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 | 11 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0042555 | MCM complex | 2 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: A4HLY1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006270 | DNA replication initiation | 5 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
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:0046483 | heterocycle metabolic process | 3 | 12 |
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 |
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:0006271 | DNA strand elongation involved in DNA replication | 6 | 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:0022616 | DNA strand elongation | 5 | 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 |
GO:0006260 | DNA replication | 5 | 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 | 11 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
GO:0016887 | ATP hydrolysis activity | 7 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 |
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: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 | 219 | 223 | PF00656 | 0.435 |
CLV_C14_Caspase3-7 | 251 | 255 | PF00656 | 0.554 |
CLV_C14_Caspase3-7 | 272 | 276 | PF00656 | 0.439 |
CLV_C14_Caspase3-7 | 548 | 552 | PF00656 | 0.570 |
CLV_C14_Caspase3-7 | 554 | 558 | PF00656 | 0.605 |
CLV_C14_Caspase3-7 | 64 | 68 | PF00656 | 0.554 |
CLV_C14_Caspase3-7 | 641 | 645 | PF00656 | 0.535 |
CLV_C14_Caspase3-7 | 737 | 741 | PF00656 | 0.481 |
CLV_C14_Caspase3-7 | 762 | 766 | PF00656 | 0.686 |
CLV_C14_Caspase3-7 | 824 | 828 | PF00656 | 0.602 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.246 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.326 |
CLV_NRD_NRD_1 | 523 | 525 | PF00675 | 0.249 |
CLV_NRD_NRD_1 | 572 | 574 | PF00675 | 0.779 |
CLV_NRD_NRD_1 | 812 | 814 | PF00675 | 0.469 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.239 |
CLV_PCSK_KEX2_1 | 523 | 525 | PF00082 | 0.249 |
CLV_PCSK_KEX2_1 | 572 | 574 | PF00082 | 0.779 |
CLV_PCSK_KEX2_1 | 617 | 619 | PF00082 | 0.318 |
CLV_PCSK_KEX2_1 | 727 | 729 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 812 | 814 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 849 | 851 | PF00082 | 0.331 |
CLV_PCSK_PC1ET2_1 | 617 | 619 | PF00082 | 0.335 |
CLV_PCSK_PC1ET2_1 | 727 | 729 | PF00082 | 0.653 |
CLV_PCSK_PC1ET2_1 | 849 | 851 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 45 | 49 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 492 | 496 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 610 | 614 | PF00082 | 0.309 |
CLV_Separin_Metazoa | 816 | 820 | PF03568 | 0.474 |
DEG_APCC_DBOX_1 | 182 | 190 | PF00400 | 0.473 |
DEG_APCC_DBOX_1 | 260 | 268 | PF00400 | 0.460 |
DEG_APCC_DBOX_1 | 505 | 513 | PF00400 | 0.449 |
DEG_Kelch_Keap1_1 | 582 | 587 | PF01344 | 0.500 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.509 |
DEG_SCF_TRCP1_1 | 779 | 784 | PF00400 | 0.769 |
DEG_SPOP_SBC_1 | 270 | 274 | PF00917 | 0.492 |
DEG_SPOP_SBC_1 | 393 | 397 | PF00917 | 0.489 |
DOC_ANK_TNKS_1 | 565 | 572 | PF00023 | 0.525 |
DOC_CKS1_1 | 185 | 190 | PF01111 | 0.449 |
DOC_CKS1_1 | 651 | 656 | PF01111 | 0.535 |
DOC_CKS1_1 | 721 | 726 | PF01111 | 0.503 |
DOC_CYCLIN_RxL_1 | 42 | 52 | PF00134 | 0.467 |
DOC_MAPK_DCC_7 | 384 | 394 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 43 | 50 | PF00069 | 0.554 |
DOC_MAPK_gen_1 | 727 | 735 | PF00069 | 0.758 |
DOC_MAPK_gen_1 | 849 | 855 | PF00069 | 0.328 |
DOC_MAPK_MEF2A_6 | 261 | 269 | PF00069 | 0.460 |
DOC_MAPK_MEF2A_6 | 343 | 350 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 364 | 371 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 43 | 50 | PF00069 | 0.460 |
DOC_MAPK_MEF2A_6 | 92 | 101 | PF00069 | 0.446 |
DOC_MAPK_NFAT4_5 | 343 | 351 | PF00069 | 0.462 |
DOC_MAPK_NFAT4_5 | 43 | 51 | PF00069 | 0.473 |
DOC_PP1_RVXF_1 | 490 | 496 | PF00149 | 0.449 |
DOC_PP2B_LxvP_1 | 792 | 795 | PF13499 | 0.489 |
DOC_PP4_FxxP_1 | 126 | 129 | PF00568 | 0.429 |
DOC_PP4_FxxP_1 | 651 | 654 | PF00568 | 0.535 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.443 |
DOC_USP7_MATH_1 | 742 | 746 | PF00917 | 0.658 |
DOC_USP7_UBL2_3 | 176 | 180 | PF12436 | 0.449 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 617 | 622 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 650 | 655 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 670 | 675 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 720 | 725 | PF00397 | 0.711 |
LIG_14-3-3_CanoR_1 | 142 | 148 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 156 | 164 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 299 | 305 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 356 | 363 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 419 | 428 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 473 | 477 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 5 | 14 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 531 | 541 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 662 | 670 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 689 | 693 | PF00244 | 0.521 |
LIG_Actin_WH2_2 | 656 | 673 | PF00022 | 0.449 |
LIG_Actin_WH2_2 | 836 | 851 | PF00022 | 0.430 |
LIG_AP2alpha_1 | 18 | 22 | PF02296 | 0.449 |
LIG_BRCT_BRCA1_1 | 275 | 279 | PF00533 | 0.470 |
LIG_BRCT_BRCA1_1 | 604 | 608 | PF00533 | 0.539 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.449 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.449 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.449 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.449 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.449 |
LIG_FHA_1 | 508 | 514 | PF00498 | 0.460 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.282 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.460 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.457 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.423 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.420 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.524 |
LIG_FHA_2 | 546 | 552 | PF00498 | 0.580 |
LIG_FHA_2 | 673 | 679 | PF00498 | 0.449 |
LIG_FHA_2 | 735 | 741 | PF00498 | 0.583 |
LIG_Integrin_RGD_1 | 364 | 366 | PF01839 | 0.249 |
LIG_Integrin_RGD_1 | 559 | 561 | PF01839 | 0.525 |
LIG_Integrin_RGD_1 | 776 | 778 | PF01839 | 0.530 |
LIG_LIR_Apic_2 | 124 | 129 | PF02991 | 0.300 |
LIG_LIR_Apic_2 | 648 | 654 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 111 | 117 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 276 | 285 | PF02991 | 0.401 |
LIG_LIR_Gen_1 | 291 | 302 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 437 | 446 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 508 | 515 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 765 | 775 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 111 | 115 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 276 | 282 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 291 | 297 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 508 | 514 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 55 | 59 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 745 | 749 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 765 | 770 | PF02991 | 0.424 |
LIG_LRP6_Inhibitor_1 | 82 | 88 | PF00058 | 0.316 |
LIG_PCNA_PIPBox_1 | 11 | 20 | PF02747 | 0.317 |
LIG_PCNA_yPIPBox_3 | 811 | 823 | PF02747 | 0.336 |
LIG_Pex14_2 | 18 | 22 | PF04695 | 0.439 |
LIG_Pex14_2 | 507 | 511 | PF04695 | 0.449 |
LIG_Pex14_2 | 608 | 612 | PF04695 | 0.535 |
LIG_PTB_Apo_2 | 478 | 485 | PF02174 | 0.449 |
LIG_PTB_Phospho_1 | 478 | 484 | PF10480 | 0.449 |
LIG_SH2_CRK | 298 | 302 | PF00017 | 0.410 |
LIG_SH2_CRK | 527 | 531 | PF00017 | 0.554 |
LIG_SH2_CRK | 767 | 771 | PF00017 | 0.508 |
LIG_SH2_NCK_1 | 541 | 545 | PF00017 | 0.672 |
LIG_SH2_PTP2 | 56 | 59 | PF00017 | 0.535 |
LIG_SH2_PTP2 | 635 | 638 | PF00017 | 0.449 |
LIG_SH2_PTP2 | 93 | 96 | PF00017 | 0.489 |
LIG_SH2_SRC | 541 | 544 | PF00017 | 0.672 |
LIG_SH2_SRC | 56 | 59 | PF00017 | 0.535 |
LIG_SH2_STAP1 | 140 | 144 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 27 | 31 | PF00017 | 0.460 |
LIG_SH2_STAT3 | 487 | 490 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 635 | 638 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.473 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.423 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.497 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.449 |
LIG_SH3_3 | 494 | 500 | PF00018 | 0.449 |
LIG_SH3_3 | 673 | 679 | PF00018 | 0.373 |
LIG_SUMO_SIM_anti_2 | 260 | 266 | PF11976 | 0.485 |
LIG_SUMO_SIM_anti_2 | 281 | 286 | PF11976 | 0.372 |
LIG_SUMO_SIM_par_1 | 146 | 151 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 368 | 374 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 390 | 397 | PF11976 | 0.440 |
LIG_SUMO_SIM_par_1 | 46 | 52 | PF11976 | 0.554 |
LIG_TRAF2_1 | 675 | 678 | PF00917 | 0.535 |
LIG_TYR_ITIM | 525 | 530 | PF00017 | 0.434 |
LIG_TYR_ITIM | 539 | 544 | PF00017 | 0.465 |
LIG_TYR_ITIM | 54 | 59 | PF00017 | 0.422 |
LIG_UBA3_1 | 433 | 441 | PF00899 | 0.317 |
LIG_WRC_WIRS_1 | 217 | 222 | PF05994 | 0.271 |
MOD_CDK_SPK_2 | 132 | 137 | PF00069 | 0.413 |
MOD_CDK_SPK_2 | 650 | 655 | PF00069 | 0.422 |
MOD_CDK_SPxxK_3 | 720 | 727 | PF00069 | 0.505 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.391 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.414 |
MOD_CK1_1 | 502 | 508 | PF00069 | 0.301 |
MOD_CK1_1 | 552 | 558 | PF00069 | 0.488 |
MOD_CK1_1 | 585 | 591 | PF00069 | 0.710 |
MOD_CK1_1 | 602 | 608 | PF00069 | 0.495 |
MOD_CK1_1 | 844 | 850 | PF00069 | 0.601 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.420 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.402 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.301 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.336 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.477 |
MOD_CK2_1 | 559 | 565 | PF00069 | 0.713 |
MOD_CK2_1 | 581 | 587 | PF00069 | 0.502 |
MOD_CK2_1 | 595 | 601 | PF00069 | 0.546 |
MOD_CK2_1 | 672 | 678 | PF00069 | 0.302 |
MOD_CK2_1 | 706 | 712 | PF00069 | 0.604 |
MOD_CK2_1 | 827 | 833 | PF00069 | 0.576 |
MOD_Cter_Amidation | 570 | 573 | PF01082 | 0.780 |
MOD_DYRK1A_RPxSP_1 | 132 | 136 | PF00069 | 0.516 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.373 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.301 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.306 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.654 |
MOD_GlcNHglycan | 584 | 587 | PF01048 | 0.649 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.319 |
MOD_GlcNHglycan | 750 | 753 | PF01048 | 0.690 |
MOD_GlcNHglycan | 761 | 764 | PF01048 | 0.637 |
MOD_GlcNHglycan | 778 | 782 | PF01048 | 0.726 |
MOD_GlcNHglycan | 783 | 786 | PF01048 | 0.698 |
MOD_GlcNHglycan | 843 | 846 | PF01048 | 0.584 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.316 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.182 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.305 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.271 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.420 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.388 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.289 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.301 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.118 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.457 |
MOD_GSK3_1 | 545 | 552 | PF00069 | 0.578 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.633 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.526 |
