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: A4H5X5
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 | 0.450 |
CLV_C14_Caspase3-7 | 55 | 59 | PF00656 | 0.398 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.282 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.226 |
CLV_NRD_NRD_1 | 447 | 449 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 516 | 518 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 544 | 546 | PF00675 | 0.348 |
CLV_NRD_NRD_1 | 547 | 549 | PF00675 | 0.348 |
CLV_NRD_NRD_1 | 556 | 558 | PF00675 | 0.348 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.286 |
CLV_NRD_NRD_1 | 749 | 751 | PF00675 | 0.272 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.226 |
CLV_PCSK_KEX2_1 | 544 | 546 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 6 | 8 | PF00082 | 0.387 |
CLV_PCSK_KEX2_1 | 749 | 751 | PF00082 | 0.272 |
CLV_PCSK_PC1ET2_1 | 254 | 256 | PF00082 | 0.390 |
CLV_PCSK_PC1ET2_1 | 402 | 404 | PF00082 | 0.197 |
CLV_PCSK_PC1ET2_1 | 566 | 568 | PF00082 | 0.680 |
CLV_PCSK_PC1ET2_1 | 6 | 8 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 532 | 536 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 591 | 595 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 597 | 601 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 684 | 688 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.395 |
CLV_Separin_Metazoa | 616 | 620 | PF03568 | 0.259 |
DEG_APCC_DBOX_1 | 89 | 97 | PF00400 | 0.567 |
DEG_APCC_KENBOX_2 | 297 | 301 | PF00400 | 0.579 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.586 |
DEG_SCF_FBW7_1 | 170 | 177 | PF00400 | 0.482 |
DEG_SCF_FBW7_1 | 286 | 293 | PF00400 | 0.343 |
DEG_SPOP_SBC_1 | 356 | 360 | PF00917 | 0.436 |
DOC_CDC14_PxL_1 | 621 | 629 | PF14671 | 0.265 |
DOC_CYCLIN_RxL_1 | 207 | 218 | PF00134 | 0.555 |
DOC_CYCLIN_RxL_1 | 424 | 437 | PF00134 | 0.323 |
DOC_CYCLIN_RxL_1 | 665 | 675 | PF00134 | 0.557 |
DOC_MAPK_DCC_7 | 619 | 629 | PF00069 | 0.261 |
DOC_MAPK_FxFP_2 | 13 | 16 | PF00069 | 0.571 |
DOC_MAPK_gen_1 | 208 | 216 | PF00069 | 0.375 |
DOC_MAPK_gen_1 | 424 | 433 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 436 | 444 | PF00069 | 0.226 |
DOC_MAPK_gen_1 | 517 | 523 | PF00069 | 0.282 |
DOC_MAPK_gen_1 | 57 | 66 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 6 | 12 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 208 | 216 | PF00069 | 0.375 |
DOC_MAPK_MEF2A_6 | 60 | 68 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 614 | 622 | PF00069 | 0.516 |
DOC_PP2B_LxvP_1 | 507 | 510 | PF13499 | 0.348 |
DOC_PP2B_LxvP_1 | 670 | 673 | PF13499 | 0.560 |
DOC_PP4_FxxP_1 | 13 | 16 | PF00568 | 0.469 |
DOC_PP4_FxxP_1 | 318 | 321 | PF00568 | 0.464 |
DOC_PP4_FxxP_1 | 353 | 356 | PF00568 | 0.518 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.383 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 723 | 727 | PF00917 | 0.323 |
DOC_USP7_MATH_2 | 117 | 123 | PF00917 | 0.482 |
DOC_USP7_UBL2_3 | 518 | 522 | PF12436 | 0.348 |
DOC_USP7_UBL2_3 | 600 | 604 | PF12436 | 0.557 |
DOC_USP7_UBL2_3 | 70 | 74 | PF12436 | 0.249 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.409 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.309 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.424 |
DOC_WW_Pin1_4 | 653 | 658 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 795 | 800 | PF00397 | 0.389 |
DOC_WW_Pin1_4 | 805 | 810 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.462 |
LIG_14-3-3_CanoR_1 | 123 | 128 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 183 | 192 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 255 | 262 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 652 | 657 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 739 | 745 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 90 | 94 | PF00244 | 0.472 |
LIG_APCC_ABBA_1 | 37 | 42 | PF00400 | 0.266 |
LIG_BRCT_BRCA1_1 | 135 | 139 | PF00533 | 0.375 |
LIG_BRCT_BRCA1_1 | 234 | 238 | PF00533 | 0.506 |
LIG_BRCT_BRCA1_1 | 460 | 464 | PF00533 | 0.348 |
LIG_BRCT_BRCA1_1 | 94 | 98 | PF00533 | 0.446 |
LIG_CSL_BTD_1 | 318 | 321 | PF09270 | 0.488 |
LIG_CSL_BTD_1 | 609 | 612 | PF09270 | 0.336 |
LIG_deltaCOP1_diTrp_1 | 132 | 139 | PF00928 | 0.482 |
LIG_deltaCOP1_diTrp_1 | 250 | 260 | PF00928 | 0.408 |
LIG_deltaCOP1_diTrp_1 | 421 | 430 | PF00928 | 0.338 |
LIG_EH1_1 | 218 | 226 | PF00400 | 0.388 |
LIG_EVH1_2 | 314 | 318 | PF00568 | 0.268 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.482 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.591 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.355 |
LIG_FHA_1 | 601 | 607 | PF00498 | 0.398 |
LIG_FHA_1 | 801 | 807 | PF00498 | 0.498 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.560 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.396 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.408 |
LIG_FHA_2 | 396 | 402 | PF00498 | 0.348 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.394 |
LIG_FHA_2 | 611 | 617 | PF00498 | 0.315 |
LIG_FHA_2 | 641 | 647 | PF00498 | 0.389 |
LIG_FHA_2 | 775 | 781 | PF00498 | 0.409 |
LIG_Integrin_RGD_1 | 366 | 368 | PF01839 | 0.341 |
LIG_LIR_Apic_2 | 11 | 16 | PF02991 | 0.461 |
LIG_LIR_Apic_2 | 316 | 321 | PF02991 | 0.490 |
LIG_LIR_Apic_2 | 350 | 356 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 132 | 142 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 173 | 180 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 196 | 205 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 215 | 224 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 647 | 658 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 693 | 704 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 206 | 212 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 215 | 219 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 250 | 256 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.212 |
LIG_LIR_Nem_3 | 285 | 291 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 461 | 466 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 647 | 653 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 693 | 699 | PF02991 | 0.495 |
LIG_MLH1_MIPbox_1 | 460 | 464 | PF16413 | 0.449 |
LIG_Pex14_1 | 135 | 139 | PF04695 | 0.482 |
LIG_PTAP_UEV_1 | 808 | 813 | PF05743 | 0.379 |
LIG_PTB_Apo_2 | 570 | 577 | PF02174 | 0.448 |
LIG_SH2_CRK | 199 | 203 | PF00017 | 0.482 |
LIG_SH2_CRK | 696 | 700 | PF00017 | 0.251 |
LIG_SH2_CRK | 752 | 756 | PF00017 | 0.394 |
LIG_SH2_GRB2like | 41 | 44 | PF00017 | 0.388 |
LIG_SH2_NCK_1 | 199 | 203 | PF00017 | 0.482 |
LIG_SH2_NCK_1 | 752 | 756 | PF00017 | 0.394 |
LIG_SH2_SRC | 31 | 34 | PF00017 | 0.459 |
LIG_SH2_SRC | 405 | 408 | PF00017 | 0.449 |
LIG_SH2_SRC | 41 | 44 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 199 | 203 | PF00017 | 0.482 |
LIG_SH2_STAP1 | 31 | 35 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 495 | 499 | PF00017 | 0.289 |
LIG_SH2_STAP1 | 696 | 700 | PF00017 | 0.299 |
LIG_SH2_STAP1 | 742 | 746 | PF00017 | 0.431 |
LIG_SH2_STAP1 | 75 | 79 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 752 | 756 | PF00017 | 0.384 |
LIG_SH2_STAT3 | 793 | 796 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 533 | 536 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 717 | 720 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 742 | 745 | PF00017 | 0.387 |
LIG_SH3_1 | 306 | 312 | PF00018 | 0.498 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.498 |
LIG_SH3_3 | 619 | 625 | PF00018 | 0.377 |
LIG_SH3_3 | 651 | 657 | PF00018 | 0.433 |
LIG_SH3_3 | 803 | 809 | PF00018 | 0.514 |
LIG_SH3_5 | 140 | 144 | PF00018 | 0.482 |
LIG_Sin3_3 | 80 | 87 | PF02671 | 0.287 |
LIG_SUMO_SIM_par_1 | 116 | 122 | PF11976 | 0.482 |
LIG_SUMO_SIM_par_1 | 176 | 182 | PF11976 | 0.482 |
LIG_SUMO_SIM_par_1 | 620 | 626 | PF11976 | 0.477 |
LIG_TRAF2_1 | 23 | 26 | PF00917 | 0.530 |
LIG_TRAF2_1 | 485 | 488 | PF00917 | 0.348 |
LIG_TRAF2_1 | 538 | 541 | PF00917 | 0.449 |
LIG_TRAF2_1 | 613 | 616 | PF00917 | 0.325 |
LIG_UBA3_1 | 419 | 424 | PF00899 | 0.348 |
LIG_UBA3_1 | 441 | 449 | PF00899 | 0.449 |
LIG_UBA3_1 | 474 | 480 | PF00899 | 0.352 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.311 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.319 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.482 |
MOD_CK1_1 | 716 | 722 | PF00069 | 0.242 |
MOD_CK1_1 | 767 | 773 | PF00069 | 0.440 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.471 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.324 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.482 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.550 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.399 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.471 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.434 |
MOD_CK2_1 | 27 | 33 | PF00069 | 0.436 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.268 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.348 |
MOD_CK2_1 | 610 | 616 | PF00069 | 0.346 |
MOD_CK2_1 | 774 | 780 | PF00069 | 0.419 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.209 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.237 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.286 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.449 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.449 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.197 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.379 |
MOD_GlcNHglycan | 725 | 728 | PF01048 | 0.343 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.393 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.447 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.482 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.631 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.482 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.482 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.541 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.460 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.453 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.374 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.414 |
MOD_GSK3_1 | 640 | 647 | PF00069 | 0.515 |
MOD_GSK3_1 | 686 | 693 | PF00069 | 0.510 |
MOD_GSK3_1 | 712 | 719 | PF00069 | 0.317 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.434 |
MOD_GSK3_1 | 740 | 747 | PF00069 | 0.376 |
MOD_GSK3_1 | 795 | 802 | PF00069 | 0.316 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.400 |
MOD_LATS_1 | 598 | 604 | PF00433 | 0.542 |
MOD_N-GLC_1 | 299 | 304 | PF02516 | 0.601 |
MOD_N-GLC_1 | 454 | 459 | PF02516 | 0.348 |
MOD_N-GLC_1 | 572 | 577 | PF02516 | 0.440 |
MOD_N-GLC_1 | 800 | 805 | PF02516 | 0.492 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.398 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.565 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.438 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.390 |
MOD_NEK2_1 | 528 | 533 | PF00069 | 0.348 |
MOD_NEK2_1 | 687 | 692 | PF00069 | 0.293 |
MOD_NEK2_1 | 713 | 718 | PF00069 | 0.242 |
MOD_NEK2_1 | 744 | 749 | PF00069 | 0.524 |
MOD_NEK2_1 | 800 | 805 | PF00069 | 0.492 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.442 |
MOD_NEK2_2 | 333 | 338 | PF00069 | 0.258 |
MOD_NEK2_2 | 490 | 495 | PF00069 | 0.449 |
MOD_PIKK_1 | 343 | 349 | PF00454 | 0.304 |
MOD_PKA_1 | 123 | 129 | PF00069 | 0.482 |
MOD_PKA_1 | 254 | 260 | PF00069 | 0.375 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.482 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.375 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.467 |
MOD_PKB_1 | 183 | 191 | PF00069 | 0.482 |
MOD_Plk_1 | 572 | 578 | PF00069 | 0.432 |
MOD_Plk_1 | 800 | 806 | PF00069 | 0.494 |
MOD_Plk_2-3 | 268 | 274 | PF00069 | 0.434 |
MOD_Plk_2-3 | 52 | 58 | PF00069 | 0.388 |
MOD_Plk_2-3 | 577 | 583 | PF00069 | 0.516 |
MOD_Plk_4 | 713 | 719 | PF00069 | 0.365 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.409 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.482 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.538 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.605 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.301 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.419 |
MOD_ProDKin_1 | 653 | 659 | PF00069 | 0.380 |
MOD_ProDKin_1 | 795 | 801 | PF00069 | 0.389 |
MOD_ProDKin_1 | 805 | 811 | PF00069 | 0.455 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.455 |
MOD_SUMO_for_1 | 485 | 488 | PF00179 | 0.449 |
MOD_SUMO_rev_2 | 116 | 122 | PF00179 | 0.482 |
MOD_SUMO_rev_2 | 200 | 209 | PF00179 | 0.375 |
MOD_SUMO_rev_2 | 247 | 256 | PF00179 | 0.452 |
MOD_SUMO_rev_2 | 368 | 372 | PF00179 | 0.604 |
MOD_SUMO_rev_2 | 432 | 441 | PF00179 | 0.226 |
MOD_SUMO_rev_2 | 632 | 638 | PF00179 | 0.608 |
TRG_DiLeu_BaEn_1 | 649 | 654 | PF01217 | 0.419 |
TRG_DiLeu_BaEn_1 | 780 | 785 | PF01217 | 0.507 |
TRG_DiLeu_BaEn_2 | 446 | 452 | PF01217 | 0.449 |
TRG_DiLeu_BaLyEn_6 | 658 | 663 | PF01217 | 0.257 |
TRG_ENDOCYTIC_2 | 149 | 152 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 696 | 699 | PF00928 | 0.251 |
TRG_ENDOCYTIC_2 | 741 | 744 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 752 | 755 | PF00928 | 0.400 |
TRG_ER_diArg_1 | 275 | 278 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 427 | 430 | PF00400 | 0.197 |
TRG_ER_diArg_1 | 544 | 546 | PF00400 | 0.348 |
TRG_ER_diArg_1 | 748 | 750 | PF00400 | 0.261 |
TRG_NES_CRM1_1 | 465 | 479 | PF08389 | 0.260 |
TRG_NLS_MonoExtC_3 | 5 | 11 | PF00514 | 0.497 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8A0 | Leptomonas seymouri | 65% | 99% |
A0A0S4JFS0 | Bodo saltans | 42% | 95% |
A0A1X0NHV5 | Trypanosomatidae | 46% | 99% |
A0A3Q8IAX2 | Leishmania donovani | 84% | 100% |
A0A422NZF9 | Trypanosoma rangeli | 47% | 99% |
A4H5X5 | Leishmania braziliensis | 100% | 100% |
A4HU70 | Leishmania infantum | 84% | 100% |
D0A9Q3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 97% |
E9AN00 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
P86937 | Trypanosoma brucei brucei | 44% | 97% |
P86938 | Trypanosoma brucei brucei (strain 927/4 GUTat10.1) | 44% | 97% |
Q4DBW3 | Trypanosoma cruzi (strain CL Brener) | 47% | 98% |
Q4DLX9 | Trypanosoma cruzi (strain CL Brener) | 48% | 98% |
Q4QHM7 | Leishmania major | 85% | 100% |
Q9U6M1 | Leishmania tarentolae | 85% | 98% |
Q9U6M2 | Crithidia fasciculata | 64% | 100% |
V5DE87 | Trypanosoma cruzi | 47% | 98% |