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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4H5L0
Term | Name | Level | Count |
---|---|---|---|
GO:0000719 | photoreactive repair | 7 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006290 | pyrimidine dimer repair | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0033554 | cellular response to stress | 3 | 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:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 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:0003824 | catalytic activity | 1 | 11 |
GO:0003904 | deoxyribodipyrimidine photo-lyase activity | 5 | 8 |
GO:0003913 | DNA photolyase activity | 4 | 8 |
GO:0016829 | lyase activity | 2 | 11 |
GO:0016830 | carbon-carbon lyase activity | 3 | 8 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 8 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 8 |
GO:0000166 | nucleotide binding | 3 | 1 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0036094 | small molecule binding | 2 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043168 | anion binding | 3 | 1 |
GO:0050660 | flavin adenine dinucleotide binding | 4 | 1 |
GO:0071949 | FAD binding | 5 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901265 | nucleoside phosphate binding | 3 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 228 | 232 | PF00656 | 0.468 |
CLV_C14_Caspase3-7 | 578 | 582 | PF00656 | 0.610 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.271 |
CLV_NRD_NRD_1 | 610 | 612 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 635 | 637 | PF00675 | 0.314 |
CLV_NRD_NRD_1 | 668 | 670 | PF00675 | 0.327 |
CLV_NRD_NRD_1 | 703 | 705 | PF00675 | 0.301 |
CLV_NRD_NRD_1 | 938 | 940 | PF00675 | 0.710 |
CLV_PCSK_FUR_1 | 608 | 612 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 610 | 612 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 668 | 670 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 955 | 957 | PF00082 | 0.683 |
CLV_PCSK_PC1ET2_1 | 955 | 957 | PF00082 | 0.683 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 546 | 550 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 651 | 655 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 682 | 686 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 738 | 742 | PF00082 | 0.274 |
CLV_Separin_Metazoa | 640 | 644 | PF03568 | 0.393 |
CLV_Separin_Metazoa | 789 | 793 | PF03568 | 0.464 |
DEG_APCC_DBOX_1 | 545 | 553 | PF00400 | 0.462 |
DEG_APCC_DBOX_1 | 659 | 667 | PF00400 | 0.349 |
DEG_APCC_DBOX_1 | 737 | 745 | PF00400 | 0.444 |
DEG_SCF_FBW7_1 | 35 | 40 | PF00400 | 0.673 |
DEG_SPOP_SBC_1 | 192 | 196 | PF00917 | 0.614 |
DEG_SPOP_SBC_1 | 259 | 263 | PF00917 | 0.561 |
DOC_CKS1_1 | 151 | 156 | PF01111 | 0.594 |
DOC_CKS1_1 | 481 | 486 | PF01111 | 0.544 |
DOC_CYCLIN_RxL_1 | 925 | 934 | PF00134 | 0.454 |
DOC_CYCLIN_yCln2_LP_2 | 339 | 345 | PF00134 | 0.444 |
DOC_CYCLIN_yCln2_LP_2 | 481 | 487 | PF00134 | 0.469 |
DOC_MAPK_DCC_7 | 349 | 359 | PF00069 | 0.457 |
DOC_MAPK_DCC_7 | 843 | 851 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 332 | 341 | PF00069 | 0.444 |
DOC_MAPK_gen_1 | 377 | 384 | PF00069 | 0.501 |
DOC_MAPK_gen_1 | 620 | 630 | PF00069 | 0.420 |
DOC_MAPK_HePTP_8 | 331 | 343 | PF00069 | 0.444 |
DOC_MAPK_MEF2A_6 | 334 | 343 | PF00069 | 0.444 |
DOC_MAPK_MEF2A_6 | 623 | 630 | PF00069 | 0.403 |
DOC_MAPK_RevD_3 | 622 | 637 | PF00069 | 0.449 |
DOC_PP1_RVXF_1 | 680 | 686 | PF00149 | 0.480 |
DOC_PP2B_LxvP_1 | 161 | 164 | PF13499 | 0.580 |
DOC_PP2B_LxvP_1 | 339 | 342 | PF13499 | 0.444 |
DOC_PP2B_PxIxI_1 | 428 | 434 | PF00149 | 0.519 |
DOC_PP4_FxxP_1 | 304 | 307 | PF00568 | 0.444 |
DOC_PP4_FxxP_1 | 77 | 80 | PF00568 | 0.499 |
DOC_PP4_FxxP_1 | 787 | 790 | PF00568 | 0.475 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 574 | 578 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 790 | 794 | PF00917 | 0.408 |
DOC_USP7_MATH_1 | 855 | 859 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 938 | 942 | PF00917 | 0.702 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 480 | 485 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 622 | 627 | PF00397 | 0.334 |
DOC_WW_Pin1_4 | 631 | 636 | PF00397 | 0.299 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 896 | 901 | PF00397 | 0.560 |
LIG_14-3-3_CanoR_1 | 212 | 216 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 235 | 243 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 450 | 455 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 457 | 465 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 539 | 545 | PF00244 | 0.354 |
LIG_14-3-3_CanoR_1 | 682 | 688 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 762 | 766 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 857 | 864 | PF00244 | 0.665 |
LIG_Actin_WH2_2 | 375 | 390 | PF00022 | 0.532 |
LIG_AP2alpha_2 | 768 | 770 | PF02296 | 0.444 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.481 |
LIG_BRCT_BRCA1_1 | 418 | 422 | PF00533 | 0.451 |
LIG_BRCT_BRCA1_1 | 73 | 77 | PF00533 | 0.535 |
LIG_Clathr_ClatBox_1 | 475 | 479 | PF01394 | 0.342 |
LIG_deltaCOP1_diTrp_1 | 670 | 679 | PF00928 | 0.308 |
LIG_deltaCOP1_diTrp_1 | 752 | 759 | PF00928 | 0.444 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.650 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.763 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.734 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.533 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.728 |
LIG_FHA_1 | 498 | 504 | PF00498 | 0.476 |
LIG_FHA_1 | 512 | 518 | PF00498 | 0.494 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.481 |
LIG_FHA_1 | 599 | 605 | PF00498 | 0.406 |
LIG_FHA_1 | 692 | 698 | PF00498 | 0.444 |
LIG_FHA_1 | 728 | 734 | PF00498 | 0.444 |
LIG_FHA_1 | 877 | 883 | PF00498 | 0.449 |
LIG_FHA_2 | 22 | 28 | PF00498 | 0.723 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.507 |
LIG_FHA_2 | 530 | 536 | PF00498 | 0.448 |
LIG_LIR_Apic_2 | 303 | 307 | PF02991 | 0.500 |
LIG_LIR_Apic_2 | 74 | 80 | PF02991 | 0.513 |
LIG_LIR_Apic_2 | 785 | 790 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 566 | 574 | PF02991 | 0.628 |
LIG_LIR_Gen_1 | 625 | 635 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 670 | 679 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 899 | 910 | PF02991 | 0.654 |
LIG_LIR_Gen_1 | 9 | 18 | PF02991 | 0.620 |
LIG_LIR_Nem_3 | 300 | 304 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 534 | 540 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 566 | 572 | PF02991 | 0.620 |
LIG_LIR_Nem_3 | 625 | 630 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 681 | 687 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 764 | 770 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 899 | 905 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 9 | 14 | PF02991 | 0.612 |
LIG_LIR_Nem_3 | 915 | 920 | PF02991 | 0.608 |
LIG_LYPXL_SIV_4 | 509 | 517 | PF13949 | 0.440 |
LIG_MYND_3 | 549 | 553 | PF01753 | 0.511 |
LIG_NRBOX | 740 | 746 | PF00104 | 0.444 |
LIG_PCNA_yPIPBox_3 | 590 | 604 | PF02747 | 0.456 |
LIG_PDZ_Class_2 | 954 | 959 | PF00595 | 0.662 |
LIG_PTB_Apo_2 | 772 | 779 | PF02174 | 0.427 |
LIG_PTB_Phospho_1 | 772 | 778 | PF10480 | 0.427 |
LIG_REV1ctd_RIR_1 | 311 | 317 | PF16727 | 0.475 |
LIG_SH2_CRK | 537 | 541 | PF00017 | 0.362 |
LIG_SH2_NCK_1 | 510 | 514 | PF00017 | 0.437 |
LIG_SH2_PTP2 | 627 | 630 | PF00017 | 0.394 |
LIG_SH2_PTP2 | 902 | 905 | PF00017 | 0.393 |
LIG_SH2_SRC | 372 | 375 | PF00017 | 0.457 |
LIG_SH2_SRC | 776 | 779 | PF00017 | 0.501 |
