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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 8 |
GO:0043226 | organelle | 2 | 8 |
GO:0043227 | membrane-bounded organelle | 3 | 8 |
GO:0043229 | intracellular organelle | 3 | 8 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0005657 | replication fork | 2 | 1 |
GO:0043596 | nuclear replication fork | 3 | 1 |
Related structures:
AlphaFold database: E9AWQ1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006259 | DNA metabolic process | 4 | 9 |
GO:0006281 | DNA repair | 5 | 9 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0006950 | response to stress | 2 | 9 |
GO:0006974 | DNA damage response | 4 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0031297 | replication fork processing | 6 | 9 |
GO:0033554 | cellular response to stress | 3 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 9 |
GO:0045005 | DNA-templated DNA replication maintenance of fidelity | 5 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0050896 | response to stimulus | 1 | 9 |
GO:0051716 | cellular response to stimulus | 2 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
GO:0006275 | regulation of DNA replication | 6 | 1 |
GO:0008156 | negative regulation of DNA replication | 7 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 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:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0048478 | obsolete replication fork protection | 6 | 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:0051052 | regulation of DNA metabolic process | 5 | 1 |
GO:0051053 | negative regulation of DNA metabolic process | 6 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:0090329 | regulation of DNA-templated DNA replication | 7 | 1 |
GO:2000104 | negative regulation of DNA-templated DNA replication | 8 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003676 | nucleic acid binding | 3 | 9 |
GO:0003677 | DNA binding | 4 | 9 |
GO:0003697 | single-stranded DNA binding | 5 | 9 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004386 | helicase activity | 2 | 7 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 10 |
GO:0016491 | oxidoreductase activity | 2 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0036310 | ATP-dependent DNA/DNA annealing activity | 2 | 9 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0051213 | dioxygenase activity | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 10 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 10 |
GO:0140657 | ATP-dependent activity | 1 | 10 |
GO:0140658 | ATP-dependent chromatin remodeler activity | 3 | 10 |
GO:0140666 | annealing activity | 4 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:1990814 | DNA/DNA annealing activity | 5 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 670 | 674 | PF00656 | 0.780 |
CLV_C14_Caspase3-7 | 985 | 989 | PF00656 | 0.638 |
CLV_NRD_NRD_1 | 1064 | 1066 | PF00675 | 0.716 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.295 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 633 | 635 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 667 | 669 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 903 | 905 | PF00675 | 0.614 |
CLV_PCSK_FUR_1 | 383 | 387 | PF00082 | 0.291 |
