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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0008023 | transcription elongation factor complex | 3 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0035101 | FACT complex | 4 | 12 |
GO:0140513 | nuclear protein-containing complex | 2 | 12 |
Related structures:
AlphaFold database: E9ADK4
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006260 | DNA replication | 5 | 12 |
GO:0006281 | DNA repair | 5 | 12 |
GO:0006325 | chromatin organization | 4 | 2 |
GO:0006354 | DNA-templated transcription elongation | 6 | 2 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 2 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 2 |
GO:0006368 | transcription elongation by RNA polymerase II | 7 | 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:0009058 | biosynthetic process | 2 | 2 |
GO:0009059 | macromolecule biosynthetic process | 4 | 2 |
GO:0009889 | regulation of biosynthetic process | 4 | 2 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 2 |
GO:0009893 | positive regulation of metabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 12 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 2 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 2 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0018130 | heterocycle biosynthetic process | 4 | 2 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 2 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 2 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 2 |
GO:0032774 | RNA biosynthetic process | 5 | 2 |
GO:0032784 | regulation of DNA-templated transcription elongation | 7 | 2 |
GO:0032786 | positive regulation of DNA-templated transcription, elongation | 8 | 2 |
GO:0032968 | positive regulation of transcription elongation by RNA polymerase II | 9 | 2 |
GO:0033554 | cellular response to stress | 3 | 12 |
GO:0034243 | regulation of transcription elongation by RNA polymerase II | 8 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 2 |
GO:0045893 | positive regulation of DNA-templated transcription | 7 | 2 |
GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 2 |
GO:0045944 | positive regulation of transcription by RNA polymerase II | 8 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0048518 | positive regulation of biological process | 3 | 2 |
GO:0048522 | positive regulation of cellular process | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0050896 | response to stimulus | 1 | 12 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 2 |
GO:0051252 | regulation of RNA metabolic process | 5 | 2 |
GO:0051254 | positive regulation of RNA metabolic process | 6 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 12 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
GO:1902680 | positive regulation of RNA biosynthetic process | 7 | 2 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 2 |
GO:1903508 | positive regulation of nucleic acid-templated transcription | 8 | 2 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003682 | chromatin binding | 2 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0031491 | nucleosome binding | 3 | 2 |
GO:0044877 | protein-containing complex binding | 2 | 2 |
GO:0003824 | catalytic activity | 1 | 3 |
GO:0004177 | aminopeptidase activity | 5 | 3 |
GO:0008233 | peptidase activity | 3 | 3 |
GO:0008238 | exopeptidase activity | 4 | 3 |
GO:0016787 | hydrolase activity | 2 | 3 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 932 | 936 | PF00656 | 0.705 |
CLV_C14_Caspase3-7 | 946 | 950 | PF00656 | 0.715 |
CLV_MEL_PAP_1 | 277 | 283 | PF00089 | 0.389 |
CLV_NRD_NRD_1 | 1002 | 1004 | PF00675 | 0.710 |
CLV_NRD_NRD_1 | 1043 | 1045 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.242 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 629 | 631 | PF00675 | 0.237 |
CLV_NRD_NRD_1 | 725 | 727 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 749 | 751 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 983 | 985 | PF00675 | 0.542 |
CLV_PCSK_KEX2_1 | 1004 | 1006 | PF00082 | 0.758 |
CLV_PCSK_KEX2_1 | 1043 | 1045 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.242 |
CLV_PCSK_KEX2_1 | 203 | 205 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 631 | 633 | PF00082 | 0.223 |
CLV_PCSK_KEX2_1 | 749 | 751 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 983 | 985 | PF00082 | 0.563 |
CLV_PCSK_PC1ET2_1 | 1004 | 1006 | PF00082 | 0.728 |
CLV_PCSK_PC1ET2_1 | 203 | 205 | PF00082 | 0.428 |
CLV_PCSK_PC1ET2_1 | 631 | 633 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 388 | 392 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 478 | 482 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 533 | 537 | PF00082 | 0.177 |
CLV_PCSK_SKI1_1 | 606 | 610 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 631 | 635 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 727 | 731 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 803 | 807 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 812 | 816 | PF00082 | 0.220 |
CLV_Separin_Metazoa | 145 | 149 | PF03568 | 0.391 |
DEG_APCC_DBOX_1 | 387 | 395 | PF00400 | 0.245 |
DEG_APCC_DBOX_1 | 477 | 485 | PF00400 | 0.496 |
DEG_APCC_DBOX_1 | 811 | 819 | PF00400 | 0.434 |
DEG_APCC_DBOX_1 | 866 | 874 | PF00400 | 0.434 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.606 |
DEG_SCF_FBW7_1 | 818 | 825 | PF00400 | 0.513 |
DOC_CDC14_PxL_1 | 157 | 165 | PF14671 | 0.444 |
DOC_CKS1_1 | 47 | 52 | PF01111 | 0.425 |
DOC_CYCLIN_RxL_1 | 291 | 300 | PF00134 | 0.389 |
DOC_CYCLIN_yCln2_LP_2 | 718 | 724 | PF00134 | 0.421 |
DOC_MAPK_DCC_7 | 641 | 651 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 541 | 548 | PF00069 | 0.517 |
DOC_MAPK_gen_1 | 726 | 734 | PF00069 | 0.335 |
DOC_MAPK_HePTP_8 | 850 | 862 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 1022 | 1030 | PF00069 | 0.642 |
DOC_MAPK_MEF2A_6 | 541 | 548 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 571 | 578 | PF00069 | 0.513 |
DOC_MAPK_MEF2A_6 | 726 | 734 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 853 | 862 | PF00069 | 0.436 |
DOC_MAPK_RevD_3 | 705 | 720 | PF00069 | 0.284 |
DOC_PP1_RVXF_1 | 509 | 515 | PF00149 | 0.419 |
DOC_PP1_RVXF_1 | 539 | 546 | PF00149 | 0.410 |
DOC_PP1_RVXF_1 | 697 | 704 | PF00149 | 0.297 |
DOC_PP1_RVXF_1 | 810 | 817 | PF00149 | 0.421 |
DOC_PP2B_LxvP_1 | 323 | 326 | PF13499 | 0.313 |
DOC_PP2B_LxvP_1 | 649 | 652 | PF13499 | 0.434 |
DOC_PP2B_PxIxI_1 | 857 | 863 | PF00149 | 0.513 |
DOC_SPAK_OSR1_1 | 280 | 284 | PF12202 | 0.313 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.268 |
DOC_USP7_MATH_1 | 633 | 637 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 706 | 710 | PF00917 | 0.367 |
DOC_USP7_MATH_1 | 748 | 752 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 866 | 870 | PF00917 | 0.434 |
DOC_USP7_UBL2_3 | 203 | 207 | PF12436 | 0.304 |
DOC_USP7_UBL2_3 | 423 | 427 | PF12436 | 0.388 |
DOC_USP7_UBL2_3 | 594 | 598 | PF12436 | 0.410 |
DOC_USP7_UBL2_3 | 853 | 857 | PF12436 | 0.434 |
DOC_WD40_RPTOR_TOS_1 | 403 | 409 | PF00400 | 0.245 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 515 | 520 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 642 | 647 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 818 | 823 | PF00397 | 0.513 |
LIG_14-3-3_CanoR_1 | 13 | 21 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 329 | 337 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 368 | 378 | PF00244 | 0.338 |
LIG_14-3-3_CanoR_1 | 458 | 467 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 478 | 488 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 511 | 515 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 632 | 642 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 682 | 686 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 749 | 753 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 803 | 808 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 894 | 898 | PF00244 | 0.535 |
LIG_Actin_WH2_2 | 667 | 684 | PF00022 | 0.420 |
LIG_AP2alpha_2 | 907 | 909 | PF02296 | 0.360 |
LIG_APCC_ABBA_1 | 270 | 275 | PF00400 | 0.389 |
LIG_BRCT_BRCA1_1 | 352 | 356 | PF00533 | 0.251 |
LIG_BRCT_BRCA1_1 | 842 | 846 | PF00533 | 0.482 |
LIG_CaM_IQ_9 | 616 | 632 | PF13499 | 0.476 |
LIG_Clathr_ClatBox_1 | 362 | 366 | PF01394 | 0.245 |
LIG_CSL_BTD_1 | 544 | 547 | PF09270 | 0.476 |
LIG_CtBP_PxDLS_1 | 1027 | 1031 | PF00389 | 0.715 |
LIG_deltaCOP1_diTrp_1 | 902 | 909 | PF00928 | 0.408 |
LIG_Dynein_DLC8_1 | 493 | 499 | PF01221 | 0.549 |
LIG_EH1_1 | 209 | 217 | PF00400 | 0.389 |
LIG_EH1_1 | 845 | 853 | PF00400 | 0.513 |
LIG_EVH1_2 | 244 | 248 | PF00568 | 0.389 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.445 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.435 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.263 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.296 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.250 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.280 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.241 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.659 |
LIG_FHA_1 | 571 | 577 | PF00498 | 0.421 |
LIG_FHA_1 | 651 | 657 | PF00498 | 0.532 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.426 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.401 |
LIG_FHA_1 | 823 | 829 | PF00498 | 0.420 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.389 |
LIG_FHA_2 | 894 | 900 | PF00498 | 0.462 |
LIG_FHA_2 | 920 | 926 | PF00498 | 0.685 |
LIG_FHA_2 | 937 | 943 | PF00498 | 0.490 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.587 |
LIG_GBD_Chelix_1 | 424 | 432 | PF00786 | 0.400 |
LIG_Integrin_isoDGR_2 | 639 | 641 | PF01839 | 0.258 |
LIG_Integrin_RGD_1 | 27 | 29 | PF01839 | 0.369 |
LIG_Integrin_RGD_1 | 911 | 913 | PF01839 | 0.565 |
LIG_LIR_Apic_2 | 854 | 858 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 141 | 151 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 235 | 245 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 286 | 296 | PF02991 | 0.268 |
LIG_LIR_Gen_1 | 36 | 42 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 430 | 441 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 513 | 522 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 575 | 586 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 692 | 703 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 835 | 844 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 913 | 921 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 977 | 986 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 141 | 146 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 235 | 240 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 286 | 291 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 331 | 337 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 36 | 41 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 430 | 436 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 513 | 517 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 692 | 698 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 709 | 714 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 796 | 800 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 835 | 839 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 913 | 918 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 977 | 981 | PF02991 | 0.598 |
