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:0000109 | nucleotide-excision repair complex | 3 | 2 |
GO:0000112 | nucleotide-excision repair factor 3 complex | 4 | 2 |
GO:0005634 | nucleus | 5 | 2 |
GO:0005654 | nucleoplasm | 2 | 2 |
GO:0005667 | transcription regulator complex | 2 | 2 |
GO:0005675 | transcription factor TFIIH holo complex | 4 | 2 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0032806 | carboxy-terminal domain protein kinase complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0032993 | protein-DNA complex | 2 | 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:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 2 |
GO:0090575 | RNA polymerase II transcription regulator complex | 3 | 2 |
GO:0097550 | transcription preinitiation complex | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1902554 | serine/threonine protein kinase complex | 6 | 2 |
GO:1902911 | protein kinase complex | 5 | 2 |
GO:1990234 | transferase complex | 3 | 2 |
Related structures:
AlphaFold database: E9ADR1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 5 |
GO:0006352 | DNA-templated transcription initiation | 6 | 5 |
GO:0006367 | transcription initiation at RNA polymerase II promoter | 7 | 5 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 5 |
GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0009058 | biosynthetic process | 2 | 5 |
GO:0009059 | macromolecule biosynthetic process | 4 | 5 |
GO:0009987 | cellular process | 1 | 5 |
GO:0016070 | RNA metabolic process | 5 | 5 |
GO:0018130 | heterocycle biosynthetic process | 4 | 5 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 5 |
GO:0032774 | RNA biosynthetic process | 5 | 5 |
GO:0033683 | obsolete nucleotide-excision repair, DNA incision | 6 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 5 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 5 |
GO:0043170 | macromolecule metabolic process | 3 | 5 |
GO:0044237 | cellular metabolic process | 2 | 5 |
GO:0044238 | primary metabolic process | 2 | 5 |
GO:0044249 | cellular biosynthetic process | 3 | 5 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 5 |
GO:0046483 | heterocycle metabolic process | 3 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 5 |
GO:0090304 | nucleic acid metabolic process | 4 | 5 |
GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 5 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 5 |
GO:1901576 | organic substance biosynthetic process | 3 | 5 |
GO:0006259 | DNA metabolic process | 4 | 3 |
GO:0006281 | DNA repair | 5 | 3 |
GO:0006289 | nucleotide-excision repair | 6 | 3 |
GO:0006950 | response to stress | 2 | 3 |
GO:0006974 | DNA damage response | 4 | 3 |
GO:0033554 | cellular response to stress | 3 | 3 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 3 |
GO:0050896 | response to stimulus | 1 | 3 |
GO:0051716 | cellular response to stimulus | 2 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003677 | DNA binding | 4 | 10 |
GO:0003678 | DNA helicase activity | 3 | 10 |
GO:0003700 | DNA-binding transcription factor activity | 2 | 2 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004386 | helicase activity | 2 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043138 | 3'-5' DNA helicase activity | 4 | 2 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 10 |
GO:0140110 | transcription regulator activity | 1 | 2 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 10 |
GO:0140657 | ATP-dependent activity | 1 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 1 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
