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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4HGJ3
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006260 | DNA replication | 5 | 2 |
GO:0006281 | DNA repair | 5 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006950 | response to stress | 2 | 12 |
GO:0006974 | DNA damage response | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0033554 | cellular response to stress | 3 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0050896 | response to stimulus | 1 | 12 |
GO:0051716 | cellular response to stimulus | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0000731 | DNA synthesis involved in DNA repair | 6 | 2 |
GO:0006301 | postreplication repair | 6 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009059 | macromolecule biosynthetic process | 4 | 2 |
GO:0018130 | heterocycle biosynthetic process | 4 | 2 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 2 |
GO:0019985 | translesion synthesis | 7 | 2 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 2 |
GO:0042276 | error-prone translesion synthesis | 8 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 2 |
GO:0071897 | DNA biosynthetic process | 5 | 2 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003684 | damaged DNA binding | 5 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0003887 | DNA-directed DNA polymerase activity | 5 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016779 | nucleotidyltransferase activity | 4 | 12 |
GO:0034061 | DNA polymerase activity | 4 | 12 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043169 | cation binding | 3 | 2 |
GO:0046872 | metal ion binding | 4 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 674 | 678 | PF00656 | 0.670 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.387 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.224 |
CLV_NRD_NRD_1 | 454 | 456 | PF00675 | 0.366 |
CLV_NRD_NRD_1 | 503 | 505 | PF00675 | 0.264 |
CLV_NRD_NRD_1 | 576 | 578 | PF00675 | 0.223 |
CLV_NRD_NRD_1 | 605 | 607 | PF00675 | 0.223 |
CLV_NRD_NRD_1 | 662 | 664 | PF00675 | 0.567 |
CLV_PCSK_FUR_1 | 183 | 187 | PF00082 | 0.315 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.168 |
CLV_PCSK_KEX2_1 | 503 | 505 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 576 | 578 | PF00082 | 0.223 |
CLV_PCSK_KEX2_1 | 604 | 606 | PF00082 | 0.223 |
CLV_PCSK_KEX2_1 | 664 | 666 | PF00082 | 0.545 |
CLV_PCSK_PC1ET2_1 | 185 | 187 | PF00082 | 0.324 |
CLV_PCSK_PC1ET2_1 | 664 | 666 | PF00082 | 0.658 |
CLV_PCSK_PC7_1 | 179 | 185 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 576 | 580 | PF00082 | 0.223 |
CLV_Separin_Metazoa | 573 | 577 | PF03568 | 0.423 |
DEG_APCC_DBOX_1 | 445 | 453 | PF00400 | 0.319 |
DEG_APCC_DBOX_1 | 518 | 526 | PF00400 | 0.435 |
DEG_APCC_DBOX_1 | 575 | 583 | PF00400 | 0.423 |
DEG_SPOP_SBC_1 | 129 | 133 | PF00917 | 0.476 |
DEG_SPOP_SBC_1 | 483 | 487 | PF00917 | 0.518 |
DOC_ANK_TNKS_1 | 418 | 425 | PF00023 | 0.368 |
DOC_CKS1_1 | 68 | 73 | PF01111 | 0.510 |
DOC_CYCLIN_RxL_1 | 557 | 571 | PF00134 | 0.368 |
DOC_MAPK_gen_1 | 183 | 193 | PF00069 | 0.375 |
DOC_MAPK_gen_1 | 515 | 522 | PF00069 | 0.368 |
DOC_MAPK_gen_1 | 576 | 584 | PF00069 | 0.397 |
DOC_MAPK_gen_1 | 592 | 600 | PF00069 | 0.360 |
DOC_MAPK_HePTP_8 | 574 | 586 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 227 | 236 | PF00069 | 0.356 |
DOC_MAPK_MEF2A_6 | 289 | 296 | PF00069 | 0.437 |
DOC_MAPK_MEF2A_6 | 577 | 586 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 592 | 600 | PF00069 | 0.419 |
DOC_MAPK_RevD_3 | 234 | 249 | PF00069 | 0.232 |
DOC_MIT_MIM_1 | 593 | 605 | PF04212 | 0.407 |
DOC_PP1_RVXF_1 | 139 | 146 | PF00149 | 0.425 |
DOC_PP2B_LxvP_1 | 582 | 585 | PF13499 | 0.442 |
