Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0042555 | MCM complex | 2 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: A0A3Q8IAX4
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006268 | DNA unwinding involved in DNA replication | 9 | 12 |
GO:0006270 | DNA replication initiation | 5 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006996 | organelle organization | 4 | 12 |
GO:0007049 | cell cycle | 2 | 11 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0010639 | negative regulation of organelle organization | 6 | 12 |
GO:0016043 | cellular component organization | 3 | 12 |
GO:0032392 | DNA geometric change | 7 | 12 |
GO:0032508 | DNA duplex unwinding | 8 | 12 |
GO:0032780 | negative regulation of ATP-dependent activity | 4 | 12 |
GO:0033043 | regulation of organelle organization | 5 | 12 |
GO:0033044 | regulation of chromosome organization | 6 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043086 | negative regulation of catalytic activity | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043462 | regulation of ATP-dependent activity | 3 | 12 |
GO:0044092 | negative regulation of molecular function | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0048519 | negative regulation of biological process | 3 | 12 |
GO:0048523 | negative regulation of cellular process | 4 | 12 |
GO:0050789 | regulation of biological process | 2 | 12 |
GO:0050790 | regulation of catalytic activity | 3 | 12 |
GO:0050794 | regulation of cellular process | 3 | 12 |
GO:0051095 | regulation of helicase activity | 4 | 12 |
GO:0051097 | negative regulation of helicase activity | 5 | 12 |
GO:0051128 | regulation of cellular component organization | 4 | 12 |
GO:0051129 | negative regulation of cellular component organization | 5 | 12 |
GO:0051276 | chromosome organization | 5 | 12 |
GO:0065007 | biological regulation | 1 | 12 |
GO:0065009 | regulation of molecular function | 2 | 12 |
GO:0071103 | DNA conformation change | 6 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1905462 | regulation of DNA duplex unwinding | 7 | 12 |
GO:1905463 | negative regulation of DNA duplex unwinding | 8 | 12 |
GO:1905774 | regulation of DNA helicase activity | 5 | 12 |
GO:1905775 | negative regulation of DNA helicase activity | 6 | 12 |
GO:2001251 | negative regulation of chromosome organization | 7 | 12 |
GO:0000724 | double-strand break repair via homologous recombination | 7 | 1 |
GO:0000725 | recombinational repair | 6 | 1 |
GO:0000727 | double-strand break repair via break-induced replication | 8 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:1902292 | cell cycle DNA replication initiation | 3 | 1 |
GO:1902315 | nuclear cell cycle DNA replication initiation | 4 | 1 |
GO:1902975 | mitotic DNA replication initiation | 4 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003678 | DNA helicase activity | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 12 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 12 |
GO:0016887 | ATP hydrolysis activity | 7 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003697 | single-stranded DNA binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 20 | 24 | PF00656 | 0.763 |
CLV_C14_Caspase3-7 | 770 | 774 | PF00656 | 0.530 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.221 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.183 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.230 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.202 |
