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 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0031261 | DNA replication preinitiation complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0032993 | protein-DNA complex | 2 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: E9AHQ0
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006259 | DNA metabolic process | 4 | 10 |
GO:0006270 | DNA replication initiation | 5 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0007049 | cell cycle | 2 | 9 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 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:0051301 | cell division | 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:0000724 | double-strand break repair via homologous recombination | 7 | 1 |
GO:0000725 | recombinational repair | 6 | 1 |
GO:0000727 | double-strand break repair via break-induced replication | 8 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0065004 | protein-DNA complex assembly | 6 | 1 |
GO:0071163 | DNA replication preinitiation complex assembly | 3 | 1 |
GO:0071824 | protein-DNA complex subunit organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1902977 | mitotic DNA replication preinitiation complex assembly | 4 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003682 | chromatin binding | 2 | 1 |
GO:0003688 | DNA replication origin binding | 7 | 1 |
GO:0003690 | double-stranded DNA binding | 5 | 1 |
GO:0003697 | single-stranded DNA binding | 5 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0043565 | sequence-specific DNA binding | 5 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
GO:1990837 | sequence-specific double-stranded DNA binding | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 208 | 212 | PF00656 | 0.505 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.286 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.267 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.197 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.170 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.187 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.341 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.231 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.265 |
CLV_NRD_NRD_1 | 448 | 450 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 500 | 502 | PF00675 | 0.267 |
CLV_NRD_NRD_1 | 582 | 584 | PF00675 | 0.295 |
CLV_NRD_NRD_1 | 600 | 602 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 603 | 605 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 760 | 762 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 763 | 765 | PF00675 | 0.679 |
CLV_PCSK_FUR_1 | 161 | 165 | PF00082 | 0.226 |
CLV_PCSK_FUR_1 | 601 | 605 | PF00082 | 0.280 |
CLV_PCSK_FUR_1 | 761 | 765 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.286 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.234 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.238 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.248 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.203 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.226 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 582 | 584 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 599 | 601 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 603 | 605 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 762 | 764 | PF00082 | 0.691 |
CLV_PCSK_PC1ET2_1 | 172 | 174 | PF00082 | 0.364 |
CLV_PCSK_PC1ET2_1 | 762 | 764 | PF00082 | 0.576 |
CLV_PCSK_PC7_1 | 162 | 168 | PF00082 | 0.236 |
CLV_PCSK_PC7_1 | 599 | 605 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 464 | 468 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 590 | 594 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.207 |
CLV_PCSK_SKI1_1 | 643 | 647 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 722 | 726 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 745 | 749 | PF00082 | 0.383 |
DEG_APCC_DBOX_1 | 385 | 393 | PF00400 | 0.480 |
DEG_APCC_DBOX_1 | 602 | 610 | PF00400 | 0.489 |
DEG_APCC_DBOX_1 | 744 | 752 | PF00400 | 0.477 |
DEG_SPOP_SBC_1 | 554 | 558 | PF00917 | 0.509 |
DOC_CKS1_1 | 717 | 722 | PF01111 | 0.562 |
DOC_CYCLIN_RxL_1 | 604 | 615 | PF00134 | 0.517 |
DOC_CYCLIN_RxL_1 | 716 | 727 | PF00134 | 0.442 |
DOC_CYCLIN_RxL_1 | 742 | 753 | PF00134 | 0.477 |
DOC_CYCLIN_yCln2_LP_2 | 96 | 102 | PF00134 | 0.468 |
DOC_MAPK_DCC_7 | 604 | 614 | PF00069 | 0.446 |
DOC_MAPK_FxFP_2 | 49 | 52 | PF00069 | 0.509 |
DOC_MAPK_gen_1 | 140 | 147 | PF00069 | 0.350 |
DOC_MAPK_gen_1 | 22 | 29 | PF00069 | 0.288 |
DOC_MAPK_MEF2A_6 | 140 | 147 | PF00069 | 0.350 |
DOC_MAPK_MEF2A_6 | 22 | 29 | PF00069 | 0.288 |
DOC_MAPK_MEF2A_6 | 396 | 403 | PF00069 | 0.480 |
DOC_MAPK_MEF2A_6 | 86 | 94 | PF00069 | 0.465 |
DOC_MAPK_RevD_3 | 488 | 502 | PF00069 | 0.428 |
DOC_PP1_RVXF_1 | 132 | 139 | PF00149 | 0.426 |
DOC_PP1_RVXF_1 | 234 | 240 | PF00149 | 0.451 |
DOC_PP1_RVXF_1 | 500 | 507 | PF00149 | 0.480 |
DOC_PP1_RVXF_1 | 588 | 594 | PF00149 | 0.509 |
DOC_PP2B_LxvP_1 | 28 | 31 | PF13499 | 0.509 |
DOC_PP2B_LxvP_1 | 96 | 99 | PF13499 | 0.468 |
DOC_PP4_FxxP_1 | 49 | 52 | PF00568 | 0.509 |
DOC_PP4_FxxP_1 | 717 | 720 | PF00568 | 0.433 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.426 |
DOC_USP7_MATH_1 | 544 | 548 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 627 | 631 | PF00917 | 0.539 |
DOC_USP7_MATH_1 | 658 | 662 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.509 |
DOC_USP7_MATH_2 | 10 | 16 | PF00917 | 0.431 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 569 | 574 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 697 | 702 | PF00397 | 0.334 |
DOC_WW_Pin1_4 | 716 | 721 | PF00397 | 0.559 |
LIG_14-3-3_CanoR_1 | 13 | 18 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 262 | 269 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 339 | 347 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 359 | 364 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 513 | 520 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 582 | 587 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 590 | 596 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 603 | 613 | PF00244 | 0.451 |
LIG_Actin_WH2_2 | 739 | 754 | PF00022 | 0.310 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.583 |
LIG_BIR_III_2 | 227 | 231 | PF00653 | 0.509 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.537 |
LIG_BIR_III_4 | 543 | 547 | PF00653 | 0.445 |
LIG_CaM_IQ_9 | 314 | 329 | PF13499 | 0.509 |
LIG_deltaCOP1_diTrp_1 | 62 | 73 | PF00928 | 0.445 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.445 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.470 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.437 |
LIG_FHA_1 | 698 | 704 | PF00498 | 0.474 |
LIG_FHA_1 | 737 | 743 | PF00498 | 0.379 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.526 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.480 |
LIG_GBD_Chelix_1 | 587 | 595 | PF00786 | 0.268 |
LIG_LIR_Apic_2 | 714 | 720 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 361 | 369 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 576 | 586 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 58 | 68 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 682 | 689 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 775 | 784 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 88 | 99 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 9 | 19 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 103 | 108 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 117 | 122 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 300 | 304 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 361 | 367 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 589 | 595 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 682 | 688 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 775 | 781 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 88 | 94 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 9 | 14 | PF02991 | 0.337 |
LIG_LRP6_Inhibitor_1 | 439 | 445 | PF00058 | 0.228 |
LIG_NBox_RRM_1 | 527 | 537 | PF00076 | 0.426 |
LIG_NRBOX | 388 | 394 | PF00104 | 0.426 |
LIG_PCNA_PIPBox_1 | 144 | 153 | PF02747 | 0.494 |
LIG_PCNA_yPIPBox_3 | 140 | 151 | PF02747 | 0.495 |
