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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HER5
Term | Name | Level | Count |
---|---|---|---|
GO:0000149 | SNARE binding | 3 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005515 | protein binding | 2 | 10 |
GO:0019905 | syntaxin binding | 4 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 48 | 52 | PF00656 | 0.405 |
CLV_NRD_NRD_1 | 153 | 155 | PF00675 | 0.334 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.306 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.281 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.388 |
CLV_PCSK_PC1ET2_1 | 116 | 118 | PF00082 | 0.277 |
CLV_PCSK_PC1ET2_1 | 152 | 154 | PF00082 | 0.369 |
CLV_PCSK_PC1ET2_1 | 305 | 307 | PF00082 | 0.284 |
CLV_PCSK_PC1ET2_1 | 77 | 79 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.241 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.466 |
CLV_Separin_Metazoa | 228 | 232 | PF03568 | 0.190 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 229 | 238 | PF00134 | 0.190 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.322 |
DOC_USP7_UBL2_3 | 66 | 70 | PF12436 | 0.246 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.621 |
LIG_14-3-3_CanoR_1 | 224 | 228 | PF00244 | 0.333 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.190 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.190 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.543 |
LIG_LIR_Gen_1 | 179 | 189 | PF02991 | 0.415 |
LIG_LIR_LC3C_4 | 198 | 201 | PF02991 | 0.190 |
LIG_LIR_Nem_3 | 179 | 185 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 242 | 248 | PF02991 | 0.305 |
LIG_Pex14_2 | 178 | 182 | PF04695 | 0.362 |
LIG_SH2_SRC | 203 | 206 | PF00017 | 0.441 |
LIG_SH2_STAP1 | 241 | 245 | PF00017 | 0.328 |
LIG_SH2_STAT3 | 241 | 244 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.337 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.376 |
LIG_SUMO_SIM_anti_2 | 214 | 221 | PF11976 | 0.397 |
LIG_TRAF2_1 | 10 | 13 | PF00917 | 0.571 |
LIG_TRAF2_1 | 109 | 112 | PF00917 | 0.350 |
LIG_TRAF2_1 | 202 | 205 | PF00917 | 0.413 |
LIG_TRAF2_1 | 23 | 26 | PF00917 | 0.453 |
LIG_TRAF2_1 | 328 | 331 | PF00917 | 0.578 |
LIG_TRAF2_1 | 98 | 101 | PF00917 | 0.369 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.654 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.239 |
MOD_CK2_1 | 178 | 184 | PF00069 | 0.244 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.511 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.738 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.659 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.190 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.635 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.376 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.345 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.628 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.635 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.324 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.336 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.406 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.315 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.388 |
MOD_PKA_1 | 174 | 180 | PF00069 | 0.423 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.441 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.336 |
MOD_Plk_1 | 178 | 184 | PF00069 | 0.379 |
MOD_Plk_2-3 | 223 | 229 | PF00069 | 0.362 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.282 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.285 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.618 |
MOD_SUMO_for_1 | 304 | 307 | PF00179 | 0.303 |
MOD_SUMO_rev_2 | 158 | 167 | PF00179 | 0.262 |
MOD_SUMO_rev_2 | 251 | 261 | PF00179 | 0.190 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.378 |
TRG_ER_diArg_1 | 220 | 222 | PF00400 | 0.323 |
TRG_NES_CRM1_1 | 209 | 223 | PF08389 | 0.190 |
TRG_NES_CRM1_1 | 228 | 242 | PF08389 | 0.190 |
TRG_NES_CRM1_1 | 71 | 83 | PF08389 | 0.337 |
TRG_NLS_Bipartite_1 | 76 | 98 | PF00514 | 0.190 |
TRG_Pf-PMV_PEXEL_1 | 306 | 310 | PF00026 | 0.342 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2W3 | Leptomonas seymouri | 64% | 99% |
A0A0S4JT11 | Bodo saltans | 30% | 91% |
A0A1X0NSF2 | Trypanosomatidae | 37% | 94% |
A0A3Q8IFN3 | Leishmania donovani | 82% | 100% |
A0A3R7M749 | Trypanosoma rangeli | 38% | 92% |
A4I1Z2 | Leishmania infantum | 82% | 100% |
C9ZS22 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 91% |
E9AY39 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4Q9D4 | Leishmania major | 82% | 100% |
V5BZC0 | Trypanosoma cruzi | 38% | 91% |