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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 7 |
GO:0043226 | organelle | 2 | 7 |
GO:0043227 | membrane-bounded organelle | 3 | 7 |
GO:0043229 | intracellular organelle | 3 | 7 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0031010 | ISWI-type complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0070603 | SWI/SNF superfamily-type complex | 3 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1904949 | ATPase complex | 3 | 1 |
Related structures:
AlphaFold database: A0A3S7XAG3
Term | Name | Level | Count |
---|---|---|---|
GO:0006325 | chromatin organization | 4 | 1 |
GO:0006338 | chromatin remodeling | 5 | 1 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009890 | negative regulation of biosynthetic process | 5 | 1 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010558 | negative regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0031327 | negative regulation of cellular biosynthetic process | 6 | 1 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 1 |
GO:0031554 | regulation of termination of DNA-templated transcription | 6 | 1 |
GO:0031555 | transcriptional attenuation | 7 | 1 |
GO:0043244 | regulation of protein-containing complex disassembly | 5 | 1 |
GO:0045892 | negative regulation of DNA-templated transcription | 7 | 1 |
GO:0045893 | positive regulation of DNA-templated transcription | 7 | 1 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051128 | regulation of cellular component organization | 4 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0051253 | negative regulation of RNA metabolic process | 6 | 1 |
GO:0051254 | positive regulation of RNA metabolic process | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1902679 | negative regulation of RNA biosynthetic process | 7 | 1 |
GO:1902680 | positive regulation of RNA biosynthetic process | 7 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:1903507 | negative regulation of nucleic acid-templated transcription | 8 | 1 |
GO:1903508 | positive regulation of nucleic acid-templated transcription | 8 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 209 | 213 | PF00656 | 0.625 |
CLV_C14_Caspase3-7 | 594 | 598 | PF00656 | 0.668 |
CLV_C14_Caspase3-7 | 600 | 604 | PF00656 | 0.547 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.589 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 580 | 582 | PF00675 | 0.658 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 755 | 757 | PF00675 | 0.642 |
CLV_NRD_NRD_1 | 823 | 825 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 855 | 857 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 892 | 894 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 914 | 916 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 957 | 959 | PF00675 | 0.284 |
CLV_PCSK_FUR_1 | 202 | 206 | PF00082 | 0.636 |
CLV_PCSK_FUR_1 | 413 | 417 | PF00082 | 0.453 |
CLV_PCSK_FUR_1 | 853 | 857 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 585 | 587 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 825 | 827 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 855 | 857 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 892 | 894 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 913 | 915 | PF00082 | 0.358 |
CLV_PCSK_KEX2_1 | 957 | 959 | PF00082 | 0.284 |
CLV_PCSK_PC1ET2_1 | 332 | 334 | PF00082 | 0.568 |
CLV_PCSK_PC1ET2_1 | 415 | 417 | PF00082 | 0.462 |
CLV_PCSK_PC1ET2_1 | 420 | 422 | PF00082 | 0.468 |
