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 | 7 |
GO:0043226 | organelle | 2 | 7 |
GO:0043227 | membrane-bounded organelle | 3 | 7 |
GO:0043229 | intracellular organelle | 3 | 7 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0005657 | replication fork | 2 | 1 |
GO:0043596 | nuclear replication fork | 3 | 1 |
Related structures:
AlphaFold database: A4HDB9
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 | 436 | 440 | PF00656 | 0.562 |
CLV_C14_Caspase3-7 | 678 | 682 | PF00656 | 0.723 |
CLV_C14_Caspase3-7 | 841 | 845 | PF00656 | 0.525 |
CLV_NRD_NRD_1 | 1073 | 1075 | PF00675 | 0.679 |
CLV_NRD_NRD_1 | 312 | 314 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 641 | 643 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 742 | 744 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 792 | 794 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 836 | 838 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 897 | 899 | PF00675 | 0.634 |
CLV_PCSK_FUR_1 | 383 | 387 | PF00082 | 0.266 |
CLV_PCSK_KEX2_1 | 1073 | 1075 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.234 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 641 | 643 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 742 | 744 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 792 | 794 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 836 | 838 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 897 | 899 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 958 | 960 | PF00082 | 0.661 |
CLV_PCSK_PC1ET2_1 | 299 | 301 | PF00082 | 0.309 |
CLV_PCSK_PC1ET2_1 | 385 | 387 | PF00082 | 0.266 |
CLV_PCSK_PC1ET2_1 | 958 | 960 | PF00082 | 0.694 |
CLV_PCSK_SKI1_1 | 1074 | 1078 | PF00082 | 0.677 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.201 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.256 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 484 | 488 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 591 | 595 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 898 | 902 | PF00082 | 0.697 |
DEG_APCC_DBOX_1 | 1072 | 1080 | PF00400 | 0.678 |
DEG_COP1_1 | 851 | 859 | PF00400 | 0.496 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.468 |
DEG_ODPH_VHL_1 | 33 | 46 | PF01847 | 0.600 |
DEG_SCF_FBW7_1 | 317 | 324 | PF00400 | 0.456 |
DEG_SCF_FBW7_1 | 912 | 918 | PF00400 | 0.521 |
DEG_SPOP_SBC_1 | 1050 | 1054 | PF00917 | 0.666 |
DEG_SPOP_SBC_1 | 1060 | 1064 | PF00917 | 0.550 |
DEG_SPOP_SBC_1 | 821 | 825 | PF00917 | 0.546 |
DEG_SPOP_SBC_1 | 920 | 924 | PF00917 | 0.604 |
DOC_CKS1_1 | 671 | 676 | PF01111 | 0.612 |
DOC_CKS1_1 | 717 | 722 | PF01111 | 0.683 |
DOC_CKS1_1 | 734 | 739 | PF01111 | 0.665 |
DOC_CKS1_1 | 761 | 766 | PF01111 | 0.591 |
DOC_CKS1_1 | 912 | 917 | PF01111 | 0.520 |
DOC_CYCLIN_RxL_1 | 1071 | 1081 | PF00134 | 0.560 |
DOC_CYCLIN_RxL_1 | 588 | 598 | PF00134 | 0.364 |
DOC_MAPK_DCC_7 | 126 | 135 | PF00069 | 0.494 |
DOC_MAPK_FxFP_2 | 111 | 114 | PF00069 | 0.379 |
DOC_MAPK_gen_1 | 126 | 135 | PF00069 | 0.412 |
DOC_MAPK_gen_1 | 299 | 307 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 309 | 317 | PF00069 | 0.448 |
DOC_MAPK_gen_1 | 395 | 404 | PF00069 | 0.468 |
DOC_MAPK_MEF2A_6 | 126 | 135 | PF00069 | 0.494 |
DOC_MAPK_MEF2A_6 | 218 | 226 | PF00069 | 0.461 |
DOC_MAPK_MEF2A_6 | 395 | 404 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 711 | 718 | PF00069 | 0.680 |
DOC_MAPK_MEF2A_6 | 86 | 94 | PF00069 | 0.528 |
DOC_MAPK_MEF2A_6 | 943 | 951 | PF00069 | 0.656 |
DOC_PP1_RVXF_1 | 482 | 489 | PF00149 | 0.469 |
DOC_PP2B_LxvP_1 | 46 | 49 | PF13499 | 0.580 |
DOC_PP2B_LxvP_1 | 936 | 939 | PF13499 | 0.505 |
DOC_PP2B_PxIxI_1 | 130 | 136 | PF00149 | 0.323 |
DOC_PP4_FxxP_1 | 111 | 114 | PF00568 | 0.379 |
DOC_PP4_FxxP_1 | 664 | 667 | PF00568 | 0.685 |
DOC_SPAK_OSR1_1 | 358 | 362 | PF12202 | 0.481 |
DOC_USP7_MATH_1 | 1016 | 1020 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 1050 | 1054 | PF00917 | 0.808 |
DOC_USP7_MATH_1 | 1067 | 1071 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 646 | 650 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 653 | 657 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 667 | 671 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 745 | 749 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 783 | 787 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 821 | 825 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 859 | 863 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 908 | 912 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 915 | 919 | PF00917 | 0.693 |
DOC_USP7_UBL2_3 | 237 | 241 | PF12436 | 0.508 |
DOC_USP7_UBL2_3 | 410 | 414 | PF12436 | 0.487 |
DOC_WW_Pin1_4 | 1026 | 1031 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 1052 | 1057 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 1061 | 1066 | PF00397 | 0.752 |
DOC_WW_Pin1_4 | 1086 | 1091 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 517 | 522 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 649 | 654 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 670 | 675 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 687 | 692 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 705 | 710 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 716 | 721 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 733 | 738 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 760 | 765 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 815 | 820 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 848 | 853 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 878 | 883 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 904 | 909 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 911 | 916 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 921 | 926 | PF00397 | 0.519 |
LIG_14-3-3_CanoR_1 | 1035 | 1044 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 1073 | 1077 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 300 | 306 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 350 | 356 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 420 | 424 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 43 | 47 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 726 | 734 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 742 | 750 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 795 | 805 | PF00244 | 0.684 |
LIG_14-3-3_CanoR_1 | 897 | 901 | PF00244 | 0.697 |
LIG_Actin_WH2_2 | 259 | 277 | PF00022 | 0.523 |
LIG_Actin_WH2_2 | 495 | 511 | PF00022 | 0.399 |
LIG_APCC_ABBA_1 | 767 | 772 | PF00400 | 0.659 |
LIG_BIR_III_2 | 712 | 716 | PF00653 | 0.616 |
LIG_CtBP_PxDLS_1 | 811 | 815 | PF00389 | 0.542 |
LIG_deltaCOP1_diTrp_1 | 101 | 111 | PF00928 | 0.503 |
LIG_deltaCOP1_diTrp_1 | 233 | 242 | PF00928 | 0.456 |
LIG_eIF4E_1 | 7 | 13 | PF01652 | 0.356 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.532 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.534 |
LIG_FHA_1 | 535 | 541 | PF00498 | 0.490 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.465 |
LIG_FHA_1 | 613 | 619 | PF00498 | 0.467 |
LIG_FHA_1 | 749 | 755 | PF00498 | 0.534 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.288 |
LIG_FHA_1 | 800 | 806 | PF00498 | 0.547 |
LIG_FHA_1 | 871 | 877 | PF00498 | 0.815 |
LIG_FHA_1 | 925 | 931 | PF00498 | 0.614 |
LIG_FHA_1 | 942 | 948 | PF00498 | 0.651 |
LIG_FHA_1 | 986 | 992 | PF00498 | 0.531 |
LIG_FHA_2 | 382 | 388 | PF00498 | 0.481 |
LIG_FHA_2 | 403 | 409 | PF00498 | 0.456 |
LIG_FHA_2 | 561 | 567 | PF00498 | 0.456 |
LIG_FHA_2 | 638 | 644 | PF00498 | 0.589 |
LIG_FHA_2 | 730 | 736 | PF00498 | 0.526 |
LIG_FHA_2 | 839 | 845 | PF00498 | 0.521 |
LIG_FHA_2 | 935 | 941 | PF00498 | 0.559 |
LIG_LIR_Apic_2 | 662 | 667 | PF02991 | 0.674 |
LIG_LIR_Gen_1 | 116 | 125 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 238 | 247 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 270 | 277 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 328 | 338 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 39 | 49 | PF02991 | 0.618 |
LIG_LIR_Gen_1 | 433 | 442 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 512 | 521 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 559 | 569 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 85 | 95 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 116 | 121 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 172 | 178 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 220 | 224 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 238 | 242 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 270 | 274 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 328 | 333 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 39 | 44 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 433 | 438 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 512 | 516 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 559 | 565 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 601 | 607 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.533 |
LIG_MYND_1 | 765 | 769 | PF01753 | 0.663 |
LIG_MYND_2 | 764 | 768 | PF01753 | 0.660 |
LIG_NRBOX | 371 | 377 | PF00104 | 0.523 |
LIG_Pex14_1 | 235 | 239 | PF04695 | 0.535 |
LIG_Pex14_2 | 100 | 104 | PF04695 | 0.439 |
LIG_Pex14_2 | 355 | 359 | PF04695 | 0.523 |
LIG_PTB_Apo_2 | 137 | 144 | PF02174 | 0.278 |
LIG_Rb_LxCxE_1 | 270 | 290 | PF01857 | 0.484 |
LIG_SH2_CRK | 175 | 179 | PF00017 | 0.460 |
LIG_SH2_CRK | 271 | 275 | PF00017 | 0.463 |
LIG_SH2_CRK | 330 | 334 | PF00017 | 0.456 |
LIG_SH2_CRK | 41 | 45 | PF00017 | 0.610 |
LIG_SH2_NCK_1 | 31 | 35 | PF00017 | 0.563 |
LIG_SH2_NCK_1 | 41 | 45 | PF00017 | 0.610 |
LIG_SH2_PTP2 | 401 | 404 | PF00017 | 0.396 |
LIG_SH2_PTP2 | 513 | 516 | PF00017 | 0.456 |
LIG_SH2_SRC | 11 | 14 | PF00017 | 0.526 |
LIG_SH2_SRC | 401 | 404 | PF00017 | 0.395 |
LIG_SH2_SRC | 513 | 516 | PF00017 | 0.523 |
LIG_SH2_STAP1 | 118 | 122 | PF00017 | 0.424 |
LIG_SH2_STAP1 | 156 | 160 | PF00017 | 0.476 |
LIG_SH2_STAP1 | 21 | 25 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 513 | 516 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 592 | 595 | PF00017 | 0.339 |
LIG_SH3_3 | 1025 | 1031 | PF00018 | 0.769 |
LIG_SH3_3 | 1084 | 1090 | PF00018 | 0.680 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.549 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.543 |
LIG_SH3_3 | 504 | 510 | PF00018 | 0.455 |
LIG_SH3_3 | 599 | 605 | PF00018 | 0.412 |
LIG_SH3_3 | 717 | 723 | PF00018 | 0.652 |
LIG_SH3_3 | 758 | 764 | PF00018 | 0.625 |
LIG_SH3_3 | 804 | 810 | PF00018 | 0.661 |
LIG_SH3_3 | 882 | 888 | PF00018 | 0.730 |
LIG_SH3_3 | 890 | 896 | PF00018 | 0.644 |
LIG_SH3_3 | 936 | 942 | PF00018 | 0.741 |
LIG_SH3_3 | 944 | 950 | PF00018 | 0.690 |
LIG_SUMO_SIM_anti_2 | 248 | 254 | PF11976 | 0.437 |
LIG_SUMO_SIM_anti_2 | 265 | 270 | PF11976 | 0.395 |
LIG_SUMO_SIM_anti_2 | 539 | 544 | PF11976 | 0.524 |
LIG_SUMO_SIM_anti_2 | 830 | 836 | PF11976 | 0.693 |
LIG_SUMO_SIM_par_1 | 265 | 270 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 283 | 290 | PF11976 | 0.481 |
LIG_SUMO_SIM_par_1 | 537 | 544 | PF11976 | 0.523 |
LIG_SUMO_SIM_par_1 | 714 | 719 | PF11976 | 0.818 |
LIG_SUMO_SIM_par_1 | 810 | 816 | PF11976 | 0.558 |
LIG_SUMO_SIM_par_1 | 934 | 940 | PF11976 | 0.504 |
LIG_TRAF2_1 | 134 | 137 | PF00917 | 0.447 |
LIG_TRAF2_2 | 153 | 158 | PF00917 | 0.458 |
LIG_TRFH_1 | 31 | 35 | PF08558 | 0.563 |
LIG_TYR_ITIM | 269 | 274 | PF00017 | 0.458 |
LIG_TYR_ITIM | 399 | 404 | PF00017 | 0.456 |
LIG_TYR_ITIM | 511 | 516 | PF00017 | 0.456 |
LIG_UBA3_1 | 121 | 126 | PF00899 | 0.343 |
LIG_UBA3_1 | 399 | 407 | PF00899 | 0.523 |
LIG_WW_3 | 894 | 898 | PF00397 | 0.596 |
MOD_CDC14_SPxK_1 | 708 | 711 | PF00782 | 0.529 |
MOD_CDK_SPK_2 | 687 | 692 | PF00069 | 0.694 |
MOD_CDK_SPxK_1 | 670 | 676 | PF00069 | 0.555 |
MOD_CDK_SPxK_1 | 705 | 711 | PF00069 | 0.540 |
MOD_CK1_1 | 1008 | 1014 | PF00069 | 0.506 |
MOD_CK1_1 | 1029 | 1035 | PF00069 | 0.558 |
MOD_CK1_1 | 1052 | 1058 | PF00069 | 0.703 |
MOD_CK1_1 | 1059 | 1065 | PF00069 | 0.653 |
MOD_CK1_1 | 1081 | 1087 | PF00069 | 0.530 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.508 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.607 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.592 |
MOD_CK1_1 | 517 | 523 | PF00069 | 0.523 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.529 |
MOD_CK1_1 | 612 | 618 | PF00069 | 0.469 |
MOD_CK1_1 | 621 | 627 | PF00069 | 0.662 |
MOD_CK1_1 | 649 | 655 | PF00069 | 0.691 |
MOD_CK1_1 | 656 | 662 | PF00069 | 0.603 |
MOD_CK1_1 | 670 | 676 | PF00069 | 0.542 |
MOD_CK1_1 | 686 | 692 | PF00069 | 0.630 |
MOD_CK1_1 | 697 | 703 | PF00069 | 0.687 |
MOD_CK1_1 | 741 | 747 | PF00069 | 0.532 |
MOD_CK1_1 | 748 | 754 | PF00069 | 0.525 |
MOD_CK1_1 | 786 | 792 | PF00069 | 0.753 |
MOD_CK1_1 | 797 | 803 | PF00069 | 0.631 |
MOD_CK1_1 | 813 | 819 | PF00069 | 0.723 |
MOD_CK1_1 | 840 | 846 | PF00069 | 0.590 |
MOD_CK1_1 | 872 | 878 | PF00069 | 0.631 |
MOD_CK1_1 | 880 | 886 | PF00069 | 0.694 |
MOD_CK1_1 | 911 | 917 | PF00069 | 0.631 |
MOD_CK1_1 | 918 | 924 | PF00069 | 0.651 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.481 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.487 |
MOD_CK2_1 | 402 | 408 | PF00069 | 0.462 |
MOD_CK2_1 | 497 | 503 | PF00069 | 0.508 |
MOD_CK2_1 | 621 | 627 | PF00069 | 0.689 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.431 |
MOD_CK2_1 | 934 | 940 | PF00069 | 0.643 |
MOD_GlcNHglycan | 1010 | 1013 | PF01048 | 0.584 |
MOD_GlcNHglycan | 1016 | 1019 | PF01048 | 0.587 |
MOD_GlcNHglycan | 1069 | 1072 | PF01048 | 0.677 |
MOD_GlcNHglycan | 1083 | 1086 | PF01048 | 0.818 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.347 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.271 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.575 |
MOD_GlcNHglycan | 439 | 443 | PF01048 | 0.530 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.456 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.323 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.323 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.217 |
MOD_GlcNHglycan | 547 | 550 | PF01048 | 0.332 |
MOD_GlcNHglycan | 623 | 626 | PF01048 | 0.595 |
MOD_GlcNHglycan | 738 | 741 | PF01048 | 0.665 |
MOD_GlcNHglycan | 743 | 746 | PF01048 | 0.639 |
MOD_GlcNHglycan | 747 | 750 | PF01048 | 0.620 |
MOD_GlcNHglycan | 788 | 791 | PF01048 | 0.749 |
MOD_GlcNHglycan | 796 | 799 | PF01048 | 0.610 |
MOD_GlcNHglycan | 824 | 827 | PF01048 | 0.700 |
MOD_GlcNHglycan | 846 | 849 | PF01048 | 0.702 |
MOD_GlcNHglycan | 857 | 860 | PF01048 | 0.662 |
MOD_GSK3_1 | 1010 | 1017 | PF00069 | 0.508 |
MOD_GSK3_1 | 1022 | 1029 | PF00069 | 0.488 |
MOD_GSK3_1 | 1050 | 1057 | PF00069 | 0.746 |
MOD_GSK3_1 | 1059 | 1066 | PF00069 | 0.688 |
MOD_GSK3_1 | 1081 | 1088 | PF00069 | 0.809 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.478 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.528 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.523 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.535 |
MOD_GSK3_1 | 617 | 624 | PF00069 | 0.613 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.710 |
MOD_GSK3_1 | 683 | 690 | PF00069 | 0.687 |
MOD_GSK3_1 | 694 | 701 | PF00069 | 0.600 |
MOD_GSK3_1 | 729 | 736 | PF00069 | 0.662 |
MOD_GSK3_1 | 741 | 748 | PF00069 | 0.570 |
MOD_GSK3_1 | 750 | 757 | PF00069 | 0.598 |
MOD_GSK3_1 | 815 | 822 | PF00069 | 0.601 |
MOD_GSK3_1 | 836 | 843 | PF00069 | 0.605 |
MOD_GSK3_1 | 844 | 851 | PF00069 | 0.574 |
MOD_GSK3_1 | 855 | 862 | PF00069 | 0.497 |
MOD_GSK3_1 | 865 | 872 | PF00069 | 0.662 |
MOD_GSK3_1 | 877 | 884 | PF00069 | 0.694 |
MOD_GSK3_1 | 899 | 906 | PF00069 | 0.728 |
MOD_GSK3_1 | 911 | 918 | PF00069 | 0.628 |
MOD_GSK3_1 | 920 | 927 | PF00069 | 0.692 |
MOD_GSK3_1 | 993 | 1000 | PF00069 | 0.567 |
MOD_N-GLC_1 | 1081 | 1086 | PF02516 | 0.549 |
MOD_N-GLC_1 | 552 | 557 | PF02516 | 0.256 |
MOD_N-GLC_1 | 621 | 626 | PF02516 | 0.592 |
MOD_N-GLC_1 | 637 | 642 | PF02516 | 0.475 |
MOD_N-GLC_1 | 786 | 791 | PF02516 | 0.685 |
MOD_N-GLC_1 | 908 | 913 | PF02516 | 0.511 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.435 |
MOD_NEK2_1 | 1049 | 1054 | PF00069 | 0.696 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.485 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.488 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.496 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.564 |
MOD_NEK2_1 | 545 | 550 | PF00069 | 0.504 |
MOD_NEK2_1 | 611 | 616 | PF00069 | 0.419 |
MOD_NEK2_1 | 617 | 622 | PF00069 | 0.480 |
MOD_NEK2_1 | 647 | 652 | PF00069 | 0.545 |
MOD_NEK2_1 | 729 | 734 | PF00069 | 0.643 |
MOD_NEK2_1 | 754 | 759 | PF00069 | 0.605 |
MOD_NEK2_1 | 777 | 782 | PF00069 | 0.746 |
MOD_NEK2_1 | 788 | 793 | PF00069 | 0.708 |
MOD_NEK2_1 | 796 | 801 | PF00069 | 0.631 |
MOD_NEK2_1 | 835 | 840 | PF00069 | 0.690 |
MOD_NEK2_1 | 867 | 872 | PF00069 | 0.607 |
MOD_NEK2_1 | 901 | 906 | PF00069 | 0.559 |
MOD_NEK2_1 | 919 | 924 | PF00069 | 0.686 |
MOD_NEK2_1 | 986 | 991 | PF00069 | 0.639 |
MOD_NEK2_2 | 1072 | 1077 | PF00069 | 0.652 |
MOD_NEK2_2 | 301 | 306 | PF00069 | 0.533 |
MOD_NEK2_2 | 74 | 79 | PF00069 | 0.280 |
MOD_NEK2_2 | 896 | 901 | PF00069 | 0.608 |
MOD_PIKK_1 | 1036 | 1042 | PF00454 | 0.661 |
MOD_PIKK_1 | 113 | 119 | PF00454 | 0.332 |
MOD_PIKK_1 | 653 | 659 | PF00454 | 0.644 |
MOD_PIKK_1 | 667 | 673 | PF00454 | 0.604 |
MOD_PIKK_1 | 694 | 700 | PF00454 | 0.618 |
MOD_PIKK_1 | 721 | 727 | PF00454 | 0.788 |
MOD_PIKK_1 | 805 | 811 | PF00454 | 0.800 |
MOD_PIKK_1 | 870 | 876 | PF00454 | 0.815 |
