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:0032300 | mismatch repair complex | 2 | 10 |
GO:0032991 | protein-containing complex | 1 | 10 |
GO:0032389 | MutLalpha complex | 3 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A4HMI7
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:0006298 | mismatch 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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003677 | DNA binding | 4 | 10 |
GO:0003690 | double-stranded DNA binding | 5 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0008094 | ATP-dependent activity, acting on DNA | 2 | 10 |
GO:0016462 | pyrophosphatase activity | 5 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 10 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 10 |
GO:0016887 | ATP hydrolysis activity | 7 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0030983 | mismatched DNA binding | 6 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 10 |
GO:0140299 | small molecule sensor activity | 1 | 10 |
GO:0140612 | DNA damage sensor activity | 2 | 10 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 10 |
GO:0140657 | ATP-dependent activity | 1 | 10 |
GO:0140664 | ATP-dependent DNA damage sensor activity | 3 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 435 | 439 | PF00656 | 0.590 |
CLV_C14_Caspase3-7 | 509 | 513 | PF00656 | 0.685 |
CLV_C14_Caspase3-7 | 544 | 548 | PF00656 | 0.512 |
CLV_C14_Caspase3-7 | 565 | 569 | PF00656 | 0.519 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.406 |
CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.299 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.586 |
CLV_PCSK_KEX2_1 | 622 | 624 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 798 | 800 | PF00082 | 0.541 |
CLV_PCSK_PC1ET2_1 | 360 | 362 | PF00082 | 0.299 |
CLV_PCSK_PC1ET2_1 | 430 | 432 | PF00082 | 0.704 |
CLV_PCSK_PC1ET2_1 | 622 | 624 | PF00082 | 0.540 |
CLV_PCSK_PC1ET2_1 | 798 | 800 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.286 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.231 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 719 | 723 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 798 | 802 | PF00082 | 0.505 |
CLV_Separin_Metazoa | 831 | 835 | PF03568 | 0.381 |
DEG_APCC_DBOX_1 | 819 | 827 | PF00400 | 0.436 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.516 |
DEG_SIAH_1 | 610 | 618 | PF03145 | 0.504 |
DEG_SPOP_SBC_1 | 461 | 465 | PF00917 | 0.761 |
DEG_SPOP_SBC_1 | 504 | 508 | PF00917 | 0.694 |
DOC_AGCK_PIF_1 | 424 | 429 | PF00069 | 0.534 |
DOC_CDC14_PxL_1 | 311 | 319 | PF14671 | 0.420 |
DOC_CKS1_1 | 238 | 243 | PF01111 | 0.535 |
DOC_CKS1_1 | 415 | 420 | PF01111 | 0.435 |
DOC_CKS1_1 | 791 | 796 | PF01111 | 0.462 |
DOC_CYCLIN_RxL_1 | 359 | 369 | PF00134 | 0.377 |
DOC_CYCLIN_yCln2_LP_2 | 699 | 705 | PF00134 | 0.377 |
DOC_MAPK_gen_1 | 360 | 366 | PF00069 | 0.209 |
DOC_MAPK_gen_1 | 783 | 791 | PF00069 | 0.321 |
DOC_MAPK_gen_1 | 798 | 804 | PF00069 | 0.393 |
DOC_MAPK_MEF2A_6 | 37 | 45 | PF00069 | 0.462 |
DOC_PP1_RVXF_1 | 273 | 279 | PF00149 | 0.321 |
DOC_PP2B_LxvP_1 | 699 | 702 | PF13499 | 0.420 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 459 | 463 | PF00917 | 0.763 |
DOC_USP7_MATH_1 | 504 | 508 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 784 | 788 | PF00917 | 0.321 |
DOC_USP7_UBL2_3 | 208 | 212 | PF12436 | 0.505 |
DOC_USP7_UBL2_3 | 645 | 649 | PF12436 | 0.420 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.423 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 496 | 501 | PF00397 | 0.761 |
DOC_WW_Pin1_4 | 692 | 697 | PF00397 | 0.404 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 790 | 795 | PF00397 | 0.431 |