CLV_PCSK_PC1ET2_1 | 579 | 581 | PF00082 | 0.600 |
CLV_PCSK_PC1ET2_1 | 825 | 827 | PF00082 | 0.537 |
CLV_PCSK_PC7_1 | 202 | 208 | PF00082 | 0.697 |
CLV_PCSK_PC7_1 | 416 | 422 | PF00082 | 0.553 |
CLV_PCSK_PC7_1 | 441 | 447 | PF00082 | 0.570 |
CLV_PCSK_PC7_1 | 581 | 587 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.628 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 554 | 558 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 738 | 742 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 897 | 901 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 918 | 922 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 966 | 970 | PF00082 | 0.400 |
DEG_APCC_DBOX_1 | 965 | 973 | PF00400 | 0.284 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.512 |
DEG_SCF_TRCP1_1 | 189 | 195 | PF00400 | 0.613 |
DEG_SPOP_SBC_1 | 604 | 608 | PF00917 | 0.619 |
DOC_ANK_TNKS_1 | 445 | 452 | PF00023 | 0.608 |
DOC_CKS1_1 | 465 | 470 | PF01111 | 0.729 |
DOC_CKS1_1 | 482 | 487 | PF01111 | 0.503 |
DOC_CKS1_1 | 550 | 555 | PF01111 | 0.581 |
DOC_CYCLIN_RxL_1 | 500 | 508 | PF00134 | 0.525 |
DOC_CYCLIN_RxL_1 | 532 | 541 | PF00134 | 0.486 |
DOC_CYCLIN_yCln2_LP_2 | 371 | 377 | PF00134 | 0.360 |
DOC_MAPK_DCC_7 | 162 | 171 | PF00069 | 0.600 |
DOC_MAPK_gen_1 | 89 | 95 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 535 | 542 | PF00069 | 0.492 |
DOC_PP1_RVXF_1 | 1000 | 1006 | PF00149 | 0.638 |
DOC_PP1_RVXF_1 | 853 | 860 | PF00149 | 0.346 |
DOC_PP4_FxxP_1 | 394 | 397 | PF00568 | 0.504 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.782 |
DOC_USP7_MATH_1 | 604 | 608 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 623 | 627 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 701 | 705 | PF00917 | 0.569 |
DOC_USP7_MATH_2 | 944 | 950 | PF00917 | 0.313 |
DOC_USP7_UBL2_3 | 426 | 430 | PF12436 | 0.563 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.559 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 481 | 486 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 546 | 551 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 629 | 634 | PF00397 | 0.794 |
LIG_14-3-3_CanoR_1 | 204 | 214 | PF00244 | 0.714 |
LIG_14-3-3_CanoR_1 | 586 | 596 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 677 | 683 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 69 | 79 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 84 | 93 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 892 | 901 | PF00244 | 0.253 |
LIG_Actin_WH2_2 | 300 | 315 | PF00022 | 0.385 |
LIG_AP2alpha_2 | 660 | 662 | PF02296 | 0.605 |
LIG_BIR_III_4 | 525 | 529 | PF00653 | 0.539 |
LIG_BRCT_BRCA1_1 | 353 | 357 | PF00533 | 0.405 |
LIG_BRCT_BRCA1_1 | 612 | 616 | PF00533 | 0.550 |
LIG_Clathr_ClatBox_1 | 1000 | 1004 | PF01394 | 0.573 |
LIG_Clathr_ClatBox_1 | 47 | 51 | PF01394 | 0.314 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.652 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.629 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.567 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.540 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.474 |
LIG_FHA_1 | 550 | 556 | PF00498 | 0.544 |
LIG_FHA_1 | 877 | 883 | PF00498 | 0.441 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.431 |
LIG_FHA_2 | 183 | 189 | PF00498 | 0.680 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.415 |
LIG_FHA_2 | 396 | 402 | PF00498 | 0.593 |
LIG_FHA_2 | 588 | 594 | PF00498 | 0.712 |
LIG_FHA_2 | 623 | 629 | PF00498 | 0.704 |
LIG_FHA_2 | 630 | 636 | PF00498 | 0.645 |
LIG_FHA_2 | 641 | 647 | PF00498 | 0.678 |
LIG_FHA_2 | 769 | 775 | PF00498 | 0.594 |
LIG_FHA_2 | 797 | 803 | PF00498 | 0.693 |
LIG_FHA_2 | 975 | 981 | PF00498 | 0.598 |
LIG_LIR_Apic_2 | 391 | 397 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 296 | 305 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 336 | 346 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 827 | 836 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 296 | 301 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 336 | 341 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 470 | 476 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 568 | 572 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 6 | 11 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 681 | 685 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 77 | 81 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 827 | 833 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 852 | 857 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 879 | 883 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 938 | 943 | PF02991 | 0.336 |
LIG_MAD2 | 865 | 873 | PF02301 | 0.379 |
LIG_NRBOX | 739 | 745 | PF00104 | 0.585 |
LIG_PALB2_WD40_1 | 558 | 566 | PF16756 | 0.553 |
LIG_PCNA_yPIPBox_3 | 231 | 245 | PF02747 | 0.595 |
LIG_PCNA_yPIPBox_3 | 89 | 99 | PF02747 | 0.388 |
LIG_Pex14_2 | 294 | 298 | PF04695 | 0.488 |
LIG_RPA_C_Fungi | 888 | 900 | PF08784 | 0.251 |
LIG_SH2_CRK | 34 | 38 | PF00017 | 0.350 |
LIG_SH2_CRK | 830 | 834 | PF00017 | 0.634 |
LIG_SH2_CRK | 854 | 858 | PF00017 | 0.344 |
LIG_SH2_CRK | 997 | 1001 | PF00017 | 0.500 |
LIG_SH2_GRB2like | 997 | 1000 | PF00017 | 0.558 |
LIG_SH2_PTP2 | 78 | 81 | PF00017 | 0.472 |
LIG_SH2_STAP1 | 245 | 249 | PF00017 | 0.464 |
LIG_SH2_STAP1 | 476 | 480 | PF00017 | 0.604 |
LIG_SH2_STAP1 | 60 | 64 | PF00017 | 0.435 |
LIG_SH2_STAP1 | 830 | 834 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 473 | 476 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 868 | 871 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 947 | 950 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 975 | 978 | PF00017 | 0.525 |
LIG_SH3_3 | 547 | 553 | PF00018 | 0.628 |
LIG_SH3_3 | 631 | 637 | PF00018 | 0.556 |
LIG_SH3_3 | 875 | 881 | PF00018 | 0.298 |
LIG_SUMO_SIM_par_1 | 167 | 174 | PF11976 | 0.659 |
LIG_SUMO_SIM_par_1 | 536 | 541 | PF11976 | 0.482 |
LIG_SxIP_EBH_1 | 72 | 84 | PF03271 | 0.389 |
LIG_TRAF2_1 | 27 | 30 | PF00917 | 0.531 |
LIG_TRAF2_1 | 38 | 41 | PF00917 | 0.443 |
LIG_TRAF2_1 | 398 | 401 | PF00917 | 0.506 |
LIG_TRAF2_1 | 626 | 629 | PF00917 | 0.732 |
LIG_TRAF2_1 | 652 | 655 | PF00917 | 0.714 |
LIG_TRAF2_1 | 978 | 981 | PF00917 | 0.619 |
LIG_TYR_ITIM | 32 | 37 | PF00017 | 0.355 |
LIG_TYR_ITIM | 76 | 81 | PF00017 | 0.454 |
LIG_UBA3_1 | 994 | 1002 | PF00899 | 0.631 |
LIG_WRC_WIRS_1 | 512 | 517 | PF05994 | 0.559 |
LIG_WRC_WIRS_1 | 948 | 953 | PF05994 | 0.391 |
MOD_CDK_SPK_2 | 549 | 554 | PF00069 | 0.593 |
MOD_CDK_SPxxK_3 | 629 | 636 | PF00069 | 0.513 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.676 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.688 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.743 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.517 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.648 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.510 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.358 |
MOD_CK1_1 | 496 | 502 | PF00069 | 0.503 |