LIG_NRBOX | 162 | 168 | PF00104 | 0.369 |
LIG_NRBOX | 319 | 325 | PF00104 | 0.290 |
LIG_NRBOX | 347 | 353 | PF00104 | 0.268 |
LIG_NRBOX | 476 | 482 | PF00104 | 0.374 |
LIG_NRBOX | 58 | 64 | PF00104 | 0.315 |
LIG_PCNA_yPIPBox_3 | 113 | 123 | PF02747 | 0.276 |
LIG_PCNA_yPIPBox_3 | 342 | 352 | PF02747 | 0.363 |
LIG_Pex14_1 | 38 | 42 | PF04695 | 0.424 |
LIG_Pex14_2 | 139 | 143 | PF04695 | 0.438 |
LIG_PTB_Apo_2 | 282 | 289 | PF02174 | 0.260 |
LIG_PTB_Phospho_1 | 282 | 288 | PF10480 | 0.260 |
LIG_REV1ctd_RIR_1 | 289 | 298 | PF16727 | 0.389 |
LIG_RPA_C_Fungi | 22 | 34 | PF08784 | 0.279 |
LIG_RPA_C_Fungi | 8 | 20 | PF08784 | 0.381 |
LIG_SH2_CRK | 334 | 338 | PF00017 | 0.301 |
LIG_SH2_CRK | 855 | 859 | PF00017 | 0.279 |
LIG_SH2_STAP1 | 288 | 292 | PF00017 | 0.260 |
LIG_SH2_STAP1 | 314 | 318 | PF00017 | 0.268 |
LIG_SH2_STAP1 | 572 | 576 | PF00017 | 0.268 |
LIG_SH2_STAT3 | 253 | 256 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.254 |
LIG_SH2_STAT5 | 572 | 575 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 711 | 714 | PF00017 | 0.435 |
LIG_SH3_3 | 1010 | 1016 | PF00018 | 0.683 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.361 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.436 |
LIG_SH3_3 | 516 | 522 | PF00018 | 0.522 |
LIG_SH3_3 | 523 | 529 | PF00018 | 0.553 |
LIG_SH3_3 | 541 | 547 | PF00018 | 0.219 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.443 |
LIG_SUMO_SIM_anti_2 | 102 | 107 | PF11976 | 0.489 |
LIG_SUMO_SIM_anti_2 | 275 | 280 | PF11976 | 0.261 |
LIG_SUMO_SIM_anti_2 | 359 | 366 | PF11976 | 0.225 |
LIG_SUMO_SIM_anti_2 | 77 | 84 | PF11976 | 0.360 |
LIG_SUMO_SIM_anti_2 | 829 | 835 | PF11976 | 0.279 |
LIG_SUMO_SIM_par_1 | 101 | 107 | PF11976 | 0.444 |
LIG_SUMO_SIM_par_1 | 294 | 300 | PF11976 | 0.279 |
LIG_SUMO_SIM_par_1 | 359 | 366 | PF11976 | 0.304 |
LIG_SUMO_SIM_par_1 | 858 | 864 | PF11976 | 0.389 |
LIG_TRAF2_1 | 133 | 136 | PF00917 | 0.354 |
LIG_TRAF2_1 | 580 | 583 | PF00917 | 0.245 |
LIG_TRAF2_1 | 751 | 754 | PF00917 | 0.435 |
LIG_TRAF2_1 | 779 | 782 | PF00917 | 0.477 |
LIG_TRFH_1 | 588 | 592 | PF08558 | 0.268 |
LIG_TYR_ITIM | 431 | 436 | PF00017 | 0.520 |
LIG_UBA3_1 | 694 | 699 | PF00899 | 0.449 |
LIG_WRC_WIRS_1 | 773 | 778 | PF05994 | 0.473 |
LIG_WRC_WIRS_1 | 833 | 838 | PF05994 | 0.389 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.388 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.355 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.375 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.248 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.332 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.616 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.510 |
MOD_CK1_1 | 936 | 942 | PF00069 | 0.604 |
MOD_CK1_1 | 947 | 953 | PF00069 | 0.652 |
MOD_CK1_1 | 961 | 967 | PF00069 | 0.639 |
MOD_CK1_1 | 974 | 980 | PF00069 | 0.508 |
MOD_CK2_1 | 497 | 503 | PF00069 | 0.575 |
MOD_CK2_1 | 510 | 516 | PF00069 | 0.259 |
MOD_CK2_1 | 748 | 754 | PF00069 | 0.460 |
MOD_CK2_1 | 824 | 830 | PF00069 | 0.347 |
MOD_CK2_1 | 893 | 899 | PF00069 | 0.505 |
MOD_CK2_1 | 919 | 925 | PF00069 | 0.647 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.502 |
MOD_CK2_1 | 936 | 942 | PF00069 | 0.472 |
MOD_CK2_1 | 951 | 957 | PF00069 | 0.610 |
MOD_CK2_1 | 974 | 980 | PF00069 | 0.638 |
MOD_CMANNOS | 906 | 909 | PF00535 | 0.388 |
MOD_Cter_Amidation | 492 | 495 | PF01082 | 0.470 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.313 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.490 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.439 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.397 |
