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 |
Related structures:
AlphaFold database: A4HC06
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 146 | 150 | PF00656 | 0.324 |
CLV_C14_Caspase3-7 | 92 | 96 | PF00656 | 0.400 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.556 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.465 |
CLV_PCSK_PC1ET2_1 | 5 | 7 | PF00082 | 0.442 |
CLV_PCSK_PC7_1 | 172 | 178 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.333 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.542 |
DOC_PP2B_LxvP_1 | 293 | 296 | PF13499 | 0.553 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.316 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.229 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.261 |
LIG_14-3-3_CanoR_1 | 124 | 129 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 233 | 238 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 55 | 59 | PF00244 | 0.410 |
LIG_BIR_III_2 | 180 | 184 | PF00653 | 0.317 |
LIG_BRCT_BRCA1_1 | 244 | 248 | PF00533 | 0.325 |
LIG_EH_1 | 80 | 84 | PF12763 | 0.324 |
LIG_FHA_2 | 131 | 137 | PF00498 | 0.409 |
LIG_FHA_2 | 144 | 150 | PF00498 | 0.380 |
LIG_FHA_2 | 41 | 47 | PF00498 | 0.339 |
LIG_FHA_2 | 70 | 76 | PF00498 | 0.267 |
LIG_LIR_Gen_1 | 114 | 123 | PF02991 | 0.366 |
LIG_LIR_Gen_1 | 240 | 251 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 114 | 120 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 236 | 242 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 245 | 251 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 64 | 69 | PF02991 | 0.321 |
LIG_MLH1_MIPbox_1 | 244 | 248 | PF16413 | 0.325 |
LIG_NRBOX | 255 | 261 | PF00104 | 0.525 |
LIG_PDZ_Class_2 | 296 | 301 | PF00595 | 0.650 |
LIG_Pex14_1 | 239 | 243 | PF04695 | 0.349 |
LIG_Pex14_2 | 41 | 45 | PF04695 | 0.412 |
LIG_PTB_Apo_2 | 78 | 85 | PF02174 | 0.328 |
LIG_SH2_NCK_1 | 153 | 157 | PF00017 | 0.229 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.229 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.360 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.272 |
LIG_SUMO_SIM_par_1 | 254 | 261 | PF11976 | 0.470 |
LIG_TRFH_1 | 204 | 208 | PF08558 | 0.459 |
LIG_WRC_WIRS_1 | 62 | 67 | PF05994 | 0.418 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.332 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.315 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.168 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.635 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.434 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.362 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.544 |
MOD_GlcNHglycan | 166 | 170 | PF01048 | 0.368 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.595 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.646 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.619 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.344 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.202 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.534 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.260 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.701 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.363 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.317 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.318 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.404 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.321 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.402 |
MOD_NEK2_2 | 50 | 55 | PF00069 | 0.226 |
MOD_PKA_1 | 124 | 130 | PF00069 | 0.237 |
MOD_PKA_2 | 143 | 149 | PF00069 | 0.168 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.382 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.259 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.202 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.452 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.298 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.378 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.353 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.266 |
MOD_SUMO_rev_2 | 57 | 63 | PF00179 | 0.405 |
MOD_SUMO_rev_2 | 92 | 99 | PF00179 | 0.250 |
TRG_AP2beta_CARGO_1 | 114 | 124 | PF09066 | 0.314 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.293 |
TRG_ER_diArg_1 | 176 | 178 | PF00400 | 0.347 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2X3 | Leptomonas seymouri | 53% | 83% |
A0A1X0NHP3 | Trypanosomatidae | 37% | 84% |
A0A3R7N7N1 | Trypanosoma rangeli | 34% | 89% |
A0A3S7WWQ5 | Leishmania donovani | 77% | 67% |
A4HZF6 | Leishmania infantum | 77% | 67% |
D0A124 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 91% |
E9AVE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 81% |
V5BLW0 | Trypanosoma cruzi | 37% | 96% |