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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 9 |
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 | 10 |
GO:0000109 | nucleotide-excision repair complex | 3 | 1 |
GO:0000111 | nucleotide-excision repair factor 2 complex | 4 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0071942 | XPC complex | 4 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: E9B6M4
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006259 | DNA metabolic process | 4 | 10 |
GO:0006281 | DNA repair | 5 | 10 |
GO:0006289 | nucleotide-excision repair | 6 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0006950 | response to stress | 2 | 10 |
GO:0006974 | DNA damage response | 4 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0033554 | cellular response to stress | 3 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0050896 | response to stimulus | 1 | 10 |
GO:0051716 | cellular response to stimulus | 2 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
GO:0006298 | mismatch repair | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003677 | DNA binding | 4 | 10 |
GO:0003684 | damaged DNA binding | 5 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0003697 | single-stranded DNA binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 400 | 404 | PF00656 | 0.753 |
CLV_C14_Caspase3-7 | 460 | 464 | PF00656 | 0.508 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.658 |
CLV_NRD_NRD_1 | 415 | 417 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 534 | 536 | PF00675 | 0.330 |
CLV_NRD_NRD_1 | 741 | 743 | PF00675 | 0.247 |
CLV_NRD_NRD_1 | 757 | 759 | PF00675 | 0.247 |
CLV_NRD_NRD_1 | 763 | 765 | PF00675 | 0.247 |
CLV_NRD_NRD_1 | 803 | 805 | PF00675 | 0.327 |
CLV_PCSK_FUR_1 | 427 | 431 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.732 |
CLV_PCSK_KEX2_1 | 415 | 417 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 429 | 431 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 449 | 451 | PF00082 | 0.155 |
CLV_PCSK_KEX2_1 | 534 | 536 | PF00082 | 0.314 |
CLV_PCSK_KEX2_1 | 641 | 643 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 741 | 743 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 756 | 758 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 763 | 765 | PF00082 | 0.250 |
CLV_PCSK_KEX2_1 | 802 | 804 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 822 | 824 | PF00082 | 0.234 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.582 |
CLV_PCSK_PC1ET2_1 | 158 | 160 | PF00082 | 0.648 |
CLV_PCSK_PC1ET2_1 | 195 | 197 | PF00082 | 0.642 |
CLV_PCSK_PC1ET2_1 | 209 | 211 | PF00082 | 0.731 |
CLV_PCSK_PC1ET2_1 | 429 | 431 | PF00082 | 0.469 |
CLV_PCSK_PC1ET2_1 | 449 | 451 | PF00082 | 0.155 |
CLV_PCSK_PC1ET2_1 | 641 | 643 | PF00082 | 0.247 |
CLV_PCSK_PC1ET2_1 | 802 | 804 | PF00082 | 0.314 |
CLV_PCSK_PC1ET2_1 | 822 | 824 | PF00082 | 0.234 |
CLV_PCSK_PC1ET2_1 | 90 | 92 | PF00082 | 0.582 |
CLV_PCSK_PC7_1 | 430 | 436 | PF00082 | 0.385 |
CLV_PCSK_PC7_1 | 637 | 643 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.632 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.688 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 470 | 474 | PF00082 | 0.300 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.689 |
CLV_PCSK_SKI1_1 | 659 | 663 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 741 | 745 | PF00082 | 0.302 |
CLV_Separin_Metazoa | 560 | 564 | PF03568 | 0.502 |
DEG_APCC_DBOX_1 | 414 | 422 | PF00400 | 0.732 |
DEG_APCC_DBOX_1 | 605 | 613 | PF00400 | 0.444 |
DEG_SPOP_SBC_1 | 289 | 293 | PF00917 | 0.500 |
DEG_SPOP_SBC_1 | 571 | 575 | PF00917 | 0.467 |
DEG_SPOP_SBC_1 | 97 | 101 | PF00917 | 0.457 |
DOC_CYCLIN_RxL_1 | 467 | 475 | PF00134 | 0.372 |
DOC_CYCLIN_yCln2_LP_2 | 283 | 289 | PF00134 | 0.371 |
DOC_CYCLIN_yCln2_LP_2 | 346 | 352 | PF00134 | 0.367 |
DOC_MAPK_gen_1 | 195 | 202 | PF00069 | 0.315 |
DOC_MAPK_gen_1 | 415 | 423 | PF00069 | 0.705 |
DOC_MAPK_gen_1 | 641 | 648 | PF00069 | 0.447 |
DOC_MAPK_gen_1 | 738 | 747 | PF00069 | 0.447 |
DOC_MAPK_gen_1 | 90 | 97 | PF00069 | 0.395 |
DOC_MAPK_MEF2A_6 | 195 | 202 | PF00069 | 0.331 |
DOC_MAPK_MEF2A_6 | 738 | 747 | PF00069 | 0.447 |
DOC_MAPK_NFAT4_5 | 195 | 203 | PF00069 | 0.336 |
DOC_PP1_RVXF_1 | 180 | 186 | PF00149 | 0.333 |
DOC_PP1_RVXF_1 | 742 | 748 | PF00149 | 0.530 |
DOC_PP2B_LxvP_1 | 200 | 203 | PF13499 | 0.362 |
DOC_PP2B_LxvP_1 | 283 | 286 | PF13499 | 0.372 |
DOC_PP2B_LxvP_1 | 344 | 347 | PF13499 | 0.333 |
DOC_PP4_FxxP_1 | 680 | 683 | PF00568 | 0.599 |
DOC_PP4_MxPP_1 | 241 | 244 | PF00568 | 0.300 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 494 | 498 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 571 | 575 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 644 | 648 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 681 | 685 | PF00917 | 0.585 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.460 |
LIG_14-3-3_CanoR_1 | 159 | 167 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 218 | 227 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 295 | 300 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 337 | 344 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 434 | 442 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 563 | 567 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 586 | 592 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 659 | 669 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 689 | 694 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 713 | 717 | PF00244 | 0.528 |
LIG_Actin_WH2_2 | 641 | 658 | PF00022 | 0.495 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.489 |
LIG_BIR_III_2 | 517 | 521 | PF00653 | 0.530 |
LIG_BRCT_BRCA1_1 | 352 | 356 | PF00533 | 0.353 |
LIG_BRCT_BRCA1_1 | 676 | 680 | PF00533 | 0.572 |
LIG_Clathr_ClatBox_1 | 106 | 110 | PF01394 | 0.538 |
LIG_deltaCOP1_diTrp_1 | 480 | 489 | PF00928 | 0.465 |
LIG_eIF4E_1 | 788 | 794 | PF01652 | 0.425 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.396 |
LIG_FHA_1 | 505 | 511 | PF00498 | 0.447 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.541 |
LIG_FHA_1 | 563 | 569 | PF00498 | 0.512 |
LIG_FHA_1 | 571 | 577 | PF00498 | 0.465 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.424 |
LIG_FHA_1 | 777 | 783 | PF00498 | 0.504 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.569 |
LIG_FHA_2 | 375 | 381 | PF00498 | 0.696 |
LIG_FHA_2 | 699 | 705 | PF00498 | 0.604 |
LIG_GBD_Chelix_1 | 175 | 183 | PF00786 | 0.544 |
LIG_LIR_Apic_2 | 316 | 321 | PF02991 | 0.375 |
LIG_LIR_Apic_2 | 677 | 683 | PF02991 | 0.603 |
LIG_LIR_Gen_1 | 122 | 129 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 142 | 149 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 169 | 179 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 221 | 231 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 33 | 42 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 353 | 363 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 475 | 484 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 487 | 494 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 714 | 725 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 789 | 795 | PF02991 | 0.587 |
LIG_LIR_LC3C_4 | 366 | 371 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 122 | 126 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 169 | 175 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 221 | 227 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 33 | 37 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 353 | 359 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 475 | 481 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 487 | 492 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 692 | 698 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 714 | 720 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 789 | 794 | PF02991 | 0.505 |
LIG_MYND_1 | 248 | 252 | PF01753 | 0.359 |
LIG_NBox_RRM_1 | 226 | 236 | PF00076 | 0.360 |
LIG_NRBOX | 170 | 176 | PF00104 | 0.352 |
LIG_Pex14_1 | 502 | 506 | PF04695 | 0.465 |
LIG_Pex14_2 | 352 | 356 | PF04695 | 0.344 |
LIG_PTB_Apo_2 | 275 | 282 | PF02174 | 0.339 |
LIG_SH2_CRK | 669 | 673 | PF00017 | 0.558 |
LIG_SH2_NCK_1 | 304 | 308 | PF00017 | 0.466 |
LIG_SH2_NCK_1 | 526 | 530 | PF00017 | 0.447 |
LIG_SH2_PTP2 | 224 | 227 | PF00017 | 0.368 |
LIG_SH2_PTP2 | 717 | 720 | PF00017 | 0.447 |
LIG_SH2_SRC | 530 | 533 | PF00017 | 0.515 |
LIG_SH2_STAP1 | 145 | 149 | PF00017 | 0.331 |
LIG_SH2_STAP1 | 506 | 510 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 526 | 530 | PF00017 | 0.355 |
LIG_SH2_STAP1 | 593 | 597 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 788 | 792 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 506 | 509 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 522 | 525 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 610 | 613 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 717 | 720 | PF00017 | 0.447 |
LIG_SH3_3 | 126 | 132 | PF00018 | 0.473 |
LIG_SH3_3 | 283 | 289 | PF00018 | 0.494 |
LIG_SH3_3 | 318 | 324 | PF00018 | 0.436 |
LIG_SH3_3 | 34 | 40 | PF00018 | 0.464 |
LIG_SH3_3 | 565 | 571 | PF00018 | 0.502 |
LIG_SH3_3 | 668 | 674 | PF00018 | 0.539 |
LIG_SH3_3 | 691 | 697 | PF00018 | 0.535 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.560 |
LIG_SH3_3 | 703 | 709 | PF00018 | 0.577 |
LIG_SUMO_SIM_anti_2 | 778 | 786 | PF11976 | 0.502 |
LIG_SUMO_SIM_anti_2 | 789 | 797 | PF11976 | 0.482 |
LIG_SUMO_SIM_anti_2 | 93 | 101 | PF11976 | 0.382 |
LIG_SUMO_SIM_par_1 | 419 | 425 | PF11976 | 0.664 |
LIG_SUMO_SIM_par_1 | 505 | 511 | PF11976 | 0.502 |
LIG_SUMO_SIM_par_1 | 643 | 650 | PF11976 | 0.543 |
LIG_SUMO_SIM_par_1 | 789 | 797 | PF11976 | 0.433 |
LIG_TRAF2_1 | 19 | 22 | PF00917 | 0.478 |
LIG_TRAF2_1 | 787 | 790 | PF00917 | 0.537 |
LIG_UBA3_1 | 273 | 282 | PF00899 | 0.419 |
LIG_UBA3_1 | 818 | 822 | PF00899 | 0.490 |
MOD_CDK_SPK_2 | 516 | 521 | PF00069 | 0.284 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.466 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.722 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.467 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.386 |
MOD_CK1_1 | 497 | 503 | PF00069 | 0.336 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.513 |
MOD_CK1_1 | 524 | 530 | PF00069 | 0.353 |
MOD_CK1_1 | 647 | 653 | PF00069 | 0.420 |
MOD_CK1_1 | 660 | 666 | PF00069 | 0.467 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.723 |
MOD_CK2_1 | 306 | 312 | PF00069 | 0.546 |
MOD_CK2_1 | 374 | 380 | PF00069 | 0.550 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.655 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.681 |
MOD_Cter_Amidation | 532 | 535 | PF01082 | 0.400 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.474 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.388 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.772 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.697 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.624 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.695 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.428 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.360 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.708 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.346 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.308 |
MOD_GlcNHglycan | 642 | 645 | PF01048 | 0.284 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.638 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.673 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.786 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.627 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.503 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.690 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.479 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.622 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.318 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.413 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.600 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.284 |
MOD_GSK3_1 | 640 | 647 | PF00069 | 0.284 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.752 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.702 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.695 |
MOD_N-GLC_1 | 17 | 22 | PF02516 | 0.762 |
MOD_N-GLC_1 | 263 | 268 | PF02516 | 0.373 |
MOD_N-GLC_1 | 395 | 400 | PF02516 | 0.747 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.743 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.466 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.399 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.581 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.179 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.418 |
MOD_NEK2_1 | 562 | 567 | PF00069 | 0.360 |
MOD_NEK2_2 | 185 | 190 | PF00069 | 0.462 |
MOD_NEK2_2 | 363 | 368 | PF00069 | 0.360 |
MOD_NEK2_2 | 644 | 649 | PF00069 | 0.446 |
MOD_NEK2_2 | 78 | 83 | PF00069 | 0.614 |
MOD_PIKK_1 | 374 | 380 | PF00454 | 0.502 |
MOD_PIKK_1 | 689 | 695 | PF00454 | 0.456 |
MOD_PIKK_1 | 729 | 735 | PF00454 | 0.393 |
MOD_PK_1 | 295 | 301 | PF00069 | 0.464 |
MOD_PK_1 | 419 | 425 | PF00069 | 0.690 |
MOD_PKA_1 | 158 | 164 | PF00069 | 0.550 |
MOD_PKA_1 | 218 | 224 | PF00069 | 0.396 |
MOD_PKA_1 | 246 | 252 | PF00069 | 0.515 |
MOD_PKA_1 | 430 | 436 | PF00069 | 0.658 |
MOD_PKA_1 | 756 | 762 | PF00069 | 0.346 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.682 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.439 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.530 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.462 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.571 |
MOD_PKA_2 | 433 | 439 | PF00069 | 0.508 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.338 |
MOD_PKA_2 | 485 | 491 | PF00069 | 0.344 |
MOD_PKA_2 | 562 | 568 | PF00069 | 0.400 |
MOD_PKA_2 | 582 | 588 | PF00069 | 0.155 |
MOD_PKA_2 | 712 | 718 | PF00069 | 0.400 |
MOD_PKA_2 | 756 | 762 | PF00069 | 0.319 |
MOD_Plk_1 | 316 | 322 | PF00069 | 0.502 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.565 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.594 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.424 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.608 |
MOD_Plk_4 | 485 | 491 | PF00069 | 0.314 |
MOD_Plk_4 | 497 | 503 | PF00069 | 0.243 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.643 |
MOD_Plk_4 | 587 | 593 | PF00069 | 0.447 |
MOD_Plk_4 | 682 | 688 | PF00069 | 0.487 |
MOD_Plk_4 | 712 | 718 | PF00069 | 0.400 |
MOD_Plk_4 | 766 | 772 | PF00069 | 0.331 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.554 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.302 |
MOD_SUMO_for_1 | 102 | 105 | PF00179 | 0.430 |
MOD_SUMO_for_1 | 281 | 284 | PF00179 | 0.335 |
MOD_SUMO_for_1 | 71 | 74 | PF00179 | 0.686 |
MOD_SUMO_for_1 | 82 | 85 | PF00179 | 0.703 |
MOD_SUMO_rev_2 | 454 | 464 | PF00179 | 0.405 |
MOD_SUMO_rev_2 | 465 | 469 | PF00179 | 0.392 |
TRG_DiLeu_BaEn_1 | 150 | 155 | PF01217 | 0.431 |
TRG_DiLeu_BaEn_1 | 53 | 58 | PF01217 | 0.553 |
TRG_DiLeu_BaEn_1 | 657 | 662 | PF01217 | 0.504 |
TRG_DiLeu_BaEn_1 | 789 | 794 | PF01217 | 0.480 |
TRG_DiLeu_BaEn_2 | 484 | 490 | PF01217 | 0.400 |
TRG_DiLeu_BaLyEn_6 | 179 | 184 | PF01217 | 0.430 |
TRG_DiLeu_BaLyEn_6 | 193 | 198 | PF01217 | 0.389 |
TRG_DiLeu_BaLyEn_6 | 814 | 819 | PF01217 | 0.424 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 669 | 672 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 717 | 720 | PF00928 | 0.284 |
TRG_ER_diArg_1 | 138 | 141 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 179 | 182 | PF00400 | 0.394 |
TRG_ER_diArg_1 | 203 | 206 | PF00400 | 0.641 |
TRG_ER_diArg_1 | 415 | 417 | PF00400 | 0.714 |
TRG_ER_diArg_1 | 450 | 453 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 534 | 536 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 648 | 651 | PF00400 | 0.358 |
TRG_ER_diArg_1 | 741 | 743 | PF00400 | 0.284 |
TRG_ER_diArg_1 | 756 | 758 | PF00400 | 0.284 |
TRG_ER_diArg_1 | 803 | 806 | PF00400 | 0.422 |
TRG_NES_CRM1_1 | 735 | 746 | PF08389 | 0.400 |
TRG_NLS_Bipartite_1 | 195 | 213 | PF00514 | 0.432 |
TRG_NLS_Bipartite_1 | 434 | 453 | PF00514 | 0.502 |
TRG_NLS_MonoExtC_3 | 208 | 214 | PF00514 | 0.702 |
TRG_NLS_MonoExtC_3 | 448 | 453 | PF00514 | 0.379 |
TRG_NLS_MonoExtC_3 | 801 | 806 | PF00514 | 0.377 |
TRG_NLS_MonoExtN_4 | 206 | 213 | PF00514 | 0.645 |
TRG_NLS_MonoExtN_4 | 446 | 453 | PF00514 | 0.393 |
TRG_Pf-PMV_PEXEL_1 | 118 | 122 | PF00026 | 0.680 |
TRG_Pf-PMV_PEXEL_1 | 182 | 187 | PF00026 | 0.381 |
TRG_Pf-PMV_PEXEL_1 | 543 | 548 | PF00026 | 0.380 |
TRG_Pf-PMV_PEXEL_1 | 556 | 560 | PF00026 | 0.433 |
TRG_Pf-PMV_PEXEL_1 | 659 | 664 | PF00026 | 0.456 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4G5 | Leptomonas seymouri | 64% | 95% |
A0A1X0P5A4 | Trypanosomatidae | 40% | 100% |
A0A3Q8IJN2 | Leishmania donovani | 92% | 100% |
A0A3R7KHS6 | Trypanosoma rangeli | 42% | 100% |
A4HN12 | Leishmania braziliensis | 81% | 100% |
A4IBN5 | Leishmania infantum | 91% | 100% |
C9ZYZ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AFG9 | Leishmania major | 91% | 100% |