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:0032991 | protein-containing complex | 1 | 2 |
GO:0042575 | DNA polymerase complex | 3 | 2 |
GO:0043625 | delta DNA polymerase complex | 3 | 2 |
GO:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:0140535 | intracellular protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1990234 | transferase complex | 3 | 2 |
GO:0005634 | nucleus | 5 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: Q4Q418
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006260 | DNA replication | 5 | 12 |
GO:0006261 | DNA-templated DNA replication | 6 | 2 |
GO:0006281 | DNA repair | 5 | 2 |
GO:0006287 | base-excision repair, gap-filling | 5 | 2 |
GO:0006297 | nucleotide-excision repair, DNA gap filling | 5 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006950 | response to stress | 2 | 2 |
GO:0006974 | DNA damage response | 4 | 2 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 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:0045004 | DNA replication proofreading | 6 | 2 |
GO:0045005 | DNA-templated DNA replication maintenance of fidelity | 5 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0003887 | DNA-directed DNA polymerase activity | 5 | 12 |
GO:0004518 | nuclease activity | 4 | 2 |
GO:0004527 | exonuclease activity | 5 | 2 |
GO:0004529 | DNA exonuclease activity | 5 | 2 |
GO:0004536 | DNA nuclease activity | 4 | 2 |
GO:0005488 | binding | 1 | 12 |
GO:0008296 | 3'-5'-DNA exonuclease activity | 7 | 2 |
GO:0008408 | 3'-5' exonuclease activity | 6 | 2 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016779 | nucleotidyltransferase activity | 4 | 12 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 2 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 2 |
GO:0016895 | DNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 2 |
GO:0034061 | DNA polymerase activity | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0051536 | iron-sulfur cluster binding | 3 | 12 |
GO:0051539 | 4 iron, 4 sulfur cluster binding | 4 | 12 |
GO:0051540 | metal cluster binding | 2 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 751 | 755 | PF00656 | 0.299 |
CLV_MEL_PAP_1 | 1022 | 1028 | PF00089 | 0.415 |
CLV_NRD_NRD_1 | 1008 | 1010 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.365 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 489 | 491 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 595 | 597 | PF00675 | 0.323 |
CLV_NRD_NRD_1 | 762 | 764 | PF00675 | 0.308 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 737 | 739 | PF00082 | 0.295 |
CLV_PCSK_KEX2_1 | 762 | 764 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 970 | 972 | PF00082 | 0.306 |
CLV_PCSK_PC1ET2_1 | 737 | 739 | PF00082 | 0.295 |
CLV_PCSK_PC1ET2_1 | 970 | 972 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 280 | 284 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 443 | 447 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 578 | 582 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 685 | 689 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 718 | 722 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 857 | 861 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 932 | 936 | PF00082 | 0.497 |
DEG_SPOP_SBC_1 | 206 | 210 | PF00917 | 0.326 |
DOC_CYCLIN_RxL_1 | 144 | 154 | PF00134 | 0.324 |
DOC_CYCLIN_yClb1_LxF_4 | 719 | 724 | PF00134 | 0.308 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 660 | 668 | PF00134 | 0.429 |
DOC_CYCLIN_yCln2_LP_2 | 552 | 558 | PF00134 | 0.455 |
DOC_MAPK_DCC_7 | 127 | 137 | PF00069 | 0.429 |
DOC_MAPK_DCC_7 | 48 | 57 | PF00069 | 0.456 |
DOC_MAPK_FxFP_2 | 329 | 332 | PF00069 | 0.308 |
DOC_MAPK_gen_1 | 120 | 126 | PF00069 | 0.429 |
DOC_MAPK_gen_1 | 46 | 54 | PF00069 | 0.517 |
DOC_MAPK_gen_1 | 490 | 499 | PF00069 | 0.324 |
DOC_MAPK_gen_1 | 695 | 704 | PF00069 | 0.325 |
DOC_MAPK_JIP1_4 | 718 | 724 | PF00069 | 0.332 |
DOC_MAPK_MEF2A_6 | 443 | 451 | PF00069 | 0.337 |
DOC_MAPK_MEF2A_6 | 48 | 57 | PF00069 | 0.396 |
DOC_MAPK_MEF2A_6 | 726 | 734 | PF00069 | 0.303 |
DOC_MAPK_RevD_3 | 582 | 597 | PF00069 | 0.308 |
DOC_PP1_RVXF_1 | 22 | 29 | PF00149 | 0.393 |
DOC_PP1_RVXF_1 | 719 | 725 | PF00149 | 0.308 |
DOC_PP2B_LxvP_1 | 15 | 18 | PF13499 | 0.474 |
DOC_PP2B_LxvP_1 | 497 | 500 | PF13499 | 0.365 |
DOC_PP2B_LxvP_1 | 891 | 894 | PF13499 | 0.324 |
DOC_PP2B_PxIxI_1 | 259 | 265 | PF00149 | 0.308 |
DOC_PP2B_PxIxI_1 | 538 | 544 | PF00149 | 0.324 |
DOC_PP4_FxxP_1 | 202 | 205 | PF00568 | 0.339 |
DOC_PP4_FxxP_1 | 253 | 256 | PF00568 | 0.324 |
DOC_PP4_FxxP_1 | 329 | 332 | PF00568 | 0.305 |
DOC_PP4_FxxP_1 | 716 | 719 | PF00568 | 0.308 |
DOC_SPAK_OSR1_1 | 1025 | 1029 | PF12202 | 0.425 |
DOC_SPAK_OSR1_1 | 181 | 185 | PF12202 | 0.308 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.488 |
DOC_USP7_MATH_1 | 607 | 611 | PF00917 | 0.324 |
DOC_USP7_MATH_2 | 40 | 46 | PF00917 | 0.505 |
DOC_USP7_UBL2_3 | 1010 | 1014 | PF12436 | 0.403 |
DOC_USP7_UBL2_3 | 364 | 368 | PF12436 | 0.343 |
DOC_USP7_UBL2_3 | 491 | 495 | PF12436 | 0.343 |
DOC_USP7_UBL2_3 | 691 | 695 | PF12436 | 0.371 |
DOC_USP7_UBL2_3 | 752 | 756 | PF12436 | 0.308 |
DOC_USP7_UBL2_3 | 814 | 818 | PF12436 | 0.308 |
DOC_USP7_UBL2_3 | 966 | 970 | PF12436 | 0.308 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.365 |
DOC_WW_Pin1_4 | 566 | 571 | PF00397 | 0.308 |
LIG_14-3-3_CanoR_1 | 120 | 124 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 149 | 157 | PF00244 | 0.314 |
LIG_14-3-3_CanoR_1 | 167 | 173 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 399 | 404 | PF00244 | 0.308 |
LIG_14-3-3_CanoR_1 | 46 | 55 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 568 | 576 | PF00244 | 0.455 |
LIG_Actin_WH2_2 | 328 | 344 | PF00022 | 0.429 |
LIG_Actin_WH2_2 | 608 | 626 | PF00022 | 0.308 |
LIG_APCC_ABBAyCdc20_2 | 249 | 255 | PF00400 | 0.343 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.633 |
LIG_BIR_III_4 | 754 | 758 | PF00653 | 0.295 |
LIG_BRCT_BRCA1_1 | 343 | 347 | PF00533 | 0.467 |
LIG_BRCT_BRCA1_1 | 406 | 410 | PF00533 | 0.410 |
LIG_BRCT_BRCA1_1 | 571 | 575 | PF00533 | 0.455 |
LIG_BRCT_BRCA1_1 | 712 | 716 | PF00533 | 0.333 |
LIG_BRCT_BRCA1_1 | 90 | 94 | PF00533 | 0.385 |
LIG_BRCT_BRCA1_2 | 571 | 577 | PF00533 | 0.455 |
LIG_BRCT_BRCA1_2 | 712 | 718 | PF00533 | 0.350 |
LIG_eIF4E_1 | 728 | 734 | PF01652 | 0.308 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.349 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.311 |
LIG_FHA_1 | 569 | 575 | PF00498 | 0.472 |
LIG_FHA_1 | 659 | 665 | PF00498 | 0.324 |
LIG_FHA_1 | 677 | 683 | PF00498 | 0.306 |
LIG_FHA_1 | 913 | 919 | PF00498 | 0.431 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.324 |
LIG_FHA_2 | 514 | 520 | PF00498 | 0.336 |
LIG_FHA_2 | 743 | 749 | PF00498 | 0.324 |
LIG_FHA_2 | 794 | 800 | PF00498 | 0.299 |
LIG_FHA_2 | 844 | 850 | PF00498 | 0.365 |
LIG_Integrin_isoDGR_2 | 617 | 619 | PF01839 | 0.308 |
LIG_IRF3_LxIS_1 | 641 | 647 | PF10401 | 0.429 |
LIG_IRF3_LxIS_1 | 801 | 808 | PF10401 | 0.308 |
