC_MAPK_FxFP_2 | 15 | 18 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 358 | 365 | PF00069 | 0.392 |
DOC_MAPK_gen_1 | 367 | 375 | PF00069 | 0.330 |
DOC_MAPK_gen_1 | 459 | 469 | PF00069 | 0.468 |
DOC_MAPK_gen_1 | 506 | 513 | PF00069 | 0.445 |
DOC_MAPK_gen_1 | 53 | 62 | PF00069 | 0.430 |
DOC_MAPK_MEF2A_6 | 236 | 245 | PF00069 | 0.357 |
DOC_MAPK_MEF2A_6 | 506 | 513 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 55 | 63 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 628 | 637 | PF00069 | 0.432 |
DOC_MAPK_MEF2A_6 | 788 | 796 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 828 | 837 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 968 | 976 | PF00069 | 0.430 |
DOC_PP2B_LxvP_1 | 297 | 300 | PF13499 | 0.393 |
DOC_PP2B_LxvP_1 | 579 | 582 | PF13499 | 0.468 |
DOC_PP4_FxxP_1 | 15 | 18 | PF00568 | 0.435 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.349 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 558 | 562 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 574 | 578 | PF00917 | 0.429 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.419 |
DOC_USP7_MATH_1 | 781 | 785 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 942 | 946 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 947 | 951 | PF00917 | 0.423 |
DOC_USP7_MATH_2 | 285 | 291 | PF00917 | 0.280 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 580 | 585 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 641 | 646 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 808 | 813 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 905 | 910 | PF00397 | 0.462 |
LIG_14-3-3_CanoR_1 | 205 | 214 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 236 | 245 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 358 | 365 | PF00244 | 0.347 |
LIG_14-3-3_CanoR_1 | 412 | 418 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 420 | 428 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 484 | 490 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 571 | 579 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 653 | 659 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 706 | 711 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 860 | 870 | PF00244 | 0.417 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.526 |
LIG_BRCT_BRCA1_1 | 11 | 15 | PF00533 | 0.461 |
LIG_BRCT_BRCA1_1 | 214 | 218 | PF00533 | 0.418 |
LIG_BRCT_BRCA1_1 | 474 | 478 | PF00533 | 0.464 |
LIG_BRCT_BRCA1_1 | 586 | 590 | PF00533 | 0.418 |
LIG_BRCT_BRCA1_1 | 953 | 957 | PF00533 | 0.458 |
LIG_Clathr_ClatBox_1 | 630 | 634 | PF01394 | 0.473 |
LIG_CtBP_PxDLS_1 | 777 | 783 | PF00389 | 0.417 |
LIG_deltaCOP1_diTrp_1 | 109 | 116 | PF00928 | 0.417 |
LIG_Dynein_DLC8_1 | 902 | 908 | PF01221 | 0.360 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.443 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.303 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.343 |
LIG_FHA_1 | 560 | 566 | PF00498 | 0.390 |
LIG_FHA_1 | 584 | 590 | PF00498 | 0.494 |
LIG_FHA_1 | 592 | 598 | PF00498 | 0.439 |
LIG_FHA_1 | 703 | 709 | PF00498 | 0.415 |
LIG_FHA_1 | 787 | 793 | PF00498 | 0.417 |
LIG_FHA_1 | 830 | 836 | PF00498 | 0.435 |
LIG_FHA_1 | 838 | 844 | PF00498 | 0.460 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.417 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.602 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.423 |
LIG_FHA_2 | 277 | 283 | PF00498 | 0.478 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.250 |
LIG_FHA_2 | 554 | 560 | PF00498 | 0.468 |
LIG_FHA_2 | 665 | 671 | PF00498 | 0.515 |
LIG_FHA_2 | 732 | 738 | PF00498 | 0.477 |
LIG_FHA_2 | 804 | 810 | PF00498 | 0.511 |
LIG_FHA_2 | 906 | 912 | PF00498 | 0.360 |
LIG_LIR_Apic_2 | 12 | 18 | PF02991 | 0.446 |
LIG_LIR_Apic_2 | 657 | 663 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 1009 | 1014 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 109 | 116 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 311 | 318 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 468 | 478 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 54 | 63 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 621 | 631 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 73 | 79 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 814 | 825 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 831 | 842 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 891 | 902 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 1009 | 1014 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 109 | 113 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 14 | 20 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 263 | 268 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 311 | 316 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 46 | 52 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 468 | 473 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 475 | 481 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 54 | 60 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 621 | 626 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 696 | 701 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 726 | 732 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 73 | 77 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 809 | 813 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 814 | 820 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 831 | 837 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 891 | 897 | PF02991 | 0.417 |
LIG_LYPXL_yS_3 | 17 | 20 | PF13949 | 0.465 |
LIG_LYPXL_yS_3 | 729 | 732 | PF13949 | 0.386 |
LIG_NRBOX | 237 | 243 | PF00104 | 0.387 |
LIG_NRBOX | 547 | 553 | PF00104 | 0.511 |
LIG_NRBOX | 710 | 716 | PF00104 | 0.360 |
LIG_PDZ_Class_2 | 1009 | 1014 | PF00595 | 0.519 |
LIG_Pex14_1 | 110 | 114 | PF04695 | 0.417 |
LIG_Pex14_1 | 525 | 529 | PF04695 | 0.511 |
LIG_Pex14_2 | 15 | 19 | PF04695 | 0.443 |
LIG_Pex14_2 | 365 | 369 | PF04695 | 0.291 |
LIG_Pex14_2 | 698 | 702 | PF04695 | 0.527 |
LIG_PTAP_UEV_1 | 24 | 29 | PF05743 | 0.521 |
LIG_PTB_Apo_2 | 201 | 208 | PF02174 | 0.380 |
LIG_PTB_Apo_2 | 77 | 84 | PF02174 | 0.500 |
LIG_Rb_pABgroove_1 | 563 | 571 | PF01858 | 0.473 |
LIG_REV1ctd_RIR_1 | 60 | 69 | PF16727 | 0.430 |
LIG_SH2_CRK | 441 | 445 | PF00017 | 0.468 |
LIG_SH2_CRK | 57 | 61 | PF00017 | 0.469 |
LIG_SH2_CRK | 74 | 78 | PF00017 | 0.388 |
LIG_SH2_CRK | 872 | 876 | PF00017 | 0.488 |
LIG_SH2_CRK | 894 | 898 | PF00017 | 0.417 |
LIG_SH2_CRK | 959 | 963 | PF00017 | 0.430 |
LIG_SH2_PTP2 | 498 | 501 | PF00017 | 0.511 |
LIG_SH2_PTP2 | 660 | 663 | PF00017 | 0.360 |
LIG_SH2_PTP2 | 834 | 837 | PF00017 | 0.430 |
LIG_SH2_SRC | 38 | 41 | PF00017 | 0.432 |
LIG_SH2_SRC | 498 | 501 | PF00017 | 0.511 |
LIG_SH2_STAP1 | 331 | 335 | PF00017 | 0.380 |
LIG_SH2_STAP1 | 72 | 76 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 660 | 663 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 710 | 713 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 834 | 837 | PF00017 | 0.450 |
LIG_SH2_STAT6 | 264 | 268 | PF00017 | 0.287 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.399 |
LIG_SH3_3 | 247 | 253 | PF00018 | 0.336 |
LIG_SH3_3 | 342 | 348 | PF00018 | 0.503 |
LIG_SH3_3 | 724 | 730 | PF00018 | 0.444 |
LIG_SH3_3 | 880 | 886 | PF00018 | 0.448 |
LIG_SUMO_SIM_anti_2 | 145 | 151 | PF11976 | 0.430 |
LIG_SUMO_SIM_anti_2 | 381 | 387 | PF11976 | 0.417 |
LIG_SUMO_SIM_anti_2 | 973 | 978 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 145 | 151 | PF11976 | 0.430 |
LIG_SUMO_SIM_par_1 | 471 | 477 | PF11976 | 0.423 |
LIG_SUMO_SIM_par_1 | 771 | 776 | PF11976 | 0.325 |
LIG_SUMO_SIM_par_1 | 885 | 892 | PF11976 | 0.417 |
LIG_TRAF2_1 | 304 | 307 | PF00917 | 0.388 |
LIG_TRAF2_1 | 573 | 576 | PF00917 | 0.511 |
LIG_TYR_ITIM | 727 | 732 | PF00017 | 0.437 |
LIG_TYR_ITIM | 870 | 875 | PF00017 | 0.488 |
LIG_UBA3_1 | 241 | 248 | PF00899 | 0.381 |
LIG_UBA3_1 | 519 | 527 | PF00899 | 0.360 |
LIG_UBA3_1 | 748 | 756 | PF00899 | 0.392 |
LIG_WRC_WIRS_1 | 312 | 317 | PF05994 | 0.368 |
LIG_WRC_WIRS_1 | 362 | 367 | PF05994 | 0.356 |
LIG_WRC_WIRS_1 | 469 | 474 | PF05994 | 0.360 |
MOD_CDK_SPxxK_3 | 808 | 815 | PF00069 | 0.511 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.423 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.669 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.447 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.443 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.479 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.502 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.421 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.355 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.446 |
MOD_CK1_1 | 483 | 489 | PF00069 | 0.463 |
MOD_CK1_1 | 538 | 544 | PF00069 | 0.360 |
MOD_CK1_1 | 583 | 589 | PF00069 | 0.490 |
MOD_CK1_1 | 689 | 695 | PF00069 | 0.568 |
MOD_CK1_1 | 848 | 854 | PF00069 | 0.543 |
MOD_CK1_1 | 950 | 956 | PF00069 | 0.478 |
MOD_CK1_1 | 996 | 1002 | PF00069 | 0.589 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.417 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.483 |
MOD_CK2_1 | 276 | 282 | PF00069 | 0.530 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.352 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.430 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.430 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.375 |
MOD_CK2_1 | 553 | 559 | PF00069 | 0.468 |
MOD_CK2_1 | 570 | 576 | PF00069 | 0.348 |
MOD_CK2_1 | 664 | 670 | PF00069 | 0.497 |
MOD_CK2_1 | 731 | 737 | PF00069 | 0.464 |
MOD_CK2_1 | 803 | 809 | PF00069 | 0.481 |
MOD_Cter_Amidation | 356 | 359 | PF01082 | 0.393 |
MOD_Cter_Amidation | 409 | 412 | PF01082 | 0.217 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.445 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.512 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.508 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.248 |
MOD_GlcNHglycan | 539 | 543 | PF01048 | 0.194 |
MOD_GlcNHglycan | 572 | 575 | PF01048 | 0.236 |
MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.230 |
MOD_GlcNHglycan | 702 | 705 | PF01048 | 0.268 |
MOD_GlcNHglycan | 845 | 848 | PF01048 | 0.319 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.644 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.406 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.521 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.466 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.449 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.468 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.536 |
MOD_GSK3_1 | 553 | 560 | PF00069 | 0.447 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.382 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.426 |
MOD_GSK3_1 | 664 | 671 | PF00069 | 0.430 |
MOD_GSK3_1 | 682 | 689 | PF00069 | 0.502 |
MOD_GSK3_1 | 702 | 709 | PF00069 | 0.397 |
MOD_GSK3_1 | 782 | 789 | PF00069 | 0.417 |
MOD_GSK3_1 | 885 | 892 | PF00069 | 0.500 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.544 |
MOD_GSK3_1 | 903 | 910 | PF00069 | 0.358 |
MOD_GSK3_1 | 947 | 954 | PF00069 | 0.397 |
MOD_GSK3_1 | 989 | 996 | PF00069 | 0.488 |
MOD_N-GLC_1 | 230 | 235 | PF02516 | 0.312 |
MOD_N-GLC_1 | 290 | 295 | PF02516 | 0.361 |
MOD_N-GLC_1 | 490 | 495 | PF02516 | 0.252 |
MOD_N-GLC_2 | 399 | 401 | PF02516 | 0.230 |
MOD_N-GLC_2 | 403 | 405 | PF02516 | 0.204 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.346 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.427 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.490 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.330 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.444 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.484 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.396 |
MOD_NEK2_1 | 668 | 673 | PF00069 | 0.572 |
MOD_NEK2_1 | 702 | 707 | PF00069 | 0.508 |
MOD_NEK2_1 | 773 | 778 | PF00069 | 0.278 |
MOD_NEK2_1 | 786 | 791 | PF00069 | 0.369 |
MOD_NEK2_1 | 837 | 842 | PF00069 | 0.474 |
MOD_NEK2_1 | 878 | 883 | PF00069 | 0.392 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.476 |
MOD_NEK2_2 | 585 | 590 | PF00069 | 0.446 |
MOD_NEK2_2 | 829 | 834 | PF00069 | 0.430 |
MOD_NEK2_2 | 871 | 876 | PF00069 | 0.473 |
MOD_OFUCOSY | 944 | 951 | PF10250 | 0.212 |
MOD_PIKK_1 | 3 | 9 | PF00454 | 0.567 |
MOD_PIKK_1 | 490 | 496 | PF00454 | 0.453 |
MOD_PIKK_1 | 903 | 909 | PF00454 | 0.499 |
MOD_PK_1 | 358 | 364 | PF00069 | 0.303 |
MOD_PKA_1 | 358 | 364 | PF00069 | 0.303 |
MOD_PKA_1 | 903 | 909 | PF00069 | 0.360 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.411 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.365 |
MOD_PKA_2 | 403 | 409 | PF00069 | 0.472 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.352 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.490 |
MOD_PKA_2 | 570 | 576 | PF00069 | 0.490 |
MOD_PKA_2 | 859 | 865 | PF00069 | 0.417 |
MOD_PKA_2 | 903 | 909 | PF00069 | 0.430 |
MOD_PKA_2 | 996 | 1002 | PF00069 | 0.589 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.417 |
MOD_Plk_1 | 230 | 236 | PF00069 | 0.374 |
MOD_Plk_1 | 290 | 296 | PF00069 | 0.449 |
MOD_Plk_1 | 375 | 381 | PF00069 | 0.283 |
MOD_Plk_1 | 673 | 679 | PF00069 | 0.468 |
MOD_Plk_2-3 | 1004 | 1010 | PF00069 | 0.454 |
MOD_Plk_2-3 | 394 | 400 | PF00069 | 0.511 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.582 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.429 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.397 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.494 |
MOD_Plk_4 | 585 | 591 | PF00069 | 0.409 |
MOD_Plk_4 | 664 | 670 | PF00069 | 0.444 |
MOD_Plk_4 | 682 | 688 | PF00069 | 0.522 |
MOD_Plk_4 | 706 | 712 | PF00069 | 0.456 |
MOD_Plk_4 | 782 | 788 | PF00069 | 0.417 |
MOD_Plk_4 | 829 | 835 | PF00069 | 0.417 |
MOD_Plk_4 | 885 | 891 | PF00069 | 0.498 |
MOD_Plk_4 | 980 | 986 | PF00069 | 0.473 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.442 |
MOD_ProDKin_1 | 580 | 586 | PF00069 | 0.496 |
MOD_ProDKin_1 | 641 | 647 | PF00069 | 0.511 |
MOD_ProDKin_1 | 808 | 814 | PF00069 | 0.511 |
MOD_ProDKin_1 | 905 | 911 | PF00069 | 0.462 |
MOD_SUMO_for_1 | 220 | 223 | PF00179 | 0.598 |
MOD_SUMO_for_1 | 926 | 929 | PF00179 | 0.511 |
MOD_SUMO_for_1 | 990 | 993 | PF00179 | 0.468 |
MOD_SUMO_rev_2 | 46 | 54 | PF00179 | 0.430 |
MOD_SUMO_rev_2 | 483 | 490 | PF00179 | 0.389 |
MOD_SUMO_rev_2 | 935 | 939 | PF00179 | 0.360 |
TRG_DiLeu_BaEn_1 | 575 | 580 | PF01217 | 0.514 |
TRG_DiLeu_BaEn_1 | 769 | 774 | PF01217 | 0.436 |