CLV_PCSK_KEX2_1 | 1064 | 1066 | PF00082 | 0.716 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.285 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.242 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 633 | 635 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 667 | 669 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 903 | 905 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 964 | 966 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 980 | 982 | PF00082 | 0.655 |
CLV_PCSK_PC1ET2_1 | 299 | 301 | PF00082 | 0.285 |
CLV_PCSK_PC1ET2_1 | 385 | 387 | PF00082 | 0.291 |
CLV_PCSK_PC1ET2_1 | 964 | 966 | PF00082 | 0.643 |
CLV_PCSK_PC1ET2_1 | 980 | 982 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 1065 | 1069 | PF00082 | 0.711 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.289 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.286 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 476 | 480 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 583 | 587 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 904 | 908 | PF00082 | 0.651 |
CLV_Separin_Metazoa | 495 | 499 | PF03568 | 0.387 |
DEG_APCC_DBOX_1 | 1063 | 1071 | PF00400 | 0.711 |
DEG_APCC_DBOX_1 | 108 | 116 | PF00400 | 0.462 |
DEG_APCC_DBOX_1 | 719 | 727 | PF00400 | 0.590 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.475 |
DEG_ODPH_VHL_1 | 1014 | 1025 | PF01847 | 0.586 |
DEG_ODPH_VHL_1 | 33 | 46 | PF01847 | 0.507 |
DEG_SCF_FBW7_1 | 317 | 324 | PF00400 | 0.470 |
DEG_SCF_FBW7_1 | 792 | 798 | PF00400 | 0.511 |
DEG_SPOP_SBC_1 | 1038 | 1042 | PF00917 | 0.721 |
DEG_SPOP_SBC_1 | 638 | 642 | PF00917 | 0.570 |
DOC_CKS1_1 | 709 | 714 | PF01111 | 0.701 |
DOC_CKS1_1 | 726 | 731 | PF01111 | 0.662 |
DOC_CKS1_1 | 746 | 751 | PF01111 | 0.563 |
DOC_CKS1_1 | 792 | 797 | PF01111 | 0.509 |
DOC_CYCLIN_RxL_1 | 578 | 590 | PF00134 | 0.389 |
DOC_MAPK_DCC_7 | 126 | 135 | PF00069 | 0.526 |
DOC_MAPK_FxFP_2 | 111 | 114 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 299 | 307 | PF00069 | 0.477 |
DOC_MAPK_gen_1 | 309 | 317 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 395 | 404 | PF00069 | 0.483 |
DOC_MAPK_MEF2A_6 | 126 | 135 | PF00069 | 0.516 |
DOC_MAPK_MEF2A_6 | 218 | 226 | PF00069 | 0.470 |
DOC_MAPK_MEF2A_6 | 703 | 710 | PF00069 | 0.730 |
DOC_MAPK_MEF2A_6 | 842 | 850 | PF00069 | 0.582 |
DOC_MAPK_MEF2A_6 | 86 | 94 | PF00069 | 0.553 |
DOC_MAPK_MEF2A_6 | 949 | 957 | PF00069 | 0.728 |
DOC_MAPK_RevD_3 | 951 | 965 | PF00069 | 0.672 |
DOC_PP1_RVXF_1 | 474 | 481 | PF00149 | 0.483 |
DOC_PP2B_LxvP_1 | 1017 | 1020 | PF13499 | 0.580 |
DOC_PP4_FxxP_1 | 111 | 114 | PF00568 | 0.446 |
DOC_PP4_FxxP_1 | 656 | 659 | PF00568 | 0.674 |
DOC_SPAK_OSR1_1 | 358 | 362 | PF12202 | 0.470 |
DOC_USP7_MATH_1 | 1038 | 1042 | PF00917 | 0.815 |
DOC_USP7_MATH_1 | 1058 | 1062 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.368 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 489 | 493 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 639 | 643 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 645 | 649 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 659 | 663 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 683 | 687 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 768 | 772 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 773 | 777 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 830 | 834 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 835 | 839 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 844 | 848 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 875 | 879 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 921 | 925 | PF00917 | 0.702 |
DOC_USP7_MATH_2 | 369 | 375 | PF00917 | 0.501 |
DOC_USP7_UBL2_3 | 237 | 241 | PF12436 | 0.543 |
DOC_USP7_UBL2_3 | 410 | 414 | PF12436 | 0.474 |
DOC_WW_Pin1_4 | 1054 | 1059 | PF00397 | 0.786 |
DOC_WW_Pin1_4 | 1077 | 1082 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 509 | 514 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 641 | 646 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 679 | 684 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 708 | 713 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 725 | 730 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 745 | 750 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 791 | 796 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 804 | 809 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 863 | 868 | PF00397 | 0.751 |
DOC_WW_Pin1_4 | 879 | 884 | PF00397 | 0.504 |
LIG_14-3-3_CanoR_1 | 1064 | 1068 | PF00244 | 0.714 |
LIG_14-3-3_CanoR_1 | 300 | 306 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 350 | 356 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 420 | 430 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 43 | 47 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 720 | 726 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 778 | 787 | PF00244 | 0.734 |
LIG_14-3-3_CanoR_1 | 86 | 91 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 903 | 907 | PF00244 | 0.617 |
LIG_Actin_WH2_2 | 259 | 277 | PF00022 | 0.536 |
LIG_APCC_ABBA_1 | 752 | 757 | PF00400 | 0.722 |
LIG_BIR_III_2 | 704 | 708 | PF00653 | 0.651 |
LIG_BRCT_BRCA1_1 | 139 | 143 | PF00533 | 0.399 |
LIG_BRCT_BRCA1_1 | 424 | 428 | PF00533 | 0.422 |
LIG_deltaCOP1_diTrp_1 | 101 | 111 | PF00928 | 0.512 |
LIG_deltaCOP1_diTrp_1 | 233 | 242 | PF00928 | 0.470 |
LIG_FHA_1 | 1020 | 1026 | PF00498 | 0.777 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.553 |
LIG_FHA_1 | 527 | 533 | PF00498 | 0.509 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.491 |
LIG_FHA_1 | 610 | 616 | PF00498 | 0.513 |
LIG_FHA_1 | 811 | 817 | PF00498 | 0.674 |
LIG_FHA_1 | 856 | 862 | PF00498 | 0.768 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.636 |
LIG_FHA_1 | 874 | 880 | PF00498 | 0.512 |
LIG_FHA_1 | 948 | 954 | PF00498 | 0.725 |
LIG_FHA_1 | 992 | 998 | PF00498 | 0.550 |
LIG_FHA_2 | 382 | 388 | PF00498 | 0.470 |
LIG_FHA_2 | 403 | 409 | PF00498 | 0.470 |
LIG_FHA_2 | 553 | 559 | PF00498 | 0.495 |
LIG_FHA_2 | 614 | 620 | PF00498 | 0.711 |
LIG_FHA_2 | 67 | 73 | PF00498 | 0.459 |
LIG_FHA_2 | 697 | 703 | PF00498 | 0.634 |
LIG_FHA_2 | 966 | 972 | PF00498 | 0.689 |
LIG_FHA_2 | 983 | 989 | PF00498 | 0.511 |
LIG_LIR_Apic_2 | 654 | 659 | PF02991 | 0.674 |
