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: A4HGC9
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 | 34 | 38 | PF00656 | 0.346 |
CLV_C14_Caspase3-7 | 769 | 773 | PF00656 | 0.531 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.221 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.182 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.342 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.230 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.202 |
CLV_NRD_NRD_1 | 469 | 471 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.206 |
CLV_NRD_NRD_1 | 782 | 784 | PF00675 | 0.212 |
CLV_NRD_NRD_1 | 879 | 881 | PF00675 | 0.358 |
CLV_NRD_NRD_1 | 948 | 950 | PF00675 | 0.513 |
CLV_PCSK_FUR_1 | 12 | 16 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.218 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.163 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.202 |
CLV_PCSK_KEX2_1 | 469 | 471 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 497 | 499 | PF00082 | 0.158 |
CLV_PCSK_PC1ET2_1 | 13 | 15 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.221 |
CLV_PCSK_SKI1_1 | 567 | 571 | PF00082 | 0.202 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 734 | 738 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 784 | 788 | PF00082 | 0.212 |
CLV_PCSK_SKI1_1 | 880 | 884 | PF00082 | 0.516 |
CLV_Separin_Metazoa | 212 | 216 | PF03568 | 0.334 |
DEG_APCC_DBOX_1 | 187 | 195 | PF00400 | 0.529 |
DEG_APCC_DBOX_1 | 497 | 505 | PF00400 | 0.370 |
DEG_APCC_DBOX_1 | 680 | 688 | PF00400 | 0.412 |
DEG_APCC_DBOX_1 | 920 | 928 | PF00400 | 0.279 |
DEG_ODPH_VHL_1 | 504 | 516 | PF01847 | 0.412 |
DEG_SCF_FBW7_1 | 674 | 680 | PF00400 | 0.402 |
DOC_CKS1_1 | 674 | 679 | PF01111 | 0.408 |
DOC_CYCLIN_RxL_1 | 492 | 503 | PF00134 | 0.433 |
DOC_MAPK_gen_1 | 298 | 306 | PF00069 | 0.413 |
DOC_MAPK_gen_1 | 318 | 327 | PF00069 | 0.315 |
DOC_MAPK_gen_1 | 412 | 421 | PF00069 | 0.402 |
DOC_MAPK_gen_1 | 428 | 437 | PF00069 | 0.402 |
DOC_MAPK_gen_1 | 469 | 476 | PF00069 | 0.419 |
DOC_MAPK_gen_1 | 537 | 544 | PF00069 | 0.402 |
DOC_MAPK_gen_1 | 894 | 901 | PF00069 | 0.476 |
DOC_MAPK_HePTP_8 | 508 | 520 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 299 | 308 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 321 | 329 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 412 | 421 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 469 | 478 | PF00069 | 0.345 |
DOC_MAPK_MEF2A_6 | 511 | 520 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 537 | 546 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 689 | 696 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 817 | 825 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 894 | 901 | PF00069 | 0.489 |
DOC_MAPK_NFAT4_5 | 511 | 519 | PF00069 | 0.406 |
DOC_MAPK_RevD_3 | 325 | 338 | PF00069 | 0.402 |
DOC_PP2B_LxvP_1 | 27 | 30 | PF13499 | 0.481 |
DOC_PP4_FxxP_1 | 477 | 480 | PF00568 | 0.409 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 664 | 668 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 761 | 765 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 854 | 858 | PF00917 | 0.448 |
