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: A4HH10
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: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 |
GO:0006325 | chromatin organization | 4 | 1 |
GO:0006354 | DNA-templated transcription elongation | 6 | 1 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 1 |
GO:0006368 | transcription elongation by RNA polymerase II | 7 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 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:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 1 |
GO:0032774 | RNA biosynthetic process | 5 | 1 |
GO:0032784 | regulation of DNA-templated transcription elongation | 7 | 1 |
GO:0032786 | positive regulation of DNA-templated transcription, elongation | 8 | 1 |
GO:0032968 | positive regulation of transcription elongation by RNA polymerase II | 9 | 1 |
GO:0034243 | regulation of transcription elongation by RNA polymerase II | 8 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0045893 | positive regulation of DNA-templated transcription | 7 | 1 |
GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0045944 | positive regulation of transcription by RNA polymerase II | 8 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 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:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
GO:1902680 | positive regulation of RNA biosynthetic process | 7 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 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:0003682 | chromatin binding | 2 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0031491 | nucleosome binding | 3 | 1 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
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 | 931 | 935 | PF00656 | 0.660 |
CLV_C14_Caspase3-7 | 967 | 971 | PF00656 | 0.510 |
CLV_MEL_PAP_1 | 277 | 283 | PF00089 | 0.373 |
CLV_NRD_NRD_1 | 1004 | 1006 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 1046 | 1048 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.223 |
CLV_NRD_NRD_1 | 425 | 427 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 450 | 452 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 629 | 631 | PF00675 | 0.210 |
CLV_NRD_NRD_1 | 725 | 727 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 749 | 751 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 985 | 987 | PF00675 | 0.510 |
CLV_PCSK_KEX2_1 | 1006 | 1008 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 1046 | 1048 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.377 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 631 | 633 | PF00082 | 0.208 |
CLV_PCSK_KEX2_1 | 749 | 751 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 985 | 987 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 1006 | 1008 | PF00082 | 0.685 |
CLV_PCSK_PC1ET2_1 | 631 | 633 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 388 | 392 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 478 | 482 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 594 | 598 | PF00082 | 0.188 |
CLV_PCSK_SKI1_1 | 606 | 610 | PF00082 | 0.223 |
CLV_PCSK_SKI1_1 | 631 | 635 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 803 | 807 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 812 | 816 | PF00082 | 0.206 |
CLV_Separin_Metazoa | 145 | 149 | PF03568 | 0.341 |
DEG_APCC_DBOX_1 | 387 | 395 | PF00400 | 0.226 |
DEG_APCC_DBOX_1 | 449 | 457 | PF00400 | 0.489 |
DEG_APCC_DBOX_1 | 477 | 485 | PF00400 | 0.472 |
DEG_APCC_DBOX_1 | 510 | 518 | PF00400 | 0.357 |
DEG_APCC_DBOX_1 | 811 | 819 | PF00400 | 0.257 |
DEG_APCC_DBOX_1 | 866 | 874 | PF00400 | 0.419 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.519 |
DEG_SCF_FBW7_1 | 818 | 825 | PF00400 | 0.501 |
DEG_SCF_SKP2-CKS1_1 | 514 | 521 | PF00560 | 0.385 |
DEG_SPOP_SBC_1 | 497 | 501 | PF00917 | 0.373 |
DOC_CDC14_PxL_1 | 157 | 165 | PF14671 | 0.426 |
DOC_CKS1_1 | 47 | 52 | PF01111 | 0.407 |
DOC_CYCLIN_RxL_1 | 291 | 300 | PF00134 | 0.373 |
DOC_CYCLIN_yCln2_LP_2 | 718 | 724 | PF00134 | 0.410 |
DOC_MAPK_DCC_7 | 641 | 651 | PF00069 | 0.461 |
DOC_MAPK_gen_1 | 541 | 548 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 589 | 597 | PF00069 | 0.344 |
DOC_MAPK_gen_1 | 726 | 734 | PF00069 | 0.321 |
DOC_MAPK_HePTP_8 | 850 | 862 | PF00069 | 0.436 |
DOC_MAPK_MEF2A_6 | 1024 | 1032 | PF00069 | 0.589 |
DOC_MAPK_MEF2A_6 | 541 | 548 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 571 | 578 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 853 | 862 | PF00069 | 0.421 |
DOC_PP1_RVXF_1 | 539 | 546 | PF00149 | 0.396 |
DOC_PP1_RVXF_1 | 697 | 704 | PF00149 | 0.278 |
DOC_PP1_RVXF_1 | 810 | 817 | PF00149 | 0.240 |
DOC_PP2B_LxvP_1 | 323 | 326 | PF13499 | 0.270 |
DOC_PP2B_LxvP_1 | 649 | 652 | PF13499 | 0.419 |
DOC_PP2B_PxIxI_1 | 857 | 863 | PF00149 | 0.501 |
DOC_PP4_FxxP_1 | 536 | 539 | PF00568 | 0.346 |
DOC_SPAK_OSR1_1 | 280 | 284 | PF12202 | 0.270 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.334 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.375 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.384 |
DOC_USP7_MATH_1 | 633 | 637 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 706 | 710 | PF00917 | 0.347 |
DOC_USP7_MATH_1 | 748 | 752 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 866 | 870 | PF00917 | 0.419 |
DOC_USP7_UBL2_3 | 203 | 207 | PF12436 | 0.282 |
DOC_USP7_UBL2_3 | 423 | 427 | PF12436 | 0.318 |
DOC_USP7_UBL2_3 | 594 | 598 | PF12436 | 0.396 |
DOC_USP7_UBL2_3 | 853 | 857 | PF12436 | 0.419 |
DOC_WD40_RPTOR_TOS_1 | 403 | 409 | PF00400 | 0.226 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 515 | 520 | PF00397 | 0.423 |
DOC_WW_Pin1_4 | 601 | 606 | PF00397 | 0.346 |
DOC_WW_Pin1_4 | 642 | 647 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 818 | 823 | PF00397 | 0.489 |
LIG_14-3-3_CanoR_1 | 13 | 21 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 329 | 337 | PF00244 | 0.339 |
LIG_14-3-3_CanoR_1 | 368 | 378 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 458 | 467 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 478 | 488 | PF00244 | 0.228 |
LIG_14-3-3_CanoR_1 | 511 | 515 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 632 | 642 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 682 | 686 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 726 | 735 | PF00244 | 0.249 |
LIG_14-3-3_CanoR_1 | 749 | 753 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 803 | 809 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 867 | 871 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 894 | 898 | PF00244 | 0.521 |
LIG_Actin_WH2_2 | 667 | 684 | PF00022 | 0.406 |
LIG_APCC_ABBA_1 | 270 | 275 | PF00400 | 0.373 |
LIG_BRCT_BRCA1_1 | 352 | 356 | PF00533 | 0.276 |
LIG_CaM_IQ_9 | 616 | 632 | PF13499 | 0.461 |
LIG_Clathr_ClatBox_1 | 362 | 366 | PF01394 | 0.226 |
LIG_CSL_BTD_1 | 544 | 547 | PF09270 | 0.461 |
LIG_CtBP_PxDLS_1 | 1029 | 1033 | PF00389 | 0.686 |
LIG_deltaCOP1_diTrp_1 | 36 | 42 | PF00928 | 0.207 |
LIG_deltaCOP1_diTrp_1 | 902 | 909 | PF00928 | 0.381 |
