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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: Q4Q8F4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 146 | 150 | PF00656 | 0.290 |
CLV_C14_Caspase3-7 | 7 | 11 | PF00656 | 0.664 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.434 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.382 |
DEG_APCC_DBOX_1 | 77 | 85 | PF00400 | 0.492 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.666 |
DOC_CKS1_1 | 101 | 106 | PF01111 | 0.351 |
DOC_CYCLIN_yCln2_LP_2 | 101 | 107 | PF00134 | 0.426 |
DOC_MAPK_gen_1 | 78 | 87 | PF00069 | 0.545 |
DOC_MAPK_MEF2A_6 | 147 | 156 | PF00069 | 0.320 |
DOC_PP1_RVXF_1 | 216 | 223 | PF00149 | 0.311 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.321 |
DOC_USP7_UBL2_3 | 39 | 43 | PF12436 | 0.605 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.296 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.683 |
LIG_14-3-3_CanoR_1 | 109 | 117 | PF00244 | 0.458 |
LIG_Actin_WH2_2 | 233 | 250 | PF00022 | 0.339 |
LIG_BIR_III_4 | 48 | 52 | PF00653 | 0.664 |
LIG_BRCT_BRCA1_1 | 118 | 122 | PF00533 | 0.259 |
LIG_EH1_1 | 182 | 190 | PF00400 | 0.555 |
LIG_eIF4E_1 | 155 | 161 | PF01652 | 0.311 |
LIG_eIF4E_1 | 183 | 189 | PF01652 | 0.458 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.358 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.724 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.565 |
LIG_FHA_1 | 229 | 235 | PF00498 | 0.320 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.604 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.433 |
LIG_FHA_2 | 144 | 150 | PF00498 | 0.284 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.664 |
LIG_GBD_Chelix_1 | 152 | 160 | PF00786 | 0.311 |
LIG_GBD_Chelix_1 | 197 | 205 | PF00786 | 0.385 |
LIG_LIR_Gen_1 | 148 | 159 | PF02991 | 0.273 |
LIG_LIR_Gen_1 | 241 | 250 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 97 | 107 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 148 | 154 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 241 | 247 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 97 | 102 | PF02991 | 0.300 |
LIG_NRBOX | 153 | 159 | PF00104 | 0.415 |
LIG_NRBOX | 233 | 239 | PF00104 | 0.446 |
LIG_PALB2_WD40_1 | 189 | 197 | PF16756 | 0.227 |
LIG_PTB_Apo_2 | 216 | 223 | PF02174 | 0.312 |
LIG_SH2_GRB2like | 60 | 63 | PF00017 | 0.667 |
LIG_SH2_PTP2 | 155 | 158 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 183 | 186 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.695 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.616 |
LIG_SH3_2 | 70 | 75 | PF14604 | 0.614 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.646 |
LIG_SUMO_SIM_anti_2 | 187 | 192 | PF11976 | 0.227 |
LIG_SUMO_SIM_anti_2 | 82 | 89 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 236 | 241 | PF11976 | 0.371 |
LIG_SUMO_SIM_par_1 | 82 | 89 | PF11976 | 0.555 |
LIG_UBA3_1 | 243 | 251 | PF00899 | 0.368 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.339 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.571 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.379 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.608 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.664 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.554 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.394 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.669 |
MOD_GlcNHglycan | 48 | 52 | PF01048 | 0.404 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.352 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.655 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.706 |
MOD_N-GLC_1 | 213 | 218 | PF02516 | 0.462 |
MOD_N-GLC_1 | 44 | 49 | PF02516 | 0.574 |
MOD_N-GLC_2 | 210 | 212 | PF02516 | 0.542 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.709 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.282 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.331 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.573 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.328 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.282 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.428 |
MOD_PK_1 | 116 | 122 | PF00069 | 0.318 |
MOD_PKA_1 | 74 | 80 | PF00069 | 0.598 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.330 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.656 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.669 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.284 |
MOD_Plk_1 | 56 | 62 | PF00069 | 0.723 |
MOD_Plk_1 | 9 | 15 | PF00069 | 0.702 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.412 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.386 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.486 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.689 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.388 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.345 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.296 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.681 |
MOD_SUMO_rev_2 | 35 | 44 | PF00179 | 0.601 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.421 |
TRG_ER_diArg_1 | 73 | 75 | PF00400 | 0.672 |
TRG_ER_diArg_1 | 78 | 81 | PF00400 | 0.599 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1D0 | Leptomonas seymouri | 47% | 100% |
A0A1X0NYY6 | Trypanosomatidae | 22% | 100% |
A0A3Q8IEK1 | Leishmania donovani | 82% | 100% |
A4I3I8 | Leishmania infantum | 83% | 100% |
D0A7V4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
E9AZT0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |