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: 25 |
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:0005737 | cytoplasm | 2 | 1 |
GO:0010494 | cytoplasmic stress granule | 5 | 1 |
GO:0035770 | ribonucleoprotein granule | 3 | 1 |
GO:0036464 | cytoplasmic ribonucleoprotein granule | 4 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ANC1
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0034063 | stress granule assembly | 7 | 1 |
GO:0070925 | organelle assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0140694 | non-membrane-bounded organelle assembly | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003723 | RNA binding | 4 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 41 | 45 | PF00656 | 0.380 |
CLV_C14_Caspase3-7 | 482 | 486 | PF00656 | 0.852 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 502 | 504 | PF00675 | 0.821 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.761 |
CLV_PCSK_KEX2_1 | 502 | 504 | PF00082 | 0.808 |
CLV_PCSK_PC1ET2_1 | 223 | 225 | PF00082 | 0.753 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.639 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.757 |
DEG_SCF_FBW7_1 | 244 | 251 | PF00400 | 0.632 |
DEG_SPOP_SBC_1 | 234 | 238 | PF00917 | 0.777 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 190 | 196 | PF00134 | 0.469 |
DOC_MAPK_MEF2A_6 | 12 | 20 | PF00069 | 0.357 |
DOC_PP1_RVXF_1 | 115 | 122 | PF00149 | 0.612 |
DOC_PP2B_LxvP_1 | 277 | 280 | PF13499 | 0.794 |
DOC_PP4_FxxP_1 | 303 | 306 | PF00568 | 0.721 |
DOC_PP4_MxPP_1 | 421 | 424 | PF00568 | 0.771 |
DOC_SPAK_OSR1_1 | 148 | 152 | PF12202 | 0.475 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.820 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 483 | 487 | PF00917 | 0.764 |
DOC_USP7_UBL2_3 | 523 | 527 | PF12436 | 0.703 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.828 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.690 |
LIG_14-3-3_CanoR_1 | 449 | 459 | PF00244 | 0.748 |
LIG_BIR_III_4 | 218 | 222 | PF00653 | 0.729 |
LIG_deltaCOP1_diTrp_1 | 330 | 337 | PF00928 | 0.708 |
LIG_eIF4E_1 | 15 | 21 | PF01652 | 0.357 |
LIG_EVH1_1 | 277 | 281 | PF00568 | 0.794 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.357 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.375 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.373 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.475 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.725 |
LIG_FHA_1 | 496 | 502 | PF00498 | 0.745 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.366 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.344 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.357 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.758 |
LIG_FHA_2 | 41 | 47 | PF00498 | 0.369 |
LIG_LIR_Apic_2 | 301 | 306 | PF02991 | 0.724 |
LIG_LIR_Apic_2 | 322 | 328 | PF02991 | 0.624 |
LIG_LIR_Apic_2 | 343 | 348 | PF02991 | 0.763 |
LIG_LIR_Gen_1 | 137 | 145 | PF02991 | 0.590 |
LIG_LIR_Gen_1 | 14 | 25 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 137 | 143 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 14 | 20 | PF02991 | 0.383 |
LIG_PAM2_1 | 294 | 306 | PF00658 | 0.659 |
LIG_RPA_C_Fungi | 37 | 49 | PF08784 | 0.469 |
LIG_SH2_CRK | 325 | 329 | PF00017 | 0.633 |
LIG_SH2_CRK | 345 | 349 | PF00017 | 0.779 |
LIG_SH2_CRK | 360 | 364 | PF00017 | 0.568 |
LIG_SH2_GRB2like | 17 | 20 | PF00017 | 0.357 |
LIG_SH2_NCK_1 | 325 | 329 | PF00017 | 0.691 |
LIG_SH2_NCK_1 | 345 | 349 | PF00017 | 0.791 |
LIG_SH2_SRC | 84 | 87 | PF00017 | 0.469 |
LIG_SH2_STAP1 | 160 | 164 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 338 | 342 | PF00017 | 0.671 |
LIG_SH2_STAP1 | 84 | 88 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.475 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.768 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.810 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.684 |
LIG_SH3_3 | 290 | 296 | PF00018 | 0.651 |
LIG_SH3_3 | 299 | 305 | PF00018 | 0.738 |
LIG_SH3_3 | 361 | 367 | PF00018 | 0.748 |
LIG_SH3_3 | 421 | 427 | PF00018 | 0.747 |
LIG_SH3_3 | 453 | 459 | PF00018 | 0.700 |
LIG_SUMO_SIM_par_1 | 23 | 29 | PF11976 | 0.475 |
LIG_TRAF2_1 | 270 | 273 | PF00917 | 0.686 |
LIG_TYR_ITIM | 13 | 18 | PF00017 | 0.357 |
LIG_UBA3_1 | 87 | 93 | PF00899 | 0.475 |
LIG_WRC_WIRS_1 | 307 | 312 | PF05994 | 0.642 |
MOD_CDC14_SPxK_1 | 434 | 437 | PF00782 | 0.760 |
MOD_CDK_SPxK_1 | 431 | 437 | PF00069 | 0.768 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.700 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.357 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.778 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.650 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.678 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.470 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.357 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.469 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.756 |
MOD_Cter_Amidation | 521 | 524 | PF01082 | 0.788 |
MOD_GlcNHglycan | 185 | 189 | PF01048 | 0.431 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.693 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.757 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.609 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.814 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.566 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.783 |
MOD_GlcNHglycan | 485 | 489 | PF01048 | 0.736 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.380 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.745 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.696 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.706 |
MOD_GSK3_1 | 459 | 466 | PF00069 | 0.847 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.549 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.659 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.367 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.418 |
MOD_PIKK_1 | 451 | 457 | PF00454 | 0.796 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.728 |
MOD_PKA_2 | 448 | 454 | PF00069 | 0.728 |
MOD_Plk_1 | 340 | 346 | PF00069 | 0.630 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.390 |
MOD_Plk_2-3 | 115 | 121 | PF00069 | 0.698 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.475 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.855 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.524 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.566 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.726 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.714 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.828 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.688 |
MOD_SUMO_rev_2 | 109 | 119 | PF00179 | 0.721 |
MOD_SUMO_rev_2 | 165 | 170 | PF00179 | 0.469 |
MOD_SUMO_rev_2 | 85 | 95 | PF00179 | 0.469 |
TRG_DiLeu_BaEn_2 | 50 | 56 | PF01217 | 0.469 |
TRG_DiLeu_BaEn_4 | 272 | 278 | PF01217 | 0.795 |
TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.357 |
TRG_ER_diArg_1 | 501 | 503 | PF00400 | 0.807 |
TRG_ER_diLys_1 | 523 | 527 | PF00400 | 0.856 |
TRG_NLS_MonoExtC_3 | 498 | 503 | PF00514 | 0.806 |
TRG_NLS_MonoExtN_4 | 496 | 503 | PF00514 | 0.747 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I433 | Leptomonas seymouri | 68% | 100% |
A0A1X0NQC5 | Trypanosomatidae | 35% | 95% |
A0A3S5H6H2 | Leishmania donovani | 96% | 100% |
A0A422NGM0 | Trypanosoma rangeli | 37% | 96% |
A4H699 | Leishmania braziliensis | 87% | 100% |
A4HUM3 | Leishmania infantum | 96% | 100% |
Q4QHA3 | Leishmania major | 94% | 100% |
V5DKQ2 | Trypanosoma cruzi | 37% | 96% |