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 | 2 |
GO:0005681 | spliceosomal complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0071013 | catalytic step 2 spliceosome | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 2 |
Related structures:
AlphaFold database: Q4Q1D7
Term | Name | Level | Count |
---|---|---|---|
GO:0000390 | spliceosomal complex disassembly | 7 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022411 | cellular component disassembly | 4 | 2 |
GO:0032984 | protein-containing complex disassembly | 5 | 2 |
GO:0032988 | ribonucleoprotein complex disassembly | 6 | 2 |
GO:0043933 | protein-containing complex organization | 4 | 2 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003723 | RNA binding | 4 | 2 |
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 54 | 58 | PF00656 | 0.618 |
CLV_C14_Caspase3-7 | 85 | 89 | PF00656 | 0.715 |
CLV_C14_Caspase3-7 | 887 | 891 | PF00656 | 0.457 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.736 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.673 |
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 | 0.336 |
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 | 0.522 |
CLV_NRD_NRD_1 | 968 | 970 | PF00675 | 0.194 |
CLV_NRD_NRD_1 | 982 | 984 | PF00675 | 0.242 |
CLV_NRD_NRD_1 | 997 | 999 | PF00675 | 0.194 |
CLV_PCSK_KEX2_1 | 1025 | 1027 | PF00082 | 0.319 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.260 |
CLV_PCSK_KEX2_1 | 660 | 662 | PF00082 | 0.354 |
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 | 0.486 |
CLV_PCSK_KEX2_1 | 982 | 984 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 997 | 999 | PF00082 | 0.249 |
CLV_PCSK_PC1ET2_1 | 1025 | 1027 | PF00082 | 0.319 |
CLV_PCSK_PC1ET2_1 | 158 | 160 | PF00082 | 0.627 |
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 | 0.753 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.499 |
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 | 0.483 |
CLV_PCSK_SKI1_1 | 697 | 701 | PF00082 | 0.249 |
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 | 0.579 |
CLV_PCSK_SKI1_1 | 970 | 974 | PF00082 | 0.259 |
CLV_Separin_Metazoa | 657 | 661 | PF03568 | 0.535 |
DEG_APCC_DBOX_1 | 616 | 624 | PF00400 | 0.472 |
DEG_APCC_DBOX_1 | 784 | 792 | PF00400 | 0.383 |
DEG_APCC_DBOX_1 | 942 | 950 | PF00400 | 0.404 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.704 |
DEG_SCF_FBW7_1 | 834 | 840 | PF00400 | 0.535 |
DOC_CKS1_1 | 663 | 668 | PF01111 | 0.535 |
DOC_CKS1_1 | 834 | 839 | PF01111 | 0.460 |
DOC_CYCLIN_RxL_1 | 399 | 412 | PF00134 | 0.458 |
DOC_CYCLIN_RxL_1 | 850 | 860 | PF00134 | 0.449 |
DOC_MAPK_gen_1 | 192 | 198 | PF00069 | 0.589 |
DOC_MAPK_gen_1 | 429 | 436 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 565 | 572 | PF00069 | 0.439 |
DOC_MAPK_MEF2A_6 | 565 | 574 | PF00069 | 0.439 |
DOC_PP1_RVXF_1 | 402 | 409 | PF00149 | 0.469 |
DOC_PP4_FxxP_1 | 408 | 411 | PF00568 | 0.700 |
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 | 0.550 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 705 | 709 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 815 | 819 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 837 | 841 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 849 | 853 | PF00917 | 0.412 |
DOC_USP7_MATH_2 | 680 | 686 | PF00917 | 0.474 |
DOC_USP7_UBL2_3 | 193 | 197 | PF12436 | 0.704 |
DOC_WW_Pin1_4 | 1063 | 1068 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 662 | 667 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 688 | 693 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 833 | 838 | PF00397 | 0.460 |
LIG_14-3-3_CanoR_1 | 421 | 425 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 441 | 445 | PF00244 | 0.318 |
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 | 0.490 |
