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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 15 |
GO:0110165 | cellular anatomical entity | 1 | 16 |
GO:0005657 | replication fork | 2 | 1 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: E9ANH9
Term | Name | Level | Count |
---|---|---|---|
GO:0000723 | telomere maintenance | 5 | 16 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 16 |
GO:0006259 | DNA metabolic process | 4 | 16 |
GO:0006281 | DNA repair | 5 | 16 |
GO:0006310 | DNA recombination | 5 | 16 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 16 |
GO:0006807 | nitrogen compound metabolic process | 2 | 16 |
GO:0006950 | response to stress | 2 | 16 |
GO:0006974 | DNA damage response | 4 | 16 |
GO:0006996 | organelle organization | 4 | 16 |
GO:0008152 | metabolic process | 1 | 16 |
GO:0009987 | cellular process | 1 | 16 |
GO:0016043 | cellular component organization | 3 | 16 |
GO:0032200 | telomere organization | 6 | 16 |
GO:0033554 | cellular response to stress | 3 | 16 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 16 |
GO:0043170 | macromolecule metabolic process | 3 | 16 |
GO:0044237 | cellular metabolic process | 2 | 16 |
GO:0044238 | primary metabolic process | 2 | 16 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 16 |
GO:0046483 | heterocycle metabolic process | 3 | 16 |
GO:0050896 | response to stimulus | 1 | 16 |
GO:0051276 | chromosome organization | 5 | 16 |
GO:0051716 | cellular response to stimulus | 2 | 16 |
GO:0071704 | organic substance metabolic process | 2 | 16 |
GO:0071840 | cellular component organization or biogenesis | 2 | 16 |
GO:0090304 | nucleic acid metabolic process | 4 | 16 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 16 |
GO:0006260 | DNA replication | 5 | 1 |
GO:0032392 | DNA geometric change | 7 | 1 |
GO:0032508 | DNA duplex unwinding | 8 | 1 |
GO:0071103 | DNA conformation change | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 16 |
GO:0003678 | DNA helicase activity | 3 | 16 |
GO:0003824 | catalytic activity | 1 | 16 |
GO:0004386 | helicase activity | 2 | 16 |
GO:0005488 | binding | 1 | 16 |
GO:0005524 | ATP binding | 5 | 16 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 16 |
GO:0016462 | pyrophosphatase activity | 5 | 16 |
GO:0016787 | hydrolase activity | 2 | 16 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 16 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 16 |
GO:0016887 | ATP hydrolysis activity | 7 | 16 |
GO:0017076 | purine nucleotide binding | 4 | 16 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 16 |
GO:0030554 | adenyl nucleotide binding | 5 | 16 |
GO:0032553 | ribonucleotide binding | 3 | 16 |
GO:0032555 | purine ribonucleotide binding | 4 | 16 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 16 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 16 |
GO:0036094 | small molecule binding | 2 | 16 |
GO:0043167 | ion binding | 2 | 16 |
GO:0043168 | anion binding | 3 | 16 |
GO:0097159 | organic cyclic compound binding | 2 | 16 |
GO:0097367 | carbohydrate derivative binding | 2 | 16 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 16 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 16 |
GO:0140657 | ATP-dependent activity | 1 | 16 |
GO:1901265 | nucleoside phosphate binding | 3 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
GO:0000287 | magnesium ion binding | 5 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 181 | 185 | PF00656 | 0.637 |
CLV_C14_Caspase3-7 | 403 | 407 | PF00656 | 0.596 |
CLV_C14_Caspase3-7 | 821 | 825 | PF00656 | 0.772 |
CLV_C14_Caspase3-7 | 839 | 843 | PF00656 | 0.614 |
CLV_C14_Caspase3-7 | 940 | 944 | PF00656 | 0.770 |
CLV_MEL_PAP_1 | 846 | 852 | PF00089 | 0.767 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.754 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 613 | 615 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 779 | 781 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 887 | 889 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 907 | 909 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 941 | 943 | PF00675 | 0.698 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.792 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.771 |
