Related to USP9X animal ubiquitin-specific proteases. Does not appear to be a TM protein.
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: A4HDH1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.543 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 102 | 104 | PF00082 | 0.368 |
CLV_PCSK_PC7_1 | 7 | 13 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.572 |
DEG_APCC_DBOX_1 | 188 | 196 | PF00400 | 0.488 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.525 |
DOC_MAPK_gen_1 | 147 | 156 | PF00069 | 0.413 |
DOC_MAPK_gen_1 | 223 | 231 | PF00069 | 0.235 |
DOC_MAPK_MEF2A_6 | 147 | 156 | PF00069 | 0.397 |
DOC_MAPK_MEF2A_6 | 205 | 214 | PF00069 | 0.460 |
DOC_MAPK_MEF2A_6 | 276 | 283 | PF00069 | 0.385 |
DOC_PP2B_LxvP_1 | 176 | 179 | PF13499 | 0.324 |
DOC_PP2B_LxvP_1 | 239 | 242 | PF13499 | 0.501 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.692 |
DOC_USP7_UBL2_3 | 102 | 106 | PF12436 | 0.640 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.295 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.663 |
LIG_14-3-3_CanoR_1 | 48 | 54 | PF00244 | 0.615 |
LIG_APCC_ABBA_1 | 251 | 256 | PF00400 | 0.320 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.520 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.767 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.730 |
LIG_FHA_2 | 162 | 168 | PF00498 | 0.304 |
LIG_FHA_2 | 40 | 46 | PF00498 | 0.485 |
LIG_LIR_Gen_1 | 167 | 176 | PF02991 | 0.284 |
LIG_LIR_LC3C_4 | 190 | 194 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 167 | 172 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 201 | 207 | PF02991 | 0.315 |
LIG_Pex14_2 | 73 | 77 | PF04695 | 0.477 |
LIG_SH2_CRK | 173 | 177 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.322 |
LIG_SH3_1 | 11 | 17 | PF00018 | 0.470 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.470 |
LIG_SUMO_SIM_anti_2 | 190 | 197 | PF11976 | 0.480 |
LIG_SUMO_SIM_par_1 | 190 | 197 | PF11976 | 0.320 |
LIG_SUMO_SIM_par_1 | 54 | 61 | PF11976 | 0.451 |
LIG_TYR_ITIM | 171 | 176 | PF00017 | 0.318 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.497 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.595 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.614 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.588 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.521 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.387 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.484 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.665 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.440 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.720 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.663 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.626 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.618 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.635 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.591 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.594 |
MOD_LATS_1 | 29 | 35 | PF00433 | 0.467 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.389 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.686 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.523 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.350 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.535 |
MOD_NEK2_2 | 19 | 24 | PF00069 | 0.552 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.565 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.480 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.473 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.396 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.614 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.293 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.659 |
TRG_DiLeu_BaEn_1 | 114 | 119 | PF01217 | 0.435 |
TRG_DiLeu_BaEn_1 | 167 | 172 | PF01217 | 0.346 |
TRG_DiLeu_LyEn_5 | 114 | 119 | PF01217 | 0.274 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.316 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.438 |
TRG_ER_diArg_1 | 222 | 225 | PF00400 | 0.282 |
TRG_ER_diArg_1 | 69 | 71 | PF00400 | 0.624 |
TRG_NES_CRM1_1 | 148 | 160 | PF08389 | 0.462 |
TRG_NES_CRM1_1 | 201 | 216 | PF08389 | 0.237 |
TRG_NLS_MonoCore_2 | 11 | 16 | PF00514 | 0.472 |
TRG_NLS_MonoExtN_4 | 11 | 16 | PF00514 | 0.472 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBQ7 | Leptomonas seymouri | 61% | 85% |
A0A1X0NX67 | Trypanosomatidae | 38% | 73% |
A0A3S7WYF3 | Leishmania donovani | 70% | 69% |
A0A422NQ90 | Trypanosoma rangeli | 44% | 89% |
A4I0V2 | Leishmania infantum | 70% | 69% |
D0A781 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 87% |
E9AWV6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 75% |
V5BR35 | Trypanosoma cruzi | 39% | 85% |