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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005783 | endoplasmic reticulum | 5 | 2 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005737 | cytoplasm | 2 | 8 |
GO:0016020 | membrane | 2 | 8 |
Related structures:
AlphaFold database: Q4QBT9
Term | Name | Level | Count |
---|---|---|---|
GO:0006621 | protein retention in ER lumen | 6 | 2 |
GO:0006810 | transport | 3 | 2 |
GO:0006890 | retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum | 6 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016192 | vesicle-mediated transport | 4 | 2 |
GO:0032507 | maintenance of protein location in cell | 3 | 2 |
GO:0035437 | maintenance of protein localization in endoplasmic reticulum | 5 | 2 |
GO:0045185 | maintenance of protein location | 3 | 2 |
GO:0048193 | Golgi vesicle transport | 5 | 2 |
GO:0051179 | localization | 1 | 10 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051235 | maintenance of location | 2 | 2 |
GO:0051651 | maintenance of location in cell | 2 | 2 |
GO:0072595 | maintenance of protein localization in organelle | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 95 | 99 | PF00656 | 0.504 |
CLV_MEL_PAP_1 | 8 | 14 | PF00089 | 0.318 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.259 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.286 |
CLV_PCSK_PC1ET2_1 | 25 | 27 | PF00082 | 0.286 |
CLV_PCSK_PC7_1 | 21 | 27 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.348 |
DEG_SPOP_SBC_1 | 179 | 183 | PF00917 | 0.683 |
DOC_CKS1_1 | 77 | 82 | PF01111 | 0.295 |
DOC_PP1_RVXF_1 | 50 | 57 | PF00149 | 0.336 |
DOC_PP2B_LxvP_1 | 134 | 137 | PF13499 | 0.256 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.494 |
DOC_USP7_UBL2_3 | 176 | 180 | PF12436 | 0.625 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.295 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.442 |
LIG_14-3-3_CanoR_1 | 11 | 17 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 21 | 25 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 52 | 57 | PF00244 | 0.368 |
LIG_CaM_IQ_9 | 150 | 166 | PF13499 | 0.295 |
LIG_eIF4E_1 | 72 | 78 | PF01652 | 0.338 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.388 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.527 |
LIG_LIR_Gen_1 | 120 | 131 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 132 | 141 | PF02991 | 0.240 |
LIG_LIR_Nem_3 | 120 | 126 | PF02991 | 0.254 |
LIG_LIR_Nem_3 | 129 | 134 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 23 | 27 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 55 | 59 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 99 | 105 | PF02991 | 0.442 |
LIG_NRBOX | 69 | 75 | PF00104 | 0.318 |
LIG_Pex14_1 | 115 | 119 | PF04695 | 0.332 |
LIG_Pex14_2 | 119 | 123 | PF04695 | 0.333 |
LIG_Pex14_2 | 127 | 131 | PF04695 | 0.257 |
LIG_Pex14_2 | 147 | 151 | PF04695 | 0.110 |
LIG_SH2_SRC | 27 | 30 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 27 | 30 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.251 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.269 |
LIG_SH3_3 | 101 | 107 | PF00018 | 0.442 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.238 |
LIG_SUMO_SIM_par_1 | 73 | 79 | PF11976 | 0.302 |
LIG_TYR_ITIM | 70 | 75 | PF00017 | 0.314 |
LIG_WRC_WIRS_1 | 130 | 135 | PF05994 | 0.339 |
LIG_WRC_WIRS_1 | 53 | 58 | PF05994 | 0.437 |
LIG_WRPW_2 | 102 | 105 | PF00400 | 0.442 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.524 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.525 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.303 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.314 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.461 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.314 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.522 |
MOD_Plk_1 | 28 | 34 | PF00069 | 0.451 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.580 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.328 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.295 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.442 |
TRG_DiLeu_BaEn_2 | 100 | 106 | PF01217 | 0.494 |
TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.522 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.355 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2L3 | Leptomonas seymouri | 79% | 100% |
A0A0S4INL9 | Bodo saltans | 57% | 100% |
A0A1X0NTI3 | Trypanosomatidae | 62% | 99% |
A0A3R7MCZ0 | Trypanosoma rangeli | 62% | 99% |
A0A3S7WX19 | Leishmania donovani | 94% | 100% |
A4HZT5 | Leishmania infantum | 94% | 100% |
A5PJ65 | Bos taurus | 34% | 93% |
C9ZRM1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E9AVP0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
O15258 | Homo sapiens | 34% | 93% |
O48670 | Arabidopsis thaliana | 40% | 96% |
O48671 | Arabidopsis thaliana | 39% | 94% |
P25560 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 97% |
P52879 | Caenorhabditis elegans | 37% | 96% |
P79003 | Saccharomyces pastorianus | 36% | 97% |
Q10358 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 99% |
Q498C8 | Rattus norvegicus | 34% | 93% |
Q54D10 | Dictyostelium discoideum | 37% | 97% |
Q5R5U4 | Pongo abelii | 34% | 93% |
Q5ZHM5 | Gallus gallus | 34% | 93% |
Q9CQU3 | Mus musculus | 34% | 93% |
Q9ZPV7 | Arabidopsis thaliana | 37% | 83% |
Q9ZWI7 | Arabidopsis thaliana | 37% | 86% |