DOC_SPAK_OSR1_1 | 351 | 355 | PF12202 | 0.423 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 607 | 611 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 638 | 642 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 710 | 714 | PF00917 | 0.564 |
DOC_USP7_UBL2_3 | 559 | 563 | PF12436 | 0.423 |
DOC_USP7_UBL2_3 | 730 | 734 | PF12436 | 0.506 |
DOC_WW_Pin1_4 | 109 | 114 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.407 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 648 | 653 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 715 | 720 | PF00397 | 0.618 |
LIG_14-3-3_CanoR_1 | 25 | 29 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 455 | 459 | PF00244 | 0.339 |
LIG_14-3-3_CanoR_1 | 503 | 508 | PF00244 | 0.230 |
LIG_14-3-3_CanoR_1 | 531 | 538 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 59 | 63 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 639 | 648 | PF00244 | 0.518 |
LIG_Actin_WH2_2 | 518 | 533 | PF00022 | 0.485 |
LIG_APCC_ABBA_1 | 232 | 237 | PF00400 | 0.236 |
LIG_APCC_ABBA_1 | 565 | 570 | PF00400 | 0.442 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.599 |
LIG_BRCT_BRCA1_1 | 122 | 126 | PF00533 | 0.459 |
LIG_BRCT_BRCA1_1 | 307 | 311 | PF00533 | 0.442 |
LIG_BRCT_BRCA1_1 | 633 | 637 | PF00533 | 0.510 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.442 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.374 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.408 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.437 |
LIG_FHA_1 | 485 | 491 | PF00498 | 0.485 |
LIG_FHA_2 | 345 | 351 | PF00498 | 0.371 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.325 |
LIG_FHA_2 | 700 | 706 | PF00498 | 0.533 |
LIG_LIR_Apic_2 | 389 | 394 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 228 | 236 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 239 | 247 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 457 | 466 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 569 | 579 | PF02991 | 0.540 |
LIG_LIR_Gen_1 | 588 | 598 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 207 | 212 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 228 | 232 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 239 | 245 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 308 | 314 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 457 | 461 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 510 | 516 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 569 | 575 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 588 | 593 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 98 | 102 | PF02991 | 0.500 |
LIG_MLH1_MIPbox_1 | 633 | 637 | PF16413 | 0.510 |
LIG_NRBOX | 578 | 584 | PF00104 | 0.442 |
LIG_PCNA_PIPBox_1 | 331 | 340 | PF02747 | 0.442 |
LIG_PCNA_PIPBox_1 | 630 | 639 | PF02747 | 0.540 |
LIG_PCNA_yPIPBox_3 | 630 | 639 | PF02747 | 0.540 |
LIG_PTB_Apo_2 | 247 | 254 | PF02174 | 0.442 |
LIG_PTB_Phospho_1 | 247 | 253 | PF10480 | 0.442 |
LIG_Rb_pABgroove_1 | 466 | 474 | PF01858 | 0.402 |
LIG_REV1ctd_RIR_1 | 634 | 643 | PF16727 | 0.569 |
LIG_SH2_CRK | 391 | 395 | PF00017 | 0.376 |
LIG_SH2_CRK | 99 | 103 | PF00017 | 0.492 |
LIG_SH2_GRB2like | 128 | 131 | PF00017 | 0.458 |
LIG_SH2_GRB2like | 174 | 177 | PF00017 | 0.323 |
LIG_SH2_NCK_1 | 242 | 246 | PF00017 | 0.452 |
LIG_SH2_NCK_1 | 253 | 257 | PF00017 | 0.440 |
LIG_SH2_NCK_1 | 318 | 322 | PF00017 | 0.368 |
LIG_SH2_PTP2 | 233 | 236 | PF00017 | 0.245 |
LIG_SH2_SRC | 233 | 236 | PF00017 | 0.295 |
LIG_SH2_SRC | 253 | 256 | PF00017 | 0.406 |
LIG_SH2_SRC | 318 | 321 | PF00017 | 0.368 |
LIG_SH2_STAP1 | 458 | 462 | PF00017 | 0.293 |
LIG_SH2_STAP1 | 568 | 572 | PF00017 | 0.381 |
