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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 11 |
GO:0016020 | membrane | 2 | 7 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: A0A3S5H7J4
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006289 | nucleotide-excision repair | 6 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022414 | reproductive process | 1 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1903046 | meiotic cell cycle process | 2 | 1 |
GO:1990918 | double-strand break repair involved in meiotic recombination | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003678 | DNA helicase activity | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 12 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 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 | 106 | 110 | PF00656 | 0.523 |
CLV_C14_Caspase3-7 | 978 | 982 | PF00656 | 0.723 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.661 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 453 | 455 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.709 |
CLV_NRD_NRD_1 | 756 | 758 | PF00675 | 0.293 |
CLV_NRD_NRD_1 | 902 | 904 | PF00675 | 0.351 |
CLV_PCSK_FUR_1 | 414 | 418 | PF00082 | 0.589 |
CLV_PCSK_FUR_1 | 58 | 62 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.687 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 514 | 516 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 66 | 68 | PF00082 | 0.669 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.781 |
CLV_PCSK_KEX2_1 | 902 | 904 | PF00082 | 0.332 |
CLV_PCSK_PC1ET2_1 | 420 | 422 | PF00082 | 0.741 |
CLV_PCSK_PC1ET2_1 | 46 | 48 | PF00082 | 0.611 |
CLV_PCSK_PC1ET2_1 | 514 | 516 | PF00082 | 0.247 |
CLV_PCSK_PC1ET2_1 | 66 | 68 | PF00082 | 0.759 |
CLV_PCSK_PC7_1 | 416 | 422 | PF00082 | 0.656 |
CLV_PCSK_SKI1_1 | 1038 | 1042 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 1050 | 1054 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.632 |
CLV_PCSK_SKI1_1 | 331 | 335 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 521 | 525 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 552 | 556 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 609 | 613 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 729 | 733 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 803 | 807 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 902 | 906 | PF00082 | 0.395 |
DEG_APCC_DBOX_1 | 330 | 338 | PF00400 | 0.289 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.246 |
DEG_SCF_TRCP1_1 | 574 | 580 | PF00400 | 0.642 |
DEG_SPOP_SBC_1 | 358 | 362 | PF00917 | 0.467 |
DEG_SPOP_SBC_1 | 657 | 661 | PF00917 | 0.582 |
DEG_SPOP_SBC_1 | 909 | 913 | PF00917 | 0.660 |
DOC_CDC14_PxL_1 | 282 | 290 | PF14671 | 0.335 |
DOC_CKS1_1 | 915 | 920 | PF01111 | 0.653 |
DOC_CYCLIN_RxL_1 | 374 | 385 | PF00134 | 0.386 |
DOC_CYCLIN_RxL_1 | 549 | 559 | PF00134 | 0.604 |
DOC_CYCLIN_yCln2_LP_2 | 683 | 689 | PF00134 | 0.528 |
DOC_CYCLIN_yCln2_LP_2 | 808 | 814 | PF00134 | 0.535 |
DOC_MAPK_gen_1 | 127 | 135 | PF00069 | 0.451 |
DOC_MAPK_gen_1 | 514 | 522 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 726 | 734 | PF00069 | 0.478 |
DOC_MAPK_gen_1 | 788 | 797 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 849 | 859 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 331 | 338 | PF00069 | 0.360 |
DOC_MAPK_MEF2A_6 | 514 | 522 | PF00069 | 0.471 |
DOC_MAPK_MEF2A_6 | 803 | 812 | PF00069 | 0.431 |
DOC_MAPK_NFAT4_5 | 331 | 339 | PF00069 | 0.364 |
DOC_MAPK_NFAT4_5 | 515 | 523 | PF00069 | 0.549 |
DOC_MAPK_NFAT4_5 | 803 | 811 | PF00069 | 0.478 |
DOC_PP1_RVXF_1 | 270 | 277 | PF00149 | 0.242 |