CLV_NRD_NRD_1 | 470 | 472 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.212 |
CLV_NRD_NRD_1 | 755 | 757 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 783 | 785 | PF00675 | 0.213 |
CLV_NRD_NRD_1 | 880 | 882 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 949 | 951 | PF00675 | 0.513 |
CLV_PCSK_FUR_1 | 11 | 15 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.218 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.163 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.202 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 755 | 757 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 13 | 15 | PF00082 | 0.561 |
CLV_PCSK_PC7_1 | 7 | 13 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 499 | 503 | PF00082 | 0.224 |
CLV_PCSK_SKI1_1 | 568 | 572 | PF00082 | 0.202 |
CLV_PCSK_SKI1_1 | 700 | 704 | PF00082 | 0.235 |
CLV_PCSK_SKI1_1 | 735 | 739 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 785 | 789 | PF00082 | 0.213 |
CLV_PCSK_SKI1_1 | 881 | 885 | PF00082 | 0.518 |
CLV_Separin_Metazoa | 213 | 217 | PF03568 | 0.334 |
DEG_APCC_DBOX_1 | 188 | 196 | PF00400 | 0.544 |
DEG_APCC_DBOX_1 | 681 | 689 | PF00400 | 0.402 |
DEG_ODPH_VHL_1 | 505 | 517 | PF01847 | 0.413 |
DEG_SCF_FBW7_1 | 675 | 681 | PF00400 | 0.402 |
DOC_CKS1_1 | 675 | 680 | PF01111 | 0.402 |
DOC_CYCLIN_RxL_1 | 493 | 504 | PF00134 | 0.434 |
DOC_MAPK_gen_1 | 299 | 307 | PF00069 | 0.413 |
DOC_MAPK_gen_1 | 319 | 328 | PF00069 | 0.409 |
DOC_MAPK_gen_1 | 413 | 422 | PF00069 | 0.402 |
DOC_MAPK_gen_1 | 429 | 438 | PF00069 | 0.402 |
DOC_MAPK_gen_1 | 538 | 545 | PF00069 | 0.402 |
DOC_MAPK_gen_1 | 895 | 902 | PF00069 | 0.476 |
DOC_MAPK_HePTP_8 | 509 | 521 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 300 | 309 | PF00069 | 0.403 |
DOC_MAPK_MEF2A_6 | 322 | 330 | PF00069 | 0.408 |
DOC_MAPK_MEF2A_6 | 413 | 422 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 512 | 521 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 538 | 547 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 690 | 697 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 818 | 826 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 895 | 902 | PF00069 | 0.488 |
DOC_MAPK_NFAT4_5 | 512 | 520 | PF00069 | 0.404 |
DOC_MAPK_RevD_3 | 326 | 339 | PF00069 | 0.402 |
DOC_PP1_RVXF_1 | 783 | 790 | PF00149 | 0.453 |
DOC_PP4_FxxP_1 | 478 | 481 | PF00568 | 0.429 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 665 | 669 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 855 | 859 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 933 | 937 | PF00917 | 0.537 |
DOC_USP7_UBL2_3 | 560 | 564 | PF12436 | 0.402 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 491 | 496 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 674 | 679 | PF00397 | 0.402 |
LIG_14-3-3_CanoR_1 | 299 | 309 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 355 | 359 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 372 | 376 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 413 | 419 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 470 | 478 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 575 | 582 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 700 | 705 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 834 | 842 | PF00244 | 0.426 |
LIG_Actin_WH2_2 | 858 | 875 | PF00022 | 0.493 |
LIG_APCC_ABBA_1 | 235 | 240 | PF00400 | 0.506 |
LIG_BIR_III_4 | 23 | 27 | PF00653 | 0.576 |
LIG_BRCT_BRCA1_1 | 193 | 197 | PF00533 | 0.554 |
LIG_BRCT_BRCA1_1 | 302 | 306 | PF00533 | 0.506 |
