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: 1, no: 10 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000315 | organellar large ribosomal subunit | 5 | 2 |
GO:0005762 | mitochondrial large ribosomal subunit | 3 | 2 |
GO:0015934 | large ribosomal subunit | 4 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0044391 | ribosomal subunit | 3 | 2 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 2 |
GO:1990904 | ribonucleoprotein complex | 2 | 2 |
GO:0005840 | ribosome | 5 | 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:0110165 | cellular anatomical entity | 1 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003735 | structural constituent of ribosome | 2 | 12 |
GO:0005198 | structural molecule activity | 1 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 195 | 199 | PF00656 | 0.440 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.454 |
CLV_PCSK_FUR_1 | 155 | 159 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.376 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.445 |
CLV_PCSK_PC1ET2_1 | 142 | 144 | PF00082 | 0.355 |
CLV_PCSK_PC1ET2_1 | 212 | 214 | PF00082 | 0.490 |
CLV_PCSK_PC1ET2_1 | 217 | 219 | PF00082 | 0.471 |
CLV_PCSK_PC7_1 | 213 | 219 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.374 |
DEG_APCC_DBOX_1 | 50 | 58 | PF00400 | 0.403 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.539 |
DOC_MAPK_gen_1 | 155 | 162 | PF00069 | 0.391 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.462 |
DOC_USP7_UBL2_3 | 165 | 169 | PF12436 | 0.422 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.538 |
LIG_14-3-3_CanoR_1 | 149 | 153 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 223 | 227 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 3 | 8 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 33 | 38 | PF00244 | 0.362 |
LIG_14-3-3_CanoR_1 | 56 | 62 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 85 | 92 | PF00244 | 0.400 |
LIG_Actin_WH2_2 | 133 | 151 | PF00022 | 0.376 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.468 |
LIG_FHA_2 | 149 | 155 | PF00498 | 0.390 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.538 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.594 |
LIG_LIR_Gen_1 | 115 | 125 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 133 | 141 | PF02991 | 0.256 |
LIG_LIR_Nem_3 | 115 | 120 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 133 | 139 | PF02991 | 0.255 |
LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.577 |
LIG_LYPXL_yS_3 | 101 | 104 | PF13949 | 0.364 |
LIG_SH2_CRK | 96 | 100 | PF00017 | 0.376 |
LIG_SH2_STAP1 | 110 | 114 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.351 |
LIG_SH3_2 | 23 | 28 | PF14604 | 0.420 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.358 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.426 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.391 |
LIG_TRAF2_1 | 192 | 195 | PF00917 | 0.567 |
LIG_TRFH_1 | 13 | 17 | PF08558 | 0.444 |
LIG_TYR_ITIM | 99 | 104 | PF00017 | 0.363 |
LIG_UBA3_1 | 127 | 132 | PF00899 | 0.501 |
LIG_WRC_WIRS_1 | 10 | 15 | PF05994 | 0.428 |
LIG_WW_3 | 25 | 29 | PF00397 | 0.406 |
MOD_CDK_SPK_2 | 58 | 63 | PF00069 | 0.538 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.452 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.400 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.378 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.497 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.500 |
MOD_CMANNOS | 42 | 45 | PF00535 | 0.347 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.396 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.447 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.399 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.376 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.498 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.443 |
MOD_PIKK_1 | 164 | 170 | PF00454 | 0.470 |
MOD_PIKK_1 | 181 | 187 | PF00454 | 0.296 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.371 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.491 |
MOD_PKA_2 | 222 | 228 | PF00069 | 0.571 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.401 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.401 |
MOD_PKB_1 | 83 | 91 | PF00069 | 0.398 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.614 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.533 |
MOD_SUMO_rev_2 | 207 | 214 | PF00179 | 0.475 |
TRG_AP2beta_CARGO_1 | 133 | 143 | PF09066 | 0.364 |
TRG_AP2beta_CARGO_1 | 209 | 218 | PF09066 | 0.487 |
TRG_DiLeu_BaEn_1 | 210 | 215 | PF01217 | 0.483 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.380 |
TRG_ER_diArg_1 | 155 | 158 | PF00400 | 0.369 |
TRG_Pf-PMV_PEXEL_1 | 178 | 182 | PF00026 | 0.448 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5G2 | Leptomonas seymouri | 86% | 99% |
A0A0S4IPI6 | Bodo saltans | 65% | 98% |
A0A1X0P1J1 | Trypanosomatidae | 72% | 99% |
A0A3Q8IEF6 | Leishmania donovani | 96% | 100% |
A0A3R7NH11 | Trypanosoma rangeli | 77% | 98% |
A4HIK7 | Leishmania braziliensis | 94% | 100% |
A4I5V2 | Leishmania infantum | 96% | 100% |
C9ZR74 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 72% | 97% |
E9B147 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
V5B7A9 | Trypanosoma cruzi | 70% | 83% |