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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0042555 | MCM complex | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HSF2
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016043 | cellular component organization | 3 | 7 |
GO:0032392 | DNA geometric change | 7 | 7 |
GO:0032508 | DNA duplex unwinding | 8 | 7 |
GO:0051276 | chromosome organization | 5 | 7 |
GO:0071103 | DNA conformation change | 6 | 7 |
GO:0071840 | cellular component organization or biogenesis | 2 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0003677 | DNA binding | 4 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0003697 | single-stranded DNA binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 268 | 272 | PF00656 | 0.448 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 710 | 712 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 757 | 759 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 925 | 927 | PF00675 | 0.683 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 757 | 759 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 925 | 927 | PF00082 | 0.683 |
CLV_PCSK_PC1ET2_1 | 180 | 182 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.632 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.234 |
CLV_PCSK_SKI1_1 | 566 | 570 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 614 | 618 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 669 | 673 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 790 | 794 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 926 | 930 | PF00082 | 0.557 |
DEG_APCC_DBOX_1 | 938 | 946 | PF00400 | 0.569 |
DEG_SCF_TRCP1_1 | 847 | 852 | PF00400 | 0.653 |
DEG_SPOP_SBC_1 | 620 | 624 | PF00917 | 0.578 |
DOC_ANK_TNKS_1 | 180 | 187 | PF00023 | 0.630 |
DOC_ANK_TNKS_1 | 3 | 10 | PF00023 | 0.700 |
DOC_ANK_TNKS_1 | 475 | 482 | PF00023 | 0.708 |
DOC_CKS1_1 | 105 | 110 | PF01111 | 0.661 |
DOC_CYCLIN_RxL_1 | 787 | 797 | PF00134 | 0.397 |
DOC_CYCLIN_yCln2_LP_2 | 102 | 108 | PF00134 | 0.517 |
DOC_CYCLIN_yCln2_LP_2 | 144 | 150 | PF00134 | 0.362 |
DOC_MAPK_MEF2A_6 | 566 | 573 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 586 | 593 | PF00069 | 0.383 |
DOC_MAPK_NFAT4_5 | 566 | 574 | PF00069 | 0.578 |
DOC_PP1_RVXF_1 | 518 | 524 | PF00149 | 0.646 |
DOC_PP1_RVXF_1 | 788 | 795 | PF00149 | 0.391 |
DOC_PP2B_LxvP_1 | 366 | 369 | PF13499 | 0.399 |
DOC_PP2B_LxvP_1 | 783 | 786 | PF13499 | 0.571 |
DOC_PP4_FxxP_1 | 689 | 692 | PF00568 | 0.493 |
DOC_SPAK_OSR1_1 | 727 | 731 | PF12202 | 0.468 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 507 | 511 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 514 | 518 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 519 | 523 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 710 | 714 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 833 | 837 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 914 | 918 | PF00917 | 0.714 |
DOC_USP7_UBL2_3 | 987 | 991 | PF12436 | 0.542 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 718 | 723 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 864 | 869 | PF00397 | 0.485 |
LIG_14-3-3_CanoR_1 | 168 | 177 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 248 | 256 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 407 | 413 | PF00244 | 0.584 |
LIG_14-3-3_CanoR_1 | 49 | 55 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 520 | 530 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 550 | 556 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 711 | 715 | PF00244 | 0.513 |
LIG_BRCT_BRCA1_1 | 523 | 527 | PF00533 | 0.587 |
LIG_CtBP_PxDLS_1 | 561 | 566 | PF00389 | 0.493 |
LIG_deltaCOP1_diTrp_1 | 29 | 36 | PF00928 | 0.531 |
LIG_EH1_1 | 147 | 155 | PF00400 | 0.329 |
LIG_EH1_1 | 96 | 104 | PF00400 | 0.494 |
LIG_eIF4E_1 | 148 | 154 | PF01652 | 0.331 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.564 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.468 |
LIG_FHA_1 | 550 | 556 | PF00498 | 0.504 |
LIG_FHA_1 | 627 | 633 | PF00498 | 0.498 |
LIG_FHA_1 | 677 | 683 | PF00498 | 0.582 |
LIG_FHA_1 | 693 | 699 | PF00498 | 0.417 |
LIG_FHA_1 | 747 | 753 | PF00498 | 0.493 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.556 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.459 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.491 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.578 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.417 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.604 |
LIG_FHA_2 | 639 | 645 | PF00498 | 0.493 |
LIG_FHA_2 | 654 | 660 | PF00498 | 0.493 |
