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. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032991 | protein-containing complex | 1 | 11 |
GO:1990904 | ribonucleoprotein complex | 2 | 11 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005681 | spliceosomal complex | 3 | 1 |
GO:0005684 | U2-type spliceosomal complex | 4 | 1 |
GO:0030532 | small nuclear ribonucleoprotein complex | 3 | 1 |
GO:0046540 | U4/U6 x U5 tri-snRNP complex | 6 | 1 |
GO:0071007 | U2-type catalytic step 2 spliceosome | 4 | 1 |
GO:0071013 | catalytic step 2 spliceosome | 3 | 1 |
GO:0097525 | spliceosomal snRNP complex | 4 | 1 |
GO:0097526 | spliceosomal tri-snRNP complex | 5 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0120114 | Sm-like protein family complex | 2 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8IFJ7
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 1 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 1 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008380 | RNA splicing | 7 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0003924 | GTPase activity | 7 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005525 | GTP binding | 5 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 12 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 12 |
GO:0019001 | guanyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032561 | guanyl 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:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0017069 | snRNA binding | 5 | 1 |
GO:0030623 | U5 snRNA binding | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 15 | 19 | PF00656 | 0.592 |
CLV_C14_Caspase3-7 | 439 | 443 | PF00656 | 0.334 |
CLV_C14_Caspase3-7 | 56 | 60 | PF00656 | 0.634 |
CLV_C14_Caspase3-7 | 728 | 732 | PF00656 | 0.474 |
CLV_C14_Caspase3-7 | 793 | 797 | PF00656 | 0.408 |
CLV_C14_Caspase3-7 | 868 | 872 | PF00656 | 0.507 |
CLV_NRD_NRD_1 | 1005 | 1007 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.683 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.208 |
CLV_NRD_NRD_1 | 779 | 781 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 787 | 789 | PF00675 | 0.233 |
CLV_NRD_NRD_1 | 919 | 921 | PF00675 | 0.208 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.614 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 787 | 789 | PF00082 | 0.267 |
CLV_PCSK_KEX2_1 | 919 | 921 | PF00082 | 0.208 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.638 |
CLV_PCSK_PC1ET2_1 | 186 | 188 | PF00082 | 0.312 |
CLV_PCSK_PC7_1 | 182 | 188 | PF00082 | 0.223 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 755 | 759 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 859 | 863 | PF00082 | 0.219 |
CLV_PCSK_SKI1_1 | 879 | 883 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 954 | 958 | PF00082 | 0.250 |
CLV_Separin_Metazoa | 851 | 855 | PF03568 | 0.459 |
DEG_APCC_DBOX_1 | 418 | 426 | PF00400 | 0.509 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.606 |
DEG_SPOP_SBC_1 | 524 | 528 | PF00917 | 0.382 |
DOC_CKS1_1 | 221 | 226 | PF01111 | 0.432 |
DOC_CYCLIN_yCln2_LP_2 | 893 | 899 | PF00134 | 0.416 |
DOC_MAPK_gen_1 | 278 | 288 | PF00069 | 0.402 |
DOC_MAPK_gen_1 | 295 | 301 | PF00069 | 0.439 |
DOC_MAPK_gen_1 | 381 | 389 | PF00069 | 0.301 |
DOC_MAPK_MEF2A_6 | 171 | 179 | PF00069 | 0.450 |
DOC_MAPK_MEF2A_6 | 278 | 286 | PF00069 | 0.420 |
DOC_MAPK_MEF2A_6 | 490 | 498 | PF00069 | 0.389 |
DOC_MAPK_MEF2A_6 | 674 | 681 | PF00069 | 0.512 |
DOC_MAPK_MEF2A_6 | 707 | 716 | PF00069 | 0.606 |
DOC_PP1_RVXF_1 | 545 | 552 | PF00149 | 0.506 |
DOC_PP1_RVXF_1 | 639 | 646 | PF00149 | 0.421 |
DOC_PP1_RVXF_1 | 857 | 863 | PF00149 | 0.419 |
DOC_PP1_RVXF_1 | 96 | 103 | PF00149 | 0.598 |
DOC_PP2B_LxvP_1 | 448 | 451 | PF13499 | 0.485 |
DOC_PP2B_LxvP_1 | 903 | 906 | PF13499 | 0.415 |
DOC_PP2B_PxIxI_1 | 810 | 816 | PF00149 | 0.475 |
DOC_PP4_FxxP_1 | 645 | 648 | PF00568 | 0.454 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.383 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.311 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 524 | 528 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 596 | 600 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 660 | 664 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 834 | 838 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 943 | 947 | PF00917 | 0.419 |
DOC_USP7_UBL2_3 | 371 | 375 | PF12436 | 0.501 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.419 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 673 | 678 | PF00397 | 0.408 |
LIG_14-3-3_CanoR_1 | 216 | 221 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 419 | 429 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 516 | 522 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 583 | 591 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 742 | 747 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 755 | 763 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 767 | 776 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 780 | 786 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 833 | 843 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 883 | 887 | PF00244 | 0.314 |
LIG_14-3-3_CanoR_1 | 954 | 962 | PF00244 | 0.408 |
LIG_Actin_WH2_2 | 410 | 428 | PF00022 | 0.318 |
LIG_Actin_WH2_2 | 812 | 830 | PF00022 | 0.512 |
LIG_AP2alpha_2 | 976 | 978 | PF02296 | 0.419 |
LIG_APCC_ABBA_1 | 679 | 684 | PF00400 | 0.512 |
LIG_BIR_III_2 | 557 | 561 | PF00653 | 0.393 |
LIG_BIR_III_4 | 49 | 53 | PF00653 | 0.608 |
LIG_BIR_III_4 | 731 | 735 | PF00653 | 0.510 |
LIG_BRCT_BRCA1_1 | 641 | 645 | PF00533 | 0.414 |
LIG_BRCT_BRCA1_1 | 718 | 722 | PF00533 | 0.341 |
LIG_BRCT_BRCA1_1 | 744 | 748 | PF00533 | 0.450 |
LIG_Clathr_ClatBox_1 | 126 | 130 | PF01394 | 0.522 |
LIG_Clathr_ClatBox_1 | 244 | 248 | PF01394 | 0.432 |
LIG_Clathr_ClatBox_1 | 548 | 552 | PF01394 | 0.361 |
LIG_eIF4E_1 | 763 | 769 | PF01652 | 0.407 |
LIG_EVH1_1 | 448 | 452 | PF00568 | 0.368 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.408 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.464 |
LIG_FHA_1 | 756 | 762 | PF00498 | 0.353 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.645 |
LIG_FHA_1 | 930 | 936 | PF00498 | 0.419 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.386 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.475 |
LIG_FHA_2 | 275 | 281 | PF00498 | 0.408 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.550 |
LIG_FHA_2 | 571 | 577 | PF00498 | 0.467 |
LIG_FHA_2 | 722 | 728 | PF00498 | 0.329 |
LIG_FHA_2 | 769 | 775 | PF00498 | 0.607 |
LIG_FHA_2 | 816 | 822 | PF00498 | 0.419 |
LIG_LIR_Apic_2 | 631 | 637 | PF02991 | 0.417 |
LIG_LIR_Apic_2 | 642 | 648 | PF02991 | 0.222 |
LIG_LIR_Gen_1 | 144 | 155 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 313 | 322 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 385 | 394 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 719 | 729 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 762 | 769 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 789 | 800 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.683 |
LIG_LIR_Nem_3 | 292 | 297 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 313 | 318 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 361 | 367 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 373 | 377 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 385 | 389 | PF02991 | 0.187 |
LIG_LIR_Nem_3 | 392 | 398 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 559 | 564 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 575 | 581 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 692 | 697 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 719 | 725 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 762 | 766 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 789 | 795 | PF02991 | 0.512 |
LIG_LYPXL_S_1 | 350 | 354 | PF13949 | 0.333 |
LIG_LYPXL_yS_3 | 351 | 354 | PF13949 | 0.359 |
LIG_NRBOX | 173 | 179 | PF00104 | 0.434 |
LIG_NRBOX | 668 | 674 | PF00104 | 0.475 |
LIG_PDZ_Class_1 | 1012 | 1017 | PF00595 | 0.564 |
LIG_SH2_CRK | 294 | 298 | PF00017 | 0.408 |
LIG_SH2_CRK | 347 | 351 | PF00017 | 0.310 |
LIG_SH2_CRK | 395 | 399 | PF00017 | 0.303 |
LIG_SH2_NCK_1 | 347 | 351 | PF00017 | 0.449 |
LIG_SH2_SRC | 147 | 150 | PF00017 | 0.460 |
LIG_SH2_STAP1 | 315 | 319 | PF00017 | 0.454 |
LIG_SH2_STAP1 | 347 | 351 | PF00017 | 0.337 |
LIG_SH2_STAP1 | 562 | 566 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 431 | 434 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 570 | 573 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 689 | 692 | PF00017 | 0.512 |
LIG_SH3_2 | 449 | 454 | PF14604 | 0.371 |
LIG_SH3_2 | 986 | 991 | PF14604 | 0.396 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.393 |
LIG_SH3_3 | 387 | 393 | PF00018 | 0.310 |
LIG_SH3_3 | 415 | 421 | PF00018 | 0.415 |
LIG_SH3_3 | 446 | 452 | PF00018 | 0.485 |
LIG_SH3_3 | 619 | 625 | PF00018 | 0.469 |
LIG_SH3_3 | 653 | 659 | PF00018 | 0.534 |
LIG_SH3_3 | 709 | 715 | PF00018 | 0.417 |
LIG_SH3_3 | 773 | 779 | PF00018 | 0.396 |
LIG_SH3_3 | 971 | 977 | PF00018 | 0.408 |
LIG_SH3_3 | 983 | 989 | PF00018 | 0.388 |
LIG_Sin3_3 | 937 | 944 | PF02671 | 0.454 |
LIG_SUMO_SIM_anti_2 | 122 | 130 | PF11976 | 0.567 |
LIG_SUMO_SIM_anti_2 | 172 | 179 | PF11976 | 0.464 |
LIG_SUMO_SIM_anti_2 | 601 | 607 | PF11976 | 0.345 |
LIG_SUMO_SIM_anti_2 | 67 | 74 | PF11976 | 0.568 |
LIG_SUMO_SIM_par_1 | 122 | 130 | PF11976 | 0.544 |
LIG_SUMO_SIM_par_1 | 271 | 277 | PF11976 | 0.419 |
LIG_SUMO_SIM_par_1 | 492 | 500 | PF11976 | 0.460 |
LIG_TRAF2_1 | 31 | 34 | PF00917 | 0.751 |
LIG_TRFH_1 | 389 | 393 | PF08558 | 0.334 |
LIG_TYR_ITIM | 761 | 766 | PF00017 | 0.394 |
LIG_UBA3_1 | 282 | 287 | PF00899 | 0.438 |
LIG_WRC_WIRS_1 | 315 | 320 | PF05994 | 0.480 |
LIG_WRC_WIRS_1 | 340 | 345 | PF05994 | 0.370 |
LIG_WRC_WIRS_1 | 722 | 727 | PF05994 | 0.279 |
LIG_WRC_WIRS_1 | 944 | 949 | PF05994 | 0.408 |
MOD_CDC14_SPxK_1 | 321 | 324 | PF00782 | 0.512 |
MOD_CDK_SPxK_1 | 318 | 324 | PF00069 | 0.512 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.465 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.450 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.348 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.638 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.517 |
MOD_CK1_1 | 527 | 533 | PF00069 | 0.514 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.627 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.549 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.556 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.695 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.605 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.693 |
MOD_CK2_1 | 721 | 727 | PF00069 | 0.304 |
MOD_CK2_1 | 815 | 821 | PF00069 | 0.419 |
MOD_Cter_Amidation | 18 | 21 | PF01082 | 0.539 |
MOD_Cter_Amidation | 95 | 98 | PF01082 | 0.620 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.672 |
MOD_GlcNHglycan | 140 | 144 | PF01048 | 0.637 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.715 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.279 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.405 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.637 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.516 |
MOD_GlcNHglycan | 536 | 539 | PF01048 | 0.602 |
MOD_GlcNHglycan | 598 | 601 | PF01048 | 0.532 |
MOD_GlcNHglycan | 691 | 694 | PF01048 | 0.275 |
MOD_GlcNHglycan | 749 | 752 | PF01048 | 0.441 |
MOD_GlcNHglycan | 836 | 839 | PF01048 | 0.222 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.723 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.414 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.450 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.666 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.437 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.425 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.647 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.390 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.410 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.601 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.565 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.390 |
MOD_GSK3_1 | 683 | 690 | PF00069 | 0.408 |
MOD_GSK3_1 | 721 | 728 | PF00069 | 0.303 |
MOD_GSK3_1 | 736 | 743 | PF00069 | 0.372 |
MOD_GSK3_1 | 805 | 812 | PF00069 | 0.414 |
MOD_GSK3_1 | 834 | 841 | PF00069 | 0.417 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.682 |
MOD_GSK3_1 | 873 | 880 | PF00069 | 0.355 |
MOD_N-GLC_1 | 524 | 529 | PF02516 | 0.646 |
MOD_N-GLC_1 | 9 | 14 | PF02516 | 0.648 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.480 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.415 |
MOD_NEK2_1 | 672 | 677 | PF00069 | 0.411 |
MOD_NEK2_1 | 725 | 730 | PF00069 | 0.319 |
MOD_NEK2_1 | 736 | 741 | PF00069 | 0.378 |
MOD_NEK2_1 | 839 | 844 | PF00069 | 0.512 |
MOD_NEK2_1 | 882 | 887 | PF00069 | 0.428 |
MOD_NEK2_1 | 978 | 983 | PF00069 | 0.487 |
MOD_NEK2_2 | 586 | 591 | PF00069 | 0.463 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.546 |
MOD_PIKK_1 | 141 | 147 | PF00454 | 0.600 |
MOD_PIKK_1 | 452 | 458 | PF00454 | 0.366 |
MOD_PIKK_1 | 716 | 722 | PF00454 | 0.365 |
MOD_PIKK_1 | 755 | 761 | PF00454 | 0.446 |
MOD_PIKK_1 | 76 | 82 | PF00454 | 0.694 |
MOD_PIKK_1 | 948 | 954 | PF00454 | 0.408 |
MOD_PK_1 | 661 | 667 | PF00069 | 0.454 |
MOD_PK_1 | 742 | 748 | PF00069 | 0.469 |
MOD_PK_1 | 809 | 815 | PF00069 | 0.442 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.641 |
MOD_PKA_2 | 323 | 329 | PF00069 | 0.512 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.729 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.386 |
MOD_PKA_2 | 515 | 521 | PF00069 | 0.385 |
MOD_PKA_2 | 582 | 588 | PF00069 | 0.453 |
MOD_PKA_2 | 839 | 845 | PF00069 | 0.497 |
MOD_PKA_2 | 882 | 888 | PF00069 | 0.327 |
MOD_Plk_1 | 193 | 199 | PF00069 | 0.419 |
MOD_Plk_1 | 687 | 693 | PF00069 | 0.408 |
MOD_Plk_1 | 815 | 821 | PF00069 | 0.415 |
MOD_Plk_1 | 978 | 984 | PF00069 | 0.486 |
MOD_Plk_2-3 | 553 | 559 | PF00069 | 0.432 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.408 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.433 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.291 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.415 |
MOD_Plk_4 | 586 | 592 | PF00069 | 0.462 |
MOD_Plk_4 | 809 | 815 | PF00069 | 0.411 |
MOD_Plk_4 | 882 | 888 | PF00069 | 0.374 |
MOD_Plk_4 | 930 | 936 | PF00069 | 0.481 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.413 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.419 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.491 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.473 |
MOD_ProDKin_1 | 673 | 679 | PF00069 | 0.408 |
MOD_SUMO_rev_2 | 280 | 289 | PF00179 | 0.419 |
MOD_SUMO_rev_2 | 370 | 377 | PF00179 | 0.415 |
MOD_SUMO_rev_2 | 500 | 510 | PF00179 | 0.416 |
TRG_DiLeu_BaEn_1 | 105 | 110 | PF01217 | 0.680 |
TRG_DiLeu_BaLyEn_6 | 256 | 261 | PF01217 | 0.432 |
TRG_DiLeu_BaLyEn_6 | 544 | 549 | PF01217 | 0.540 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.460 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 315 | 318 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 347 | 350 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 395 | 398 | PF00928 | 0.294 |
TRG_ENDOCYTIC_2 | 561 | 564 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 763 | 766 | PF00928 | 0.411 |
TRG_ER_diArg_1 | 380 | 383 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 544 | 547 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 786 | 788 | PF00400 | 0.465 |
TRG_ER_diArg_1 | 890 | 893 | PF00400 | 0.438 |
TRG_ER_diArg_1 | 935 | 938 | PF00400 | 0.462 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJN8 | Leptomonas seymouri | 75% | 100% |
A0A0N1PBS6 | Leptomonas seymouri | 27% | 100% |
A0A0S4JM05 | Bodo saltans | 27% | 100% |
A0A0S4JNU7 | Bodo saltans | 41% | 100% |
A0A1X0NU75 | Trypanosomatidae | 50% | 100% |
A0A1X0P8P3 | Trypanosomatidae | 27% | 100% |
A0A3Q8IIX7 | Leishmania donovani | 27% | 100% |
A0A3R7NHC0 | Trypanosoma rangeli | 27% | 100% |
A0A422N8J1 | Trypanosoma rangeli | 48% | 100% |
A4FUD3 | Bos taurus | 31% | 100% |
A4HKL0 | Leishmania braziliensis | 85% | 100% |
A4HNM7 | Leishmania braziliensis | 27% | 100% |
A4I843 | Leishmania infantum | 100% | 100% |
A4ICW8 | Leishmania infantum | 27% | 100% |
A5DI11 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 25% | 100% |
C4YJQ8 | Candida albicans (strain WO-1) | 25% | 100% |
D0A2I0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D0AAB0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9ASD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B301 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
F4JWP9 | Arabidopsis thaliana | 30% | 100% |
O08810 | Mus musculus | 31% | 100% |
O14460 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
O74945 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 100% |
O94316 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 100% |
P15112 | Dictyostelium discoideum | 26% | 100% |
P29691 | Caenorhabditis elegans | 25% | 100% |
P32324 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
Q06193 | Entamoeba histolytica | 26% | 100% |
Q15029 | Homo sapiens | 31% | 100% |
Q23716 | Cryptosporidium parvum | 27% | 100% |
Q4Q259 | Leishmania major | 27% | 100% |
Q4Q555 | Leishmania major | 94% | 100% |
Q5A0M4 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 25% | 100% |
Q5F3X4 | Gallus gallus | 32% | 100% |
Q5R6E0 | Pongo abelii | 31% | 100% |
Q6BJ25 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 25% | 100% |
Q6CPQ9 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 25% | 100% |
Q6FYA7 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 26% | 100% |
Q754C8 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 26% | 100% |
Q874B9 | Komagataella pastoris | 25% | 100% |
Q875S0 | Lachancea kluyveri (strain ATCC 58438 / CBS 3082 / BCRC 21498 / NBRC 1685 / JCM 7257 / NCYC 543 / NRRL Y-12651) | 26% | 100% |
Q875Z2 | Naumovozyma castellii (strain ATCC 76901 / BCRC 22586 / CBS 4309 / NBRC 1992 / NRRL Y-12630) | 26% | 100% |
Q96X45 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 26% | 100% |
Q9LNC5 | Arabidopsis thaliana | 31% | 100% |
V5AW74 | Trypanosoma cruzi | 49% | 100% |
V5DRS6 | Trypanosoma cruzi | 26% | 100% |