LIG_14-3-3_CanoR_1 | 165 | 169 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 259 | 268 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 275 | 281 | PF00244 | 0.316 |
LIG_14-3-3_CanoR_1 | 297 | 305 | PF00244 | 0.266 |
LIG_14-3-3_CanoR_1 | 416 | 424 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 523 | 528 | PF00244 | 0.734 |
LIG_14-3-3_CanoR_1 | 576 | 584 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 625 | 631 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 834 | 840 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 87 | 94 | PF00244 | 0.494 |
LIG_Actin_WH2_2 | 570 | 587 | PF00022 | 0.516 |
LIG_Actin_WH2_2 | 60 | 78 | PF00022 | 0.330 |
LIG_BIR_III_4 | 449 | 453 | PF00653 | 0.502 |
LIG_BRCT_BRCA1_1 | 132 | 136 | PF00533 | 0.521 |
LIG_BRCT_BRCA1_1 | 278 | 282 | PF00533 | 0.423 |
LIG_eIF4E_1 | 683 | 689 | PF01652 | 0.462 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.513 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.462 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.379 |
LIG_FHA_1 | 172 | 178 | PF00498 | 0.405 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.305 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.399 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.404 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.248 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.196 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.572 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.524 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.604 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.729 |
LIG_FHA_1 | 541 | 547 | PF00498 | 0.657 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.576 |
LIG_FHA_1 | 707 | 713 | PF00498 | 0.209 |
LIG_FHA_1 | 768 | 774 | PF00498 | 0.377 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.523 |
LIG_FHA_1 | 820 | 826 | PF00498 | 0.484 |
LIG_FHA_2 | 487 | 493 | PF00498 | 0.795 |
LIG_FHA_2 | 529 | 535 | PF00498 | 0.530 |
LIG_FHA_2 | 563 | 569 | PF00498 | 0.520 |
LIG_FHA_2 | 595 | 601 | PF00498 | 0.629 |
LIG_FHA_2 | 633 | 639 | PF00498 | 0.500 |
LIG_LIR_Apic_2 | 455 | 459 | PF02991 | 0.503 |
LIG_LIR_Apic_2 | 811 | 817 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 422 | 432 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 262 | 268 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 279 | 285 | PF02991 | 0.197 |
LIG_LIR_Nem_3 | 422 | 427 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 597 | 601 | PF02991 | 0.534 |
LIG_MYND_1 | 500 | 504 | PF01753 | 0.797 |
LIG_MYND_1 | 538 | 542 | PF01753 | 0.539 |
LIG_Pex14_1 | 278 | 282 | PF04695 | 0.321 |
LIG_Pex14_2 | 657 | 661 | PF04695 | 0.309 |
LIG_RPA_C_Fungi | 171 | 183 | PF08784 | 0.331 |
LIG_SH2_CRK | 265 | 269 | PF00017 | 0.420 |
LIG_SH2_CRK | 741 | 745 | PF00017 | 0.356 |
LIG_SH2_CRK | 748 | 752 | PF00017 | 0.331 |
LIG_SH2_CRK | 766 | 770 | PF00017 | 0.321 |
LIG_SH2_GRB2like | 642 | 645 | PF00017 | 0.392 |
LIG_SH2_NCK_1 | 100 | 104 | PF00017 | 0.480 |
LIG_SH2_NCK_1 | 748 | 752 | PF00017 | 0.321 |
LIG_SH2_SRC | 168 | 171 | PF00017 | 0.378 |
LIG_SH2_STAP1 | 168 | 172 | PF00017 | 0.483 |
LIG_SH2_STAP1 | 352 | 356 | PF00017 | 0.321 |
LIG_SH2_STAP1 | 477 | 481 | PF00017 | 0.642 |
LIG_SH2_STAP1 | 685 | 689 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.572 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.671 |
LIG_SH2_STAT5 | 642 | 645 | PF00017 | 0.477 |
LIG_SH3_1 | 741 | 747 | PF00018 | 0.462 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.493 |
LIG_SH3_3 | 309 | 315 | PF00018 | 0.321 |
LIG_SH3_3 | 599 | 605 | PF00018 | 0.707 |