LIG_FHA_2 | 724 | 730 | PF00498 | 0.448 |
LIG_FHA_2 | 889 | 895 | PF00498 | 0.493 |
LIG_Integrin_RGD_1 | 476 | 478 | PF01839 | 0.715 |
LIG_LIR_Apic_2 | 275 | 279 | PF02991 | 0.578 |
LIG_LIR_Gen_1 | 145 | 156 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 221 | 231 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 57 | 66 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 726 | 734 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 91 | 102 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 145 | 151 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 155 | 160 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 221 | 226 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 57 | 62 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 726 | 731 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 908 | 912 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 91 | 97 | PF02991 | 0.563 |
LIG_PALB2_WD40_1 | 543 | 551 | PF16756 | 0.493 |
LIG_Pex14_1 | 161 | 165 | PF04695 | 0.427 |
LIG_Pex14_2 | 157 | 161 | PF04695 | 0.401 |
LIG_Pex14_2 | 523 | 527 | PF04695 | 0.587 |
LIG_SH2_CRK | 210 | 214 | PF00017 | 0.450 |
LIG_SH2_NCK_1 | 210 | 214 | PF00017 | 0.450 |
LIG_SH2_PTP2 | 148 | 151 | PF00017 | 0.339 |
LIG_SH2_STAP1 | 50 | 54 | PF00017 | 0.591 |
LIG_SH2_STAP1 | 897 | 901 | PF00017 | 0.493 |
LIG_SH2_STAT3 | 815 | 818 | PF00017 | 0.437 |
LIG_SH2_STAT3 | 897 | 900 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 815 | 818 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 870 | 873 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 992 | 995 | PF00017 | 0.395 |
LIG_SH3_2 | 105 | 110 | PF14604 | 0.722 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.671 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.513 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.441 |
LIG_SH3_3 | 591 | 597 | PF00018 | 0.497 |
LIG_SH3_3 | 848 | 854 | PF00018 | 0.646 |
LIG_SUMO_SIM_par_1 | 149 | 155 | PF11976 | 0.390 |
LIG_SUMO_SIM_par_1 | 360 | 365 | PF11976 | 0.443 |
LIG_SUMO_SIM_par_1 | 590 | 596 | PF11976 | 0.493 |
LIG_SUMO_SIM_par_1 | 670 | 676 | PF11976 | 0.493 |
LIG_SUMO_SIM_par_1 | 72 | 78 | PF11976 | 0.715 |
LIG_SUMO_SIM_par_1 | 958 | 965 | PF11976 | 0.529 |
LIG_TRAF2_1 | 531 | 534 | PF00917 | 0.466 |
LIG_UBA3_1 | 559 | 566 | PF00899 | 0.493 |
LIG_WRC_WIRS_1 | 906 | 911 | PF05994 | 0.458 |
MOD_CDC14_SPxK_1 | 245 | 248 | PF00782 | 0.493 |
MOD_CDK_SPK_2 | 864 | 869 | PF00069 | 0.493 |
MOD_CDK_SPxK_1 | 104 | 110 | PF00069 | 0.652 |
MOD_CDK_SPxK_1 | 242 | 248 | PF00069 | 0.493 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.624 |
MOD_CK1_1 | 319 | 325 | PF00069 | 0.791 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.671 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.583 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.573 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.629 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.528 |
MOD_CK1_1 | 638 | 644 | PF00069 | 0.493 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.327 |
MOD_CK2_1 | 528 | 534 | PF00069 | 0.477 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.600 |
MOD_CK2_1 | 638 | 644 | PF00069 | 0.493 |
MOD_Cter_Amidation | 178 | 181 | PF01082 | 0.594 |
MOD_Cter_Amidation | 923 | 926 | PF01082 | 0.746 |
MOD_DYRK1A_RPxSP_1 | 190 | 194 | PF00069 | 0.677 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.608 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.738 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.367 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.501 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.378 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.695 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.739 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.587 |
MOD_GlcNHglycan | 416 | 420 | PF01048 | 0.627 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.653 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.738 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.617 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.469 |
MOD_GlcNHglycan | 530 | 533 | PF01048 | 0.391 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.285 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.293 |
MOD_GlcNHglycan | 740 | 743 | PF01048 | 0.268 |
MOD_GlcNHglycan | 847 | 850 | PF01048 | 0.720 |
MOD_GlcNHglycan | 851 | 854 | PF01048 | 0.597 |
MOD_GlcNHglycan | 914 | 917 | PF01048 | 0.601 |
MOD_GlcNHglycan | 946 | 951 | PF01048 | 0.529 |
