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: 15 |
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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0010494 | cytoplasmic stress granule | 5 | 2 |
GO:0016281 | eukaryotic translation initiation factor 4F complex | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000339 | RNA cap binding | 5 | 2 |
GO:0000340 | RNA 7-methylguanosine cap binding | 6 | 2 |
GO:0003676 | nucleic acid binding | 3 | 14 |
GO:0003723 | RNA binding | 4 | 14 |
GO:0003743 | translation initiation factor activity | 4 | 14 |
GO:0005488 | binding | 1 | 14 |
GO:0008135 | translation factor activity, RNA binding | 3 | 14 |
GO:0045182 | translation regulator activity | 1 | 14 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 14 |
GO:0097159 | organic cyclic compound binding | 2 | 14 |
GO:1901363 | heterocyclic compound binding | 2 | 14 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 222 | 226 | PF00656 | 0.536 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.728 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.705 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.728 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.705 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.669 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.544 |
DEG_ODPH_VHL_1 | 111 | 124 | PF01847 | 0.543 |
DOC_ANK_TNKS_1 | 12 | 19 | PF00023 | 0.717 |
DOC_MAPK_gen_1 | 243 | 251 | PF00069 | 0.506 |
DOC_MAPK_MEF2A_6 | 245 | 253 | PF00069 | 0.517 |
DOC_PP4_FxxP_1 | 133 | 136 | PF00568 | 0.465 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.535 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.601 |
LIG_14-3-3_CanoR_1 | 100 | 106 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 54 | 58 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 67 | 71 | PF00244 | 0.566 |
LIG_APCC_ABBA_1 | 180 | 185 | PF00400 | 0.511 |
LIG_CSL_BTD_1 | 267 | 270 | PF09270 | 0.486 |
LIG_deltaCOP1_diTrp_1 | 127 | 133 | PF00928 | 0.470 |
LIG_EH1_1 | 153 | 161 | PF00400 | 0.442 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.511 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.484 |
LIG_FHA_2 | 136 | 142 | PF00498 | 0.585 |
LIG_FHA_2 | 220 | 226 | PF00498 | 0.479 |
LIG_LIR_Apic_2 | 188 | 194 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 127 | 136 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 212 | 223 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 127 | 133 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 161 | 166 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 212 | 218 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 266 | 271 | PF02991 | 0.540 |
LIG_MAD2 | 100 | 108 | PF02301 | 0.616 |
LIG_MAD2 | 164 | 172 | PF02301 | 0.549 |
LIG_PAM2_1 | 83 | 95 | PF00658 | 0.568 |
LIG_PCNA_PIPBox_1 | 261 | 270 | PF02747 | 0.549 |
LIG_PCNA_yPIPBox_3 | 255 | 268 | PF02747 | 0.549 |
LIG_Pex14_1 | 130 | 134 | PF04695 | 0.507 |
LIG_SH2_STAT3 | 92 | 95 | PF00017 | 0.664 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.664 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.561 |
LIG_WRC_WIRS_1 | 159 | 164 | PF05994 | 0.468 |
MOD_CDK_SPxxK_3 | 225 | 232 | PF00069 | 0.486 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.490 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.444 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.577 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.492 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.490 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.521 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.485 |
MOD_Cter_Amidation | 10 | 13 | PF01082 | 0.726 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.384 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.551 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.552 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.457 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.451 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.549 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.591 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.620 |
MOD_N-GLC_1 | 255 | 260 | PF02516 | 0.257 |
MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.646 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.573 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.499 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.582 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.612 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.660 |
MOD_PK_1 | 155 | 161 | PF00069 | 0.511 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.468 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.699 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.561 |
MOD_Plk_1 | 255 | 261 | PF00069 | 0.486 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.513 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.499 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.570 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.526 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.553 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.505 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.658 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.600 |
MOD_SUMO_for_1 | 143 | 146 | PF00179 | 0.549 |
MOD_SUMO_for_1 | 189 | 192 | PF00179 | 0.468 |
TRG_DiLeu_BaEn_1 | 213 | 218 | PF01217 | 0.549 |
TRG_ER_diArg_1 | 305 | 307 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 53 | 55 | PF00400 | 0.614 |
TRG_NLS_MonoExtC_3 | 301 | 306 | PF00514 | 0.584 |
TRG_NLS_MonoExtN_4 | 300 | 306 | PF00514 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 221 | 225 | PF00026 | 0.281 |
TRG_Pf-PMV_PEXEL_1 | 262 | 266 | PF00026 | 0.356 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7F6 | Leptomonas seymouri | 78% | 68% |
A0A1X0P285 | Trypanosomatidae | 45% | 74% |
A0A3Q8IE78 | Leishmania donovani | 27% | 100% |
A0A3Q8IEL7 | Leishmania donovani | 99% | 69% |
A0A3R7L212 | Trypanosoma rangeli | 26% | 68% |
A0A422N533 | Trypanosoma rangeli | 49% | 75% |
A4HHZ6 | Leishmania braziliensis | 89% | 100% |
A4I2V4 | Leishmania infantum | 27% | 100% |
A4I573 | Leishmania infantum | 99% | 100% |
C9ZQJ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 72% |
E9AZ65 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9B0H0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |