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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005783 | endoplasmic reticulum | 5 | 2 |
GO:0016020 | membrane | 2 | 10 |
GO:0031201 | SNARE complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0098796 | membrane protein complex | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: Q4QH50
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 10 |
GO:0006890 | retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum | 6 | 10 |
GO:0016192 | vesicle-mediated transport | 4 | 10 |
GO:0048193 | Golgi vesicle transport | 5 | 10 |
GO:0051179 | localization | 1 | 10 |
GO:0051234 | establishment of localization | 2 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005484 | SNAP receptor activity | 3 | 10 |
GO:0030674 | protein-macromolecule adaptor activity | 2 | 10 |
GO:0060090 | molecular adaptor activity | 1 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 193 | 199 | PF00089 | 0.485 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.440 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.440 |
CLV_PCSK_PC7_1 | 89 | 95 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.459 |
DEG_APCC_DBOX_1 | 88 | 96 | PF00400 | 0.704 |
DEG_SPOP_SBC_1 | 114 | 118 | PF00917 | 0.723 |
DOC_CYCLIN_RxL_1 | 127 | 137 | PF00134 | 0.488 |
DOC_CYCLIN_RxL_1 | 178 | 189 | PF00134 | 0.490 |
DOC_MAPK_gen_1 | 10 | 20 | PF00069 | 0.707 |
DOC_MAPK_gen_1 | 179 | 187 | PF00069 | 0.509 |
DOC_MAPK_gen_1 | 76 | 85 | PF00069 | 0.718 |
DOC_MAPK_MEF2A_6 | 136 | 143 | PF00069 | 0.465 |
DOC_MAPK_MEF2A_6 | 190 | 197 | PF00069 | 0.502 |
DOC_MAPK_NFAT4_5 | 190 | 198 | PF00069 | 0.514 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.821 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.734 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.742 |
LIG_14-3-3_CanoR_1 | 120 | 129 | PF00244 | 0.687 |
LIG_14-3-3_CanoR_1 | 136 | 142 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 179 | 185 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 196 | 204 | PF00244 | 0.285 |
LIG_Actin_WH2_2 | 180 | 198 | PF00022 | 0.490 |
LIG_Actin_WH2_2 | 78 | 95 | PF00022 | 0.705 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.491 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.742 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.775 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.618 |
LIG_FHA_2 | 73 | 79 | PF00498 | 0.758 |
LIG_LIR_Gen_1 | 220 | 229 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.494 |
LIG_NRBOX | 128 | 134 | PF00104 | 0.490 |
LIG_PDZ_Class_3 | 224 | 229 | PF00595 | 0.476 |
LIG_SH2_PTP2 | 223 | 226 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.424 |
LIG_SUMO_SIM_par_1 | 137 | 142 | PF11976 | 0.543 |
LIG_SUMO_SIM_par_1 | 183 | 189 | PF11976 | 0.474 |
LIG_TRAF2_1 | 75 | 78 | PF00917 | 0.757 |
LIG_TRFH_1 | 215 | 219 | PF08558 | 0.489 |
MOD_CDK_SPxxK_3 | 56 | 63 | PF00069 | 0.753 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.719 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.531 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.401 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.761 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.693 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.563 |
MOD_CK2_1 | 31 | 37 | PF00069 | 0.631 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.734 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.532 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.444 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.585 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.716 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.427 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.784 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.516 |
MOD_N-GLC_1 | 8 | 13 | PF02516 | 0.557 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.490 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.508 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.496 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.235 |
MOD_PIKK_1 | 8 | 14 | PF00454 | 0.693 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.344 |
MOD_Plk_2-3 | 107 | 113 | PF00069 | 0.706 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.462 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.735 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.740 |
MOD_SUMO_rev_2 | 137 | 146 | PF00179 | 0.561 |
TRG_ENDOCYTIC_2 | 223 | 226 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.697 |
TRG_ER_diArg_1 | 92 | 94 | PF00400 | 0.640 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1V7 | Leptomonas seymouri | 64% | 89% |
A0A1X0NV60 | Trypanosomatidae | 47% | 100% |
A0A3S5ISC5 | Trypanosoma rangeli | 42% | 100% |
A0A3S7WRJ0 | Leishmania donovani | 95% | 84% |
A4H9S8 | Leishmania braziliensis | 82% | 72% |
A4HUU1 | Leishmania infantum | 95% | 84% |
E9ANH6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 84% |
V5BBG4 | Trypanosoma cruzi | 44% | 100% |