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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q883
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006259 | DNA metabolic process | 4 | 2 |
GO:0006281 | DNA repair | 5 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006950 | response to stress | 2 | 2 |
GO:0006974 | DNA damage response | 4 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0005524 | ATP binding | 5 | 8 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 8 |
GO:0016491 | oxidoreductase activity | 2 | 8 |
GO:0017076 | purine nucleotide binding | 4 | 8 |
GO:0030554 | adenyl nucleotide binding | 5 | 8 |
GO:0032553 | ribonucleotide binding | 3 | 8 |
GO:0032555 | purine ribonucleotide binding | 4 | 8 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 8 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 8 |
GO:0036094 | small molecule binding | 2 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043168 | anion binding | 3 | 8 |
GO:0043169 | cation binding | 3 | 8 |
GO:0046872 | metal ion binding | 4 | 8 |
GO:0051213 | dioxygenase activity | 3 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:0097367 | carbohydrate derivative binding | 2 | 8 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 8 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 8 |
GO:0140657 | ATP-dependent activity | 1 | 8 |
GO:0140658 | ATP-dependent chromatin remodeler activity | 3 | 8 |
GO:1901265 | nucleoside phosphate binding | 3 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 447 | 451 | PF00656 | 0.464 |
CLV_NRD_NRD_1 | 254 | 256 | PF00675 | 0.238 |
CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.293 |
CLV_NRD_NRD_1 | 442 | 444 | PF00675 | 0.239 |
CLV_NRD_NRD_1 | 531 | 533 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 591 | 593 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 651 | 653 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 862 | 864 | PF00675 | 0.458 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.280 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 442 | 444 | PF00082 | 0.239 |
CLV_PCSK_KEX2_1 | 460 | 462 | PF00082 | 0.239 |
CLV_PCSK_KEX2_1 | 531 | 533 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 591 | 593 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 651 | 653 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 657 | 659 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 864 | 866 | PF00082 | 0.468 |
CLV_PCSK_PC1ET2_1 | 256 | 258 | PF00082 | 0.264 |
CLV_PCSK_PC1ET2_1 | 460 | 462 | PF00082 | 0.281 |
CLV_PCSK_PC1ET2_1 | 657 | 659 | PF00082 | 0.514 |
CLV_PCSK_PC1ET2_1 | 864 | 866 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 350 | 354 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.281 |
CLV_PCSK_SKI1_1 | 452 | 456 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 461 | 465 | PF00082 | 0.221 |
CLV_PCSK_SKI1_1 | 543 | 547 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 594 | 598 | PF00082 | 0.708 |
CLV_PCSK_SKI1_1 | 644 | 648 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 793 | 797 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 840 | 844 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 864 | 868 | PF00082 | 0.482 |
CLV_Separin_Metazoa | 11 | 15 | PF03568 | 0.489 |
CLV_Separin_Metazoa | 414 | 418 | PF03568 | 0.481 |
DEG_APCC_DBOX_1 | 792 | 800 | PF00400 | 0.444 |
DEG_MDM2_SWIB_1 | 344 | 352 | PF02201 | 0.481 |
DEG_SPOP_SBC_1 | 680 | 684 | PF00917 | 0.595 |
DOC_CYCLIN_yCln2_LP_2 | 666 | 672 | PF00134 | 0.540 |
DOC_MAPK_gen_1 | 189 | 196 | PF00069 | 0.439 |
DOC_MAPK_gen_1 | 255 | 261 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 657 | 668 | PF00069 | 0.483 |
DOC_MAPK_gen_1 | 774 | 782 | PF00069 | 0.527 |
DOC_MAPK_gen_1 | 888 | 897 | PF00069 | 0.492 |
DOC_MAPK_MEF2A_6 | 427 | 436 | PF00069 | 0.439 |
DOC_MAPK_MEF2A_6 | 661 | 670 | PF00069 | 0.548 |
DOC_MAPK_MEF2A_6 | 788 | 796 | PF00069 | 0.475 |
DOC_PP1_RVXF_1 | 737 | 744 | PF00149 | 0.439 |
DOC_PP1_RVXF_1 | 838 | 845 | PF00149 | 0.376 |
DOC_PP2B_LxvP_1 | 400 | 403 | PF13499 | 0.439 |
DOC_PP2B_LxvP_1 | 455 | 458 | PF13499 | 0.439 |
DOC_PP2B_LxvP_1 | 666 | 669 | PF13499 | 0.525 |
DOC_PP2B_LxvP_1 | 897 | 900 | PF13499 | 0.481 |
DOC_PP2B_PxIxI_1 | 522 | 528 | PF00149 | 0.439 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 680 | 684 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 760 | 764 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 879 | 883 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 900 | 904 | PF00917 | 0.618 |
DOC_USP7_UBL2_3 | 483 | 487 | PF12436 | 0.481 |
DOC_USP7_UBL2_3 | 657 | 661 | PF12436 | 0.413 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 381 | 386 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 498 | 503 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 545 | 550 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 788 | 793 | PF00397 | 0.481 |
LIG_14-3-3_CanoR_1 | 137 | 146 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 257 | 262 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 334 | 344 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 378 | 386 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 427 | 436 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 461 | 466 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 515 | 525 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 543 | 552 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 694 | 702 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 888 | 897 | PF00244 | 0.492 |
LIG_Actin_WH2_2 | 428 | 444 | PF00022 | 0.481 |
LIG_Actin_WH2_2 | 578 | 596 | PF00022 | 0.564 |
LIG_APCC_ABBA_1 | 704 | 709 | PF00400 | 0.566 |
LIG_APCC_ABBA_1 | 780 | 785 | PF00400 | 0.493 |
LIG_APCC_ABBAyCdc20_2 | 177 | 183 | PF00400 | 0.481 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.465 |
LIG_BRCT_BRCA1_1 | 432 | 436 | PF00533 | 0.481 |
LIG_Clathr_ClatBox_1 | 21 | 25 | PF01394 | 0.375 |
LIG_Clathr_ClatBox_1 | 667 | 671 | PF01394 | 0.535 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.464 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.529 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.398 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.439 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.439 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.413 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.446 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.481 |
LIG_FHA_1 | 483 | 489 | PF00498 | 0.481 |
LIG_FHA_1 | 585 | 591 | PF00498 | 0.504 |
LIG_FHA_1 | 69 | 75 | PF00498 | 0.488 |
LIG_FHA_1 | 722 | 728 | PF00498 | 0.335 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.429 |
LIG_FHA_1 | 837 | 843 | PF00498 | 0.376 |
LIG_FHA_1 | 889 | 895 | PF00498 | 0.449 |
LIG_FHA_2 | 336 | 342 | PF00498 | 0.493 |
LIG_FHA_2 | 506 | 512 | PF00498 | 0.439 |
LIG_HP1_1 | 792 | 796 | PF01393 | 0.481 |
LIG_Integrin_RGD_1 | 91 | 93 | PF01839 | 0.241 |