LIG_EH1_1 | 209 | 217 | PF00400 | 0.373 |
LIG_EH1_1 | 845 | 853 | PF00400 | 0.501 |
LIG_EVH1_2 | 244 | 248 | PF00568 | 0.373 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.491 |
LIG_FHA_1 | 1008 | 1014 | PF00498 | 0.529 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.368 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.297 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.298 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.352 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.279 |
LIG_FHA_1 | 462 | 468 | PF00498 | 0.613 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.282 |
LIG_FHA_1 | 651 | 657 | PF00498 | 0.524 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.451 |
LIG_FHA_1 | 717 | 723 | PF00498 | 0.397 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.432 |
LIG_FHA_1 | 823 | 829 | PF00498 | 0.406 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.498 |
LIG_FHA_2 | 140 | 146 | PF00498 | 0.216 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.398 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.411 |
LIG_FHA_2 | 261 | 267 | PF00498 | 0.156 |
LIG_FHA_2 | 497 | 503 | PF00498 | 0.434 |
LIG_FHA_2 | 894 | 900 | PF00498 | 0.411 |
LIG_FHA_2 | 920 | 926 | PF00498 | 0.657 |
LIG_FHA_2 | 938 | 944 | PF00498 | 0.485 |
LIG_FHA_2 | 94 | 100 | PF00498 | 0.596 |
LIG_GBD_Chelix_1 | 424 | 432 | PF00786 | 0.364 |
LIG_Integrin_isoDGR_2 | 639 | 641 | PF01839 | 0.228 |
LIG_LIR_Apic_2 | 599 | 605 | PF02991 | 0.363 |
LIG_LIR_Apic_2 | 854 | 858 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 141 | 151 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 235 | 245 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 36 | 42 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 430 | 441 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 575 | 586 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 692 | 703 | PF02991 | 0.276 |
LIG_LIR_Gen_1 | 835 | 844 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 913 | 921 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 979 | 988 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 141 | 146 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 235 | 240 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 331 | 337 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 36 | 41 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 430 | 436 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 501 | 507 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 692 | 698 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 709 | 714 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 796 | 800 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 835 | 839 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 913 | 918 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 979 | 983 | PF02991 | 0.569 |
LIG_MYND_3 | 526 | 530 | PF01753 | 0.370 |
LIG_NRBOX | 162 | 168 | PF00104 | 0.345 |
LIG_NRBOX | 319 | 325 | PF00104 | 0.253 |
LIG_NRBOX | 476 | 482 | PF00104 | 0.345 |
LIG_PCNA_yPIPBox_3 | 345 | 354 | PF02747 | 0.335 |
LIG_Pex14_1 | 38 | 42 | PF04695 | 0.411 |
LIG_Pex14_2 | 139 | 143 | PF04695 | 0.424 |
LIG_PTB_Apo_2 | 282 | 289 | PF02174 | 0.239 |
LIG_PTB_Phospho_1 | 282 | 288 | PF10480 | 0.239 |
LIG_REV1ctd_RIR_1 | 289 | 298 | PF16727 | 0.373 |
LIG_RPA_C_Fungi | 8 | 20 | PF08784 | 0.325 |
LIG_SH2_CRK | 334 | 338 | PF00017 | 0.279 |
LIG_SH2_CRK | 602 | 606 | PF00017 | 0.202 |
LIG_SH2_CRK | 855 | 859 | PF00017 | 0.257 |