MOD_GSK3_1 | 617 | 624 | PF00069 | 0.386 |
MOD_GSK3_1 | 683 | 690 | PF00069 | 0.450 |
MOD_GSK3_1 | 759 | 766 | PF00069 | 0.710 |
MOD_GSK3_1 | 777 | 784 | PF00069 | 0.614 |
MOD_GSK3_1 | 844 | 851 | PF00069 | 0.596 |
MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.480 |
MOD_N-GLC_1 | 596 | 601 | PF02516 | 0.649 |
MOD_N-GLC_1 | 869 | 874 | PF02516 | 0.353 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.301 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.276 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.306 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.317 |
MOD_NEK2_1 | 592 | 597 | PF00069 | 0.551 |
MOD_NEK2_1 | 687 | 692 | PF00069 | 0.394 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.407 |
MOD_NEK2_1 | 848 | 853 | PF00069 | 0.529 |
MOD_PIKK_1 | 220 | 226 | PF00454 | 0.301 |
MOD_PIKK_1 | 288 | 294 | PF00454 | 0.510 |
MOD_PIKK_1 | 377 | 383 | PF00454 | 0.301 |
MOD_PIKK_1 | 441 | 447 | PF00454 | 0.448 |
MOD_PIKK_1 | 696 | 702 | PF00454 | 0.612 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.301 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.556 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.422 |
MOD_PKA_2 | 472 | 478 | PF00069 | 0.301 |
MOD_PKA_2 | 565 | 571 | PF00069 | 0.761 |
MOD_PKA_2 | 592 | 598 | PF00069 | 0.533 |
MOD_PKA_2 | 661 | 667 | PF00069 | 0.277 |
MOD_PKA_2 | 688 | 694 | PF00069 | 0.403 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.317 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.478 |
MOD_Plk_1 | 417 | 423 | PF00069 | 0.301 |
MOD_Plk_1 | 507 | 513 | PF00069 | 0.317 |
MOD_Plk_1 | 869 | 875 | PF00069 | 0.414 |
MOD_Plk_2-3 | 545 | 551 | PF00069 | 0.681 |
MOD_Plk_2-3 | 827 | 833 | PF00069 | 0.570 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.324 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.262 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.418 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.322 |
MOD_Plk_4 | 472 | 478 | PF00069 | 0.293 |
MOD_Plk_4 | 499 | 505 | PF00069 | 0.301 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.301 |
MOD_Plk_4 | 599 | 605 | PF00069 | 0.534 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.430 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.414 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.288 |
MOD_ProDKin_1 | 617 | 623 | PF00069 | 0.386 |
MOD_ProDKin_1 | 650 | 656 | PF00069 | 0.389 |
MOD_ProDKin_1 | 670 | 676 | PF00069 | 0.422 |
MOD_ProDKin_1 | 720 | 726 | PF00069 | 0.712 |
MOD_SUMO_rev_2 | 274 | 279 | PF00179 | 0.534 |
MOD_SUMO_rev_2 | 755 | 762 | PF00179 | 0.495 |
TRG_DiLeu_BaLyEn_6 | 42 | 47 | PF01217 | 0.301 |
TRG_DiLeu_BaLyEn_6 | 618 | 623 | PF01217 | 0.386 |
TRG_DiLeu_BaLyEn_6 | 92 | 97 | PF01217 | 0.301 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 298 | 301 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 527 | 530 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 541 | 544 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 635 | 638 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 746 | 749 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 767 | 770 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.358 |
TRG_ER_diArg_1 | 117 | 120 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 14 | 16 | PF00400 | 0.301 |
TRG_ER_diArg_1 | 161 | 164 | PF00400 | 0.302 |
TRG_ER_diArg_1 | 523 | 525 | PF00400 | 0.301 |
TRG_ER_diArg_1 | 812 | 814 | PF00400 | 0.477 |
TRG_NES_CRM1_1 | 501 | 515 | PF08389 | 0.301 |
TRG_Pf-PMV_PEXEL_1 | 45 | 49 | PF00026 | 0.301 |
TRG_Pf-PMV_PEXEL_1 | 5 | 9 | PF00026 | 0.444 |
TRG_Pf-PMV_PEXEL_1 | 628 | 633 | PF00026 | 0.380 |
TRG_Pf-PMV_PEXEL_1 | 819 | 824 | PF00026 | 0.357 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P686 | Leptomonas seymouri | 78% | 100% |
A0A0N0P860 | Leptomonas seymouri | 33% | 88% |
A0A0S4IW18 | Bodo saltans | 32% | 100% |
A0A0S4JM41 | Bodo saltans | 66% | 100% |
A0A1X0NSY3 | Trypanosomatidae | 65% | 100% |
A0A1X0NT66 | Trypanosomatidae | 33% | 100% |
A0A1X0NZT6 | Trypanosomatidae | 33% | 93% |
A0A3Q8IAX4 | Leishmania donovani | 31% | 90% |
A0A3R7K9K0 | Trypanosoma rangeli | 67% | 100% |
A0A3R7NBN0 | Trypanosoma rangeli | 33% | 92% |
A0A3S5H7S8 | Leishmania donovani | 34% | 100% |
A0A3S7X726 | Leishmania donovani | 88% | 99% |
A0A422NDD9 | Trypanosoma rangeli | 32% | 100% |
A0A422NDR0 | Trypanosoma rangeli | 28% | 100% |
A0A422NZW3 | Trypanosoma rangeli | 34% | 100% |
A4FUD9 | Bos taurus | 40% | 100% |
A4H5K0 | Leishmania braziliensis | 30% | 95% |
A4HGC9 | Leishmania braziliensis | 32% | 90% |
A4HKT9 | Leishmania braziliensis | 34% | 100% |
A4I3G2 | Leishmania infantum | 31% | 90% |
A4I8B8 | Leishmania infantum | 34% | 100% |
A4I9B0 | Leishmania infantum | 88% | 99% |
B8AEH3 | Oryza sativa subsp. indica | 31% | 100% |
B8AZ14 | Oryza sativa subsp. indica | 31% | 100% |
B8AZ99 | Oryza sativa subsp. indica | 41% | 100% |
B8BKI8 | Oryza sativa subsp. indica | 32% | 91% |
B9FKM7 | Oryza sativa subsp. japonica | 31% | 100% |
C9ZJB6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 65% | 100% |
D0A4I0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
D0A7X6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 92% |
D0A999 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
D3ZVK1 | Rattus norvegicus | 28% | 100% |
E9AZQ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 90% |
E9B377 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9B4B0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
O80786 | Arabidopsis thaliana | 33% | 100% |
P24279 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 44% | 90% |
P25205 | Homo sapiens | 40% | 100% |
P25206 | Mus musculus | 40% | 100% |
P29469 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
P29496 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 100% |
P30664 | Xenopus laevis | 31% | 100% |
P30666 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 43% | 100% |
P33991 | Homo sapiens | 32% | 100% |
P33993 | Homo sapiens | 34% | 100% |
P49717 | Mus musculus | 32% | 100% |
P49736 | Homo sapiens | 32% | 97% |
P49739 | Xenopus laevis | 41% | 100% |
P55861 | Xenopus laevis | 32% | 99% |
P97310 | Mus musculus | 32% | 97% |
Q0DHC4 | Oryza sativa subsp. japonica | 41% | 100% |
Q0V9Q6 | Xenopus tropicalis | 29% | 100% |
Q21902 | Caenorhabditis elegans | 31% | 100% |
Q24849 | Entamoeba histolytica | 37% | 100% |
Q28BS0 | Xenopus tropicalis | 41% | 100% |
Q29JI9 | Drosophila pseudoobscura pseudoobscura | 31% | 100% |
Q2R482 | Oryza sativa subsp. japonica | 32% | 91% |
Q3ZBH9 | Bos taurus | 34% | 100% |
Q43704 | Zea mays | 40% | 100% |
Q4Q3R6 | Leishmania major | 89% | 100% |
Q4Q8I2 | Leishmania major | 32% | 90% |
Q54CP4 | Dictyostelium discoideum | 31% | 100% |
Q561P5 | Xenopus tropicalis | 30% | 100% |
Q5F310 | Xenopus laevis | 27% | 100% |
Q5R8G6 | Pongo abelii | 40% | 100% |
Q5XK83 | Xenopus laevis | 31% | 100% |
Q5ZMN2 | Gallus gallus | 42% | 100% |
Q61881 | Mus musculus | 33% | 100% |
Q6DIH3 | Xenopus tropicalis | 31% | 99% |
Q6GL41 | Xenopus tropicalis | 31% | 100% |
Q6KAJ4 | Oryza sativa subsp. japonica | 31% | 100% |
Q6PCI7 | Xenopus laevis | 30% | 100% |
Q7ZXZ0 | Xenopus laevis | 41% | 100% |
Q9FL33 | Arabidopsis thaliana | 41% | 100% |
Q9LPD9 | Arabidopsis thaliana | 31% | 94% |
Q9SF37 | Arabidopsis thaliana | 30% | 100% |
Q9SX03 | Zea mays | 41% | 100% |
Q9SX04 | Zea mays | 41% | 100% |
Q9U1E0 | Leishmania major | 34% | 100% |
Q9V461 | Drosophila melanogaster | 31% | 100% |
Q9XYU1 | Drosophila melanogaster | 40% | 100% |
V5BAH7 | Trypanosoma cruzi | 67% | 100% |
V5BQA9 | Trypanosoma cruzi | 32% | 100% |
V5BSG2 | Trypanosoma cruzi | 34% | 100% |