LIG_LIR_Gen_1 | 267 | 275 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 507 | 514 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 843 | 849 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 183 | 187 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 267 | 271 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 273 | 278 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 392 | 397 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 433 | 439 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 507 | 513 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 744 | 749 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 843 | 847 | PF02991 | 0.356 |
LIG_LYPXL_S_1 | 393 | 397 | PF13949 | 0.281 |
LIG_LYPXL_yS_3 | 394 | 397 | PF13949 | 0.481 |
LIG_NRBOX | 49 | 55 | PF00104 | 0.439 |
LIG_PCNA_PIPBox_1 | 337 | 346 | PF02747 | 0.481 |
LIG_PCNA_PIPBox_1 | 387 | 396 | PF02747 | 0.473 |
LIG_PCNA_yPIPBox_3 | 334 | 344 | PF02747 | 0.481 |
LIG_PCNA_yPIPBox_3 | 387 | 398 | PF02747 | 0.473 |
LIG_Pex14_2 | 344 | 348 | PF04695 | 0.481 |
LIG_Pex14_2 | 506 | 510 | PF04695 | 0.481 |
LIG_SH2_CRK | 184 | 188 | PF00017 | 0.481 |
LIG_SH2_CRK | 268 | 272 | PF00017 | 0.509 |
LIG_SH2_CRK | 275 | 279 | PF00017 | 0.509 |
LIG_SH2_CRK | 477 | 481 | PF00017 | 0.439 |
LIG_SH2_GRB2like | 418 | 421 | PF00017 | 0.481 |
LIG_SH2_PTP2 | 524 | 527 | PF00017 | 0.550 |
LIG_SH2_SRC | 268 | 271 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 268 | 272 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 465 | 468 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 524 | 527 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 726 | 729 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 749 | 752 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 870 | 873 | PF00017 | 0.489 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.480 |
LIG_SH3_3 | 235 | 241 | PF00018 | 0.449 |
LIG_SH3_3 | 420 | 426 | PF00018 | 0.481 |
LIG_SH3_3 | 623 | 629 | PF00018 | 0.335 |
LIG_SH3_3 | 699 | 705 | PF00018 | 0.610 |
LIG_SH3_3 | 786 | 792 | PF00018 | 0.481 |
LIG_SUMO_SIM_anti_2 | 430 | 436 | PF11976 | 0.481 |
LIG_SUMO_SIM_anti_2 | 663 | 669 | PF11976 | 0.458 |
LIG_SUMO_SIM_par_1 | 192 | 200 | PF11976 | 0.439 |
LIG_SUMO_SIM_par_1 | 668 | 674 | PF11976 | 0.550 |
LIG_TRAF2_1 | 470 | 473 | PF00917 | 0.481 |
LIG_TRAF2_1 | 912 | 915 | PF00917 | 0.752 |
LIG_TRFH_1 | 419 | 423 | PF08558 | 0.476 |
LIG_TYR_ITIM | 416 | 421 | PF00017 | 0.493 |
LIG_UBA3_1 | 454 | 460 | PF00899 | 0.439 |
LIG_UBA3_1 | 894 | 902 | PF00899 | 0.472 |
LIG_WRC_WIRS_1 | 503 | 508 | PF05994 | 0.473 |
LIG_WRC_WIRS_1 | 743 | 748 | PF05994 | 0.443 |
MOD_CDC14_SPxK_1 | 304 | 307 | PF00782 | 0.441 |
MOD_CDK_SPK_2 | 788 | 793 | PF00069 | 0.481 |
MOD_CDK_SPxK_1 | 301 | 307 | PF00069 | 0.441 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.500 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.439 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.439 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.588 |
MOD_CK1_1 | 660 | 666 | PF00069 | 0.510 |
MOD_CK1_1 | 711 | 717 | PF00069 | 0.614 |
MOD_CK1_1 | 721 | 727 | PF00069 | 0.349 |
MOD_CK1_1 | 745 | 751 | PF00069 | 0.457 |
MOD_CK1_1 | 903 | 909 | PF00069 | 0.651 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.533 |
MOD_CK2_1 | 467 | 473 | PF00069 | 0.481 |
MOD_CK2_1 | 505 | 511 | PF00069 | 0.439 |
MOD_CK2_1 | 601 | 607 | PF00069 | 0.558 |
MOD_CK2_1 | 693 | 699 | PF00069 | 0.719 |
MOD_CK2_1 | 775 | 781 | PF00069 | 0.493 |
MOD_CK2_1 | 909 | 915 | PF00069 | 0.641 |
MOD_DYRK1A_RPxSP_1 | 788 | 792 | PF00069 | 0.458 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.197 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.336 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.315 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.381 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.189 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.268 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.641 |
