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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032991 | protein-containing complex | 1 | 8 |
GO:0043564 | Ku70:Ku80 complex | 3 | 8 |
GO:0140513 | nuclear protein-containing complex | 2 | 8 |
Related structures:
AlphaFold database: A4HHB7
Term | Name | Level | Count |
---|---|---|---|
GO:0000723 | telomere maintenance | 5 | 8 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
GO:0006259 | DNA metabolic process | 4 | 8 |
GO:0006281 | DNA repair | 5 | 8 |
GO:0006302 | double-strand break repair | 6 | 8 |
GO:0006303 | double-strand break repair via nonhomologous end joining | 7 | 8 |
GO:0006310 | DNA recombination | 5 | 8 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0006950 | response to stress | 2 | 8 |
GO:0006974 | DNA damage response | 4 | 8 |
GO:0006996 | organelle organization | 4 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016043 | cellular component organization | 3 | 8 |
GO:0032200 | telomere organization | 6 | 8 |
GO:0033554 | cellular response to stress | 3 | 8 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 8 |
GO:0046483 | heterocycle metabolic process | 3 | 8 |
GO:0050896 | response to stimulus | 1 | 8 |
GO:0051276 | chromosome organization | 5 | 8 |
GO:0051716 | cellular response to stimulus | 2 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0071840 | cellular component organization or biogenesis | 2 | 8 |
GO:0090304 | nucleic acid metabolic process | 4 | 8 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
GO:0009314 | response to radiation | 3 | 1 |
GO:0009628 | response to abiotic stimulus | 2 | 1 |
GO:0010165 | response to X-ray | 5 | 1 |
GO:0010212 | response to ionizing radiation | 4 | 1 |
GO:0010332 | response to gamma radiation | 5 | 1 |
GO:0071214 | cellular response to abiotic stimulus | 3 | 1 |
GO:0071478 | cellular response to radiation | 4 | 1 |
GO:0071479 | cellular response to ionizing radiation | 5 | 1 |
GO:0071480 | cellular response to gamma radiation | 6 | 1 |
GO:0071481 | cellular response to X-ray | 6 | 1 |
GO:0104004 | cellular response to environmental stimulus | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0003676 | nucleic acid binding | 3 | 8 |
GO:0003677 | DNA binding | 4 | 8 |
GO:0003684 | damaged DNA binding | 5 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0004386 | helicase activity | 2 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 8 |
GO:0016787 | hydrolase activity | 2 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0042162 | telomeric DNA binding | 6 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0043565 | sequence-specific DNA binding | 5 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 8 |
GO:0140657 | ATP-dependent activity | 1 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 319 | 323 | PF00656 | 0.534 |
CLV_C14_Caspase3-7 | 381 | 385 | PF00656 | 0.622 |
CLV_C14_Caspase3-7 | 548 | 552 | PF00656 | 0.462 |
CLV_C14_Caspase3-7 | 635 | 639 | PF00656 | 0.508 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 459 | 461 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 612 | 614 | PF00675 | 0.285 |
CLV_NRD_NRD_1 | 672 | 674 | PF00675 | 0.302 |
CLV_NRD_NRD_1 | 710 | 712 | PF00675 | 0.250 |
CLV_NRD_NRD_1 | 790 | 792 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 798 | 800 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 882 | 884 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 947 | 949 | PF00675 | 0.471 |
CLV_PCSK_FUR_1 | 256 | 260 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 459 | 461 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 528 | 530 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 614 | 616 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 641 | 643 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 672 | 674 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 710 | 712 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 798 | 800 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 882 | 884 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 933 | 935 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 947 | 949 | PF00082 | 0.471 |
CLV_PCSK_PC1ET2_1 | 528 | 530 | PF00082 | 0.348 |
CLV_PCSK_PC1ET2_1 | 614 | 616 | PF00082 | 0.337 |
CLV_PCSK_PC1ET2_1 | 641 | 643 | PF00082 | 0.308 |
CLV_PCSK_PC1ET2_1 | 933 | 935 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 746 | 750 | PF00082 | 0.688 |
CLV_PCSK_SKI1_1 | 798 | 802 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 858 | 862 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 934 | 938 | PF00082 | 0.370 |
