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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 7 |
GO:0043226 | organelle | 2 | 7 |
GO:0043227 | membrane-bounded organelle | 3 | 7 |
GO:0043229 | intracellular organelle | 3 | 7 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
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: A4HLU5
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006259 | DNA metabolic process | 4 | 7 |
GO:0006270 | DNA replication initiation | 5 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0007049 | cell cycle | 2 | 6 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0051301 | cell division | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
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 | 198 | 202 | PF00656 | 0.395 |
CLV_C14_Caspase3-7 | 234 | 238 | PF00656 | 0.497 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.234 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.347 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.217 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.187 |
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.235 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.229 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.294 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 524 | 526 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 624 | 626 | PF00675 | 0.322 |
CLV_NRD_NRD_1 | 627 | 629 | PF00675 | 0.253 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.191 |
CLV_NRD_NRD_1 | 748 | 750 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 789 | 791 | PF00675 | 0.643 |
CLV_PCSK_FUR_1 | 161 | 165 | PF00082 | 0.253 |
CLV_PCSK_FUR_1 | 174 | 178 | PF00082 | 0.253 |
CLV_PCSK_FUR_1 | 184 | 188 | PF00082 | 0.178 |
CLV_PCSK_FUR_1 | 625 | 629 | PF00082 | 0.307 |
CLV_PCSK_FUR_1 | 787 | 791 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.234 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.161 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 623 | 625 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 627 | 629 | PF00082 | 0.253 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.191 |
CLV_PCSK_KEX2_1 | 748 | 750 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 789 | 791 | PF00082 | 0.648 |
CLV_PCSK_PC1ET2_1 | 172 | 174 | PF00082 | 0.307 |
CLV_PCSK_PC7_1 | 162 | 168 | PF00082 | 0.256 |
CLV_PCSK_PC7_1 | 182 | 188 | PF00082 | 0.161 |
CLV_PCSK_PC7_1 | 623 | 629 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.253 |
CLV_PCSK_SKI1_1 | 614 | 618 | PF00082 | 0.254 |
CLV_PCSK_SKI1_1 | 628 | 632 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 771 | 775 | PF00082 | 0.487 |
DEG_APCC_DBOX_1 | 409 | 417 | PF00400 | 0.507 |
DEG_APCC_DBOX_1 | 770 | 778 | PF00400 | 0.488 |
DEG_COP1_1 | 785 | 794 | PF00400 | 0.521 |
DEG_SPOP_SBC_1 | 578 | 582 | PF00917 | 0.453 |
DOC_CKS1_1 | 743 | 748 | PF01111 | 0.566 |
DOC_CYCLIN_RxL_1 | 628 | 639 | PF00134 | 0.463 |
DOC_CYCLIN_RxL_1 | 768 | 779 | PF00134 | 0.484 |
DOC_CYCLIN_yCln2_LP_2 | 96 | 102 | PF00134 | 0.453 |
DOC_MAPK_DCC_7 | 628 | 638 | PF00069 | 0.507 |
DOC_MAPK_FxFP_2 | 49 | 52 | PF00069 | 0.453 |
DOC_MAPK_MEF2A_6 | 420 | 427 | PF00069 | 0.507 |
DOC_MAPK_MEF2A_6 | 86 | 94 | PF00069 | 0.492 |
DOC_PP1_RVXF_1 | 132 | 139 | PF00149 | 0.453 |
DOC_PP1_RVXF_1 | 524 | 531 | PF00149 | 0.507 |
DOC_PP1_RVXF_1 | 612 | 618 | PF00149 | 0.453 |
DOC_PP2B_LxvP_1 | 28 | 31 | PF13499 | 0.453 |
DOC_PP2B_LxvP_1 | 96 | 99 | PF13499 | 0.453 |
DOC_PP4_FxxP_1 | 49 | 52 | PF00568 | 0.453 |
DOC_PP4_FxxP_1 | 743 | 746 | PF00568 | 0.543 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 568 | 572 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 587 | 591 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 651 | 655 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 671 | 675 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 686 | 690 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.453 |
DOC_USP7_MATH_2 | 508 | 514 | PF00917 | 0.395 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 512 | 517 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 593 | 598 | PF00397 | 0.453 |
DOC_WW_Pin1_4 | 742 | 747 | PF00397 | 0.563 |
LIG_14-3-3_CanoR_1 | 13 | 18 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 286 | 293 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 362 | 371 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 383 | 388 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 446 | 455 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 537 | 544 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 607 | 611 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 614 | 620 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 627 | 637 | PF00244 | 0.438 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.617 |
LIG_BIR_III_2 | 251 | 255 | PF00653 | 0.453 |
LIG_CaM_IQ_9 | 338 | 353 | PF13499 | 0.453 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.453 |
LIG_FHA_1 | 481 | 487 | PF00498 | 0.526 |
LIG_FHA_1 | 567 | 573 | PF00498 | 0.425 |
LIG_FHA_1 | 692 | 698 | PF00498 | 0.538 |
LIG_FHA_1 | 707 | 713 | PF00498 | 0.370 |
LIG_FHA_1 | 763 | 769 | PF00498 | 0.474 |
LIG_FHA_1 | 786 | 792 | PF00498 | 0.538 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.475 |
LIG_FHA_2 | 234 | 240 | PF00498 | 0.428 |
LIG_FHA_2 | 384 | 390 | PF00498 | 0.508 |
LIG_FHA_2 | 791 | 797 | PF00498 | 0.562 |
LIG_GBD_Chelix_1 | 611 | 619 | PF00786 | 0.253 |
LIG_LIR_Apic_2 | 389 | 395 | PF02991 | 0.391 |
LIG_LIR_Apic_2 | 740 | 746 | PF02991 | 0.543 |
LIG_LIR_Gen_1 | 385 | 395 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 58 | 68 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 600 | 610 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 708 | 715 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 88 | 99 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 9 | 19 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 103 | 108 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 117 | 122 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 324 | 328 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 385 | 391 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 600 | 605 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 613 | 619 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 708 | 714 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 88 | 94 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 9 | 14 | PF02991 | 0.369 |
LIG_NBox_RRM_1 | 551 | 561 | PF00076 | 0.453 |
LIG_NRBOX | 412 | 418 | PF00104 | 0.453 |
LIG_PCNA_yPIPBox_3 | 446 | 455 | PF02747 | 0.505 |
LIG_PCNA_yPIPBox_3 | 79 | 91 | PF02747 | 0.395 |
LIG_Pex14_2 | 49 | 53 | PF04695 | 0.453 |
LIG_REV1ctd_RIR_1 | 148 | 157 | PF16727 | 0.453 |
LIG_SH2_CRK | 586 | 590 | PF00017 | 0.453 |
LIG_SH2_NCK_1 | 586 | 590 | PF00017 | 0.471 |
LIG_SH2_PTP2 | 711 | 714 | PF00017 | 0.530 |
LIG_SH2_SRC | 273 | 276 | PF00017 | 0.456 |
LIG_SH2_STAP1 | 293 | 297 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 325 | 329 | PF00017 | 0.507 |
LIG_SH2_STAP1 | 477 | 481 | PF00017 | 0.453 |
LIG_SH2_STAT3 | 393 | 396 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 503 | 506 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 711 | 714 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 732 | 735 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 750 | 753 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 767 | 770 | PF00017 | 0.575 |
LIG_SH3_1 | 586 | 592 | PF00018 | 0.507 |
LIG_SH3_2 | 589 | 594 | PF14604 | 0.507 |
LIG_SH3_3 | 502 | 508 | PF00018 | 0.398 |
LIG_SH3_3 | 586 | 592 | PF00018 | 0.507 |
LIG_SH3_3 | 661 | 667 | PF00018 | 0.660 |
LIG_SH3_3 | 724 | 730 | PF00018 | 0.509 |
LIG_SUMO_SIM_anti_2 | 294 | 299 | PF11976 | 0.453 |
LIG_SUMO_SIM_anti_2 | 706 | 716 | PF11976 | 0.499 |
LIG_SUMO_SIM_anti_2 | 805 | 811 | PF11976 | 0.612 |
LIG_SUMO_SIM_par_1 | 111 | 117 | PF11976 | 0.453 |
LIG_SUMO_SIM_par_1 | 539 | 545 | PF11976 | 0.456 |
LIG_SUMO_SIM_par_1 | 634 | 639 | PF11976 | 0.453 |
LIG_SUMO_SIM_par_1 | 674 | 680 | PF11976 | 0.484 |
LIG_SUMO_SIM_par_1 | 706 | 716 | PF11976 | 0.517 |
LIG_SUMO_SIM_par_1 | 770 | 776 | PF11976 | 0.483 |
LIG_SUMO_SIM_par_1 | 805 | 811 | PF11976 | 0.576 |
LIG_SUMO_SIM_par_1 | 98 | 104 | PF11976 | 0.453 |
LIG_TRAF2_1 | 227 | 230 | PF00917 | 0.507 |
LIG_TRAF2_1 | 334 | 337 | PF00917 | 0.429 |
LIG_TRAF2_2 | 254 | 259 | PF00917 | 0.453 |
LIG_TRFH_1 | 53 | 57 | PF08558 | 0.453 |
LIG_TYR_ITSM | 707 | 714 | PF00017 | 0.389 |
LIG_UBA3_1 | 772 | 778 | PF00899 | 0.488 |
LIG_WRC_WIRS_1 | 599 | 604 | PF05994 | 0.453 |
LIG_WRPW_2 | 119 | 122 | PF00400 | 0.453 |
LIG_WW_3 | 745 | 749 | PF00397 | 0.591 |
MOD_CDK_SPxK_1 | 742 | 748 | PF00069 | 0.563 |
MOD_CDK_SPxxK_3 | 742 | 749 | PF00069 | 0.528 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.463 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.431 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.395 |
MOD_CK1_1 | 509 | 515 | PF00069 | 0.421 |
MOD_CK1_1 | 590 | 596 | PF00069 | 0.529 |
MOD_CK1_1 | 601 | 607 | PF00069 | 0.489 |
MOD_CK1_1 | 689 | 695 | PF00069 | 0.677 |
MOD_CK1_1 | 776 | 782 | PF00069 | 0.634 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.475 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.453 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.456 |
MOD_CK2_1 | 512 | 518 | PF00069 | 0.563 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.453 |
MOD_CK2_1 | 671 | 677 | PF00069 | 0.553 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.453 |
MOD_CK2_1 | 790 | 796 | PF00069 | 0.639 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.344 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.307 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.232 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.246 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.563 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.307 |
MOD_GlcNHglycan | 654 | 657 | PF01048 | 0.579 |
MOD_GlcNHglycan | 658 | 661 | PF01048 | 0.666 |
MOD_GlcNHglycan | 664 | 667 | PF01048 | 0.595 |
MOD_GlcNHglycan | 679 | 682 | PF01048 | 0.591 |
MOD_GlcNHglycan | 686 | 689 | PF01048 | 0.732 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.374 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.415 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.475 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.453 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.453 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.453 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.507 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.419 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.453 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.449 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.456 |
MOD_GSK3_1 | 652 | 659 | PF00069 | 0.713 |
MOD_GSK3_1 | 689 | 696 | PF00069 | 0.515 |
MOD_GSK3_1 | 773 | 780 | PF00069 | 0.506 |
MOD_N-GLC_1 | 656 | 661 | PF02516 | 0.617 |
MOD_N-GLC_1 | 763 | 768 | PF02516 | 0.556 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.453 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.453 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.530 |
MOD_NEK2_1 | 382 | 387 | PF00069 | 0.416 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.455 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.475 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.395 |
MOD_NEK2_1 | 615 | 620 | PF00069 | 0.453 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.453 |
MOD_NEK2_1 | 773 | 778 | PF00069 | 0.496 |
MOD_PIKK_1 | 252 | 258 | PF00454 | 0.453 |
MOD_PIKK_1 | 411 | 417 | PF00454 | 0.395 |
MOD_PIKK_1 | 530 | 536 | PF00454 | 0.395 |
MOD_PKA_1 | 362 | 368 | PF00069 | 0.395 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.385 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.395 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.396 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.468 |
MOD_PKA_2 | 361 | 367 | PF00069 | 0.528 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.469 |
MOD_PKA_2 | 411 | 417 | PF00069 | 0.471 |
MOD_PKA_2 | 506 | 512 | PF00069 | 0.395 |
MOD_PKA_2 | 536 | 542 | PF00069 | 0.507 |
MOD_PKA_2 | 606 | 612 | PF00069 | 0.453 |
MOD_PKB_1 | 467 | 475 | PF00069 | 0.450 |
MOD_PKB_1 | 760 | 768 | PF00069 | 0.564 |
MOD_Plk_1 | 219 | 225 | PF00069 | 0.507 |
MOD_Plk_1 | 293 | 299 | PF00069 | 0.453 |
MOD_Plk_1 | 479 | 485 | PF00069 | 0.455 |
MOD_Plk_1 | 509 | 515 | PF00069 | 0.447 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.431 |
MOD_Plk_1 | 762 | 768 | PF00069 | 0.485 |
MOD_Plk_2-3 | 216 | 222 | PF00069 | 0.507 |
MOD_Plk_2-3 | 231 | 237 | PF00069 | 0.397 |
MOD_Plk_2-3 | 480 | 486 | PF00069 | 0.507 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.369 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.453 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.453 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.471 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.453 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.395 |
MOD_Plk_4 | 498 | 504 | PF00069 | 0.453 |
MOD_Plk_4 | 568 | 574 | PF00069 | 0.507 |
MOD_Plk_4 | 606 | 612 | PF00069 | 0.453 |
MOD_Plk_4 | 671 | 677 | PF00069 | 0.486 |
MOD_Plk_4 | 693 | 699 | PF00069 | 0.540 |
MOD_Plk_4 | 763 | 769 | PF00069 | 0.474 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.446 |
MOD_ProDKin_1 | 512 | 518 | PF00069 | 0.474 |
MOD_ProDKin_1 | 593 | 599 | PF00069 | 0.453 |
MOD_ProDKin_1 | 742 | 748 | PF00069 | 0.563 |
TRG_AP2beta_CARGO_1 | 613 | 623 | PF09066 | 0.453 |
TRG_DiLeu_BaEn_1 | 377 | 382 | PF01217 | 0.453 |
TRG_DiLeu_BaEn_1 | 770 | 775 | PF01217 | 0.486 |
TRG_DiLeu_BaEn_2 | 62 | 68 | PF01217 | 0.453 |
TRG_DiLeu_BaLyEn_6 | 632 | 637 | PF01217 | 0.502 |
TRG_DiLeu_BaLyEn_6 | 724 | 729 | PF01217 | 0.583 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 711 | 714 | PF00928 | 0.454 |
TRG_ER_diArg_1 | 127 | 129 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 161 | 164 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 165 | 168 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 173 | 176 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 183 | 186 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 187 | 190 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 319 | 321 | PF00400 | 0.453 |
TRG_ER_diArg_1 | 361 | 363 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 410 | 413 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 464 | 467 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 623 | 625 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 64 | 66 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 747 | 749 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 759 | 762 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 786 | 789 | PF00400 | 0.631 |
TRG_NES_CRM1_1 | 331 | 343 | PF08389 | 0.453 |
TRG_NLS_Bipartite_1 | 161 | 176 | PF00514 | 0.395 |
TRG_NLS_MonoExtC_3 | 171 | 176 | PF00514 | 0.395 |
TRG_Pf-PMV_PEXEL_1 | 320 | 324 | PF00026 | 0.253 |
TRG_Pf-PMV_PEXEL_1 | 525 | 529 | PF00026 | 0.273 |
TRG_Pf-PMV_PEXEL_1 | 66 | 70 | PF00026 | 0.191 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5R4 | Leptomonas seymouri | 65% | 98% |
A0A3Q8IF06 | Leishmania donovani | 81% | 100% |
E9AHQ0 | Leishmania infantum | 81% | 100% |
E9B471 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q08032 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 22% | 100% |
Q4Q3V5 | Leishmania major | 82% | 99% |