MOD_GlcNHglycan | 695 | 698 | PF01048 | 0.621 |
MOD_GlcNHglycan | 767 | 770 | PF01048 | 0.257 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.315 |
MOD_GlcNHglycan | 867 | 870 | PF01048 | 0.516 |
MOD_GlcNHglycan | 881 | 884 | PF01048 | 0.475 |
MOD_GlcNHglycan | 903 | 906 | PF01048 | 0.551 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.480 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.444 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.356 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.473 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.524 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.451 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.482 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.424 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.459 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.481 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.446 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.520 |
MOD_GSK3_1 | 714 | 721 | PF00069 | 0.521 |
MOD_GSK3_1 | 741 | 748 | PF00069 | 0.440 |
MOD_GSK3_1 | 765 | 772 | PF00069 | 0.436 |
MOD_GSK3_1 | 836 | 843 | PF00069 | 0.546 |
MOD_GSK3_1 | 900 | 907 | PF00069 | 0.624 |
MOD_LATS_1 | 425 | 431 | PF00433 | 0.481 |
MOD_LATS_1 | 611 | 617 | PF00433 | 0.471 |
MOD_N-GLC_1 | 680 | 685 | PF02516 | 0.614 |
MOD_N-GLC_1 | 714 | 719 | PF02516 | 0.488 |
MOD_N-GLC_1 | 806 | 811 | PF02516 | 0.239 |
MOD_N-GLC_1 | 855 | 860 | PF02516 | 0.420 |
MOD_N-GLC_2 | 812 | 814 | PF02516 | 0.281 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.505 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.522 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.378 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.439 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.415 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.464 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.498 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.461 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.495 |
MOD_NEK2_1 | 584 | 589 | PF00069 | 0.540 |
MOD_NEK2_1 | 601 | 606 | PF00069 | 0.424 |
MOD_NEK2_1 | 647 | 652 | PF00069 | 0.335 |
MOD_NEK2_1 | 673 | 678 | PF00069 | 0.606 |
MOD_NEK2_1 | 718 | 723 | PF00069 | 0.488 |
MOD_NEK2_1 | 727 | 732 | PF00069 | 0.578 |
MOD_NEK2_1 | 795 | 800 | PF00069 | 0.439 |
MOD_NEK2_1 | 806 | 811 | PF00069 | 0.439 |
MOD_NEK2_1 | 872 | 877 | PF00069 | 0.558 |
MOD_NEK2_2 | 769 | 774 | PF00069 | 0.481 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.439 |
MOD_PIKK_1 | 721 | 727 | PF00454 | 0.351 |
MOD_PIKK_1 | 855 | 861 | PF00454 | 0.420 |
MOD_PKA_1 | 657 | 663 | PF00069 | 0.498 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.484 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.626 |
MOD_PKA_2 | 516 | 522 | PF00069 | 0.481 |
MOD_PKA_2 | 553 | 559 | PF00069 | 0.629 |
MOD_PKA_2 | 657 | 663 | PF00069 | 0.498 |
MOD_PKA_2 | 68 | 74 | PF00069 | 0.389 |
MOD_PKA_2 | 693 | 699 | PF00069 | 0.575 |
MOD_PKB_1 | 255 | 263 | PF00069 | 0.481 |
MOD_PKB_1 | 863 | 871 | PF00069 | 0.495 |
MOD_Plk_1 | 160 | 166 | PF00069 | 0.482 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.467 |
MOD_Plk_1 | 714 | 720 | PF00069 | 0.537 |
MOD_Plk_1 | 855 | 861 | PF00069 | 0.420 |
MOD_Plk_2-3 | 910 | 916 | PF00069 | 0.682 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.454 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.420 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.400 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.439 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.467 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.447 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.419 |
MOD_Plk_4 | 584 | 590 | PF00069 | 0.643 |
MOD_Plk_4 | 601 | 607 | PF00069 | 0.454 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.441 |
MOD_Plk_4 | 742 | 748 | PF00069 | 0.491 |
MOD_Plk_4 | 775 | 781 | PF00069 | 0.493 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.493 |
MOD_ProDKin_1 | 381 | 387 | PF00069 | 0.442 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.481 |
MOD_ProDKin_1 | 498 | 504 | PF00069 | 0.491 |
MOD_ProDKin_1 | 545 | 551 | PF00069 | 0.559 |
MOD_ProDKin_1 | 788 | 794 | PF00069 | 0.481 |
MOD_SUMO_rev_2 | 446 | 454 | PF00179 | 0.440 |
MOD_SUMO_rev_2 | 733 | 741 | PF00179 | 0.491 |
MOD_SUMO_rev_2 | 858 | 866 | PF00179 | 0.449 |
TRG_DiLeu_BaEn_1 | 17 | 22 | PF01217 | 0.365 |
TRG_DiLeu_BaEn_2 | 10 | 16 | PF01217 | 0.493 |
TRG_DiLeu_BaLyEn_6 | 392 | 397 | PF01217 | 0.439 |
TRG_DiLeu_LyEn_5 | 57 | 62 | PF01217 | 0.458 |
TRG_ENDOCYTIC_2 | 184 | 187 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 394 | 397 | PF00928 | 0.509 |
TRG_ENDOCYTIC_2 | 418 | 421 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 477 | 480 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 524 | 527 | PF00928 | 0.550 |
TRG_ER_diArg_1 | 334 | 336 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 441 | 443 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 514 | 517 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 530 | 532 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 590 | 592 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 62 | 65 | PF00400 | 0.441 |
TRG_NES_CRM1_1 | 11 | 25 | PF08389 | 0.362 |
TRG_Pf-PMV_PEXEL_1 | 334 | 339 | PF00026 | 0.281 |
TRG_Pf-PMV_PEXEL_1 | 350 | 354 | PF00026 | 0.183 |
TRG_Pf-PMV_PEXEL_1 | 579 | 583 | PF00026 | 0.629 |
TRG_Pf-PMV_PEXEL_1 | 732 | 737 | PF00026 | 0.293 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFY0 | Leptomonas seymouri | 67% | 74% |
A0A0S4IS76 | Bodo saltans | 40% | 83% |
A0A3S7X1L6 | Leishmania donovani | 93% | 73% |
A4HGN6 | Leishmania braziliensis | 80% | 72% |
A4I3Q9 | Leishmania infantum | 93% | 73% |
D0A899 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 100% |
E9B002 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
O13762 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 100% |
O60177 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 27% | 89% |
P0CQ66 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 26% | 77% |
P0CQ67 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 26% | 77% |
P32849 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 79% |
Q14527 | Homo sapiens | 29% | 91% |
Q4IJ84 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 26% | 80% |
Q4PGG5 | Ustilago maydis (strain 521 / FGSC 9021) | 26% | 66% |
Q4WVM1 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 28% | 74% |
Q5BHD6 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 26% | 77% |
Q6BIP2 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 26% | 77% |
Q6C2R8 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 27% | 90% |
Q6CJM4 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 25% | 83% |
Q6FY76 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 27% | 80% |
Q6PCN7 | Mus musculus | 28% | 92% |
Q753V5 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 26% | 85% |
Q7S1P9 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 26% | 75% |
Q94BR5 | Arabidopsis thaliana | 25% | 94% |
Q95216 | Oryctolagus cuniculus | 26% | 92% |
Q9FIY7 | Arabidopsis thaliana | 27% | 72% |
Q9FNI6 | Arabidopsis thaliana | 28% | 90% |
Q9LHE4 | Arabidopsis thaliana | 27% | 88% |