LIG_LIR_Apic_2 | 713 | 719 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 191 | 201 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 230 | 239 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 25 | 32 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 374 | 380 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 531 | 542 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 63 | 72 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 723 | 732 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 747 | 758 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 75 | 84 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 1024 | 1029 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 191 | 196 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 197 | 201 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 230 | 234 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 25 | 31 | PF02991 | 0.153 |
LIG_LIR_Nem_3 | 330 | 334 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 374 | 378 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 444 | 449 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 531 | 537 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 579 | 584 | PF02991 | 0.324 |
LIG_LIR_Nem_3 | 610 | 616 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 63 | 68 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 7 | 12 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 723 | 727 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 747 | 753 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 75 | 80 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 962 | 967 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 975 | 981 | PF02991 | 0.308 |
LIG_LYPXL_S_1 | 537 | 541 | PF13949 | 0.308 |
LIG_LYPXL_yS_3 | 538 | 541 | PF13949 | 0.308 |
LIG_MYND_3 | 641 | 645 | PF01753 | 0.308 |
LIG_NRBOX | 147 | 153 | PF00104 | 0.324 |
LIG_NRBOX | 588 | 594 | PF00104 | 0.324 |
LIG_PCNA_yPIPBox_3 | 478 | 488 | PF02747 | 0.324 |
LIG_Pex14_1 | 86 | 90 | PF04695 | 0.214 |
LIG_Pex14_2 | 178 | 182 | PF04695 | 0.303 |
LIG_PTB_Apo_2 | 325 | 332 | PF02174 | 0.324 |
LIG_PTB_Apo_2 | 369 | 376 | PF02174 | 0.308 |
LIG_PTB_Phospho_1 | 369 | 375 | PF10480 | 0.308 |
LIG_SH2_CRK | 525 | 529 | PF00017 | 0.324 |
LIG_SH2_CRK | 549 | 553 | PF00017 | 0.308 |
LIG_SH2_CRK | 613 | 617 | PF00017 | 0.308 |
LIG_SH2_CRK | 739 | 743 | PF00017 | 0.308 |
LIG_SH2_CRK | 964 | 968 | PF00017 | 0.308 |
LIG_SH2_NCK_1 | 90 | 94 | PF00017 | 0.222 |
LIG_SH2_NCK_1 | 974 | 978 | PF00017 | 0.308 |
LIG_SH2_PTP2 | 853 | 856 | PF00017 | 0.324 |
LIG_SH2_SRC | 853 | 856 | PF00017 | 0.324 |
LIG_SH2_SRC | 886 | 889 | PF00017 | 0.308 |
LIG_SH2_STAP1 | 299 | 303 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 549 | 553 | PF00017 | 0.308 |
LIG_SH2_STAP1 | 90 | 94 | PF00017 | 0.239 |
LIG_SH2_STAP1 | 974 | 978 | PF00017 | 0.308 |
LIG_SH2_STAT3 | 653 | 656 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 728 | 731 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 853 | 856 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 873 | 876 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 886 | 889 | PF00017 | 0.308 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.308 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.308 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.324 |
LIG_SH3_3 | 514 | 520 | PF00018 | 0.308 |
LIG_SH3_3 | 724 | 730 | PF00018 | 0.297 |
LIG_SH3_5 | 227 | 231 | PF00018 | 0.429 |
LIG_SUMO_SIM_par_1 | 238 | 243 | PF11976 | 0.308 |
LIG_TYR_ITIM | 547 | 552 | PF00017 | 0.308 |
LIG_TYR_ITIM | 611 | 616 | PF00017 | 0.308 |
LIG_TYR_ITIM | 851 | 856 | PF00017 | 0.324 |
LIG_UBA3_1 | 282 | 286 | PF00899 | 0.308 |
LIG_WRC_WIRS_1 | 169 | 174 | PF05994 | 0.343 |
MOD_CDC14_SPxK_1 | 204 | 207 | PF00782 | 0.408 |