MOD_GlcNHglycan | 3 | 6 | PF01048 | 0.459 |
MOD_GlcNHglycan | 315 | 319 | PF01048 | 0.418 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.374 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.340 |
MOD_GlcNHglycan | 611 | 614 | PF01048 | 0.413 |
MOD_GlcNHglycan | 635 | 638 | PF01048 | 0.320 |
MOD_GlcNHglycan | 746 | 749 | PF01048 | 0.620 |
MOD_GlcNHglycan | 842 | 845 | PF01048 | 0.268 |
MOD_GlcNHglycan | 878 | 881 | PF01048 | 0.389 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.329 |
MOD_GlcNHglycan | 964 | 967 | PF01048 | 0.695 |
MOD_GlcNHglycan | 971 | 976 | PF01048 | 0.600 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.528 |
MOD_GSK3_1 | 1017 | 1024 | PF00069 | 0.731 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.375 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.237 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.659 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.522 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.256 |
MOD_GSK3_1 | 739 | 746 | PF00069 | 0.468 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.366 |
MOD_GSK3_1 | 781 | 788 | PF00069 | 0.434 |
MOD_GSK3_1 | 789 | 796 | PF00069 | 0.445 |
MOD_GSK3_1 | 818 | 825 | PF00069 | 0.354 |
MOD_GSK3_1 | 842 | 849 | PF00069 | 0.337 |
MOD_GSK3_1 | 931 | 938 | PF00069 | 0.644 |
MOD_GSK3_1 | 947 | 954 | PF00069 | 0.574 |
MOD_GSK3_1 | 958 | 965 | PF00069 | 0.542 |
MOD_GSK3_1 | 967 | 974 | PF00069 | 0.635 |
MOD_LATS_1 | 801 | 807 | PF00433 | 0.393 |
MOD_N-GLC_1 | 369 | 374 | PF02516 | 0.200 |
MOD_N-GLC_1 | 5 | 10 | PF02516 | 0.483 |
MOD_N-GLC_1 | 919 | 924 | PF02516 | 0.660 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.361 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.274 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.278 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.546 |
MOD_NEK2_1 | 555 | 560 | PF00069 | 0.254 |
MOD_NEK2_1 | 574 | 579 | PF00069 | 0.413 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.301 |
MOD_NEK2_1 | 609 | 614 | PF00069 | 0.233 |
MOD_NEK2_1 | 681 | 686 | PF00069 | 0.309 |
MOD_NEK2_1 | 744 | 749 | PF00069 | 0.445 |
MOD_NEK2_1 | 846 | 851 | PF00069 | 0.304 |
MOD_NEK2_2 | 706 | 711 | PF00069 | 0.369 |
MOD_NEK2_2 | 714 | 719 | PF00069 | 0.292 |
MOD_NEK2_2 | 893 | 898 | PF00069 | 0.527 |
MOD_PIKK_1 | 252 | 258 | PF00454 | 0.389 |
MOD_PIKK_1 | 494 | 500 | PF00454 | 0.581 |
MOD_PIKK_1 | 785 | 791 | PF00454 | 0.395 |
MOD_PIKK_1 | 822 | 828 | PF00454 | 0.279 |
MOD_PKA_1 | 494 | 500 | PF00069 | 0.482 |
MOD_PKA_2 | 1021 | 1027 | PF00069 | 0.713 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.423 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.401 |
MOD_PKA_2 | 510 | 516 | PF00069 | 0.471 |
MOD_PKA_2 | 640 | 646 | PF00069 | 0.400 |
MOD_PKA_2 | 681 | 687 | PF00069 | 0.314 |
MOD_PKA_2 | 748 | 754 | PF00069 | 0.463 |
MOD_PKA_2 | 766 | 772 | PF00069 | 0.304 |
MOD_PKA_2 | 866 | 872 | PF00069 | 0.279 |
MOD_PKA_2 | 893 | 899 | PF00069 | 0.532 |
MOD_PKB_1 | 630 | 638 | PF00069 | 0.304 |
MOD_PKB_1 | 990 | 998 | PF00069 | 0.681 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.248 |
MOD_Plk_1 | 260 | 266 | PF00069 | 0.313 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.425 |
MOD_Plk_1 | 5 | 11 | PF00069 | 0.367 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.433 |
MOD_Plk_1 | 846 | 852 | PF00069 | 0.304 |
MOD_Plk_1 | 936 | 942 | PF00069 | 0.625 |
MOD_Plk_1 | 950 | 956 | PF00069 | 0.550 |
MOD_Plk_2-3 | 205 | 211 | PF00069 | 0.313 |
MOD_Plk_2-3 | 832 | 838 | PF00069 | 0.260 |
MOD_Plk_2-3 | 931 | 937 | PF00069 | 0.600 |
MOD_Plk_2-3 | 945 | 951 | PF00069 | 0.682 |