CLV_PCSK_KEX2_1 | 613 | 615 | PF00082 | 0.434 |
CLV_PCSK_KEX2_1 | 762 | 764 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 779 | 781 | PF00082 | 0.505 |
CLV_PCSK_KEX2_1 | 887 | 889 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 906 | 908 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 941 | 943 | PF00082 | 0.698 |
CLV_PCSK_PC1ET2_1 | 214 | 216 | PF00082 | 0.438 |
CLV_PCSK_PC1ET2_1 | 5 | 7 | PF00082 | 0.637 |
CLV_PCSK_PC1ET2_1 | 762 | 764 | PF00082 | 0.484 |
CLV_PCSK_PC7_1 | 241 | 247 | PF00082 | 0.403 |
CLV_PCSK_PC7_1 | 6 | 12 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 471 | 475 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 499 | 503 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 743 | 747 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 779 | 783 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 898 | 902 | PF00082 | 0.559 |
DEG_APCC_DBOX_1 | 481 | 489 | PF00400 | 0.538 |
DEG_APCC_DBOX_1 | 778 | 786 | PF00400 | 0.674 |
DEG_SCF_FBW7_2 | 544 | 550 | PF00400 | 0.451 |
DEG_SPOP_SBC_1 | 162 | 166 | PF00917 | 0.473 |
DOC_CKS1_1 | 544 | 549 | PF01111 | 0.458 |
DOC_CYCLIN_RxL_1 | 468 | 477 | PF00134 | 0.481 |
DOC_CYCLIN_RxL_1 | 91 | 102 | PF00134 | 0.575 |
DOC_CYCLIN_yClb1_LxF_4 | 377 | 383 | PF00134 | 0.231 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 575 | 584 | PF00134 | 0.398 |
DOC_CYCLIN_yCln2_LP_2 | 398 | 401 | PF00134 | 0.507 |
DOC_MAPK_gen_1 | 214 | 221 | PF00069 | 0.403 |
DOC_MAPK_gen_1 | 569 | 576 | PF00069 | 0.335 |
DOC_MAPK_gen_1 | 740 | 750 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 214 | 221 | PF00069 | 0.372 |
DOC_MAPK_MEF2A_6 | 357 | 364 | PF00069 | 0.367 |
DOC_MAPK_MEF2A_6 | 743 | 750 | PF00069 | 0.551 |
DOC_MAPK_NFAT4_5 | 743 | 751 | PF00069 | 0.463 |
DOC_PP1_RVXF_1 | 92 | 99 | PF00149 | 0.419 |
DOC_PP2B_LxvP_1 | 398 | 401 | PF13499 | 0.581 |
DOC_PP2B_LxvP_1 | 478 | 481 | PF13499 | 0.485 |
DOC_PP2B_LxvP_1 | 919 | 922 | PF13499 | 0.476 |
DOC_PP4_MxPP_1 | 501 | 504 | PF00568 | 0.582 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 504 | 508 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 813 | 817 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 818 | 822 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 922 | 926 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 977 | 981 | PF00917 | 0.722 |
DOC_USP7_UBL2_3 | 357 | 361 | PF12436 | 0.371 |
DOC_USP7_UBL2_3 | 555 | 559 | PF12436 | 0.445 |
DOC_USP7_UBL2_3 | 910 | 914 | PF12436 | 0.690 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.375 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 543 | 548 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 790 | 795 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 973 | 978 | PF00397 | 0.585 |
LIG_14-3-3_CanoR_1 | 138 | 144 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 169 | 179 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 253 | 262 | PF00244 | 0.300 |
LIG_14-3-3_CanoR_1 | 369 | 376 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 468 | 474 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 482 | 486 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 577 | 585 | PF00244 | 0.401 |
LIG_14-3-3_CanoR_1 | 774 | 779 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 81 | 90 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 960 | 965 | PF00244 | 0.713 |
LIG_Actin_WH2_2 | 240 | 255 | PF00022 | 0.334 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.595 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.595 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.595 |
LIG_BRCT_BRCA1_1 | 351 | 355 | PF00533 | 0.306 |
LIG_BRCT_BRCA1_2 | 351 | 357 | PF00533 | 0.371 |
LIG_CtBP_PxDLS_1 | 671 | 675 | PF00389 | 0.389 |
LIG_DLG_GKlike_1 | 774 | 781 | PF00625 | 0.580 |
LIG_EH1_1 | 495 | 503 | PF00400 | 0.514 |
