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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A4H9C2
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 |
GO:0003727 | single-stranded RNA binding | 5 | 1 |
GO:0003729 | mRNA binding | 5 | 1 |
GO:0003730 | mRNA 3'-UTR binding | 6 | 1 |
GO:0008143 | poly(A) binding | 7 | 1 |
GO:0008187 | poly-pyrimidine tract binding | 6 | 1 |
GO:0008266 | poly(U) RNA binding | 7 | 1 |
GO:0070717 | poly-purine tract binding | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.398 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.298 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.625 |
CLV_PCSK_PC1ET2_1 | 210 | 212 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 120 | 124 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 146 | 150 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 43 | 47 | PF00082 | 0.362 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.591 |
DEG_SCF_FBW7_1 | 279 | 286 | PF00400 | 0.633 |
DEG_SPOP_SBC_1 | 321 | 325 | PF00917 | 0.620 |
DOC_CDC14_PxL_1 | 265 | 273 | PF14671 | 0.592 |
DOC_CKS1_1 | 20 | 25 | PF01111 | 0.534 |
DOC_MAPK_DCC_7 | 240 | 248 | PF00069 | 0.488 |
DOC_MAPK_gen_1 | 115 | 123 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 163 | 171 | PF00069 | 0.527 |
DOC_MAPK_gen_1 | 82 | 92 | PF00069 | 0.502 |
DOC_MAPK_MEF2A_6 | 163 | 171 | PF00069 | 0.527 |
DOC_PP1_RVXF_1 | 162 | 169 | PF00149 | 0.523 |
DOC_PP2B_LxvP_1 | 246 | 249 | PF13499 | 0.478 |
DOC_PP4_FxxP_1 | 20 | 23 | PF00568 | 0.565 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.715 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.423 |
DOC_WW_Pin1_4 | 227 | 232 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.667 |
LIG_14-3-3_CanoR_1 | 301 | 307 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 322 | 331 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 43 | 52 | PF00244 | 0.409 |
LIG_Actin_WH2_2 | 30 | 45 | PF00022 | 0.527 |
LIG_APCC_ABBA_1 | 148 | 153 | PF00400 | 0.484 |
LIG_APCC_ABBAyCdc20_2 | 147 | 153 | PF00400 | 0.527 |
LIG_BIR_III_4 | 86 | 90 | PF00653 | 0.502 |
LIG_BRCT_BRCA1_1 | 329 | 333 | PF00533 | 0.638 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.488 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.580 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.540 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.527 |
LIG_FHA_2 | 256 | 262 | PF00498 | 0.479 |
LIG_IBAR_NPY_1 | 336 | 338 | PF08397 | 0.562 |
LIG_LIR_Gen_1 | 300 | 311 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 141 | 145 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 26 | 32 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 47 | 52 | PF02991 | 0.556 |
LIG_LIR_Nem_3 | 69 | 74 | PF02991 | 0.519 |
LIG_PDZ_Class_2 | 342 | 347 | PF00595 | 0.492 |
LIG_SH2_CRK | 142 | 146 | PF00017 | 0.562 |
LIG_SH2_CRK | 303 | 307 | PF00017 | 0.495 |
LIG_SH2_CRK | 338 | 342 | PF00017 | 0.543 |
LIG_SH2_NCK_1 | 303 | 307 | PF00017 | 0.495 |
LIG_SH2_STAP1 | 329 | 333 | PF00017 | 0.681 |
LIG_SH2_STAT3 | 62 | 65 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 32 | 35 | PF00017 | 0.527 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.702 |
LIG_SUMO_SIM_anti_2 | 131 | 141 | PF11976 | 0.536 |
LIG_SUMO_SIM_par_1 | 126 | 134 | PF11976 | 0.512 |
LIG_SUMO_SIM_par_1 | 244 | 250 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 5 | 11 | PF11976 | 0.455 |
LIG_TRAF2_1 | 111 | 114 | PF00917 | 0.670 |
LIG_WRC_WIRS_1 | 168 | 173 | PF05994 | 0.527 |
LIG_WRC_WIRS_1 | 260 | 265 | PF05994 | 0.675 |
MOD_CDK_SPK_2 | 227 | 232 | PF00069 | 0.510 |
MOD_CDK_SPxK_1 | 279 | 285 | PF00069 | 0.634 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.512 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.689 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.687 |
MOD_CK1_1 | 259 | 265 | PF00069 | 0.573 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.666 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.546 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.506 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.527 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.540 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.733 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.457 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.735 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.419 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.247 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.559 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.669 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.608 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.586 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.710 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.673 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.480 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.616 |
MOD_LATS_1 | 299 | 305 | PF00433 | 0.493 |
MOD_N-GLC_1 | 151 | 156 | PF02516 | 0.327 |
MOD_N-GLC_1 | 316 | 321 | PF02516 | 0.723 |
MOD_N-GLC_1 | 50 | 55 | PF02516 | 0.224 |
MOD_N-GLC_2 | 186 | 188 | PF02516 | 0.362 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.417 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.665 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.520 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.481 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.552 |
MOD_PIKK_1 | 13 | 19 | PF00454 | 0.660 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.662 |
MOD_PIKK_1 | 287 | 293 | PF00454 | 0.632 |
MOD_PK_1 | 213 | 219 | PF00069 | 0.601 |
MOD_PK_1 | 95 | 101 | PF00069 | 0.548 |
MOD_PKA_1 | 146 | 152 | PF00069 | 0.527 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.695 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.691 |
MOD_PKB_1 | 211 | 219 | PF00069 | 0.527 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.743 |
MOD_Plk_1 | 316 | 322 | PF00069 | 0.738 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.680 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.562 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.550 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.415 |
MOD_ProDKin_1 | 227 | 233 | PF00069 | 0.688 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.670 |
TRG_DiLeu_BaLyEn_6 | 88 | 93 | PF01217 | 0.502 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.562 |
TRG_ENDOCYTIC_2 | 303 | 306 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 338 | 341 | PF00928 | 0.535 |
TRG_ER_diArg_1 | 115 | 118 | PF00400 | 0.620 |
TRG_ER_diArg_1 | 163 | 165 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 211 | 214 | PF00400 | 0.635 |
TRG_NLS_MonoExtC_3 | 209 | 215 | PF00514 | 0.462 |
TRG_NLS_MonoExtN_4 | 208 | 214 | PF00514 | 0.619 |
TRG_Pf-PMV_PEXEL_1 | 31 | 36 | PF00026 | 0.327 |
TRG_Pf-PMV_PEXEL_1 | 82 | 86 | PF00026 | 0.334 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P516 | Leptomonas seymouri | 61% | 93% |
A0A3Q8IAV4 | Leishmania donovani | 47% | 100% |
A0A3Q8IAX1 | Leishmania donovani | 79% | 100% |
A4HXP3 | Leishmania infantum | 79% | 100% |
A4HXP5 | Leishmania infantum | 47% | 100% |
E9ARF4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4QE25 | Leishmania major | 78% | 100% |
V5B1R5 | Trypanosoma cruzi | 40% | 84% |