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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 9 |
GO:0020023 | kinetoplast | 2 | 2 |
GO:0043226 | organelle | 2 | 9 |
GO:0043227 | membrane-bounded organelle | 3 | 9 |
GO:0043229 | intracellular organelle | 3 | 9 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: Q4Q3N1
Term | Name | Level | Count |
---|---|---|---|
GO:0000012 | single strand break repair | 6 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006259 | DNA metabolic process | 4 | 9 |
GO:0006281 | DNA repair | 5 | 9 |
GO:0006302 | double-strand break repair | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0006950 | response to stress | 2 | 9 |
GO:0006974 | DNA damage response | 4 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0033554 | cellular response to stress | 3 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0050896 | response to stimulus | 1 | 9 |
GO:0051716 | cellular response to stimulus | 2 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003677 | DNA binding | 4 | 2 |
GO:0003690 | double-stranded DNA binding | 5 | 2 |
GO:0003697 | single-stranded DNA binding | 5 | 2 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004518 | nuclease activity | 4 | 9 |
GO:0005488 | binding | 1 | 2 |
GO:0008081 | phosphoric diester hydrolase activity | 5 | 9 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 9 |
GO:0017005 | 3'-tyrosyl-DNA phosphodiesterase activity | 5 | 2 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 9 |
GO:0070259 | tyrosyl-DNA phosphodiesterase activity | 4 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 2 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 512 | 516 | PF00656 | 0.422 |
CLV_C14_Caspase3-7 | 597 | 601 | PF00656 | 0.493 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 244 | 246 | PF00675 | 0.274 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 619 | 621 | PF00675 | 0.176 |
CLV_NRD_NRD_1 | 658 | 660 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 821 | 823 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 87 | 89 | PF00675 | 0.413 |
CLV_PCSK_FUR_1 | 119 | 123 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 466 | 468 | PF00082 | 0.315 |
CLV_PCSK_KEX2_1 | 574 | 576 | PF00082 | 0.295 |
CLV_PCSK_KEX2_1 | 619 | 621 | PF00082 | 0.176 |
CLV_PCSK_KEX2_1 | 823 | 825 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.413 |
CLV_PCSK_PC1ET2_1 | 574 | 576 | PF00082 | 0.238 |
CLV_PCSK_PC1ET2_1 | 823 | 825 | PF00082 | 0.645 |
CLV_PCSK_PC7_1 | 117 | 123 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 574 | 578 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 579 | 583 | PF00082 | 0.213 |
CLV_PCSK_SKI1_1 | 620 | 624 | PF00082 | 0.176 |
CLV_PCSK_SKI1_1 | 640 | 644 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 711 | 715 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 87 | 91 | PF00082 | 0.408 |
CLV_Separin_Metazoa | 463 | 467 | PF03568 | 0.490 |
DEG_APCC_DBOX_1 | 214 | 222 | PF00400 | 0.443 |
DEG_APCC_DBOX_1 | 286 | 294 | PF00400 | 0.469 |
DEG_APCC_DBOX_1 | 454 | 462 | PF00400 | 0.490 |
DEG_APCC_DBOX_1 | 619 | 627 | PF00400 | 0.376 |
DEG_APCC_DBOX_1 | 72 | 80 | PF00400 | 0.388 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.393 |
DEG_SCF_FBW7_1 | 735 | 742 | PF00400 | 0.392 |
DEG_SPOP_SBC_1 | 366 | 370 | PF00917 | 0.435 |
DOC_CDC14_PxL_1 | 218 | 226 | PF14671 | 0.447 |
DOC_CDC14_PxL_1 | 254 | 262 | PF14671 | 0.376 |
DOC_CKS1_1 | 715 | 720 | PF01111 | 0.474 |
DOC_CKS1_1 | 728 | 733 | PF01111 | 0.422 |
DOC_CYCLIN_RxL_1 | 176 | 189 | PF00134 | 0.180 |
DOC_CYCLIN_yCln2_LP_2 | 293 | 299 | PF00134 | 0.454 |
DOC_CYCLIN_yCln2_LP_2 | 728 | 734 | PF00134 | 0.490 |
DOC_MAPK_gen_1 | 779 | 788 | PF00069 | 0.368 |
DOC_MAPK_MEF2A_6 | 541 | 550 | PF00069 | 0.447 |
DOC_MAPK_RevD_3 | 74 | 88 | PF00069 | 0.396 |
DOC_PP2B_LxvP_1 | 293 | 296 | PF13499 | 0.433 |
DOC_PP2B_LxvP_1 | 774 | 777 | PF13499 | 0.490 |
DOC_PP4_FxxP_1 | 577 | 580 | PF00568 | 0.422 |
DOC_PP4_FxxP_1 | 621 | 624 | PF00568 | 0.469 |
DOC_USP7_MATH_1 | 105 | 109 | PF00917 | 0.395 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 634 | 638 | PF00917 | 0.458 |
DOC_USP7_MATH_1 | 653 | 657 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 707 | 711 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 739 | 743 | PF00917 | 0.345 |
DOC_USP7_MATH_1 | 791 | 795 | PF00917 | 0.546 |
DOC_WW_Pin1_4 | 110 | 115 | PF00397 | 0.396 |
DOC_WW_Pin1_4 | 249 | 254 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.464 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 604 | 609 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 714 | 719 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 727 | 732 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 735 | 740 | PF00397 | 0.495 |
DOC_WW_Pin1_4 | 794 | 799 | PF00397 | 0.421 |
LIG_14-3-3_CanoR_1 | 244 | 250 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 395 | 401 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 467 | 476 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 51 | 56 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 534 | 538 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 73 | 82 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 87 | 96 | PF00244 | 0.390 |
LIG_Actin_WH2_2 | 305 | 320 | PF00022 | 0.469 |
LIG_BIR_III_2 | 56 | 60 | PF00653 | 0.399 |
LIG_BIR_III_4 | 782 | 786 | PF00653 | 0.427 |
LIG_BRCT_BRCA1_1 | 111 | 115 | PF00533 | 0.397 |
LIG_BRCT_BRCA1_1 | 375 | 379 | PF00533 | 0.447 |
LIG_BRCT_BRCA1_1 | 690 | 694 | PF00533 | 0.471 |
LIG_BRCT_BRCA1_1 | 77 | 81 | PF00533 | 0.388 |
LIG_BRCT_BRCA1_2 | 375 | 381 | PF00533 | 0.422 |
LIG_CtBP_PxDLS_1 | 608 | 612 | PF00389 | 0.376 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.395 |
LIG_deltaCOP1_diTrp_1 | 328 | 333 | PF00928 | 0.463 |
LIG_EH_1 | 264 | 268 | PF12763 | 0.490 |
LIG_eIF4E_1 | 729 | 735 | PF01652 | 0.469 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.490 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.497 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.389 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.497 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.483 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.390 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.450 |
LIG_FHA_1 | 721 | 727 | PF00498 | 0.480 |
LIG_FHA_1 | 741 | 747 | PF00498 | 0.440 |
LIG_FHA_1 | 810 | 816 | PF00498 | 0.692 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.389 |
LIG_FHA_2 | 218 | 224 | PF00498 | 0.541 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.469 |
LIG_FHA_2 | 527 | 533 | PF00498 | 0.447 |
LIG_LIR_Gen_1 | 200 | 210 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 251 | 261 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 628 | 634 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 691 | 702 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 730 | 740 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 789 | 800 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 99 | 105 | PF02991 | 0.386 |
LIG_LIR_LC3C_4 | 228 | 233 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 200 | 205 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 251 | 257 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 342 | 348 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 628 | 632 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 691 | 697 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 730 | 735 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 78 | 84 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 789 | 795 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 99 | 104 | PF02991 | 0.389 |
LIG_LYPXL_yS_3 | 68 | 71 | PF13949 | 0.383 |
LIG_MYND_1 | 134 | 138 | PF01753 | 0.408 |
LIG_NRBOX | 213 | 219 | PF00104 | 0.436 |
LIG_Pex14_2 | 420 | 424 | PF04695 | 0.490 |
LIG_PTB_Apo_2 | 489 | 496 | PF02174 | 0.422 |
LIG_Rb_pABgroove_1 | 674 | 682 | PF01858 | 0.483 |
LIG_SH2_CRK | 254 | 258 | PF00017 | 0.376 |
LIG_SH2_CRK | 629 | 633 | PF00017 | 0.461 |
LIG_SH2_CRK | 732 | 736 | PF00017 | 0.537 |
LIG_SH2_NCK_1 | 254 | 258 | PF00017 | 0.422 |
LIG_SH2_NCK_1 | 629 | 633 | PF00017 | 0.469 |
LIG_SH2_SRC | 445 | 448 | PF00017 | 0.422 |
LIG_SH2_STAP1 | 629 | 633 | PF00017 | 0.469 |
LIG_SH2_STAP1 | 740 | 744 | PF00017 | 0.394 |
LIG_SH2_STAP1 | 85 | 89 | PF00017 | 0.410 |
LIG_SH2_STAT3 | 485 | 488 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 392 | 395 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 729 | 732 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.411 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.399 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.422 |
LIG_SH3_3 | 247 | 253 | PF00018 | 0.391 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.463 |
LIG_SH3_3 | 341 | 347 | PF00018 | 0.522 |
LIG_SH3_3 | 522 | 528 | PF00018 | 0.447 |
LIG_SH3_3 | 56 | 62 | PF00018 | 0.396 |
LIG_SUMO_SIM_anti_2 | 288 | 294 | PF11976 | 0.490 |
LIG_SUMO_SIM_anti_2 | 506 | 513 | PF11976 | 0.422 |
LIG_SUMO_SIM_par_1 | 230 | 235 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 358 | 364 | PF11976 | 0.376 |
LIG_TRAF2_1 | 528 | 531 | PF00917 | 0.469 |
LIG_WW_2 | 295 | 298 | PF00397 | 0.447 |
MOD_CDK_SPxxK_3 | 110 | 117 | PF00069 | 0.398 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.395 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.510 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.463 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.490 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.458 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.496 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.492 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.485 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.433 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.571 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.403 |
MOD_CK1_1 | 689 | 695 | PF00069 | 0.508 |
MOD_CK1_1 | 77 | 83 | PF00069 | 0.484 |
MOD_CK1_1 | 794 | 800 | PF00069 | 0.422 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.397 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.532 |
MOD_CK2_1 | 526 | 532 | PF00069 | 0.447 |
MOD_CK2_1 | 697 | 703 | PF00069 | 0.438 |
MOD_CMANNOS | 537 | 540 | PF00535 | 0.269 |
MOD_Cter_Amidation | 119 | 122 | PF01082 | 0.406 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.566 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.394 |
MOD_GlcNHglycan | 223 | 227 | PF01048 | 0.300 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.223 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.261 |
MOD_GlcNHglycan | 354 | 358 | PF01048 | 0.301 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.273 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.330 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.301 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.287 |
MOD_GlcNHglycan | 645 | 648 | PF01048 | 0.247 |
MOD_GlcNHglycan | 683 | 686 | PF01048 | 0.290 |
MOD_GlcNHglycan | 688 | 691 | PF01048 | 0.253 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.412 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.371 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.487 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.532 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.558 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.579 |
MOD_GSK3_1 | 349 | 356 | PF00069 | 0.497 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.555 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.407 |
MOD_GSK3_1 | 399 | 406 | PF00069 | 0.435 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.548 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.371 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.509 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.440 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.452 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.559 |
MOD_GSK3_1 | 643 | 650 | PF00069 | 0.423 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.489 |
MOD_GSK3_1 | 735 | 742 | PF00069 | 0.430 |
MOD_GSK3_1 | 794 | 801 | PF00069 | 0.536 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.406 |
MOD_N-GLC_1 | 373 | 378 | PF02516 | 0.269 |
MOD_N-GLC_1 | 647 | 652 | PF02516 | 0.225 |
MOD_N-GLC_1 | 798 | 803 | PF02516 | 0.489 |
MOD_N-GLC_2 | 706 | 708 | PF02516 | 0.176 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.378 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.498 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.492 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.515 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.535 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.535 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.459 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.436 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.554 |
MOD_NEK2_1 | 611 | 616 | PF00069 | 0.469 |
MOD_NEK2_1 | 642 | 647 | PF00069 | 0.428 |
MOD_NEK2_1 | 679 | 684 | PF00069 | 0.454 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.389 |
MOD_NEK2_2 | 239 | 244 | PF00069 | 0.492 |
MOD_NEK2_2 | 46 | 51 | PF00069 | 0.397 |
MOD_OFUCOSY | 103 | 109 | PF10250 | 0.381 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.389 |
MOD_PIKK_1 | 332 | 338 | PF00454 | 0.447 |
MOD_PIKK_1 | 484 | 490 | PF00454 | 0.423 |
MOD_PIKK_1 | 647 | 653 | PF00454 | 0.483 |
MOD_PIKK_1 | 720 | 726 | PF00454 | 0.438 |
MOD_PIKK_1 | 88 | 94 | PF00454 | 0.397 |
MOD_PK_1 | 51 | 57 | PF00069 | 0.411 |
MOD_PKA_1 | 244 | 250 | PF00069 | 0.438 |
MOD_PKA_1 | 822 | 828 | PF00069 | 0.527 |
MOD_PKA_1 | 87 | 93 | PF00069 | 0.403 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.469 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.512 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.489 |
MOD_PKA_2 | 465 | 471 | PF00069 | 0.509 |
MOD_PKA_2 | 533 | 539 | PF00069 | 0.476 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.409 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.522 |
MOD_Plk_1 | 222 | 228 | PF00069 | 0.490 |
MOD_Plk_1 | 479 | 485 | PF00069 | 0.439 |
MOD_Plk_1 | 634 | 640 | PF00069 | 0.497 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.515 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.474 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.439 |
MOD_Plk_4 | 689 | 695 | PF00069 | 0.455 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.380 |
MOD_Plk_4 | 791 | 797 | PF00069 | 0.384 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.506 |
MOD_ProDKin_1 | 110 | 116 | PF00069 | 0.395 |
MOD_ProDKin_1 | 249 | 255 | PF00069 | 0.446 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.464 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.489 |
MOD_ProDKin_1 | 604 | 610 | PF00069 | 0.390 |
MOD_ProDKin_1 | 714 | 720 | PF00069 | 0.471 |
MOD_ProDKin_1 | 727 | 733 | PF00069 | 0.506 |
MOD_ProDKin_1 | 735 | 741 | PF00069 | 0.495 |
MOD_ProDKin_1 | 794 | 800 | PF00069 | 0.417 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 618 | 621 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 629 | 632 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 68 | 71 | PF00928 | 0.383 |
TRG_ENDOCYTIC_2 | 732 | 735 | PF00928 | 0.488 |
TRG_ER_diArg_1 | 116 | 119 | PF00400 | 0.405 |
TRG_ER_diArg_1 | 121 | 124 | PF00400 | 0.404 |
TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.450 |
TRG_ER_diArg_1 | 185 | 188 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 243 | 245 | PF00400 | 0.474 |
TRG_ER_diArg_1 | 465 | 467 | PF00400 | 0.519 |
TRG_ER_diArg_1 | 618 | 620 | PF00400 | 0.376 |
TRG_ER_diArg_1 | 805 | 808 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 821 | 824 | PF00400 | 0.658 |
TRG_NES_CRM1_1 | 223 | 237 | PF08389 | 0.490 |
TRG_NLS_MonoExtC_3 | 821 | 826 | PF00514 | 0.585 |
TRG_NLS_MonoExtN_4 | 821 | 826 | PF00514 | 0.585 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3C9 | Leptomonas seymouri | 49% | 100% |
A0A0S4JE96 | Bodo saltans | 29% | 100% |
A0A3Q8IMS2 | Leishmania donovani | 90% | 100% |
A4HM15 | Leishmania braziliensis | 73% | 100% |
A4I9E7 | Leishmania infantum | 90% | 100% |
C9ZJR8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9B4E6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q8H1D9 | Arabidopsis thaliana | 25% | 100% |