DEG_APCC_DBOX_1 | 467 | 475 | PF00400 | 0.443 |
DEG_COP1_1 | 387 | 397 | PF00400 | 0.431 |
DEG_COP1_1 | 730 | 738 | PF00400 | 0.505 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.665 |
DOC_CDC14_PxL_1 | 732 | 740 | PF14671 | 0.502 |
DOC_CKS1_1 | 223 | 228 | PF01111 | 0.485 |
DOC_CKS1_1 | 511 | 516 | PF01111 | 0.422 |
DOC_CYCLIN_RxL_1 | 255 | 264 | PF00134 | 0.334 |
DOC_CYCLIN_RxL_1 | 792 | 804 | PF00134 | 0.407 |
DOC_CYCLIN_yCln2_LP_2 | 223 | 229 | PF00134 | 0.481 |
DOC_MAPK_gen_1 | 465 | 474 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 613 | 619 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 672 | 682 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 710 | 716 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 78 | 87 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 798 | 805 | PF00069 | 0.358 |
DOC_MAPK_gen_1 | 947 | 955 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 135 | 142 | PF00069 | 0.459 |
DOC_MAPK_MEF2A_6 | 289 | 296 | PF00069 | 0.444 |
DOC_MAPK_MEF2A_6 | 78 | 87 | PF00069 | 0.506 |
DOC_MAPK_RevD_3 | 245 | 259 | PF00069 | 0.464 |
DOC_PP1_RVXF_1 | 603 | 609 | PF00149 | 0.505 |
DOC_PP2B_LxvP_1 | 927 | 930 | PF13499 | 0.463 |
DOC_PP4_FxxP_1 | 204 | 207 | PF00568 | 0.482 |
DOC_PP4_FxxP_1 | 398 | 401 | PF00568 | 0.432 |
DOC_PP4_FxxP_1 | 960 | 963 | PF00568 | 0.557 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 889 | 893 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 894 | 898 | PF00917 | 0.583 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 382 | 387 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 510 | 515 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 698 | 703 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 746 | 751 | PF00397 | 0.583 |
LIG_14-3-3_CanoR_1 | 248 | 253 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 327 | 336 | PF00244 | 0.641 |
LIG_14-3-3_CanoR_1 | 346 | 354 | PF00244 | 0.631 |
LIG_14-3-3_CanoR_1 | 459 | 467 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 572 | 579 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 605 | 611 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 648 | 652 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 739 | 744 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 934 | 941 | PF00244 | 0.337 |
LIG_Actin_WH2_2 | 717 | 735 | PF00022 | 0.502 |
LIG_BRCT_BRCA1_1 | 110 | 114 | PF00533 | 0.363 |
LIG_BRCT_BRCA1_1 | 150 | 154 | PF00533 | 0.508 |
LIG_BRCT_BRCA1_1 | 229 | 233 | PF00533 | 0.466 |
LIG_BRCT_BRCA1_1 | 356 | 360 | PF00533 | 0.589 |
LIG_BRCT_BRCA1_1 | 409 | 413 | PF00533 | 0.519 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.603 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.587 |
LIG_FHA_1 | 389 | 395 | PF00498 | 0.634 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.641 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.411 |
LIG_FHA_1 | 578 | 584 | PF00498 | 0.429 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.528 |
LIG_FHA_1 | 747 | 753 | PF00498 | 0.571 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.664 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.640 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.647 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.516 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.439 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.658 |
LIG_FHA_2 | 487 | 493 | PF00498 | 0.586 |
LIG_FHA_2 | 583 | 589 | PF00498 | 0.403 |
LIG_FHA_2 | 607 | 613 | PF00498 | 0.463 |
LIG_FHA_2 | 837 | 843 | PF00498 | 0.446 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.588 |
LIG_FHA_2 | 900 | 906 | PF00498 | 0.798 |
LIG_GBD_Chelix_1 | 764 | 772 | PF00786 | 0.407 |
LIG_LIR_Apic_2 | 202 | 207 | PF02991 | 0.473 |
LIG_LIR_Apic_2 | 396 | 401 | PF02991 | 0.468 |
LIG_LIR_Apic_2 | 594 | 600 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 185 | 195 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 625 | 636 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 848 | 856 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 864 | 872 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 185 | 191 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 26 | 30 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 396 | 402 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 510 | 515 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 625 | 631 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 848 | 852 | PF02991 | 0.397 |
LIG_LIR_Nem_3 | 864 | 868 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 921 | 927 | PF02991 | 0.628 |