LIG_14-3-3_CanoR_1 | 764 | 771 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 785 | 789 | PF00244 | 0.489 |
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 | 0.474 |
LIG_Clathr_ClatBox_1 | 802 | 806 | PF01394 | 0.395 |
LIG_deltaCOP1_diTrp_1 | 923 | 930 | PF00928 | 0.400 |
LIG_EH1_1 | 439 | 447 | PF00400 | 0.308 |
LIG_FHA_1 | 1028 | 1034 | PF00498 | 0.535 |
LIG_FHA_1 | 1064 | 1070 | PF00498 | 0.598 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.569 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.450 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.452 |
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 | 0.376 |
LIG_FHA_1 | 771 | 777 | PF00498 | 0.573 |
LIG_FHA_1 | 790 | 796 | PF00498 | 0.249 |
LIG_FHA_2 | 1022 | 1028 | PF00498 | 0.449 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.582 |
LIG_FHA_2 | 414 | 420 | PF00498 | 0.649 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.637 |
LIG_FHA_2 | 638 | 644 | PF00498 | 0.449 |
LIG_FHA_2 | 777 | 783 | PF00498 | 0.406 |
LIG_FHA_2 | 855 | 861 | PF00498 | 0.449 |
LIG_FHA_2 | 991 | 997 | PF00498 | 0.454 |
LIG_HCF-1_HBM_1 | 463 | 466 | PF13415 | 0.460 |
LIG_LIR_Apic_2 | 362 | 368 | PF02991 | 0.526 |
LIG_LIR_Apic_2 | 999 | 1004 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 37 | 47 | PF02991 | 0.544 |
LIG_LIR_Gen_1 | 554 | 564 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 612 | 623 | PF02991 | 0.272 |
LIG_LIR_Gen_1 | 988 | 996 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 1063 | 1068 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 37 | 43 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 504 | 510 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 532 | 538 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 554 | 560 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 581 | 587 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 612 | 618 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 712 | 718 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 988 | 994 | PF02991 | 0.454 |
LIG_NRP_CendR_1 | 1085 | 1088 | PF00754 | 0.592 |
LIG_Pex14_2 | 584 | 588 | PF04695 | 0.360 |
LIG_PTB_Apo_2 | 247 | 254 | PF02174 | 0.599 |
LIG_PTB_Apo_2 | 710 | 717 | PF02174 | 0.449 |
LIG_PTB_Phospho_1 | 710 | 716 | PF10480 | 0.474 |
LIG_Rb_LxCxE_1 | 64 | 85 | PF01857 | 0.627 |
LIG_Rb_LxCxE_1 | 857 | 872 | PF01857 | 0.535 |
LIG_SH2_CRK | 1048 | 1052 | PF00017 | 0.428 |
LIG_SH2_CRK | 263 | 267 | PF00017 | 0.485 |
LIG_SH2_CRK | 365 | 369 | PF00017 | 0.517 |
LIG_SH2_CRK | 538 | 542 | PF00017 | 0.449 |
LIG_SH2_NCK_1 | 365 | 369 | PF00017 | 0.517 |
LIG_SH2_PTP2 | 1001 | 1004 | PF00017 | 0.417 |
LIG_SH2_PTP2 | 615 | 618 | PF00017 | 0.270 |
LIG_SH2_PTP2 | 991 | 994 | PF00017 | 0.474 |
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 | 0.379 |
LIG_SH2_STAT3 | 169 | 172 | PF00017 | 0.705 |
LIG_SH2_STAT3 | 766 | 769 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 1001 | 1004 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 1015 | 1018 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 587 | 590 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.220 |
LIG_SH2_STAT5 | 615 | 618 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 716 | 719 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 766 | 769 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 825 | 828 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 976 | 979 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 991 | 994 | PF00017 | 0.439 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.674 |
LIG_SH3_3 | 660 | 666 | PF00018 | 0.512 |
LIG_SH3_3 | 684 | 690 | PF00018 | 0.457 |
LIG_SH3_5 | 611 | 615 | PF00018 | 0.379 |
LIG_SUMO_SIM_anti_2 | 539 | 545 | PF11976 | 0.449 |
LIG_SUMO_SIM_anti_2 | 669 | 674 | PF11976 | 0.510 |
LIG_SUMO_SIM_anti_2 | 905 | 911 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 1030 | 1036 | PF11976 | 0.463 |
LIG_SUMO_SIM_par_1 | 442 | 449 | PF11976 | 0.450 |
LIG_SUMO_SIM_par_1 | 539 | 545 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 864 | 872 | PF11976 | 0.451 |
LIG_TRAF2_1 | 160 | 163 | PF00917 | 0.641 |
LIG_TRAF2_1 | 199 | 202 | PF00917 | 0.657 |
LIG_TRAF2_1 | 416 | 419 | PF00917 | 0.605 |
LIG_TRAF2_1 | 51 | 54 | PF00917 | 0.663 |
LIG_TRAF2_1 | 640 | 643 | PF00917 | 0.449 |
LIG_TYR_ITIM | 1016 | 1021 | PF00017 | 0.301 |
LIG_TYR_ITIM | 38 | 43 | PF00017 | 0.541 |
LIG_TYR_ITSM | 611 | 618 | PF00017 | 0.287 |
LIG_UBA3_1 | 1032 | 1038 | PF00899 | 0.455 |
LIG_WW_1 | 1012 | 1015 | PF00397 | 0.336 |
MOD_CDK_SPxxK_3 | 1063 | 1070 | PF00069 | 0.597 |
MOD_CDK_SPxxK_3 | 274 | 281 | PF00069 | 0.526 |
MOD_CK1_1 | 1071 | 1077 | PF00069 | 0.482 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.631 |
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 | 0.315 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.638 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.708 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.667 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.563 |
MOD_CK2_1 | 413 | 419 | PF00069 | 0.580 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.627 |
MOD_CK2_1 | 637 | 643 | PF00069 | 0.301 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.259 |
MOD_CK2_1 | 815 | 821 | PF00069 | 0.479 |
MOD_Cter_Amidation | 353 | 356 | PF01082 | 0.679 |
MOD_Cter_Amidation | 402 | 405 | PF01082 | 0.649 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.661 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.571 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.660 |
MOD_GlcNHglycan | 363 | 368 | PF01048 | 0.739 |
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 | 0.414 |
MOD_GSK3_1 | 1074 | 1081 | PF00069 | 0.446 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.729 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.610 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.549 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.759 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.695 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.310 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.637 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.301 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.509 |
MOD_GSK3_1 | 705 | 712 | PF00069 | 0.298 |
MOD_GSK3_1 | 833 | 840 | PF00069 | 0.372 |
MOD_GSK3_1 | 843 | 850 | PF00069 | 0.266 |
MOD_GSK3_1 | 919 | 926 | PF00069 | 0.515 |
MOD_GSK3_1 | 983 | 990 | PF00069 | 0.422 |
MOD_LATS_1 | 547 | 553 | PF00433 | 0.448 |
MOD_N-GLC_1 | 22 | 27 | PF02516 | 0.613 |
MOD_NEK2_1 | 1021 | 1026 | PF00069 | 0.317 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.710 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.621 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.632 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.509 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.301 |
MOD_NEK2_1 | 573 | 578 | PF00069 | 0.422 |
MOD_NEK2_1 | 675 | 680 | PF00069 | 0.315 |
MOD_NEK2_1 | 784 | 789 | PF00069 | 0.495 |
MOD_PIKK_1 | 266 | 272 | PF00454 | 0.590 |
MOD_PIKK_1 | 323 | 329 | PF00454 | 0.673 |
MOD_PIKK_1 | 452 | 458 | PF00454 | 0.293 |
MOD_PIKK_1 | 472 | 478 | PF00454 | 0.118 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.651 |
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 | 0.556 |
MOD_PKA_2 | 1078 | 1084 | PF00069 | 0.455 |
MOD_PKA_2 | 420 | 426 | PF00069 | 0.423 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.118 |
MOD_PKA_2 | 536 | 542 | PF00069 | 0.301 |
MOD_PKA_2 | 784 | 790 | PF00069 | 0.495 |
MOD_PKA_2 | 939 | 945 | PF00069 | 0.396 |
MOD_PKA_2 | 968 | 974 | PF00069 | 0.414 |
