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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005851 | eukaryotic translation initiation factor 2B complex | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: Q4QGU3
Term | Name | Level | Count |
---|---|---|---|
GO:0006413 | translational initiation | 3 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0050790 | regulation of catalytic activity | 3 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065009 | regulation of molecular function | 2 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003743 | translation initiation factor activity | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008135 | translation factor activity, RNA binding | 3 | 12 |
GO:0045182 | translation regulator activity | 1 | 12 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.533 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.517 |
CLV_PCSK_PC1ET2_1 | 114 | 116 | PF00082 | 0.548 |
CLV_PCSK_PC1ET2_1 | 334 | 336 | PF00082 | 0.661 |
CLV_PCSK_PC1ET2_1 | 79 | 81 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.549 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.407 |
DEG_SCF_TRCP1_1 | 215 | 220 | PF00400 | 0.538 |
DOC_CKS1_1 | 194 | 199 | PF01111 | 0.548 |
DOC_PP4_FxxP_1 | 297 | 300 | PF00568 | 0.452 |
DOC_SPAK_OSR1_1 | 168 | 172 | PF12202 | 0.471 |
DOC_SPAK_OSR1_1 | 90 | 94 | PF12202 | 0.383 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.494 |
DOC_USP7_UBL2_3 | 110 | 114 | PF12436 | 0.562 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.459 |
LIG_14-3-3_CanoR_1 | 139 | 146 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 324 | 329 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 62 | 68 | PF00244 | 0.495 |
LIG_AP2alpha_1 | 84 | 88 | PF02296 | 0.485 |
LIG_APCC_ABBA_1 | 22 | 27 | PF00400 | 0.414 |
LIG_BRCT_BRCA1_1 | 223 | 227 | PF00533 | 0.400 |
LIG_BRCT_BRCA1_1 | 3 | 7 | PF00533 | 0.659 |
LIG_BRCT_BRCA1_1 | 60 | 64 | PF00533 | 0.432 |
LIG_EH1_1 | 42 | 50 | PF00400 | 0.390 |
LIG_eIF4E_1 | 10 | 16 | PF01652 | 0.376 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.363 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.463 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.452 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.397 |
LIG_GBD_Chelix_1 | 11 | 19 | PF00786 | 0.375 |
LIG_LIR_Apic_2 | 296 | 300 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 224 | 235 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 267 | 276 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 61 | 70 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 86 | 95 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 267 | 273 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 4 | 10 | PF02991 | 0.654 |
LIG_LIR_Nem_3 | 61 | 67 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 86 | 91 | PF02991 | 0.383 |
LIG_NRP_CendR_1 | 334 | 336 | PF00754 | 0.752 |
LIG_OCRL_FandH_1 | 12 | 24 | PF00620 | 0.388 |
LIG_Pex14_2 | 270 | 274 | PF04695 | 0.452 |
LIG_Pex14_2 | 84 | 88 | PF04695 | 0.485 |
LIG_PTAP_UEV_1 | 328 | 333 | PF05743 | 0.625 |
LIG_SH2_CRK | 209 | 213 | PF00017 | 0.390 |
LIG_SH2_STAP1 | 43 | 47 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.452 |
LIG_SH3_2 | 329 | 334 | PF14604 | 0.641 |
LIG_SH3_3 | 326 | 332 | PF00018 | 0.614 |
LIG_SH3_5 | 39 | 43 | PF00018 | 0.406 |
LIG_SUMO_SIM_anti_2 | 301 | 309 | PF11976 | 0.452 |
LIG_SUMO_SIM_anti_2 | 44 | 49 | PF11976 | 0.403 |
LIG_SUMO_SIM_par_1 | 151 | 156 | PF11976 | 0.485 |
LIG_TRAF2_1 | 160 | 163 | PF00917 | 0.371 |
LIG_WRC_WIRS_1 | 64 | 69 | PF05994 | 0.525 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.538 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.463 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.470 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.494 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.392 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.417 |
MOD_Cter_Amidation | 332 | 335 | PF01082 | 0.604 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.445 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.446 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.313 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.385 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.368 |
MOD_GlcNHglycan | 329 | 332 | PF01048 | 0.504 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.557 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.478 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.530 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.452 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.453 |
MOD_N-GLC_1 | 139 | 144 | PF02516 | 0.451 |
MOD_N-GLC_1 | 28 | 33 | PF02516 | 0.396 |
MOD_N-GLC_1 | 93 | 98 | PF02516 | 0.503 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.557 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.419 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.462 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.410 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.461 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.442 |
MOD_PIKK_1 | 123 | 129 | PF00454 | 0.398 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.429 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.519 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.369 |
MOD_Plk_2-3 | 37 | 43 | PF00069 | 0.487 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.642 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.464 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.290 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.467 |
MOD_Plk_4 | 298 | 304 | PF00069 | 0.459 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.487 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.452 |
MOD_SUMO_rev_2 | 277 | 284 | PF00179 | 0.463 |
TRG_DiLeu_BaEn_1 | 237 | 242 | PF01217 | 0.452 |
TRG_ENDOCYTIC_2 | 10 | 13 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.470 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5D7 | Leptomonas seymouri | 87% | 100% |
A0A0S4KHS3 | Bodo saltans | 54% | 100% |
A0A1X0NMS5 | Trypanosomatidae | 70% | 100% |
A0A3Q8IBD6 | Leishmania donovani | 98% | 100% |
A0A3R7NDG3 | Trypanosoma rangeli | 67% | 100% |
A4H6R5 | Leishmania braziliensis | 91% | 100% |
A4HV45 | Leishmania infantum | 98% | 100% |
C9ZQE1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 68% | 90% |
E9ANS6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
P34604 | Caenorhabditis elegans | 24% | 100% |
Q0IIF2 | Bos taurus | 31% | 100% |
Q14232 | Homo sapiens | 29% | 100% |
Q4R4V8 | Macaca fascicularis | 30% | 100% |
Q54I81 | Dictyostelium discoideum | 29% | 100% |
Q57586 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 25% | 100% |
Q5RAR0 | Pongo abelii | 29% | 100% |
Q64270 | Rattus norvegicus | 30% | 100% |
Q99LC8 | Mus musculus | 31% | 100% |
Q9USP0 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 99% |
V5BMF9 | Trypanosoma cruzi | 68% | 91% |