DOC_PP2B_LxvP_1 | 146 | 149 | PF13499 | 0.381 |
DOC_PP2B_LxvP_1 | 672 | 675 | PF13499 | 0.494 |
DOC_PP2B_LxvP_1 | 713 | 716 | PF13499 | 0.446 |
DOC_PP2B_LxvP_1 | 808 | 811 | PF13499 | 0.535 |
DOC_PP2B_LxvP_1 | 958 | 961 | PF13499 | 0.657 |
DOC_PP4_FxxP_1 | 145 | 148 | PF00568 | 0.415 |
DOC_PP4_FxxP_1 | 473 | 476 | PF00568 | 0.417 |
DOC_PP4_FxxP_1 | 753 | 756 | PF00568 | 0.456 |
DOC_USP7_MATH_1 | 1003 | 1007 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 1044 | 1048 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.391 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 479 | 483 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 533 | 537 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 657 | 661 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 814 | 818 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 916 | 920 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 977 | 981 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 984 | 988 | PF00917 | 0.626 |
DOC_USP7_UBL2_3 | 68 | 72 | PF12436 | 0.509 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.276 |
DOC_WW_Pin1_4 | 1013 | 1018 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.367 |
DOC_WW_Pin1_4 | 615 | 620 | PF00397 | 0.541 |
DOC_WW_Pin1_4 | 740 | 745 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 910 | 915 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 980 | 985 | PF00397 | 0.778 |
LIG_14-3-3_CanoR_1 | 1004 | 1014 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 122 | 129 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 464 | 473 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 677 | 683 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 788 | 797 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 878 | 882 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 895 | 905 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 991 | 997 | PF00244 | 0.736 |
LIG_Actin_WH2_2 | 148 | 165 | PF00022 | 0.278 |
LIG_Actin_WH2_2 | 591 | 607 | PF00022 | 0.508 |
LIG_Actin_WH2_2 | 689 | 706 | PF00022 | 0.574 |
LIG_Actin_WH2_2 | 833 | 851 | PF00022 | 0.491 |
LIG_APCC_ABBA_1 | 308 | 313 | PF00400 | 0.242 |
LIG_APCC_ABBA_1 | 400 | 405 | PF00400 | 0.308 |
LIG_BRCT_BRCA1_1 | 400 | 404 | PF00533 | 0.273 |
LIG_BRCT_BRCA1_1 | 596 | 600 | PF00533 | 0.457 |
LIG_CSL_BTD_1 | 964 | 967 | PF09270 | 0.596 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.241 |
LIG_deltaCOP1_diTrp_1 | 109 | 118 | PF00928 | 0.337 |
LIG_EH_1 | 500 | 504 | PF12763 | 0.266 |
LIG_eIF4E_1 | 269 | 275 | PF01652 | 0.225 |
LIG_eIF4E_1 | 287 | 293 | PF01652 | 0.275 |
LIG_eIF4E_1 | 854 | 860 | PF01652 | 0.439 |
LIG_EVH1_2 | 114 | 118 | PF00568 | 0.372 |
LIG_FHA_1 | 1031 | 1037 | PF00498 | 0.685 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.337 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.243 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.229 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.300 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.514 |
LIG_FHA_1 | 578 | 584 | PF00498 | 0.708 |
LIG_FHA_1 | 586 | 592 | PF00498 | 0.504 |
LIG_FHA_1 | 667 | 673 | PF00498 | 0.581 |
LIG_FHA_1 | 698 | 704 | PF00498 | 0.589 |
LIG_FHA_1 | 726 | 732 | PF00498 | 0.499 |
LIG_FHA_1 | 761 | 767 | PF00498 | 0.501 |
LIG_FHA_1 | 778 | 784 | PF00498 | 0.404 |
LIG_FHA_1 | 832 | 838 | PF00498 | 0.498 |
LIG_FHA_1 | 910 | 916 | PF00498 | 0.588 |
LIG_FHA_1 | 947 | 953 | PF00498 | 0.738 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.557 |
LIG_FHA_2 | 295 | 301 | PF00498 | 0.335 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.281 |
LIG_FHA_2 | 444 | 450 | PF00498 | 0.391 |
LIG_FHA_2 | 700 | 706 | PF00498 | 0.545 |
LIG_FHA_2 | 976 | 982 | PF00498 | 0.748 |
LIG_Integrin_isoDGR_2 | 434 | 436 | PF01839 | 0.640 |
LIG_Integrin_RGD_1 | 423 | 425 | PF01839 | 0.646 |
LIG_LIR_Apic_2 | 108 | 114 | PF02991 | 0.373 |
LIG_LIR_Apic_2 | 750 | 756 | PF02991 | 0.525 |
LIG_LIR_Apic_2 | 861 | 867 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 229 | 239 | PF02991 | 0.275 |
LIG_LIR_Gen_1 | 368 | 376 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 388 | 397 | PF02991 | 0.187 |
LIG_LIR_Gen_1 | 597 | 607 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 116 | 121 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 229 | 234 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 279 | 285 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 388 | 393 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 395 | 400 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 401 | 406 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 499 | 503 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 597 | 603 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 618 | 623 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 632 | 637 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 817 | 821 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 851 | 857 | PF02991 | 0.440 |
LIG_LYPXL_yS_3 | 285 | 288 | PF13949 | 0.335 |
LIG_MLH1_MIPbox_1 | 400 | 404 | PF16413 | 0.273 |
LIG_MYND_1 | 671 | 675 | PF01753 | 0.557 |
LIG_NRBOX | 519 | 525 | PF00104 | 0.532 |
LIG_Pex14_1 | 901 | 905 | PF04695 | 0.549 |
LIG_Pex14_2 | 117 | 121 | PF04695 | 0.338 |
LIG_PTB_Apo_2 | 682 | 689 | PF02174 | 0.584 |
LIG_REV1ctd_RIR_1 | 115 | 123 | PF16727 | 0.367 |
LIG_SH2_CRK | 490 | 494 | PF00017 | 0.231 |
LIG_SH2_CRK | 718 | 722 | PF00017 | 0.522 |
LIG_SH2_CRK | 854 | 858 | PF00017 | 0.457 |
LIG_SH2_NCK_1 | 1027 | 1031 | PF00017 | 0.638 |
LIG_SH2_NCK_1 | 277 | 281 | PF00017 | 0.282 |
LIG_SH2_NCK_1 | 864 | 868 | PF00017 | 0.498 |
LIG_SH2_SRC | 277 | 280 | PF00017 | 0.322 |
LIG_SH2_STAP1 | 1027 | 1031 | PF00017 | 0.703 |
LIG_SH2_STAP1 | 648 | 652 | PF00017 | 0.510 |
LIG_SH2_STAP1 | 832 | 836 | PF00017 | 0.498 |
LIG_SH2_STAT3 | 56 | 59 | PF00017 | 0.378 |
LIG_SH2_STAT3 | 767 | 770 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.256 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.242 |
LIG_SH2_STAT5 | 287 | 290 | PF00017 | 0.249 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 602 | 605 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 832 | 835 | PF00017 | 0.442 |
LIG_SH3_2 | 811 | 816 | PF14604 | 0.439 |
LIG_SH3_3 | 1011 | 1017 | PF00018 | 0.665 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.312 |
LIG_SH3_3 | 639 | 645 | PF00018 | 0.549 |
LIG_SH3_3 | 808 | 814 | PF00018 | 0.439 |
LIG_SUMO_SIM_anti_2 | 730 | 735 | PF11976 | 0.462 |
LIG_SUMO_SIM_par_1 | 17 | 23 | PF11976 | 0.321 |
LIG_SUMO_SIM_par_1 | 385 | 391 | PF11976 | 0.300 |
LIG_SUMO_SIM_par_1 | 856 | 862 | PF11976 | 0.431 |
LIG_TRAF2_1 | 1058 | 1061 | PF00917 | 0.760 |
LIG_TRFH_1 | 287 | 291 | PF08558 | 0.231 |
LIG_TYR_ITIM | 275 | 280 | PF00017 | 0.272 |
LIG_UBA3_1 | 519 | 526 | PF00899 | 0.510 |
LIG_WRC_WIRS_1 | 389 | 394 | PF05994 | 0.315 |
MOD_CDC14_SPxK_1 | 983 | 986 | PF00782 | 0.641 |
MOD_CDK_SPK_2 | 46 | 51 | PF00069 | 0.447 |
MOD_CDK_SPxK_1 | 980 | 986 | PF00069 | 0.647 |
MOD_CK1_1 | 1055 | 1061 | PF00069 | 0.700 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.235 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.518 |
MOD_CK1_1 | 659 | 665 | PF00069 | 0.680 |
MOD_CK1_1 | 980 | 986 | PF00069 | 0.774 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.544 |
MOD_CK2_1 | 1055 | 1061 | PF00069 | 0.736 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.335 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.294 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.291 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.386 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.370 |
MOD_CK2_1 | 545 | 551 | PF00069 | 0.748 |
MOD_CK2_1 | 699 | 705 | PF00069 | 0.587 |
MOD_Cter_Amidation | 417 | 420 | PF01082 | 0.597 |
MOD_Cter_Amidation | 72 | 75 | PF01082 | 0.740 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.595 |
MOD_GlcNHglycan | 1005 | 1008 | PF01048 | 0.501 |
MOD_GlcNHglycan | 1054 | 1058 | PF01048 | 0.492 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.439 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.506 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.706 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.379 |
MOD_GlcNHglycan | 545 | 548 | PF01048 | 0.553 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.479 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.448 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.263 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.685 |
MOD_GlcNHglycan | 705 | 709 | PF01048 | 0.320 |
MOD_GlcNHglycan | 826 | 829 | PF01048 | 0.231 |
MOD_GlcNHglycan | 918 | 921 | PF01048 | 0.499 |
MOD_GlcNHglycan | 961 | 964 | PF01048 | 0.490 |
MOD_GlcNHglycan | 986 | 989 | PF01048 | 0.496 |
MOD_GSK3_1 | 1026 | 1033 | PF00069 | 0.650 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.487 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.509 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.323 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.704 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.565 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.374 |
MOD_GSK3_1 | 629 | 636 | PF00069 | 0.451 |
MOD_GSK3_1 | 656 | 663 | PF00069 | 0.612 |
MOD_GSK3_1 | 699 | 706 | PF00069 | 0.516 |
MOD_GSK3_1 | 826 | 833 | PF00069 | 0.407 |
MOD_GSK3_1 | 910 | 917 | PF00069 | 0.694 |
MOD_GSK3_1 | 938 | 945 | PF00069 | 0.641 |
MOD_GSK3_1 | 975 | 982 | PF00069 | 0.751 |
MOD_LATS_1 | 120 | 126 | PF00433 | 0.423 |
MOD_N-GLC_1 | 201 | 206 | PF02516 | 0.481 |
MOD_N-GLC_1 | 770 | 775 | PF02516 | 0.342 |
MOD_N-GLC_2 | 281 | 283 | PF02516 | 0.528 |
MOD_NEK2_1 | 1018 | 1023 | PF00069 | 0.643 |
MOD_NEK2_1 | 1026 | 1031 | PF00069 | 0.638 |
MOD_NEK2_1 | 1052 | 1057 | PF00069 | 0.747 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.298 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.335 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.311 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.287 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.378 |
MOD_NEK2_1 | 496 | 501 | PF00069 | 0.278 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.266 |
MOD_NEK2_1 | 543 | 548 | PF00069 | 0.672 |
MOD_NEK2_1 | 594 | 599 | PF00069 | 0.468 |
MOD_NEK2_1 | 603 | 608 | PF00069 | 0.521 |
MOD_NEK2_1 | 676 | 681 | PF00069 | 0.557 |
MOD_NEK2_1 | 688 | 693 | PF00069 | 0.515 |
MOD_NEK2_1 | 699 | 704 | PF00069 | 0.505 |
MOD_NEK2_1 | 782 | 787 | PF00069 | 0.518 |
MOD_NEK2_1 | 894 | 899 | PF00069 | 0.526 |
MOD_NEK2_1 | 908 | 913 | PF00069 | 0.589 |
MOD_NEK2_1 | 942 | 947 | PF00069 | 0.709 |
MOD_NEK2_1 | 975 | 980 | PF00069 | 0.812 |
MOD_NEK2_1 | 992 | 997 | PF00069 | 0.715 |
MOD_NEK2_2 | 509 | 514 | PF00069 | 0.210 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.520 |
MOD_PIKK_1 | 135 | 141 | PF00454 | 0.431 |
MOD_PIKK_1 | 443 | 449 | PF00454 | 0.451 |
MOD_PIKK_1 | 643 | 649 | PF00454 | 0.610 |
MOD_PIKK_1 | 666 | 672 | PF00454 | 0.725 |
MOD_PIKK_1 | 697 | 703 | PF00454 | 0.552 |
MOD_PIKK_1 | 747 | 753 | PF00454 | 0.490 |
MOD_PIKK_1 | 770 | 776 | PF00454 | 0.545 |
MOD_PIKK_1 | 896 | 902 | PF00454 | 0.472 |
MOD_PKA_1 | 60 | 66 | PF00069 | 0.556 |
MOD_PKA_2 | 1003 | 1009 | PF00069 | 0.737 |
MOD_PKA_2 | 60 | 66 | PF00069 | 0.561 |
MOD_PKA_2 | 676 | 682 | PF00069 | 0.593 |
MOD_PKA_2 | 703 | 709 | PF00069 | 0.513 |
MOD_PKA_2 | 848 | 854 | PF00069 | 0.413 |
MOD_PKA_2 | 871 | 877 | PF00069 | 0.474 |
MOD_PKA_2 | 894 | 900 | PF00069 | 0.618 |
MOD_PKB_1 | 58 | 66 | PF00069 | 0.379 |
MOD_PKB_1 | 944 | 952 | PF00069 | 0.741 |
MOD_Plk_1 | 201 | 207 | PF00069 | 0.281 |
MOD_Plk_1 | 550 | 556 | PF00069 | 0.718 |
MOD_Plk_1 | 629 | 635 | PF00069 | 0.536 |
MOD_Plk_1 | 883 | 889 | PF00069 | 0.574 |
MOD_Plk_2-3 | 100 | 106 | PF00069 | 0.441 |
MOD_Plk_2-3 | 323 | 329 | PF00069 | 0.242 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.381 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.277 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.332 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.317 |
MOD_Plk_4 | 629 | 635 | PF00069 | 0.536 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.277 |
MOD_ProDKin_1 | 1013 | 1019 | PF00069 | 0.708 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.368 |
MOD_ProDKin_1 | 615 | 621 | PF00069 | 0.547 |
MOD_ProDKin_1 | 740 | 746 | PF00069 | 0.474 |
MOD_ProDKin_1 | 910 | 916 | PF00069 | 0.637 |
MOD_ProDKin_1 | 980 | 986 | PF00069 | 0.779 |
MOD_SUMO_rev_2 | 290 | 299 | PF00179 | 0.225 |
TRG_DiLeu_BaEn_2 | 387 | 393 | PF01217 | 0.315 |
TRG_DiLeu_BaLyEn_6 | 288 | 293 | PF01217 | 0.242 |
TRG_DiLeu_BaLyEn_6 | 668 | 673 | PF01217 | 0.681 |
TRG_ENDOCYTIC_2 | 231 | 234 | PF00928 | 0.256 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.269 |
TRG_ENDOCYTIC_2 | 285 | 288 | PF00928 | 0.263 |
TRG_ENDOCYTIC_2 | 490 | 493 | PF00928 | 0.231 |
TRG_ENDOCYTIC_2 | 718 | 721 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 854 | 857 | PF00928 | 0.439 |
TRG_ER_diArg_1 | 141 | 144 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 169 | 171 | PF00400 | 0.298 |
TRG_ER_diArg_1 | 452 | 454 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 463 | 466 | PF00400 | 0.445 |
TRG_ER_diArg_1 | 57 | 60 | PF00400 | 0.398 |
TRG_ER_diArg_1 | 901 | 903 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 944 | 947 | PF00400 | 0.745 |
TRG_NES_CRM1_1 | 249 | 259 | PF08389 | 0.303 |
TRG_NES_CRM1_1 | 340 | 354 | PF08389 | 0.392 |
TRG_NES_CRM1_1 | 398 | 412 | PF08389 | 0.296 |
TRG_NES_CRM1_1 | 799 | 813 | PF08389 | 0.439 |
TRG_NLS_MonoExtC_3 | 126 | 132 | PF00514 | 0.397 |
TRG_NLS_MonoExtC_3 | 418 | 423 | PF00514 | 0.478 |
TRG_NLS_MonoExtC_3 | 45 | 50 | PF00514 | 0.466 |
TRG_NLS_MonoExtN_4 | 416 | 423 | PF00514 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 1024 | 1028 | PF00026 | 0.396 |
TRG_Pf-PMV_PEXEL_1 | 3 | 7 | PF00026 | 0.523 |
TRG_Pf-PMV_PEXEL_1 | 521 | 525 | PF00026 | 0.321 |
TRG_Pf-PMV_PEXEL_1 | 625 | 630 | PF00026 | 0.337 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8F0 | Leptomonas seymouri | 56% | 84% |
A0A0S4IQT3 | Bodo saltans | 38% | 97% |
A0A1X0NRE3 | Trypanosomatidae | 42% | 100% |
A0A3R7P0G4 | Trypanosoma rangeli | 43% | 100% |
A4HGL3 | Leishmania braziliensis | 80% | 100% |
A4I3N9 | Leishmania infantum | 99% | 100% |
D0A8C5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9AZY0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q8A5 | Leishmania major | 92% | 100% |
V5BAP9 | Trypanosoma cruzi | 42% | 100% |