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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0016604 | nuclear body | 2 | 2 |
GO:0016605 | PML body | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q6T443
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006259 | DNA metabolic process | 4 | 2 |
GO:0006281 | DNA repair | 5 | 2 |
GO:0006302 | double-strand break repair | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006950 | response to stress | 2 | 2 |
GO:0006974 | DNA damage response | 4 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003677 | DNA binding | 4 | 2 |
GO:0003697 | single-stranded DNA binding | 5 | 2 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0005488 | binding | 1 | 2 |
GO:0008081 | phosphoric diester hydrolase activity | 5 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 2 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 2 |
GO:0070259 | tyrosyl-DNA phosphodiesterase activity | 4 | 2 |
GO:0070260 | 5'-tyrosyl-DNA phosphodiesterase activity | 5 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 2 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 218 | 222 | PF00656 | 0.561 |
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 772 | 774 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 827 | 829 | PF00675 | 0.482 |
CLV_PCSK_KEX2_1 | 111 | 113 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 711 | 713 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 772 | 774 | PF00082 | 0.347 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.287 |
CLV_PCSK_PC1ET2_1 | 711 | 713 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.691 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 447 | 451 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 536 | 540 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 605 | 609 | PF00082 | 0.632 |
CLV_PCSK_SKI1_1 | 682 | 686 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 864 | 868 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 934 | 938 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 949 | 953 | PF00082 | 0.344 |
CLV_Separin_Metazoa | 533 | 537 | PF03568 | 0.620 |
DEG_APCC_DBOX_1 | 435 | 443 | PF00400 | 0.552 |
DEG_APCC_DBOX_1 | 604 | 612 | PF00400 | 0.657 |
DEG_APCC_DBOX_1 | 68 | 76 | PF00400 | 0.513 |
DEG_APCC_DBOX_1 | 775 | 783 | PF00400 | 0.485 |
DEG_APCC_DBOX_1 | 948 | 956 | PF00400 | 0.630 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.704 |
DEG_SPOP_SBC_1 | 355 | 359 | PF00917 | 0.689 |
DOC_CKS1_1 | 507 | 512 | PF01111 | 0.533 |
DOC_CKS1_1 | 696 | 701 | PF01111 | 0.423 |
DOC_CYCLIN_RxL_1 | 602 | 612 | PF00134 | 0.656 |
DOC_CYCLIN_yCln2_LP_2 | 890 | 893 | PF00134 | 0.485 |
DOC_MAPK_DCC_7 | 692 | 702 | PF00069 | 0.369 |
DOC_MAPK_gen_1 | 921 | 929 | PF00069 | 0.369 |
DOC_MAPK_MEF2A_6 | 244 | 252 | PF00069 | 0.363 |
DOC_MAPK_MEF2A_6 | 563 | 570 | PF00069 | 0.587 |
DOC_MAPK_MEF2A_6 | 85 | 92 | PF00069 | 0.384 |
DOC_MAPK_NFAT4_5 | 85 | 93 | PF00069 | 0.482 |
DOC_MAPK_RevD_3 | 760 | 773 | PF00069 | 0.380 |
DOC_PP1_RVXF_1 | 680 | 687 | PF00149 | 0.379 |
DOC_PP2B_LxvP_1 | 335 | 338 | PF13499 | 0.702 |
DOC_PP2B_LxvP_1 | 481 | 484 | PF13499 | 0.512 |
DOC_PP2B_LxvP_1 | 700 | 703 | PF13499 | 0.369 |
DOC_PP2B_LxvP_1 | 785 | 788 | PF13499 | 0.369 |
DOC_PP2B_LxvP_1 | 844 | 847 | PF13499 | 0.344 |
DOC_PP2B_LxvP_1 | 890 | 893 | PF13499 | 0.485 |
DOC_PP4_FxxP_1 | 352 | 355 | PF00568 | 0.741 |
DOC_PP4_FxxP_1 | 889 | 892 | PF00568 | 0.344 |
DOC_PP4_FxxP_1 | 92 | 95 | PF00568 | 0.440 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 529 | 533 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 537 | 541 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 564 | 568 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 609 | 613 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 657 | 661 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 669 | 673 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 676 | 680 | PF00917 | 0.330 |
DOC_USP7_MATH_1 | 808 | 812 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 822 | 826 | PF00917 | 0.308 |
DOC_USP7_MATH_1 | 942 | 946 | PF00917 | 0.447 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 506 | 511 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 524 | 529 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 55 | 60 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 695 | 700 | PF00397 | 0.344 |
DOC_WW_Pin1_4 | 706 | 711 | PF00397 | 0.344 |
