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 | 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 |
Related structures:
AlphaFold database: A0A3Q8IAX2
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006259 | DNA metabolic process | 4 | 7 |
GO:0006304 | DNA modification | 5 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0070580 | base J metabolic process | 6 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006283 | transcription-coupled nucleotide-excision repair | 7 | 1 |
GO:0006289 | nucleotide-excision repair | 6 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0003677 | DNA binding | 4 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0016491 | oxidoreductase activity | 2 | 7 |
GO:0016705 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen | 3 | 7 |
GO:0016706 | 2-oxoglutarate-dependent dioxygenase activity | 4 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0050341 | thymine dioxygenase activity | 5 | 7 |
GO:0051213 | dioxygenase activity | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0005506 | iron ion binding | 6 | 1 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 1 |
GO:0008198 | ferrous iron binding | 7 | 1 |
GO:0046914 | transition metal ion binding | 5 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
GO:0140657 | ATP-dependent activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 358 | 362 | PF00656 | 0.446 |
CLV_C14_Caspase3-7 | 55 | 59 | PF00656 | 0.315 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.215 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 447 | 449 | PF00675 | 0.339 |
CLV_NRD_NRD_1 | 516 | 518 | PF00675 | 0.244 |
CLV_NRD_NRD_1 | 544 | 546 | PF00675 | 0.254 |
CLV_NRD_NRD_1 | 547 | 549 | PF00675 | 0.254 |
CLV_NRD_NRD_1 | 556 | 558 | PF00675 | 0.254 |
CLV_NRD_NRD_1 | 720 | 722 | PF00675 | 0.351 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 543 | 545 | PF00082 | 0.257 |
CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.245 |
CLV_PCSK_KEX2_1 | 567 | 569 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 720 | 722 | PF00082 | 0.351 |
CLV_PCSK_PC1ET2_1 | 254 | 256 | PF00082 | 0.286 |
CLV_PCSK_PC1ET2_1 | 543 | 545 | PF00082 | 0.287 |
CLV_PCSK_PC1ET2_1 | 567 | 569 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 532 | 536 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 601 | 605 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 685 | 689 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.299 |
DEG_APCC_DBOX_1 | 89 | 97 | PF00400 | 0.562 |
DEG_APCC_KENBOX_2 | 297 | 301 | PF00400 | 0.463 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.521 |
DEG_SCF_FBW7_1 | 170 | 177 | PF00400 | 0.415 |
DEG_SPOP_SBC_1 | 356 | 360 | PF00917 | 0.420 |
DOC_CYCLIN_RxL_1 | 207 | 218 | PF00134 | 0.476 |
DOC_CYCLIN_RxL_1 | 424 | 437 | PF00134 | 0.262 |
DOC_CYCLIN_RxL_1 | 666 | 676 | PF00134 | 0.454 |
DOC_CYCLIN_yCln2_LP_2 | 266 | 272 | PF00134 | 0.341 |
DOC_MAPK_DCC_7 | 306 | 315 | PF00069 | 0.267 |
DOC_MAPK_FxFP_2 | 13 | 16 | PF00069 | 0.478 |
DOC_MAPK_gen_1 | 424 | 433 | PF00069 | 0.332 |
DOC_MAPK_gen_1 | 517 | 523 | PF00069 | 0.244 |
DOC_MAPK_gen_1 | 57 | 66 | PF00069 | 0.329 |
DOC_MAPK_gen_1 | 6 | 12 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 60 | 68 | PF00069 | 0.318 |
DOC_MAPK_MEF2A_6 | 615 | 623 | PF00069 | 0.433 |
DOC_PP2B_LxvP_1 | 507 | 510 | PF13499 | 0.254 |
DOC_PP2B_LxvP_1 | 671 | 674 | PF13499 | 0.458 |
DOC_PP4_FxxP_1 | 13 | 16 | PF00568 | 0.393 |
DOC_PP4_FxxP_1 | 314 | 317 | PF00568 | 0.348 |
DOC_PP4_FxxP_1 | 318 | 321 | PF00568 | 0.337 |
DOC_PP4_FxxP_1 | 353 | 356 | PF00568 | 0.401 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.370 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 687 | 691 | PF00917 | 0.377 |
DOC_USP7_MATH_1 | 724 | 728 | PF00917 | 0.276 |
DOC_USP7_MATH_2 | 117 | 123 | PF00917 | 0.415 |
DOC_USP7_UBL2_3 | 518 | 522 | PF12436 | 0.254 |
DOC_USP7_UBL2_3 | 601 | 605 | PF12436 | 0.461 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.346 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.230 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.289 |
DOC_WW_Pin1_4 | 654 | 659 | PF00397 | 0.295 |
DOC_WW_Pin1_4 | 796 | 801 | PF00397 | 0.283 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.365 |
LIG_14-3-3_CanoR_1 | 123 | 128 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 183 | 192 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 255 | 262 | PF00244 | 0.267 |
LIG_14-3-3_CanoR_1 | 646 | 654 | PF00244 | 0.353 |
LIG_14-3-3_CanoR_1 | 740 | 746 | PF00244 | 0.297 |
LIG_14-3-3_CanoR_1 | 766 | 770 | PF00244 | 0.292 |
LIG_14-3-3_CanoR_1 | 90 | 94 | PF00244 | 0.408 |
LIG_Actin_WH2_2 | 730 | 748 | PF00022 | 0.293 |
LIG_BIR_III_2 | 162 | 166 | PF00653 | 0.439 |
LIG_BRCT_BRCA1_1 | 234 | 238 | PF00533 | 0.383 |
LIG_BRCT_BRCA1_1 | 36 | 40 | PF00533 | 0.331 |
LIG_BRCT_BRCA1_1 | 460 | 464 | PF00533 | 0.339 |
LIG_BRCT_BRCA1_1 | 94 | 98 | PF00533 | 0.378 |
LIG_CSL_BTD_1 | 318 | 321 | PF09270 | 0.352 |
LIG_deltaCOP1_diTrp_1 | 132 | 139 | PF00928 | 0.415 |
LIG_deltaCOP1_diTrp_1 | 251 | 260 | PF00928 | 0.295 |
LIG_deltaCOP1_diTrp_1 | 421 | 430 | PF00928 | 0.244 |
LIG_EH1_1 | 218 | 226 | PF00400 | 0.437 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.430 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.546 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.290 |
LIG_FHA_1 | 602 | 608 | PF00498 | 0.383 |
LIG_FHA_1 | 802 | 808 | PF00498 | 0.445 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.500 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.323 |
LIG_FHA_2 | 396 | 402 | PF00498 | 0.254 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.311 |
LIG_FHA_2 | 776 | 782 | PF00498 | 0.312 |
LIG_FXI_DFP_1 | 12 | 16 | PF00024 | 0.326 |
LIG_LIR_Apic_2 | 11 | 16 | PF02991 | 0.385 |
LIG_LIR_Apic_2 | 316 | 321 | PF02991 | 0.352 |
LIG_LIR_Apic_2 | 350 | 356 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 173 | 180 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 196 | 205 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 437 | 446 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 648 | 659 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 698 | 706 | PF02991 | 0.292 |
LIG_LIR_Gen_1 | 752 | 761 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 206 | 212 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 251 | 256 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 271 | 275 | PF02991 | 0.230 |
LIG_LIR_Nem_3 | 285 | 291 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 308 | 314 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 461 | 466 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 648 | 654 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 698 | 702 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 752 | 756 | PF02991 | 0.313 |
LIG_LYPXL_S_1 | 310 | 314 | PF13949 | 0.275 |
LIG_MAD2 | 620 | 628 | PF02301 | 0.345 |
LIG_MLH1_MIPbox_1 | 460 | 464 | PF16413 | 0.339 |
LIG_Pex14_1 | 135 | 139 | PF04695 | 0.415 |
LIG_Pex14_2 | 314 | 318 | PF04695 | 0.228 |
LIG_Pex14_2 | 410 | 414 | PF04695 | 0.261 |
LIG_PTB_Apo_2 | 404 | 411 | PF02174 | 0.287 |
LIG_PTB_Apo_2 | 571 | 578 | PF02174 | 0.379 |
LIG_SH2_CRK | 199 | 203 | PF00017 | 0.415 |
LIG_SH2_CRK | 41 | 45 | PF00017 | 0.338 |
LIG_SH2_CRK | 753 | 757 | PF00017 | 0.305 |
LIG_SH2_GRB2like | 405 | 408 | PF00017 | 0.287 |
LIG_SH2_GRB2like | 41 | 44 | PF00017 | 0.295 |
LIG_SH2_NCK_1 | 199 | 203 | PF00017 | 0.415 |