DOC_USP7_UBL2_3 | 559 | 563 | PF12436 | 0.402 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 490 | 495 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 673 | 678 | PF00397 | 0.408 |
LIG_14-3-3_CanoR_1 | 298 | 308 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 354 | 358 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 371 | 375 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 412 | 418 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 469 | 478 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 574 | 581 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 833 | 841 | PF00244 | 0.426 |
LIG_Actin_WH2_2 | 857 | 874 | PF00022 | 0.472 |
LIG_APCC_ABBA_1 | 234 | 239 | PF00400 | 0.505 |
LIG_BIR_III_4 | 8 | 12 | PF00653 | 0.504 |
LIG_BRCT_BRCA1_1 | 301 | 305 | PF00533 | 0.505 |
LIG_BRCT_BRCA1_1 | 664 | 668 | PF00533 | 0.412 |
LIG_BRCT_BRCA1_1 | 790 | 794 | PF00533 | 0.505 |
LIG_BRCT_BRCA1_1 | 944 | 948 | PF00533 | 0.362 |
LIG_BRCT_BRCA1_2 | 944 | 950 | PF00533 | 0.360 |
LIG_Clathr_ClatBox_1 | 328 | 332 | PF01394 | 0.402 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.505 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.448 |
LIG_FHA_1 | 396 | 402 | PF00498 | 0.430 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.430 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.328 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.404 |
LIG_FHA_1 | 580 | 586 | PF00498 | 0.402 |
LIG_FHA_1 | 631 | 637 | PF00498 | 0.409 |
LIG_FHA_1 | 673 | 679 | PF00498 | 0.402 |
LIG_FHA_1 | 717 | 723 | PF00498 | 0.592 |
LIG_FHA_1 | 851 | 857 | PF00498 | 0.505 |
LIG_FHA_1 | 885 | 891 | PF00498 | 0.431 |
LIG_FHA_1 | 929 | 935 | PF00498 | 0.347 |
LIG_FHA_2 | 664 | 670 | PF00498 | 0.505 |
LIG_FHA_2 | 713 | 719 | PF00498 | 0.486 |
LIG_FHA_2 | 740 | 746 | PF00498 | 0.473 |
LIG_FHA_2 | 846 | 852 | PF00498 | 0.505 |
LIG_GBD_Chelix_1 | 205 | 213 | PF00786 | 0.367 |
LIG_Integrin_RGD_1 | 188 | 190 | PF01839 | 0.541 |
LIG_Integrin_RGD_1 | 539 | 541 | PF01839 | 0.202 |
LIG_LIR_Apic_2 | 175 | 181 | PF02991 | 0.683 |
LIG_LIR_Apic_2 | 195 | 201 | PF02991 | 0.336 |
LIG_LIR_Apic_2 | 65 | 69 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 128 | 138 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 255 | 263 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 302 | 313 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 555 | 565 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 612 | 621 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 680 | 688 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 729 | 737 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 255 | 259 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 260 | 266 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 290 | 294 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 302 | 308 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 319 | 323 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 555 | 560 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 680 | 685 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 729 | 733 | PF02991 | 0.297 |
LIG_LIR_Nem_3 | 791 | 797 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 876 | 882 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 951 | 955 | PF02991 | 0.392 |
LIG_LYPXL_S_1 | 341 | 345 | PF13949 | 0.202 |
LIG_LYPXL_yS_3 | 342 | 345 | PF13949 | 0.402 |
LIG_NRBOX | 515 | 521 | PF00104 | 0.412 |
LIG_PCNA_PIPBox_1 | 936 | 945 | PF02747 | 0.508 |
LIG_PCNA_yPIPBox_3 | 199 | 209 | PF02747 | 0.371 |
LIG_PCNA_yPIPBox_3 | 775 | 786 | PF02747 | 0.341 |
LIG_PCNA_yPIPBox_3 | 936 | 950 | PF02747 | 0.513 |
LIG_PDZ_Class_1 | 966 | 971 | PF00595 | 0.384 |
LIG_Pex14_2 | 682 | 686 | PF04695 | 0.402 |
LIG_Pex14_2 | 859 | 863 | PF04695 | 0.402 |
LIG_PTB_Apo_2 | 217 | 224 | PF02174 | 0.313 |
LIG_PTB_Phospho_1 | 217 | 223 | PF10480 | 0.308 |
LIG_SH2_CRK | 263 | 267 | PF00017 | 0.402 |
LIG_SH2_CRK | 297 | 301 | PF00017 | 0.405 |
LIG_SH2_CRK | 350 | 354 | PF00017 | 0.348 |
LIG_SH2_CRK | 952 | 956 | PF00017 | 0.352 |
LIG_SH2_GRB2like | 226 | 229 | PF00017 | 0.412 |
LIG_SH2_NCK_1 | 943 | 947 | PF00017 | 0.501 |
LIG_SH2_PTP2 | 785 | 788 | PF00017 | 0.346 |
LIG_SH2_PTP2 | 809 | 812 | PF00017 | 0.505 |
LIG_SH2_SRC | 357 | 360 | PF00017 | 0.426 |
LIG_SH2_SRC | 66 | 69 | PF00017 | 0.354 |
LIG_SH2_SRC | 662 | 665 | PF00017 | 0.412 |
LIG_SH2_STAP1 | 237 | 241 | PF00017 | 0.402 |
LIG_SH2_STAP1 | 263 | 267 | PF00017 | 0.412 |
LIG_SH2_STAP1 | 749 | 753 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 930 | 934 | PF00017 | 0.519 |
LIG_SH2_STAT3 | 749 | 752 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 785 | 788 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 809 | 812 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 930 | 933 | PF00017 | 0.526 |
LIG_SH3_1 | 337 | 343 | PF00018 | 0.402 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.412 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.402 |
LIG_SH3_3 | 544 | 550 | PF00018 | 0.429 |
LIG_SH3_4 | 775 | 782 | PF00018 | 0.370 |
LIG_SUMO_SIM_anti_2 | 416 | 422 | PF11976 | 0.435 |
LIG_SUMO_SIM_par_1 | 276 | 284 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 397 | 404 | PF11976 | 0.412 |
LIG_SUMO_SIM_par_1 | 486 | 491 | PF11976 | 0.470 |
LIG_SUMO_SIM_par_1 | 543 | 549 | PF11976 | 0.402 |
LIG_TRAF2_1 | 431 | 434 | PF00917 | 0.412 |
LIG_TRAF2_1 | 69 | 72 | PF00917 | 0.462 |
LIG_TRAF2_1 | 715 | 718 | PF00917 | 0.459 |
LIG_TRFH_1 | 291 | 295 | PF08558 | 0.224 |
LIG_TYR_ITIM | 254 | 259 | PF00017 | 0.236 |
LIG_TYR_ITIM | 348 | 353 | PF00017 | 0.161 |
LIG_UBA3_1 | 487 | 492 | PF00899 | 0.251 |
LIG_UBA3_1 | 519 | 528 | PF00899 | 0.236 |
LIG_WRC_WIRS_1 | 288 | 293 | PF05994 | 0.382 |
LIG_WW_3 | 28 | 32 | PF00397 | 0.712 |
MOD_CDC14_SPxK_1 | 404 | 407 | PF00782 | 0.161 |
MOD_CDK_SPxK_1 | 401 | 407 | PF00069 | 0.161 |
MOD_CDK_SPxxK_3 | 490 | 497 | PF00069 | 0.382 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.734 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.672 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.251 |
MOD_CK1_1 | 870 | 876 | PF00069 | 0.350 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.251 |
MOD_CK1_1 | 935 | 941 | PF00069 | 0.433 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.579 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.270 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.332 |