MOD_CDK_SPxK_1 | 201 | 207 | PF00069 | 0.408 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.452 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.385 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.320 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.428 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.567 |
MOD_CK1_1 | 402 | 408 | PF00069 | 0.363 |
MOD_CK1_1 | 421 | 427 | PF00069 | 0.268 |
MOD_CK1_1 | 569 | 575 | PF00069 | 0.408 |
MOD_CK1_1 | 626 | 632 | PF00069 | 0.316 |
MOD_CK1_1 | 785 | 791 | PF00069 | 0.352 |
MOD_CK1_1 | 843 | 849 | PF00069 | 0.393 |
MOD_CK1_1 | 921 | 927 | PF00069 | 0.507 |
MOD_CK2_1 | 298 | 304 | PF00069 | 0.285 |
MOD_CK2_1 | 690 | 696 | PF00069 | 0.343 |
MOD_CK2_1 | 785 | 791 | PF00069 | 0.299 |
MOD_CK2_1 | 814 | 820 | PF00069 | 0.324 |
MOD_Cter_Amidation | 247 | 250 | PF01082 | 0.308 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.603 |
MOD_GlcNHglycan | 625 | 628 | PF01048 | 0.308 |
MOD_GlcNHglycan | 645 | 649 | PF01048 | 0.393 |
MOD_GlcNHglycan | 773 | 776 | PF01048 | 0.308 |
MOD_GlcNHglycan | 787 | 790 | PF01048 | 0.295 |
MOD_GlcNHglycan | 842 | 845 | PF01048 | 0.308 |
MOD_GlcNHglycan | 920 | 923 | PF01048 | 0.478 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.368 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.249 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.369 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.494 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.341 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.308 |
MOD_GSK3_1 | 644 | 651 | PF00069 | 0.303 |
MOD_GSK3_1 | 810 | 817 | PF00069 | 0.320 |
MOD_GSK3_1 | 976 | 983 | PF00069 | 0.324 |
MOD_N-GLC_1 | 103 | 108 | PF02516 | 0.415 |
MOD_N-GLC_2 | 266 | 268 | PF02516 | 0.324 |
MOD_N-GLC_2 | 325 | 327 | PF02516 | 0.365 |
MOD_N-GLC_2 | 546 | 548 | PF02516 | 0.308 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.626 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.396 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.429 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.324 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.308 |
MOD_NEK2_1 | 623 | 628 | PF00069 | 0.308 |
MOD_NEK2_1 | 644 | 649 | PF00069 | 0.308 |
MOD_NEK2_1 | 742 | 747 | PF00069 | 0.308 |
MOD_NEK2_1 | 805 | 810 | PF00069 | 0.308 |
MOD_NEK2_2 | 757 | 762 | PF00069 | 0.308 |
MOD_PIKK_1 | 4 | 10 | PF00454 | 0.529 |
MOD_PIKK_1 | 404 | 410 | PF00454 | 0.405 |
MOD_PIKK_1 | 88 | 94 | PF00454 | 0.365 |
MOD_PIKK_1 | 880 | 886 | PF00454 | 0.308 |
MOD_PIKK_1 | 976 | 982 | PF00454 | 0.311 |
MOD_PK_1 | 238 | 244 | PF00069 | 0.314 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.324 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.416 |
MOD_PKA_2 | 465 | 471 | PF00069 | 0.338 |
MOD_PKA_2 | 47 | 53 | PF00069 | 0.518 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.390 |
MOD_Plk_1 | 355 | 361 | PF00069 | 0.301 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.343 |
MOD_Plk_2-3 | 513 | 519 | PF00069 | 0.324 |
MOD_Plk_2-3 | 690 | 696 | PF00069 | 0.365 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.337 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.475 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.395 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.429 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.410 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.308 |
MOD_Plk_4 | 533 | 539 | PF00069 | 0.125 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.308 |
MOD_Plk_4 | 626 | 632 | PF00069 | 0.308 |
MOD_Plk_4 | 678 | 684 | PF00069 | 0.308 |
MOD_Plk_4 | 904 | 910 | PF00069 | 0.415 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.365 |