LIG_BRCT_BRCA1_1 | 665 | 669 | PF00533 | 0.438 |
LIG_BRCT_BRCA1_1 | 763 | 767 | PF00533 | 0.507 |
LIG_BRCT_BRCA1_1 | 791 | 795 | PF00533 | 0.506 |
LIG_BRCT_BRCA1_1 | 945 | 949 | PF00533 | 0.362 |
LIG_BRCT_BRCA1_2 | 945 | 951 | PF00533 | 0.360 |
LIG_Clathr_ClatBox_1 | 329 | 333 | PF01394 | 0.402 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.506 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.413 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.402 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.379 |
LIG_FHA_1 | 470 | 476 | PF00498 | 0.462 |
LIG_FHA_1 | 581 | 587 | PF00498 | 0.406 |
LIG_FHA_1 | 632 | 638 | PF00498 | 0.415 |
LIG_FHA_1 | 674 | 680 | PF00498 | 0.402 |
LIG_FHA_1 | 718 | 724 | PF00498 | 0.589 |
LIG_FHA_1 | 852 | 858 | PF00498 | 0.512 |
LIG_FHA_1 | 886 | 892 | PF00498 | 0.431 |
LIG_FHA_2 | 665 | 671 | PF00498 | 0.506 |
LIG_FHA_2 | 714 | 720 | PF00498 | 0.477 |
LIG_FHA_2 | 741 | 747 | PF00498 | 0.451 |
LIG_FHA_2 | 847 | 853 | PF00498 | 0.506 |
LIG_GBD_Chelix_1 | 206 | 214 | PF00786 | 0.366 |
LIG_Integrin_RGD_1 | 189 | 191 | PF01839 | 0.556 |
LIG_Integrin_RGD_1 | 366 | 368 | PF01839 | 0.189 |
LIG_Integrin_RGD_1 | 540 | 542 | PF01839 | 0.207 |
LIG_LIR_Apic_2 | 176 | 182 | PF02991 | 0.683 |
LIG_LIR_Apic_2 | 65 | 69 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 128 | 138 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 256 | 264 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 303 | 314 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 556 | 566 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 613 | 622 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 681 | 689 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 256 | 260 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 261 | 267 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 291 | 295 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 303 | 309 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 320 | 324 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 556 | 561 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 681 | 686 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 792 | 798 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 877 | 883 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 952 | 956 | PF02991 | 0.358 |
LIG_LYPXL_S_1 | 342 | 346 | PF13949 | 0.202 |
LIG_LYPXL_yS_3 | 343 | 346 | PF13949 | 0.402 |
LIG_NRBOX | 516 | 522 | PF00104 | 0.413 |
LIG_PCNA_PIPBox_1 | 937 | 946 | PF02747 | 0.508 |
LIG_PCNA_yPIPBox_3 | 200 | 210 | PF02747 | 0.373 |
LIG_PCNA_yPIPBox_3 | 776 | 787 | PF02747 | 0.345 |
LIG_PCNA_yPIPBox_3 | 937 | 951 | PF02747 | 0.513 |
LIG_PDZ_Class_1 | 967 | 972 | PF00595 | 0.398 |
LIG_Pex14_2 | 683 | 687 | PF04695 | 0.402 |
LIG_Pex14_2 | 860 | 864 | PF04695 | 0.402 |
LIG_PTB_Apo_2 | 218 | 225 | PF02174 | 0.252 |
LIG_PTB_Phospho_1 | 218 | 224 | PF10480 | 0.252 |
LIG_SH2_CRK | 228 | 232 | PF00017 | 0.417 |
LIG_SH2_CRK | 264 | 268 | PF00017 | 0.402 |
LIG_SH2_CRK | 298 | 302 | PF00017 | 0.406 |
LIG_SH2_CRK | 953 | 957 | PF00017 | 0.354 |
LIG_SH2_GRB2like | 227 | 230 | PF00017 | 0.413 |
LIG_SH2_NCK_1 | 944 | 948 | PF00017 | 0.502 |
LIG_SH2_PTP2 | 810 | 813 | PF00017 | 0.506 |
LIG_SH2_SRC | 358 | 361 | PF00017 | 0.426 |
LIG_SH2_SRC | 663 | 666 | PF00017 | 0.413 |
LIG_SH2_STAP1 | 238 | 242 | PF00017 | 0.404 |
LIG_SH2_STAP1 | 264 | 268 | PF00017 | 0.433 |
