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:0005634 | nucleus | 5 | 7 |
GO:0043226 | organelle | 2 | 7 |
GO:0043227 | membrane-bounded organelle | 3 | 7 |
GO:0043229 | intracellular organelle | 3 | 7 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0031010 | ISWI-type complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0070603 | SWI/SNF superfamily-type complex | 3 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1904949 | ATPase complex | 3 | 1 |
Related structures:
AlphaFold database: A4HNW6
Term | Name | Level | Count |
---|---|---|---|
GO:0006325 | chromatin organization | 4 | 1 |
GO:0006338 | chromatin remodeling | 5 | 1 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009890 | negative regulation of biosynthetic process | 5 | 1 |
GO:0009891 | positive regulation of biosynthetic process | 5 | 1 |
GO:0009892 | negative regulation of metabolic process | 4 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010557 | positive regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010558 | negative regulation of macromolecule biosynthetic process | 6 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031324 | negative regulation of cellular metabolic process | 5 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0031327 | negative regulation of cellular biosynthetic process | 6 | 1 |
GO:0031328 | positive regulation of cellular biosynthetic process | 6 | 1 |
GO:0031554 | regulation of termination of DNA-templated transcription | 6 | 1 |
GO:0031555 | transcriptional attenuation | 7 | 1 |
GO:0043244 | regulation of protein-containing complex disassembly | 5 | 1 |
GO:0045892 | negative regulation of DNA-templated transcription | 7 | 1 |
GO:0045893 | positive regulation of DNA-templated transcription | 7 | 1 |
GO:0045934 | negative regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0045935 | positive regulation of nucleobase-containing compound metabolic process | 6 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051128 | regulation of cellular component organization | 4 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051172 | negative regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0051253 | negative regulation of RNA metabolic process | 6 | 1 |
GO:0051254 | positive regulation of RNA metabolic process | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1902679 | negative regulation of RNA biosynthetic process | 7 | 1 |
GO:1902680 | positive regulation of RNA biosynthetic process | 7 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:1903507 | negative regulation of nucleic acid-templated transcription | 8 | 1 |
GO:1903508 | positive regulation of nucleic acid-templated transcription | 8 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 522 | 526 | PF00656 | 0.445 |
CLV_C14_Caspase3-7 | 601 | 605 | PF00656 | 0.635 |
CLV_C14_Caspase3-7 | 840 | 844 | PF00656 | 0.538 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.680 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 580 | 582 | PF00675 | 0.658 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.700 |
CLV_NRD_NRD_1 | 770 | 772 | PF00675 | 0.722 |
CLV_NRD_NRD_1 | 828 | 830 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 860 | 862 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 897 | 899 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 918 | 920 | PF00675 | 0.360 |
CLV_NRD_NRD_1 | 961 | 963 | PF00675 | 0.284 |
CLV_PCSK_FUR_1 | 202 | 206 | PF00082 | 0.649 |
CLV_PCSK_FUR_1 | 413 | 417 | PF00082 | 0.450 |
CLV_PCSK_FUR_1 | 768 | 772 | PF00082 | 0.531 |
CLV_PCSK_FUR_1 | 858 | 862 | PF00082 | 0.308 |
CLV_PCSK_FUR_1 | 916 | 920 | PF00082 | 0.203 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 585 | 587 | PF00082 | 0.659 |
CLV_PCSK_KEX2_1 | 770 | 772 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 830 | 832 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 860 | 862 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 897 | 899 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 916 | 918 | PF00082 | 0.352 |
CLV_PCSK_KEX2_1 | 961 | 963 | PF00082 | 0.284 |
CLV_PCSK_PC1ET2_1 | 332 | 334 | PF00082 | 0.560 |
CLV_PCSK_PC1ET2_1 | 415 | 417 | PF00082 | 0.463 |
CLV_PCSK_PC1ET2_1 | 420 | 422 | PF00082 | 0.471 |
CLV_PCSK_PC1ET2_1 | 579 | 581 | PF00082 | 0.594 |
CLV_PCSK_PC1ET2_1 | 770 | 772 | PF00082 | 0.646 |
CLV_PCSK_PC1ET2_1 | 830 | 832 | PF00082 | 0.492 |
CLV_PCSK_PC1ET2_1 | 89 | 91 | PF00082 | 0.504 |
CLV_PCSK_PC7_1 | 202 | 208 | PF00082 | 0.705 |
CLV_PCSK_PC7_1 | 416 | 422 | PF00082 | 0.555 |
CLV_PCSK_PC7_1 | 441 | 447 | PF00082 | 0.581 |
CLV_PCSK_PC7_1 | 581 | 587 | PF00082 | 0.667 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.535 |
CLV_PCSK_SKI1_1 | 554 | 558 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 732 | 736 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 743 | 747 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 902 | 906 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 970 | 974 | PF00082 | 0.400 |
DEG_APCC_DBOX_1 | 969 | 977 | PF00400 | 0.284 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.510 |
DEG_SPOP_SBC_1 | 754 | 758 | PF00917 | 0.483 |
DOC_ANK_TNKS_1 | 445 | 452 | PF00023 | 0.612 |
DOC_CKS1_1 | 465 | 470 | PF01111 | 0.724 |
DOC_CKS1_1 | 482 | 487 | PF01111 | 0.493 |
DOC_CYCLIN_RxL_1 | 402 | 410 | PF00134 | 0.381 |
DOC_CYCLIN_RxL_1 | 500 | 508 | PF00134 | 0.520 |
DOC_CYCLIN_RxL_1 | 532 | 541 | PF00134 | 0.495 |
DOC_CYCLIN_RxL_1 | 831 | 843 | PF00134 | 0.368 |
DOC_CYCLIN_RxL_1 | 897 | 910 | PF00134 | 0.203 |
DOC_CYCLIN_yCln2_LP_2 | 371 | 377 | PF00134 | 0.363 |
DOC_MAPK_gen_1 | 721 | 730 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 535 | 542 | PF00069 | 0.497 |
DOC_PP1_RVXF_1 | 858 | 865 | PF00149 | 0.346 |
DOC_PP4_FxxP_1 | 394 | 397 | PF00568 | 0.509 |
DOC_PP4_FxxP_1 | 547 | 550 | PF00568 | 0.430 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.363 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.780 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 617 | 621 | PF00917 | 0.808 |
DOC_USP7_MATH_1 | 627 | 631 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 706 | 710 | PF00917 | 0.591 |
DOC_USP7_UBL2_3 | 426 | 430 | PF12436 | 0.567 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 464 | 469 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 481 | 486 | PF00397 | 0.532 |
DOC_WW_Pin1_4 | 546 | 551 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 613 | 618 | PF00397 | 0.727 |
LIG_14-3-3_CanoR_1 | 204 | 214 | PF00244 | 0.697 |
LIG_14-3-3_CanoR_1 | 268 | 273 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 503 | 508 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 511 | 516 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 682 | 688 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 837 | 842 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 84 | 93 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 922 | 930 | PF00244 | 0.227 |
LIG_AP2alpha_2 | 665 | 667 | PF02296 | 0.580 |
LIG_BIR_III_4 | 219 | 223 | PF00653 | 0.542 |
LIG_BIR_III_4 | 525 | 529 | PF00653 | 0.550 |
LIG_BRCT_BRCA1_1 | 353 | 357 | PF00533 | 0.432 |
LIG_CtBP_PxDLS_1 | 399 | 403 | PF00389 | 0.410 |