LIG_LIR_Gen_1 | 238 | 247 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 270 | 277 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 328 | 338 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 39 | 49 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 504 | 513 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 551 | 561 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 85 | 95 | PF02991 | 0.548 |
LIG_LIR_LC3C_4 | 760 | 764 | PF02991 | 0.497 |
LIG_LIR_LC3C_4 | 847 | 850 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 172 | 178 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 219 | 224 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 238 | 242 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 270 | 274 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 328 | 333 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 39 | 44 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 504 | 508 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 551 | 557 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 593 | 599 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.554 |
LIG_MLH1_MIPbox_1 | 139 | 143 | PF16413 | 0.399 |
LIG_MYND_1 | 338 | 342 | PF01753 | 0.501 |
LIG_MYND_1 | 750 | 754 | PF01753 | 0.711 |
LIG_MYND_2 | 749 | 753 | PF01753 | 0.718 |
LIG_NRBOX | 371 | 377 | PF00104 | 0.536 |
LIG_Pex14_1 | 235 | 239 | PF04695 | 0.547 |
LIG_Pex14_2 | 100 | 104 | PF04695 | 0.408 |
LIG_Pex14_2 | 355 | 359 | PF04695 | 0.495 |
LIG_PTB_Apo_2 | 276 | 283 | PF02174 | 0.439 |
LIG_Rb_LxCxE_1 | 270 | 290 | PF01857 | 0.498 |
LIG_SH2_CRK | 118 | 122 | PF00017 | 0.380 |
LIG_SH2_CRK | 175 | 179 | PF00017 | 0.430 |
LIG_SH2_CRK | 271 | 275 | PF00017 | 0.476 |
LIG_SH2_CRK | 330 | 334 | PF00017 | 0.495 |
LIG_SH2_CRK | 401 | 405 | PF00017 | 0.501 |
LIG_SH2_CRK | 41 | 45 | PF00017 | 0.494 |
LIG_SH2_NCK_1 | 31 | 35 | PF00017 | 0.522 |
LIG_SH2_NCK_1 | 41 | 45 | PF00017 | 0.494 |
LIG_SH2_PTP2 | 505 | 508 | PF00017 | 0.470 |
LIG_SH2_SRC | 11 | 14 | PF00017 | 0.551 |
LIG_SH2_SRC | 505 | 508 | PF00017 | 0.495 |
LIG_SH2_STAP1 | 118 | 122 | PF00017 | 0.368 |
LIG_SH2_STAP1 | 156 | 160 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 505 | 508 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 584 | 587 | PF00017 | 0.357 |
LIG_SH3_1 | 877 | 883 | PF00018 | 0.510 |
LIG_SH3_2 | 872 | 877 | PF14604 | 0.591 |
LIG_SH3_3 | 1013 | 1019 | PF00018 | 0.779 |
LIG_SH3_3 | 1075 | 1081 | PF00018 | 0.729 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.548 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.489 |
LIG_SH3_3 | 493 | 499 | PF00018 | 0.472 |
LIG_SH3_3 | 591 | 597 | PF00018 | 0.427 |
LIG_SH3_3 | 709 | 715 | PF00018 | 0.671 |
LIG_SH3_3 | 743 | 749 | PF00018 | 0.602 |
LIG_SH3_3 | 789 | 795 | PF00018 | 0.717 |
LIG_SH3_3 | 800 | 806 | PF00018 | 0.727 |
LIG_SH3_3 | 859 | 865 | PF00018 | 0.697 |
LIG_SH3_3 | 869 | 875 | PF00018 | 0.662 |
LIG_SH3_3 | 877 | 883 | PF00018 | 0.563 |
LIG_SH3_3 | 896 | 902 | PF00018 | 0.533 |
LIG_SH3_3 | 935 | 941 | PF00018 | 0.700 |
LIG_SH3_3 | 942 | 948 | PF00018 | 0.754 |
LIG_SH3_3 | 950 | 956 | PF00018 | 0.728 |
LIG_SUMO_SIM_anti_2 | 492 | 498 | PF11976 | 0.387 |
LIG_SUMO_SIM_anti_2 | 531 | 536 | PF11976 | 0.536 |
LIG_SUMO_SIM_anti_2 | 722 | 728 | PF11976 | 0.537 |
LIG_SUMO_SIM_anti_2 | 813 | 818 | PF11976 | 0.716 |
LIG_SUMO_SIM_par_1 | 283 | 290 | PF11976 | 0.470 |
LIG_SUMO_SIM_par_1 | 313 | 318 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 529 | 536 | PF11976 | 0.536 |
