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:0005654 | nucleoplasm | 2 | 1 |
GO:0005681 | spliceosomal complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0071013 | catalytic step 2 spliceosome | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: E9AT60
Term | Name | Level | Count |
---|---|---|---|
GO:0000390 | spliceosomal complex disassembly | 7 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022411 | cellular component disassembly | 4 | 1 |
GO:0032984 | protein-containing complex disassembly | 5 | 1 |
GO:0032988 | ribonucleoprotein complex disassembly | 6 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 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:0016787 | hydrolase activity | 2 | 11 |
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: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:0003723 | RNA binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 85 | 89 | PF00656 | 0.725 |
CLV_C14_Caspase3-7 | 887 | 891 | PF00656 | 0.456 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.741 |
CLV_NRD_NRD_1 | 478 | 480 | PF00675 | 0.249 |
CLV_NRD_NRD_1 | 564 | 566 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 660 | 662 | PF00675 | 0.330 |
CLV_NRD_NRD_1 | 695 | 697 | PF00675 | 0.249 |
CLV_NRD_NRD_1 | 896 | 898 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 952 | 954 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 968 | 970 | PF00675 | 0.179 |
CLV_NRD_NRD_1 | 982 | 984 | PF00675 | 0.239 |
CLV_NRD_NRD_1 | 997 | 999 | PF00675 | 0.194 |
CLV_PCSK_KEX2_1 | 1025 | 1027 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.740 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.260 |
CLV_PCSK_KEX2_1 | 660 | 662 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 878 | 880 | PF00082 | 0.259 |
CLV_PCSK_KEX2_1 | 896 | 898 | PF00082 | 0.194 |
CLV_PCSK_KEX2_1 | 952 | 954 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 982 | 984 | PF00082 | 0.282 |
CLV_PCSK_KEX2_1 | 997 | 999 | PF00082 | 0.249 |
CLV_PCSK_PC1ET2_1 | 1025 | 1027 | PF00082 | 0.335 |
CLV_PCSK_PC1ET2_1 | 158 | 160 | PF00082 | 0.655 |
CLV_PCSK_PC1ET2_1 | 878 | 880 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 1014 | 1018 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.738 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 508 | 512 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 518 | 522 | PF00082 | 0.239 |
CLV_PCSK_SKI1_1 | 527 | 531 | PF00082 | 0.191 |
CLV_PCSK_SKI1_1 | 561 | 565 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 617 | 621 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 697 | 701 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 769 | 773 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 853 | 857 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 879 | 883 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 947 | 951 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 970 | 974 | PF00082 | 0.259 |
CLV_Separin_Metazoa | 657 | 661 | PF03568 | 0.535 |
DEG_APCC_DBOX_1 | 616 | 624 | PF00400 | 0.477 |
DEG_APCC_DBOX_1 | 784 | 792 | PF00400 | 0.381 |
DEG_APCC_DBOX_1 | 942 | 950 | PF00400 | 0.409 |
DEG_COP1_1 | 772 | 783 | PF00400 | 0.272 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.670 |
DEG_SCF_FBW7_1 | 834 | 840 | PF00400 | 0.535 |
DEG_SCF_FBW7_2 | 80 | 85 | PF00400 | 0.438 |
DEG_SPOP_SBC_1 | 180 | 184 | PF00917 | 0.487 |
DOC_CKS1_1 | 663 | 668 | PF01111 | 0.535 |
DOC_CKS1_1 | 834 | 839 | PF01111 | 0.460 |
DOC_CYCLIN_RxL_1 | 850 | 860 | PF00134 | 0.449 |
