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: 8 |
NetGPI | no | yes: 0, no: 8 |
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: A4H699
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 | 9 |
GO:0003723 | RNA binding | 4 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 41 | 45 | PF00656 | 0.350 |
CLV_C14_Caspase3-7 | 474 | 478 | PF00656 | 0.826 |
CLV_C14_Caspase3-7 | 68 | 72 | PF00656 | 0.399 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.793 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.749 |
CLV_PCSK_KEX2_1 | 494 | 496 | PF00082 | 0.776 |
CLV_PCSK_PC1ET2_1 | 223 | 225 | PF00082 | 0.749 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.613 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.715 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 190 | 196 | PF00134 | 0.438 |
DOC_MAPK_MEF2A_6 | 12 | 20 | PF00069 | 0.377 |
DOC_PP1_RVXF_1 | 115 | 122 | PF00149 | 0.579 |
DOC_PP2B_LxvP_1 | 276 | 279 | PF13499 | 0.711 |
DOC_PP4_FxxP_1 | 302 | 305 | PF00568 | 0.662 |
DOC_PP4_MxPP_1 | 421 | 424 | PF00568 | 0.717 |
DOC_SPAK_OSR1_1 | 148 | 152 | PF12202 | 0.424 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.789 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.770 |
DOC_USP7_UBL2_3 | 515 | 519 | PF12436 | 0.728 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.651 |
LIG_14-3-3_CanoR_1 | 442 | 448 | PF00244 | 0.867 |
LIG_BIR_III_4 | 218 | 222 | PF00653 | 0.711 |
LIG_deltaCOP1_diTrp_1 | 329 | 336 | PF00928 | 0.666 |
LIG_eIF4E_1 | 15 | 21 | PF01652 | 0.344 |
LIG_EVH1_1 | 276 | 280 | PF00568 | 0.709 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.344 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.344 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.344 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.509 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.784 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.672 |
LIG_FHA_1 | 454 | 460 | PF00498 | 0.593 |
LIG_FHA_2 | 152 | 158 | PF00498 | 0.356 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.328 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.344 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.741 |
LIG_FHA_2 | 41 | 47 | PF00498 | 0.344 |
LIG_LIR_Apic_2 | 300 | 305 | PF02991 | 0.668 |
LIG_LIR_Apic_2 | 321 | 327 | PF02991 | 0.610 |
LIG_LIR_Apic_2 | 342 | 347 | PF02991 | 0.711 |
LIG_LIR_Gen_1 | 137 | 145 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 14 | 25 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 210 | 219 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 137 | 143 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 14 | 20 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 210 | 215 | PF02991 | 0.317 |
LIG_PAM2_1 | 293 | 305 | PF00658 | 0.586 |
LIG_RPA_C_Fungi | 37 | 49 | PF08784 | 0.438 |
LIG_SH2_CRK | 324 | 328 | PF00017 | 0.564 |
LIG_SH2_CRK | 344 | 348 | PF00017 | 0.512 |
LIG_SH2_CRK | 359 | 363 | PF00017 | 0.542 |
LIG_SH2_GRB2like | 17 | 20 | PF00017 | 0.344 |
LIG_SH2_NCK_1 | 324 | 328 | PF00017 | 0.610 |
LIG_SH2_NCK_1 | 344 | 348 | PF00017 | 0.512 |
LIG_SH2_SRC | 84 | 87 | PF00017 | 0.438 |
LIG_SH2_STAP1 | 160 | 164 | PF00017 | 0.344 |
LIG_SH2_STAP1 | 337 | 341 | PF00017 | 0.659 |
LIG_SH2_STAP1 | 84 | 88 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.424 |
LIG_SH3_1 | 344 | 350 | PF00018 | 0.560 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.751 |
LIG_SH3_3 | 271 | 277 | PF00018 | 0.651 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.549 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.658 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.654 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.764 |
LIG_SH3_3 | 421 | 427 | PF00018 | 0.687 |
LIG_SH3_3 | 445 | 451 | PF00018 | 0.688 |
LIG_SUMO_SIM_par_1 | 23 | 29 | PF11976 | 0.424 |
LIG_TRAF2_1 | 269 | 272 | PF00917 | 0.709 |
LIG_TYR_ITIM | 13 | 18 | PF00017 | 0.344 |
LIG_UBA3_1 | 87 | 93 | PF00899 | 0.424 |
LIG_WRC_WIRS_1 | 306 | 311 | PF05994 | 0.625 |
MOD_CDC14_SPxK_1 | 434 | 437 | PF00782 | 0.749 |
MOD_CDK_SPxK_1 | 431 | 437 | PF00069 | 0.742 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.645 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.344 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.400 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.663 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.438 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.344 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.438 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.740 |
MOD_Cter_Amidation | 221 | 224 | PF01082 | 0.546 |
MOD_GlcNHglycan | 185 | 189 | PF01048 | 0.379 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.582 |
MOD_GlcNHglycan | 283 | 287 | PF01048 | 0.809 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.572 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.579 |
MOD_GlcNHglycan | 473 | 476 | PF01048 | 0.801 |
MOD_GlcNHglycan | 477 | 481 | PF01048 | 0.752 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.674 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.638 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.399 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.349 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.655 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.665 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.721 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.820 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.432 |
MOD_N-GLC_1 | 389 | 394 | PF02516 | 0.639 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.641 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.351 |
MOD_NEK2_1 | 38 | 43 | PF00069 | 0.467 |
MOD_PIKK_1 | 443 | 449 | PF00454 | 0.770 |
MOD_PIKK_1 | 453 | 459 | PF00454 | 0.773 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.588 |
MOD_Plk_1 | 282 | 288 | PF00069 | 0.557 |
MOD_Plk_1 | 339 | 345 | PF00069 | 0.621 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.351 |
MOD_Plk_2-3 | 115 | 121 | PF00069 | 0.673 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.317 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.424 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.717 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.576 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.489 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.646 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.704 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.651 |
MOD_SUMO_rev_2 | 109 | 119 | PF00179 | 0.706 |
MOD_SUMO_rev_2 | 165 | 170 | PF00179 | 0.438 |
MOD_SUMO_rev_2 | 85 | 95 | PF00179 | 0.438 |
TRG_DiLeu_BaEn_2 | 50 | 56 | PF01217 | 0.438 |
TRG_DiLeu_BaEn_4 | 271 | 277 | PF01217 | 0.738 |
TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.344 |
TRG_ER_diArg_1 | 493 | 495 | PF00400 | 0.773 |
TRG_ER_diLys_1 | 515 | 519 | PF00400 | 0.757 |
TRG_NLS_MonoExtC_3 | 490 | 495 | PF00514 | 0.768 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I433 | Leptomonas seymouri | 68% | 100% |
A0A3S5H6H2 | Leishmania donovani | 89% | 99% |
A0A422NGM0 | Trypanosoma rangeli | 39% | 95% |
A4HUM3 | Leishmania infantum | 89% | 99% |
E9ANC1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 98% |
Q4QHA3 | Leishmania major | 87% | 100% |
V5DKQ2 | Trypanosoma cruzi | 37% | 94% |