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: 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: A4HPS2
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 | 404 | 406 | PF00675 | 0.602 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 424 | 426 | PF00082 | 0.629 |
CLV_PCSK_PC1ET2_1 | 409 | 411 | PF00082 | 0.691 |
CLV_PCSK_PC1ET2_1 | 424 | 426 | PF00082 | 0.629 |
CLV_PCSK_PC7_1 | 405 | 411 | PF00082 | 0.691 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.453 |
DEG_APCC_DBOX_1 | 171 | 179 | PF00400 | 0.251 |
DEG_APCC_DBOX_1 | 196 | 204 | PF00400 | 0.236 |
DEG_APCC_DBOX_1 | 269 | 277 | PF00400 | 0.440 |
DEG_SPOP_SBC_1 | 52 | 56 | PF00917 | 0.763 |
DOC_CKS1_1 | 325 | 330 | PF01111 | 0.635 |
DOC_CYCLIN_yCln2_LP_2 | 360 | 366 | PF00134 | 0.647 |
DOC_PP2B_LxvP_1 | 360 | 363 | PF13499 | 0.562 |
DOC_PP2B_LxvP_1 | 384 | 387 | PF13499 | 0.603 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.668 |
DOC_USP7_MATH_2 | 328 | 334 | PF00917 | 0.592 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.704 |
LIG_14-3-3_CanoR_1 | 145 | 150 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 268 | 274 | PF00244 | 0.460 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.741 |
LIG_BIR_III_2 | 229 | 233 | PF00653 | 0.481 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.412 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.259 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.614 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.477 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.505 |
LIG_FHA_2 | 409 | 415 | PF00498 | 0.700 |
LIG_FHA_2 | 53 | 59 | PF00498 | 0.817 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.499 |
LIG_GBD_Chelix_1 | 284 | 292 | PF00786 | 0.510 |
LIG_LIR_Gen_1 | 163 | 173 | PF02991 | 0.332 |
LIG_LIR_Gen_1 | 356 | 366 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 108 | 114 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 163 | 168 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 330 | 334 | PF02991 | 0.598 |
LIG_NRBOX | 291 | 297 | PF00104 | 0.440 |
LIG_PCNA_PIPBox_1 | 110 | 119 | PF02747 | 0.357 |
LIG_PCNA_yPIPBox_3 | 141 | 153 | PF02747 | 0.577 |
LIG_SH2_CRK | 111 | 115 | PF00017 | 0.364 |
LIG_SH2_CRK | 224 | 228 | PF00017 | 0.388 |
LIG_SH2_GRB2like | 165 | 168 | PF00017 | 0.478 |
LIG_SH2_PTP2 | 165 | 168 | PF00017 | 0.478 |
LIG_SH2_SRC | 103 | 106 | PF00017 | 0.414 |
LIG_SH2_STAP1 | 103 | 107 | PF00017 | 0.431 |
LIG_SH2_STAP1 | 210 | 214 | PF00017 | 0.369 |
LIG_SH2_STAP1 | 217 | 221 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.664 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.625 |
LIG_SH3_3 | 392 | 398 | PF00018 | 0.708 |
LIG_SUMO_SIM_anti_2 | 233 | 241 | PF11976 | 0.592 |
LIG_TRAF2_1 | 231 | 234 | PF00917 | 0.626 |
LIG_TRAF2_1 | 27 | 30 | PF00917 | 0.594 |
LIG_TRAF2_1 | 327 | 330 | PF00917 | 0.514 |
LIG_TRAF2_1 | 38 | 41 | PF00917 | 0.694 |
LIG_TRAF2_1 | 56 | 59 | PF00917 | 0.653 |
LIG_TRAF2_1 | 83 | 86 | PF00917 | 0.495 |
LIG_TYR_ITIM | 109 | 114 | PF00017 | 0.354 |
LIG_TYR_ITIM | 222 | 227 | PF00017 | 0.395 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.571 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.731 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.691 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.417 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.508 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.676 |
MOD_CK2_1 | 52 | 58 | PF00069 | 0.607 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.535 |
MOD_DYRK1A_RPxSP_1 | 391 | 395 | PF00069 | 0.726 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.597 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.513 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.571 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.629 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.701 |
MOD_GlcNHglycan | 395 | 398 | PF01048 | 0.622 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.751 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.786 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.697 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.540 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.579 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.598 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.558 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.718 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.743 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.665 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.519 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.571 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.580 |
MOD_PIKK_1 | 135 | 141 | PF00454 | 0.320 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.685 |
MOD_PKA_2 | 144 | 150 | PF00069 | 0.437 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.463 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.328 |
MOD_PKB_1 | 425 | 433 | PF00069 | 0.739 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.425 |
MOD_Plk_1 | 355 | 361 | PF00069 | 0.600 |
MOD_Plk_1 | 412 | 418 | PF00069 | 0.747 |
MOD_Plk_1 | 75 | 81 | PF00069 | 0.699 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.315 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.466 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.490 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.694 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.599 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.535 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.520 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.639 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.704 |
MOD_SUMO_for_1 | 27 | 30 | PF00179 | 0.522 |
MOD_SUMO_rev_2 | 229 | 238 | PF00179 | 0.489 |
MOD_SUMO_rev_2 | 274 | 278 | PF00179 | 0.496 |
MOD_SUMO_rev_2 | 333 | 341 | PF00179 | 0.628 |
MOD_SUMO_rev_2 | 417 | 426 | PF00179 | 0.636 |
TRG_DiLeu_BaEn_1 | 291 | 296 | PF01217 | 0.437 |
TRG_DiLeu_BaLyEn_6 | 138 | 143 | PF01217 | 0.429 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.384 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.478 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 359 | 362 | PF00928 | 0.586 |
TRG_ER_diArg_1 | 153 | 156 | PF00400 | 0.402 |
TRG_NLS_Bipartite_1 | 406 | 428 | PF00514 | 0.696 |
TRG_NLS_MonoCore_2 | 423 | 428 | PF00514 | 0.628 |
TRG_NLS_MonoExtC_3 | 404 | 409 | PF00514 | 0.615 |
TRG_NLS_MonoExtC_3 | 423 | 429 | PF00514 | 0.597 |
TRG_NLS_MonoExtN_4 | 405 | 410 | PF00514 | 0.597 |
TRG_NLS_MonoExtN_4 | 421 | 428 | PF00514 | 0.655 |
TRG_Pf-PMV_PEXEL_1 | 141 | 146 | PF00026 | 0.529 |
TRG_Pf-PMV_PEXEL_1 | 225 | 229 | PF00026 | 0.379 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXN4 | Leptomonas seymouri | 82% | 100% |
A0A0S4IPT5 | Bodo saltans | 48% | 100% |
A0A1X0P488 | Trypanosomatidae | 49% | 89% |
A0A3R7NPK3 | Trypanosoma rangeli | 50% | 95% |
A0A3S7XBE8 | Leishmania donovani | 87% | 100% |
A4ICZ1 | Leishmania infantum | 87% | 100% |
D0A8N7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9ATI7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q111 | Leishmania major | 84% | 99% |
V5BS19 | Trypanosoma cruzi | 54% | 95% |