LIG_SH2_STAP1 | 557 | 561 | PF00017 | 0.503 |
LIG_SH2_STAP1 | 617 | 621 | PF00017 | 0.418 |
LIG_SH2_STAP1 | 878 | 882 | PF00017 | 0.492 |
LIG_SH2_STAT3 | 17 | 20 | PF00017 | 0.635 |
LIG_SH2_STAT3 | 867 | 870 | PF00017 | 0.618 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 627 | 630 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 796 | 799 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 807 | 810 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 822 | 825 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 840 | 843 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 878 | 881 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 902 | 905 | PF00017 | 0.606 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.662 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.678 |
LIG_SH3_3 | 503 | 509 | PF00018 | 0.419 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.697 |
LIG_SH3_3 | 820 | 826 | PF00018 | 0.410 |
LIG_SH3_3 | 870 | 876 | PF00018 | 0.575 |
LIG_SH3_3 | 885 | 891 | PF00018 | 0.613 |
LIG_SUMO_SIM_anti_2 | 24 | 30 | PF11976 | 0.505 |
LIG_SUMO_SIM_anti_2 | 500 | 505 | PF11976 | 0.353 |
LIG_SUMO_SIM_par_1 | 159 | 165 | PF11976 | 0.650 |
LIG_SUMO_SIM_par_1 | 2 | 7 | PF11976 | 0.660 |
LIG_SUMO_SIM_par_1 | 255 | 264 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 425 | 435 | PF11976 | 0.595 |
LIG_TRAF2_1 | 394 | 397 | PF00917 | 0.501 |
LIG_TRAF2_1 | 531 | 534 | PF00917 | 0.491 |
LIG_TRAF2_1 | 568 | 571 | PF00917 | 0.555 |
LIG_UBA3_1 | 139 | 144 | PF00899 | 0.611 |
LIG_WRC_WIRS_1 | 301 | 306 | PF05994 | 0.360 |
LIG_WW_1 | 819 | 822 | PF00397 | 0.281 |
MOD_CDC14_SPxK_1 | 317 | 320 | PF00782 | 0.296 |
MOD_CDC14_SPxK_1 | 634 | 637 | PF00782 | 0.306 |
MOD_CDK_SPK_2 | 631 | 636 | PF00069 | 0.299 |
MOD_CDK_SPxK_1 | 314 | 320 | PF00069 | 0.296 |
MOD_CDK_SPxK_1 | 631 | 637 | PF00069 | 0.304 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.700 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.734 |
MOD_CK1_1 | 453 | 459 | PF00069 | 0.626 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.717 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.646 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.732 |
MOD_CK2_1 | 391 | 397 | PF00069 | 0.362 |
MOD_CK2_1 | 529 | 535 | PF00069 | 0.424 |
MOD_CK2_1 | 857 | 863 | PF00069 | 0.552 |
MOD_CK2_1 | 928 | 934 | PF00069 | 0.707 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.683 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.537 |
MOD_GlcNHglycan | 186 | 190 | PF01048 | 0.785 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.734 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.352 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.682 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.686 |
MOD_GlcNHglycan | 452 | 455 | PF01048 | 0.599 |
MOD_GlcNHglycan | 559 | 562 | PF01048 | 0.574 |
MOD_GlcNHglycan | 859 | 862 | PF01048 | 0.581 |
MOD_GlcNHglycan | 885 | 888 | PF01048 | 0.598 |
MOD_GlcNHglycan | 914 | 917 | PF01048 | 0.500 |
MOD_GlcNHglycan | 940 | 943 | PF01048 | 0.682 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.708 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.699 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.645 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.480 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.613 |
MOD_N-GLC_1 | 457 | 462 | PF02516 | 0.607 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.611 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.512 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.598 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.300 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.300 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.274 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.442 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.374 |