MOD_CK2_1 | 621 | 627 | PF00069 | 0.236 |
MOD_CK2_1 | 712 | 718 | PF00069 | 0.442 |
MOD_CK2_1 | 739 | 745 | PF00069 | 0.508 |
MOD_CK2_1 | 761 | 767 | PF00069 | 0.582 |
MOD_CK2_1 | 870 | 876 | PF00069 | 0.350 |
MOD_CK2_1 | 882 | 888 | PF00069 | 0.402 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.382 |
MOD_Cter_Amidation | 10 | 13 | PF01082 | 0.595 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.602 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.593 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.385 |
MOD_GlcNHglycan | 645 | 648 | PF01048 | 0.251 |
MOD_GlcNHglycan | 872 | 875 | PF01048 | 0.365 |
MOD_GlcNHglycan | 911 | 914 | PF01048 | 0.413 |
MOD_GlcNHglycan | 944 | 947 | PF01048 | 0.497 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.236 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.272 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.236 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.270 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.204 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.236 |
MOD_GSK3_1 | 712 | 719 | PF00069 | 0.488 |
MOD_GSK3_1 | 756 | 763 | PF00069 | 0.582 |
MOD_GSK3_1 | 850 | 857 | PF00069 | 0.294 |
MOD_GSK3_1 | 863 | 870 | PF00069 | 0.265 |
MOD_GSK3_1 | 882 | 889 | PF00069 | 0.402 |
MOD_GSK3_1 | 928 | 935 | PF00069 | 0.393 |
MOD_N-GLC_1 | 565 | 570 | PF02516 | 0.159 |
MOD_N-GLC_1 | 672 | 677 | PF02516 | 0.235 |
MOD_N-GLC_1 | 738 | 743 | PF02516 | 0.426 |
MOD_N-GLC_1 | 932 | 937 | PF02516 | 0.410 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.575 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.374 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.245 |
MOD_NEK2_1 | 581 | 586 | PF00069 | 0.236 |
MOD_NEK2_1 | 756 | 761 | PF00069 | 0.409 |
MOD_NEK2_1 | 788 | 793 | PF00069 | 0.382 |
MOD_NEK2_1 | 863 | 868 | PF00069 | 0.301 |
MOD_NEK2_2 | 565 | 570 | PF00069 | 0.382 |
MOD_NEK2_2 | 854 | 859 | PF00069 | 0.251 |
MOD_NEK2_2 | 900 | 905 | PF00069 | 0.367 |
MOD_PIKK_1 | 552 | 558 | PF00454 | 0.236 |
MOD_PIKK_1 | 863 | 869 | PF00454 | 0.311 |
MOD_PIKK_1 | 915 | 921 | PF00454 | 0.459 |
MOD_PIKK_1 | 932 | 938 | PF00454 | 0.371 |
MOD_PKA_1 | 469 | 475 | PF00069 | 0.498 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.762 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.277 |
MOD_PKA_2 | 370 | 376 | PF00069 | 0.341 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.300 |
MOD_PKA_2 | 468 | 474 | PF00069 | 0.386 |
MOD_PKA_2 | 573 | 579 | PF00069 | 0.236 |
MOD_PKA_2 | 621 | 627 | PF00069 | 0.262 |
MOD_PKA_2 | 756 | 762 | PF00069 | 0.468 |
MOD_PKA_2 | 795 | 801 | PF00069 | 0.236 |
MOD_PKA_2 | 832 | 838 | PF00069 | 0.270 |
MOD_PKB_1 | 5 | 13 | PF00069 | 0.479 |
MOD_PKB_1 | 726 | 734 | PF00069 | 0.308 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.750 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.339 |
MOD_Plk_1 | 248 | 254 | PF00069 | 0.155 |
MOD_Plk_1 | 565 | 571 | PF00069 | 0.382 |
MOD_Plk_1 | 620 | 626 | PF00069 | 0.251 |
MOD_Plk_1 | 716 | 722 | PF00069 | 0.638 |