LIG_SH2_NCK_1 | 753 | 757 | PF00017 | 0.308 |
LIG_SH2_SRC | 31 | 34 | PF00017 | 0.370 |
LIG_SH2_SRC | 405 | 408 | PF00017 | 0.339 |
LIG_SH2_SRC | 41 | 44 | PF00017 | 0.295 |
LIG_SH2_STAP1 | 129 | 133 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 199 | 203 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 31 | 35 | PF00017 | 0.367 |
LIG_SH2_STAP1 | 495 | 499 | PF00017 | 0.254 |
LIG_SH2_STAP1 | 75 | 79 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 753 | 757 | PF00017 | 0.289 |
LIG_SH2_STAT3 | 794 | 797 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.254 |
LIG_SH2_STAT5 | 533 | 536 | PF00017 | 0.254 |
LIG_SH2_STAT5 | 718 | 721 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 743 | 746 | PF00017 | 0.314 |
LIG_SH3_1 | 306 | 312 | PF00018 | 0.351 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.375 |
LIG_SH3_3 | 620 | 626 | PF00018 | 0.303 |
LIG_SH3_3 | 804 | 810 | PF00018 | 0.402 |
LIG_SH3_5 | 140 | 144 | PF00018 | 0.415 |
LIG_SUMO_SIM_par_1 | 116 | 122 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 176 | 182 | PF11976 | 0.417 |
LIG_SUMO_SIM_par_1 | 621 | 627 | PF11976 | 0.384 |
LIG_TRAF2_1 | 23 | 26 | PF00917 | 0.442 |
LIG_TRAF2_1 | 485 | 488 | PF00917 | 0.254 |
LIG_TRAF2_1 | 538 | 541 | PF00917 | 0.348 |
LIG_UBA3_1 | 419 | 424 | PF00899 | 0.339 |
LIG_UBA3_1 | 441 | 449 | PF00899 | 0.339 |
LIG_UBA3_1 | 474 | 480 | PF00899 | 0.258 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.367 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.416 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.415 |
MOD_CK1_1 | 768 | 774 | PF00069 | 0.353 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.448 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.288 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.431 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.488 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.318 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.329 |
MOD_CK2_1 | 27 | 33 | PF00069 | 0.353 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.265 |
MOD_CK2_1 | 775 | 781 | PF00069 | 0.322 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.447 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.499 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.522 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.365 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.316 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.339 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.296 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.530 |
MOD_GlcNHglycan | 608 | 611 | PF01048 | 0.420 |
MOD_GlcNHglycan | 715 | 718 | PF01048 | 0.332 |
MOD_GlcNHglycan | 721 | 724 | PF01048 | 0.308 |
MOD_GlcNHglycan | 726 | 729 | PF01048 | 0.249 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.416 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.415 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.562 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.430 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.422 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.427 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.399 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.474 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.406 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.332 |
MOD_GSK3_1 | 641 | 648 | PF00069 | 0.528 |
MOD_GSK3_1 | 687 | 694 | PF00069 | 0.412 |
MOD_GSK3_1 | 741 | 748 | PF00069 | 0.311 |
MOD_GSK3_1 | 781 | 788 | PF00069 | 0.412 |
MOD_GSK3_1 | 796 | 803 | PF00069 | 0.223 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.387 |
MOD_LATS_1 | 599 | 605 | PF00433 | 0.444 |
MOD_LATS_1 | 689 | 695 | PF00433 | 0.346 |
MOD_N-GLC_1 | 299 | 304 | PF02516 | 0.470 |