MOD_NEK2_1 | 555 | 560 | PF00069 | 0.552 |
MOD_NEK2_1 | 664 | 669 | PF00069 | 0.338 |
MOD_NEK2_1 | 683 | 688 | PF00069 | 0.350 |
MOD_NEK2_1 | 727 | 732 | PF00069 | 0.281 |
MOD_NEK2_2 | 790 | 795 | PF00069 | 0.242 |
MOD_NEK2_2 | 950 | 955 | PF00069 | 0.548 |
MOD_PIKK_1 | 171 | 177 | PF00454 | 0.690 |
MOD_PIKK_1 | 29 | 35 | PF00454 | 0.543 |
MOD_PIKK_1 | 367 | 373 | PF00454 | 0.281 |
MOD_PIKK_1 | 572 | 578 | PF00454 | 0.492 |
MOD_PIKK_1 | 615 | 621 | PF00454 | 0.412 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.461 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.444 |
MOD_PKA_2 | 449 | 455 | PF00069 | 0.617 |
MOD_PKA_2 | 504 | 510 | PF00069 | 0.384 |
MOD_PKA_2 | 562 | 568 | PF00069 | 0.669 |
MOD_PKA_2 | 609 | 615 | PF00069 | 0.502 |
MOD_PKA_2 | 664 | 670 | PF00069 | 0.333 |
MOD_PKA_2 | 761 | 767 | PF00069 | 0.281 |
MOD_PKA_2 | 938 | 944 | PF00069 | 0.699 |
MOD_PKB_1 | 386 | 394 | PF00069 | 0.404 |
MOD_Plk_1 | 497 | 503 | PF00069 | 0.460 |
MOD_Plk_1 | 862 | 868 | PF00069 | 0.501 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.773 |
MOD_Plk_2-3 | 396 | 402 | PF00069 | 0.337 |
MOD_Plk_2-3 | 761 | 767 | PF00069 | 0.281 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.418 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.374 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.348 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.413 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.336 |
MOD_Plk_4 | 499 | 505 | PF00069 | 0.473 |
MOD_Plk_4 | 540 | 546 | PF00069 | 0.601 |
MOD_Plk_4 | 599 | 605 | PF00069 | 0.406 |
MOD_Plk_4 | 898 | 904 | PF00069 | 0.648 |
MOD_Plk_4 | 928 | 934 | PF00069 | 0.582 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.597 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.658 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.307 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.665 |
MOD_ProDKin_1 | 480 | 486 | PF00069 | 0.541 |
MOD_ProDKin_1 | 622 | 628 | PF00069 | 0.331 |
MOD_ProDKin_1 | 631 | 637 | PF00069 | 0.304 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.699 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.567 |
MOD_ProDKin_1 | 896 | 902 | PF00069 | 0.560 |
MOD_SUMO_for_1 | 333 | 336 | PF00179 | 0.242 |
MOD_SUMO_rev_2 | 699 | 707 | PF00179 | 0.281 |
MOD_SUMO_rev_2 | 921 | 927 | PF00179 | 0.439 |
TRG_DiLeu_BaEn_1 | 584 | 589 | PF01217 | 0.307 |
TRG_DiLeu_BaLyEn_6 | 157 | 162 | PF01217 | 0.700 |
TRG_DiLeu_BaLyEn_6 | 173 | 178 | PF01217 | 0.718 |
TRG_DiLeu_BaLyEn_6 | 205 | 210 | PF01217 | 0.584 |
TRG_DiLeu_BaLyEn_6 | 339 | 344 | PF01217 | 0.281 |
TRG_DiLeu_LyEn_5 | 426 | 431 | PF01217 | 0.551 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.281 |
TRG_ENDOCYTIC_2 | 537 | 540 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 627 | 630 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 638 | 641 | PF00928 | 0.287 |
TRG_ENDOCYTIC_2 | 767 | 770 | PF00928 | 0.281 |
TRG_ENDOCYTIC_2 | 902 | 905 | PF00928 | 0.393 |
TRG_ER_diArg_1 | 377 | 379 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 384 | 386 | PF00400 | 0.389 |
TRG_NES_CRM1_1 | 322 | 336 | PF08389 | 0.295 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXX3 | Leptomonas seymouri | 63% | 95% |
A0A1X0NMQ9 | Trypanosomatidae | 56% | 100% |
A0A3S7WQJ5 | Leishmania donovani | 83% | 100% |
A0A422N7E2 | Trypanosoma rangeli | 56% | 100% |
A4HTU9 | Leishmania infantum | 83% | 100% |
D0A9A9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 100% |
E9AMN6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4QHY9 | Leishmania major | 83% | 100% |
V5B2X6 | Trypanosoma cruzi | 58% | 100% |