Structurally similar to the amastin family proteins, but with a rather divergent sequence. Also seems to be related to mammalian clarin proteins.
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) | yes | yes: 6 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 4 |
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A4HVZ0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.758 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.464 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.506 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.805 |
DOC_MAPK_gen_1 | 45 | 52 | PF00069 | 0.578 |
DOC_MAPK_MEF2A_6 | 45 | 52 | PF00069 | 0.578 |
DOC_PP2B_LxvP_1 | 40 | 43 | PF13499 | 0.629 |
DOC_USP7_UBL2_3 | 216 | 220 | PF12436 | 0.446 |
LIG_14-3-3_CanoR_1 | 22 | 28 | PF00244 | 0.821 |
LIG_14-3-3_CanoR_1 | 256 | 261 | PF00244 | 0.678 |
LIG_BRCT_BRCA1_1 | 101 | 105 | PF00533 | 0.423 |
LIG_BRCT_BRCA1_1 | 225 | 229 | PF00533 | 0.476 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.414 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.467 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.561 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.467 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.421 |
LIG_LIR_Gen_1 | 139 | 150 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 156 | 166 | PF02991 | 0.500 |
LIG_LIR_Gen_1 | 174 | 181 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 185 | 195 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 221 | 230 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 244 | 253 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 60 | 69 | PF02991 | 0.539 |
LIG_LIR_Nem_3 | 156 | 161 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 174 | 178 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 185 | 190 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 221 | 225 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 226 | 232 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 244 | 248 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 60 | 64 | PF02991 | 0.539 |
LIG_Pex14_2 | 225 | 229 | PF04695 | 0.423 |
LIG_Pex14_2 | 241 | 245 | PF04695 | 0.444 |
LIG_PTB_Apo_2 | 130 | 137 | PF02174 | 0.372 |
LIG_Rb_LxCxE_1 | 38 | 60 | PF01857 | 0.564 |
LIG_SH2_CRK | 158 | 162 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 142 | 146 | PF00017 | 0.414 |
LIG_SH2_STAP1 | 201 | 205 | PF00017 | 0.450 |
LIG_SH2_STAP1 | 249 | 253 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 249 | 252 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.639 |
LIG_Sin3_3 | 61 | 68 | PF02671 | 0.423 |
LIG_SUMO_SIM_anti_2 | 60 | 66 | PF11976 | 0.505 |
LIG_SUMO_SIM_par_1 | 187 | 193 | PF11976 | 0.444 |
LIG_WRC_WIRS_1 | 58 | 63 | PF05994 | 0.423 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.398 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.325 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.777 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.546 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.507 |
MOD_Cter_Amidation | 213 | 216 | PF01082 | 0.763 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.618 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.760 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.431 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.401 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.765 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.382 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.479 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.543 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.753 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.352 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.838 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.556 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.302 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.444 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.444 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.468 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.470 |
MOD_NEK2_2 | 116 | 121 | PF00069 | 0.521 |
MOD_PKA_1 | 22 | 28 | PF00069 | 0.740 |
MOD_PKA_1 | 29 | 35 | PF00069 | 0.706 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.768 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.628 |
MOD_Plk_1 | 13 | 19 | PF00069 | 0.761 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.578 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.557 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.400 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.402 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.543 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.529 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.672 |
MOD_SUMO_rev_2 | 259 | 267 | PF00179 | 0.666 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.504 |
TRG_ER_diArg_1 | 22 | 24 | PF00400 | 0.841 |
TRG_NES_CRM1_1 | 86 | 100 | PF08389 | 0.504 |
TRG_NLS_MonoExtN_4 | 29 | 34 | PF00514 | 0.743 |
TRG_Pf-PMV_PEXEL_1 | 269 | 273 | PF00026 | 0.459 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2B8 | Leptomonas seymouri | 71% | 99% |
A0A3S5H6R5 | Leishmania donovani | 98% | 100% |
A0A3S7WSV8 | Leishmania donovani | 100% | 100% |
A4H7K8 | Leishmania braziliensis | 77% | 100% |
A4H7K9 | Leishmania braziliensis | 78% | 100% |
A4HVZ1 | Leishmania infantum | 97% | 100% |
E9APP2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
E9APP3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4QFT6 | Leishmania major | 92% | 100% |
Q4QFT7 | Leishmania major | 93% | 100% |