Uncharacterized Protein, Uncharacterized
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: A4ICZ1
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 | 0.625 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.643 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.646 |
CLV_PCSK_PC1ET2_1 | 406 | 408 | PF00082 | 0.707 |
CLV_PCSK_PC1ET2_1 | 421 | 423 | PF00082 | 0.646 |
CLV_PCSK_PC7_1 | 402 | 408 | PF00082 | 0.709 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.674 |
DEG_APCC_DBOX_1 | 266 | 274 | PF00400 | 0.461 |
DEG_SPOP_SBC_1 | 50 | 54 | PF00917 | 0.683 |
DOC_CKS1_1 | 322 | 327 | PF01111 | 0.652 |
DOC_CYCLIN_yCln2_LP_2 | 357 | 363 | PF00134 | 0.632 |
DOC_PP1_RVXF_1 | 167 | 173 | PF00149 | 0.329 |
DOC_PP2B_LxvP_1 | 357 | 360 | PF13499 | 0.542 |
DOC_PP2B_LxvP_1 | 381 | 384 | PF13499 | 0.615 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.751 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.672 |
DOC_USP7_MATH_2 | 325 | 331 | PF00917 | 0.618 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.714 |
LIG_14-3-3_CanoR_1 | 265 | 271 | PF00244 | 0.481 |
LIG_Actin_WH2_2 | 239 | 257 | PF00022 | 0.377 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.783 |
LIG_BIR_III_2 | 226 | 230 | PF00653 | 0.498 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.426 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.751 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.635 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.640 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.482 |
LIG_FHA_2 | 322 | 328 | PF00498 | 0.548 |
LIG_FHA_2 | 406 | 412 | PF00498 | 0.715 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.813 |
LIG_FHA_2 | 78 | 84 | PF00498 | 0.514 |
LIG_GBD_Chelix_1 | 281 | 289 | PF00786 | 0.532 |
LIG_LIR_Gen_1 | 160 | 170 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 353 | 363 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 105 | 111 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 160 | 165 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 327 | 331 | PF02991 | 0.645 |
LIG_NRBOX | 288 | 294 | PF00104 | 0.465 |
LIG_PCNA_PIPBox_1 | 107 | 116 | PF02747 | 0.375 |
LIG_PCNA_yPIPBox_3 | 138 | 150 | PF02747 | 0.602 |
LIG_SH2_CRK | 108 | 112 | PF00017 | 0.381 |
LIG_SH2_CRK | 221 | 225 | PF00017 | 0.443 |
LIG_SH2_GRB2like | 162 | 165 | PF00017 | 0.493 |
LIG_SH2_PTP2 | 162 | 165 | PF00017 | 0.493 |
LIG_SH2_SRC | 100 | 103 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 100 | 104 | PF00017 | 0.415 |
LIG_SH2_STAP1 | 207 | 211 | PF00017 | 0.386 |
LIG_SH2_STAP1 | 214 | 218 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.656 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.647 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.760 |
LIG_SUMO_SIM_anti_2 | 230 | 238 | PF11976 | 0.608 |
LIG_TRAF2_1 | 228 | 231 | PF00917 | 0.640 |
LIG_TRAF2_1 | 324 | 327 | PF00917 | 0.517 |
LIG_TRAF2_1 | 45 | 48 | PF00917 | 0.711 |
LIG_TRAF2_1 | 80 | 83 | PF00917 | 0.510 |
LIG_TYR_ITIM | 106 | 111 | PF00017 | 0.373 |
LIG_TYR_ITIM | 219 | 224 | PF00017 | 0.403 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.586 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.751 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.661 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.567 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.452 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.525 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.694 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.619 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.550 |
MOD_DYRK1A_RPxSP_1 | 388 | 392 | PF00069 | 0.760 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.537 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.566 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.614 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.692 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.652 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.729 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.494 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.539 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.519 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.798 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.747 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.758 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.631 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.611 |
MOD_NEK2_2 | 157 | 162 | PF00069 | 0.409 |
MOD_PIKK_1 | 132 | 138 | PF00454 | 0.342 |
MOD_PIKK_1 | 43 | 49 | PF00454 | 0.693 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.485 |
MOD_PKB_1 | 422 | 430 | PF00069 | 0.748 |
MOD_Plk_1 | 29 | 35 | PF00069 | 0.528 |
MOD_Plk_1 | 352 | 358 | PF00069 | 0.593 |
MOD_Plk_1 | 409 | 415 | PF00069 | 0.771 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.727 |
MOD_Plk_1 | 72 | 78 | PF00069 | 0.709 |
MOD_Plk_2-3 | 327 | 333 | PF00069 | 0.608 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.483 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.529 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.702 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.611 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.653 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.713 |
MOD_SUMO_for_1 | 35 | 38 | PF00179 | 0.685 |
MOD_SUMO_rev_2 | 226 | 235 | PF00179 | 0.504 |
MOD_SUMO_rev_2 | 271 | 275 | PF00179 | 0.517 |
MOD_SUMO_rev_2 | 330 | 338 | PF00179 | 0.659 |
MOD_SUMO_rev_2 | 414 | 423 | PF00179 | 0.647 |
TRG_DiLeu_BaEn_1 | 21 | 26 | PF01217 | 0.725 |
TRG_DiLeu_BaEn_1 | 288 | 293 | PF01217 | 0.462 |
TRG_DiLeu_BaLyEn_6 | 135 | 140 | PF01217 | 0.452 |
TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.579 |
TRG_NLS_Bipartite_1 | 403 | 425 | PF00514 | 0.708 |
TRG_NLS_MonoExtC_3 | 401 | 406 | PF00514 | 0.634 |
TRG_NLS_MonoExtC_3 | 420 | 426 | PF00514 | 0.606 |
TRG_NLS_MonoExtN_4 | 402 | 407 | PF00514 | 0.616 |
TRG_NLS_MonoExtN_4 | 418 | 425 | PF00514 | 0.662 |
TRG_Pf-PMV_PEXEL_1 | 138 | 143 | PF00026 | 0.554 |
TRG_Pf-PMV_PEXEL_1 | 222 | 226 | PF00026 | 0.397 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXN4 | Leptomonas seymouri | 83% | 100% |
A0A0S4IPT5 | Bodo saltans | 46% | 100% |
A0A1X0P488 | Trypanosomatidae | 49% | 89% |
A0A3R7NPK3 | Trypanosoma rangeli | 49% | 95% |
A0A3S7XBE8 | Leishmania donovani | 100% | 100% |
A4HPS2 | Leishmania braziliensis | 87% | 100% |
D0A8N7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9ATI7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
Q4Q111 | Leishmania major | 97% | 100% |
V5BS19 | Trypanosoma cruzi | 53% | 94% |