DOC_MAPK_gen_1 | 192 | 198 | PF00069 | 0.614 |
DOC_MAPK_gen_1 | 429 | 436 | PF00069 | 0.479 |
DOC_MAPK_gen_1 | 565 | 572 | PF00069 | 0.439 |
DOC_MAPK_MEF2A_6 | 565 | 574 | PF00069 | 0.439 |
DOC_PP4_FxxP_1 | 408 | 411 | PF00568 | 0.702 |
DOC_PP4_FxxP_1 | 882 | 885 | PF00568 | 0.449 |
DOC_PP4_FxxP_1 | 899 | 902 | PF00568 | 0.449 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 705 | 709 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 815 | 819 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 837 | 841 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 849 | 853 | PF00917 | 0.411 |
DOC_USP7_MATH_2 | 680 | 686 | PF00917 | 0.473 |
DOC_USP7_UBL2_3 | 193 | 197 | PF12436 | 0.725 |
DOC_WW_Pin1_4 | 1063 | 1068 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 662 | 667 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 688 | 693 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 833 | 838 | PF00397 | 0.460 |
LIG_14-3-3_CanoR_1 | 421 | 425 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 441 | 445 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 537 | 541 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 549 | 559 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 660 | 666 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 764 | 771 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 785 | 789 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 969 | 978 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 989 | 995 | PF00244 | 0.318 |
LIG_Actin_WH2_2 | 513 | 529 | PF00022 | 0.449 |
LIG_APCC_ABBAyCdc20_2 | 1014 | 1020 | PF00400 | 0.449 |
LIG_BRCT_BRCA1_1 | 590 | 594 | PF00533 | 0.507 |
LIG_BRCT_BRCA1_1 | 684 | 688 | PF00533 | 0.460 |
LIG_Clathr_ClatBox_1 | 1032 | 1036 | PF01394 | 0.473 |
LIG_Clathr_ClatBox_1 | 802 | 806 | PF01394 | 0.393 |
LIG_deltaCOP1_diTrp_1 | 923 | 930 | PF00928 | 0.397 |
LIG_EH1_1 | 439 | 447 | PF00400 | 0.308 |
LIG_FHA_1 | 1028 | 1034 | PF00498 | 0.535 |
LIG_FHA_1 | 1064 | 1070 | PF00498 | 0.584 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.587 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.450 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.441 |
LIG_FHA_1 | 509 | 515 | PF00498 | 0.449 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.449 |
LIG_FHA_1 | 598 | 604 | PF00498 | 0.432 |
LIG_FHA_1 | 611 | 617 | PF00498 | 0.396 |
LIG_FHA_1 | 771 | 777 | PF00498 | 0.559 |
LIG_FHA_1 | 790 | 796 | PF00498 | 0.465 |
LIG_FHA_2 | 1022 | 1028 | PF00498 | 0.449 |
LIG_FHA_2 | 414 | 420 | PF00498 | 0.634 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.635 |
LIG_FHA_2 | 638 | 644 | PF00498 | 0.449 |
LIG_FHA_2 | 777 | 783 | PF00498 | 0.394 |
LIG_FHA_2 | 855 | 861 | PF00498 | 0.439 |
LIG_FHA_2 | 961 | 967 | PF00498 | 0.567 |
LIG_FHA_2 | 991 | 997 | PF00498 | 0.453 |
LIG_HCF-1_HBM_1 | 463 | 466 | PF13415 | 0.460 |
LIG_LIR_Apic_2 | 999 | 1004 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 37 | 47 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 554 | 564 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 988 | 996 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 1063 | 1068 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 332 | 338 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 37 | 43 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 504 | 510 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 532 | 538 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 554 | 560 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 581 | 587 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 712 | 718 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 988 | 994 | PF02991 | 0.453 |
