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:0005737 | cytoplasm | 2 | 2 |
GO:0032300 | mismatch repair complex | 2 | 12 |
GO:0032301 | MutSalpha complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 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 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
Related structures:
AlphaFold database: Q4Q4J6
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006281 | DNA repair | 5 | 12 |
GO:0006298 | mismatch repair | 6 | 12 |
GO:0006310 | DNA recombination | 5 | 2 |
GO:0006312 | mitotic recombination | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006950 | response to stress | 2 | 12 |
GO:0006974 | DNA damage response | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0033554 | cellular response to stress | 3 | 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:0050896 | response to stimulus | 1 | 12 |
GO:0051716 | cellular response to stimulus | 2 | 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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003690 | double-stranded DNA binding | 5 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0030983 | mismatched DNA binding | 6 | 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:0140299 | small molecule sensor activity | 1 | 12 |
GO:0140612 | DNA damage sensor activity | 2 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:0140664 | ATP-dependent DNA damage sensor activity | 3 | 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 | 176 | 180 | PF00656 | 0.358 |
CLV_C14_Caspase3-7 | 3 | 7 | PF00656 | 0.483 |
CLV_C14_Caspase3-7 | 545 | 549 | PF00656 | 0.424 |
CLV_MEL_PAP_1 | 725 | 731 | PF00089 | 0.205 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.254 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.279 |
CLV_NRD_NRD_1 | 527 | 529 | PF00675 | 0.205 |
CLV_NRD_NRD_1 | 565 | 567 | PF00675 | 0.234 |
CLV_NRD_NRD_1 | 579 | 581 | PF00675 | 0.216 |
CLV_NRD_NRD_1 | 89 | 91 | PF00675 | 0.387 |
CLV_NRD_NRD_1 | 892 | 894 | PF00675 | 0.569 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.225 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.262 |
CLV_PCSK_KEX2_1 | 565 | 567 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 900 | 902 | PF00082 | 0.430 |
CLV_PCSK_PC1ET2_1 | 386 | 388 | PF00082 | 0.309 |
CLV_PCSK_PC1ET2_1 | 579 | 581 | PF00082 | 0.251 |
CLV_PCSK_PC1ET2_1 | 900 | 902 | PF00082 | 0.430 |
CLV_PCSK_PC7_1 | 396 | 402 | PF00082 | 0.216 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.229 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 510 | 514 | PF00082 | 0.263 |
CLV_Separin_Metazoa | 253 | 257 | PF03568 | 0.467 |
DEG_APCC_DBOX_1 | 656 | 664 | PF00400 | 0.316 |
DEG_SCF_FBW7_1 | 194 | 200 | PF00400 | 0.353 |
DEG_SPOP_SBC_1 | 62 | 66 | PF00917 | 0.355 |
DOC_CKS1_1 | 194 | 199 | PF01111 | 0.473 |
DOC_CYCLIN_RxL_1 | 159 | 170 | PF00134 | 0.370 |
DOC_CYCLIN_RxL_1 | 396 | 408 | PF00134 | 0.509 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 182 | 191 | PF00134 | 0.347 |
DOC_CYCLIN_yCln2_LP_2 | 855 | 861 | PF00134 | 0.357 |
DOC_MAPK_gen_1 | 396 | 405 | PF00069 | 0.405 |
DOC_MAPK_gen_1 | 535 | 543 | PF00069 | 0.416 |
DOC_MAPK_gen_1 | 654 | 663 | PF00069 | 0.364 |
DOC_MAPK_gen_1 | 790 | 797 | PF00069 | 0.447 |
DOC_MAPK_HePTP_8 | 651 | 663 | PF00069 | 0.360 |
DOC_MAPK_MEF2A_6 | 222 | 229 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 363 | 371 | PF00069 | 0.416 |
DOC_MAPK_MEF2A_6 | 654 | 663 | PF00069 | 0.364 |
DOC_MAPK_MEF2A_6 | 697 | 705 | PF00069 | 0.405 |
DOC_PP1_RVXF_1 | 160 | 167 | PF00149 | 0.413 |
DOC_PP2B_LxvP_1 | 255 | 258 | PF13499 | 0.318 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.358 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.396 |
DOC_USP7_MATH_1 | 878 | 882 | PF00917 | 0.666 |
DOC_USP7_MATH_2 | 258 | 264 | PF00917 | 0.350 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.325 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.408 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.532 |