MOD_Plk_1 | 728 | 734 | PF00069 | 0.446 |
MOD_Plk_1 | 761 | 767 | PF00069 | 0.616 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.281 |
MOD_Plk_2-3 | 615 | 621 | PF00069 | 0.236 |
MOD_Plk_2-3 | 845 | 851 | PF00069 | 0.382 |
MOD_Plk_2-3 | 90 | 96 | PF00069 | 0.382 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.270 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.240 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.277 |
MOD_Plk_4 | 395 | 401 | PF00069 | 0.251 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.328 |
MOD_Plk_4 | 827 | 833 | PF00069 | 0.236 |
MOD_Plk_4 | 854 | 860 | PF00069 | 0.301 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.236 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.161 |
MOD_ProDKin_1 | 490 | 496 | PF00069 | 0.382 |
MOD_ProDKin_1 | 673 | 679 | PF00069 | 0.246 |
MOD_SUMO_rev_2 | 233 | 241 | PF00179 | 0.277 |
MOD_SUMO_rev_2 | 507 | 516 | PF00179 | 0.236 |
TRG_DiLeu_BaEn_1 | 597 | 602 | PF01217 | 0.236 |
TRG_DiLeu_BaEn_1 | 717 | 722 | PF01217 | 0.513 |
TRG_DiLeu_BaEn_2 | 472 | 478 | PF01217 | 0.370 |
TRG_DiLeu_BaEn_4 | 121 | 127 | PF01217 | 0.284 |
TRG_DiLeu_BaEn_4 | 52 | 58 | PF01217 | 0.378 |
TRG_DiLeu_BaEn_4 | 717 | 723 | PF01217 | 0.592 |
TRG_DiLeu_BaLyEn_6 | 444 | 449 | PF01217 | 0.364 |
TRG_DiLeu_BaLyEn_6 | 950 | 955 | PF01217 | 0.506 |
TRG_DiLeu_LyEn_5 | 717 | 722 | PF01217 | 0.513 |
TRG_DiLeu_LyEn_5 | 888 | 893 | PF01217 | 0.396 |
TRG_ENDOCYTIC_2 | 256 | 259 | PF00928 | 0.236 |
TRG_ENDOCYTIC_2 | 263 | 266 | PF00928 | 0.236 |
TRG_ENDOCYTIC_2 | 288 | 291 | PF00928 | 0.238 |
TRG_ENDOCYTIC_2 | 297 | 300 | PF00928 | 0.232 |
TRG_ENDOCYTIC_2 | 342 | 345 | PF00928 | 0.236 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.242 |
TRG_ENDOCYTIC_2 | 785 | 788 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 809 | 812 | PF00928 | 0.236 |
TRG_ENDOCYTIC_2 | 952 | 955 | PF00928 | 0.395 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.343 |
TRG_ER_diArg_1 | 12 | 15 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 214 | 216 | PF00400 | 0.341 |
TRG_ER_diArg_1 | 30 | 32 | PF00400 | 0.492 |
TRG_ER_diArg_1 | 336 | 338 | PF00400 | 0.236 |
TRG_ER_diArg_1 | 468 | 470 | PF00400 | 0.348 |
TRG_ER_diArg_1 | 484 | 487 | PF00400 | 0.201 |
TRG_ER_diArg_1 | 496 | 498 | PF00400 | 0.235 |
TRG_ER_diArg_1 | 732 | 735 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 893 | 896 | PF00400 | 0.509 |
TRG_ER_FFAT_2 | 923 | 935 | PF00635 | 0.440 |
TRG_NES_CRM1_1 | 683 | 698 | PF08389 | 0.251 |
TRG_NLS_MonoCore_2 | 11 | 16 | PF00514 | 0.666 |
TRG_NLS_MonoExtC_3 | 11 | 16 | PF00514 | 0.666 |
TRG_NLS_MonoExtN_4 | 12 | 17 | PF00514 | 0.692 |
TRG_Pf-PMV_PEXEL_1 | 124 | 128 | PF00026 | 0.316 |
TRG_Pf-PMV_PEXEL_1 | 168 | 172 | PF00026 | 0.489 |
TRG_Pf-PMV_PEXEL_1 | 498 | 502 | PF00026 | 0.382 |
TRG_Pf-PMV_PEXEL_1 | 720 | 725 | PF00026 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 754 | 758 | PF00026 | 0.530 |
TRG_Pf-PMV_PEXEL_1 | 953 | 957 | PF00026 | 0.503 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P860 | Leptomonas seymouri | 86% | 98% |
A0A0N1I383 | Leptomonas seymouri | 32% | 95% |
A0A0S4IK09 | Bodo saltans | 63% | 98% |