GO:0016887 | ATP hydrolysis activity | 7 | 1 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1033 | 1037 | PF00656 | 0.514 |
CLV_C14_Caspase3-7 | 730 | 734 | PF00656 | 0.639 |
CLV_MEL_PAP_1 | 837 | 843 | PF00089 | 0.274 |
CLV_NRD_NRD_1 | 1058 | 1060 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 1061 | 1063 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 264 | 266 | PF00675 | 0.488 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.329 |
CLV_NRD_NRD_1 | 703 | 705 | PF00675 | 0.690 |
CLV_NRD_NRD_1 | 864 | 866 | PF00675 | 0.312 |
CLV_PCSK_FUR_1 | 1056 | 1060 | PF00082 | 0.560 |
CLV_PCSK_FUR_1 | 291 | 295 | PF00082 | 0.563 |
CLV_PCSK_FUR_1 | 489 | 493 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 1058 | 1060 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 1061 | 1063 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 577 | 579 | PF00082 | 0.298 |
CLV_PCSK_KEX2_1 | 703 | 705 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 715 | 717 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 864 | 866 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 905 | 907 | PF00082 | 0.431 |
CLV_PCSK_PC1ET2_1 | 173 | 175 | PF00082 | 0.619 |
CLV_PCSK_PC1ET2_1 | 577 | 579 | PF00082 | 0.333 |
CLV_PCSK_PC1ET2_1 | 715 | 717 | PF00082 | 0.620 |
CLV_PCSK_PC1ET2_1 | 905 | 907 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.665 |
CLV_PCSK_SKI1_1 | 357 | 361 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 509 | 513 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 539 | 543 | PF00082 | 0.298 |
CLV_PCSK_SKI1_1 | 590 | 594 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 627 | 631 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 695 | 699 | PF00082 | 0.522 |
CLV_Separin_Metazoa | 408 | 412 | PF03568 | 0.503 |
DEG_APCC_DBOX_1 | 345 | 353 | PF00400 | 0.530 |
DEG_APCC_DBOX_1 | 589 | 597 | PF00400 | 0.391 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.527 |
DOC_ANK_TNKS_1 | 577 | 584 | PF00023 | 0.268 |
DOC_CDC14_PxL_1 | 1017 | 1025 | PF14671 | 0.535 |
DOC_CKS1_1 | 222 | 227 | PF01111 | 0.606 |
DOC_CYCLIN_RxL_1 | 213 | 224 | PF00134 | 0.717 |
DOC_CYCLIN_RxL_1 | 755 | 764 | PF00134 | 0.336 |
DOC_CYCLIN_yCln2_LP_2 | 217 | 223 | PF00134 | 0.665 |
DOC_MAPK_DCC_7 | 357 | 365 | PF00069 | 0.424 |
DOC_MAPK_gen_1 | 491 | 502 | PF00069 | 0.331 |
DOC_MAPK_gen_1 | 560 | 568 | PF00069 | 0.391 |
DOC_MAPK_gen_1 | 625 | 632 | PF00069 | 0.303 |
DOC_MAPK_JIP1_4 | 399 | 405 | PF00069 | 0.630 |
DOC_MAPK_MEF2A_6 | 250 | 257 | PF00069 | 0.612 |
DOC_MAPK_MEF2A_6 | 840 | 848 | PF00069 | 0.274 |
DOC_PP1_RVXF_1 | 1027 | 1033 | PF00149 | 0.494 |
DOC_PP1_RVXF_1 | 1079 | 1086 | PF00149 | 0.403 |
DOC_PP1_RVXF_1 | 786 | 793 | PF00149 | 0.274 |
DOC_PP2B_LxvP_1 | 466 | 469 | PF13499 | 0.429 |
DOC_PP2B_LxvP_1 | 806 | 809 | PF13499 | 0.274 |
DOC_PP2B_LxvP_1 | 846 | 849 | PF13499 | 0.274 |
DOC_PP4_FxxP_1 | 359 | 362 | PF00568 | 0.391 |
DOC_USP7_MATH_1 | 1010 | 1014 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.786 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 586 | 590 | PF00917 | 0.391 |
DOC_USP7_MATH_1 | 754 | 758 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 849 | 853 | PF00917 | 0.274 |
DOC_USP7_MATH_1 | 898 | 902 | PF00917 | 0.336 |
DOC_USP7_MATH_1 | 954 | 958 | PF00917 | 0.637 |
DOC_WW_Pin1_4 | 1006 | 1011 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 1050 | 1055 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 419 | 424 | PF00397 | 0.651 |
DOC_WW_Pin1_4 | 781 | 786 | PF00397 | 0.274 |
DOC_WW_Pin1_4 | 952 | 957 | PF00397 | 0.659 |
LIG_14-3-3_CanoR_1 | 1011 | 1020 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 107 | 113 | PF00244 | 0.608 |
LIG_14-3-3_CanoR_1 | 1081 | 1086 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 1087 | 1091 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 147 | 154 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 250 | 256 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 302 | 307 | PF00244 | 0.744 |
LIG_14-3-3_CanoR_1 | 314 | 318 | PF00244 | 0.551 |
LIG_14-3-3_CanoR_1 | 370 | 380 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 761 | 770 | PF00244 | 0.394 |
LIG_14-3-3_CanoR_1 | 906 | 910 | PF00244 | 0.315 |
LIG_14-3-3_CanoR_1 | 924 | 932 | PF00244 | 0.489 |
LIG_APCC_ABBA_1 | 789 | 794 | PF00400 | 0.280 |
LIG_APCC_ABBAyCdc20_2 | 718 | 724 | PF00400 | 0.632 |
LIG_APCC_ABBAyCdc20_2 | 788 | 794 | PF00400 | 0.274 |
LIG_BIR_III_4 | 750 | 754 | PF00653 | 0.493 |
LIG_BRCT_BRCA1_1 | 118 | 122 | PF00533 | 0.626 |
LIG_Clathr_ClatBox_1 | 1022 | 1026 | PF01394 | 0.379 |
LIG_Clathr_ClatBox_1 | 603 | 607 | PF01394 | 0.298 |
LIG_CtBP_PxDLS_1 | 268 | 272 | PF00389 | 0.537 |
LIG_deltaCOP1_diTrp_1 | 1026 | 1032 | PF00928 | 0.396 |
LIG_deltaCOP1_diTrp_1 | 965 | 974 | PF00928 | 0.360 |
LIG_FHA_1 | 1041 | 1047 | PF00498 | 0.469 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.761 |
LIG_FHA_1 | 209 | 215 | PF00498 | 0.691 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.570 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.610 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.401 |
LIG_FHA_1 | 520 | 526 | PF00498 | 0.392 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.484 |
LIG_FHA_1 | 554 | 560 | PF00498 | 0.298 |
LIG_FHA_1 | 692 | 698 | PF00498 | 0.516 |
LIG_FHA_1 | 819 | 825 | PF00498 | 0.352 |
LIG_FHA_1 | 895 | 901 | PF00498 | 0.313 |
LIG_FHA_1 | 995 | 1001 | PF00498 | 0.546 |
LIG_FHA_2 | 146 | 152 | PF00498 | 0.594 |
LIG_FHA_2 | 412 | 418 | PF00498 | 0.687 |
LIG_IBAR_NPY_1 | 766 | 768 | PF08397 | 0.298 |
LIG_LIR_Apic_2 | 358 | 362 | PF02991 | 0.401 |
LIG_LIR_Apic_2 | 972 | 978 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 1031 | 1038 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 444 | 454 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 455 | 466 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 569 | 576 | PF02991 | 0.309 |
LIG_LIR_Gen_1 | 656 | 667 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 927 | 936 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 1031 | 1035 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 1040 | 1044 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 444 | 450 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 455 | 460 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 569 | 574 | PF02991 | 0.309 |
LIG_LIR_Nem_3 | 623 | 629 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 656 | 662 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 687 | 691 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 750 | 755 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 927 | 932 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 965 | 971 | PF02991 | 0.495 |
LIG_LYPXL_SIV_4 | 17 | 25 | PF13949 | 0.488 |
LIG_LYPXL_yS_3 | 1020 | 1023 | PF13949 | 0.531 |
LIG_PCNA_yPIPBox_3 | 165 | 176 | PF02747 | 0.544 |
LIG_Pex14_1 | 1028 | 1032 | PF04695 | 0.388 |
LIG_Pex14_1 | 537 | 541 | PF04695 | 0.274 |
LIG_Rb_LxCxE_1 | 23 | 39 | PF01857 | 0.466 |
LIG_RPA_C_Fungi | 1082 | 1094 | PF08784 | 0.355 |
LIG_SH2_CRK | 571 | 575 | PF00017 | 0.274 |
LIG_SH2_CRK | 626 | 630 | PF00017 | 0.333 |
LIG_SH2_CRK | 752 | 756 | PF00017 | 0.455 |
LIG_SH2_CRK | 890 | 894 | PF00017 | 0.274 |
LIG_SH2_CRK | 917 | 921 | PF00017 | 0.298 |
LIG_SH2_NCK_1 | 416 | 420 | PF00017 | 0.532 |
LIG_SH2_NCK_1 | 890 | 894 | PF00017 | 0.274 |
LIG_SH2_SRC | 18 | 21 | PF00017 | 0.424 |
LIG_SH2_SRC | 407 | 410 | PF00017 | 0.581 |
LIG_SH2_STAP1 | 18 | 22 | PF00017 | 0.494 |
LIG_SH2_STAP1 | 57 | 61 | PF00017 | 0.443 |
LIG_SH2_STAP1 | 571 | 575 | PF00017 | 0.391 |
LIG_SH2_STAP1 | 655 | 659 | PF00017 | 0.356 |
LIG_SH2_STAT3 | 339 | 342 | PF00017 | 0.483 |
LIG_SH2_STAT3 | 430 | 433 | PF00017 | 0.379 |
LIG_SH2_STAT3 | 689 | 692 | PF00017 | 0.300 |
LIG_SH2_STAT3 | 904 | 907 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 795 | 798 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 826 | 829 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 888 | 891 | PF00017 | 0.276 |
LIG_SH3_2 | 1051 | 1056 | PF14604 | 0.497 |
LIG_SH3_3 | 1032 | 1038 | PF00018 | 0.481 |
LIG_SH3_3 | 1048 | 1054 | PF00018 | 0.438 |
LIG_SH3_3 | 217 | 223 | PF00018 | 0.732 |
LIG_SH3_3 | 254 | 260 | PF00018 | 0.660 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.420 |
LIG_SH3_3 | 673 | 679 | PF00018 | 0.343 |
LIG_SH3_3 | 874 | 880 | PF00018 | 0.321 |
LIG_SH3_3 | 936 | 942 | PF00018 | 0.400 |
LIG_Sin3_3 | 983 | 990 | PF02671 | 0.426 |
LIG_SUMO_SIM_anti_2 | 254 | 259 | PF11976 | 0.612 |
LIG_SUMO_SIM_par_1 | 1042 | 1048 | PF11976 | 0.490 |
LIG_SUMO_SIM_par_1 | 602 | 608 | PF11976 | 0.274 |
LIG_SUMO_SIM_par_1 | 76 | 82 | PF11976 | 0.492 |
LIG_TRAF2_1 | 1013 | 1016 | PF00917 | 0.651 |
LIG_TRAF2_1 | 1076 | 1079 | PF00917 | 0.488 |
LIG_TRAF2_1 | 548 | 551 | PF00917 | 0.292 |
LIG_TRAF2_1 | 585 | 588 | PF00917 | 0.391 |
LIG_TRAF2_1 | 73 | 76 | PF00917 | 0.545 |
LIG_TYR_ITIM | 624 | 629 | PF00017 | 0.333 |
LIG_TYR_ITSM | 567 | 574 | PF00017 | 0.391 |
LIG_WRC_WIRS_1 | 1022 | 1027 | PF05994 | 0.372 |
LIG_WW_3 | 408 | 412 | PF00397 | 0.503 |
MOD_CDC14_SPxK_1 | 1053 | 1056 | PF00782 | 0.482 |
MOD_CDK_SPK_2 | 1006 | 1011 | PF00069 | 0.470 |
MOD_CDK_SPxK_1 | 1050 | 1056 | PF00069 | 0.497 |
MOD_CDK_SPxxK_3 | 206 | 213 | PF00069 | 0.683 |
MOD_CDK_SPxxK_3 | 231 | 238 | PF00069 | 0.551 |
MOD_CDK_SPxxK_3 | 781 | 788 | PF00069 | 0.274 |
MOD_CK1_1 | 1024 | 1030 | PF00069 | 0.471 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.706 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.803 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.685 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.684 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.660 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.599 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.561 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.458 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.395 |
MOD_CK1_1 | 894 | 900 | PF00069 | 0.291 |
MOD_CK1_1 | 957 | 963 | PF00069 | 0.676 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.660 |
MOD_CK2_1 | 1010 | 1016 | PF00069 | 0.593 |
MOD_CK2_1 | 1100 | 1106 | PF00069 | 0.619 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.766 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.422 |
MOD_CK2_1 | 411 | 417 | PF00069 | 0.634 |
MOD_CK2_1 | 731 | 737 | PF00069 | 0.785 |
MOD_CK2_1 | 813 | 819 | PF00069 | 0.332 |
MOD_Cter_Amidation | 492 | 495 | PF01082 | 0.279 |
MOD_Cter_Amidation | 713 | 716 | PF01082 | 0.608 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.613 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.761 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.787 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.707 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.681 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.821 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.578 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.426 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.575 |
MOD_GlcNHglycan | 579 | 582 | PF01048 | 0.336 |
MOD_GlcNHglycan | 632 | 635 | PF01048 | 0.274 |
MOD_GlcNHglycan | 857 | 860 | PF01048 | 0.298 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.658 |
MOD_GlcNHglycan | 952 | 955 | PF01048 | 0.671 |
MOD_GlcNHglycan | 979 | 982 | PF01048 | 0.366 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.665 |
MOD_GSK3_1 | 1006 | 1013 | PF00069 | 0.467 |
MOD_GSK3_1 | 1024 | 1031 | PF00069 | 0.446 |
MOD_GSK3_1 | 1077 | 1084 | PF00069 | 0.595 |
MOD_GSK3_1 | 1096 | 1103 | PF00069 | 0.595 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.746 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.640 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.688 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.667 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.789 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.717 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.673 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.702 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.631 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.463 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.337 |
MOD_GSK3_1 | 878 | 885 | PF00069 | 0.280 |
MOD_GSK3_1 | 894 | 901 | PF00069 | 0.294 |
MOD_GSK3_1 | 948 | 955 | PF00069 | 0.561 |
MOD_N-GLC_1 | 145 | 150 | PF02516 | 0.591 |
MOD_N-GLC_1 | 164 | 169 | PF02516 | 0.496 |
MOD_N-GLC_1 | 279 | 284 | PF02516 | 0.460 |
MOD_N-GLC_1 | 469 | 474 | PF02516 | 0.418 |
MOD_N-GLC_2 | 884 | 886 | PF02516 | 0.298 |
MOD_NEK2_1 | 1065 | 1070 | PF00069 | 0.573 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.654 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.656 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.466 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.421 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.604 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.795 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.531 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.455 |
MOD_NEK2_1 | 520 | 525 | PF00069 | 0.411 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.248 |
MOD_NEK2_1 | 567 | 572 | PF00069 | 0.280 |
MOD_NEK2_1 | 630 | 635 | PF00069 | 0.309 |
MOD_NEK2_1 | 660 | 665 | PF00069 | 0.376 |
MOD_NEK2_1 | 860 | 865 | PF00069 | 0.274 |
MOD_NEK2_1 | 882 | 887 | PF00069 | 0.333 |
MOD_NEK2_2 | 717 | 722 | PF00069 | 0.570 |
MOD_PIKK_1 | 106 | 112 | PF00454 | 0.711 |
MOD_PIKK_1 | 236 | 242 | PF00454 | 0.609 |
MOD_PIKK_1 | 32 | 38 | PF00454 | 0.505 |
MOD_PIKK_1 | 411 | 417 | PF00454 | 0.643 |
MOD_PIKK_1 | 891 | 897 | PF00454 | 0.322 |
MOD_PKA_1 | 577 | 583 | PF00069 | 0.279 |
MOD_PKA_1 | 905 | 911 | PF00069 | 0.401 |
MOD_PKA_2 | 1010 | 1016 | PF00069 | 0.350 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.768 |
MOD_PKA_2 | 1086 | 1092 | PF00069 | 0.545 |
MOD_PKA_2 | 1093 | 1099 | PF00069 | 0.638 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.560 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.747 |
MOD_PKA_2 | 313 | 319 | PF00069 | 0.784 |
MOD_PKA_2 | 542 | 548 | PF00069 | 0.274 |
MOD_PKA_2 | 577 | 583 | PF00069 | 0.370 |
MOD_PKA_2 | 717 | 723 | PF00069 | 0.685 |
MOD_PKA_2 | 813 | 819 | PF00069 | 0.389 |
MOD_PKA_2 | 905 | 911 | PF00069 | 0.316 |
MOD_PKA_2 | 994 | 1000 | PF00069 | 0.553 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.616 |