LIG_SUMO_SIM_par_1 | 706 | 711 | PF11976 | 0.682 |
LIG_SUMO_SIM_par_1 | 812 | 818 | PF11976 | 0.526 |
LIG_SUMO_SIM_par_1 | 847 | 853 | PF11976 | 0.640 |
LIG_TRAF2_1 | 134 | 137 | PF00917 | 0.472 |
LIG_TRAF2_1 | 678 | 681 | PF00917 | 0.664 |
LIG_TRAF2_2 | 153 | 158 | PF00917 | 0.497 |
LIG_TRAF2_2 | 499 | 504 | PF00917 | 0.478 |
LIG_TRFH_1 | 31 | 35 | PF08558 | 0.464 |
LIG_TYR_ITIM | 269 | 274 | PF00017 | 0.472 |
LIG_TYR_ITIM | 399 | 404 | PF00017 | 0.470 |
LIG_TYR_ITIM | 503 | 508 | PF00017 | 0.470 |
LIG_UBA3_1 | 399 | 407 | PF00899 | 0.536 |
LIG_WRC_WIRS_1 | 138 | 143 | PF05994 | 0.396 |
LIG_WW_3 | 900 | 904 | PF00397 | 0.616 |
MOD_CDK_SPK_2 | 679 | 684 | PF00069 | 0.711 |
MOD_CDK_SPK_2 | 804 | 809 | PF00069 | 0.739 |
MOD_CK1_1 | 1040 | 1046 | PF00069 | 0.727 |
MOD_CK1_1 | 1047 | 1053 | PF00069 | 0.694 |
MOD_CK1_1 | 1054 | 1060 | PF00069 | 0.633 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.507 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.618 |
MOD_CK1_1 | 509 | 515 | PF00069 | 0.536 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.501 |
MOD_CK1_1 | 613 | 619 | PF00069 | 0.648 |
MOD_CK1_1 | 643 | 649 | PF00069 | 0.689 |
MOD_CK1_1 | 686 | 692 | PF00069 | 0.696 |
MOD_CK1_1 | 771 | 777 | PF00069 | 0.691 |
MOD_CK1_1 | 782 | 788 | PF00069 | 0.643 |
MOD_CK1_1 | 797 | 803 | PF00069 | 0.800 |
MOD_CK1_1 | 810 | 816 | PF00069 | 0.715 |
MOD_CK1_1 | 825 | 831 | PF00069 | 0.614 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.452 |
MOD_CK1_1 | 878 | 884 | PF00069 | 0.637 |
MOD_CK1_1 | 924 | 930 | PF00069 | 0.748 |
MOD_CK1_1 | 975 | 981 | PF00069 | 0.690 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.495 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.476 |
MOD_CK2_1 | 402 | 408 | PF00069 | 0.470 |
MOD_CK2_1 | 489 | 495 | PF00069 | 0.543 |
MOD_CK2_1 | 613 | 619 | PF00069 | 0.640 |
MOD_CK2_1 | 675 | 681 | PF00069 | 0.652 |
MOD_CK2_1 | 696 | 702 | PF00069 | 0.637 |
MOD_CK2_1 | 830 | 836 | PF00069 | 0.681 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.601 |
MOD_CK2_1 | 965 | 971 | PF00069 | 0.688 |
MOD_GlcNHglycan | 1046 | 1049 | PF01048 | 0.736 |
MOD_GlcNHglycan | 1053 | 1056 | PF01048 | 0.733 |
MOD_GlcNHglycan | 1060 | 1063 | PF01048 | 0.702 |
MOD_GlcNHglycan | 1074 | 1077 | PF01048 | 0.821 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.279 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.461 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.336 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.336 |
MOD_GlcNHglycan | 508 | 511 | PF01048 | 0.226 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.348 |
MOD_GlcNHglycan | 685 | 688 | PF01048 | 0.546 |
MOD_GlcNHglycan | 730 | 733 | PF01048 | 0.607 |
MOD_GlcNHglycan | 737 | 740 | PF01048 | 0.615 |
MOD_GlcNHglycan | 765 | 768 | PF01048 | 0.788 |
MOD_GlcNHglycan | 773 | 776 | PF01048 | 0.737 |
MOD_GlcNHglycan | 781 | 784 | PF01048 | 0.604 |
MOD_GlcNHglycan | 827 | 830 | PF01048 | 0.542 |
MOD_GlcNHglycan | 832 | 835 | PF01048 | 0.707 |
MOD_GlcNHglycan | 839 | 842 | PF01048 | 0.595 |
MOD_GlcNHglycan | 894 | 897 | PF01048 | 0.634 |
MOD_GlcNHglycan | 974 | 977 | PF01048 | 0.737 |
MOD_GlcNHglycan | 985 | 988 | PF01048 | 0.724 |
MOD_GSK3_1 | 1037 | 1044 | PF00069 | 0.749 |