MOD_PKB_1 | 506 | 514 | PF00069 | 0.317 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.508 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.751 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.750 |
MOD_Plk_1 | 531 | 537 | PF00069 | 0.301 |
MOD_Plk_1 | 547 | 553 | PF00069 | 0.301 |
MOD_Plk_1 | 705 | 711 | PF00069 | 0.301 |
MOD_Plk_2-3 | 343 | 349 | PF00069 | 0.751 |
MOD_Plk_4 | 1003 | 1009 | PF00069 | 0.422 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.644 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.581 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.641 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.498 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.655 |
MOD_Plk_4 | 440 | 446 | PF00069 | 0.310 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.301 |
MOD_Plk_4 | 602 | 608 | PF00069 | 0.502 |
MOD_Plk_4 | 619 | 625 | PF00069 | 0.276 |
MOD_Plk_4 | 784 | 790 | PF00069 | 0.495 |
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 | 0.599 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.667 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.528 |
MOD_ProDKin_1 | 662 | 668 | PF00069 | 0.422 |
MOD_ProDKin_1 | 688 | 694 | PF00069 | 0.301 |
MOD_ProDKin_1 | 833 | 839 | PF00069 | 0.317 |
MOD_SUMO_for_1 | 428 | 431 | PF00179 | 0.567 |
MOD_SUMO_rev_2 | 1031 | 1040 | PF00179 | 0.422 |
MOD_SUMO_rev_2 | 150 | 160 | PF00179 | 0.632 |
MOD_SUMO_rev_2 | 186 | 195 | PF00179 | 0.668 |
TRG_DiLeu_BaEn_1 | 1036 | 1041 | PF01217 | 0.317 |
TRG_DiLeu_BaEn_2 | 242 | 248 | PF01217 | 0.623 |
TRG_DiLeu_BaEn_4 | 162 | 168 | PF01217 | 0.658 |
TRG_DiLeu_BaEn_4 | 201 | 207 | PF01217 | 0.530 |
TRG_DiLeu_BaEn_4 | 243 | 249 | PF01217 | 0.509 |
TRG_ENDOCYTIC_2 | 1018 | 1021 | PF00928 | 0.290 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 538 | 541 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 615 | 618 | PF00928 | 0.270 |
TRG_ENDOCYTIC_2 | 715 | 718 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 991 | 994 | PF00928 | 0.301 |
TRG_ER_diArg_1 | 259 | 261 | PF00400 | 0.576 |
TRG_ER_diArg_1 | 316 | 318 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 477 | 479 | PF00400 | 0.290 |
TRG_ER_diArg_1 | 659 | 661 | PF00400 | 0.448 |
TRG_ER_diArg_1 | 883 | 886 | PF00400 | 0.301 |
TRG_ER_diArg_1 | 951 | 953 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 982 | 984 | PF00400 | 0.380 |
TRG_ER_diLys_1 | 1084 | 1088 | PF00400 | 0.619 |
TRG_NES_CRM1_1 | 782 | 794 | PF08389 | 0.484 |
TRG_NLS_MonoExtC_3 | 1083 | 1088 | PF00514 | 0.612 |
TRG_NLS_MonoExtC_3 | 77 | 82 | PF00514 | 0.432 |
TRG_NLS_MonoExtN_4 | 1082 | 1088 | PF00514 | 0.601 |
TRG_Pf-PMV_PEXEL_1 | 1038 | 1042 | PF00026 | 0.386 |
TRG_Pf-PMV_PEXEL_1 | 934 | 938 | PF00026 | 0.396 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0Z0 | Leptomonas seymouri | 83% | 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% |
A0A3S7XB01 | Leishmania donovani | 97% | 100% |
A0A422MXB1 | Trypanosoma rangeli | 61% | 100% |
A1Z9L3 | Drosophila melanogaster | 48% | 88% |
A2A4P0 | Mus musculus | 49% | 87% |
A4HAT8 | Leishmania braziliensis | 35% | 100% |
A4HNU7 | Leishmania braziliensis | 35% | 100% |
A4HPE9 | Leishmania braziliensis | 94% | 100% |
A4IA06 | Leishmania infantum | 34% | 100% |
A4ICJ0 | Leishmania infantum | 97% | 100% |
A4ICP7 | Leishmania infantum | 35% | 100% |
C9ZMU8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 76% |
D0A3F8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 100% |
E9ASK7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9AT60 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
E9B512 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
Q09530 | Caenorhabditis elegans | 43% | 91% |
Q14562 | Homo sapiens | 49% | 89% |
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 | 36% | 100% |