LIG_SH2_STAP1 | 288 | 292 | PF00017 | 0.239 |
LIG_SH2_STAP1 | 7 | 11 | PF00017 | 0.311 |
LIG_SH2_STAT3 | 253 | 256 | PF00017 | 0.239 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.156 |
LIG_SH2_STAT5 | 288 | 291 | PF00017 | 0.230 |
LIG_SH2_STAT5 | 572 | 575 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 711 | 714 | PF00017 | 0.411 |
LIG_SH3_2 | 1022 | 1027 | PF14604 | 0.479 |
LIG_SH3_3 | 1019 | 1025 | PF00018 | 0.547 |
LIG_SH3_3 | 1038 | 1044 | PF00018 | 0.510 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.513 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.407 |
LIG_SH3_3 | 516 | 522 | PF00018 | 0.489 |
LIG_SH3_3 | 541 | 547 | PF00018 | 0.202 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.465 |
LIG_SUMO_SIM_anti_2 | 102 | 107 | PF11976 | 0.472 |
LIG_SUMO_SIM_anti_2 | 275 | 280 | PF11976 | 0.240 |
LIG_SUMO_SIM_anti_2 | 359 | 366 | PF11976 | 0.208 |
LIG_SUMO_SIM_anti_2 | 79 | 84 | PF11976 | 0.326 |
LIG_SUMO_SIM_anti_2 | 830 | 835 | PF11976 | 0.258 |
LIG_SUMO_SIM_par_1 | 101 | 107 | PF11976 | 0.428 |
LIG_SUMO_SIM_par_1 | 294 | 300 | PF11976 | 0.257 |
LIG_SUMO_SIM_par_1 | 359 | 366 | PF11976 | 0.299 |
LIG_SUMO_SIM_par_1 | 462 | 468 | PF11976 | 0.606 |
LIG_SUMO_SIM_par_1 | 858 | 864 | PF11976 | 0.373 |
LIG_SxIP_EBH_1 | 1021 | 1035 | PF03271 | 0.474 |
LIG_TRAF2_1 | 133 | 136 | PF00917 | 0.349 |
LIG_TRAF2_1 | 500 | 503 | PF00917 | 0.450 |
LIG_TRAF2_1 | 580 | 583 | PF00917 | 0.226 |
LIG_TRAF2_1 | 779 | 782 | PF00917 | 0.458 |
LIG_TRAF2_1 | 827 | 830 | PF00917 | 0.156 |
LIG_TRAF2_1 | 922 | 925 | PF00917 | 0.471 |
LIG_TYR_ITIM | 431 | 436 | PF00017 | 0.522 |
LIG_UBA3_1 | 58 | 66 | PF00899 | 0.380 |
LIG_UBA3_1 | 694 | 699 | PF00899 | 0.438 |
LIG_WRC_WIRS_1 | 348 | 353 | PF05994 | 0.398 |
LIG_WRC_WIRS_1 | 773 | 778 | PF05994 | 0.456 |
LIG_WRC_WIRS_1 | 805 | 810 | PF05994 | 0.245 |
LIG_WRC_WIRS_1 | 833 | 838 | PF05994 | 0.373 |
MOD_CDK_SPK_2 | 601 | 606 | PF00069 | 0.156 |
MOD_CDK_SPxK_1 | 515 | 521 | PF00069 | 0.388 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.413 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.262 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.288 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.311 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.515 |
MOD_CK1_1 | 804 | 810 | PF00069 | 0.275 |
MOD_CK1_1 | 937 | 943 | PF00069 | 0.583 |
MOD_CK1_1 | 949 | 955 | PF00069 | 0.594 |
MOD_CK1_1 | 969 | 975 | PF00069 | 0.616 |
MOD_CK1_1 | 976 | 982 | PF00069 | 0.482 |
MOD_CK1_1 | 994 | 1000 | PF00069 | 0.544 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.216 |
MOD_CK2_1 | 215 | 221 | PF00069 | 0.271 |
MOD_CK2_1 | 260 | 266 | PF00069 | 0.277 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.238 |
MOD_CK2_1 | 496 | 502 | PF00069 | 0.530 |
MOD_CK2_1 | 510 | 516 | PF00069 | 0.450 |
MOD_CK2_1 | 577 | 583 | PF00069 | 0.167 |
MOD_CK2_1 | 824 | 830 | PF00069 | 0.326 |
MOD_CK2_1 | 893 | 899 | PF00069 | 0.475 |
MOD_CK2_1 | 919 | 925 | PF00069 | 0.605 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.490 |
MOD_CK2_1 | 937 | 943 | PF00069 | 0.480 |
MOD_CK2_1 | 953 | 959 | PF00069 | 0.589 |
MOD_CK2_1 | 960 | 966 | PF00069 | 0.583 |
MOD_CK2_1 | 976 | 982 | PF00069 | 0.606 |
MOD_CMANNOS | 906 | 909 | PF00535 | 0.361 |
MOD_Cter_Amidation | 492 | 495 | PF01082 | 0.438 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.360 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.311 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.380 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.337 |