MOD_GSK3_1 | 1047 | 1054 | PF00069 | 0.724 |
MOD_GSK3_1 | 1072 | 1079 | PF00069 | 0.815 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.476 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.444 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.501 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.577 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.521 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.536 |
MOD_GSK3_1 | 609 | 616 | PF00069 | 0.633 |
MOD_GSK3_1 | 637 | 644 | PF00069 | 0.650 |
MOD_GSK3_1 | 645 | 652 | PF00069 | 0.587 |
MOD_GSK3_1 | 675 | 682 | PF00069 | 0.677 |
MOD_GSK3_1 | 686 | 693 | PF00069 | 0.641 |
MOD_GSK3_1 | 721 | 728 | PF00069 | 0.644 |
MOD_GSK3_1 | 733 | 740 | PF00069 | 0.639 |
MOD_GSK3_1 | 741 | 748 | PF00069 | 0.481 |
MOD_GSK3_1 | 782 | 789 | PF00069 | 0.645 |
MOD_GSK3_1 | 791 | 798 | PF00069 | 0.520 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.575 |
MOD_GSK3_1 | 821 | 828 | PF00069 | 0.630 |
MOD_GSK3_1 | 850 | 857 | PF00069 | 0.654 |
MOD_GSK3_1 | 875 | 882 | PF00069 | 0.601 |
MOD_GSK3_1 | 905 | 912 | PF00069 | 0.798 |
MOD_GSK3_1 | 917 | 924 | PF00069 | 0.798 |
MOD_GSK3_1 | 926 | 933 | PF00069 | 0.782 |
MOD_GSK3_1 | 967 | 974 | PF00069 | 0.719 |
MOD_N-GLC_1 | 1072 | 1077 | PF02516 | 0.571 |
MOD_N-GLC_1 | 544 | 549 | PF02516 | 0.270 |
MOD_N-GLC_1 | 613 | 618 | PF02516 | 0.571 |
MOD_N-GLC_1 | 771 | 776 | PF02516 | 0.724 |
MOD_N-GLC_1 | 976 | 981 | PF02516 | 0.699 |
MOD_N-GLC_1 | 982 | 987 | PF02516 | 0.742 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.456 |
MOD_NEK2_1 | 1037 | 1042 | PF00069 | 0.718 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.483 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.517 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.524 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.535 |
MOD_NEK2_1 | 537 | 542 | PF00069 | 0.523 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.414 |
MOD_NEK2_1 | 609 | 614 | PF00069 | 0.477 |
MOD_NEK2_1 | 721 | 726 | PF00069 | 0.610 |
MOD_NEK2_1 | 733 | 738 | PF00069 | 0.569 |
MOD_NEK2_1 | 762 | 767 | PF00069 | 0.717 |
MOD_NEK2_1 | 799 | 804 | PF00069 | 0.619 |
MOD_NEK2_1 | 820 | 825 | PF00069 | 0.669 |
MOD_NEK2_1 | 852 | 857 | PF00069 | 0.635 |
MOD_NEK2_1 | 890 | 895 | PF00069 | 0.699 |
MOD_NEK2_1 | 907 | 912 | PF00069 | 0.560 |
MOD_NEK2_1 | 917 | 922 | PF00069 | 0.707 |
MOD_NEK2_1 | 926 | 931 | PF00069 | 0.682 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.491 |
MOD_NEK2_2 | 1063 | 1068 | PF00069 | 0.719 |
MOD_NEK2_2 | 301 | 306 | PF00069 | 0.545 |
MOD_NEK2_2 | 902 | 907 | PF00069 | 0.611 |
MOD_PIKK_1 | 1024 | 1030 | PF00454 | 0.722 |
MOD_PIKK_1 | 1047 | 1053 | PF00454 | 0.614 |
MOD_PIKK_1 | 342 | 348 | PF00454 | 0.427 |
MOD_PIKK_1 | 645 | 651 | PF00454 | 0.666 |
MOD_PIKK_1 | 659 | 665 | PF00454 | 0.605 |
MOD_PIKK_1 | 686 | 692 | PF00454 | 0.660 |
MOD_PIKK_1 | 713 | 719 | PF00454 | 0.655 |
MOD_PIKK_1 | 855 | 861 | PF00454 | 0.722 |
MOD_PIKK_1 | 911 | 917 | PF00454 | 0.580 |
MOD_PIKK_1 | 95 | 101 | PF00454 | 0.459 |
MOD_PKA_2 | 1063 | 1069 | PF00069 | 0.709 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.511 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.470 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.515 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.531 |