MOD_PKA_1 | 836 | 842 | PF00069 | 0.590 |
MOD_PKA_2 | 1072 | 1078 | PF00069 | 0.674 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.479 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.481 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.490 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.594 |
MOD_PKA_2 | 741 | 747 | PF00069 | 0.633 |
MOD_PKA_2 | 794 | 800 | PF00069 | 0.774 |
MOD_PKA_2 | 835 | 841 | PF00069 | 0.675 |
MOD_PKA_2 | 896 | 902 | PF00069 | 0.690 |
MOD_Plk_1 | 287 | 293 | PF00069 | 0.456 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.526 |
MOD_Plk_1 | 908 | 914 | PF00069 | 0.514 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.465 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.472 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.523 |
MOD_Plk_4 | 556 | 562 | PF00069 | 0.475 |
MOD_Plk_4 | 598 | 604 | PF00069 | 0.401 |
MOD_Plk_4 | 683 | 689 | PF00069 | 0.529 |
MOD_Plk_4 | 729 | 735 | PF00069 | 0.671 |
MOD_Plk_4 | 827 | 833 | PF00069 | 0.688 |
MOD_Plk_4 | 851 | 857 | PF00069 | 0.535 |
MOD_Plk_4 | 872 | 878 | PF00069 | 0.561 |
MOD_Plk_4 | 915 | 921 | PF00069 | 0.553 |
MOD_ProDKin_1 | 1026 | 1032 | PF00069 | 0.504 |
MOD_ProDKin_1 | 1052 | 1058 | PF00069 | 0.690 |
MOD_ProDKin_1 | 1061 | 1067 | PF00069 | 0.744 |
MOD_ProDKin_1 | 1086 | 1092 | PF00069 | 0.675 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.471 |
MOD_ProDKin_1 | 517 | 523 | PF00069 | 0.487 |
MOD_ProDKin_1 | 649 | 655 | PF00069 | 0.685 |
MOD_ProDKin_1 | 670 | 676 | PF00069 | 0.555 |
MOD_ProDKin_1 | 687 | 693 | PF00069 | 0.662 |
MOD_ProDKin_1 | 705 | 711 | PF00069 | 0.684 |
MOD_ProDKin_1 | 716 | 722 | PF00069 | 0.623 |
MOD_ProDKin_1 | 733 | 739 | PF00069 | 0.607 |
MOD_ProDKin_1 | 760 | 766 | PF00069 | 0.608 |
MOD_ProDKin_1 | 815 | 821 | PF00069 | 0.600 |
MOD_ProDKin_1 | 848 | 854 | PF00069 | 0.542 |
MOD_ProDKin_1 | 878 | 884 | PF00069 | 0.680 |
MOD_ProDKin_1 | 904 | 910 | PF00069 | 0.576 |
MOD_ProDKin_1 | 911 | 917 | PF00069 | 0.634 |
MOD_ProDKin_1 | 921 | 927 | PF00069 | 0.519 |
MOD_SUMO_rev_2 | 14 | 19 | PF00179 | 0.549 |
MOD_SUMO_rev_2 | 406 | 412 | PF00179 | 0.523 |
TRG_DiLeu_BaEn_1 | 220 | 225 | PF01217 | 0.456 |
TRG_DiLeu_BaEn_1 | 371 | 376 | PF01217 | 0.481 |
TRG_DiLeu_BaLyEn_6 | 602 | 607 | PF01217 | 0.385 |
TRG_DiLeu_BaLyEn_6 | 712 | 717 | PF01217 | 0.718 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.469 |
TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.611 |
TRG_ENDOCYTIC_2 | 513 | 516 | PF00928 | 0.456 |
TRG_ER_diArg_1 | 1072 | 1074 | PF00400 | 0.672 |
TRG_ER_diArg_1 | 27 | 30 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 381 | 383 | PF00400 | 0.469 |
TRG_ER_diArg_1 | 792 | 795 | PF00400 | 0.648 |
TRG_ER_diArg_1 | 835 | 837 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 896 | 898 | PF00400 | 0.589 |
TRG_NLS_MonoCore_2 | 957 | 962 | PF00514 | 0.721 |
TRG_NLS_MonoExtC_3 | 957 | 963 | PF00514 | 0.693 |
TRG_Pf-PMV_PEXEL_1 | 150 | 155 | PF00026 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 386 | 391 | PF00026 | 0.266 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1Z2 | Leptomonas seymouri | 60% | 94% |
A0A0S4JHP8 | Bodo saltans | 43% | 100% |
A0A3Q8IC06 | Leishmania donovani | 76% | 99% |
A4H349 | Leishmania braziliensis | 22% | 100% |
A4I0P9 | Leishmania infantum | 76% | 99% |
D0A725 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AWQ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q4QAS2 | Leishmania major | 73% | 94% |