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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0010494 | cytoplasmic stress granule | 5 | 2 |
GO:0035770 | ribonucleoprotein granule | 3 | 2 |
GO:0036464 | cytoplasmic ribonucleoprotein granule | 4 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0099080 | supramolecular complex | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QHK5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
DEG_SCF_FBW7_1 | 262 | 267 | PF00400 | 0.607 |
DEG_SPOP_SBC_1 | 270 | 274 | PF00917 | 0.772 |
DOC_CDC14_PxL_1 | 183 | 191 | PF14671 | 0.683 |
DOC_CKS1_1 | 168 | 173 | PF01111 | 0.713 |
DOC_CKS1_1 | 265 | 270 | PF01111 | 0.616 |
DOC_CYCLIN_yCln2_LP_2 | 115 | 121 | PF00134 | 0.617 |
DOC_PP2B_LxvP_1 | 152 | 155 | PF13499 | 0.682 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 269 | 273 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.680 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.713 |
LIG_14-3-3_CanoR_1 | 282 | 286 | PF00244 | 0.693 |
LIG_14-3-3_CanoR_1 | 312 | 320 | PF00244 | 0.713 |
LIG_14-3-3_CterR_2 | 366 | 371 | PF00244 | 0.646 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.684 |
LIG_BRCT_BRCA1_1 | 20 | 24 | PF00533 | 0.773 |
LIG_BRCT_BRCA1_1 | 50 | 54 | PF00533 | 0.750 |
LIG_CtBP_PxDLS_1 | 112 | 117 | PF00389 | 0.618 |
LIG_EVH1_1 | 152 | 156 | PF00568 | 0.678 |
LIG_EVH1_2 | 198 | 202 | PF00568 | 0.620 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.717 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.590 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.654 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.708 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.623 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.681 |
LIG_LIR_Apic_2 | 263 | 269 | PF02991 | 0.609 |
LIG_LIR_Gen_1 | 51 | 60 | PF02991 | 0.748 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.670 |
LIG_NRBOX | 72 | 78 | PF00104 | 0.549 |
LIG_PCNA_yPIPBox_3 | 70 | 81 | PF02747 | 0.613 |
LIG_PROFILIN_1 | 153 | 159 | PF00235 | 0.666 |
LIG_PROFILIN_1 | 160 | 166 | PF00235 | 0.664 |
LIG_PTB_Apo_2 | 9 | 16 | PF02174 | 0.646 |
LIG_PTB_Phospho_1 | 9 | 15 | PF10480 | 0.644 |
LIG_SH2_CRK | 119 | 123 | PF00017 | 0.763 |
LIG_SH2_CRK | 168 | 172 | PF00017 | 0.662 |
LIG_SH2_CRK | 183 | 187 | PF00017 | 0.642 |
LIG_SH2_CRK | 266 | 270 | PF00017 | 0.618 |
LIG_SH2_CRK | 283 | 287 | PF00017 | 0.638 |
LIG_SH2_GRB2like | 179 | 182 | PF00017 | 0.767 |
LIG_SH2_NCK_1 | 123 | 127 | PF00017 | 0.771 |
LIG_SH2_NCK_1 | 146 | 150 | PF00017 | 0.716 |
LIG_SH2_NCK_1 | 168 | 172 | PF00017 | 0.787 |
LIG_SH2_NCK_1 | 266 | 270 | PF00017 | 0.618 |
LIG_SH2_NCK_1 | 283 | 287 | PF00017 | 0.638 |
LIG_SH2_PTP2 | 233 | 236 | PF00017 | 0.674 |
LIG_SH2_SRC | 233 | 236 | PF00017 | 0.620 |
LIG_SH2_STAP1 | 146 | 150 | PF00017 | 0.697 |
LIG_SH2_STAP1 | 179 | 183 | PF00017 | 0.699 |
LIG_SH2_STAP1 | 340 | 344 | PF00017 | 0.708 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.760 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.691 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.674 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.735 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.683 |
LIG_SH3_3 | 150 | 156 | PF00018 | 0.690 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.642 |
LIG_SH3_3 | 172 | 178 | PF00018 | 0.522 |
LIG_SH3_3 | 194 | 200 | PF00018 | 0.762 |
LIG_SH3_3 | 232 | 238 | PF00018 | 0.625 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.604 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.636 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.765 |
LIG_SH3_3 | 362 | 368 | PF00018 | 0.735 |
LIG_TRAF2_1 | 222 | 225 | PF00917 | 0.695 |
LIG_TRAF2_1 | 240 | 243 | PF00917 | 0.663 |
LIG_TRFH_1 | 254 | 258 | PF08558 | 0.558 |
LIG_TRFH_1 | 283 | 287 | PF08558 | 0.638 |
LIG_UBA3_1 | 255 | 261 | PF00899 | 0.583 |
LIG_WW_1 | 165 | 168 | PF00397 | 0.637 |
LIG_WW_1 | 357 | 360 | PF00397 | 0.631 |
MOD_CDK_SPxxK_3 | 189 | 196 | PF00069 | 0.782 |
MOD_CDK_SPxxK_3 | 275 | 282 | PF00069 | 0.687 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.698 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.701 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.738 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.629 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.714 |
MOD_CK1_1 | 352 | 358 | PF00069 | 0.654 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.707 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.621 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.738 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.525 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.721 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.735 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.696 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.667 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.764 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.725 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.787 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.623 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.635 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.605 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.641 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.677 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.706 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.722 |
MOD_N-GLC_1 | 142 | 147 | PF02516 | 0.684 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.753 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.595 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.637 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.699 |
MOD_NEK2_2 | 49 | 54 | PF00069 | 0.751 |
MOD_PIKK_1 | 220 | 226 | PF00454 | 0.697 |
MOD_PK_1 | 312 | 318 | PF00069 | 0.702 |
MOD_PKA_2 | 247 | 253 | PF00069 | 0.610 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.692 |
MOD_PKA_2 | 311 | 317 | PF00069 | 0.710 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.691 |
MOD_Plk_2-3 | 96 | 102 | PF00069 | 0.707 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.788 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.627 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.718 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.689 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.629 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.588 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.720 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.442 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.671 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.606 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.644 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.678 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.712 |
TRG_DiLeu_BaLyEn_6 | 72 | 77 | PF01217 | 0.600 |
TRG_ENDOCYTIC_2 | 123 | 126 | PF00928 | 0.775 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.703 |
TRG_ENDOCYTIC_2 | 322 | 325 | PF00928 | 0.693 |
TRG_Pf-PMV_PEXEL_1 | 75 | 79 | PF00026 | 0.555 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCX5 | Leptomonas seymouri | 56% | 100% |
A0A3Q8IAY2 | Leishmania donovani | 96% | 100% |
A4H5Z6 | Leishmania braziliensis | 78% | 100% |
A4HUC2 | Leishmania infantum | 95% | 100% |
E9AN21 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5BE36 | Trypanosoma cruzi | 37% | 100% |