LIG_NRP_CendR_1 | 1085 | 1088 | PF00754 | 0.590 |
LIG_PCNA_PIPBox_1 | 123 | 132 | PF02747 | 0.493 |
LIG_Pex14_2 | 584 | 588 | PF04695 | 0.361 |
LIG_PTB_Apo_2 | 247 | 254 | PF02174 | 0.661 |
LIG_PTB_Apo_2 | 710 | 717 | PF02174 | 0.449 |
LIG_PTB_Phospho_1 | 710 | 716 | PF10480 | 0.473 |
LIG_Rb_LxCxE_1 | 64 | 86 | PF01857 | 0.634 |
LIG_Rb_LxCxE_1 | 857 | 872 | PF01857 | 0.535 |
LIG_SH2_CRK | 1048 | 1052 | PF00017 | 0.454 |
LIG_SH2_CRK | 130 | 134 | PF00017 | 0.514 |
LIG_SH2_CRK | 263 | 267 | PF00017 | 0.579 |
LIG_SH2_CRK | 538 | 542 | PF00017 | 0.449 |
LIG_SH2_PTP2 | 1001 | 1004 | PF00017 | 0.417 |
LIG_SH2_PTP2 | 991 | 994 | PF00017 | 0.473 |
LIG_SH2_SRC | 1001 | 1004 | PF00017 | 0.460 |
LIG_SH2_SRC | 825 | 828 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 503 | 507 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 538 | 542 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 913 | 917 | PF00017 | 0.381 |
LIG_SH2_STAT3 | 169 | 172 | PF00017 | 0.713 |
LIG_SH2_STAT3 | 365 | 368 | PF00017 | 0.650 |
LIG_SH2_STAT5 | 1001 | 1004 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 1015 | 1018 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 587 | 590 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.219 |
LIG_SH2_STAT5 | 615 | 618 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 716 | 719 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 766 | 769 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 825 | 828 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 976 | 979 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 991 | 994 | PF00017 | 0.432 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.665 |
LIG_SH3_3 | 660 | 666 | PF00018 | 0.512 |
LIG_SH3_3 | 684 | 690 | PF00018 | 0.443 |
LIG_SH3_5 | 611 | 615 | PF00018 | 0.403 |
LIG_SUMO_SIM_anti_2 | 539 | 545 | PF11976 | 0.445 |
LIG_SUMO_SIM_anti_2 | 669 | 674 | PF11976 | 0.509 |
LIG_SUMO_SIM_anti_2 | 905 | 911 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 1030 | 1036 | PF11976 | 0.462 |
LIG_SUMO_SIM_par_1 | 442 | 449 | PF11976 | 0.440 |
LIG_SUMO_SIM_par_1 | 539 | 545 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 864 | 872 | PF11976 | 0.451 |
LIG_TRAF2_1 | 115 | 118 | PF00917 | 0.726 |
LIG_TRAF2_1 | 160 | 163 | PF00917 | 0.662 |
LIG_TRAF2_1 | 199 | 202 | PF00917 | 0.675 |
LIG_TRAF2_1 | 416 | 419 | PF00917 | 0.589 |
LIG_TRAF2_1 | 51 | 54 | PF00917 | 0.663 |
LIG_TRAF2_1 | 640 | 643 | PF00917 | 0.449 |
LIG_TYR_ITIM | 1016 | 1021 | PF00017 | 0.317 |
LIG_TYR_ITIM | 38 | 43 | PF00017 | 0.522 |
LIG_UBA3_1 | 1032 | 1038 | PF00899 | 0.462 |
LIG_WW_1 | 1012 | 1015 | PF00397 | 0.336 |
MOD_CDK_SPxxK_3 | 1063 | 1070 | PF00069 | 0.583 |
MOD_CDK_SPxxK_3 | 274 | 281 | PF00069 | 0.550 |
MOD_CK1_1 | 1071 | 1077 | PF00069 | 0.468 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.651 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.301 |
MOD_CK1_1 | 512 | 518 | PF00069 | 0.301 |
MOD_CK1_1 | 550 | 556 | PF00069 | 0.301 |
MOD_CK1_1 | 990 | 996 | PF00069 | 0.422 |
MOD_CK2_1 | 1021 | 1027 | PF00069 | 0.314 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.660 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.734 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.687 |
MOD_CK2_1 | 413 | 419 | PF00069 | 0.567 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.624 |
MOD_CK2_1 | 637 | 643 | PF00069 | 0.301 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.247 |
MOD_CK2_1 | 815 | 821 | PF00069 | 0.490 |
MOD_Cter_Amidation | 353 | 356 | PF01082 | 0.667 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.684 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.614 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.659 |
MOD_GlcNHglycan | 381 | 385 | PF01048 | 0.538 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.301 |
MOD_GlcNHglycan | 575 | 578 | PF01048 | 0.301 |
MOD_GlcNHglycan | 719 | 722 | PF01048 | 0.317 |
MOD_GlcNHglycan | 750 | 753 | PF01048 | 0.386 |
MOD_GlcNHglycan | 817 | 820 | PF01048 | 0.410 |
MOD_GSK3_1 | 1074 | 1081 | PF00069 | 0.438 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.738 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.669 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.574 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.748 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.691 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.307 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.634 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.301 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.510 |
MOD_GSK3_1 | 705 | 712 | PF00069 | 0.287 |
MOD_GSK3_1 | 770 | 777 | PF00069 | 0.264 |
MOD_GSK3_1 | 833 | 840 | PF00069 | 0.371 |
MOD_GSK3_1 | 843 | 850 | PF00069 | 0.266 |
MOD_GSK3_1 | 919 | 926 | PF00069 | 0.516 |
MOD_GSK3_1 | 983 | 990 | PF00069 | 0.422 |
MOD_LATS_1 | 547 | 553 | PF00433 | 0.448 |
MOD_N-GLC_1 | 185 | 190 | PF02516 | 0.586 |
MOD_N-GLC_1 | 960 | 965 | PF02516 | 0.523 |
MOD_NEK2_1 | 1021 | 1026 | PF00069 | 0.317 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.735 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.665 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.495 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.301 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.422 |
MOD_NEK2_1 | 675 | 680 | PF00069 | 0.313 |
MOD_NEK2_1 | 784 | 789 | PF00069 | 0.493 |
MOD_PIKK_1 | 266 | 272 | PF00454 | 0.655 |
MOD_PIKK_1 | 323 | 329 | PF00454 | 0.702 |
MOD_PIKK_1 | 364 | 370 | PF00454 | 0.535 |
MOD_PIKK_1 | 452 | 458 | PF00454 | 0.301 |
MOD_PIKK_1 | 472 | 478 | PF00454 | 0.118 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.648 |
MOD_PIKK_1 | 740 | 746 | PF00454 | 0.301 |
MOD_PIKK_1 | 847 | 853 | PF00454 | 0.317 |
MOD_PKA_2 | 1021 | 1027 | PF00069 | 0.422 |
MOD_PKA_2 | 1054 | 1060 | PF00069 | 0.611 |
MOD_PKA_2 | 1078 | 1084 | PF00069 | 0.448 |
MOD_PKA_2 | 420 | 426 | PF00069 | 0.408 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.390 |
MOD_PKA_2 | 536 | 542 | PF00069 | 0.301 |
MOD_PKA_2 | 784 | 790 | PF00069 | 0.493 |
MOD_PKA_2 | 939 | 945 | PF00069 | 0.401 |
MOD_PKA_2 | 968 | 974 | PF00069 | 0.383 |
MOD_PKB_1 | 506 | 514 | PF00069 | 0.317 |
MOD_Plk_1 | 180 | 186 | PF00069 | 0.550 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.518 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.733 |
MOD_Plk_1 | 531 | 537 | PF00069 | 0.301 |
MOD_Plk_1 | 547 | 553 | PF00069 | 0.301 |
MOD_Plk_1 | 705 | 711 | PF00069 | 0.293 |
MOD_Plk_2-3 | 343 | 349 | PF00069 | 0.733 |
MOD_Plk_4 | 1003 | 1009 | PF00069 | 0.422 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.671 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.591 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.693 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.489 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.652 |
MOD_Plk_4 | 440 | 446 | PF00069 | 0.306 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.301 |
MOD_Plk_4 | 602 | 608 | PF00069 | 0.504 |
MOD_Plk_4 | 619 | 625 | PF00069 | 0.280 |
MOD_Plk_4 | 784 | 790 | PF00069 | 0.493 |
MOD_Plk_4 | 851 | 857 | PF00069 | 0.301 |
MOD_Plk_4 | 866 | 872 | PF00069 | 0.301 |
MOD_Plk_4 | 905 | 911 | PF00069 | 0.386 |
MOD_ProDKin_1 | 1063 | 1069 | PF00069 | 0.586 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.687 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.551 |
MOD_ProDKin_1 | 662 | 668 | PF00069 | 0.422 |
MOD_ProDKin_1 | 688 | 694 | PF00069 | 0.301 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.565 |
MOD_ProDKin_1 | 833 | 839 | PF00069 | 0.317 |
MOD_SUMO_for_1 | 428 | 431 | PF00179 | 0.556 |
MOD_SUMO_rev_2 | 1031 | 1040 | PF00179 | 0.422 |
MOD_SUMO_rev_2 | 150 | 160 | PF00179 | 0.657 |
MOD_SUMO_rev_2 | 188 | 195 | PF00179 | 0.697 |
TRG_DiLeu_BaEn_1 | 1036 | 1041 | PF01217 | 0.317 |
TRG_DiLeu_BaEn_2 | 242 | 248 | PF01217 | 0.711 |
TRG_DiLeu_BaEn_4 | 162 | 168 | PF01217 | 0.674 |
TRG_DiLeu_BaEn_4 | 201 | 207 | PF01217 | 0.566 |
TRG_DiLeu_BaEn_4 | 243 | 249 | PF01217 | 0.592 |
TRG_ENDOCYTIC_2 | 1018 | 1021 | PF00928 | 0.303 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 538 | 541 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 715 | 718 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 991 | 994 | PF00928 | 0.301 |
TRG_ER_diArg_1 | 259 | 261 | PF00400 | 0.655 |
TRG_ER_diArg_1 | 316 | 318 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 477 | 479 | PF00400 | 0.301 |
TRG_ER_diArg_1 | 659 | 661 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 883 | 886 | PF00400 | 0.301 |
TRG_ER_diArg_1 | 982 | 984 | PF00400 | 0.379 |
TRG_ER_diLys_1 | 1084 | 1088 | PF00400 | 0.618 |
TRG_NES_CRM1_1 | 58 | 73 | PF08389 | 0.356 |
TRG_NES_CRM1_1 | 782 | 794 | PF08389 | 0.481 |
TRG_NLS_MonoExtC_3 | 1083 | 1088 | PF00514 | 0.610 |
TRG_NLS_MonoExtN_4 | 1082 | 1088 | PF00514 | 0.604 |
TRG_Pf-PMV_PEXEL_1 | 1038 | 1042 | PF00026 | 0.386 |
TRG_Pf-PMV_PEXEL_1 | 934 | 938 | PF00026 | 0.398 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8Y1 | Leptomonas seymouri | 34% | 100% |
A0A0N1I0Z0 | Leptomonas seymouri | 84% | 100% |
A0A0N1PEU4 | Leptomonas seymouri | 35% | 100% |
A0A0S4JCY8 | Bodo saltans | 55% | 100% |
A0A1X0NKY7 | Trypanosomatidae | 59% | 100% |
A0A3Q8II71 | Leishmania donovani | 34% | 100% |
A0A3Q8IJ24 | Leishmania donovani | 35% | 100% |
A0A3S7XB01 | Leishmania donovani | 98% | 100% |
A0A422MXB1 | Trypanosoma rangeli | 60% | 100% |
A4HAT8 | Leishmania braziliensis | 35% | 100% |
A4HNU7 | Leishmania braziliensis | 35% | 100% |
A4HPE9 | Leishmania braziliensis | 94% | 100% |
A4IA06 | Leishmania infantum | 34% | 100% |
A4ICJ0 | Leishmania infantum | 98% | 100% |
A4ICP7 | Leishmania infantum | 35% | 100% |
D0A3F8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 100% |
E9ASK7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
E9B512 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
O60114 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 76% |
Q09530 | Caenorhabditis elegans | 42% | 91% |
Q296Q5 | Drosophila pseudoobscura pseudoobscura | 28% | 76% |
Q4Q1D7 | Leishmania major | 96% | 100% |
Q4Q1Y9 | Leishmania major | 35% | 100% |
Q4Q2X4 | Leishmania major | 34% | 100% |
Q9HDY4 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 92% |
Q9VF26 | Drosophila melanogaster | 27% | 76% |
V5BPV3 | Trypanosoma cruzi | 62% | 100% |
V5BV22 | Trypanosoma cruzi | 37% | 100% |