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: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: A4H9C3
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 |
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 | 138 | 140 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.225 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.475 |
CLV_PCSK_FUR_1 | 247 | 251 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 249 | 251 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 113 | 117 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.682 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.362 |
DEG_SCF_FBW7_1 | 308 | 314 | PF00400 | 0.430 |
DEG_SCF_FBW7_2 | 232 | 237 | PF00400 | 0.522 |
DEG_SCF_TRCP1_1 | 328 | 334 | PF00400 | 0.582 |
DOC_CKS1_1 | 203 | 208 | PF01111 | 0.506 |
DOC_CKS1_1 | 265 | 270 | PF01111 | 0.592 |
DOC_CKS1_1 | 308 | 313 | PF01111 | 0.492 |
DOC_MAPK_gen_1 | 108 | 116 | PF00069 | 0.434 |
DOC_MAPK_gen_1 | 156 | 164 | PF00069 | 0.496 |
DOC_MAPK_gen_1 | 202 | 211 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 75 | 85 | PF00069 | 0.585 |
DOC_MAPK_MEF2A_6 | 156 | 164 | PF00069 | 0.497 |
DOC_MAPK_MEF2A_6 | 235 | 244 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 327 | 335 | PF00069 | 0.526 |
DOC_PP1_RVXF_1 | 155 | 162 | PF00149 | 0.493 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.593 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.542 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.459 |
LIG_14-3-3_CanoR_1 | 222 | 227 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 36 | 45 | PF00244 | 0.467 |
LIG_Actin_WH2_2 | 23 | 38 | PF00022 | 0.497 |
LIG_APCC_ABBA_1 | 141 | 146 | PF00400 | 0.493 |
LIG_APCC_ABBAyCdc20_2 | 140 | 146 | PF00400 | 0.497 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.678 |
LIG_BIR_III_4 | 79 | 83 | PF00653 | 0.497 |
LIG_BRCT_BRCA1_1 | 10 | 14 | PF00533 | 0.534 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.597 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.624 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.652 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.582 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.493 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.586 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.417 |
LIG_FHA_2 | 161 | 167 | PF00498 | 0.581 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.448 |
LIG_LIR_Nem_3 | 134 | 138 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 19 | 25 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 214 | 220 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 313 | 318 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 40 | 45 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 62 | 67 | PF02991 | 0.485 |
LIG_SH2_CRK | 135 | 139 | PF00017 | 0.562 |
LIG_SH2_GRB2like | 199 | 202 | PF00017 | 0.443 |
LIG_SH2_STAP1 | 199 | 203 | PF00017 | 0.523 |
LIG_SH2_STAP1 | 228 | 232 | PF00017 | 0.530 |
LIG_SH2_STAT3 | 55 | 58 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 199 | 202 | PF00017 | 0.601 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.514 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.468 |
LIG_SH3_3 | 305 | 311 | PF00018 | 0.530 |
LIG_SUMO_SIM_anti_2 | 124 | 134 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 119 | 127 | PF11976 | 0.493 |
LIG_TRAF2_1 | 104 | 107 | PF00917 | 0.506 |
LIG_WRC_WIRS_1 | 161 | 166 | PF05994 | 0.497 |
MOD_CDK_SPK_2 | 230 | 235 | PF00069 | 0.528 |
MOD_CDK_SPK_2 | 264 | 269 | PF00069 | 0.581 |
MOD_CDK_SPxxK_3 | 223 | 230 | PF00069 | 0.511 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.399 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.598 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.582 |
MOD_CK1_1 | 270 | 276 | PF00069 | 0.631 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.660 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.492 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.497 |
MOD_DYRK1A_RPxSP_1 | 202 | 206 | PF00069 | 0.476 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.524 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.587 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.589 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.338 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.301 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.484 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.591 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.615 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.623 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.538 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.563 |
MOD_N-GLC_1 | 144 | 149 | PF02516 | 0.297 |
MOD_N-GLC_1 | 292 | 297 | PF02516 | 0.451 |
MOD_N-GLC_1 | 43 | 48 | PF02516 | 0.311 |
MOD_N-GLC_2 | 179 | 181 | PF02516 | 0.297 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.484 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.624 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.497 |
MOD_NEK2_2 | 320 | 325 | PF00069 | 0.426 |
MOD_PIKK_1 | 294 | 300 | PF00454 | 0.549 |
MOD_PIKK_1 | 341 | 347 | PF00454 | 0.522 |
MOD_PK_1 | 88 | 94 | PF00069 | 0.556 |
MOD_PKA_1 | 139 | 145 | PF00069 | 0.497 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.611 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.618 |
MOD_Plk_1 | 236 | 242 | PF00069 | 0.563 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.497 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.472 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.578 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.573 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.568 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.611 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.543 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.457 |
MOD_SUMO_for_1 | 248 | 251 | PF00179 | 0.504 |
TRG_DiLeu_BaLyEn_6 | 81 | 86 | PF01217 | 0.497 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.571 |
TRG_ER_diArg_1 | 108 | 111 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 156 | 158 | PF00400 | 0.496 |
TRG_ER_diArg_1 | 335 | 338 | PF00400 | 0.590 |
TRG_Pf-PMV_PEXEL_1 | 24 | 29 | PF00026 | 0.334 |
TRG_Pf-PMV_PEXEL_1 | 75 | 79 | PF00026 | 0.199 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8II02 | Leishmania donovani | 26% | 69% |
A0A3S7WUT6 | Leishmania donovani | 69% | 100% |
A4HXP4 | Leishmania infantum | 69% | 100% |
A4I5P8 | Leishmania infantum | 25% | 69% |
E9ARF5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 100% |
Q4QE24 | Leishmania major | 68% | 100% |
Q9C652 | Arabidopsis thaliana | 25% | 96% |
Q9SAB3 | Arabidopsis thaliana | 23% | 86% |
V5BLA5 | Trypanosoma cruzi | 25% | 89% |