MOD_Plk_1 | 279 | 285 | PF00069 | 0.451 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.499 |
MOD_Plk_1 | 462 | 468 | PF00069 | 0.424 |
MOD_Plk_1 | 469 | 475 | PF00069 | 0.385 |
MOD_Plk_1 | 550 | 556 | PF00069 | 0.211 |
MOD_Plk_2-3 | 1100 | 1106 | PF00069 | 0.596 |
MOD_Plk_2-3 | 731 | 737 | PF00069 | 0.638 |
MOD_Plk_4 | 1040 | 1046 | PF00069 | 0.473 |
MOD_Plk_4 | 1086 | 1092 | PF00069 | 0.513 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.679 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.771 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.313 |
MOD_Plk_4 | 521 | 527 | PF00069 | 0.322 |
MOD_Plk_4 | 530 | 536 | PF00069 | 0.240 |
MOD_Plk_4 | 569 | 575 | PF00069 | 0.357 |
MOD_Plk_4 | 632 | 638 | PF00069 | 0.274 |
MOD_Plk_4 | 717 | 723 | PF00069 | 0.685 |
MOD_Plk_4 | 849 | 855 | PF00069 | 0.293 |
MOD_Plk_4 | 888 | 894 | PF00069 | 0.287 |
MOD_Plk_4 | 905 | 911 | PF00069 | 0.196 |
MOD_ProDKin_1 | 1006 | 1012 | PF00069 | 0.475 |
MOD_ProDKin_1 | 1050 | 1056 | PF00069 | 0.497 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.646 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.674 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.636 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.698 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.620 |
MOD_ProDKin_1 | 419 | 425 | PF00069 | 0.646 |
MOD_ProDKin_1 | 781 | 787 | PF00069 | 0.274 |
MOD_ProDKin_1 | 952 | 958 | PF00069 | 0.658 |
MOD_SUMO_for_1 | 172 | 175 | PF00179 | 0.775 |
MOD_SUMO_rev_2 | 639 | 643 | PF00179 | 0.435 |
TRG_DiLeu_BaEn_1 | 819 | 824 | PF01217 | 0.274 |
TRG_DiLeu_BaEn_3 | 587 | 593 | PF01217 | 0.391 |
TRG_DiLeu_BaLyEn_6 | 1018 | 1023 | PF01217 | 0.543 |
TRG_DiLeu_BaLyEn_6 | 210 | 215 | PF01217 | 0.567 |
TRG_DiLeu_BaLyEn_6 | 217 | 222 | PF01217 | 0.513 |
TRG_DiLeu_BaLyEn_6 | 248 | 253 | PF01217 | 0.622 |
TRG_DiLeu_BaLyEn_6 | 401 | 406 | PF01217 | 0.577 |
TRG_ENDOCYTIC_2 | 1020 | 1023 | PF00928 | 0.531 |
TRG_ENDOCYTIC_2 | 18 | 21 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 458 | 461 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 571 | 574 | PF00928 | 0.274 |
TRG_ENDOCYTIC_2 | 626 | 629 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 688 | 691 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 752 | 755 | PF00928 | 0.463 |
TRG_ENDOCYTIC_2 | 890 | 893 | PF00928 | 0.274 |
TRG_ENDOCYTIC_2 | 917 | 920 | PF00928 | 0.274 |
TRG_ENDOCYTIC_2 | 971 | 974 | PF00928 | 0.511 |
TRG_ER_diArg_1 | 1058 | 1061 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 1091 | 1094 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 263 | 265 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 290 | 293 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 477 | 480 | PF00400 | 0.274 |
TRG_ER_diArg_1 | 490 | 492 | PF00400 | 0.274 |
TRG_Pf-PMV_PEXEL_1 | 130 | 134 | PF00026 | 0.570 |
TRG_Pf-PMV_PEXEL_1 | 265 | 269 | PF00026 | 0.657 |
TRG_Pf-PMV_PEXEL_1 | 404 | 408 | PF00026 | 0.607 |
TRG_Pf-PMV_PEXEL_1 | 590 | 594 | PF00026 | 0.336 |
TRG_Pf-PMV_PEXEL_1 | 918 | 923 | PF00026 | 0.282 |
TRG_Pf-PMV_PEXEL_1 | 924 | 928 | PF00026 | 0.356 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM24 | Leptomonas seymouri | 64% | 100% |
A0A0S4JHE3 | Bodo saltans | 38% | 100% |
A0A1X0P056 | Trypanosomatidae | 48% | 100% |
A0A3S5H7K7 | Leishmania donovani | 93% | 100% |
A4HH67 | Leishmania braziliensis | 82% | 100% |
A4I4B1 | Leishmania infantum | 92% | 100% |
C9ZKL6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9AM19 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q580W5 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 46% | 100% |