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. | yes | yes: 15 |
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7XBE8
Term | Name | Level | Count |
---|---|---|---|
GO:0006325 | chromatin organization | 4 | 1 |
GO:0006335 | DNA replication-dependent chromatin assembly | 5 | 1 |
GO:0006338 | chromatin remodeling | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0031055 | chromatin remodeling at centromere | 6 | 1 |
GO:0034080 | CENP-A containing chromatin assembly | 7 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0042393 | histone binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 401 | 403 | PF00675 | 0.760 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.786 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.793 |
CLV_PCSK_PC1ET2_1 | 406 | 408 | PF00082 | 0.841 |
CLV_PCSK_PC1ET2_1 | 421 | 423 | PF00082 | 0.793 |
CLV_PCSK_PC7_1 | 402 | 408 | PF00082 | 0.841 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.580 |
DEG_APCC_DBOX_1 | 266 | 274 | PF00400 | 0.662 |
DEG_SPOP_SBC_1 | 50 | 54 | PF00917 | 0.915 |
DOC_CKS1_1 | 322 | 327 | PF01111 | 0.759 |
DOC_CYCLIN_yCln2_LP_2 | 357 | 363 | PF00134 | 0.793 |
DOC_PP1_RVXF_1 | 167 | 173 | PF00149 | 0.463 |
DOC_PP2B_LxvP_1 | 357 | 360 | PF13499 | 0.701 |
DOC_PP2B_LxvP_1 | 381 | 384 | PF13499 | 0.765 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.875 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.794 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.807 |
DOC_USP7_MATH_2 | 27 | 33 | PF00917 | 0.668 |
DOC_USP7_MATH_2 | 325 | 331 | PF00917 | 0.735 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.835 |
LIG_14-3-3_CanoR_1 | 265 | 271 | PF00244 | 0.593 |
LIG_Actin_WH2_2 | 239 | 257 | PF00022 | 0.549 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.871 |
LIG_BIR_III_2 | 226 | 230 | PF00653 | 0.703 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.554 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.869 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.818 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.746 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.605 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.653 |
LIG_FHA_2 | 406 | 412 | PF00498 | 0.842 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.927 |
LIG_FHA_2 | 78 | 84 | PF00498 | 0.646 |
LIG_GBD_Chelix_1 | 281 | 289 | PF00786 | 0.639 |
LIG_LIR_Gen_1 | 160 | 170 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 353 | 363 | PF02991 | 0.755 |
LIG_LIR_Nem_3 | 105 | 111 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 160 | 165 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 327 | 331 | PF02991 | 0.705 |
LIG_NRBOX | 288 | 294 | PF00104 | 0.666 |
LIG_PCNA_PIPBox_1 | 107 | 116 | PF02747 | 0.507 |
LIG_PCNA_yPIPBox_3 | 138 | 150 | PF02747 | 0.709 |
LIG_SH2_CRK | 108 | 112 | PF00017 | 0.513 |
LIG_SH2_CRK | 221 | 225 | PF00017 | 0.533 |
LIG_SH2_GRB2like | 162 | 165 | PF00017 | 0.602 |
LIG_SH2_PTP2 | 162 | 165 | PF00017 | 0.602 |
LIG_SH2_SRC | 100 | 103 | PF00017 | 0.572 |
LIG_SH2_STAP1 | 100 | 104 | PF00017 | 0.548 |
LIG_SH2_STAP1 | 207 | 211 | PF00017 | 0.517 |
LIG_SH2_STAP1 | 214 | 218 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.779 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.752 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.866 |
LIG_SUMO_SIM_anti_2 | 230 | 238 | PF11976 | 0.702 |
LIG_TRAF2_1 | 228 | 231 | PF00917 | 0.711 |
LIG_TRAF2_1 | 27 | 30 | PF00917 | 0.904 |
LIG_TRAF2_1 | 324 | 327 | PF00917 | 0.636 |
LIG_TRAF2_1 | 45 | 48 | PF00917 | 0.797 |
LIG_TRAF2_1 | 80 | 83 | PF00917 | 0.644 |
LIG_TYR_ITIM | 106 | 111 | PF00017 | 0.504 |
LIG_TYR_ITIM | 219 | 224 | PF00017 | 0.539 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.710 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.863 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.796 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.661 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.580 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.653 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.827 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.779 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.680 |
MOD_DYRK1A_RPxSP_1 | 388 | 392 | PF00069 | 0.866 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.599 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.723 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.775 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.889 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.907 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.843 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.697 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.703 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.678 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.632 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.866 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.875 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.768 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.727 |
MOD_NEK2_2 | 157 | 162 | PF00069 | 0.539 |
MOD_PIKK_1 | 132 | 138 | PF00454 | 0.472 |
MOD_PIKK_1 | 43 | 49 | PF00454 | 0.913 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.604 |
MOD_PKB_1 | 422 | 430 | PF00069 | 0.869 |
MOD_Plk_1 | 29 | 35 | PF00069 | 0.706 |
MOD_Plk_1 | 352 | 358 | PF00069 | 0.740 |
MOD_Plk_1 | 409 | 415 | PF00069 | 0.879 |
MOD_Plk_1 | 72 | 78 | PF00069 | 0.805 |
MOD_Plk_2-3 | 327 | 333 | PF00069 | 0.708 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.686 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.671 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.821 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.736 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.761 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.835 |
MOD_SUMO_for_1 | 35 | 38 | PF00179 | 0.827 |
MOD_SUMO_rev_2 | 226 | 235 | PF00179 | 0.709 |
MOD_SUMO_rev_2 | 271 | 275 | PF00179 | 0.634 |
MOD_SUMO_rev_2 | 330 | 338 | PF00179 | 0.762 |
MOD_SUMO_rev_2 | 414 | 423 | PF00179 | 0.794 |
TRG_DiLeu_BaEn_1 | 21 | 26 | PF01217 | 0.910 |
TRG_DiLeu_BaEn_1 | 288 | 293 | PF01217 | 0.663 |
TRG_DiLeu_BaLyEn_6 | 135 | 140 | PF01217 | 0.574 |
TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.507 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.602 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.736 |
TRG_NLS_Bipartite_1 | 403 | 425 | PF00514 | 0.843 |
TRG_NLS_MonoExtC_3 | 401 | 406 | PF00514 | 0.774 |
TRG_NLS_MonoExtC_3 | 420 | 426 | PF00514 | 0.752 |
TRG_NLS_MonoExtN_4 | 402 | 407 | PF00514 | 0.756 |
TRG_NLS_MonoExtN_4 | 418 | 425 | PF00514 | 0.808 |
TRG_Pf-PMV_PEXEL_1 | 138 | 143 | PF00026 | 0.660 |
TRG_Pf-PMV_PEXEL_1 | 222 | 226 | PF00026 | 0.524 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXN4 | Leptomonas seymouri | 83% | 100% |
A0A0S4IPT5 | Bodo saltans | 46% | 100% |
A0A1X0P488 | Trypanosomatidae | 49% | 89% |
A0A3R7NPK3 | Trypanosoma rangeli | 49% | 95% |
A4HPS2 | Leishmania braziliensis | 87% | 100% |
A4ICZ1 | Leishmania infantum | 100% | 100% |
D0A8N7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9ATI7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
Q4Q111 | Leishmania major | 97% | 100% |
V5BS19 | Trypanosoma cruzi | 52% | 94% |