LIG_PCNA_yPIPBox_3 | 422 | 431 | PF02747 | 0.478 |
LIG_Pex14_2 | 49 | 53 | PF04695 | 0.509 |
LIG_REV1ctd_RIR_1 | 148 | 157 | PF16727 | 0.443 |
LIG_SH2_CRK | 562 | 566 | PF00017 | 0.443 |
LIG_SH2_NCK_1 | 562 | 566 | PF00017 | 0.462 |
LIG_SH2_PTP2 | 685 | 688 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 269 | 273 | PF00017 | 0.426 |
LIG_SH2_STAP1 | 301 | 305 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 369 | 373 | PF00017 | 0.461 |
LIG_SH2_STAP1 | 453 | 457 | PF00017 | 0.426 |
LIG_SH2_STAT3 | 369 | 372 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 304 | 307 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 685 | 688 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 741 | 744 | PF00017 | 0.532 |
LIG_SH3_1 | 562 | 568 | PF00018 | 0.443 |
LIG_SH3_2 | 565 | 570 | PF14604 | 0.480 |
LIG_SH3_2 | 638 | 643 | PF14604 | 0.385 |
LIG_SH3_3 | 562 | 568 | PF00018 | 0.443 |
LIG_SH3_3 | 635 | 641 | PF00018 | 0.480 |
LIG_SH3_3 | 698 | 704 | PF00018 | 0.391 |
LIG_SUMO_SIM_anti_2 | 270 | 275 | PF11976 | 0.426 |
LIG_SUMO_SIM_anti_2 | 684 | 690 | PF11976 | 0.456 |
LIG_SUMO_SIM_anti_2 | 779 | 785 | PF11976 | 0.648 |
LIG_SUMO_SIM_par_1 | 111 | 117 | PF11976 | 0.392 |
LIG_SUMO_SIM_par_1 | 515 | 521 | PF11976 | 0.511 |
LIG_SUMO_SIM_par_1 | 610 | 615 | PF11976 | 0.462 |
LIG_SUMO_SIM_par_1 | 684 | 690 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 744 | 750 | PF11976 | 0.433 |
LIG_SUMO_SIM_par_1 | 98 | 104 | PF11976 | 0.449 |
LIG_TRAF2_1 | 203 | 206 | PF00917 | 0.536 |
LIG_TRAF2_1 | 491 | 494 | PF00917 | 0.497 |
LIG_TRAF2_2 | 230 | 235 | PF00917 | 0.509 |
LIG_TRFH_1 | 53 | 57 | PF08558 | 0.426 |
LIG_UBA3_1 | 746 | 752 | PF00899 | 0.474 |
LIG_WRC_WIRS_1 | 457 | 462 | PF05994 | 0.427 |
LIG_WRC_WIRS_1 | 575 | 580 | PF05994 | 0.426 |
LIG_WRPW_2 | 119 | 122 | PF00400 | 0.426 |
LIG_WW_3 | 719 | 723 | PF00397 | 0.582 |
MOD_CDK_SPxK_1 | 716 | 722 | PF00069 | 0.562 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.458 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.427 |
MOD_CK1_1 | 577 | 583 | PF00069 | 0.511 |
MOD_CK1_1 | 630 | 636 | PF00069 | 0.463 |
MOD_CK1_1 | 653 | 659 | PF00069 | 0.519 |
MOD_CK1_1 | 663 | 669 | PF00069 | 0.558 |
MOD_CK1_1 | 750 | 756 | PF00069 | 0.617 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.526 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.468 |
MOD_CK2_1 | 488 | 494 | PF00069 | 0.527 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.509 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.509 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.280 |
MOD_GlcNHglycan | 245 | 249 | PF01048 | 0.358 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.244 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.302 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.535 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.280 |
MOD_GlcNHglycan | 630 | 633 | PF01048 | 0.311 |
MOD_GlcNHglycan | 634 | 637 | PF01048 | 0.323 |
MOD_GlcNHglycan | 638 | 641 | PF01048 | 0.297 |
MOD_GlcNHglycan | 655 | 658 | PF01048 | 0.364 |
MOD_GlcNHglycan | 660 | 663 | PF01048 | 0.373 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.458 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.457 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.426 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.509 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.426 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.553 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.480 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.333 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.449 |
MOD_GSK3_1 | 591 | 598 | PF00069 | 0.511 |
MOD_GSK3_1 | 628 | 635 | PF00069 | 0.568 |
MOD_GSK3_1 | 747 | 754 | PF00069 | 0.448 |
MOD_N-GLC_1 | 737 | 742 | PF02516 | 0.439 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.468 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.445 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.525 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.455 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.526 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.468 |