LIG_SH2_STAP1 | 931 | 935 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 786 | 789 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 810 | 813 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 847 | 850 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 931 | 934 | PF00017 | 0.533 |
LIG_SH3_1 | 338 | 344 | PF00018 | 0.402 |
LIG_SH3_2 | 27 | 32 | PF14604 | 0.692 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.689 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.413 |
LIG_SH3_3 | 338 | 344 | PF00018 | 0.402 |
LIG_SH3_3 | 545 | 551 | PF00018 | 0.402 |
LIG_SH3_4 | 776 | 783 | PF00018 | 0.372 |
LIG_SUMO_SIM_anti_2 | 417 | 423 | PF11976 | 0.402 |
LIG_SUMO_SIM_par_1 | 277 | 285 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 398 | 404 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 487 | 492 | PF11976 | 0.471 |
LIG_SUMO_SIM_par_1 | 544 | 550 | PF11976 | 0.402 |
LIG_TRAF2_1 | 148 | 151 | PF00917 | 0.569 |
LIG_TRAF2_1 | 432 | 435 | PF00917 | 0.413 |
LIG_TRAF2_1 | 69 | 72 | PF00917 | 0.496 |
LIG_TRAF2_1 | 716 | 719 | PF00917 | 0.490 |
LIG_TRAF2_1 | 76 | 79 | PF00917 | 0.498 |
LIG_TRFH_1 | 292 | 296 | PF08558 | 0.224 |
LIG_TYR_ITIM | 255 | 260 | PF00017 | 0.237 |
LIG_UBA3_1 | 488 | 493 | PF00899 | 0.252 |
LIG_UBA3_1 | 520 | 529 | PF00899 | 0.237 |
LIG_WRC_WIRS_1 | 289 | 294 | PF05994 | 0.382 |
LIG_WRC_WIRS_1 | 701 | 706 | PF05994 | 0.216 |
LIG_WW_3 | 28 | 32 | PF00397 | 0.718 |
MOD_CDK_SPxxK_3 | 491 | 498 | PF00069 | 0.382 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.728 |
MOD_CK1_1 | 378 | 384 | PF00069 | 0.252 |
MOD_CK1_1 | 871 | 877 | PF00069 | 0.350 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.252 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.271 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.341 |
MOD_CK2_1 | 622 | 628 | PF00069 | 0.237 |
MOD_CK2_1 | 713 | 719 | PF00069 | 0.433 |
MOD_CK2_1 | 740 | 746 | PF00069 | 0.474 |
MOD_CK2_1 | 762 | 768 | PF00069 | 0.588 |
MOD_CK2_1 | 871 | 877 | PF00069 | 0.350 |
MOD_CK2_1 | 883 | 889 | PF00069 | 0.401 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.382 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.615 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.385 |
MOD_GlcNHglycan | 646 | 649 | PF01048 | 0.252 |
MOD_GlcNHglycan | 873 | 876 | PF01048 | 0.367 |
MOD_GlcNHglycan | 912 | 915 | PF01048 | 0.415 |
MOD_GlcNHglycan | 945 | 948 | PF01048 | 0.497 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.237 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.245 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.264 |
MOD_GSK3_1 | 562 | 569 | PF00069 | 0.271 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.204 |
MOD_GSK3_1 | 674 | 681 | PF00069 | 0.237 |
MOD_GSK3_1 | 713 | 720 | PF00069 | 0.481 |
MOD_GSK3_1 | 757 | 764 | PF00069 | 0.599 |
MOD_GSK3_1 | 851 | 858 | PF00069 | 0.306 |
MOD_GSK3_1 | 864 | 871 | PF00069 | 0.291 |
MOD_GSK3_1 | 883 | 890 | PF00069 | 0.538 |
MOD_GSK3_1 | 929 | 936 | PF00069 | 0.426 |
MOD_N-GLC_1 | 673 | 678 | PF02516 | 0.235 |
MOD_N-GLC_1 | 739 | 744 | PF02516 | 0.462 |
MOD_N-GLC_1 | 933 | 938 | PF02516 | 0.464 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.602 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.432 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.249 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.273 |
MOD_NEK2_1 | 789 | 794 | PF00069 | 0.382 |
MOD_NEK2_1 | 864 | 869 | PF00069 | 0.310 |
MOD_NEK2_2 | 566 | 571 | PF00069 | 0.382 |
MOD_NEK2_2 | 855 | 860 | PF00069 | 0.252 |
MOD_NEK2_2 | 901 | 906 | PF00069 | 0.363 |
MOD_PIKK_1 | 553 | 559 | PF00454 | 0.237 |
MOD_PIKK_1 | 713 | 719 | PF00454 | 0.411 |
MOD_PIKK_1 | 864 | 870 | PF00454 | 0.312 |
MOD_PIKK_1 | 916 | 922 | PF00454 | 0.464 |
MOD_PIKK_1 | 933 | 939 | PF00454 | 0.377 |
MOD_PKA_1 | 470 | 476 | PF00069 | 0.508 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.744 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.267 |
MOD_PKA_2 | 371 | 377 | PF00069 | 0.196 |
MOD_PKA_2 | 389 | 395 | PF00069 | 0.396 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.399 |
MOD_PKA_2 | 574 | 580 | PF00069 | 0.237 |
MOD_PKA_2 | 622 | 628 | PF00069 | 0.263 |
MOD_PKA_2 | 757 | 763 | PF00069 | 0.474 |
MOD_PKA_2 | 796 | 802 | PF00069 | 0.265 |
MOD_PKA_2 | 833 | 839 | PF00069 | 0.271 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.751 |
MOD_Plk_1 | 233 | 239 | PF00069 | 0.339 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.155 |
MOD_Plk_1 | 566 | 572 | PF00069 | 0.382 |
MOD_Plk_1 | 621 | 627 | PF00069 | 0.252 |
MOD_Plk_1 | 717 | 723 | PF00069 | 0.631 |
MOD_Plk_1 | 729 | 735 | PF00069 | 0.462 |
MOD_Plk_1 | 762 | 768 | PF00069 | 0.623 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.281 |
MOD_Plk_2-3 | 166 | 172 | PF00069 | 0.502 |
MOD_Plk_2-3 | 616 | 622 | PF00069 | 0.237 |
MOD_Plk_2-3 | 846 | 852 | PF00069 | 0.382 |
MOD_Plk_2-3 | 90 | 96 | PF00069 | 0.382 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.271 |
MOD_Plk_4 | 263 | 269 | PF00069 | 0.240 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.252 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.252 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.331 |
MOD_Plk_4 | 700 | 706 | PF00069 | 0.216 |
MOD_Plk_4 | 778 | 784 | PF00069 | 0.408 |
MOD_Plk_4 | 828 | 834 | PF00069 | 0.237 |
MOD_Plk_4 | 855 | 861 | PF00069 | 0.323 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.237 |
MOD_ProDKin_1 | 491 | 497 | PF00069 | 0.392 |
MOD_ProDKin_1 | 674 | 680 | PF00069 | 0.237 |
MOD_SUMO_rev_2 | 234 | 242 | PF00179 | 0.281 |
MOD_SUMO_rev_2 | 508 | 517 | PF00179 | 0.237 |
TRG_DiLeu_BaEn_1 | 598 | 603 | PF01217 | 0.237 |
TRG_DiLeu_BaEn_1 | 718 | 723 | PF01217 | 0.508 |
TRG_DiLeu_BaEn_4 | 121 | 127 | PF01217 | 0.285 |
TRG_DiLeu_BaEn_4 | 52 | 58 | PF01217 | 0.379 |
TRG_DiLeu_BaEn_4 | 718 | 724 | PF01217 | 0.589 |
TRG_DiLeu_BaEn_4 | 729 | 735 | PF01217 | 0.532 |
TRG_DiLeu_BaLyEn_6 | 445 | 450 | PF01217 | 0.374 |
TRG_DiLeu_BaLyEn_6 | 951 | 956 | PF01217 | 0.507 |
TRG_DiLeu_LyEn_5 | 718 | 723 | PF01217 | 0.508 |
TRG_DiLeu_LyEn_5 | 889 | 894 | PF01217 | 0.395 |
TRG_ENDOCYTIC_2 | 228 | 231 | PF00928 | 0.258 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.237 |
TRG_ENDOCYTIC_2 | 264 | 267 | PF00928 | 0.237 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.281 |
TRG_ENDOCYTIC_2 | 298 | 301 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.237 |
TRG_ENDOCYTIC_2 | 786 | 789 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 810 | 813 | PF00928 | 0.237 |
TRG_ENDOCYTIC_2 | 953 | 956 | PF00928 | 0.349 |
TRG_ER_diArg_1 | 11 | 14 | PF00400 | 0.597 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 15 | 18 | PF00400 | 0.603 |
TRG_ER_diArg_1 | 215 | 217 | PF00400 | 0.343 |
TRG_ER_diArg_1 | 30 | 32 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 337 | 339 | PF00400 | 0.237 |
TRG_ER_diArg_1 | 469 | 471 | PF00400 | 0.366 |
TRG_ER_diArg_1 | 485 | 488 | PF00400 | 0.202 |
TRG_ER_diArg_1 | 733 | 736 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 754 | 756 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 894 | 897 | PF00400 | 0.510 |
TRG_ER_FFAT_2 | 924 | 936 | PF00635 | 0.447 |
TRG_NES_CRM1_1 | 684 | 699 | PF08389 | 0.252 |
TRG_NLS_MonoCore_2 | 11 | 16 | PF00514 | 0.641 |
TRG_NLS_MonoExtC_3 | 11 | 16 | PF00514 | 0.641 |
TRG_NLS_MonoExtN_4 | 11 | 17 | PF00514 | 0.662 |
TRG_NLS_MonoExtN_4 | 495 | 502 | PF00514 | 0.218 |
TRG_Pf-PMV_PEXEL_1 | 124 | 128 | PF00026 | 0.317 |
TRG_Pf-PMV_PEXEL_1 | 721 | 726 | PF00026 | 0.459 |
TRG_Pf-PMV_PEXEL_1 | 755 | 759 | PF00026 | 0.543 |
TRG_Pf-PMV_PEXEL_1 | 954 | 958 | PF00026 | 0.505 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P860 | Leptomonas seymouri | 87% | 98% |
A0A0N1I383 | Leptomonas seymouri | 32% | 95% |
A0A0S4IK09 | Bodo saltans | 64% | 99% |
A0A1X0NZT6 | Trypanosomatidae | 75% | 100% |
A0A3Q8IQ79 | Leishmania donovani | 28% | 100% |
A0A3R7K9K0 | Trypanosoma rangeli | 31% | 100% |
A0A3R7NBN0 | Trypanosoma rangeli | 76% | 100% |
A0A3S7WY81 | Leishmania donovani | 30% | 100% |
A0A3S7X726 | Leishmania donovani | 32% | 100% |
A0A422NDD9 | Trypanosoma rangeli | 29% | 100% |
A4FUD9 | Bos taurus | 33% | 100% |
A4H5K0 | Leishmania braziliensis | 31% | 100% |
A4HDE7 | Leishmania braziliensis | 31% | 100% |
A4HGC9 | Leishmania braziliensis | 92% | 100% |
A4HLY1 | Leishmania braziliensis | 31% | 100% |
A4I0T0 | Leishmania infantum | 30% | 100% |
A4I3G2 | Leishmania infantum | 100% | 100% |
A4I9B0 | Leishmania infantum | 32% | 100% |
A4IC27 | Leishmania infantum | 28% | 100% |
B8AZ99 | Oryza sativa subsp. indica | 34% | 100% |
B8BKI8 | Oryza sativa subsp. indica | 42% | 100% |
D0A7X6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 71% | 100% |
E9AMM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9AWT2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
E9AZQ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
E9B4B0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
F1M5F3 | Rattus norvegicus | 31% | 86% |
F1N2W9 | Bos taurus | 30% | 85% |
P25205 | Homo sapiens | 33% | 100% |
P25206 | Mus musculus | 33% | 100% |
P29469 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 47% | 100% |
P30666 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 100% |
P33991 | Homo sapiens | 30% | 100% |
P40377 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 42% | 100% |
P41389 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 100% |
P49735 | Drosophila melanogaster | 43% | 100% |
P49736 | Homo sapiens | 45% | 100% |
P55861 | Xenopus laevis | 43% | 100% |
P97310 | Mus musculus | 44% | 100% |
Q0DHC4 | Oryza sativa subsp. japonica | 34% | 100% |
Q21902 | Caenorhabditis elegans | 29% | 100% |
Q28BS0 | Xenopus tropicalis | 34% | 100% |
Q29JI9 | Drosophila pseudoobscura pseudoobscura | 31% | 100% |
Q2KHI9 | Mus musculus | 32% | 86% |
Q2R482 | Oryza sativa subsp. japonica | 42% | 100% |
Q43704 | Zea mays | 35% | 100% |
Q4Q3R6 | Leishmania major | 32% | 100% |
Q4Q8I2 | Leishmania major | 98% | 100% |
Q4QAP2 | Leishmania major | 30% | 100% |
Q54CP4 | Dictyostelium discoideum | 31% | 100% |
Q5R8G6 | Pongo abelii | 33% | 100% |
Q6DIH3 | Xenopus tropicalis | 43% | 100% |
Q6NRM6 | Xenopus laevis | 30% | 85% |
Q7ZXZ0 | Xenopus laevis | 35% | 100% |
Q9LPD9 | Arabidopsis thaliana | 45% | 100% |
Q9NXL9 | Homo sapiens | 30% | 85% |
Q9SF37 | Arabidopsis thaliana | 31% | 100% |
Q9SX03 | Zea mays | 35% | 100% |
Q9SX04 | Zea mays | 35% | 100% |
Q9V461 | Drosophila melanogaster | 32% | 100% |
Q9VGW6 | Drosophila melanogaster | 32% | 100% |
Q9XYU0 | Drosophila melanogaster | 33% | 100% |
V5BQA9 | Trypanosoma cruzi | 80% | 100% |