MOD_GlcNHglycan | 635 | 638 | PF01048 | 0.290 |
MOD_GlcNHglycan | 746 | 749 | PF01048 | 0.600 |
MOD_GlcNHglycan | 878 | 881 | PF01048 | 0.373 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.342 |
MOD_GlcNHglycan | 973 | 978 | PF01048 | 0.571 |
MOD_GlcNHglycan | 993 | 996 | PF01048 | 0.415 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.512 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.275 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.553 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.633 |
MOD_GSK3_1 | 660 | 667 | PF00069 | 0.156 |
MOD_GSK3_1 | 739 | 746 | PF00069 | 0.446 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.354 |
MOD_GSK3_1 | 781 | 788 | PF00069 | 0.390 |
MOD_GSK3_1 | 789 | 796 | PF00069 | 0.422 |
MOD_GSK3_1 | 818 | 825 | PF00069 | 0.322 |
MOD_GSK3_1 | 842 | 849 | PF00069 | 0.315 |
MOD_GSK3_1 | 932 | 939 | PF00069 | 0.599 |
MOD_GSK3_1 | 949 | 956 | PF00069 | 0.532 |
MOD_GSK3_1 | 960 | 967 | PF00069 | 0.524 |
MOD_GSK3_1 | 969 | 976 | PF00069 | 0.587 |
MOD_LATS_1 | 801 | 807 | PF00433 | 0.378 |
MOD_N-GLC_1 | 590 | 595 | PF02516 | 0.167 |
MOD_N-GLC_1 | 919 | 924 | PF02516 | 0.642 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.456 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.287 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.212 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.329 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.295 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.298 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.557 |
MOD_NEK2_1 | 555 | 560 | PF00069 | 0.226 |
MOD_NEK2_1 | 590 | 595 | PF00069 | 0.178 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.271 |
MOD_NEK2_1 | 681 | 686 | PF00069 | 0.295 |
MOD_NEK2_1 | 744 | 749 | PF00069 | 0.419 |
MOD_NEK2_1 | 824 | 829 | PF00069 | 0.287 |
MOD_NEK2_1 | 846 | 851 | PF00069 | 0.282 |
MOD_NEK2_1 | 885 | 890 | PF00069 | 0.332 |
MOD_NEK2_2 | 706 | 711 | PF00069 | 0.348 |
MOD_NEK2_2 | 893 | 898 | PF00069 | 0.512 |
MOD_PIKK_1 | 252 | 258 | PF00454 | 0.373 |
MOD_PIKK_1 | 785 | 791 | PF00454 | 0.371 |
MOD_PIKK_1 | 822 | 828 | PF00454 | 0.257 |
MOD_PKA_2 | 1023 | 1029 | PF00069 | 0.684 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.388 |
MOD_PKA_2 | 249 | 255 | PF00069 | 0.167 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.359 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.202 |
MOD_PKA_2 | 510 | 516 | PF00069 | 0.443 |
MOD_PKA_2 | 640 | 646 | PF00069 | 0.373 |
MOD_PKA_2 | 664 | 670 | PF00069 | 0.221 |
MOD_PKA_2 | 681 | 687 | PF00069 | 0.293 |
MOD_PKA_2 | 725 | 731 | PF00069 | 0.285 |
MOD_PKA_2 | 748 | 754 | PF00069 | 0.436 |
MOD_PKA_2 | 766 | 772 | PF00069 | 0.291 |
MOD_PKA_2 | 866 | 872 | PF00069 | 0.257 |
MOD_PKA_2 | 893 | 899 | PF00069 | 0.516 |
MOD_PKA_2 | 991 | 997 | PF00069 | 0.554 |
MOD_PKB_1 | 1005 | 1013 | PF00069 | 0.612 |
MOD_PKB_1 | 630 | 638 | PF00069 | 0.282 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.320 |
MOD_Plk_1 | 260 | 266 | PF00069 | 0.270 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.393 |
MOD_Plk_1 | 598 | 604 | PF00069 | 0.153 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.418 |
MOD_Plk_1 | 846 | 852 | PF00069 | 0.282 |
MOD_Plk_1 | 885 | 891 | PF00069 | 0.315 |
MOD_Plk_1 | 937 | 943 | PF00069 | 0.596 |
MOD_Plk_1 | 952 | 958 | PF00069 | 0.537 |
MOD_Plk_2-3 | 205 | 211 | PF00069 | 0.282 |
MOD_Plk_2-3 | 260 | 266 | PF00069 | 0.156 |
MOD_Plk_2-3 | 503 | 509 | PF00069 | 0.384 |
MOD_Plk_2-3 | 832 | 838 | PF00069 | 0.239 |
MOD_Plk_2-3 | 947 | 953 | PF00069 | 0.638 |
MOD_Plk_2-3 | 960 | 966 | PF00069 | 0.567 |
MOD_Plk_2-3 | 99 | 105 | PF00069 | 0.437 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.497 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.373 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.413 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.309 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.373 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.584 |
MOD_Plk_4 | 572 | 578 | PF00069 | 0.253 |
MOD_Plk_4 | 706 | 712 | PF00069 | 0.415 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.382 |
MOD_Plk_4 | 846 | 852 | PF00069 | 0.282 |
MOD_Plk_4 | 937 | 943 | PF00069 | 0.616 |
MOD_Plk_4 | 953 | 959 | PF00069 | 0.488 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.387 |
MOD_ProDKin_1 | 515 | 521 | PF00069 | 0.432 |
MOD_ProDKin_1 | 601 | 607 | PF00069 | 0.156 |
MOD_ProDKin_1 | 642 | 648 | PF00069 | 0.282 |
MOD_ProDKin_1 | 818 | 824 | PF00069 | 0.356 |
MOD_SUMO_for_1 | 623 | 626 | PF00179 | 0.373 |
MOD_SUMO_rev_2 | 199 | 209 | PF00179 | 0.256 |
TRG_DiLeu_BaEn_1 | 476 | 481 | PF01217 | 0.373 |
TRG_DiLeu_BaEn_2 | 346 | 352 | PF01217 | 0.156 |
TRG_ENDOCYTIC_2 | 217 | 220 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 288 | 291 | PF00928 | 0.239 |
TRG_ENDOCYTIC_2 | 334 | 337 | PF00928 | 0.279 |
TRG_ENDOCYTIC_2 | 433 | 436 | PF00928 | 0.554 |
TRG_ER_diArg_1 | 1004 | 1007 | PF00400 | 0.623 |
TRG_ER_diArg_1 | 1046 | 1048 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 147 | 149 | PF00400 | 0.381 |
TRG_ER_diArg_1 | 189 | 191 | PF00400 | 0.235 |
TRG_ER_diArg_1 | 764 | 767 | PF00400 | 0.410 |
TRG_NLS_MonoCore_2 | 1005 | 1010 | PF00514 | 0.589 |
TRG_NLS_MonoExtC_3 | 1004 | 1009 | PF00514 | 0.615 |
TRG_NLS_MonoExtN_4 | 1004 | 1010 | PF00514 | 0.598 |
TRG_Pf-PMV_PEXEL_1 | 118 | 122 | PF00026 | 0.452 |
TRG_Pf-PMV_PEXEL_1 | 294 | 299 | PF00026 | 0.174 |
TRG_Pf-PMV_PEXEL_1 | 426 | 430 | PF00026 | 0.355 |
TRG_Pf-PMV_PEXEL_1 | 478 | 483 | PF00026 | 0.360 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHS5 | Leptomonas seymouri | 74% | 100% |
A0A0S4JAR0 | Bodo saltans | 38% | 100% |
A0A1X0NZD4 | Trypanosomatidae | 53% | 100% |
A0A3S7X235 | Leishmania donovani | 84% | 100% |
A0A422NUY4 | Trypanosoma rangeli | 52% | 100% |
A4I439 | Leishmania infantum | 84% | 100% |
C9ZKS3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
E9ADK4 | Leishmania major | 84% | 100% |
E9AM77 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
O82491 | Arabidopsis thaliana | 26% | 98% |
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) | 24% | 100% |
Q2UBF1 | Aspergillus oryzae (strain ATCC 42149 / RIB 40) | 27% | 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) | 24% | 100% |
Q4WJ02 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 26% | 100% |
Q54S43 | Dictyostelium discoideum | 24% | 98% |
Q5A1D5 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 24% | 99% |
Q5B2X8 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 26% | 100% |
Q61E63 | Caenorhabditis briggsae | 26% | 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) | 24% | 100% |
Q756A7 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 25% | 100% |
Q7X923 | Oryza sativa subsp. japonica | 27% | 99% |
Q8H6B1 | Zea mays | 27% | 99% |
Q8IRG6 | Drosophila melanogaster | 25% | 97% |
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 | 51% | 100% |