MOD_ProDKin_1 | 566 | 572 | PF00069 | 0.308 |
MOD_SUMO_for_1 | 576 | 579 | PF00179 | 0.301 |
MOD_SUMO_for_1 | 720 | 723 | PF00179 | 0.324 |
MOD_SUMO_rev_2 | 356 | 365 | PF00179 | 0.324 |
MOD_SUMO_rev_2 | 610 | 616 | PF00179 | 0.329 |
MOD_SUMO_rev_2 | 748 | 758 | PF00179 | 0.310 |
TRG_DiLeu_BaEn_1 | 1018 | 1023 | PF01217 | 0.401 |
TRG_DiLeu_BaEn_1 | 302 | 307 | PF01217 | 0.320 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.381 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 375 | 378 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 538 | 541 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 549 | 552 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 613 | 616 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 731 | 734 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 739 | 742 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 853 | 856 | PF00928 | 0.324 |
TRG_ENDOCYTIC_2 | 964 | 967 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 974 | 977 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 978 | 981 | PF00928 | 0.308 |
TRG_ER_diArg_1 | 434 | 436 | PF00400 | 0.370 |
TRG_ER_diArg_1 | 761 | 763 | PF00400 | 0.308 |
TRG_ER_diArg_1 | 836 | 839 | PF00400 | 0.310 |
TRG_NLS_MonoExtN_4 | 491 | 498 | PF00514 | 0.455 |
TRG_Pf-PMV_PEXEL_1 | 1014 | 1018 | PF00026 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 149 | 154 | PF00026 | 0.343 |
TRG_Pf-PMV_PEXEL_1 | 181 | 185 | PF00026 | 0.324 |
TRG_Pf-PMV_PEXEL_1 | 238 | 243 | PF00026 | 0.296 |
TRG_Pf-PMV_PEXEL_1 | 383 | 387 | PF00026 | 0.324 |
TRG_Pf-PMV_PEXEL_1 | 662 | 666 | PF00026 | 0.322 |
TRG_Pf-PMV_PEXEL_1 | 673 | 678 | PF00026 | 0.324 |
TRG_Pf-PMV_PEXEL_1 | 96 | 100 | PF00026 | 0.429 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P846 | Leptomonas seymouri | 90% | 100% |
A0A0N1I597 | Leptomonas seymouri | 26% | 77% |
A0A0S4J863 | Bodo saltans | 73% | 95% |
A0A1X0P2A8 | Trypanosomatidae | 82% | 100% |
A0A3S5H6Z2 | Leishmania donovani | 25% | 77% |
A0A3S7X6W2 | Leishmania donovani | 98% | 100% |
A0A422N236 | Trypanosoma rangeli | 79% | 100% |
A4HLN0 | Leishmania braziliensis | 95% | 100% |
A4HX52 | Leishmania infantum | 25% | 77% |
A4I965 | Leishmania infantum | 98% | 100% |
A7U6F2 | Pyramimonas orientalis virus | 30% | 86% |
C9ZIW0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 74% | 100% |
E9AQW7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 77% |
E9B406 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
O00874 | Leishmania donovani | 25% | 77% |
O05706 | Saccharolobus shibatae | 22% | 100% |
O29753 | Archaeoglobus fulgidus (strain ATCC 49558 / DSM 4304 / JCM 9628 / NBRC 100126 / VC-16) | 26% | 100% |
O36363 | Alcelaphine herpesvirus 1 (strain C500) | 31% | 100% |
O48901 | Glycine max | 54% | 95% |
O54747 | Rattus norvegicus | 54% | 94% |
O70736 | Red sea bream iridovirus | 25% | 100% |
O71121 | Rhesus cytomegalovirus (strain 68-1) | 29% | 100% |
O89042 | Rattus norvegicus | 26% | 71% |
O93746 | Aeropyrum pernix (strain ATCC 700893 / DSM 11879 / JCM 9820 / NBRC 100138 / K1) | 27% | 100% |
P03198 | Epstein-Barr virus (strain B95-8) | 32% | 100% |
P04292 | Human herpesvirus 1 (strain KOS) | 28% | 84% |
P04293 | Human herpesvirus 1 (strain 17) | 28% | 84% |
P07917 | Human herpesvirus 1 (strain Angelotti) | 28% | 84% |
P07918 | Human herpesvirus 2 (strain 186) | 28% | 83% |
P09252 | Varicella-zoster virus (strain Dumas) | 27% | 86% |
P09854 | Human herpesvirus 1 (strain SC16) | 28% | 84% |
P09884 | Homo sapiens | 26% | 71% |
P0C971 | African swine fever virus (isolate Tick/South Africa/Pretoriuskop Pr4/1996) | 23% | 86% |
P0C972 | African swine fever virus (isolate Tick/Malawi/Lil 20-1/1983) | 23% | 86% |
P0C973 | African swine fever virus (isolate Warthog/Namibia/Wart80/1980) | 23% | 86% |
P0C974 | African swine fever virus (isolate Pig/Kenya/KEN-50/1950) | 23% | 86% |
P0CL76 | Pyrococcus abyssi | 30% | 100% |
P0CL77 | Pyrococcus abyssi (strain GE5 / Orsay) | 30% | 100% |
P13382 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 70% |
P14284 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 27% | 69% |
P15436 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 47% | 94% |
P24907 | Saimiriine herpesvirus 2 (strain 11) | 31% | 100% |
P26019 | Drosophila melanogaster | 24% | 69% |
P26811 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 25% | 100% |
P27172 | Murid herpesvirus 1 (strain Smith) | 28% | 94% |
P28040 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 23% | 73% |
P28339 | Bos taurus | 53% | 93% |
P28340 | Homo sapiens | 54% | 93% |
P28857 | Human herpesvirus 6A (strain Uganda-1102) | 29% | 100% |
P28858 | Equine herpesvirus 1 (strain Ab4p) | 29% | 85% |
P30315 | Plasmodium falciparum (isolate K1 / Thailand) | 45% | 94% |
P30316 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 50% | 95% |
P30320 | Paramecium bursaria Chlorella virus NY2A | 31% | 100% |
P30321 | Paramecium bursaria Chlorella virus 1 | 32% | 100% |
P33609 | Mus musculus | 26% | 70% |
P42489 | African swine fever virus (strain Badajoz 1971 Vero-adapted) | 23% | 85% |
P43139 | African swine fever virus (isolate Pig/Portugal/Lis 60/1960) | 23% | 83% |
P46588 | Candida albicans | 49% | 99% |
P52025 | Methanococcus voltae | 23% | 100% |
P52342 | Human herpesvirus 7 (strain JI) | 29% | 100% |
P52367 | Equine herpesvirus 2 (strain 86/87) | 30% | 100% |
P52431 | Mus musculus | 54% | 93% |
P54358 | Drosophila melanogaster | 50% | 95% |
P56689 | Thermococcus gorgonarius | 29% | 100% |
P61875 | Pyrococcus furiosus (strain ATCC 43587 / DSM 3638 / JCM 8422 / Vc1) | 28% | 100% |
P61876 | Pyrococcus woesei | 28% | 100% |
P89453 | Human herpesvirus 2 (strain HG52) | 28% | 83% |
P90829 | Caenorhabditis elegans | 48% | 95% |
P95690 | Sulfolobus acidocaldarius (strain ATCC 33909 / DSM 639 / JCM 8929 / NBRC 15157 / NCIMB 11770) | 24% | 100% |
P95979 | Saccharolobus solfataricus (strain ATCC 35092 / DSM 1617 / JCM 11322 / P2) | 20% | 100% |
P97283 | Mesocricetus auratus | 54% | 94% |
Q196U0 | Invertebrate iridescent virus 3 | 28% | 90% |
Q1HVC1 | Epstein-Barr virus (strain AG876) | 33% | 100% |
Q2HRD0 | Human herpesvirus 8 type P (isolate GK18) | 31% | 100% |
Q38087 | Escherichia phage RB69 | 23% | 100% |
Q3KSP1 | Epstein-Barr virus (strain GD1) | 33% | 100% |
Q4JQU7 | Varicella-zoster virus (strain Oka vaccine) | 27% | 86% |
Q4QEL1 | Leishmania major | 25% | 77% |
Q54N97 | Dictyostelium discoideum | 47% | 93% |
Q69025 | Guinea pig cytomegalovirus (strain 22122) | 30% | 92% |
Q6S6P1 | Equine herpesvirus 1 (strain V592) | 29% | 85% |
Q6UDK1 | Psittacid herpesvirus 1 (isolate Amazon parrot/-/97-0001/1997) | 29% | 95% |
Q9DE46 | Xenopus laevis | 25% | 71% |
Q9DKT8 | Elephantid herpesvirus 1 (isolate Asian elephant/Berlin/Kiba/1998) | 32% | 99% |
Q9E6N9 | Gallid herpesvirus 2 (strain Chicken/Md5/ATCC VR-987) | 26% | 85% |
Q9HH06 | Pyrococcus glycovorans | 29% | 100% |
Q9LRE6 | Oryza sativa subsp. japonica | 52% | 93% |
Q9LVN7 | Arabidopsis thaliana | 53% | 94% |
Q9P6L6 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 70% |
Q9QJ32 | Human herpesvirus 6B (strain Z29) | 30% | 100% |
V5B2M9 | Trypanosoma cruzi | 25% | 77% |
V5BH96 | Trypanosoma cruzi | 80% | 100% |