LIG_EVH1_2 | 648 | 652 | PF00568 | 0.338 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.484 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.661 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.659 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.305 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.310 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.375 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.562 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.394 |
LIG_FHA_1 | 468 | 474 | PF00498 | 0.502 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.482 |
LIG_FHA_1 | 533 | 539 | PF00498 | 0.449 |
LIG_FHA_1 | 607 | 613 | PF00498 | 0.513 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.651 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.700 |
LIG_FHA_2 | 24 | 30 | PF00498 | 0.518 |
LIG_FHA_2 | 401 | 407 | PF00498 | 0.531 |
LIG_FHA_2 | 412 | 418 | PF00498 | 0.418 |
LIG_FHA_2 | 455 | 461 | PF00498 | 0.453 |
LIG_FHA_2 | 589 | 595 | PF00498 | 0.385 |
LIG_FHA_2 | 747 | 753 | PF00498 | 0.535 |
LIG_LIR_Gen_1 | 170 | 179 | PF02991 | 0.575 |
LIG_LIR_Gen_1 | 292 | 301 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 307 | 316 | PF02991 | 0.262 |
LIG_LIR_Gen_1 | 337 | 344 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 379 | 389 | PF02991 | 0.224 |
LIG_LIR_Gen_1 | 49 | 59 | PF02991 | 0.705 |
LIG_LIR_Gen_1 | 516 | 525 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 72 | 82 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 170 | 175 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 292 | 296 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 307 | 312 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 324 | 330 | PF02991 | 0.225 |
LIG_LIR_Nem_3 | 337 | 341 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 379 | 385 | PF02991 | 0.218 |
LIG_LIR_Nem_3 | 487 | 492 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 49 | 55 | PF02991 | 0.697 |
LIG_LIR_Nem_3 | 516 | 521 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 600 | 606 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 617 | 622 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 660 | 665 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 72 | 78 | PF02991 | 0.463 |
LIG_LYPXL_yS_3 | 110 | 113 | PF13949 | 0.288 |
LIG_NBox_RRM_1 | 738 | 748 | PF00076 | 0.372 |
LIG_NRBOX | 777 | 783 | PF00104 | 0.578 |
LIG_PCNA_PIPBox_1 | 633 | 642 | PF02747 | 0.359 |
LIG_PCNA_yPIPBox_3 | 586 | 599 | PF02747 | 0.410 |
LIG_Pex14_2 | 355 | 359 | PF04695 | 0.300 |
LIG_SH2_CRK | 172 | 176 | PF00017 | 0.539 |
LIG_SH2_CRK | 293 | 297 | PF00017 | 0.338 |
LIG_SH2_CRK | 75 | 79 | PF00017 | 0.471 |
LIG_SH2_SRC | 492 | 495 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 172 | 176 | PF00017 | 0.531 |
LIG_SH2_STAP1 | 293 | 297 | PF00017 | 0.331 |
LIG_SH2_STAP1 | 676 | 680 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 552 | 555 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 606 | 609 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 707 | 710 | PF00017 | 0.334 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.671 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.285 |
LIG_SH3_3 | 427 | 433 | PF00018 | 0.506 |
LIG_SH3_3 | 497 | 503 | PF00018 | 0.387 |
LIG_SH3_3 | 629 | 635 | PF00018 | 0.386 |
LIG_SH3_3 | 665 | 671 | PF00018 | 0.319 |
LIG_SH3_3 | 710 | 716 | PF00018 | 0.367 |
LIG_SUMO_SIM_anti_2 | 294 | 300 | PF11976 | 0.320 |
LIG_SUMO_SIM_par_1 | 294 | 300 | PF11976 | 0.310 |
LIG_SUMO_SIM_par_1 | 432 | 437 | PF11976 | 0.575 |
LIG_SUMO_SIM_par_1 | 448 | 458 | PF11976 | 0.360 |
LIG_SUMO_SIM_par_1 | 793 | 798 | PF11976 | 0.684 |
LIG_TRAF2_1 | 13 | 16 | PF00917 | 0.625 |
LIG_TYR_ITIM | 291 | 296 | PF00017 | 0.334 |
LIG_TYR_ITIM | 73 | 78 | PF00017 | 0.475 |
LIG_WRC_WIRS_1 | 721 | 726 | PF05994 | 0.405 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.625 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.307 |
MOD_CK1_1 | 484 | 490 | PF00069 | 0.451 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.653 |
MOD_CK1_1 | 578 | 584 | PF00069 | 0.453 |
MOD_CK1_1 | 588 | 594 | PF00069 | 0.365 |
MOD_CK1_1 | 664 | 670 | PF00069 | 0.381 |
MOD_CK1_1 | 720 | 726 | PF00069 | 0.428 |
MOD_CK1_1 | 816 | 822 | PF00069 | 0.615 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.446 |
MOD_CK1_1 | 841 | 847 | PF00069 | 0.691 |
MOD_CK1_1 | 855 | 861 | PF00069 | 0.530 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.655 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.613 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.522 |
MOD_CK2_1 | 277 | 283 | PF00069 | 0.375 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.391 |
MOD_CK2_1 | 411 | 417 | PF00069 | 0.428 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.657 |
MOD_CK2_1 | 599 | 605 | PF00069 | 0.503 |
MOD_CK2_1 | 820 | 826 | PF00069 | 0.764 |
MOD_CK2_1 | 830 | 836 | PF00069 | 0.793 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.585 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.307 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.450 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.772 |
MOD_GlcNHglycan | 640 | 643 | PF01048 | 0.417 |
MOD_GlcNHglycan | 758 | 761 | PF01048 | 0.527 |
MOD_GlcNHglycan | 788 | 791 | PF01048 | 0.738 |
MOD_GlcNHglycan | 797 | 800 | PF01048 | 0.737 |
MOD_GlcNHglycan | 832 | 835 | PF01048 | 0.802 |
MOD_GlcNHglycan | 854 | 857 | PF01048 | 0.745 |
MOD_GlcNHglycan | 876 | 879 | PF01048 | 0.637 |
MOD_GlcNHglycan | 923 | 927 | PF01048 | 0.729 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.764 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.555 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.515 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.335 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.438 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.376 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.477 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.645 |
MOD_GSK3_1 | 575 | 582 | PF00069 | 0.423 |
MOD_GSK3_1 | 657 | 664 | PF00069 | 0.406 |
MOD_GSK3_1 | 720 | 727 | PF00069 | 0.467 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.485 |
MOD_GSK3_1 | 784 | 791 | PF00069 | 0.644 |
MOD_GSK3_1 | 816 | 823 | PF00069 | 0.760 |
MOD_GSK3_1 | 837 | 844 | PF00069 | 0.724 |
MOD_GSK3_1 | 932 | 939 | PF00069 | 0.750 |
MOD_GSK3_1 | 973 | 980 | PF00069 | 0.644 |
MOD_N-GLC_1 | 145 | 150 | PF02516 | 0.576 |
MOD_N-GLC_1 | 578 | 583 | PF02516 | 0.411 |
MOD_N-GLC_1 | 585 | 590 | PF02516 | 0.372 |
MOD_N-GLC_1 | 764 | 769 | PF02516 | 0.508 |
MOD_N-GLC_1 | 932 | 937 | PF02516 | 0.762 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.389 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.628 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.278 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.275 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.317 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.377 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.466 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.464 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.651 |
MOD_NEK2_1 | 575 | 580 | PF00069 | 0.402 |
MOD_NEK2_1 | 694 | 699 | PF00069 | 0.358 |
MOD_NEK2_1 | 719 | 724 | PF00069 | 0.369 |
MOD_NEK2_1 | 788 | 793 | PF00069 | 0.691 |
MOD_NEK2_1 | 795 | 800 | PF00069 | 0.748 |
MOD_NEK2_1 | 965 | 970 | PF00069 | 0.696 |
MOD_NEK2_2 | 268 | 273 | PF00069 | 0.331 |
MOD_NEK2_2 | 676 | 681 | PF00069 | 0.341 |
MOD_NEK2_2 | 764 | 769 | PF00069 | 0.521 |
MOD_PIKK_1 | 10 | 16 | PF00454 | 0.817 |
MOD_PIKK_1 | 363 | 369 | PF00454 | 0.334 |
MOD_PK_1 | 163 | 169 | PF00069 | 0.616 |
MOD_PK_1 | 171 | 177 | PF00069 | 0.583 |
MOD_PK_1 | 608 | 614 | PF00069 | 0.472 |
MOD_PK_1 | 960 | 966 | PF00069 | 0.617 |
MOD_PKA_1 | 10 | 16 | PF00069 | 0.655 |
MOD_PKA_1 | 906 | 912 | PF00069 | 0.580 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.804 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.614 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.440 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.374 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.743 |
MOD_PKA_2 | 467 | 473 | PF00069 | 0.581 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.517 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.590 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.398 |
MOD_PKA_2 | 819 | 825 | PF00069 | 0.476 |
MOD_PKA_2 | 906 | 912 | PF00069 | 0.588 |
