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:0031261 | DNA replication preinitiation complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0032993 | protein-DNA complex | 2 | 2 |
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:0140513 | nuclear protein-containing complex | 2 | 2 |
Related structures:
AlphaFold database: Q4Q3V5
Term | Name | Level | Count |
---|---|---|---|
GO:0000724 | double-strand break repair via homologous recombination | 7 | 2 |
GO:0000725 | recombinational repair | 6 | 2 |
GO:0000727 | double-strand break repair via break-induced replication | 8 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006259 | DNA metabolic process | 4 | 10 |
GO:0006270 | DNA replication initiation | 5 | 10 |
GO:0006281 | DNA repair | 5 | 2 |
GO:0006302 | double-strand break repair | 6 | 2 |
GO:0006310 | DNA recombination | 5 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0006950 | response to stress | 2 | 2 |
GO:0006974 | DNA damage response | 4 | 2 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022402 | cell cycle process | 2 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043933 | protein-containing complex organization | 4 | 2 |
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 | 2 |
GO:0051301 | cell division | 2 | 10 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0065003 | protein-containing complex assembly | 5 | 2 |
GO:0065004 | protein-DNA complex assembly | 6 | 2 |
GO:0071163 | DNA replication preinitiation complex assembly | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0071824 | protein-DNA complex subunit organization | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
GO:1902977 | mitotic DNA replication preinitiation complex assembly | 4 | 2 |
GO:1903047 | mitotic cell cycle process | 3 | 2 |
GO:0007049 | cell cycle | 2 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003677 | DNA binding | 4 | 2 |
GO:0003682 | chromatin binding | 2 | 2 |
GO:0003688 | DNA replication origin binding | 7 | 2 |
GO:0003690 | double-stranded DNA binding | 5 | 2 |
GO:0003697 | single-stranded DNA binding | 5 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0043565 | sequence-specific DNA binding | 5 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
GO:1990837 | sequence-specific double-stranded DNA binding | 6 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 208 | 212 | PF00656 | 0.499 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.260 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.192 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.167 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.183 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.241 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.285 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.172 |
CLV_NRD_NRD_1 | 448 | 450 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 500 | 502 | PF00675 | 0.282 |
CLV_NRD_NRD_1 | 582 | 584 | PF00675 | 0.288 |
CLV_NRD_NRD_1 | 600 | 602 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 603 | 605 | PF00675 | 0.303 |
CLV_NRD_NRD_1 | 722 | 724 | PF00675 | 0.406 |
CLV_NRD_NRD_1 | 760 | 762 | PF00675 | 0.659 |
CLV_NRD_NRD_1 | 763 | 765 | PF00675 | 0.663 |
CLV_PCSK_FUR_1 | 161 | 165 | PF00082 | 0.220 |
CLV_PCSK_FUR_1 | 601 | 605 | PF00082 | 0.266 |
CLV_PCSK_FUR_1 | 761 | 765 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.229 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.232 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.242 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.199 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.242 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.172 |
CLV_PCSK_KEX2_1 | 582 | 584 | PF00082 | 0.288 |
CLV_PCSK_KEX2_1 | 599 | 601 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 603 | 605 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 722 | 724 | PF00082 | 0.406 |
CLV_PCSK_KEX2_1 | 762 | 764 | PF00082 | 0.668 |
CLV_PCSK_PC1ET2_1 | 172 | 174 | PF00082 | 0.362 |
CLV_PCSK_PC1ET2_1 | 762 | 764 | PF00082 | 0.568 |
CLV_PCSK_PC7_1 | 162 | 168 | PF00082 | 0.230 |
CLV_PCSK_PC7_1 | 599 | 605 | PF00082 | 0.266 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 464 | 468 | PF00082 | 0.306 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 590 | 594 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.166 |
CLV_PCSK_SKI1_1 | 722 | 726 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 745 | 749 | PF00082 | 0.385 |
DEG_APCC_DBOX_1 | 385 | 393 | PF00400 | 0.466 |
DEG_APCC_DBOX_1 | 602 | 610 | PF00400 | 0.478 |
DEG_APCC_DBOX_1 | 744 | 752 | PF00400 | 0.480 |
DEG_COP1_1 | 653 | 662 | PF00400 | 0.388 |
DEG_SPOP_SBC_1 | 554 | 558 | PF00917 | 0.503 |
DOC_CKS1_1 | 717 | 722 | PF01111 | 0.509 |
DOC_CYCLIN_RxL_1 | 604 | 615 | PF00134 | 0.512 |
DOC_CYCLIN_RxL_1 | 716 | 727 | PF00134 | 0.444 |
DOC_CYCLIN_RxL_1 | 742 | 753 | PF00134 | 0.478 |
DOC_CYCLIN_yCln2_LP_2 | 96 | 102 | PF00134 | 0.462 |
DOC_MAPK_DCC_7 | 604 | 614 | PF00069 | 0.440 |
DOC_MAPK_FxFP_2 | 49 | 52 | PF00069 | 0.503 |
DOC_MAPK_gen_1 | 22 | 29 | PF00069 | 0.275 |
DOC_MAPK_gen_1 | 421 | 427 | PF00069 | 0.372 |
DOC_MAPK_MEF2A_6 | 22 | 29 | PF00069 | 0.275 |
DOC_MAPK_MEF2A_6 | 396 | 403 | PF00069 | 0.466 |
DOC_MAPK_MEF2A_6 | 79 | 87 | PF00069 | 0.433 |
DOC_MAPK_RevD_3 | 488 | 502 | PF00069 | 0.419 |
DOC_PP1_RVXF_1 | 132 | 139 | PF00149 | 0.420 |
DOC_PP1_RVXF_1 | 234 | 240 | PF00149 | 0.445 |
DOC_PP1_RVXF_1 | 500 | 507 | PF00149 | 0.466 |
DOC_PP1_RVXF_1 | 588 | 594 | PF00149 | 0.503 |
DOC_PP2B_LxvP_1 | 28 | 31 | PF13499 | 0.503 |
DOC_PP2B_LxvP_1 | 623 | 626 | PF13499 | 0.429 |
DOC_PP2B_LxvP_1 | 96 | 99 | PF13499 | 0.462 |
DOC_PP4_FxxP_1 | 49 | 52 | PF00568 | 0.503 |
DOC_PP4_FxxP_1 | 717 | 720 | PF00568 | 0.394 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 544 | 548 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 563 | 567 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 627 | 631 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 660 | 664 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.503 |
DOC_USP7_MATH_2 | 10 | 16 | PF00917 | 0.410 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 481 | 486 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 569 | 574 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 716 | 721 | PF00397 | 0.507 |
LIG_14-3-3_CanoR_1 | 13 | 18 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 262 | 269 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 339 | 347 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 359 | 364 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 513 | 520 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 582 | 587 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 590 | 596 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 603 | 613 | PF00244 | 0.462 |
LIG_Actin_WH2_2 | 408 | 423 | PF00022 | 0.376 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.547 |
LIG_BIR_III_2 | 227 | 231 | PF00653 | 0.503 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.495 |
LIG_BIR_III_4 | 543 | 547 | PF00653 | 0.435 |
LIG_CaM_IQ_9 | 314 | 329 | PF13499 | 0.503 |
LIG_deltaCOP1_diTrp_1 | 62 | 73 | PF00928 | 0.435 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.435 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.486 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.426 |
LIG_FHA_1 | 641 | 647 | PF00498 | 0.385 |
LIG_FHA_1 | 737 | 743 | PF00498 | 0.363 |
LIG_FHA_1 | 776 | 782 | PF00498 | 0.469 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.521 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.466 |
LIG_GBD_Chelix_1 | 587 | 595 | PF00786 | 0.262 |
LIG_LIR_Apic_2 | 714 | 720 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 361 | 369 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 576 | 586 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 58 | 68 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 682 | 692 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 88 | 99 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 9 | 19 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 103 | 108 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 117 | 122 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 300 | 304 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 361 | 367 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 589 | 595 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 682 | 688 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 88 | 94 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 9 | 14 | PF02991 | 0.314 |
LIG_LRP6_Inhibitor_1 | 439 | 445 | PF00058 | 0.219 |
LIG_NBox_RRM_1 | 527 | 537 | PF00076 | 0.420 |
LIG_NRBOX | 388 | 394 | PF00104 | 0.420 |
LIG_PCNA_PIPBox_1 | 144 | 153 | PF02747 | 0.488 |
LIG_PCNA_yPIPBox_3 | 142 | 151 | PF02747 | 0.487 |
LIG_PCNA_yPIPBox_3 | 421 | 431 | PF02747 | 0.461 |
LIG_Pex14_2 | 49 | 53 | PF04695 | 0.503 |
LIG_REV1ctd_RIR_1 | 148 | 157 | PF16727 | 0.437 |
LIG_SH2_CRK | 562 | 566 | PF00017 | 0.437 |
LIG_SH2_NCK_1 | 562 | 566 | PF00017 | 0.437 |
LIG_SH2_PTP2 | 685 | 688 | PF00017 | 0.466 |
LIG_SH2_SRC | 249 | 252 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 269 | 273 | PF00017 | 0.430 |
LIG_SH2_STAP1 | 301 | 305 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 369 | 373 | PF00017 | 0.435 |
LIG_SH2_STAP1 | 453 | 457 | PF00017 | 0.420 |
LIG_SH2_STAT3 | 369 | 372 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 304 | 307 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 685 | 688 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 741 | 744 | PF00017 | 0.532 |
LIG_SH3_1 | 562 | 568 | PF00018 | 0.437 |
LIG_SH3_2 | 565 | 570 | PF14604 | 0.466 |
LIG_SH3_3 | 562 | 568 | PF00018 | 0.437 |
LIG_SH3_3 | 635 | 641 | PF00018 | 0.537 |
LIG_SH3_3 | 698 | 704 | PF00018 | 0.391 |
LIG_SUMO_SIM_anti_2 | 270 | 275 | PF11976 | 0.420 |
LIG_SUMO_SIM_anti_2 | 684 | 690 | PF11976 | 0.444 |
LIG_SUMO_SIM_anti_2 | 778 | 785 | PF11976 | 0.680 |
LIG_SUMO_SIM_par_1 | 111 | 117 | PF11976 | 0.387 |
LIG_SUMO_SIM_par_1 | 515 | 521 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 610 | 615 | PF11976 | 0.420 |
LIG_SUMO_SIM_par_1 | 684 | 690 | PF11976 | 0.459 |
LIG_SUMO_SIM_par_1 | 744 | 750 | PF11976 | 0.435 |
LIG_SUMO_SIM_par_1 | 778 | 785 | PF11976 | 0.531 |
LIG_SUMO_SIM_par_1 | 98 | 104 | PF11976 | 0.443 |
LIG_TRAF2_1 | 203 | 206 | PF00917 | 0.532 |
LIG_TRAF2_1 | 310 | 313 | PF00917 | 0.478 |
LIG_TRAF2_1 | 491 | 494 | PF00917 | 0.435 |
LIG_TRAF2_2 | 230 | 235 | PF00917 | 0.503 |
LIG_TRFH_1 | 53 | 57 | PF08558 | 0.420 |
LIG_UBA3_1 | 746 | 752 | PF00899 | 0.477 |
LIG_WRC_WIRS_1 | 457 | 462 | PF05994 | 0.421 |
LIG_WRC_WIRS_1 | 575 | 580 | PF05994 | 0.420 |
LIG_WRPW_2 | 119 | 122 | PF00400 | 0.420 |
LIG_WW_3 | 719 | 723 | PF00397 | 0.519 |
MOD_CDK_SPxK_1 | 716 | 722 | PF00069 | 0.511 |
MOD_CDK_SPxxK_3 | 716 | 723 | PF00069 | 0.375 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.452 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.406 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.421 |
MOD_CK1_1 | 566 | 572 | PF00069 | 0.480 |
MOD_CK1_1 | 577 | 583 | PF00069 | 0.482 |
MOD_CK1_1 | 630 | 636 | PF00069 | 0.419 |
MOD_CK1_1 | 653 | 659 | PF00069 | 0.514 |
MOD_CK1_1 | 663 | 669 | PF00069 | 0.563 |
MOD_CK1_1 | 750 | 756 | PF00069 | 0.618 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.521 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.462 |
MOD_CK2_1 | 345 | 351 | PF00069 | 0.478 |
MOD_CK2_1 | 488 | 494 | PF00069 | 0.486 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.503 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.503 |
MOD_GlcNHglycan | 205 | 211 | PF01048 | 0.199 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.266 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.286 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.306 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.467 |
MOD_GlcNHglycan | 514 | 517 | PF01048 | 0.266 |
MOD_GlcNHglycan | 630 | 633 | PF01048 | 0.305 |
MOD_GlcNHglycan | 634 | 637 | PF01048 | 0.310 |
MOD_GlcNHglycan | 655 | 658 | PF01048 | 0.377 |
MOD_GlcNHglycan | 660 | 663 | PF01048 | 0.354 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.437 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.451 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.420 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.503 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.465 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.420 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.456 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.466 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.465 |
MOD_GSK3_1 | 591 | 598 | PF00069 | 0.503 |
MOD_GSK3_1 | 628 | 635 | PF00069 | 0.561 |
MOD_GSK3_1 | 747 | 754 | PF00069 | 0.447 |
MOD_N-GLC_1 | 278 | 283 | PF02516 | 0.188 |
MOD_N-GLC_1 | 486 | 491 | PF02516 | 0.229 |
MOD_N-GLC_1 | 737 | 742 | PF02516 | 0.411 |
MOD_N-GLC_2 | 126 | 128 | PF02516 | 0.172 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.462 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.435 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.506 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.474 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.476 |
MOD_NEK2_1 | 392 | 397 | PF00069 | 0.521 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.462 |
MOD_NEK2_1 | 591 | 596 | PF00069 | 0.454 |
MOD_NEK2_1 | 612 | 617 | PF00069 | 0.522 |
MOD_NEK2_1 | 747 | 752 | PF00069 | 0.485 |
MOD_PIKK_1 | 228 | 234 | PF00454 | 0.421 |
MOD_PIKK_1 | 368 | 374 | PF00454 | 0.435 |
MOD_PIKK_1 | 387 | 393 | PF00454 | 0.503 |
MOD_PK_1 | 582 | 588 | PF00069 | 0.488 |
MOD_PKA_1 | 582 | 588 | PF00069 | 0.488 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.433 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.420 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.503 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.535 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.503 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.527 |
MOD_PKA_2 | 512 | 518 | PF00069 | 0.466 |
MOD_PKA_2 | 582 | 588 | PF00069 | 0.462 |
MOD_PKA_2 | 653 | 659 | PF00069 | 0.435 |
MOD_PKB_1 | 443 | 451 | PF00069 | 0.500 |
MOD_PKB_1 | 734 | 742 | PF00069 | 0.420 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.466 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.509 |
MOD_Plk_1 | 278 | 284 | PF00069 | 0.521 |
MOD_Plk_1 | 455 | 461 | PF00069 | 0.420 |
MOD_Plk_1 | 486 | 492 | PF00069 | 0.442 |
MOD_Plk_1 | 736 | 742 | PF00069 | 0.469 |
MOD_Plk_1 | 81 | 87 | PF00069 | 0.428 |
MOD_Plk_2-3 | 192 | 198 | PF00069 | 0.512 |
MOD_Plk_2-3 | 456 | 462 | PF00069 | 0.437 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.431 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.505 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.508 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.444 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.420 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.439 |
MOD_Plk_4 | 474 | 480 | PF00069 | 0.460 |
MOD_Plk_4 | 544 | 550 | PF00069 | 0.466 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.462 |
MOD_Plk_4 | 737 | 743 | PF00069 | 0.402 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.413 |
MOD_ProDKin_1 | 481 | 487 | PF00069 | 0.439 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.447 |
MOD_ProDKin_1 | 569 | 575 | PF00069 | 0.503 |
MOD_ProDKin_1 | 716 | 722 | PF00069 | 0.511 |
MOD_SUMO_rev_2 | 59 | 67 | PF00179 | 0.448 |
TRG_AP2beta_CARGO_1 | 589 | 599 | PF09066 | 0.503 |
TRG_DiLeu_BaEn_1 | 353 | 358 | PF01217 | 0.503 |
TRG_DiLeu_BaEn_1 | 744 | 749 | PF01217 | 0.472 |
TRG_DiLeu_BaEn_2 | 62 | 68 | PF01217 | 0.503 |
TRG_DiLeu_BaEn_4 | 312 | 318 | PF01217 | 0.372 |
TRG_DiLeu_BaEn_4 | 493 | 499 | PF01217 | 0.435 |
TRG_DiLeu_BaLyEn_6 | 608 | 613 | PF01217 | 0.478 |
TRG_DiLeu_BaLyEn_6 | 698 | 703 | PF01217 | 0.489 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 685 | 688 | PF00928 | 0.503 |
TRG_ER_diArg_1 | 161 | 164 | PF00400 | 0.424 |
TRG_ER_diArg_1 | 166 | 168 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 179 | 182 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 295 | 297 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 321 | 323 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 386 | 389 | PF00400 | 0.578 |
TRG_ER_diArg_1 | 420 | 422 | PF00400 | 0.432 |
TRG_ER_diArg_1 | 440 | 443 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 581 | 583 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 599 | 601 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 721 | 723 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 733 | 736 | PF00400 | 0.389 |
TRG_ER_diArg_1 | 760 | 763 | PF00400 | 0.652 |
TRG_NES_CRM1_1 | 307 | 319 | PF08389 | 0.503 |
TRG_NLS_MonoCore_2 | 760 | 765 | PF00514 | 0.565 |
TRG_NLS_MonoExtC_3 | 151 | 157 | PF00514 | 0.435 |
TRG_NLS_MonoExtC_3 | 761 | 766 | PF00514 | 0.564 |
TRG_NLS_MonoExtN_4 | 761 | 766 | PF00514 | 0.564 |
TRG_Pf-PMV_PEXEL_1 | 296 | 300 | PF00026 | 0.220 |
TRG_Pf-PMV_PEXEL_1 | 501 | 505 | PF00026 | 0.296 |
TRG_Pf-PMV_PEXEL_1 | 722 | 727 | PF00026 | 0.473 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5R4 | Leptomonas seymouri | 66% | 95% |
A0A3Q8IF06 | Leishmania donovani | 94% | 100% |
A0A422P0B5 | Trypanosoma rangeli | 45% | 100% |
A4HLU5 | Leishmania braziliensis | 82% | 97% |
D0A683 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AHQ0 | Leishmania infantum | 94% | 100% |
E9B471 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
O74113 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 22% | 100% |
V5BP84 | Trypanosoma cruzi | 44% | 100% |