DOC_WW_Pin1_4 | 753 | 758 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 830 | 835 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 943 | 948 | PF00397 | 0.489 |
LIG_14-3-3_CanoR_1 | 105 | 115 | PF00244 | 0.295 |
LIG_14-3-3_CanoR_1 | 11 | 16 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 161 | 170 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 215 | 220 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 350 | 355 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 425 | 429 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 536 | 542 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 549 | 553 | PF00244 | 0.284 |
LIG_14-3-3_CanoR_1 | 602 | 608 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 682 | 687 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 750 | 760 | PF00244 | 0.393 |
LIG_14-3-3_CanoR_1 | 85 | 89 | PF00244 | 0.421 |
LIG_Actin_WH2_2 | 534 | 551 | PF00022 | 0.526 |
LIG_AP2alpha_2 | 763 | 765 | PF02296 | 0.429 |
LIG_BRCT_BRCA1_1 | 885 | 889 | PF00533 | 0.436 |
LIG_BRCT_BRCA1_1 | 915 | 919 | PF00533 | 0.444 |
LIG_BRCT_BRCA1_1 | 986 | 990 | PF00533 | 0.376 |
LIG_BRCT_BRCA1_2 | 915 | 921 | PF00533 | 0.444 |
LIG_Clathr_ClatBox_1 | 89 | 93 | PF01394 | 0.468 |
LIG_deltaCOP1_diTrp_1 | 433 | 437 | PF00928 | 0.467 |
LIG_deltaCOP1_diTrp_1 | 883 | 889 | PF00928 | 0.369 |
LIG_DLG_GKlike_1 | 11 | 19 | PF00625 | 0.580 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.527 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.472 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.463 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.365 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.458 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.499 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.625 |
LIG_FHA_1 | 678 | 684 | PF00498 | 0.402 |
LIG_FHA_1 | 799 | 805 | PF00498 | 0.369 |
LIG_FHA_1 | 866 | 872 | PF00498 | 0.362 |
LIG_FHA_1 | 946 | 952 | PF00498 | 0.423 |
LIG_FHA_1 | 960 | 966 | PF00498 | 0.355 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.501 |
LIG_FHA_2 | 428 | 434 | PF00498 | 0.563 |
LIG_FHA_2 | 498 | 504 | PF00498 | 0.390 |
LIG_FHA_2 | 641 | 647 | PF00498 | 0.762 |
LIG_FHA_2 | 855 | 861 | PF00498 | 0.345 |
LIG_FHA_2 | 910 | 916 | PF00498 | 0.369 |
LIG_LIR_Apic_2 | 351 | 355 | PF02991 | 0.662 |
LIG_LIR_Apic_2 | 706 | 710 | PF02991 | 0.369 |
LIG_LIR_Apic_2 | 886 | 892 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 190 | 200 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 222 | 233 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 23 | 33 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 268 | 277 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 296 | 304 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 35 | 46 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 433 | 442 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 503 | 512 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 586 | 596 | PF02991 | 0.554 |
LIG_LIR_Gen_1 | 638 | 644 | PF02991 | 0.726 |
LIG_LIR_Gen_1 | 685 | 693 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 916 | 927 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 987 | 993 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 179 | 183 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 190 | 195 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 222 | 228 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 23 | 28 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 268 | 273 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 296 | 300 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 433 | 437 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 486 | 492 | PF02991 | 0.656 |
LIG_LIR_Nem_3 | 503 | 507 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 586 | 592 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 638 | 642 | PF02991 | 0.678 |
LIG_LIR_Nem_3 | 734 | 740 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 763 | 768 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 899 | 904 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 916 | 922 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 987 | 993 | PF02991 | 0.461 |
LIG_LYPXL_yS_3 | 713 | 716 | PF13949 | 0.369 |
LIG_MYND_1 | 760 | 764 | PF01753 | 0.408 |
LIG_NRBOX | 248 | 254 | PF00104 | 0.463 |
LIG_NRBOX | 381 | 387 | PF00104 | 0.494 |
LIG_PCNA_PIPBox_1 | 309 | 318 | PF02747 | 0.295 |
LIG_Pex14_1 | 585 | 589 | PF04695 | 0.456 |
LIG_Pex14_1 | 686 | 690 | PF04695 | 0.344 |
LIG_REV1ctd_RIR_1 | 926 | 935 | PF16727 | 0.344 |