MOD_GlcNHglycan | 969 | 972 | PF01048 | 0.445 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.493 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.576 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.668 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.604 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.710 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.495 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.510 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.566 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.649 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.587 |
MOD_GSK3_1 | 843 | 850 | PF00069 | 0.629 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.612 |
MOD_GSK3_1 | 901 | 908 | PF00069 | 0.493 |
MOD_N-GLC_1 | 718 | 723 | PF02516 | 0.293 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.668 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.578 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.743 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.503 |
MOD_NEK2_1 | 569 | 574 | PF00069 | 0.493 |
MOD_NEK2_1 | 599 | 604 | PF00069 | 0.493 |
MOD_NEK2_1 | 628 | 633 | PF00069 | 0.541 |
MOD_NEK2_1 | 687 | 692 | PF00069 | 0.493 |
MOD_NEK2_1 | 794 | 799 | PF00069 | 0.399 |
MOD_NEK2_1 | 845 | 850 | PF00069 | 0.679 |
MOD_NEK2_1 | 862 | 867 | PF00069 | 0.336 |
MOD_NEK2_1 | 901 | 906 | PF00069 | 0.493 |
MOD_NEK2_1 | 912 | 917 | PF00069 | 0.587 |
MOD_NEK2_2 | 408 | 413 | PF00069 | 0.535 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.690 |
MOD_OFUCOSY | 619 | 626 | PF10250 | 0.293 |
MOD_PIKK_1 | 170 | 176 | PF00454 | 0.614 |
MOD_PIKK_1 | 266 | 272 | PF00454 | 0.470 |
MOD_PIKK_1 | 330 | 336 | PF00454 | 0.768 |
MOD_PIKK_1 | 347 | 353 | PF00454 | 0.533 |
MOD_PIKK_1 | 411 | 417 | PF00454 | 0.675 |
MOD_PIKK_1 | 599 | 605 | PF00454 | 0.493 |
MOD_PIKK_1 | 794 | 800 | PF00454 | 0.404 |
MOD_PKA_1 | 168 | 174 | PF00069 | 0.610 |
MOD_PKA_1 | 265 | 271 | PF00069 | 0.448 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.488 |
MOD_PKA_2 | 48 | 54 | PF00069 | 0.476 |
MOD_PKA_2 | 519 | 525 | PF00069 | 0.697 |
MOD_PKA_2 | 549 | 555 | PF00069 | 0.493 |
MOD_PKA_2 | 585 | 591 | PF00069 | 0.493 |
MOD_PKA_2 | 693 | 699 | PF00069 | 0.572 |
MOD_PKA_2 | 710 | 716 | PF00069 | 0.412 |
MOD_PKB_1 | 190 | 198 | PF00069 | 0.581 |
MOD_Plk_1 | 308 | 314 | PF00069 | 0.493 |
MOD_Plk_1 | 639 | 645 | PF00069 | 0.493 |
MOD_Plk_1 | 862 | 868 | PF00069 | 0.457 |
MOD_Plk_2-3 | 309 | 315 | PF00069 | 0.578 |
MOD_Plk_2-3 | 372 | 378 | PF00069 | 0.424 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.318 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.493 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.578 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.558 |
MOD_Plk_4 | 555 | 561 | PF00069 | 0.493 |
MOD_Plk_4 | 569 | 575 | PF00069 | 0.493 |
MOD_Plk_4 | 693 | 699 | PF00069 | 0.493 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.652 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.674 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.624 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.493 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.535 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.489 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.588 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.669 |
MOD_ProDKin_1 | 718 | 724 | PF00069 | 0.493 |
MOD_ProDKin_1 | 864 | 870 | PF00069 | 0.485 |
MOD_SUMO_for_1 | 882 | 885 | PF00179 | 0.493 |
MOD_SUMO_rev_2 | 662 | 671 | PF00179 | 0.493 |
TRG_DiLeu_BaEn_1 | 300 | 305 | PF01217 | 0.578 |
TRG_DiLeu_BaEn_1 | 667 | 672 | PF01217 | 0.493 |
TRG_DiLeu_BaEn_1 | 980 | 985 | PF01217 | 0.429 |
TRG_DiLeu_BaEn_4 | 300 | 306 | PF01217 | 0.578 |
TRG_DiLeu_BaLyEn_6 | 61 | 66 | PF01217 | 0.448 |
TRG_DiLeu_BaLyEn_6 | 98 | 103 | PF01217 | 0.569 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.448 |
TRG_ER_diArg_1 | 206 | 208 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 404 | 407 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 432 | 435 | PF00400 | 0.644 |
TRG_ER_diArg_1 | 925 | 927 | PF00400 | 0.683 |
TRG_NLS_Bipartite_1 | 168 | 184 | PF00514 | 0.547 |
TRG_NLS_MonoExtC_3 | 179 | 185 | PF00514 | 0.599 |
TRG_NLS_MonoExtN_4 | 177 | 184 | PF00514 | 0.593 |
TRG_Pf-PMV_PEXEL_1 | 410 | 415 | PF00026 | 0.647 |
TRG_Pf-PMV_PEXEL_1 | 669 | 673 | PF00026 | 0.293 |
TRG_Pf-PMV_PEXEL_1 | 976 | 980 | PF00026 | 0.433 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAM6 | Leptomonas seymouri | 63% | 99% |
A0A3S5H5H2 | Leishmania donovani | 99% | 100% |
A4H477 | Leishmania braziliensis | 79% | 99% |
E9AKD9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QJG9 | Leishmania major | 91% | 99% |