MOD_N-GLC_1 | 454 | 459 | PF02516 | 0.285 |
MOD_N-GLC_1 | 573 | 578 | PF02516 | 0.384 |
MOD_N-GLC_1 | 801 | 806 | PF02516 | 0.387 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.455 |
MOD_NEK2_1 | 389 | 394 | PF00069 | 0.546 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.384 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.307 |
MOD_NEK2_1 | 528 | 533 | PF00069 | 0.276 |
MOD_NEK2_1 | 745 | 750 | PF00069 | 0.395 |
MOD_NEK2_1 | 801 | 806 | PF00069 | 0.392 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.391 |
MOD_NEK2_2 | 490 | 495 | PF00069 | 0.339 |
MOD_PKA_1 | 123 | 129 | PF00069 | 0.415 |
MOD_PKA_1 | 254 | 260 | PF00069 | 0.275 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.415 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.504 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.275 |
MOD_PKA_2 | 645 | 651 | PF00069 | 0.423 |
MOD_PKA_2 | 719 | 725 | PF00069 | 0.250 |
MOD_PKA_2 | 765 | 771 | PF00069 | 0.292 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.380 |
MOD_PKB_1 | 183 | 191 | PF00069 | 0.415 |
MOD_Plk_1 | 244 | 250 | PF00069 | 0.408 |
MOD_Plk_1 | 284 | 290 | PF00069 | 0.492 |
MOD_Plk_1 | 436 | 442 | PF00069 | 0.375 |
MOD_Plk_1 | 573 | 579 | PF00069 | 0.372 |
MOD_Plk_1 | 801 | 807 | PF00069 | 0.378 |
MOD_Plk_2-3 | 268 | 274 | PF00069 | 0.329 |
MOD_Plk_2-3 | 52 | 58 | PF00069 | 0.306 |
MOD_Plk_2-3 | 578 | 584 | PF00069 | 0.441 |
MOD_Plk_4 | 781 | 787 | PF00069 | 0.292 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.346 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.415 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.488 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.599 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.225 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.287 |
MOD_ProDKin_1 | 654 | 660 | PF00069 | 0.292 |
MOD_ProDKin_1 | 796 | 802 | PF00069 | 0.283 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.362 |
MOD_SUMO_for_1 | 485 | 488 | PF00179 | 0.339 |
MOD_SUMO_rev_2 | 116 | 122 | PF00179 | 0.415 |
MOD_SUMO_rev_2 | 2 | 8 | PF00179 | 0.483 |
MOD_SUMO_rev_2 | 247 | 256 | PF00179 | 0.356 |
MOD_SUMO_rev_2 | 368 | 372 | PF00179 | 0.540 |
MOD_SUMO_rev_2 | 630 | 639 | PF00179 | 0.526 |
TRG_DiLeu_BaEn_1 | 650 | 655 | PF01217 | 0.302 |
TRG_DiLeu_BaEn_1 | 781 | 786 | PF01217 | 0.391 |
TRG_DiLeu_BaEn_2 | 446 | 452 | PF01217 | 0.339 |
TRG_ENDOCYTIC_2 | 149 | 152 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 311 | 314 | PF00928 | 0.275 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 742 | 745 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 753 | 756 | PF00928 | 0.332 |
TRG_ER_diArg_1 | 275 | 278 | PF00400 | 0.359 |
TRG_ER_diArg_1 | 544 | 546 | PF00400 | 0.254 |
TRG_ER_diArg_1 | 719 | 721 | PF00400 | 0.350 |
TRG_NLS_MonoExtC_3 | 5 | 11 | PF00514 | 0.425 |
TRG_NLS_MonoExtN_4 | 3 | 10 | PF00514 | 0.415 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8A0 | Leptomonas seymouri | 66% | 99% |
A0A0S4JFS0 | Bodo saltans | 42% | 95% |
A0A1X0NHV5 | Trypanosomatidae | 47% | 99% |
A0A422NZF9 | Trypanosoma rangeli | 48% | 99% |
A4H5X5 | Leishmania braziliensis | 84% | 100% |
A4HU70 | Leishmania infantum | 100% | 100% |
D0A9Q3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 97% |
E9AN00 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
P86937 | Trypanosoma brucei brucei | 44% | 97% |
P86938 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 44% | 97% |
Q4DBW3 | Trypanosoma cruzi (strain CL Brener) | 49% | 98% |
Q4DLX9 | Trypanosoma cruzi (strain CL Brener) | 49% | 98% |
Q4QHM7 | Leishmania major | 96% | 100% |
Q9U6M1 | Leishmania tarentolae | 90% | 98% |
Q9U6M2 | Crithidia fasciculata | 64% | 100% |
V5DE87 | Trypanosoma cruzi | 48% | 98% |