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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
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: A4HUC2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
DEG_SCF_FBW7_1 | 260 | 265 | PF00400 | 0.525 |
DEG_SPOP_SBC_1 | 268 | 272 | PF00917 | 0.642 |
DOC_CDC14_PxL_1 | 181 | 189 | PF14671 | 0.617 |
DOC_CKS1_1 | 166 | 171 | PF01111 | 0.681 |
DOC_CKS1_1 | 263 | 268 | PF01111 | 0.537 |
DOC_PP2B_LxvP_1 | 152 | 155 | PF13499 | 0.638 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.626 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 207 | 212 | PF00397 | 0.425 |
DOC_WW_Pin1_4 | 222 | 227 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.520 |
DOC_WW_Pin1_4 | 269 | 274 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.452 |
LIG_14-3-3_CanoR_1 | 280 | 284 | PF00244 | 0.646 |
LIG_14-3-3_CanoR_1 | 310 | 318 | PF00244 | 0.664 |
LIG_14-3-3_CterR_2 | 364 | 369 | PF00244 | 0.561 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.655 |
LIG_BRCT_BRCA1_1 | 20 | 24 | PF00533 | 0.690 |
LIG_BRCT_BRCA1_1 | 50 | 54 | PF00533 | 0.611 |
LIG_EVH1_1 | 152 | 156 | PF00568 | 0.633 |
LIG_EVH1_2 | 196 | 200 | PF00568 | 0.507 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.586 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.520 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.556 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.677 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.657 |
LIG_LIR_Apic_2 | 261 | 267 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 51 | 60 | PF02991 | 0.651 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.584 |
LIG_NRBOX | 72 | 78 | PF00104 | 0.500 |
LIG_PCNA_yPIPBox_3 | 70 | 81 | PF02747 | 0.568 |
LIG_PROFILIN_1 | 153 | 159 | PF00235 | 0.619 |
LIG_PTB_Apo_2 | 9 | 16 | PF02174 | 0.554 |
LIG_PTB_Phospho_1 | 9 | 15 | PF10480 | 0.554 |
LIG_SH2_CRK | 119 | 123 | PF00017 | 0.639 |
LIG_SH2_CRK | 166 | 170 | PF00017 | 0.623 |
LIG_SH2_CRK | 181 | 185 | PF00017 | 0.574 |
LIG_SH2_CRK | 264 | 268 | PF00017 | 0.540 |
LIG_SH2_CRK | 281 | 285 | PF00017 | 0.552 |
LIG_SH2_GRB2like | 177 | 180 | PF00017 | 0.616 |
LIG_SH2_NCK_1 | 123 | 127 | PF00017 | 0.641 |
LIG_SH2_NCK_1 | 146 | 150 | PF00017 | 0.686 |
LIG_SH2_NCK_1 | 166 | 170 | PF00017 | 0.657 |
LIG_SH2_NCK_1 | 264 | 268 | PF00017 | 0.574 |
LIG_SH2_NCK_1 | 281 | 285 | PF00017 | 0.586 |
LIG_SH2_PTP2 | 231 | 234 | PF00017 | 0.613 |
LIG_SH2_SRC | 231 | 234 | PF00017 | 0.554 |
LIG_SH2_STAP1 | 146 | 150 | PF00017 | 0.663 |
LIG_SH2_STAP1 | 177 | 181 | PF00017 | 0.653 |
LIG_SH2_STAP1 | 338 | 342 | PF00017 | 0.592 |
LIG_SH2_STAP1 | 40 | 44 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.637 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.583 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.606 |
LIG_SH3_3 | 112 | 118 | PF00018 | 0.603 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.589 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.558 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.537 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.729 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.524 |
LIG_SH3_3 | 257 | 263 | PF00018 | 0.518 |
LIG_SH3_3 | 271 | 277 | PF00018 | 0.565 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.622 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.691 |
LIG_SH3_5 | 36 | 40 | PF00018 | 0.520 |
LIG_SUMO_SIM_anti_2 | 88 | 96 | PF11976 | 0.550 |
LIG_TRAF2_1 | 220 | 223 | PF00917 | 0.639 |
LIG_TRAF2_1 | 238 | 241 | PF00917 | 0.605 |
LIG_TRAF2_1 | 59 | 62 | PF00917 | 0.641 |
LIG_TRFH_1 | 252 | 256 | PF08558 | 0.459 |
LIG_TRFH_1 | 281 | 285 | PF08558 | 0.586 |
LIG_UBA3_1 | 253 | 259 | PF00899 | 0.517 |
LIG_WW_1 | 163 | 166 | PF00397 | 0.596 |
LIG_WW_1 | 355 | 358 | PF00397 | 0.550 |
MOD_CDK_SPxxK_3 | 187 | 194 | PF00069 | 0.631 |
MOD_CDK_SPxxK_3 | 273 | 280 | PF00069 | 0.639 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.655 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.711 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.699 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.580 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.652 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.659 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.769 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.543 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.673 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.696 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.647 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.636 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.655 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.558 |
MOD_GlcNHglycan | 41 | 45 | PF01048 | 0.539 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.680 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.649 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.507 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.539 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.521 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.558 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.588 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.593 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.581 |
MOD_N-GLC_1 | 142 | 147 | PF02516 | 0.657 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.522 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.712 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.520 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.575 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.655 |
MOD_NEK2_2 | 49 | 54 | PF00069 | 0.611 |
MOD_PIKK_1 | 218 | 224 | PF00454 | 0.645 |
MOD_PK_1 | 310 | 316 | PF00069 | 0.579 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.539 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.645 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.652 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.661 |
MOD_Plk_2-3 | 96 | 102 | PF00069 | 0.631 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.639 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.565 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.668 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.624 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.587 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.548 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.576 |
MOD_ProDKin_1 | 207 | 213 | PF00069 | 0.427 |
MOD_ProDKin_1 | 222 | 228 | PF00069 | 0.580 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.521 |
MOD_ProDKin_1 | 269 | 275 | PF00069 | 0.561 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.586 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.454 |
TRG_DiLeu_BaLyEn_6 | 72 | 77 | PF01217 | 0.599 |
TRG_ENDOCYTIC_2 | 123 | 126 | PF00928 | 0.646 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.634 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.579 |
TRG_Pf-PMV_PEXEL_1 | 75 | 79 | PF00026 | 0.492 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCX5 | Leptomonas seymouri | 58% | 100% |
A0A3Q8IAY2 | Leishmania donovani | 99% | 99% |
A4H5Z6 | Leishmania braziliensis | 80% | 100% |
C9ZVG8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AN21 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QHK5 | Leishmania major | 95% | 100% |
V5BE36 | Trypanosoma cruzi | 36% | 100% |