LIG_MLH1_MIPbox_1 | 111 | 115 | PF16413 | 0.403 |
LIG_NBox_RRM_1 | 235 | 245 | PF00076 | 0.419 |
LIG_NRBOX | 449 | 455 | PF00104 | 0.473 |
LIG_PCNA_yPIPBox_3 | 451 | 465 | PF02747 | 0.460 |
LIG_PCNA_yPIPBox_3 | 528 | 538 | PF02747 | 0.492 |
LIG_Pex14_2 | 393 | 397 | PF04695 | 0.495 |
LIG_Pex14_2 | 849 | 853 | PF04695 | 0.458 |
LIG_PTB_Apo_2 | 803 | 810 | PF02174 | 0.430 |
LIG_PTB_Phospho_1 | 803 | 809 | PF10480 | 0.426 |
LIG_Rb_pABgroove_1 | 354 | 362 | PF01858 | 0.506 |
LIG_RPA_C_Fungi | 668 | 680 | PF08784 | 0.354 |
LIG_SH2_CRK | 790 | 794 | PF00017 | 0.396 |
LIG_SH2_NCK_1 | 598 | 602 | PF00017 | 0.343 |
LIG_SH2_PTP2 | 722 | 725 | PF00017 | 0.295 |
LIG_SH2_SRC | 598 | 601 | PF00017 | 0.318 |
LIG_SH2_SRC | 809 | 812 | PF00017 | 0.458 |
LIG_SH2_STAP1 | 728 | 732 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 865 | 869 | PF00017 | 0.366 |
LIG_SH2_STAT3 | 158 | 161 | PF00017 | 0.354 |
LIG_SH2_STAT3 | 30 | 33 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 512 | 515 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 685 | 688 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 722 | 725 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 809 | 812 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 870 | 873 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 935 | 938 | PF00017 | 0.398 |
LIG_SH3_3 | 696 | 702 | PF00018 | 0.297 |
LIG_SH3_3 | 721 | 727 | PF00018 | 0.295 |
LIG_SH3_3 | 778 | 784 | PF00018 | 0.470 |
LIG_SUMO_SIM_anti_2 | 121 | 128 | PF11976 | 0.216 |
LIG_SUMO_SIM_anti_2 | 136 | 142 | PF11976 | 0.354 |
LIG_SUMO_SIM_anti_2 | 951 | 957 | PF11976 | 0.475 |
LIG_TRAF2_1 | 187 | 190 | PF00917 | 0.363 |
LIG_TRAF2_1 | 579 | 582 | PF00917 | 0.302 |
LIG_TRAF2_1 | 585 | 588 | PF00917 | 0.236 |
LIG_TRAF2_1 | 901 | 904 | PF00917 | 0.678 |
LIG_UBA3_1 | 122 | 129 | PF00899 | 0.363 |
LIG_UBA3_1 | 928 | 933 | PF00899 | 0.470 |
LIG_UBA3_1 | 952 | 957 | PF00899 | 0.468 |
LIG_WRC_WIRS_1 | 846 | 851 | PF05994 | 0.447 |
LIG_WRC_WIRS_1 | 853 | 858 | PF05994 | 0.416 |
LIG_WW_3 | 520 | 524 | PF00397 | 0.216 |
MOD_CDC14_SPxK_1 | 75 | 78 | PF00782 | 0.508 |
MOD_CDK_SPxK_1 | 146 | 152 | PF00069 | 0.216 |
MOD_CDK_SPxK_1 | 72 | 78 | PF00069 | 0.515 |
MOD_CDK_SPxxK_3 | 227 | 234 | PF00069 | 0.430 |
MOD_CDK_SPxxK_3 | 510 | 517 | PF00069 | 0.243 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.340 |
MOD_CK1_1 | 19 | 25 | PF00069 | 0.724 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.632 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.720 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.656 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.676 |
MOD_CK1_1 | 378 | 384 | PF00069 | 0.734 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.685 |
MOD_CK1_1 | 486 | 492 | PF00069 | 0.667 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.464 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.625 |
MOD_CK1_1 | 688 | 694 | PF00069 | 0.356 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.651 |
MOD_CK1_1 | 770 | 776 | PF00069 | 0.425 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.577 |
MOD_CK2_1 | 384 | 390 | PF00069 | 0.536 |
MOD_CK2_1 | 486 | 492 | PF00069 | 0.575 |
MOD_CK2_1 | 582 | 588 | PF00069 | 0.216 |
MOD_CK2_1 | 606 | 612 | PF00069 | 0.340 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.583 |
MOD_CK2_1 | 898 | 904 | PF00069 | 0.712 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.403 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.643 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.447 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.530 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.711 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.677 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.803 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.779 |
MOD_GlcNHglycan | 387 | 390 | PF01048 | 0.617 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.493 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.587 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.556 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.588 |
MOD_GlcNHglycan | 485 | 488 | PF01048 | 0.704 |
MOD_GlcNHglycan | 687 | 690 | PF01048 | 0.216 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.697 |
MOD_GlcNHglycan | 890 | 894 | PF01048 | 0.639 |
MOD_GlcNHglycan | 896 | 899 | PF01048 | 0.611 |
MOD_GlcNHglycan | 941 | 944 | PF01048 | 0.535 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.634 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.290 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.415 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.500 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.401 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.383 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.748 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.597 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.774 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.735 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.697 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.408 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.617 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.686 |
MOD_GSK3_1 | 642 | 649 | PF00069 | 0.309 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.795 |
MOD_GSK3_1 | 684 | 691 | PF00069 | 0.363 |
MOD_GSK3_1 | 698 | 705 | PF00069 | 0.363 |
MOD_GSK3_1 | 768 | 775 | PF00069 | 0.376 |
MOD_GSK3_1 | 894 | 901 | PF00069 | 0.659 |
MOD_N-GLC_1 | 939 | 944 | PF02516 | 0.498 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.360 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.378 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.501 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.278 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.368 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.609 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.542 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.463 |
MOD_NEK2_1 | 477 | 482 | PF00069 | 0.662 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.295 |
MOD_NEK2_1 | 651 | 656 | PF00069 | 0.366 |
MOD_NEK2_1 | 752 | 757 | PF00069 | 0.571 |
MOD_NEK2_1 | 768 | 773 | PF00069 | 0.337 |
MOD_NEK2_1 | 836 | 841 | PF00069 | 0.473 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.615 |
MOD_NEK2_1 | 852 | 857 | PF00069 | 0.347 |
MOD_NEK2_1 | 936 | 941 | PF00069 | 0.344 |
MOD_PIKK_1 | 378 | 384 | PF00454 | 0.556 |
MOD_PK_1 | 642 | 648 | PF00069 | 0.216 |
MOD_PKA_1 | 346 | 352 | PF00069 | 0.515 |
MOD_PKA_1 | 459 | 465 | PF00069 | 0.367 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.760 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.512 |
MOD_PKA_2 | 411 | 417 | PF00069 | 0.582 |
MOD_PKA_2 | 459 | 465 | PF00069 | 0.444 |
MOD_PKA_2 | 496 | 502 | PF00069 | 0.452 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.555 |
MOD_PKA_2 | 647 | 653 | PF00069 | 0.375 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.633 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.383 |
MOD_Plk_1 | 360 | 366 | PF00069 | 0.646 |
MOD_Plk_1 | 642 | 648 | PF00069 | 0.240 |
MOD_Plk_1 | 753 | 759 | PF00069 | 0.640 |
MOD_Plk_1 | 812 | 818 | PF00069 | 0.504 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.570 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.379 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.371 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.578 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.519 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.295 |
MOD_Plk_4 | 647 | 653 | PF00069 | 0.285 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.240 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.503 |
MOD_ProDKin_1 | 382 | 388 | PF00069 | 0.695 |
MOD_ProDKin_1 | 510 | 516 | PF00069 | 0.243 |
MOD_ProDKin_1 | 698 | 704 | PF00069 | 0.297 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.560 |
MOD_ProDKin_1 | 746 | 752 | PF00069 | 0.581 |
MOD_SUMO_for_1 | 640 | 643 | PF00179 | 0.363 |
MOD_SUMO_rev_2 | 185 | 193 | PF00179 | 0.216 |
TRG_DiLeu_BaLyEn_6 | 398 | 403 | PF01217 | 0.426 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 512 | 515 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 607 | 610 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 790 | 793 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 809 | 812 | PF00928 | 0.458 |
TRG_ENDOCYTIC_2 | 843 | 846 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 865 | 868 | PF00928 | 0.507 |
TRG_ER_diArg_1 | 247 | 250 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 255 | 258 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 458 | 460 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 516 | 519 | PF00400 | 0.375 |
TRG_ER_diArg_1 | 613 | 616 | PF00400 | 0.350 |
TRG_ER_diArg_1 | 671 | 673 | PF00400 | 0.354 |
TRG_ER_diArg_1 | 798 | 800 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 882 | 885 | PF00400 | 0.700 |
TRG_NES_CRM1_1 | 763 | 777 | PF08389 | 0.459 |
TRG_NLS_MonoExtN_4 | 675 | 681 | PF00514 | 0.216 |
TRG_Pf-PMV_PEXEL_1 | 791 | 795 | PF00026 | 0.586 |