LIG_SH2_STAT3 | 337 | 340 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.278 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 411 | 414 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 568 | 571 | PF00017 | 0.430 |
LIG_SH3_2 | 38 | 43 | PF14604 | 0.476 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.442 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.568 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.563 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.523 |
LIG_SH3_3 | 704 | 710 | PF00018 | 0.643 |
LIG_SH3_4 | 393 | 400 | PF00018 | 0.334 |
LIG_SUMO_SIM_anti_2 | 747 | 754 | PF11976 | 0.521 |
LIG_SUMO_SIM_par_1 | 293 | 300 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 616 | 623 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 691 | 699 | PF11976 | 0.584 |
LIG_SUMO_SIM_par_1 | 747 | 754 | PF11976 | 0.634 |
LIG_UBA3_1 | 163 | 169 | PF00899 | 0.369 |
LIG_UBA3_1 | 449 | 456 | PF00899 | 0.388 |
LIG_UBA3_1 | 595 | 602 | PF00899 | 0.174 |
LIG_UBA3_1 | 659 | 664 | PF00899 | 0.482 |
LIG_WRC_WIRS_1 | 226 | 231 | PF05994 | 0.279 |
LIG_WW_3 | 40 | 44 | PF00397 | 0.469 |
MOD_CDK_SPxK_1 | 648 | 654 | PF00069 | 0.505 |
MOD_CDK_SPxK_1 | 67 | 73 | PF00069 | 0.541 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.461 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.541 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.374 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.329 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.481 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.290 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.521 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.252 |
MOD_CK1_1 | 696 | 702 | PF00069 | 0.573 |
MOD_CK1_1 | 742 | 748 | PF00069 | 0.531 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.606 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.565 |
MOD_CK2_1 | 344 | 350 | PF00069 | 0.192 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.308 |
MOD_CK2_1 | 619 | 625 | PF00069 | 0.499 |
MOD_CK2_1 | 699 | 705 | PF00069 | 0.549 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.590 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.483 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.485 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.284 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.369 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.234 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.702 |
MOD_GlcNHglycan | 6 | 10 | PF01048 | 0.621 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.534 |
MOD_GlcNHglycan | 640 | 643 | PF01048 | 0.614 |
MOD_GlcNHglycan | 671 | 674 | PF01048 | 0.501 |
MOD_GlcNHglycan | 677 | 681 | PF01048 | 0.526 |
MOD_GlcNHglycan | 743 | 747 | PF01048 | 0.700 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.582 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.547 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.524 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.647 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.575 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.602 |
MOD_GSK3_1 | 616 | 623 | PF00069 | 0.498 |
MOD_GSK3_1 | 625 | 632 | PF00069 | 0.531 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.569 |
MOD_GSK3_1 | 676 | 683 | PF00069 | 0.506 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.687 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.630 |
MOD_LATS_1 | 557 | 563 | PF00433 | 0.279 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.493 |
MOD_N-GLC_1 | 675 | 680 | PF02516 | 0.504 |
MOD_N-GLC_1 | 85 | 90 | PF02516 | 0.570 |