A0A1X0NNF6 | Trypanosomatidae | 30% | 100% |
A0A1X0NT66 | Trypanosomatidae | 31% | 100% |
A0A1X0NZT6 | Trypanosomatidae | 76% | 100% |
A0A3Q8IAX4 | Leishmania donovani | 92% | 100% |
A0A3Q8IQ79 | Leishmania donovani | 29% | 100% |
A0A3R7K9K0 | Trypanosoma rangeli | 32% | 100% |
A0A3R7NBN0 | Trypanosoma rangeli | 75% | 100% |
A0A3S5H7S8 | Leishmania donovani | 34% | 100% |
A0A3S7WQI8 | Leishmania donovani | 30% | 100% |
A0A3S7WY81 | Leishmania donovani | 30% | 100% |
A0A3S7X726 | Leishmania donovani | 32% | 100% |
A0A422NDD9 | Trypanosoma rangeli | 30% | 100% |
A0A422NZW3 | Trypanosoma rangeli | 30% | 100% |
A4FUD9 | Bos taurus | 33% | 100% |
A4H5K0 | Leishmania braziliensis | 32% | 100% |
A4HDE7 | Leishmania braziliensis | 31% | 100% |
A4HKT9 | Leishmania braziliensis | 34% | 100% |
A4HLY1 | Leishmania braziliensis | 32% | 100% |
A4HNF5 | Leishmania braziliensis | 28% | 100% |
A4HTX2 | Leishmania infantum | 30% | 100% |
A4I0T0 | Leishmania infantum | 30% | 100% |
A4I3G2 | Leishmania infantum | 92% | 100% |
A4I8B8 | Leishmania infantum | 34% | 100% |
A4I9B0 | Leishmania infantum | 32% | 100% |
A4IC27 | Leishmania infantum | 29% | 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% |
E9AFW6 | Leishmania major | 29% | 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) | 92% | 100% |
E9B377 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
E9B4B0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
F1M5F3 | Rattus norvegicus | 31% | 86% |
P25205 | Homo sapiens | 33% | 100% |
P25206 | Mus musculus | 32% | 100% |
P29469 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 47% | 100% |
P30666 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 100% |
P40377 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 43% | 100% |
P49731 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 100% |
P49735 | Drosophila melanogaster | 45% | 100% |
P49736 | Homo sapiens | 45% | 100% |
P55861 | Xenopus laevis | 40% | 100% |
P97310 | Mus musculus | 44% | 100% |
Q0DHC4 | Oryza sativa subsp. japonica | 34% | 100% |
Q21902 | Caenorhabditis elegans | 30% | 100% |
Q28BS0 | Xenopus tropicalis | 35% | 100% |
Q29JI9 | Drosophila pseudoobscura pseudoobscura | 31% | 100% |
Q2KHI9 | Mus musculus | 31% | 86% |
Q2R482 | Oryza sativa subsp. japonica | 42% | 100% |
Q43704 | Zea mays | 35% | 100% |
Q4Q3R6 | Leishmania major | 32% | 100% |
Q4Q8I2 | Leishmania major | 92% | 100% |
Q4QAP2 | Leishmania major | 30% | 100% |
Q4QI01 | Leishmania major | 30% | 100% |
Q54CP4 | Dictyostelium discoideum | 32% | 100% |
Q5R8G6 | Pongo abelii | 33% | 100% |
Q6DIH3 | Xenopus tropicalis | 42% | 100% |
Q6NRM6 | Xenopus laevis | 30% | 85% |
Q7ZXZ0 | Xenopus laevis | 35% | 100% |
Q9LPD9 | Arabidopsis thaliana | 45% | 100% |
Q9NXL9 | Homo sapiens | 30% | 85% |
Q9SX03 | Zea mays | 34% | 100% |
Q9SX04 | Zea mays | 34% | 100% |
Q9U1E0 | Leishmania major | 32% | 100% |
Q9UXG1 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 33% | 100% |
Q9V461 | Drosophila melanogaster | 32% | 100% |
Q9VGW6 | Drosophila melanogaster | 31% | 100% |
V5BQA9 | Trypanosoma cruzi | 80% | 100% |
V5BSG2 | Trypanosoma cruzi | 30% | 100% |