LIG_SH2_CRK | 25 | 29 | PF00017 | 0.535 |
LIG_SH2_CRK | 36 | 40 | PF00017 | 0.465 |
LIG_SH2_CRK | 504 | 508 | PF00017 | 0.421 |
LIG_SH2_GRB2like | 693 | 696 | PF00017 | 0.444 |
LIG_SH2_NCK_1 | 558 | 562 | PF00017 | 0.543 |
LIG_SH2_PTP2 | 38 | 41 | PF00017 | 0.384 |
LIG_SH2_PTP2 | 589 | 592 | PF00017 | 0.480 |
LIG_SH2_SRC | 36 | 39 | PF00017 | 0.467 |
LIG_SH2_SRC | 522 | 525 | PF00017 | 0.538 |
LIG_SH2_STAP1 | 36 | 40 | PF00017 | 0.465 |
LIG_SH2_STAT3 | 693 | 696 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 316 | 319 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 504 | 507 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 522 | 525 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 554 | 557 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 589 | 592 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 740 | 743 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 751 | 754 | PF00017 | 0.306 |
LIG_SH2_STAT5 | 897 | 900 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 977 | 980 | PF00017 | 0.422 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.499 |
LIG_SH3_3 | 730 | 736 | PF00018 | 0.485 |
LIG_SH3_3 | 754 | 760 | PF00018 | 0.408 |
LIG_SH3_3 | 948 | 954 | PF00018 | 0.485 |
LIG_SUMO_SIM_par_1 | 194 | 199 | PF11976 | 0.470 |
LIG_SUMO_SIM_par_1 | 427 | 433 | PF11976 | 0.488 |
LIG_SUMO_SIM_par_1 | 516 | 521 | PF11976 | 0.572 |
LIG_SUMO_SIM_par_1 | 800 | 805 | PF11976 | 0.403 |
LIG_TYR_ITIM | 34 | 39 | PF00017 | 0.482 |
LIG_WRC_WIRS_1 | 349 | 354 | PF05994 | 0.659 |
MOD_CDC14_SPxK_1 | 709 | 712 | PF00782 | 0.401 |
MOD_CDC14_SPxK_1 | 946 | 949 | PF00782 | 0.369 |
MOD_CDK_SPK_2 | 706 | 711 | PF00069 | 0.401 |
MOD_CDK_SPK_2 | 830 | 835 | PF00069 | 0.369 |
MOD_CDK_SPxK_1 | 706 | 712 | PF00069 | 0.369 |
MOD_CDK_SPxK_1 | 943 | 949 | PF00069 | 0.489 |
MOD_CDK_SPxxK_3 | 524 | 531 | PF00069 | 0.518 |
MOD_CDK_SPxxK_3 | 55 | 62 | PF00069 | 0.664 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.568 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.722 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.536 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.410 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.725 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.623 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.628 |
MOD_CK1_1 | 660 | 666 | PF00069 | 0.723 |
MOD_CK1_1 | 756 | 762 | PF00069 | 0.485 |
MOD_CK1_1 | 811 | 817 | PF00069 | 0.485 |
MOD_CK1_1 | 945 | 951 | PF00069 | 0.447 |
MOD_CK2_1 | 497 | 503 | PF00069 | 0.392 |
MOD_CK2_1 | 640 | 646 | PF00069 | 0.743 |
MOD_CK2_1 | 909 | 915 | PF00069 | 0.347 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.406 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.406 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.453 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.747 |
MOD_GlcNHglycan | 417 | 421 | PF01048 | 0.636 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.645 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.700 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.507 |
MOD_GlcNHglycan | 671 | 674 | PF01048 | 0.566 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.508 |
MOD_GlcNHglycan | 790 | 793 | PF01048 | 0.440 |
MOD_GlcNHglycan | 803 | 807 | PF01048 | 0.397 |
MOD_GlcNHglycan | 812 | 816 | PF01048 | 0.417 |
MOD_GlcNHglycan | 820 | 823 | PF01048 | 0.381 |
MOD_GlcNHglycan | 824 | 827 | PF01048 | 0.441 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.502 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.433 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.565 |
MOD_GSK3_1 | 350 | 357 | PF00069 | 0.748 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.589 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.688 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.657 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.707 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.468 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.622 |
MOD_GSK3_1 | 579 | 586 | PF00069 | 0.604 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.452 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.645 |
MOD_GSK3_1 | 657 | 664 | PF00069 | 0.751 |
MOD_GSK3_1 | 665 | 672 | PF00069 | 0.675 |
MOD_GSK3_1 | 691 | 698 | PF00069 | 0.344 |
MOD_GSK3_1 | 788 | 795 | PF00069 | 0.351 |
MOD_GSK3_1 | 798 | 805 | PF00069 | 0.335 |
MOD_GSK3_1 | 813 | 820 | PF00069 | 0.401 |
MOD_GSK3_1 | 909 | 916 | PF00069 | 0.369 |