TRG_DiLeu_BaLyEn_6 | 748 | 753 | PF01217 | 0.427 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 312 | 315 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 49 | 52 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 729 | 732 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 74 | 77 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 834 | 837 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 872 | 875 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 894 | 897 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 921 | 924 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 959 | 962 | PF00928 | 0.430 |
TRG_ER_diArg_1 | 192 | 194 | PF00400 | 0.349 |
TRG_ER_diArg_1 | 202 | 205 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 367 | 369 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 411 | 413 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 607 | 609 | PF00400 | 0.514 |
TRG_NES_CRM1_1 | 307 | 321 | PF08389 | 0.459 |
TRG_NES_CRM1_1 | 465 | 479 | PF08389 | 0.468 |
TRG_Pf-PMV_PEXEL_1 | 144 | 148 | PF00026 | 0.217 |
TRG_Pf-PMV_PEXEL_1 | 609 | 613 | PF00026 | 0.284 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6K5 | Leptomonas seymouri | 66% | 98% |
A0A0S4IMQ7 | Bodo saltans | 41% | 100% |
A0A3Q8IK49 | Leishmania donovani | 85% | 100% |
A0A3R7LRN7 | Trypanosoma rangeli | 47% | 100% |
A0KPG5 | Aeromonas hydrophila subsp. hydrophila (strain ATCC 7966 / DSM 30187 / BCRC 13018 / CCUG 14551 / JCM 1027 / KCTC 2358 / NCIMB 9240 / NCTC 8049) | 27% | 100% |
A0L7L5 | Magnetococcus marinus (strain ATCC BAA-1437 / JCM 17883 / MC-1) | 28% | 100% |
A0Q809 | Francisella tularensis subsp. novicida (strain U112) | 23% | 100% |
A3N2Q0 | Actinobacillus pleuropneumoniae serotype 5b (strain L20) | 26% | 100% |
A4HL76 | Leishmania braziliensis | 26% | 100% |
A4IDG7 | Leishmania infantum | 85% | 100% |
A4IXL2 | Francisella tularensis subsp. tularensis (strain WY96-3418) | 23% | 100% |
A4SFT1 | Chlorobium phaeovibrioides (strain DSM 265 / 1930) | 26% | 100% |
A4SIL2 | Aeromonas salmonicida (strain A449) | 26% | 100% |
A5CDU2 | Orientia tsutsugamushi (strain Boryong) | 25% | 100% |
A5N8I5 | Clostridium kluyveri (strain ATCC 8527 / DSM 555 / NCIMB 10680) | 24% | 100% |
A6VL76 | Actinobacillus succinogenes (strain ATCC 55618 / DSM 22257 / CCUG 43843 / 130Z) | 26% | 100% |
A6W1Q6 | Marinomonas sp. (strain MWYL1) | 26% | 100% |
A7N9Y6 | Francisella tularensis subsp. holarctica (strain FTNF002-00 / FTA) | 23% | 100% |
A8EZG1 | Rickettsia canadensis (strain McKiel) | 25% | 100% |
A8F164 | Rickettsia massiliae (strain Mtu5) | 23% | 100% |
A8GMX2 | Rickettsia akari (strain Hartford) | 24% | 100% |
A8GRI6 | Rickettsia rickettsii (strain Sheila Smith) | 23% | 100% |
A8GX86 | Rickettsia bellii (strain OSU 85-389) | 24% | 100% |
A8I275 | Azorhizobium caulinodans (strain ATCC 43989 / DSM 5975 / JCM 20966 / LMG 6465 / NBRC 14845 / NCIMB 13405 / ORS 571) | 26% | 100% |
A9WFZ9 | Chloroflexus aurantiacus (strain ATCC 29366 / DSM 635 / J-10-fl) | 27% | 100% |
B0BRS8 | Actinobacillus pleuropneumoniae serotype 3 (strain JL03) | 26% | 100% |
B0BWY8 | Rickettsia rickettsii (strain Iowa) | 23% | 100% |
B0CF30 | Acaryochloris marina (strain MBIC 11017) | 24% | 100% |
B0CIQ5 | Brucella suis (strain ATCC 23445 / NCTC 10510) | 25% | 100% |
B0UWV7 | Histophilus somni (strain 2336) | 25% | 100% |
B1N025 | Leuconostoc citreum (strain KM20) | 26% | 100% |
B2GB17 | Limosilactobacillus fermentum (strain NBRC 3956 / LMG 18251) | 23% | 100% |
B2SEQ6 | Francisella tularensis subsp. mediasiatica (strain FSC147) | 23% | 100% |
B3CQY2 | Orientia tsutsugamushi (strain Ikeda) | 25% | 100% |
B3H2J9 | Actinobacillus pleuropneumoniae serotype 7 (strain AP76) | 26% | 100% |
B3QPY5 | Chlorobaculum parvum (strain DSM 263 / NCIMB 8327) | 27% | 100% |
B9E1Z0 | Clostridium kluyveri (strain NBRC 12016) | 24% | 100% |
B9LB04 | Chloroflexus aurantiacus (strain ATCC 29364 / DSM 637 / Y-400-fl) | 27% | 100% |
C0QPF0 | Persephonella marina (strain DSM 14350 / EX-H1) | 25% | 100% |
C3PN02 | Rickettsia africae (strain ESF-5) | 24% | 100% |
C6DAK6 | Pectobacterium carotovorum subsp. carotovorum (strain PC1) | 24% | 100% |
D0A350 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E1BYJ2 | Gallus gallus | 28% | 76% |
E9ASW9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
O65607 | Arabidopsis thaliana | 29% | 94% |
O74502 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 81% |
P13705 | Mus musculus | 26% | 93% |
P25846 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 100% |
P61670 | Rhodopseudomonas palustris (strain ATCC BAA-98 / CGA009) | 26% | 100% |
Q0BNM7 | Francisella tularensis subsp. holarctica (strain OSU18) | 23% | 100% |
Q0BV38 | Granulibacter bethesdensis (strain ATCC BAA-1260 / CGDNIH1) | 27% | 100% |
Q0I1B8 | Haemophilus somnus (strain 129Pt) | 25% | 100% |
Q14GB1 | Francisella tularensis subsp. tularensis (strain FSC 198) | 23% | 100% |
Q1MMA5 | Rhizobium leguminosarum bv. viciae (strain 3841) | 26% | 100% |
Q1QQJ4 | Nitrobacter hamburgensis (strain DSM 10229 / NCIMB 13809 / X14) | 25% | 100% |
Q1RJJ5 | Rickettsia bellii (strain RML369-C) | 24% | 100% |
Q1WT15 | Ligilactobacillus salivarius (strain UCC118) | 24% | 100% |
Q21LB1 | Saccharophagus degradans (strain 2-40 / ATCC 43961 / DSM 17024) | 25% | 100% |
Q24X61 | Desulfitobacterium hafniense (strain Y51) | 26% | 100% |
Q28VY6 | Jannaschia sp. (strain CCS1) | 27% | 100% |
Q2A5B5 | Francisella tularensis subsp. holarctica (strain LVS) | 23% | 100% |
Q2KD76 | Rhizobium etli (strain CFN 42 / ATCC 51251) | 25% | 100% |
Q2RNG0 | Rhodospirillum rubrum (strain ATCC 11170 / ATH 1.1.1 / DSM 467 / LMG 4362 / NCIMB 8255 / S1) | 30% | 100% |
Q2YB94 | Nitrosospira multiformis (strain ATCC 25196 / NCIMB 11849 / C 71) | 25% | 100% |
Q31F87 | Hydrogenovibrio crunogenus (strain DSM 25203 / XCL-2) | 23% | 100% |
Q3M892 | Trichormus variabilis (strain ATCC 29413 / PCC 7937) | 24% | 100% |
Q3SVD4 | Nitrobacter winogradskyi (strain ATCC 25391 / DSM 10237 / CIP 104748 / NCIMB 11846 / Nb-255) | 25% | 100% |
Q3YSJ8 | Ehrlichia canis (strain Jake) | 24% | 100% |
Q46CE2 | Methanosarcina barkeri (strain Fusaro / DSM 804) | 25% | 100% |
Q47DJ8 | Dechloromonas aromatica (strain RCB) | 26% | 100% |
Q47WN0 | Colwellia psychrerythraea (strain 34H / ATCC BAA-681) | 24% | 100% |
Q4Q1M8 | Leishmania major | 85% | 100% |
Q4UM86 | Rickettsia felis (strain ATCC VR-1525 / URRWXCal2) | 24% | 100% |
Q5NEV8 | Francisella tularensis subsp. tularensis (strain SCHU S4 / Schu 4) | 23% | 100% |
Q5NYP9 | Aromatoleum aromaticum (strain EbN1) | 27% | 100% |
Q6BW83 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 23% | 99% |
Q6CSR1 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 24% | 99% |
Q6G542 | Bartonella henselae (strain ATCC 49882 / DSM 28221 / Houston 1) | 24% | 100% |
Q7NRW7 | Chromobacterium violaceum (strain ATCC 12472 / DSM 30191 / JCM 1249 / NBRC 12614 / NCIMB 9131 / NCTC 9757) | 27% | 100% |
Q7VKA1 | Haemophilus ducreyi (strain 35000HP / ATCC 700724) | 26% | 100% |
Q7W880 | Bordetella parapertussis (strain 12822 / ATCC BAA-587 / NCTC 13253) | 26% | 100% |
Q7WLT5 | Bordetella bronchiseptica (strain ATCC BAA-588 / NCTC 13252 / RB50) | 26% | 100% |
Q8KCC0 | Chlorobaculum tepidum (strain ATCC 49652 / DSM 12025 / NBRC 103806 / TLS) | 27% | 100% |
Q8TTB4 | Methanosarcina acetivorans (strain ATCC 35395 / DSM 2834 / JCM 12185 / C2A) | 27% | 100% |
Q8UIF2 | Agrobacterium fabrum (strain C58 / ATCC 33970) | 26% | 100% |
Q92IL9 | Rickettsia conorii (strain ATCC VR-613 / Malish 7) | 24% | 100% |
Q9VUM0 | Drosophila melanogaster | 29% | 85% |
V5DCH4 | Trypanosoma cruzi | 48% | 100% |