MOD_N-GLC_2 | 201 | 203 | PF02516 | 0.274 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.360 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.393 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.274 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.249 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.325 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.356 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.248 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.535 |
MOD_PIKK_1 | 542 | 548 | PF00454 | 0.263 |
MOD_PIKK_1 | 626 | 632 | PF00454 | 0.471 |
MOD_PIKK_1 | 696 | 702 | PF00454 | 0.530 |
MOD_PK_1 | 503 | 509 | PF00069 | 0.174 |
MOD_PKA_1 | 503 | 509 | PF00069 | 0.174 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.478 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.592 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.252 |
MOD_PKA_2 | 454 | 460 | PF00069 | 0.339 |
MOD_PKA_2 | 503 | 509 | PF00069 | 0.229 |
MOD_PKA_2 | 530 | 536 | PF00069 | 0.252 |
MOD_PKA_2 | 58 | 64 | PF00069 | 0.518 |
MOD_PKA_2 | 638 | 644 | PF00069 | 0.470 |
MOD_PKA_2 | 666 | 672 | PF00069 | 0.620 |
MOD_PKB_1 | 665 | 673 | PF00069 | 0.485 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.442 |
MOD_Plk_1 | 219 | 225 | PF00069 | 0.259 |
MOD_Plk_1 | 509 | 515 | PF00069 | 0.271 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.297 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.548 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.279 |
MOD_Plk_4 | 533 | 539 | PF00069 | 0.267 |
MOD_ProDKin_1 | 109 | 115 | PF00069 | 0.478 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.625 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.574 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.229 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.567 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.546 |
MOD_ProDKin_1 | 648 | 654 | PF00069 | 0.505 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.625 |
MOD_ProDKin_1 | 715 | 721 | PF00069 | 0.615 |
MOD_SUMO_for_1 | 158 | 161 | PF00179 | 0.285 |
MOD_SUMO_rev_2 | 172 | 181 | PF00179 | 0.398 |
MOD_SUMO_rev_2 | 389 | 394 | PF00179 | 0.266 |
TRG_DiLeu_BaLyEn_6 | 591 | 596 | PF01217 | 0.266 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.274 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.254 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.151 |
TRG_ENDOCYTIC_2 | 458 | 461 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 472 | 475 | PF00928 | 0.627 |
TRG_ENDOCYTIC_2 | 572 | 575 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.498 |
TRG_ER_diArg_1 | 183 | 186 | PF00400 | 0.372 |
TRG_ER_diArg_1 | 363 | 365 | PF00400 | 0.261 |
TRG_ER_diArg_1 | 417 | 419 | PF00400 | 0.174 |
TRG_ER_diArg_1 | 446 | 449 | PF00400 | 0.315 |
TRG_ER_diArg_1 | 502 | 504 | PF00400 | 0.340 |
TRG_ER_diArg_1 | 575 | 577 | PF00400 | 0.252 |
TRG_ER_diArg_1 | 603 | 606 | PF00400 | 0.252 |
TRG_ER_diArg_1 | 662 | 665 | PF00400 | 0.556 |
TRG_NES_CRM1_1 | 521 | 532 | PF08389 | 0.174 |
TRG_NES_CRM1_1 | 573 | 588 | PF08389 | 0.269 |
TRG_NLS_MonoExtC_3 | 183 | 189 | PF00514 | 0.288 |
TRG_NLS_MonoExtC_3 | 662 | 667 | PF00514 | 0.562 |
TRG_NLS_MonoExtN_4 | 183 | 188 | PF00514 | 0.287 |
TRG_Pf-PMV_PEXEL_1 | 210 | 215 | PF00026 | 0.339 |
TRG_Pf-PMV_PEXEL_1 | 357 | 361 | PF00026 | 0.252 |
TRG_Pf-PMV_PEXEL_1 | 577 | 581 | PF00026 | 0.279 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7I6 | Leptomonas seymouri | 61% | 100% |
A0A0S4JDU0 | Bodo saltans | 38% | 85% |
A0A3Q8IEM0 | Leishmania donovani | 72% | 100% |
A0A3S7X1J7 | Leishmania donovani | 37% | 100% |
A4I3M0 | Leishmania infantum | 72% | 100% |
A4I3M1 | Leishmania infantum | 37% | 100% |
E9AZW1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |
E9AZW2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
P34409 | Caenorhabditis elegans | 31% | 100% |
Q4Q8C4 | Leishmania major | 37% | 100% |
Q4Q8C5 | Leishmania major | 71% | 99% |