LIG_eIF4E_1 | 493 | 499 | PF01652 | 0.441 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.526 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.593 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.390 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.632 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.532 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.491 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.486 |
LIG_FHA_1 | 725 | 731 | PF00498 | 0.511 |
LIG_FHA_1 | 771 | 777 | PF00498 | 0.531 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.433 |
LIG_FHA_2 | 17 | 23 | PF00498 | 0.334 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.727 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.412 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.230 |
LIG_FHA_2 | 396 | 402 | PF00498 | 0.586 |
LIG_FHA_2 | 588 | 594 | PF00498 | 0.725 |
LIG_FHA_2 | 627 | 633 | PF00498 | 0.694 |
LIG_FHA_2 | 776 | 782 | PF00498 | 0.598 |
LIG_FHA_2 | 979 | 985 | PF00498 | 0.516 |
LIG_LIR_Apic_2 | 391 | 397 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 21 | 31 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 296 | 305 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 832 | 841 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 21 | 26 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 296 | 301 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 336 | 341 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 470 | 476 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 568 | 572 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 6 | 11 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 686 | 690 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 77 | 81 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 832 | 838 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 857 | 862 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 942 | 947 | PF02991 | 0.336 |
LIG_NRBOX | 744 | 750 | PF00104 | 0.561 |
LIG_PALB2_WD40_1 | 558 | 566 | PF16756 | 0.573 |
LIG_Pex14_2 | 294 | 298 | PF04695 | 0.579 |
LIG_PTB_Apo_2 | 541 | 548 | PF02174 | 0.388 |
LIG_RPA_C_Fungi | 64 | 76 | PF08784 | 0.247 |
LIG_SH2_CRK | 835 | 839 | PF00017 | 0.564 |
LIG_SH2_CRK | 859 | 863 | PF00017 | 0.344 |
LIG_SH2_GRB2like | 1001 | 1004 | PF00017 | 0.525 |
LIG_SH2_PTP2 | 78 | 81 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 455 | 459 | PF00017 | 0.499 |
LIG_SH2_STAP1 | 476 | 480 | PF00017 | 0.571 |
LIG_SH2_STAP1 | 60 | 64 | PF00017 | 0.433 |
LIG_SH2_STAP1 | 835 | 839 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 1001 | 1004 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 473 | 476 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 873 | 876 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 951 | 954 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 979 | 982 | PF00017 | 0.440 |
LIG_SH3_1 | 897 | 903 | PF00018 | 0.203 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.584 |
LIG_SH3_3 | 496 | 502 | PF00018 | 0.406 |
LIG_SH3_3 | 547 | 553 | PF00018 | 0.626 |
LIG_SH3_3 | 897 | 903 | PF00018 | 0.338 |
LIG_SUMO_SIM_anti_2 | 46 | 51 | PF11976 | 0.412 |
LIG_SUMO_SIM_par_1 | 837 | 843 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 901 | 910 | PF11976 | 0.203 |
LIG_TRAF2_1 | 27 | 30 | PF00917 | 0.540 |
LIG_TRAF2_1 | 38 | 41 | PF00917 | 0.459 |
LIG_TRAF2_1 | 398 | 401 | PF00917 | 0.498 |
LIG_TRAF2_1 | 589 | 592 | PF00917 | 0.597 |
LIG_TRAF2_1 | 597 | 600 | PF00917 | 0.551 |
LIG_TRAF2_1 | 630 | 633 | PF00917 | 0.718 |
LIG_TRAF2_1 | 658 | 661 | PF00917 | 0.691 |
LIG_TRAF2_1 | 982 | 985 | PF00917 | 0.545 |
LIG_TYR_ITIM | 76 | 81 | PF00017 | 0.457 |
LIG_UBA3_1 | 304 | 310 | PF00899 | 0.308 |