MOD_GSK3_1 | 936 | 943 | PF00069 | 0.478 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.545 |
MOD_N-GLC_1 | 268 | 273 | PF02516 | 0.571 |
MOD_N-GLC_1 | 55 | 60 | PF02516 | 0.519 |
MOD_N-GLC_1 | 657 | 662 | PF02516 | 0.562 |
MOD_N-GLC_2 | 838 | 840 | PF02516 | 0.444 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.428 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.477 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.553 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.531 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.525 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.725 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.463 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.383 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.451 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.599 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.607 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.544 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.568 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.546 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.525 |
MOD_NEK2_1 | 665 | 670 | PF00069 | 0.706 |
MOD_NEK2_1 | 802 | 807 | PF00069 | 0.444 |
MOD_NEK2_1 | 913 | 918 | PF00069 | 0.369 |
MOD_NEK2_1 | 936 | 941 | PF00069 | 0.344 |
MOD_NEK2_1 | 959 | 964 | PF00069 | 0.450 |
MOD_NEK2_2 | 176 | 181 | PF00069 | 0.364 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.486 |
MOD_PIKK_1 | 16 | 22 | PF00454 | 0.376 |
MOD_PIKK_1 | 626 | 632 | PF00454 | 0.637 |
MOD_PKA_1 | 161 | 167 | PF00069 | 0.520 |
MOD_PKA_2 | 104 | 110 | PF00069 | 0.272 |
MOD_PKA_2 | 424 | 430 | PF00069 | 0.628 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.572 |
MOD_PKA_2 | 548 | 554 | PF00069 | 0.553 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.585 |
MOD_PKA_2 | 691 | 697 | PF00069 | 0.344 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.483 |
MOD_Plk_1 | 219 | 225 | PF00069 | 0.542 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.537 |
MOD_Plk_1 | 340 | 346 | PF00069 | 0.506 |
MOD_Plk_1 | 432 | 438 | PF00069 | 0.513 |
MOD_Plk_1 | 456 | 462 | PF00069 | 0.770 |
MOD_Plk_1 | 502 | 508 | PF00069 | 0.386 |
MOD_Plk_1 | 676 | 682 | PF00069 | 0.476 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.448 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.373 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.509 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.628 |
MOD_Plk_4 | 502 | 508 | PF00069 | 0.396 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.503 |
MOD_Plk_4 | 792 | 798 | PF00069 | 0.344 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.335 |
MOD_Plk_4 | 872 | 878 | PF00069 | 0.439 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.411 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.499 |
MOD_ProDKin_1 | 506 | 512 | PF00069 | 0.528 |
MOD_ProDKin_1 | 524 | 530 | PF00069 | 0.492 |
MOD_ProDKin_1 | 55 | 61 | PF00069 | 0.663 |
MOD_ProDKin_1 | 695 | 701 | PF00069 | 0.344 |
MOD_ProDKin_1 | 706 | 712 | PF00069 | 0.344 |
MOD_ProDKin_1 | 753 | 759 | PF00069 | 0.412 |
MOD_ProDKin_1 | 830 | 836 | PF00069 | 0.447 |
MOD_ProDKin_1 | 943 | 949 | PF00069 | 0.489 |
MOD_SUMO_for_1 | 339 | 342 | PF00179 | 0.543 |
MOD_SUMO_for_1 | 922 | 925 | PF00179 | 0.369 |
MOD_SUMO_rev_2 | 156 | 164 | PF00179 | 0.489 |
MOD_SUMO_rev_2 | 359 | 368 | PF00179 | 0.527 |
MOD_SUMO_rev_2 | 408 | 413 | PF00179 | 0.490 |
TRG_DiLeu_BaLyEn_6 | 514 | 519 | PF01217 | 0.570 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 489 | 492 | PF00928 | 0.631 |
TRG_ENDOCYTIC_2 | 504 | 507 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 589 | 592 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 713 | 716 | PF00928 | 0.335 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.609 |
TRG_ER_diArg_1 | 280 | 282 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 400 | 403 | PF00400 | 0.492 |
TRG_ER_diArg_1 | 771 | 773 | PF00400 | 0.375 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.474 |
TRG_Pf-PMV_PEXEL_1 | 869 | 874 | PF00026 | 0.444 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HU57 | Leptomonas seymouri | 54% | 97% |
A0A3Q8IDQ4 | Leishmania donovani | 95% | 100% |
A0A3R7NI16 | Trypanosoma rangeli | 40% | 100% |
A0A422NMS5 | Trypanosoma rangeli | 29% | 100% |
A4HEU1 | Leishmania braziliensis | 80% | 97% |
A4I216 | Leishmania infantum | 95% | 100% |
C9ZRZ3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AY64 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |