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: 1, no: 10 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4H6I3
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:0006412 | translation | 4 | 1 |
GO:0006518 | peptide metabolic process | 4 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 1 |
GO:0043043 | peptide biosynthetic process | 5 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043603 | amide metabolic process | 3 | 1 |
GO:0043604 | amide biosynthetic process | 4 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0003729 | mRNA binding | 5 | 1 |
GO:0003735 | structural constituent of ribosome | 2 | 1 |
GO:0005198 | structural molecule activity | 1 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 1008 | 1012 | PF00656 | 0.478 |
CLV_C14_Caspase3-7 | 33 | 37 | PF00656 | 0.619 |
CLV_C14_Caspase3-7 | 830 | 834 | PF00656 | 0.596 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.289 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.731 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.373 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.463 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.380 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.738 |
CLV_NRD_NRD_1 | 567 | 569 | PF00675 | 0.302 |
CLV_NRD_NRD_1 | 645 | 647 | PF00675 | 0.311 |
CLV_NRD_NRD_1 | 655 | 657 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 695 | 697 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 788 | 790 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 886 | 888 | PF00675 | 0.708 |
CLV_NRD_NRD_1 | 939 | 941 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 942 | 944 | PF00675 | 0.644 |
CLV_PCSK_FUR_1 | 940 | 944 | PF00082 | 0.671 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.708 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.719 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 417 | 419 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 487 | 489 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 567 | 569 | PF00082 | 0.302 |
CLV_PCSK_KEX2_1 | 633 | 635 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 655 | 657 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 695 | 697 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 788 | 790 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 854 | 856 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 886 | 888 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 941 | 943 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 983 | 985 | PF00082 | 0.680 |
CLV_PCSK_PC1ET2_1 | 20 | 22 | PF00082 | 0.726 |
CLV_PCSK_PC1ET2_1 | 3 | 5 | PF00082 | 0.656 |
CLV_PCSK_PC1ET2_1 | 633 | 635 | PF00082 | 0.347 |
CLV_PCSK_PC1ET2_1 | 854 | 856 | PF00082 | 0.568 |
CLV_PCSK_PC1ET2_1 | 941 | 943 | PF00082 | 0.615 |
CLV_PCSK_PC1ET2_1 | 983 | 985 | PF00082 | 0.704 |
CLV_PCSK_PC7_1 | 21 | 27 | PF00082 | 0.765 |
CLV_PCSK_PC7_1 | 651 | 657 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.652 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 567 | 571 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 857 | 861 | PF00082 | 0.543 |
CLV_Separin_Metazoa | 597 | 601 | PF03568 | 0.437 |
CLV_Separin_Metazoa | 764 | 768 | PF03568 | 0.420 |
DEG_APCC_DBOX_1 | 566 | 574 | PF00400 | 0.427 |
DEG_APCC_DBOX_1 | 650 | 658 | PF00400 | 0.318 |
DEG_COP1_1 | 370 | 377 | PF00400 | 0.568 |
DEG_SPOP_SBC_1 | 368 | 372 | PF00917 | 0.424 |
DEG_SPOP_SBC_1 | 951 | 955 | PF00917 | 0.482 |
DOC_AGCK_PIF_1 | 387 | 392 | PF00069 | 0.348 |
DOC_ANK_TNKS_1 | 581 | 588 | PF00023 | 0.405 |
DOC_CKS1_1 | 173 | 178 | PF01111 | 0.423 |
DOC_CYCLIN_RxL_1 | 362 | 373 | PF00134 | 0.468 |
DOC_CYCLIN_RxL_1 | 883 | 894 | PF00134 | 0.714 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 431 | 440 | PF00134 | 0.443 |
DOC_CYCLIN_yCln2_LP_2 | 105 | 111 | PF00134 | 0.423 |
DOC_MAPK_FxFP_2 | 672 | 675 | PF00069 | 0.389 |
DOC_MAPK_gen_1 | 485 | 493 | PF00069 | 0.429 |
DOC_MAPK_gen_1 | 497 | 504 | PF00069 | 0.409 |
DOC_MAPK_gen_1 | 522 | 531 | PF00069 | 0.423 |
DOC_MAPK_gen_1 | 633 | 641 | PF00069 | 0.333 |
DOC_MAPK_gen_1 | 854 | 861 | PF00069 | 0.527 |
DOC_MAPK_JIP1_4 | 855 | 861 | PF00069 | 0.433 |
DOC_MAPK_MEF2A_6 | 138 | 146 | PF00069 | 0.197 |
DOC_MAPK_MEF2A_6 | 320 | 329 | PF00069 | 0.443 |
DOC_MAPK_MEF2A_6 | 549 | 557 | PF00069 | 0.387 |
DOC_PP2B_LxvP_1 | 105 | 108 | PF13499 | 0.423 |
DOC_PP4_FxxP_1 | 1032 | 1035 | PF00568 | 0.476 |
DOC_PP4_FxxP_1 | 672 | 675 | PF00568 | 0.389 |
DOC_USP7_MATH_1 | 1005 | 1009 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 1021 | 1025 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 1037 | 1041 | PF00917 | 0.777 |
DOC_USP7_MATH_1 | 177 | 181 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.302 |
DOC_USP7_MATH_1 | 537 | 541 | PF00917 | 0.302 |
DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.384 |
DOC_USP7_MATH_1 | 777 | 781 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 947 | 951 | PF00917 | 0.676 |
DOC_USP7_UBL2_3 | 287 | 291 | PF12436 | 0.482 |
DOC_USP7_UBL2_3 | 3 | 7 | PF12436 | 0.662 |
DOC_USP7_UBL2_3 | 335 | 339 | PF12436 | 0.539 |
DOC_USP7_UBL2_3 | 497 | 501 | PF12436 | 0.197 |
DOC_WW_Pin1_4 | 1017 | 1022 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.423 |
DOC_WW_Pin1_4 | 674 | 679 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 741 | 746 | PF00397 | 0.423 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 976 | 981 | PF00397 | 0.711 |
LIG_14-3-3_CanoR_1 | 1013 | 1019 | PF00244 | 0.733 |
LIG_14-3-3_CanoR_1 | 201 | 206 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 25 | 32 | PF00244 | 0.701 |
LIG_14-3-3_CanoR_1 | 279 | 285 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 512 | 520 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 6 | 15 | PF00244 | 0.760 |
LIG_14-3-3_CanoR_1 | 778 | 782 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 901 | 909 | PF00244 | 0.737 |
LIG_14-3-3_CanoR_1 | 99 | 108 | PF00244 | 0.472 |
LIG_Actin_WH2_1 | 487 | 502 | PF00022 | 0.449 |
LIG_Actin_WH2_2 | 486 | 502 | PF00022 | 0.340 |
LIG_Actin_WH2_2 | 784 | 800 | PF00022 | 0.527 |
LIG_APCC_ABBA_1 | 214 | 219 | PF00400 | 0.449 |
LIG_BIR_III_2 | 1011 | 1015 | PF00653 | 0.697 |
LIG_BIR_III_4 | 718 | 722 | PF00653 | 0.197 |
LIG_BRCT_BRCA1_1 | 383 | 387 | PF00533 | 0.656 |
LIG_FHA_1 | 1002 | 1008 | PF00498 | 0.571 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.312 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.381 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.409 |
LIG_FHA_1 | 512 | 518 | PF00498 | 0.425 |
LIG_FHA_1 | 659 | 665 | PF00498 | 0.356 |
LIG_FHA_1 | 760 | 766 | PF00498 | 0.310 |
LIG_FHA_1 | 929 | 935 | PF00498 | 0.675 |
LIG_FHA_1 | 952 | 958 | PF00498 | 0.493 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.423 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.491 |
LIG_FHA_2 | 353 | 359 | PF00498 | 0.540 |
LIG_FHA_2 | 401 | 407 | PF00498 | 0.260 |
LIG_FHA_2 | 477 | 483 | PF00498 | 0.387 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.707 |
LIG_FHA_2 | 969 | 975 | PF00498 | 0.521 |
LIG_Integrin_isoDGR_2 | 899 | 901 | PF01839 | 0.746 |
LIG_LIR_Gen_1 | 298 | 309 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 384 | 392 | PF02991 | 0.580 |
LIG_LIR_Gen_1 | 403 | 412 | PF02991 | 0.197 |
LIG_LIR_Gen_1 | 528 | 539 | PF02991 | 0.321 |
LIG_LIR_Gen_1 | 662 | 672 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 1016 | 1022 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 192 | 198 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 298 | 304 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 358 | 363 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 384 | 390 | PF02991 | 0.639 |
LIG_LIR_Nem_3 | 403 | 408 | PF02991 | 0.218 |
LIG_LIR_Nem_3 | 528 | 534 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 550 | 555 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 662 | 668 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 689 | 694 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 811 | 816 | PF02991 | 0.371 |
LIG_LYPXL_yS_3 | 360 | 363 | PF13949 | 0.540 |
LIG_LYPXL_yS_3 | 691 | 694 | PF13949 | 0.387 |
LIG_MYND_1 | 773 | 777 | PF01753 | 0.318 |
LIG_PDZ_Class_2 | 1067 | 1072 | PF00595 | 0.615 |
LIG_REV1ctd_RIR_1 | 669 | 674 | PF16727 | 0.318 |
LIG_SH2_CRK | 1019 | 1023 | PF00017 | 0.481 |
LIG_SH2_CRK | 665 | 669 | PF00017 | 0.217 |
LIG_SH2_GRB2like | 840 | 843 | PF00017 | 0.285 |
LIG_SH2_NCK_1 | 383 | 387 | PF00017 | 0.656 |
LIG_SH2_SRC | 217 | 220 | PF00017 | 0.449 |
LIG_SH2_STAP1 | 217 | 221 | PF00017 | 0.423 |
LIG_SH2_STAP1 | 23 | 27 | PF00017 | 0.765 |
LIG_SH2_STAP1 | 383 | 387 | PF00017 | 0.656 |
LIG_SH2_STAP1 | 405 | 409 | PF00017 | 0.379 |
LIG_SH2_STAP1 | 914 | 918 | PF00017 | 0.519 |
LIG_SH2_STAT3 | 489 | 492 | PF00017 | 0.423 |
LIG_SH2_STAT3 | 731 | 734 | PF00017 | 0.197 |
LIG_SH2_STAT3 | 840 | 843 | PF00017 | 0.538 |
LIG_SH2_STAT3 | 914 | 917 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.742 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 604 | 607 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 701 | 704 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 731 | 734 | PF00017 | 0.197 |
LIG_SH2_STAT5 | 840 | 843 | PF00017 | 0.505 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.458 |
LIG_SH3_3 | 566 | 572 | PF00018 | 0.302 |
LIG_SH3_3 | 574 | 580 | PF00018 | 0.352 |
LIG_SH3_3 | 672 | 678 | PF00018 | 0.484 |
LIG_SH3_3 | 858 | 864 | PF00018 | 0.380 |
LIG_SH3_4 | 287 | 294 | PF00018 | 0.568 |
LIG_SUMO_SIM_anti_2 | 637 | 643 | PF11976 | 0.197 |
LIG_SUMO_SIM_anti_2 | 761 | 767 | PF11976 | 0.340 |
LIG_SUMO_SIM_par_1 | 696 | 702 | PF11976 | 0.407 |
LIG_TRAF2_1 | 548 | 551 | PF00917 | 0.318 |
LIG_TRAF2_1 | 79 | 82 | PF00917 | 0.704 |
LIG_TRAF2_1 | 93 | 96 | PF00917 | 0.541 |
LIG_TRFH_1 | 90 | 94 | PF08558 | 0.606 |
LIG_UBA3_1 | 516 | 525 | PF00899 | 0.449 |
LIG_UBA3_1 | 956 | 961 | PF00899 | 0.507 |
LIG_WRC_WIRS_1 | 472 | 477 | PF05994 | 0.423 |
MOD_CDK_SPxxK_3 | 976 | 983 | PF00069 | 0.725 |
MOD_CK1_1 | 1024 | 1030 | PF00069 | 0.715 |
MOD_CK1_1 | 1040 | 1046 | PF00069 | 0.711 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.342 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.401 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.702 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.753 |
MOD_CK1_1 | 540 | 546 | PF00069 | 0.302 |
MOD_CK1_1 | 869 | 875 | PF00069 | 0.708 |
MOD_CK1_1 | 950 | 956 | PF00069 | 0.563 |
MOD_CK1_1 | 979 | 985 | PF00069 | 0.694 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.389 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.413 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.393 |
MOD_CK2_1 | 352 | 358 | PF00069 | 0.534 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.728 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.696 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.463 |
MOD_CK2_1 | 968 | 974 | PF00069 | 0.771 |
MOD_Cter_Amidation | 18 | 21 | PF01082 | 0.760 |
MOD_Cter_Amidation | 392 | 395 | PF01082 | 0.420 |
MOD_Cter_Amidation | 565 | 568 | PF01082 | 0.302 |
MOD_GlcNHglycan | 1008 | 1011 | PF01048 | 0.699 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.449 |
MOD_GlcNHglycan | 1035 | 1038 | PF01048 | 0.705 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.197 |
MOD_GlcNHglycan | 236 | 241 | PF01048 | 0.464 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.240 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.580 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.389 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.362 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.687 |
MOD_GlcNHglycan | 618 | 621 | PF01048 | 0.404 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.725 |
MOD_GlcNHglycan | 803 | 806 | PF01048 | 0.437 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.554 |
MOD_GlcNHglycan | 868 | 871 | PF01048 | 0.711 |
MOD_GlcNHglycan | 881 | 884 | PF01048 | 0.710 |
MOD_GlcNHglycan | 949 | 952 | PF01048 | 0.685 |
MOD_GSK3_1 | 1001 | 1008 | PF00069 | 0.669 |
MOD_GSK3_1 | 1013 | 1020 | PF00069 | 0.652 |
MOD_GSK3_1 | 1033 | 1040 | PF00069 | 0.711 |
MOD_GSK3_1 | 1058 | 1065 | PF00069 | 0.655 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.449 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.701 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.395 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.761 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.337 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.578 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.615 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.401 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.663 |
MOD_GSK3_1 | 750 | 757 | PF00069 | 0.383 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.581 |
MOD_GSK3_1 | 947 | 954 | PF00069 | 0.637 |
MOD_GSK3_1 | 965 | 972 | PF00069 | 0.611 |
MOD_N-GLC_1 | 1037 | 1042 | PF02516 | 0.515 |
MOD_N-GLC_1 | 49 | 54 | PF02516 | 0.488 |
MOD_N-GLC_1 | 505 | 510 | PF02516 | 0.302 |
MOD_N-GLC_1 | 682 | 687 | PF02516 | 0.381 |
MOD_N-GLC_1 | 951 | 956 | PF02516 | 0.682 |
MOD_N-GLC_1 | 968 | 973 | PF02516 | 0.778 |
MOD_N-GLC_2 | 621 | 623 | PF02516 | 0.197 |
MOD_N-GLC_2 | 842 | 844 | PF02516 | 0.287 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.415 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.472 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.475 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.538 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.468 |
MOD_NEK2_1 | 476 | 481 | PF00069 | 0.341 |
MOD_NEK2_1 | 660 | 665 | PF00069 | 0.387 |
MOD_NEK2_1 | 681 | 686 | PF00069 | 0.302 |
MOD_NEK2_1 | 699 | 704 | PF00069 | 0.302 |
MOD_NEK2_1 | 821 | 826 | PF00069 | 0.458 |
MOD_NEK2_1 | 916 | 921 | PF00069 | 0.588 |
MOD_NEK2_2 | 1014 | 1019 | PF00069 | 0.480 |
MOD_NEK2_2 | 412 | 417 | PF00069 | 0.410 |
MOD_NEK2_2 | 471 | 476 | PF00069 | 0.423 |
MOD_NEK2_2 | 537 | 542 | PF00069 | 0.318 |
MOD_NEK2_2 | 930 | 935 | PF00069 | 0.443 |
MOD_PIKK_1 | 1037 | 1043 | PF00454 | 0.730 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.449 |
MOD_PIKK_1 | 186 | 192 | PF00454 | 0.423 |
MOD_PIKK_1 | 61 | 67 | PF00454 | 0.741 |
MOD_PIKK_1 | 743 | 749 | PF00454 | 0.397 |
MOD_PIKK_1 | 902 | 908 | PF00454 | 0.737 |
MOD_PIKK_1 | 963 | 969 | PF00454 | 0.759 |
MOD_PK_1 | 314 | 320 | PF00069 | 0.411 |
MOD_PKA_1 | 201 | 207 | PF00069 | 0.337 |
MOD_PKA_1 | 21 | 27 | PF00069 | 0.765 |
MOD_PKA_1 | 6 | 12 | PF00069 | 0.764 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.423 |
MOD_PKA_2 | 25 | 31 | PF00069 | 0.659 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.314 |
MOD_PKA_2 | 511 | 517 | PF00069 | 0.449 |
MOD_PKA_2 | 777 | 783 | PF00069 | 0.511 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.501 |
MOD_PKB_1 | 4 | 12 | PF00069 | 0.728 |
MOD_Plk_1 | 236 | 242 | PF00069 | 0.425 |
MOD_Plk_1 | 297 | 303 | PF00069 | 0.544 |
MOD_Plk_1 | 39 | 45 | PF00069 | 0.484 |
MOD_Plk_1 | 681 | 687 | PF00069 | 0.417 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.557 |
MOD_Plk_1 | 951 | 957 | PF00069 | 0.599 |
MOD_Plk_4 | 1014 | 1020 | PF00069 | 0.625 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.474 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.395 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.302 |
MOD_Plk_4 | 660 | 666 | PF00069 | 0.361 |
MOD_Plk_4 | 808 | 814 | PF00069 | 0.480 |
MOD_Plk_4 | 821 | 827 | PF00069 | 0.388 |
MOD_Plk_4 | 952 | 958 | PF00069 | 0.493 |
MOD_ProDKin_1 | 1017 | 1023 | PF00069 | 0.710 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.423 |
MOD_ProDKin_1 | 674 | 680 | PF00069 | 0.496 |
MOD_ProDKin_1 | 741 | 747 | PF00069 | 0.423 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.589 |
MOD_ProDKin_1 | 976 | 982 | PF00069 | 0.710 |
MOD_SUMO_for_1 | 548 | 551 | PF00179 | 0.359 |
MOD_SUMO_for_1 | 960 | 963 | PF00179 | 0.513 |
MOD_SUMO_rev_2 | 227 | 233 | PF00179 | 0.410 |
MOD_SUMO_rev_2 | 415 | 423 | PF00179 | 0.431 |
MOD_SUMO_rev_2 | 482 | 486 | PF00179 | 0.387 |
MOD_SUMO_rev_2 | 790 | 797 | PF00179 | 0.548 |
TRG_DiLeu_BaEn_1 | 169 | 174 | PF01217 | 0.387 |
TRG_DiLeu_BaEn_1 | 237 | 242 | PF01217 | 0.388 |
TRG_DiLeu_BaEn_1 | 761 | 766 | PF01217 | 0.423 |
TRG_DiLeu_BaEn_4 | 550 | 556 | PF01217 | 0.318 |
TRG_DiLeu_BaLyEn_6 | 101 | 106 | PF01217 | 0.548 |
TRG_DiLeu_BaLyEn_6 | 247 | 252 | PF01217 | 0.364 |
TRG_DiLeu_BaLyEn_6 | 362 | 367 | PF01217 | 0.555 |
TRG_ENDOCYTIC_2 | 1019 | 1022 | PF00928 | 0.485 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 383 | 386 | PF00928 | 0.655 |
TRG_ENDOCYTIC_2 | 405 | 408 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 665 | 668 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 691 | 694 | PF00928 | 0.302 |
TRG_ER_diArg_1 | 159 | 161 | PF00400 | 0.290 |
TRG_ER_diArg_1 | 266 | 269 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 304 | 306 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 416 | 418 | PF00400 | 0.403 |
TRG_ER_diArg_1 | 447 | 450 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 486 | 488 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 567 | 569 | PF00400 | 0.302 |
TRG_ER_diArg_1 | 654 | 656 | PF00400 | 0.307 |
TRG_ER_diArg_1 | 694 | 696 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 787 | 789 | PF00400 | 0.416 |
TRG_ER_diArg_1 | 855 | 858 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 885 | 887 | PF00400 | 0.755 |
TRG_ER_diArg_1 | 940 | 943 | PF00400 | 0.638 |
TRG_NES_CRM1_1 | 754 | 769 | PF08389 | 0.423 |
TRG_NLS_Bipartite_1 | 3 | 24 | PF00514 | 0.745 |
TRG_NLS_MonoCore_2 | 853 | 858 | PF00514 | 0.527 |
TRG_NLS_MonoExtC_3 | 2 | 7 | PF00514 | 0.654 |
TRG_NLS_MonoExtC_3 | 940 | 946 | PF00514 | 0.671 |
TRG_NLS_MonoExtC_3 | 982 | 988 | PF00514 | 0.507 |
TRG_NLS_MonoExtN_4 | 2 | 7 | PF00514 | 0.654 |
TRG_NLS_MonoExtN_4 | 287 | 293 | PF00514 | 0.483 |
TRG_NLS_MonoExtN_4 | 940 | 945 | PF00514 | 0.636 |
TRG_NLS_MonoExtN_4 | 980 | 987 | PF00514 | 0.594 |
TRG_Pf-PMV_PEXEL_1 | 268 | 272 | PF00026 | 0.389 |
TRG_Pf-PMV_PEXEL_1 | 294 | 298 | PF00026 | 0.605 |
TRG_Pf-PMV_PEXEL_1 | 449 | 454 | PF00026 | 0.318 |
TRG_Pf-PMV_PEXEL_1 | 886 | 891 | PF00026 | 0.677 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4M8 | Leptomonas seymouri | 68% | 84% |
A0A0S4J4V2 | Bodo saltans | 35% | 72% |
A0A1X0NVJ9 | Trypanosomatidae | 51% | 100% |
A0A3S5H6I7 | Leishmania donovani | 83% | 99% |
A0A422MV81 | Trypanosoma rangeli | 50% | 100% |
A4HUW1 | Leishmania infantum | 82% | 99% |
D0A7I8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9ANK2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 99% |
O31489 | Bacillus subtilis (strain 168) | 29% | 100% |
P46837 | Escherichia coli (strain K12) | 32% | 100% |
P71353 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 31% | 100% |
Q45388 | Bordetella pertussis (strain Tohama I / ATCC BAA-589 / NCTC 13251) | 33% | 100% |
Q497V5 | Mus musculus | 27% | 100% |
Q4QH24 | Leishmania major | 82% | 100% |
Q5RDI0 | Pongo abelii | 27% | 100% |
Q8N5C6 | Homo sapiens | 26% | 100% |
V5C139 | Trypanosoma cruzi | 49% | 100% |