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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 12 |
GO:0032991 | protein-containing complex | 1 | 13 |
GO:0043226 | organelle | 2 | 12 |
GO:0043228 | non-membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
GO:1990904 | ribonucleoprotein complex | 2 | 13 |
GO:0000315 | organellar large ribosomal subunit | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005762 | mitochondrial large ribosomal subunit | 3 | 1 |
GO:0015934 | large ribosomal subunit | 4 | 1 |
GO:0044391 | ribosomal subunit | 3 | 1 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7X0Z8
Term | Name | Level | Count |
---|---|---|---|
GO:0006412 | translation | 4 | 13 |
GO:0006518 | peptide metabolic process | 4 | 13 |
GO:0006807 | nitrogen compound metabolic process | 2 | 13 |
GO:0008152 | metabolic process | 1 | 13 |
GO:0009058 | biosynthetic process | 2 | 13 |
GO:0009059 | macromolecule biosynthetic process | 4 | 13 |
GO:0009987 | cellular process | 1 | 13 |
GO:0019538 | protein metabolic process | 3 | 13 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 13 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 13 |
GO:0043043 | peptide biosynthetic process | 5 | 13 |
GO:0043170 | macromolecule metabolic process | 3 | 13 |
GO:0043603 | amide metabolic process | 3 | 13 |
GO:0043604 | amide biosynthetic process | 4 | 13 |
GO:0044237 | cellular metabolic process | 2 | 13 |
GO:0044238 | primary metabolic process | 2 | 13 |
GO:0044249 | cellular biosynthetic process | 3 | 13 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 13 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 13 |
GO:0071704 | organic substance metabolic process | 2 | 13 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 13 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 13 |
GO:1901576 | organic substance biosynthetic process | 3 | 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003735 | structural constituent of ribosome | 2 | 13 |
GO:0005198 | structural molecule activity | 1 | 13 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0019843 | rRNA binding | 5 | 1 |
GO:0070180 | large ribosomal subunit rRNA binding | 6 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.323 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.323 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.323 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.602 |
CLV_PCSK_FUR_1 | 130 | 134 | PF00082 | 0.323 |
CLV_PCSK_FUR_1 | 176 | 180 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.602 |
CLV_PCSK_PC1ET2_1 | 132 | 134 | PF00082 | 0.323 |
CLV_PCSK_PC7_1 | 285 | 291 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 203 | 207 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.674 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.661 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.574 |
DOC_CYCLIN_RxL_1 | 270 | 282 | PF00134 | 0.596 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 259 | 268 | PF00134 | 0.522 |
DOC_MAPK_gen_1 | 11 | 19 | PF00069 | 0.535 |
DOC_MAPK_gen_1 | 185 | 191 | PF00069 | 0.323 |
DOC_MAPK_MEF2A_6 | 167 | 175 | PF00069 | 0.450 |
DOC_MAPK_MEF2A_6 | 95 | 104 | PF00069 | 0.323 |
DOC_MAPK_NFAT4_5 | 95 | 103 | PF00069 | 0.450 |
DOC_PP1_RVXF_1 | 305 | 311 | PF00149 | 0.458 |
DOC_PP4_FxxP_1 | 26 | 29 | PF00568 | 0.572 |
DOC_PP4_FxxP_1 | 39 | 42 | PF00568 | 0.408 |
DOC_SPAK_OSR1_1 | 54 | 58 | PF12202 | 0.323 |
DOC_USP7_UBL2_3 | 11 | 15 | PF12436 | 0.628 |
DOC_USP7_UBL2_3 | 74 | 78 | PF12436 | 0.323 |
DOC_USP7_UBL2_3 | 91 | 95 | PF12436 | 0.323 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 340 | 345 | PF00397 | 0.729 |
LIG_14-3-3_CanoR_1 | 13 | 18 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 3 | 10 | PF00244 | 0.599 |
LIG_APCC_ABBA_1 | 104 | 109 | PF00400 | 0.323 |
LIG_APCC_ABBAyCdc20_2 | 103 | 109 | PF00400 | 0.323 |
LIG_BRCT_BRCA1_1 | 110 | 114 | PF00533 | 0.391 |
LIG_BRCT_BRCA1_1 | 22 | 26 | PF00533 | 0.578 |
LIG_BRCT_BRCA1_1 | 332 | 336 | PF00533 | 0.440 |
LIG_CtBP_PxDLS_1 | 303 | 307 | PF00389 | 0.458 |
LIG_FHA_1 | 134 | 140 | PF00498 | 0.342 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.515 |
LIG_FHA_2 | 251 | 257 | PF00498 | 0.575 |
LIG_FHA_2 | 300 | 306 | PF00498 | 0.427 |
LIG_LIR_Apic_2 | 23 | 29 | PF02991 | 0.573 |
LIG_LIR_Apic_2 | 37 | 42 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 71 | 80 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 121 | 126 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 164 | 168 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 169 | 173 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.317 |
LIG_LYPXL_yS_3 | 170 | 173 | PF13949 | 0.336 |
LIG_Pex14_2 | 82 | 86 | PF04695 | 0.323 |
LIG_PTB_Apo_2 | 49 | 56 | PF02174 | 0.394 |
LIG_REV1ctd_RIR_1 | 53 | 62 | PF16727 | 0.323 |
LIG_SH2_GRB2like | 291 | 294 | PF00017 | 0.444 |
LIG_SH2_SRC | 155 | 158 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.721 |
LIG_SH3_2 | 42 | 47 | PF14604 | 0.417 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.336 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.412 |
LIG_SH3_4 | 91 | 98 | PF00018 | 0.323 |
LIG_SUMO_SIM_anti_2 | 96 | 102 | PF11976 | 0.336 |
LIG_TRAF2_1 | 302 | 305 | PF00917 | 0.464 |
LIG_TYR_ITIM | 168 | 173 | PF00017 | 0.450 |
LIG_TYR_ITIM | 223 | 228 | PF00017 | 0.499 |
LIG_UBA3_1 | 125 | 132 | PF00899 | 0.336 |
LIG_UBA3_1 | 264 | 270 | PF00899 | 0.507 |
MOD_CDC14_SPxK_1 | 200 | 203 | PF00782 | 0.464 |
MOD_CDK_SPxK_1 | 197 | 203 | PF00069 | 0.465 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.573 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.435 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.545 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.686 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.441 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.430 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.470 |
MOD_N-GLC_1 | 324 | 329 | PF02516 | 0.580 |
MOD_N-GLC_2 | 144 | 146 | PF02516 | 0.472 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.323 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.660 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.585 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.472 |
MOD_NEK2_2 | 193 | 198 | PF00069 | 0.475 |
MOD_PIKK_1 | 250 | 256 | PF00454 | 0.525 |
MOD_PIKK_1 | 330 | 336 | PF00454 | 0.646 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.651 |
MOD_Plk_1 | 108 | 114 | PF00069 | 0.323 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.336 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.500 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.485 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.471 |
MOD_SUMO_rev_2 | 28 | 35 | PF00179 | 0.565 |
TRG_DiLeu_LyEn_5 | 234 | 239 | PF01217 | 0.503 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.450 |
TRG_ER_diArg_1 | 175 | 178 | PF00400 | 0.327 |
TRG_ER_diArg_1 | 185 | 187 | PF00400 | 0.315 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.588 |
TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.480 |
TRG_NLS_MonoCore_2 | 129 | 134 | PF00514 | 0.323 |
TRG_NLS_MonoExtC_3 | 129 | 135 | PF00514 | 0.323 |
TRG_NLS_MonoExtN_4 | 127 | 134 | PF00514 | 0.323 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMB3 | Leptomonas seymouri | 84% | 100% |
A0A0S4IQP6 | Bodo saltans | 63% | 100% |
A0A1X0NR49 | Trypanosomatidae | 71% | 100% |
A0A3R7NDU6 | Trypanosoma rangeli | 72% | 100% |
A4HFZ9 | Leishmania braziliensis | 93% | 100% |
A4I318 | Leishmania infantum | 99% | 100% |
C9ZJH2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 70% | 100% |
C9ZJI7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 70% | 100% |
E9ACT9 | Leishmania major | 97% | 100% |
E9AZC8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
V5AS82 | Trypanosoma cruzi | 72% | 100% |