LIG_SH3_3 | 611 | 617 | PF00018 | 0.622 |
LIG_SH3_3 | 741 | 747 | PF00018 | 0.345 |
LIG_SUMO_SIM_par_1 | 148 | 154 | PF11976 | 0.294 |
LIG_SUMO_SIM_par_1 | 242 | 250 | PF11976 | 0.447 |
LIG_SUMO_SIM_par_1 | 362 | 369 | PF11976 | 0.209 |
LIG_TRAF2_1 | 379 | 382 | PF00917 | 0.438 |
LIG_TRAF2_1 | 386 | 389 | PF00917 | 0.491 |
LIG_TRAF2_1 | 542 | 545 | PF00917 | 0.741 |
LIG_TYR_ITIM | 746 | 751 | PF00017 | 0.321 |
LIG_TYR_ITIM | 764 | 769 | PF00017 | 0.345 |
LIG_WRC_WIRS_1 | 472 | 477 | PF05994 | 0.646 |
MOD_CDK_SPK_2 | 496 | 501 | PF00069 | 0.547 |
MOD_CDK_SPxK_1 | 354 | 360 | PF00069 | 0.423 |
MOD_CDK_SPxxK_3 | 354 | 361 | PF00069 | 0.423 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.448 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.436 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.377 |
MOD_CK1_1 | 420 | 426 | PF00069 | 0.578 |
MOD_CK1_1 | 455 | 461 | PF00069 | 0.721 |
MOD_CK1_1 | 462 | 468 | PF00069 | 0.653 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.705 |
MOD_CK1_1 | 627 | 633 | PF00069 | 0.632 |
MOD_CK1_1 | 733 | 739 | PF00069 | 0.417 |
MOD_CK1_1 | 779 | 785 | PF00069 | 0.321 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.570 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.739 |
MOD_CK2_1 | 172 | 178 | PF00069 | 0.580 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.509 |
MOD_CK2_1 | 523 | 529 | PF00069 | 0.657 |
MOD_CK2_1 | 594 | 600 | PF00069 | 0.472 |
MOD_CK2_1 | 644 | 650 | PF00069 | 0.491 |
MOD_CK2_1 | 705 | 711 | PF00069 | 0.462 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.623 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.536 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.446 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.427 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.405 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.373 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.385 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.599 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.571 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.737 |
MOD_GlcNHglycan | 560 | 563 | PF01048 | 0.676 |
MOD_GlcNHglycan | 606 | 609 | PF01048 | 0.745 |
MOD_GlcNHglycan | 751 | 754 | PF01048 | 0.451 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.755 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.523 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.436 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.416 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.521 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.463 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.463 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.298 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.655 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.715 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.658 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.512 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.667 |
MOD_GSK3_1 | 701 | 708 | PF00069 | 0.423 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.528 |
MOD_N-GLC_1 | 276 | 281 | PF02516 | 0.356 |
MOD_N-GLC_1 | 330 | 335 | PF02516 | 0.420 |
MOD_N-GLC_1 | 346 | 351 | PF02516 | 0.420 |
MOD_N-GLC_1 | 354 | 359 | PF02516 | 0.414 |
MOD_N-GLC_2 | 551 | 553 | PF02516 | 0.492 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.561 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.209 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.420 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.557 |
MOD_NEK2_1 | 739 | 744 | PF00069 | 0.269 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.406 |
