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: A0A3S7XB01
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 | 53 | 57 | PF00656 | 0.492 |
CLV_C14_Caspase3-7 | 84 | 88 | PF00656 | 0.712 |
CLV_C14_Caspase3-7 | 886 | 890 | PF00656 | 0.418 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.762 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 477 | 479 | PF00675 | 0.211 |
CLV_NRD_NRD_1 | 563 | 565 | PF00675 | 0.281 |
CLV_NRD_NRD_1 | 659 | 661 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 694 | 696 | PF00675 | 0.211 |
CLV_NRD_NRD_1 | 895 | 897 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 951 | 953 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 967 | 969 | PF00675 | 0.166 |
CLV_NRD_NRD_1 | 981 | 983 | PF00675 | 0.205 |
CLV_NRD_NRD_1 | 996 | 998 | PF00675 | 0.166 |
CLV_PCSK_KEX2_1 | 1024 | 1026 | PF00082 | 0.313 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 258 | 260 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.568 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.761 |
CLV_PCSK_KEX2_1 | 477 | 479 | PF00082 | 0.231 |
CLV_PCSK_KEX2_1 | 659 | 661 | PF00082 | 0.265 |
CLV_PCSK_KEX2_1 | 877 | 879 | PF00082 | 0.230 |
CLV_PCSK_KEX2_1 | 895 | 897 | PF00082 | 0.227 |
CLV_PCSK_KEX2_1 | 951 | 953 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 981 | 983 | PF00082 | 0.245 |
CLV_PCSK_KEX2_1 | 996 | 998 | PF00082 | 0.211 |
CLV_PCSK_PC1ET2_1 | 1024 | 1026 | PF00082 | 0.313 |
CLV_PCSK_PC1ET2_1 | 157 | 159 | PF00082 | 0.598 |
CLV_PCSK_PC1ET2_1 | 877 | 879 | PF00082 | 0.230 |
CLV_PCSK_SKI1_1 | 1013 | 1017 | PF00082 | 0.221 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 507 | 511 | PF00082 | 0.231 |
CLV_PCSK_SKI1_1 | 517 | 521 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 526 | 530 | PF00082 | 0.239 |
CLV_PCSK_SKI1_1 | 560 | 564 | PF00082 | 0.221 |
CLV_PCSK_SKI1_1 | 616 | 620 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 696 | 700 | PF00082 | 0.211 |
CLV_PCSK_SKI1_1 | 768 | 772 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 852 | 856 | PF00082 | 0.211 |
CLV_PCSK_SKI1_1 | 878 | 882 | PF00082 | 0.215 |
CLV_PCSK_SKI1_1 | 946 | 950 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 969 | 973 | PF00082 | 0.220 |
CLV_Separin_Metazoa | 656 | 660 | PF03568 | 0.513 |
DEG_APCC_DBOX_1 | 615 | 623 | PF00400 | 0.450 |
DEG_APCC_DBOX_1 | 783 | 791 | PF00400 | 0.328 |
DEG_APCC_DBOX_1 | 941 | 949 | PF00400 | 0.357 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.560 |
DEG_SCF_FBW7_1 | 833 | 839 | PF00400 | 0.513 |
DOC_AGCK_PIF_2 | 329 | 334 | PF00069 | 0.476 |
DOC_CKS1_1 | 662 | 667 | PF01111 | 0.513 |
DOC_CKS1_1 | 833 | 838 | PF01111 | 0.423 |
DOC_CYCLIN_RxL_1 | 849 | 859 | PF00134 | 0.411 |
DOC_MAPK_gen_1 | 191 | 197 | PF00069 | 0.557 |
DOC_MAPK_gen_1 | 428 | 435 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 564 | 571 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 564 | 573 | PF00069 | 0.402 |
DOC_PP4_FxxP_1 | 407 | 410 | PF00568 | 0.661 |
DOC_PP4_FxxP_1 | 881 | 884 | PF00568 | 0.411 |
DOC_PP4_FxxP_1 | 898 | 901 | PF00568 | 0.411 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 146 | 150 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 704 | 708 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 814 | 818 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 836 | 840 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 848 | 852 | PF00917 | 0.423 |
DOC_USP7_MATH_2 | 679 | 685 | PF00917 | 0.435 |
DOC_USP7_UBL2_3 | 192 | 196 | PF12436 | 0.692 |
DOC_WW_Pin1_4 | 1062 | 1067 | PF00397 | 0.569 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 661 | 666 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 687 | 692 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 832 | 837 | PF00397 | 0.439 |
LIG_14-3-3_CanoR_1 | 420 | 424 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 440 | 444 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 536 | 540 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 548 | 558 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 659 | 665 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 763 | 770 | PF00244 | 0.325 |
LIG_14-3-3_CanoR_1 | 784 | 788 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 968 | 977 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 988 | 994 | PF00244 | 0.318 |
LIG_Actin_WH2_2 | 512 | 528 | PF00022 | 0.411 |
LIG_APCC_ABBAyCdc20_2 | 1013 | 1019 | PF00400 | 0.411 |
LIG_BRCT_BRCA1_1 | 589 | 593 | PF00533 | 0.478 |
LIG_BRCT_BRCA1_1 | 683 | 687 | PF00533 | 0.421 |
LIG_Clathr_ClatBox_1 | 1031 | 1035 | PF01394 | 0.435 |
LIG_Clathr_ClatBox_1 | 801 | 805 | PF01394 | 0.339 |
LIG_deltaCOP1_diTrp_1 | 922 | 929 | PF00928 | 0.346 |
LIG_EH1_1 | 438 | 446 | PF00400 | 0.263 |
LIG_FHA_1 | 1027 | 1033 | PF00498 | 0.513 |
LIG_FHA_1 | 1063 | 1069 | PF00498 | 0.559 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.519 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.415 |
LIG_FHA_1 | 451 | 457 | PF00498 | 0.452 |
LIG_FHA_1 | 508 | 514 | PF00498 | 0.411 |
LIG_FHA_1 | 550 | 556 | PF00498 | 0.411 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.380 |
LIG_FHA_1 | 610 | 616 | PF00498 | 0.342 |
LIG_FHA_1 | 770 | 776 | PF00498 | 0.578 |
LIG_FHA_1 | 789 | 795 | PF00498 | 0.215 |
LIG_FHA_2 | 1021 | 1027 | PF00498 | 0.411 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.508 |
LIG_FHA_2 | 49 | 55 | PF00498 | 0.587 |
LIG_FHA_2 | 637 | 643 | PF00498 | 0.411 |
LIG_FHA_2 | 776 | 782 | PF00498 | 0.351 |
LIG_FHA_2 | 854 | 860 | PF00498 | 0.411 |
LIG_FHA_2 | 960 | 966 | PF00498 | 0.547 |
LIG_FHA_2 | 990 | 996 | PF00498 | 0.415 |
LIG_HCF-1_HBM_1 | 462 | 465 | PF13415 | 0.421 |
LIG_LIR_Apic_2 | 998 | 1003 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 36 | 46 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 553 | 563 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 987 | 995 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 1062 | 1067 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 503 | 509 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 531 | 537 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 553 | 559 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 580 | 586 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 987 | 993 | PF02991 | 0.415 |
LIG_NRP_CendR_1 | 1084 | 1087 | PF00754 | 0.537 |
LIG_Pex14_2 | 583 | 587 | PF04695 | 0.309 |
LIG_PTB_Apo_2 | 246 | 253 | PF02174 | 0.604 |
LIG_PTB_Apo_2 | 709 | 716 | PF02174 | 0.411 |
LIG_PTB_Phospho_1 | 709 | 715 | PF10480 | 0.435 |
LIG_Rb_LxCxE_1 | 63 | 85 | PF01857 | 0.498 |
LIG_Rb_LxCxE_1 | 856 | 871 | PF01857 | 0.513 |
LIG_SH2_CRK | 1047 | 1051 | PF00017 | 0.394 |
LIG_SH2_CRK | 129 | 133 | PF00017 | 0.477 |
LIG_SH2_CRK | 262 | 266 | PF00017 | 0.550 |
LIG_SH2_CRK | 537 | 541 | PF00017 | 0.429 |
LIG_SH2_PTP2 | 1000 | 1003 | PF00017 | 0.383 |
LIG_SH2_PTP2 | 990 | 993 | PF00017 | 0.435 |
LIG_SH2_SRC | 1000 | 1003 | PF00017 | 0.421 |
LIG_SH2_SRC | 824 | 827 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 502 | 506 | PF00017 | 0.414 |
LIG_SH2_STAP1 | 537 | 541 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 912 | 916 | PF00017 | 0.327 |
LIG_SH2_STAT3 | 168 | 171 | PF00017 | 0.574 |
LIG_SH2_STAT3 | 364 | 367 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 1000 | 1003 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 1014 | 1017 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 58 | 61 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 586 | 589 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 606 | 609 | PF00017 | 0.219 |
LIG_SH2_STAT5 | 614 | 617 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 715 | 718 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 765 | 768 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 824 | 827 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 975 | 978 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 990 | 993 | PF00017 | 0.402 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.642 |
LIG_SH3_3 | 659 | 665 | PF00018 | 0.481 |
LIG_SH3_3 | 683 | 689 | PF00018 | 0.419 |
LIG_SH3_5 | 610 | 614 | PF00018 | 0.348 |
LIG_SUMO_SIM_anti_2 | 538 | 544 | PF11976 | 0.411 |
LIG_SUMO_SIM_anti_2 | 668 | 673 | PF11976 | 0.478 |
LIG_SUMO_SIM_anti_2 | 904 | 910 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 1029 | 1035 | PF11976 | 0.424 |
LIG_SUMO_SIM_par_1 | 441 | 448 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 538 | 544 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 863 | 871 | PF11976 | 0.413 |
LIG_TRAF2_1 | 159 | 162 | PF00917 | 0.609 |
LIG_TRAF2_1 | 198 | 201 | PF00917 | 0.654 |
LIG_TRAF2_1 | 415 | 418 | PF00917 | 0.557 |
LIG_TRAF2_1 | 50 | 53 | PF00917 | 0.618 |
LIG_TRAF2_1 | 639 | 642 | PF00917 | 0.411 |
LIG_TYR_ITIM | 1015 | 1020 | PF00017 | 0.263 |
LIG_TYR_ITIM | 37 | 42 | PF00017 | 0.482 |
LIG_UBA3_1 | 1031 | 1037 | PF00899 | 0.445 |
LIG_WW_1 | 1011 | 1014 | PF00397 | 0.282 |
MOD_CDK_SPxxK_3 | 1062 | 1069 | PF00069 | 0.559 |
MOD_CDK_SPxxK_3 | 273 | 280 | PF00069 | 0.510 |
MOD_CK1_1 | 1070 | 1076 | PF00069 | 0.417 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.589 |
MOD_CK1_1 | 450 | 456 | PF00069 | 0.248 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.248 |
MOD_CK1_1 | 549 | 555 | PF00069 | 0.249 |
MOD_CK1_1 | 989 | 995 | PF00069 | 0.391 |
MOD_CK2_1 | 1020 | 1026 | PF00069 | 0.260 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.607 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.689 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.663 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.516 |
MOD_CK2_1 | 48 | 54 | PF00069 | 0.570 |
MOD_CK2_1 | 636 | 642 | PF00069 | 0.248 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.244 |
MOD_CK2_1 | 814 | 820 | PF00069 | 0.450 |
MOD_Cter_Amidation | 352 | 355 | PF01082 | 0.579 |
MOD_Cter_Amidation | 401 | 404 | PF01082 | 0.628 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.538 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.562 |
MOD_GlcNHglycan | 362 | 367 | PF01048 | 0.704 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.248 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.248 |
MOD_GlcNHglycan | 718 | 721 | PF01048 | 0.263 |
MOD_GlcNHglycan | 749 | 752 | PF01048 | 0.341 |
MOD_GlcNHglycan | 816 | 819 | PF01048 | 0.364 |
MOD_GSK3_1 | 1073 | 1080 | PF00069 | 0.385 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.693 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.654 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.721 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.651 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.266 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.586 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.256 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.473 |
MOD_GSK3_1 | 832 | 839 | PF00069 | 0.346 |
MOD_GSK3_1 | 842 | 849 | PF00069 | 0.277 |
MOD_GSK3_1 | 918 | 925 | PF00069 | 0.486 |
MOD_GSK3_1 | 982 | 989 | PF00069 | 0.391 |
MOD_LATS_1 | 546 | 552 | PF00433 | 0.324 |
MOD_N-GLC_1 | 184 | 189 | PF02516 | 0.515 |
MOD_N-GLC_1 | 21 | 26 | PF02516 | 0.570 |
MOD_N-GLC_1 | 959 | 964 | PF02516 | 0.475 |
MOD_NEK2_1 | 1020 | 1025 | PF00069 | 0.263 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.691 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.624 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.555 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.471 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.280 |
MOD_NEK2_1 | 572 | 577 | PF00069 | 0.391 |
MOD_NEK2_1 | 674 | 679 | PF00069 | 0.261 |
MOD_NEK2_1 | 783 | 788 | PF00069 | 0.463 |
MOD_PIKK_1 | 265 | 271 | PF00454 | 0.652 |
MOD_PIKK_1 | 322 | 328 | PF00454 | 0.564 |
MOD_PIKK_1 | 451 | 457 | PF00454 | 0.248 |
MOD_PIKK_1 | 471 | 477 | PF00454 | 0.118 |
MOD_PIKK_1 | 48 | 54 | PF00454 | 0.604 |
MOD_PIKK_1 | 739 | 745 | PF00454 | 0.248 |
MOD_PIKK_1 | 846 | 852 | PF00454 | 0.303 |
MOD_PKA_2 | 1020 | 1026 | PF00069 | 0.391 |
MOD_PKA_2 | 1053 | 1059 | PF00069 | 0.591 |
MOD_PKA_2 | 1077 | 1083 | PF00069 | 0.394 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.355 |
MOD_PKA_2 | 439 | 445 | PF00069 | 0.391 |
MOD_PKA_2 | 535 | 541 | PF00069 | 0.248 |
MOD_PKA_2 | 783 | 789 | PF00069 | 0.463 |
MOD_PKA_2 | 938 | 944 | PF00069 | 0.346 |
MOD_PKA_2 | 967 | 973 | PF00069 | 0.379 |
MOD_PKB_1 | 505 | 513 | PF00069 | 0.263 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.443 |
MOD_Plk_1 | 342 | 348 | PF00069 | 0.625 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.692 |
MOD_Plk_1 | 530 | 536 | PF00069 | 0.248 |
MOD_Plk_1 | 546 | 552 | PF00069 | 0.248 |
MOD_Plk_1 | 704 | 710 | PF00069 | 0.248 |
MOD_Plk_2-3 | 342 | 348 | PF00069 | 0.649 |
MOD_Plk_4 | 1002 | 1008 | PF00069 | 0.391 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.606 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.525 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.666 |
MOD_Plk_4 | 33 | 39 | PF00069 | 0.431 |
MOD_Plk_4 | 366 | 372 | PF00069 | 0.601 |
MOD_Plk_4 | 439 | 445 | PF00069 | 0.276 |
MOD_Plk_4 | 535 | 541 | PF00069 | 0.256 |
MOD_Plk_4 | 601 | 607 | PF00069 | 0.466 |
MOD_Plk_4 | 618 | 624 | PF00069 | 0.242 |
MOD_Plk_4 | 783 | 789 | PF00069 | 0.463 |
MOD_Plk_4 | 850 | 856 | PF00069 | 0.248 |
MOD_Plk_4 | 865 | 871 | PF00069 | 0.282 |
MOD_Plk_4 | 904 | 910 | PF00069 | 0.348 |
MOD_ProDKin_1 | 1062 | 1068 | PF00069 | 0.563 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.663 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.513 |
MOD_ProDKin_1 | 661 | 667 | PF00069 | 0.391 |
MOD_ProDKin_1 | 687 | 693 | PF00069 | 0.248 |
MOD_ProDKin_1 | 832 | 838 | PF00069 | 0.287 |
MOD_SUMO_for_1 | 427 | 430 | PF00179 | 0.428 |
MOD_SUMO_rev_2 | 1030 | 1039 | PF00179 | 0.391 |
MOD_SUMO_rev_2 | 149 | 159 | PF00179 | 0.590 |
MOD_SUMO_rev_2 | 187 | 194 | PF00179 | 0.642 |
TRG_DiLeu_BaEn_1 | 1035 | 1040 | PF01217 | 0.263 |
TRG_DiLeu_BaEn_2 | 241 | 247 | PF01217 | 0.524 |
TRG_DiLeu_BaEn_4 | 161 | 167 | PF01217 | 0.620 |
TRG_DiLeu_BaEn_4 | 200 | 206 | PF01217 | 0.520 |
TRG_DiLeu_BaEn_4 | 242 | 248 | PF01217 | 0.482 |
TRG_ENDOCYTIC_2 | 1017 | 1020 | PF00928 | 0.250 |
TRG_ENDOCYTIC_2 | 129 | 132 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 537 | 540 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 714 | 717 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 990 | 993 | PF00928 | 0.248 |
TRG_ER_diArg_1 | 258 | 260 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 315 | 317 | PF00400 | 0.565 |
TRG_ER_diArg_1 | 476 | 478 | PF00400 | 0.248 |
TRG_ER_diArg_1 | 658 | 660 | PF00400 | 0.324 |
TRG_ER_diArg_1 | 882 | 885 | PF00400 | 0.248 |
TRG_ER_diArg_1 | 981 | 983 | PF00400 | 0.334 |
TRG_ER_diLys_1 | 1083 | 1087 | PF00400 | 0.579 |
TRG_NES_CRM1_1 | 613 | 629 | PF08389 | 0.199 |
TRG_NES_CRM1_1 | 781 | 793 | PF08389 | 0.453 |
TRG_NLS_MonoCore_2 | 402 | 407 | PF00514 | 0.619 |
TRG_NLS_MonoExtC_3 | 1082 | 1087 | PF00514 | 0.573 |
TRG_NLS_MonoExtN_4 | 1081 | 1087 | PF00514 | 0.567 |
TRG_Pf-PMV_PEXEL_1 | 1037 | 1041 | PF00026 | 0.341 |
TRG_Pf-PMV_PEXEL_1 | 933 | 937 | PF00026 | 0.352 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0Z0 | Leptomonas seymouri | 84% | 100% |
A0A0N1PEU4 | Leptomonas seymouri | 35% | 100% |
A0A0S4JCY8 | Bodo saltans | 55% | 100% |
A0A1X0NKY7 | Trypanosomatidae | 60% | 100% |
A0A3Q8II71 | Leishmania donovani | 34% | 100% |
A0A3Q8IJ24 | Leishmania donovani | 35% | 100% |
A0A422MXB1 | Trypanosoma rangeli | 61% | 100% |
A1Z9L3 | Drosophila melanogaster | 49% | 88% |
A4HAT8 | Leishmania braziliensis | 34% | 100% |
A4HNU7 | Leishmania braziliensis | 35% | 100% |
A4HPE9 | Leishmania braziliensis | 95% | 100% |
A4IA06 | Leishmania infantum | 34% | 100% |
A4ICJ0 | Leishmania infantum | 100% | 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) | 37% | 100% |
E9AT60 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
E9AWV1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B512 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
O60114 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 76% |
Q09530 | Caenorhabditis elegans | 43% | 91% |
Q4Q1D7 | Leishmania major | 97% | 100% |
Q4Q1Y9 | Leishmania major | 35% | 100% |
Q4Q2X4 | Leishmania major | 34% | 100% |
Q6PGC1 | Mus musculus | 27% | 80% |
Q9HDY4 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 92% |
Q9VF26 | Drosophila melanogaster | 27% | 76% |
V5BPV3 | Trypanosoma cruzi | 62% | 100% |
V5BV22 | Trypanosoma cruzi | 36% | 100% |