MOD_NEK2_1 | 591 | 596 | PF00069 | 0.453 |
MOD_NEK2_1 | 612 | 617 | PF00069 | 0.509 |
MOD_NEK2_1 | 747 | 752 | PF00069 | 0.481 |
MOD_PIKK_1 | 228 | 234 | PF00454 | 0.427 |
MOD_PIKK_1 | 368 | 374 | PF00454 | 0.577 |
MOD_PIKK_1 | 387 | 393 | PF00454 | 0.431 |
MOD_PIKK_1 | 430 | 436 | PF00454 | 0.429 |
MOD_PK_1 | 582 | 588 | PF00069 | 0.494 |
MOD_PKA_1 | 582 | 588 | PF00069 | 0.494 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.452 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.509 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.532 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.521 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.523 |
MOD_PKA_2 | 512 | 518 | PF00069 | 0.480 |
MOD_PKA_2 | 582 | 588 | PF00069 | 0.468 |
MOD_PKA_2 | 653 | 659 | PF00069 | 0.467 |
MOD_PKB_1 | 443 | 451 | PF00069 | 0.505 |
MOD_PKB_1 | 734 | 742 | PF00069 | 0.445 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.480 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.509 |
MOD_Plk_1 | 455 | 461 | PF00069 | 0.427 |
MOD_Plk_1 | 736 | 742 | PF00069 | 0.483 |
MOD_Plk_1 | 80 | 86 | PF00069 | 0.440 |
MOD_Plk_2-3 | 192 | 198 | PF00069 | 0.517 |
MOD_Plk_2-3 | 456 | 462 | PF00069 | 0.443 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.454 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.509 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.509 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.426 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.444 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.445 |
MOD_Plk_4 | 474 | 480 | PF00069 | 0.509 |
MOD_Plk_4 | 544 | 550 | PF00069 | 0.484 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.468 |
MOD_Plk_4 | 737 | 743 | PF00069 | 0.417 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.418 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.447 |
MOD_ProDKin_1 | 569 | 575 | PF00069 | 0.509 |
MOD_ProDKin_1 | 697 | 703 | PF00069 | 0.336 |
MOD_ProDKin_1 | 716 | 722 | PF00069 | 0.562 |
MOD_SUMO_rev_2 | 59 | 67 | PF00179 | 0.455 |
TRG_AP2beta_CARGO_1 | 589 | 599 | PF09066 | 0.509 |
TRG_DiLeu_BaEn_1 | 353 | 358 | PF01217 | 0.509 |
TRG_DiLeu_BaEn_1 | 744 | 749 | PF01217 | 0.469 |
TRG_DiLeu_BaEn_2 | 62 | 68 | PF01217 | 0.509 |
TRG_DiLeu_BaEn_4 | 493 | 499 | PF01217 | 0.445 |
TRG_DiLeu_BaLyEn_6 | 608 | 613 | PF01217 | 0.484 |
TRG_DiLeu_BaLyEn_6 | 698 | 703 | PF01217 | 0.487 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 685 | 688 | PF00928 | 0.509 |
TRG_ER_diArg_1 | 127 | 129 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 161 | 164 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 166 | 168 | PF00400 | 0.432 |
TRG_ER_diArg_1 | 179 | 182 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 295 | 297 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 321 | 323 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 386 | 389 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 440 | 443 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 581 | 583 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 599 | 601 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 733 | 736 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 760 | 763 | PF00400 | 0.671 |
TRG_NES_CRM1_1 | 307 | 319 | PF08389 | 0.509 |
TRG_NLS_MonoCore_2 | 760 | 765 | PF00514 | 0.563 |
TRG_NLS_MonoExtC_3 | 151 | 157 | PF00514 | 0.445 |
TRG_NLS_MonoExtC_3 | 761 | 766 | PF00514 | 0.567 |
TRG_NLS_MonoExtN_4 | 761 | 766 | PF00514 | 0.567 |
TRG_Pf-PMV_PEXEL_1 | 296 | 300 | PF00026 | 0.226 |
TRG_Pf-PMV_PEXEL_1 | 501 | 505 | PF00026 | 0.314 |
TRG_Pf-PMV_PEXEL_1 | 722 | 727 | PF00026 | 0.431 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5R4 | Leptomonas seymouri | 66% | 95% |
A0A3Q8IF06 | Leishmania donovani | 100% | 100% |
A0A422P0B5 | Trypanosoma rangeli | 43% | 100% |
A4HLU5 | Leishmania braziliensis | 81% | 100% |
D0A683 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9B471 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
O74113 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 100% |
Q4Q3V5 | Leishmania major | 94% | 100% |
V5BP84 | Trypanosoma cruzi | 42% | 100% |