LIG_UBA3_1 | 668 | 672 | PF00899 | 0.412 |
LIG_UBA3_1 | 998 | 1006 | PF00899 | 0.592 |
LIG_WRC_WIRS_1 | 512 | 517 | PF05994 | 0.541 |
LIG_WRC_WIRS_1 | 952 | 957 | PF05994 | 0.391 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.667 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.714 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.727 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.652 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.509 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.374 |
MOD_CK1_1 | 611 | 617 | PF00069 | 0.750 |
MOD_CK1_1 | 619 | 625 | PF00069 | 0.767 |
MOD_CK1_1 | 683 | 689 | PF00069 | 0.634 |
MOD_CK1_1 | 775 | 781 | PF00069 | 0.529 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.502 |
MOD_CK1_1 | 928 | 934 | PF00069 | 0.348 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.493 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.420 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.443 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.592 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.387 |
MOD_CK2_1 | 585 | 591 | PF00069 | 0.733 |
MOD_CK2_1 | 594 | 600 | PF00069 | 0.676 |
MOD_CK2_1 | 626 | 632 | PF00069 | 0.639 |
MOD_CK2_1 | 633 | 639 | PF00069 | 0.571 |
MOD_CK2_1 | 649 | 655 | PF00069 | 0.654 |
MOD_CK2_1 | 782 | 788 | PF00069 | 0.643 |
MOD_CK2_1 | 978 | 984 | PF00069 | 0.442 |
MOD_Cter_Amidation | 914 | 917 | PF01082 | 0.352 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.522 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.601 |
MOD_GlcNHglycan | 573 | 576 | PF01048 | 0.485 |
MOD_GlcNHglycan | 619 | 622 | PF01048 | 0.713 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.447 |
MOD_GlcNHglycan | 629 | 632 | PF01048 | 0.813 |
MOD_GlcNHglycan | 651 | 654 | PF01048 | 0.727 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.330 |
MOD_GlcNHglycan | 935 | 940 | PF01048 | 0.216 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.635 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.709 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.418 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.553 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.440 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.623 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.688 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.687 |
MOD_GSK3_1 | 756 | 763 | PF00069 | 0.636 |
MOD_GSK3_1 | 766 | 773 | PF00069 | 0.670 |
MOD_GSK3_1 | 921 | 928 | PF00069 | 0.268 |
MOD_GSK3_1 | 935 | 942 | PF00069 | 0.286 |
MOD_GSK3_1 | 951 | 958 | PF00069 | 0.380 |
MOD_N-GLC_1 | 121 | 126 | PF02516 | 0.642 |
MOD_N-GLC_1 | 195 | 200 | PF02516 | 0.696 |
MOD_N-GLC_1 | 538 | 543 | PF02516 | 0.512 |
MOD_N-GLC_1 | 627 | 632 | PF02516 | 0.531 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.571 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.529 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.298 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.474 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.523 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.515 |
MOD_NEK2_1 | 671 | 676 | PF00069 | 0.484 |
MOD_NEK2_1 | 748 | 753 | PF00069 | 0.519 |
MOD_NEK2_2 | 126 | 131 | PF00069 | 0.348 |
MOD_NEK2_2 | 252 | 257 | PF00069 | 0.506 |
MOD_PIKK_1 | 205 | 211 | PF00454 | 0.596 |
MOD_PIKK_1 | 505 | 511 | PF00454 | 0.489 |
MOD_PIKK_1 | 82 | 88 | PF00454 | 0.567 |
MOD_PK_1 | 772 | 778 | PF00069 | 0.528 |
MOD_PKA_1 | 205 | 211 | PF00069 | 0.725 |
MOD_PKA_1 | 585 | 591 | PF00069 | 0.676 |
MOD_PKA_1 | 770 | 776 | PF00069 | 0.699 |
MOD_PKA_2 | 205 | 211 | PF00069 | 0.713 |
MOD_PKA_2 | 510 | 516 | PF00069 | 0.372 |
MOD_PKA_2 | 585 | 591 | PF00069 | 0.676 |
MOD_PKA_2 | 760 | 766 | PF00069 | 0.621 |
MOD_PKA_2 | 770 | 776 | PF00069 | 0.587 |
MOD_PKA_2 | 921 | 927 | PF00069 | 0.203 |
MOD_PKA_2 | 989 | 995 | PF00069 | 0.584 |
MOD_PKB_1 | 205 | 213 | PF00069 | 0.742 |
MOD_PKB_1 | 268 | 276 | PF00069 | 0.444 |
MOD_Plk_1 | 39 | 45 | PF00069 | 0.347 |
MOD_Plk_1 | 460 | 466 | PF00069 | 0.604 |
MOD_Plk_1 | 538 | 544 | PF00069 | 0.568 |
MOD_Plk_1 | 724 | 730 | PF00069 | 0.674 |
MOD_Plk_1 | 812 | 818 | PF00069 | 0.495 |
MOD_Plk_1 | 909 | 915 | PF00069 | 0.356 |
MOD_Plk_1 | 935 | 941 | PF00069 | 0.203 |
MOD_Plk_2-3 | 594 | 600 | PF00069 | 0.717 |
MOD_Plk_4 | 378 | 384 | PF00069 | 0.330 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.347 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.611 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.526 |
MOD_Plk_4 | 939 | 945 | PF00069 | 0.415 |
MOD_Plk_4 | 951 | 957 | PF00069 | 0.377 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.643 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.673 |
MOD_ProDKin_1 | 245 | 251 | PF00069 | 0.660 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.489 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.552 |
MOD_ProDKin_1 | 464 | 470 | PF00069 | 0.733 |
MOD_ProDKin_1 | 481 | 487 | PF00069 | 0.527 |
MOD_ProDKin_1 | 546 | 552 | PF00069 | 0.616 |
MOD_ProDKin_1 | 613 | 619 | PF00069 | 0.727 |
MOD_SUMO_for_1 | 230 | 233 | PF00179 | 0.591 |
MOD_SUMO_for_1 | 429 | 432 | PF00179 | 0.484 |
MOD_SUMO_for_1 | 776 | 779 | PF00179 | 0.553 |
MOD_SUMO_rev_2 | 271 | 280 | PF00179 | 0.470 |
MOD_SUMO_rev_2 | 425 | 431 | PF00179 | 0.567 |
MOD_SUMO_rev_2 | 665 | 674 | PF00179 | 0.583 |
MOD_SUMO_rev_2 | 725 | 734 | PF00179 | 0.503 |
MOD_SUMO_rev_2 | 739 | 748 | PF00179 | 0.375 |
MOD_SUMO_rev_2 | 796 | 805 | PF00179 | 0.512 |
MOD_SUMO_rev_2 | 929 | 939 | PF00179 | 0.300 |
TRG_DiLeu_BaEn_1 | 439 | 444 | PF01217 | 0.509 |
TRG_DiLeu_BaEn_1 | 461 | 466 | PF01217 | 0.637 |
TRG_DiLeu_BaEn_1 | 744 | 749 | PF01217 | 0.462 |
TRG_DiLeu_BaEn_4 | 908 | 914 | PF01217 | 0.323 |
TRG_DiLeu_BaLyEn_6 | 834 | 839 | PF01217 | 0.494 |
TRG_DiLeu_BaLyEn_6 | 900 | 905 | PF01217 | 0.451 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 835 | 838 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 859 | 862 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 863 | 866 | PF00928 | 0.284 |
TRG_ER_diArg_1 | 201 | 204 | PF00400 | 0.660 |
TRG_ER_diArg_1 | 205 | 207 | PF00400 | 0.685 |
TRG_ER_diArg_1 | 421 | 423 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 444 | 447 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 859 | 861 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 916 | 919 | PF00400 | 0.352 |
TRG_NLS_Bipartite_1 | 404 | 424 | PF00514 | 0.564 |
TRG_NLS_MonoCore_2 | 576 | 581 | PF00514 | 0.600 |
TRG_NLS_MonoExtC_3 | 419 | 425 | PF00514 | 0.562 |
TRG_NLS_MonoExtC_3 | 576 | 581 | PF00514 | 0.555 |
TRG_NLS_MonoExtN_4 | 577 | 583 | PF00514 | 0.623 |
TRG_Pf-PMV_PEXEL_1 | 446 | 450 | PF00026 | 0.657 |
TRG_Pf-PMV_PEXEL_1 | 732 | 736 | PF00026 | 0.516 |
TRG_Pf-PMV_PEXEL_1 | 837 | 842 | PF00026 | 0.611 |
TRG_Pf-PMV_PEXEL_1 | 902 | 907 | PF00026 | 0.430 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD66 | Leptomonas seymouri | 56% | 94% |
A0A1X0P937 | Trypanosomatidae | 37% | 100% |
A0A3S7XAG3 | Leishmania donovani | 75% | 100% |
A0A422NTX5 | Trypanosoma rangeli | 38% | 100% |
A4ICM8 | Leishmania infantum | 76% | 100% |
D0A2T4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9ASM6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
Q4Q1X0 | Leishmania major | 75% | 100% |