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: A4HGL3
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 | 1041 | 1045 | PF00656 | 0.716 |
CLV_C14_Caspase3-7 | 842 | 846 | PF00656 | 0.413 |
CLV_NRD_NRD_1 | 105 | 107 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.722 |
CLV_NRD_NRD_1 | 195 | 197 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 469 | 471 | PF00675 | 0.702 |
CLV_NRD_NRD_1 | 475 | 477 | PF00675 | 0.710 |
CLV_NRD_NRD_1 | 517 | 519 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 802 | 804 | PF00675 | 0.293 |
CLV_NRD_NRD_1 | 940 | 942 | PF00675 | 0.290 |
CLV_PCSK_FUR_1 | 103 | 107 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 469 | 471 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 517 | 519 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 560 | 562 | PF00082 | 0.249 |
CLV_PCSK_PC1ET2_1 | 118 | 120 | PF00082 | 0.762 |
CLV_PCSK_PC1ET2_1 | 473 | 475 | PF00082 | 0.748 |
CLV_PCSK_PC1ET2_1 | 560 | 562 | PF00082 | 0.249 |
CLV_PCSK_PC7_1 | 469 | 475 | PF00082 | 0.680 |
CLV_PCSK_SKI1_1 | 1084 | 1088 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 135 | 139 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 454 | 458 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 529 | 533 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 561 | 565 | PF00082 | 0.244 |
CLV_PCSK_SKI1_1 | 567 | 571 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 598 | 602 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 655 | 659 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 775 | 779 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 849 | 853 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 895 | 899 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 924 | 928 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 942 | 946 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 948 | 952 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 970 | 974 | PF00082 | 0.403 |
DEG_APCC_DBOX_1 | 1083 | 1091 | PF00400 | 0.550 |
DEG_SPOP_SBC_1 | 411 | 415 | PF00917 | 0.460 |
DOC_CDC14_PxL_1 | 334 | 342 | PF14671 | 0.335 |
DOC_CDC14_PxL_1 | 699 | 707 | PF14671 | 0.461 |
DOC_CKS1_1 | 36 | 41 | PF01111 | 0.405 |
DOC_CYCLIN_RxL_1 | 427 | 438 | PF00134 | 0.380 |
DOC_CYCLIN_RxL_1 | 595 | 605 | PF00134 | 0.613 |
DOC_CYCLIN_yCln2_LP_2 | 33 | 39 | PF00134 | 0.421 |
DOC_CYCLIN_yCln2_LP_2 | 582 | 588 | PF00134 | 0.657 |
DOC_CYCLIN_yCln2_LP_2 | 729 | 735 | PF00134 | 0.519 |
DOC_CYCLIN_yCln2_LP_2 | 854 | 860 | PF00134 | 0.535 |
DOC_MAPK_gen_1 | 179 | 187 | PF00069 | 0.478 |
DOC_MAPK_gen_1 | 560 | 568 | PF00069 | 0.456 |
DOC_MAPK_gen_1 | 772 | 780 | PF00069 | 0.478 |
DOC_MAPK_gen_1 | 834 | 843 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 895 | 905 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 560 | 568 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 849 | 858 | PF00069 | 0.431 |
DOC_MAPK_NFAT4_5 | 561 | 569 | PF00069 | 0.548 |
DOC_MAPK_NFAT4_5 | 849 | 857 | PF00069 | 0.478 |
DOC_PP1_RVXF_1 | 322 | 329 | PF00149 | 0.242 |
DOC_PP1_RVXF_1 | 452 | 458 | PF00149 | 0.211 |
DOC_PP2B_LxvP_1 | 198 | 201 | PF13499 | 0.371 |
DOC_PP2B_LxvP_1 | 33 | 36 | PF13499 | 0.404 |
DOC_PP2B_LxvP_1 | 582 | 585 | PF13499 | 0.504 |
DOC_PP2B_LxvP_1 | 854 | 857 | PF13499 | 0.535 |
DOC_PP4_FxxP_1 | 197 | 200 | PF00568 | 0.409 |
DOC_PP4_FxxP_1 | 759 | 762 | PF00568 | 0.452 |
DOC_PP4_FxxP_1 | 799 | 802 | PF00568 | 0.456 |
DOC_USP7_MATH_1 | 1008 | 1012 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 1013 | 1017 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 1053 | 1057 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.376 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 463 | 467 | PF00917 | 0.317 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 591 | 595 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 596 | 600 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 860 | 864 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 955 | 959 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 962 | 966 | PF00917 | 0.761 |
DOC_USP7_UBL2_3 | 120 | 124 | PF12436 | 0.506 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 1004 | 1009 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 1059 | 1064 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.298 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.265 |
DOC_WW_Pin1_4 | 661 | 666 | PF00397 | 0.538 |
DOC_WW_Pin1_4 | 714 | 719 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.356 |
LIG_14-3-3_CanoR_1 | 1012 | 1018 | PF00244 | 0.757 |
LIG_14-3-3_CanoR_1 | 1037 | 1043 | PF00244 | 0.737 |
LIG_14-3-3_CanoR_1 | 1050 | 1056 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 518 | 524 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 723 | 727 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 834 | 843 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 941 | 947 | PF00244 | 0.583 |
LIG_Actin_WH2_2 | 200 | 217 | PF00022 | 0.278 |
LIG_Actin_WH2_2 | 735 | 752 | PF00022 | 0.567 |
LIG_Actin_WH2_2 | 879 | 897 | PF00022 | 0.526 |
LIG_APCC_ABBA_1 | 360 | 365 | PF00400 | 0.245 |
LIG_APCC_ABBA_1 | 453 | 458 | PF00400 | 0.316 |
LIG_APCC_ABBA_1 | 796 | 801 | PF00400 | 0.413 |
LIG_BH_BH3_1 | 256 | 272 | PF00452 | 0.177 |
LIG_BRCT_BRCA1_1 | 642 | 646 | PF00533 | 0.458 |
LIG_deltaCOP1_diTrp_1 | 161 | 170 | PF00928 | 0.327 |
LIG_EH_1 | 546 | 550 | PF12763 | 0.266 |
LIG_EH1_1 | 739 | 747 | PF00400 | 0.402 |
LIG_eIF4E_1 | 321 | 327 | PF01652 | 0.225 |
LIG_eIF4E_1 | 339 | 345 | PF01652 | 0.275 |
LIG_EVH1_2 | 166 | 170 | PF00568 | 0.360 |
LIG_FHA_1 | 1033 | 1039 | PF00498 | 0.691 |
LIG_FHA_1 | 1050 | 1056 | PF00498 | 0.557 |
LIG_FHA_1 | 1077 | 1083 | PF00498 | 0.698 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.337 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.251 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.382 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.436 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.520 |
LIG_FHA_1 | 632 | 638 | PF00498 | 0.526 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.288 |
LIG_FHA_1 | 772 | 778 | PF00498 | 0.499 |
LIG_FHA_1 | 807 | 813 | PF00498 | 0.501 |
LIG_FHA_1 | 878 | 884 | PF00498 | 0.498 |
LIG_FHA_1 | 993 | 999 | PF00498 | 0.721 |
LIG_FHA_2 | 1039 | 1045 | PF00498 | 0.805 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.335 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.273 |
LIG_FHA_2 | 707 | 713 | PF00498 | 0.566 |
LIG_FHA_2 | 746 | 752 | PF00498 | 0.545 |
LIG_LIR_Apic_2 | 161 | 166 | PF02991 | 0.353 |
LIG_LIR_Apic_2 | 907 | 913 | PF02991 | 0.478 |
LIG_LIR_Apic_2 | 99 | 104 | PF02991 | 0.278 |
LIG_LIR_Gen_1 | 281 | 291 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 421 | 428 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 441 | 450 | PF02991 | 0.187 |
LIG_LIR_Gen_1 | 643 | 653 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 664 | 673 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 725 | 734 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 281 | 286 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 331 | 337 | PF02991 | 0.245 |
LIG_LIR_Nem_3 | 441 | 446 | PF02991 | 0.270 |
LIG_LIR_Nem_3 | 488 | 494 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 545 | 549 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 599 | 604 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 643 | 649 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 664 | 669 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 678 | 683 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 725 | 729 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 826 | 832 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 863 | 867 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 945 | 950 | PF02991 | 0.472 |
LIG_LYPXL_yS_3 | 337 | 340 | PF13949 | 0.335 |
LIG_NRBOX | 565 | 571 | PF00104 | 0.534 |
LIG_Pex14_1 | 947 | 951 | PF04695 | 0.544 |
LIG_Pex14_2 | 169 | 173 | PF04695 | 0.332 |
LIG_PTB_Apo_2 | 728 | 735 | PF02174 | 0.575 |
LIG_REV1ctd_RIR_1 | 167 | 175 | PF16727 | 0.359 |
LIG_SH2_CRK | 491 | 495 | PF00017 | 0.318 |
LIG_SH2_CRK | 536 | 540 | PF00017 | 0.231 |
LIG_SH2_CRK | 726 | 730 | PF00017 | 0.523 |
LIG_SH2_CRK | 764 | 768 | PF00017 | 0.522 |
LIG_SH2_NCK_1 | 1073 | 1077 | PF00017 | 0.645 |
LIG_SH2_NCK_1 | 910 | 914 | PF00017 | 0.498 |
LIG_SH2_STAP1 | 428 | 432 | PF00017 | 0.338 |
LIG_SH2_STAP1 | 694 | 698 | PF00017 | 0.502 |
LIG_SH2_STAP1 | 878 | 882 | PF00017 | 0.498 |
LIG_SH2_STAT3 | 40 | 43 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.256 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.242 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.231 |
LIG_SH2_STAT5 | 878 | 881 | PF00017 | 0.453 |
LIG_SH3_1 | 101 | 107 | PF00018 | 0.380 |
LIG_SH3_2 | 718 | 723 | PF14604 | 0.474 |
LIG_SH3_3 | 101 | 107 | PF00018 | 0.340 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.413 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.504 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.321 |
LIG_SH3_3 | 700 | 706 | PF00018 | 0.610 |
LIG_SH3_3 | 715 | 721 | PF00018 | 0.494 |
LIG_SH3_3 | 789 | 795 | PF00018 | 0.508 |
LIG_SH3_3 | 854 | 860 | PF00018 | 0.439 |
LIG_SUMO_SIM_anti_2 | 776 | 781 | PF11976 | 0.462 |
LIG_SUMO_SIM_par_1 | 62 | 68 | PF11976 | 0.319 |
LIG_SUMO_SIM_par_1 | 902 | 908 | PF11976 | 0.431 |
LIG_TRFH_1 | 339 | 343 | PF08558 | 0.231 |
LIG_UBA3_1 | 565 | 572 | PF00899 | 0.512 |
LIG_WRC_WIRS_1 | 442 | 447 | PF05994 | 0.318 |
MOD_CDK_SPK_2 | 119 | 124 | PF00069 | 0.419 |
MOD_CDK_SPK_2 | 91 | 96 | PF00069 | 0.436 |
MOD_CDK_SPxxK_3 | 119 | 126 | PF00069 | 0.420 |
MOD_CK1_1 | 1029 | 1035 | PF00069 | 0.759 |
MOD_CK1_1 | 1101 | 1107 | PF00069 | 0.669 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.513 |
MOD_CK1_1 | 623 | 629 | PF00069 | 0.673 |
MOD_CK1_1 | 664 | 670 | PF00069 | 0.483 |
MOD_CK2_1 | 1099 | 1105 | PF00069 | 0.721 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.335 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.294 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.283 |
MOD_CK2_1 | 591 | 597 | PF00069 | 0.747 |
MOD_CK2_1 | 706 | 712 | PF00069 | 0.561 |
MOD_CK2_1 | 745 | 751 | PF00069 | 0.578 |
MOD_CK2_1 | 870 | 876 | PF00069 | 0.377 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.333 |
MOD_Cter_Amidation | 115 | 118 | PF01082 | 0.707 |
MOD_Cter_Amidation | 177 | 180 | PF01082 | 0.615 |
MOD_GlcNHglycan | 1055 | 1058 | PF01048 | 0.517 |
MOD_GlcNHglycan | 1100 | 1104 | PF01048 | 0.461 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.766 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.549 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.439 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.506 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.583 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.588 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.609 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.778 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.593 |
MOD_GlcNHglycan | 603 | 607 | PF01048 | 0.521 |
MOD_GlcNHglycan | 620 | 623 | PF01048 | 0.468 |
MOD_GlcNHglycan | 659 | 662 | PF01048 | 0.258 |
MOD_GlcNHglycan | 751 | 755 | PF01048 | 0.320 |
MOD_GlcNHglycan | 872 | 875 | PF01048 | 0.231 |
MOD_GlcNHglycan | 957 | 960 | PF01048 | 0.425 |
MOD_GSK3_1 | 1004 | 1011 | PF00069 | 0.579 |
MOD_GSK3_1 | 1021 | 1028 | PF00069 | 0.747 |
MOD_GSK3_1 | 1049 | 1056 | PF00069 | 0.687 |
MOD_GSK3_1 | 1072 | 1079 | PF00069 | 0.658 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.595 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.502 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.512 |
MOD_GSK3_1 | 640 | 647 | PF00069 | 0.537 |
MOD_GSK3_1 | 657 | 664 | PF00069 | 0.415 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.514 |
MOD_GSK3_1 | 745 | 752 | PF00069 | 0.507 |
MOD_GSK3_1 | 962 | 969 | PF00069 | 0.713 |
MOD_GSK3_1 | 984 | 991 | PF00069 | 0.650 |
MOD_LATS_1 | 172 | 178 | PF00433 | 0.416 |
MOD_N-GLC_1 | 1026 | 1031 | PF02516 | 0.449 |
MOD_N-GLC_1 | 1032 | 1037 | PF02516 | 0.430 |
MOD_N-GLC_1 | 174 | 179 | PF02516 | 0.589 |
MOD_N-GLC_1 | 253 | 258 | PF02516 | 0.481 |
MOD_N-GLC_2 | 333 | 335 | PF02516 | 0.528 |
MOD_NEK2_1 | 1022 | 1027 | PF00069 | 0.807 |
MOD_NEK2_1 | 1038 | 1043 | PF00069 | 0.715 |
MOD_NEK2_1 | 1064 | 1069 | PF00069 | 0.641 |
MOD_NEK2_1 | 1072 | 1077 | PF00069 | 0.645 |
MOD_NEK2_1 | 1098 | 1103 | PF00069 | 0.719 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.573 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.177 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.374 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.301 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.335 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.355 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.333 |
MOD_NEK2_1 | 519 | 524 | PF00069 | 0.336 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.278 |
MOD_NEK2_1 | 549 | 554 | PF00069 | 0.266 |
MOD_NEK2_1 | 640 | 645 | PF00069 | 0.463 |
MOD_NEK2_1 | 649 | 654 | PF00069 | 0.477 |
MOD_NEK2_1 | 722 | 727 | PF00069 | 0.556 |
MOD_NEK2_1 | 745 | 750 | PF00069 | 0.495 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.302 |
MOD_NEK2_1 | 828 | 833 | PF00069 | 0.518 |
MOD_NEK2_1 | 940 | 945 | PF00069 | 0.528 |
MOD_NEK2_1 | 954 | 959 | PF00069 | 0.592 |
MOD_NEK2_1 | 988 | 993 | PF00069 | 0.713 |
MOD_NEK2_2 | 596 | 601 | PF00069 | 0.552 |
MOD_PIKK_1 | 1092 | 1098 | PF00454 | 0.603 |
MOD_PIKK_1 | 187 | 193 | PF00454 | 0.428 |
MOD_PIKK_1 | 396 | 402 | PF00454 | 0.289 |
MOD_PIKK_1 | 628 | 634 | PF00454 | 0.566 |
MOD_PIKK_1 | 664 | 670 | PF00454 | 0.458 |
MOD_PIKK_1 | 689 | 695 | PF00454 | 0.605 |
MOD_PIKK_1 | 712 | 718 | PF00454 | 0.726 |
MOD_PIKK_1 | 816 | 822 | PF00454 | 0.545 |
MOD_PKA_2 | 1049 | 1055 | PF00069 | 0.722 |
MOD_PKA_2 | 613 | 619 | PF00069 | 0.648 |
MOD_PKA_2 | 722 | 728 | PF00069 | 0.591 |
MOD_PKA_2 | 749 | 755 | PF00069 | 0.513 |
MOD_PKA_2 | 816 | 822 | PF00069 | 0.417 |
MOD_PKA_2 | 917 | 923 | PF00069 | 0.474 |
MOD_PKA_2 | 940 | 946 | PF00069 | 0.618 |
MOD_PKB_1 | 133 | 141 | PF00069 | 0.412 |
MOD_PKB_1 | 990 | 998 | PF00069 | 0.731 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.274 |
MOD_Plk_1 | 253 | 259 | PF00069 | 0.313 |
MOD_Plk_1 | 44 | 50 | PF00069 | 0.248 |
MOD_Plk_1 | 596 | 602 | PF00069 | 0.722 |
MOD_Plk_1 | 675 | 681 | PF00069 | 0.525 |
MOD_Plk_1 | 929 | 935 | PF00069 | 0.571 |
MOD_Plk_2-3 | 375 | 381 | PF00069 | 0.242 |
MOD_Plk_4 | 1055 | 1061 | PF00069 | 0.552 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.270 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.307 |
MOD_Plk_4 | 554 | 560 | PF00069 | 0.224 |
MOD_Plk_4 | 675 | 681 | PF00069 | 0.525 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.301 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.515 |
MOD_ProDKin_1 | 1004 | 1010 | PF00069 | 0.652 |
MOD_ProDKin_1 | 1059 | 1065 | PF00069 | 0.690 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.585 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.449 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.300 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.267 |
MOD_ProDKin_1 | 661 | 667 | PF00069 | 0.544 |
MOD_ProDKin_1 | 714 | 720 | PF00069 | 0.610 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.357 |
MOD_SUMO_rev_2 | 342 | 351 | PF00179 | 0.225 |
TRG_DiLeu_BaEn_2 | 440 | 446 | PF01217 | 0.314 |
TRG_DiLeu_BaLyEn_6 | 340 | 345 | PF01217 | 0.242 |
TRG_DiLeu_BaLyEn_6 | 715 | 720 | PF01217 | 0.658 |
TRG_DiLeu_BaLyEn_6 | 854 | 859 | PF01217 | 0.462 |
TRG_ENDOCYTIC_2 | 283 | 286 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.219 |
TRG_ENDOCYTIC_2 | 447 | 450 | PF00928 | 0.201 |
TRG_ENDOCYTIC_2 | 491 | 494 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 536 | 539 | PF00928 | 0.231 |
TRG_ENDOCYTIC_2 | 726 | 729 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 764 | 767 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 872 | 875 | PF00928 | 0.376 |
TRG_ER_diArg_1 | 102 | 105 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 132 | 135 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 193 | 196 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 221 | 223 | PF00400 | 0.298 |
TRG_ER_diArg_1 | 315 | 317 | PF00400 | 0.176 |
TRG_ER_diArg_1 | 474 | 476 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 517 | 519 | PF00400 | 0.505 |
TRG_ER_diArg_1 | 990 | 993 | PF00400 | 0.747 |
TRG_NES_CRM1_1 | 301 | 311 | PF08389 | 0.303 |
TRG_NES_CRM1_1 | 392 | 406 | PF08389 | 0.386 |
TRG_NLS_Bipartite_1 | 105 | 122 | PF00514 | 0.502 |
TRG_NLS_MonoCore_2 | 116 | 121 | PF00514 | 0.482 |
TRG_NLS_MonoExtC_3 | 178 | 184 | PF00514 | 0.400 |
TRG_NLS_MonoExtN_4 | 114 | 121 | PF00514 | 0.458 |
TRG_Pf-PMV_PEXEL_1 | 1070 | 1074 | PF00026 | 0.400 |
TRG_Pf-PMV_PEXEL_1 | 48 | 52 | PF00026 | 0.521 |
TRG_Pf-PMV_PEXEL_1 | 529 | 533 | PF00026 | 0.504 |
TRG_Pf-PMV_PEXEL_1 | 567 | 571 | PF00026 | 0.304 |
TRG_Pf-PMV_PEXEL_1 | 598 | 603 | PF00026 | 0.349 |
TRG_Pf-PMV_PEXEL_1 | 671 | 676 | PF00026 | 0.331 |
TRG_Pf-PMV_PEXEL_1 | 865 | 869 | PF00026 | 0.176 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8F0 | Leptomonas seymouri | 57% | 87% |
A0A0S4IQT3 | Bodo saltans | 36% | 100% |
A0A1X0NRE3 | Trypanosomatidae | 42% | 100% |
A0A3R7P0G4 | Trypanosoma rangeli | 44% | 100% |
A0A3S5H7J4 | Leishmania donovani | 80% | 100% |
A4I3N9 | Leishmania infantum | 80% | 87% |
D0A8C5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AZY0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4Q8A5 | Leishmania major | 79% | 100% |
V5BAP9 | Trypanosoma cruzi | 40% | 100% |