MOD_Plk_2-3 | 99 | 105 | PF00069 | 0.452 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.503 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.383 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.279 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.412 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.665 |
MOD_Plk_4 | 706 | 712 | PF00069 | 0.437 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.400 |
MOD_Plk_4 | 803 | 809 | PF00069 | 0.268 |
MOD_Plk_4 | 846 | 852 | PF00069 | 0.304 |
MOD_Plk_4 | 936 | 942 | PF00069 | 0.638 |
MOD_Plk_4 | 951 | 957 | PF00069 | 0.496 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.387 |
MOD_ProDKin_1 | 515 | 521 | PF00069 | 0.487 |
MOD_ProDKin_1 | 642 | 648 | PF00069 | 0.304 |
MOD_ProDKin_1 | 818 | 824 | PF00069 | 0.389 |
MOD_SUMO_for_1 | 218 | 221 | PF00179 | 0.268 |
MOD_SUMO_for_1 | 565 | 568 | PF00179 | 0.231 |
MOD_SUMO_for_1 | 623 | 626 | PF00179 | 0.402 |
MOD_SUMO_rev_2 | 200 | 209 | PF00179 | 0.299 |
MOD_SUMO_rev_2 | 558 | 567 | PF00179 | 0.238 |
TRG_DiLeu_BaEn_1 | 476 | 481 | PF01217 | 0.424 |
TRG_DiLeu_BaEn_1 | 78 | 83 | PF01217 | 0.341 |
TRG_ENDOCYTIC_2 | 217 | 220 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 288 | 291 | PF00928 | 0.260 |
TRG_ENDOCYTIC_2 | 334 | 337 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 433 | 436 | PF00928 | 0.548 |
TRG_ER_diArg_1 | 1002 | 1005 | PF00400 | 0.681 |
TRG_ER_diArg_1 | 1043 | 1045 | PF00400 | 0.633 |
TRG_ER_diArg_1 | 189 | 191 | PF00400 | 0.255 |
TRG_ER_diArg_1 | 764 | 767 | PF00400 | 0.456 |
TRG_NES_CRM1_1 | 381 | 392 | PF08389 | 0.256 |
TRG_NLS_MonoExtC_3 | 1002 | 1007 | PF00514 | 0.648 |
TRG_NLS_MonoExtN_4 | 1002 | 1008 | PF00514 | 0.634 |
TRG_Pf-PMV_PEXEL_1 | 426 | 430 | PF00026 | 0.379 |
TRG_Pf-PMV_PEXEL_1 | 478 | 483 | PF00026 | 0.391 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHS5 | Leptomonas seymouri | 75% | 99% |
A0A0S4JAR0 | Bodo saltans | 38% | 100% |
A0A1X0NZD4 | Trypanosomatidae | 54% | 100% |
A0A3S7X235 | Leishmania donovani | 95% | 100% |
A0A422NUY4 | Trypanosoma rangeli | 53% | 100% |
A4HH10 | Leishmania braziliensis | 84% | 100% |
A4I439 | Leishmania infantum | 95% | 100% |
C9ZKS3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
E9AM77 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
O82491 | Arabidopsis thaliana | 26% | 97% |
O94267 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
P0CQ22 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 28% | 100% |
P0CQ23 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 28% | 100% |
P32558 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 25% | 100% |
Q2UBF1 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 25% | 100% |
Q4HYB8 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 24% | 100% |
Q4P2U5 | Ustilago maydis (strain 521 / FGSC 9021) | 26% | 100% |
Q4WJ02 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 25% | 100% |
Q54S43 | Dictyostelium discoideum | 25% | 97% |
Q5A1D5 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 24% | 99% |
Q5B2X8 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 24% | 100% |
Q61E63 | Caenorhabditis briggsae | 27% | 100% |
Q6BXE5 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 25% | 100% |
Q6C931 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 28% | 100% |
Q6FWT4 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 26% | 100% |
Q756A7 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 26% | 100% |
Q7X923 | Oryza sativa subsp. japonica | 26% | 99% |
Q8H6B1 | Zea mays | 27% | 99% |
Q8IRG6 | Drosophila melanogaster | 27% | 96% |
Q8X0X6 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 24% | 100% |
Q920B9 | Mus musculus | 28% | 100% |
Q9N5R9 | Caenorhabditis elegans | 27% | 100% |
Q9W603 | Xenopus laevis | 27% | 100% |
Q9Y5B9 | Homo sapiens | 28% | 100% |
V5DLC1 | Trypanosoma cruzi | 52% | 100% |