MOD_CK1_1 | 541 | 547 | PF00069 | 0.581 |
MOD_CK1_1 | 549 | 555 | PF00069 | 0.540 |
MOD_CK1_1 | 602 | 608 | PF00069 | 0.711 |
MOD_CK1_1 | 609 | 615 | PF00069 | 0.749 |
MOD_CK1_1 | 618 | 624 | PF00069 | 0.741 |
MOD_CK1_1 | 678 | 684 | PF00069 | 0.630 |
MOD_CK1_1 | 749 | 755 | PF00069 | 0.561 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.481 |
MOD_CK1_1 | 895 | 901 | PF00069 | 0.490 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.524 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.595 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.420 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.424 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.597 |
MOD_CK2_1 | 585 | 591 | PF00069 | 0.724 |
MOD_CK2_1 | 614 | 620 | PF00069 | 0.724 |
MOD_CK2_1 | 622 | 628 | PF00069 | 0.651 |
MOD_CK2_1 | 629 | 635 | PF00069 | 0.576 |
MOD_CK2_1 | 640 | 646 | PF00069 | 0.680 |
MOD_CK2_1 | 974 | 980 | PF00069 | 0.531 |
MOD_Cter_Amidation | 911 | 914 | PF01082 | 0.358 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.528 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.667 |
MOD_GlcNHglycan | 188 | 192 | PF01048 | 0.660 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.597 |
MOD_GlcNHglycan | 573 | 576 | PF01048 | 0.484 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.450 |
MOD_GlcNHglycan | 625 | 628 | PF01048 | 0.822 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.316 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.673 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.627 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.425 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.573 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.471 |
MOD_GSK3_1 | 595 | 602 | PF00069 | 0.695 |
MOD_GSK3_1 | 603 | 610 | PF00069 | 0.552 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.706 |
MOD_GSK3_1 | 656 | 663 | PF00069 | 0.631 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.318 |
MOD_GSK3_1 | 746 | 753 | PF00069 | 0.526 |
MOD_GSK3_1 | 757 | 764 | PF00069 | 0.623 |
MOD_GSK3_1 | 792 | 799 | PF00069 | 0.579 |
MOD_GSK3_1 | 947 | 954 | PF00069 | 0.380 |
MOD_N-GLC_1 | 121 | 126 | PF02516 | 0.663 |
MOD_N-GLC_1 | 16 | 21 | PF02516 | 0.514 |
MOD_N-GLC_1 | 195 | 200 | PF02516 | 0.687 |
MOD_N-GLC_1 | 505 | 510 | PF02516 | 0.573 |
MOD_N-GLC_1 | 761 | 766 | PF02516 | 0.595 |
MOD_N-GLC_1 | 873 | 878 | PF02516 | 0.379 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.558 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.550 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.466 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.499 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.500 |
MOD_NEK2_1 | 743 | 748 | PF00069 | 0.523 |
MOD_PIKK_1 | 175 | 181 | PF00454 | 0.677 |
MOD_PIKK_1 | 505 | 511 | PF00454 | 0.484 |
MOD_PIKK_1 | 757 | 763 | PF00454 | 0.563 |
MOD_PIKK_1 | 82 | 88 | PF00454 | 0.547 |
MOD_PKA_1 | 205 | 211 | PF00069 | 0.726 |
MOD_PKA_1 | 585 | 591 | PF00069 | 0.667 |
MOD_PKA_1 | 757 | 763 | PF00069 | 0.635 |
MOD_PKA_1 | 892 | 898 | PF00069 | 0.251 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.716 |
MOD_PKA_2 | 585 | 591 | PF00069 | 0.667 |
MOD_PKA_2 | 803 | 809 | PF00069 | 0.453 |
MOD_PKA_2 | 892 | 898 | PF00069 | 0.290 |
MOD_PKA_2 | 985 | 991 | PF00069 | 0.644 |
MOD_PKB_1 | 205 | 213 | PF00069 | 0.739 |
MOD_PKB_1 | 268 | 276 | PF00069 | 0.440 |
MOD_Plk_1 | 339 | 345 | PF00069 | 0.470 |
MOD_Plk_1 | 39 | 45 | PF00069 | 0.331 |
MOD_Plk_1 | 460 | 466 | PF00069 | 0.599 |
MOD_Plk_1 | 505 | 511 | PF00069 | 0.579 |
MOD_Plk_1 | 538 | 544 | PF00069 | 0.553 |
MOD_Plk_1 | 873 | 879 | PF00069 | 0.312 |
MOD_Plk_1 | 905 | 911 | PF00069 | 0.354 |
MOD_Plk_2-3 | 126 | 132 | PF00069 | 0.505 |
MOD_Plk_2-3 | 595 | 601 | PF00069 | 0.695 |
MOD_Plk_2-3 | 660 | 666 | PF00069 | 0.555 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.331 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.609 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.544 |
MOD_Plk_4 | 947 | 953 | PF00069 | 0.377 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.697 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.495 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.557 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.730 |
MOD_ProDKin_1 | 481 | 487 | PF00069 | 0.504 |
MOD_ProDKin_1 | 546 | 552 | PF00069 | 0.613 |
MOD_ProDKin_1 | 629 | 635 | PF00069 | 0.796 |
MOD_SUMO_for_1 | 230 | 233 | PF00179 | 0.591 |
MOD_SUMO_for_1 | 414 | 417 | PF00179 | 0.422 |
MOD_SUMO_for_1 | 429 | 432 | PF00179 | 0.480 |
MOD_SUMO_rev_2 | 425 | 431 | PF00179 | 0.563 |
MOD_SUMO_rev_2 | 617 | 626 | PF00179 | 0.600 |
MOD_SUMO_rev_2 | 660 | 669 | PF00179 | 0.602 |
MOD_SUMO_rev_2 | 720 | 729 | PF00179 | 0.534 |
MOD_SUMO_rev_2 | 734 | 743 | PF00179 | 0.404 |
MOD_SUMO_rev_2 | 782 | 788 | PF00179 | 0.599 |
MOD_SUMO_rev_2 | 925 | 935 | PF00179 | 0.300 |
TRG_DiLeu_BaEn_1 | 439 | 444 | PF01217 | 0.495 |
TRG_DiLeu_BaEn_1 | 461 | 466 | PF01217 | 0.632 |
TRG_DiLeu_BaEn_1 | 739 | 744 | PF01217 | 0.488 |
TRG_DiLeu_BaEn_3 | 904 | 910 | PF01217 | 0.288 |
TRG_DiLeu_BaEn_4 | 905 | 911 | PF01217 | 0.355 |
TRG_DiLeu_BaLyEn_6 | 829 | 834 | PF01217 | 0.561 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 830 | 833 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 854 | 857 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 858 | 861 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 997 | 1000 | PF00928 | 0.586 |
TRG_ER_diArg_1 | 202 | 205 | PF00400 | 0.660 |
TRG_ER_diArg_1 | 421 | 423 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 444 | 447 | PF00400 | 0.576 |
TRG_ER_diArg_1 | 545 | 548 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 585 | 587 | PF00400 | 0.744 |
TRG_ER_diArg_1 | 854 | 856 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 913 | 915 | PF00400 | 0.358 |
TRG_NLS_Bipartite_1 | 404 | 424 | PF00514 | 0.561 |
TRG_NLS_MonoCore_2 | 576 | 581 | PF00514 | 0.608 |
TRG_NLS_MonoCore_2 | 755 | 760 | PF00514 | 0.589 |
TRG_NLS_MonoExtC_3 | 419 | 425 | PF00514 | 0.559 |
TRG_NLS_MonoExtC_3 | 576 | 581 | PF00514 | 0.563 |
TRG_NLS_MonoExtN_4 | 577 | 583 | PF00514 | 0.627 |
TRG_NLS_MonoExtN_4 | 756 | 761 | PF00514 | 0.595 |
TRG_Pf-PMV_PEXEL_1 | 421 | 425 | PF00026 | 0.471 |
TRG_Pf-PMV_PEXEL_1 | 446 | 450 | PF00026 | 0.650 |
TRG_Pf-PMV_PEXEL_1 | 457 | 461 | PF00026 | 0.695 |
TRG_Pf-PMV_PEXEL_1 | 727 | 731 | PF00026 | 0.552 |
TRG_Pf-PMV_PEXEL_1 | 832 | 837 | PF00026 | 0.678 |
TRG_Pf-PMV_PEXEL_1 | 897 | 902 | PF00026 | 0.430 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD66 | Leptomonas seymouri | 58% | 94% |
A0A1X0P937 | Trypanosomatidae | 39% | 100% |
A0A422NTX5 | Trypanosoma rangeli | 39% | 100% |
A4HNW6 | Leishmania braziliensis | 75% | 100% |
A4ICM8 | Leishmania infantum | 99% | 100% |
D0A2T4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9ASM6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q1X0 | Leishmania major | 91% | 100% |