LIG_14-3-3_CanoR_1 | 162 | 167 | PF00244 | 0.306 |
LIG_14-3-3_CanoR_1 | 212 | 219 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 261 | 265 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 295 | 299 | PF00244 | 0.353 |
LIG_14-3-3_CanoR_1 | 363 | 367 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 387 | 394 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 400 | 404 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 471 | 477 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 532 | 541 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 551 | 560 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 769 | 775 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 790 | 796 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 831 | 837 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 89 | 95 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 893 | 902 | PF00244 | 0.454 |
LIG_Actin_WH2_2 | 391 | 408 | PF00022 | 0.472 |
LIG_Actin_WH2_2 | 519 | 537 | PF00022 | 0.509 |
LIG_Actin_WH2_2 | 75 | 91 | PF00022 | 0.327 |
LIG_Actin_WH2_2 | 816 | 833 | PF00022 | 0.416 |
LIG_APCC_ABBA_1 | 367 | 372 | PF00400 | 0.509 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.455 |
LIG_BIR_III_2 | 646 | 650 | PF00653 | 0.398 |
LIG_BRCT_BRCA1_1 | 138 | 142 | PF00533 | 0.337 |
LIG_BRCT_BRCA1_1 | 20 | 24 | PF00533 | 0.365 |
LIG_BRCT_BRCA1_1 | 797 | 801 | PF00533 | 0.400 |
LIG_CaM_IQ_9 | 232 | 248 | PF13499 | 0.423 |
LIG_Clathr_ClatBox_1 | 124 | 128 | PF01394 | 0.401 |
LIG_CtBP_PxDLS_1 | 686 | 692 | PF00389 | 0.405 |
LIG_deltaCOP1_diTrp_1 | 869 | 873 | PF00928 | 0.543 |
LIG_eIF4E_1 | 606 | 612 | PF01652 | 0.404 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.480 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.345 |
LIG_FHA_1 | 535 | 541 | PF00498 | 0.554 |
LIG_FHA_1 | 600 | 606 | PF00498 | 0.513 |
LIG_FHA_1 | 629 | 635 | PF00498 | 0.641 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.306 |
LIG_FHA_1 | 677 | 683 | PF00498 | 0.366 |
LIG_FHA_1 | 730 | 736 | PF00498 | 0.405 |
LIG_FHA_1 | 739 | 745 | PF00498 | 0.405 |
LIG_FHA_1 | 758 | 764 | PF00498 | 0.405 |
LIG_FHA_2 | 116 | 122 | PF00498 | 0.382 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.349 |
LIG_FHA_2 | 204 | 210 | PF00498 | 0.523 |
LIG_FHA_2 | 229 | 235 | PF00498 | 0.362 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.496 |
LIG_FHA_2 | 454 | 460 | PF00498 | 0.456 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.472 |
LIG_FHA_2 | 543 | 549 | PF00498 | 0.461 |
LIG_GBD_Chelix_1 | 582 | 590 | PF00786 | 0.251 |
LIG_LIR_Apic_2 | 427 | 431 | PF02991 | 0.484 |
LIG_LIR_Apic_2 | 438 | 443 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 151 | 161 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 172 | 183 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 300 | 310 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 408 | 419 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 495 | 505 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 798 | 808 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 869 | 878 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 165 | 169 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 172 | 178 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 21 | 27 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 300 | 305 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 328 | 334 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 408 | 414 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 495 | 501 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 519 | 523 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 561 | 567 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 588 | 592 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 652 | 656 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 771 | 777 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 798 | 804 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 844 | 848 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 869 | 873 | PF02991 | 0.522 |