MOD_PKA_2 | 683 | 689 | PF00069 | 0.707 |
MOD_PKA_2 | 719 | 725 | PF00069 | 0.521 |
MOD_PKA_2 | 779 | 785 | PF00069 | 0.790 |
MOD_PKA_2 | 820 | 826 | PF00069 | 0.633 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.335 |
MOD_PKA_2 | 902 | 908 | PF00069 | 0.607 |
MOD_PKB_1 | 965 | 973 | PF00069 | 0.619 |
MOD_Plk_1 | 287 | 293 | PF00069 | 0.470 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.557 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.412 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.482 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.595 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.486 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.536 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.522 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.513 |
MOD_Plk_4 | 590 | 596 | PF00069 | 0.379 |
MOD_Plk_4 | 721 | 727 | PF00069 | 0.630 |
MOD_Plk_4 | 844 | 850 | PF00069 | 0.617 |
MOD_ProDKin_1 | 1054 | 1060 | PF00069 | 0.786 |
MOD_ProDKin_1 | 1077 | 1083 | PF00069 | 0.731 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.483 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.468 |
MOD_ProDKin_1 | 509 | 515 | PF00069 | 0.501 |
MOD_ProDKin_1 | 641 | 647 | PF00069 | 0.672 |
MOD_ProDKin_1 | 679 | 685 | PF00069 | 0.651 |
MOD_ProDKin_1 | 708 | 714 | PF00069 | 0.685 |
MOD_ProDKin_1 | 725 | 731 | PF00069 | 0.538 |
MOD_ProDKin_1 | 745 | 751 | PF00069 | 0.654 |
MOD_ProDKin_1 | 791 | 797 | PF00069 | 0.590 |
MOD_ProDKin_1 | 804 | 810 | PF00069 | 0.609 |
MOD_ProDKin_1 | 863 | 869 | PF00069 | 0.755 |
MOD_ProDKin_1 | 879 | 885 | PF00069 | 0.507 |
MOD_SUMO_rev_2 | 14 | 19 | PF00179 | 0.575 |
MOD_SUMO_rev_2 | 406 | 412 | PF00179 | 0.536 |
TRG_DiLeu_BaEn_1 | 220 | 225 | PF01217 | 0.470 |
TRG_DiLeu_BaEn_1 | 371 | 376 | PF01217 | 0.495 |
TRG_DiLeu_BaLyEn_6 | 594 | 599 | PF01217 | 0.436 |
TRG_DiLeu_BaLyEn_6 | 704 | 709 | PF01217 | 0.733 |
TRG_DiLeu_BaLyEn_6 | 748 | 753 | PF01217 | 0.589 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 505 | 508 | PF00928 | 0.470 |
TRG_ER_diArg_1 | 1063 | 1065 | PF00400 | 0.704 |
TRG_ER_diArg_1 | 27 | 30 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 312 | 314 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 381 | 383 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 419 | 421 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 497 | 500 | PF00400 | 0.521 |
TRG_ER_diArg_1 | 666 | 668 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 778 | 781 | PF00400 | 0.684 |
TRG_ER_diArg_1 | 902 | 904 | PF00400 | 0.605 |
TRG_NLS_MonoCore_2 | 963 | 968 | PF00514 | 0.732 |
TRG_NLS_MonoExtC_3 | 963 | 969 | PF00514 | 0.703 |
TRG_Pf-PMV_PEXEL_1 | 150 | 155 | PF00026 | 0.486 |
TRG_Pf-PMV_PEXEL_1 | 386 | 391 | PF00026 | 0.294 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1Z2 | Leptomonas seymouri | 61% | 93% |
A0A3Q8IC06 | Leishmania donovani | 89% | 99% |
A0A3R7MWL4 | Trypanosoma rangeli | 53% | 100% |
A4H349 | Leishmania braziliensis | 22% | 100% |
A4HDB9 | Leishmania braziliensis | 76% | 98% |
A4I0P9 | Leishmania infantum | 89% | 99% |
D0A725 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
Q4QAS2 | Leishmania major | 84% | 94% |