MOD_NEK2_2 | 160 | 165 | PF00069 | 0.563 |
MOD_NEK2_2 | 217 | 222 | PF00069 | 0.477 |
MOD_NEK2_2 | 39 | 44 | PF00069 | 0.209 |
MOD_NEK2_2 | 586 | 591 | PF00069 | 0.698 |
MOD_NEK2_2 | 835 | 840 | PF00069 | 0.456 |
MOD_OFUCOSY | 590 | 595 | PF10250 | 0.488 |
MOD_PIKK_1 | 112 | 118 | PF00454 | 0.758 |
MOD_PIKK_1 | 323 | 329 | PF00454 | 0.428 |
MOD_PIKK_1 | 330 | 336 | PF00454 | 0.413 |
MOD_PIKK_1 | 422 | 428 | PF00454 | 0.656 |
MOD_PK_1 | 523 | 529 | PF00069 | 0.642 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.464 |
MOD_PKA_2 | 296 | 302 | PF00069 | 0.321 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.658 |
MOD_PKA_2 | 575 | 581 | PF00069 | 0.695 |
MOD_PKA_2 | 624 | 630 | PF00069 | 0.680 |
MOD_PKA_2 | 730 | 736 | PF00069 | 0.461 |
MOD_PKA_2 | 785 | 791 | PF00069 | 0.310 |
MOD_PKA_2 | 819 | 825 | PF00069 | 0.317 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.520 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.587 |
MOD_PKB_1 | 623 | 631 | PF00069 | 0.580 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.513 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.345 |
MOD_Plk_1 | 276 | 282 | PF00069 | 0.262 |
MOD_Plk_1 | 346 | 352 | PF00069 | 0.414 |
MOD_Plk_1 | 572 | 578 | PF00069 | 0.741 |
MOD_Plk_2-3 | 126 | 132 | PF00069 | 0.485 |
MOD_Plk_2-3 | 517 | 523 | PF00069 | 0.529 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.321 |
MOD_Plk_4 | 452 | 458 | PF00069 | 0.778 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.509 |
MOD_Plk_4 | 785 | 791 | PF00069 | 0.321 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.484 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.423 |
MOD_ProDKin_1 | 414 | 420 | PF00069 | 0.581 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.605 |
MOD_ProDKin_1 | 496 | 502 | PF00069 | 0.762 |
MOD_ProDKin_1 | 692 | 698 | PF00069 | 0.404 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.564 |
MOD_ProDKin_1 | 790 | 796 | PF00069 | 0.431 |
MOD_SUMO_for_1 | 105 | 108 | PF00179 | 0.772 |
MOD_SUMO_rev_2 | 31 | 39 | PF00179 | 0.449 |
MOD_SUMO_rev_2 | 711 | 721 | PF00179 | 0.420 |
MOD_SUMO_rev_2 | 733 | 739 | PF00179 | 0.417 |
TRG_DiLeu_BaLyEn_6 | 41 | 46 | PF01217 | 0.462 |
TRG_DiLeu_BaLyEn_6 | 498 | 503 | PF01217 | 0.547 |
TRG_DiLeu_BaLyEn_6 | 79 | 84 | PF01217 | 0.456 |
TRG_DiLeu_BaLyEn_6 | 821 | 826 | PF01217 | 0.499 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 685 | 688 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 748 | 751 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 766 | 769 | PF00928 | 0.321 |
TRG_ER_diArg_1 | 180 | 183 | PF00400 | 0.572 |
TRG_ER_diArg_1 | 201 | 204 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 376 | 378 | PF00400 | 0.209 |
TRG_ER_diArg_1 | 431 | 434 | PF00400 | 0.515 |
TRG_NLS_MonoExtC_3 | 429 | 435 | PF00514 | 0.701 |
TRG_NLS_MonoExtN_4 | 358 | 364 | PF00514 | 0.377 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.321 |
TRG_Pf-PMV_PEXEL_1 | 378 | 382 | PF00026 | 0.402 |
TRG_Pf-PMV_PEXEL_1 | 629 | 634 | PF00026 | 0.642 |
TRG_Pf-PMV_PEXEL_1 | 652 | 656 | PF00026 | 0.420 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4H3 | Leptomonas seymouri | 62% | 100% |
A0A1X0P5S1 | Trypanosomatidae | 45% | 100% |
A0A3Q8IM41 | Leishmania donovani | 81% | 100% |
A4IB67 | Leishmania infantum | 80% | 100% |
C9ZZH7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AEY8 | Leishmania major | 82% | 100% |
E9B644 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q12J93 | Shewanella denitrificans (strain OS217 / ATCC BAA-1090 / DSM 15013) | 23% | 100% |
V5BJF3 | Trypanosoma cruzi | 46% | 100% |