LIG_NRBOX | 186 | 192 | PF00104 | 0.342 |
LIG_PCNA_yPIPBox_3 | 373 | 387 | PF02747 | 0.509 |
LIG_PDZ_Class_3 | 934 | 939 | PF00595 | 0.474 |
LIG_Pex14_1 | 40 | 44 | PF04695 | 0.400 |
LIG_Pex14_2 | 777 | 781 | PF04695 | 0.405 |
LIG_Pex14_2 | 797 | 801 | PF04695 | 0.318 |
LIG_PTB_Apo_2 | 813 | 820 | PF02174 | 0.405 |
LIG_SH2_CRK | 428 | 432 | PF00017 | 0.451 |
LIG_SH2_CRK | 498 | 502 | PF00017 | 0.420 |
LIG_SH2_CRK | 520 | 524 | PF00017 | 0.405 |
LIG_SH2_CRK | 564 | 568 | PF00017 | 0.464 |
LIG_SH2_PTP2 | 302 | 305 | PF00017 | 0.264 |
LIG_SH2_PTP2 | 440 | 443 | PF00017 | 0.413 |
LIG_SH2_SRC | 589 | 592 | PF00017 | 0.429 |
LIG_SH2_STAP1 | 498 | 502 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 898 | 902 | PF00017 | 0.370 |
LIG_SH2_STAT3 | 834 | 837 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 428 | 431 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 440 | 443 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 522 | 525 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 589 | 592 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 606 | 609 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 834 | 837 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 848 | 851 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 934 | 937 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.368 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.479 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.502 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.416 |
LIG_SUMO_SIM_anti_2 | 631 | 636 | PF11976 | 0.590 |
LIG_SUMO_SIM_anti_2 | 68 | 73 | PF11976 | 0.347 |
LIG_SUMO_SIM_anti_2 | 759 | 766 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 539 | 546 | PF11976 | 0.429 |
LIG_SUMO_SIM_par_1 | 70 | 76 | PF11976 | 0.352 |
LIG_SUMO_SIM_par_1 | 759 | 766 | PF11976 | 0.447 |
LIG_TRFH_1 | 834 | 838 | PF08558 | 0.405 |
LIG_Vh1_VBS_1 | 746 | 764 | PF01044 | 0.472 |
LIG_WRC_WIRS_1 | 650 | 655 | PF05994 | 0.444 |
LIG_WRC_WIRS_1 | 739 | 744 | PF05994 | 0.405 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.502 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.386 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.426 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.540 |
MOD_CK1_1 | 751 | 757 | PF00069 | 0.479 |
MOD_CK1_1 | 826 | 832 | PF00069 | 0.420 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.369 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.311 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.399 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.428 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.485 |
MOD_CK2_1 | 524 | 530 | PF00069 | 0.421 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.407 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.390 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.537 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.449 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.321 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.452 |
MOD_GlcNHglycan | 640 | 643 | PF01048 | 0.666 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.493 |
MOD_GlcNHglycan | 748 | 751 | PF01048 | 0.205 |
MOD_GlcNHglycan | 811 | 814 | PF01048 | 0.322 |
MOD_GlcNHglycan | 824 | 828 | PF01048 | 0.237 |
MOD_GlcNHglycan | 881 | 884 | PF01048 | 0.648 |
MOD_GlcNHglycan | 895 | 898 | PF01048 | 0.317 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.416 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.496 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.396 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.416 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.463 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.439 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.435 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.491 |
MOD_GSK3_1 | 691 | 698 | PF00069 | 0.405 |
MOD_GSK3_1 | 791 | 798 | PF00069 | 0.478 |
MOD_GSK3_1 | 826 | 833 | PF00069 | 0.428 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.507 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.388 |
MOD_N-GLC_1 | 157 | 162 | PF02516 | 0.318 |
MOD_N-GLC_1 | 472 | 477 | PF02516 | 0.244 |
MOD_N-GLC_2 | 335 | 337 | PF02516 | 0.205 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.364 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.298 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.318 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.438 |
MOD_NEK2_1 | 405 | 410 | PF00069 | 0.433 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.509 |
MOD_NEK2_1 | 524 | 529 | PF00069 | 0.416 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.407 |
MOD_NEK2_1 | 673 | 678 | PF00069 | 0.401 |
MOD_NEK2_1 | 682 | 687 | PF00069 | 0.383 |
MOD_NEK2_1 | 746 | 751 | PF00069 | 0.405 |
MOD_NEK2_1 | 795 | 800 | PF00069 | 0.407 |
MOD_NEK2_1 | 830 | 835 | PF00069 | 0.411 |
MOD_NEK2_2 | 649 | 654 | PF00069 | 0.372 |
MOD_PIKK_1 | 18 | 24 | PF00454 | 0.336 |
MOD_PIKK_1 | 405 | 411 | PF00454 | 0.529 |
MOD_PIKK_1 | 487 | 493 | PF00454 | 0.451 |
MOD_PIKK_1 | 754 | 760 | PF00454 | 0.456 |
MOD_PIKK_1 | 802 | 808 | PF00454 | 0.416 |
MOD_PK_1 | 90 | 96 | PF00069 | 0.321 |
MOD_PKA_1 | 386 | 392 | PF00069 | 0.378 |
MOD_PKA_1 | 565 | 571 | PF00069 | 0.451 |
MOD_PKA_1 | 57 | 63 | PF00069 | 0.383 |
MOD_PKA_1 | 893 | 899 | PF00069 | 0.557 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.396 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.398 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.432 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.352 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.434 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.405 |
MOD_PKA_2 | 386 | 392 | PF00069 | 0.393 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.415 |
MOD_PKA_2 | 524 | 530 | PF00069 | 0.445 |
MOD_PKA_2 | 534 | 540 | PF00069 | 0.430 |
MOD_PKA_2 | 565 | 571 | PF00069 | 0.509 |
MOD_PKA_2 | 768 | 774 | PF00069 | 0.417 |
MOD_PKA_2 | 791 | 797 | PF00069 | 0.504 |
MOD_PKA_2 | 830 | 836 | PF00069 | 0.416 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.436 |
MOD_Plk_1 | 120 | 126 | PF00069 | 0.372 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.304 |
MOD_Plk_1 | 203 | 209 | PF00069 | 0.592 |
MOD_Plk_1 | 458 | 464 | PF00069 | 0.456 |
MOD_Plk_1 | 472 | 478 | PF00069 | 0.434 |
MOD_Plk_1 | 496 | 502 | PF00069 | 0.544 |
MOD_Plk_1 | 802 | 808 | PF00069 | 0.416 |
MOD_Plk_2-3 | 260 | 266 | PF00069 | 0.359 |
MOD_Plk_2-3 | 869 | 875 | PF00069 | 0.503 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.571 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.286 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.236 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.330 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.405 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.405 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.372 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.451 |
MOD_Plk_4 | 585 | 591 | PF00069 | 0.445 |
MOD_Plk_4 | 630 | 636 | PF00069 | 0.641 |
MOD_Plk_4 | 691 | 697 | PF00069 | 0.405 |
MOD_Plk_4 | 738 | 744 | PF00069 | 0.405 |
MOD_Plk_4 | 748 | 754 | PF00069 | 0.405 |
MOD_Plk_4 | 791 | 797 | PF00069 | 0.472 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.325 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.403 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.542 |
MOD_SUMO_for_1 | 436 | 439 | PF00179 | 0.509 |
MOD_SUMO_for_1 | 512 | 515 | PF00179 | 0.405 |
MOD_SUMO_for_1 | 635 | 638 | PF00179 | 0.677 |
MOD_SUMO_for_1 | 921 | 924 | PF00179 | 0.491 |
MOD_SUMO_rev_2 | 594 | 599 | PF00179 | 0.405 |
TRG_DiLeu_BaEn_1 | 311 | 316 | PF01217 | 0.509 |
TRG_DiLeu_BaEn_4 | 259 | 265 | PF01217 | 0.429 |
TRG_DiLeu_BaLyEn_6 | 646 | 651 | PF01217 | 0.403 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 498 | 501 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 520 | 523 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 564 | 567 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 589 | 592 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 774 | 777 | PF00928 | 0.405 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 294 | 296 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 564 | 566 | PF00400 | 0.509 |
TRG_ER_diArg_1 | 789 | 792 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 88 | 90 | PF00400 | 0.377 |
TRG_NES_CRM1_1 | 358 | 372 | PF08389 | 0.416 |
TRG_NES_CRM1_1 | 733 | 748 | PF08389 | 0.405 |
TRG_NLS_Bipartite_1 | 565 | 583 | PF00514 | 0.509 |
TRG_NLS_MonoExtC_3 | 578 | 584 | PF00514 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 217 | 221 | PF00026 | 0.366 |
TRG_Pf-PMV_PEXEL_1 | 230 | 234 | PF00026 | 0.381 |
TRG_Pf-PMV_PEXEL_1 | 455 | 459 | PF00026 | 0.247 |
TRG_Pf-PMV_PEXEL_1 | 565 | 569 | PF00026 | 0.299 |
TRG_Pf-PMV_PEXEL_1 | 580 | 584 | PF00026 | 0.329 |
TRG_Pf-PMV_PEXEL_1 | 903 | 907 | PF00026 | 0.497 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6N3 | Leptomonas seymouri | 80% | 99% |
A0A0S4J224 | Bodo saltans | 50% | 100% |
A0A1X0P1A3 | Trypanosomatidae | 59% | 98% |
A0A3Q8IGP6 | Leishmania donovani | 96% | 100% |
A0A3Q8IK49 | Leishmania donovani | 26% | 93% |
A0A3R7KEP9 | Trypanosoma rangeli | 58% | 98% |
A4HL76 | Leishmania braziliensis | 89% | 100% |
A4I8Q5 | Leishmania infantum | 96% | 100% |
A4IDG7 | Leishmania infantum | 26% | 93% |
A4JFW7 | Burkholderia vietnamiensis (strain G4 / LMG 22486) | 30% | 100% |
A9NGL6 | Acholeplasma laidlawii (strain PG-8A) | 28% | 100% |
B0TK13 | Shewanella halifaxensis (strain HAW-EB4) | 28% | 100% |
B0VAU7 | Acinetobacter baumannii (strain AYE) | 29% | 100% |
B0VUC9 | Acinetobacter baumannii (strain SDF) | 29% | 100% |
B2HX50 | Acinetobacter baumannii (strain ACICU) | 29% | 100% |
B7GW85 | Acinetobacter baumannii (strain AB307-0294) | 29% | 100% |
B7IBV9 | Acinetobacter baumannii (strain AB0057) | 29% | 100% |
D0A4P2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 99% |
E9B3L9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
O13396 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 31% | 100% |
O24617 | Arabidopsis thaliana | 33% | 100% |
O74773 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 96% |
P25847 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 97% |
P43246 | Homo sapiens | 33% | 100% |
P43247 | Mus musculus | 33% | 100% |
P43248 | Drosophila melanogaster | 31% | 100% |
P54275 | Rattus norvegicus | 32% | 100% |
P61672 | Treponema denticola (strain ATCC 35405 / DSM 14222 / CIP 103919 / JCM 8153 / KCTC 15104) | 29% | 100% |
Q03R33 | Levilactobacillus brevis (strain ATCC 367 / BCRC 12310 / CIP 105137 / JCM 1170 / LMG 11437 / NCIMB 947 / NCTC 947) | 30% | 100% |
Q07V29 | Rhodopseudomonas palustris (strain BisA53) | 30% | 100% |
Q10YG4 | Trichodesmium erythraeum (strain IMS101) | 27% | 100% |
Q1WT15 | Ligilactobacillus salivarius (strain UCC118) | 30% | 100% |
Q24X61 | Desulfitobacterium hafniense (strain Y51) | 31% | 100% |
Q2JT35 | Synechococcus sp. (strain JA-3-3Ab) | 31% | 100% |
Q3IUH3 | Natronomonas pharaonis (strain ATCC 35678 / DSM 2160 / CIP 103997 / JCM 8858 / NBRC 14720 / NCIMB 2260 / Gabara) | 30% | 100% |
Q3MHE4 | Bos taurus | 33% | 100% |
Q49X88 | Staphylococcus saprophyticus subsp. saprophyticus (strain ATCC 15305 / DSM 20229 / NCIMB 8711 / NCTC 7292 / S-41) | 29% | 100% |
Q553L4 | Dictyostelium discoideum | 30% | 100% |
Q5LWH0 | Ruegeria pomeroyi (strain ATCC 700808 / DSM 15171 / DSS-3) | 29% | 100% |
Q5NYP9 | Aromatoleum aromaticum (strain EbN1) | 30% | 100% |
Q5QUB6 | Idiomarina loihiensis (strain ATCC BAA-735 / DSM 15497 / L2-TR) | 31% | 100% |
Q5XXB5 | Chlorocebus aethiops | 33% | 100% |
Q6G542 | Bartonella henselae (strain ATCC 49882 / DSM 28221 / Houston 1) | 28% | 100% |
Q8RFK2 | Fusobacterium nucleatum subsp. nucleatum (strain ATCC 25586 / DSM 15643 / BCRC 10681 / CIP 101130 / JCM 8532 / KCTC 2640 / LMG 13131 / VPI 4355) | 26% | 100% |
Q9XGC9 | Zea mays | 32% | 100% |
V5BB82 | Trypanosoma cruzi | 57% | 98% |