MOD_PKB_1 | 120 | 128 | PF00069 | 0.543 |
MOD_PKB_1 | 169 | 177 | PF00069 | 0.618 |
MOD_PKB_1 | 772 | 780 | PF00069 | 0.578 |
MOD_PKB_1 | 906 | 914 | PF00069 | 0.700 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.402 |
MOD_Plk_1 | 299 | 305 | PF00069 | 0.287 |
MOD_Plk_1 | 345 | 351 | PF00069 | 0.354 |
MOD_Plk_1 | 47 | 53 | PF00069 | 0.692 |
MOD_Plk_1 | 599 | 605 | PF00069 | 0.502 |
MOD_Plk_1 | 650 | 656 | PF00069 | 0.467 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.533 |
MOD_Plk_1 | 694 | 700 | PF00069 | 0.384 |
MOD_Plk_1 | 764 | 770 | PF00069 | 0.510 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.389 |
MOD_Plk_2-3 | 863 | 869 | PF00069 | 0.617 |
MOD_Plk_4 | 139 | 145 | PF00069 | 0.289 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.583 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.568 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.309 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.296 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.358 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.467 |
MOD_Plk_4 | 449 | 455 | PF00069 | 0.378 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.671 |
MOD_Plk_4 | 481 | 487 | PF00069 | 0.425 |
MOD_Plk_4 | 588 | 594 | PF00069 | 0.394 |
MOD_Plk_4 | 684 | 690 | PF00069 | 0.383 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.500 |
MOD_Plk_4 | 724 | 730 | PF00069 | 0.446 |
MOD_Plk_4 | 764 | 770 | PF00069 | 0.529 |
MOD_Plk_4 | 879 | 885 | PF00069 | 0.572 |
MOD_Plk_4 | 960 | 966 | PF00069 | 0.684 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.762 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.375 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.625 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.438 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.445 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.549 |
MOD_ProDKin_1 | 543 | 549 | PF00069 | 0.430 |
MOD_ProDKin_1 | 790 | 796 | PF00069 | 0.670 |
MOD_ProDKin_1 | 973 | 979 | PF00069 | 0.587 |
MOD_SUMO_for_1 | 607 | 610 | PF00179 | 0.538 |
MOD_SUMO_rev_2 | 208 | 216 | PF00179 | 0.383 |
TRG_DiLeu_BaEn_1 | 520 | 525 | PF01217 | 0.434 |
TRG_DiLeu_BaLyEn_6 | 777 | 782 | PF01217 | 0.662 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.288 |
TRG_ENDOCYTIC_2 | 172 | 175 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 619 | 622 | PF00928 | 0.362 |
TRG_ENDOCYTIC_2 | 707 | 710 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 75 | 78 | PF00928 | 0.439 |
TRG_ER_diArg_1 | 10 | 12 | PF00400 | 0.596 |
TRG_ER_diArg_1 | 168 | 171 | PF00400 | 0.608 |
TRG_ER_diArg_1 | 245 | 247 | PF00400 | 0.354 |
TRG_ER_diArg_1 | 251 | 254 | PF00400 | 0.304 |
TRG_ER_diArg_1 | 285 | 287 | PF00400 | 0.353 |
TRG_ER_diArg_1 | 612 | 614 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 771 | 774 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 778 | 780 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 887 | 890 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 906 | 908 | PF00400 | 0.670 |
TRG_NES_CRM1_1 | 684 | 695 | PF08389 | 0.371 |
TRG_Pf-PMV_PEXEL_1 | 314 | 318 | PF00026 | 0.330 |
TRG_Pf-PMV_PEXEL_1 | 424 | 428 | PF00026 | 0.505 |
TRG_Pf-PMV_PEXEL_1 | 471 | 475 | PF00026 | 0.480 |
TRG_Pf-PMV_PEXEL_1 | 779 | 783 | PF00026 | 0.664 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3Q4 | Leptomonas seymouri | 74% | 86% |
A0A0S4ITU4 | Bodo saltans | 46% | 100% |
A0A0S4IUA9 | Bodo saltans | 39% | 100% |
A0A1X0NV89 | Trypanosomatidae | 67% | 100% |
A0A1X0NVS9 | Trypanosomatidae | 40% | 94% |
A0A3R7MZY3 | Trypanosoma rangeli | 40% | 94% |
A0A3S7WRL1 | Leishmania donovani | 94% | 99% |
A0A422NYP6 | Trypanosoma rangeli | 68% | 100% |
A4H6F0 | Leishmania braziliensis | 86% | 100% |
A4HUU4 | Leishmania infantum | 94% | 99% |
D0A7L1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 100% |
D0A7L2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 94% |
Q384Y0 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 41% | 94% |
Q384Y1 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 62% | 100% |
Q4QH47 | Leishmania major | 93% | 100% |
V5BW80 | Trypanosoma cruzi | 70% | 100% |