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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AWV6
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005509 | calcium ion binding | 5 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 133 | 137 | PF00656 | 0.416 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.513 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 252 | 256 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.538 |
DEG_APCC_DBOX_1 | 181 | 189 | PF00400 | 0.420 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.519 |
DEG_SPOP_SBC_1 | 49 | 53 | PF00917 | 0.507 |
DOC_MAPK_gen_1 | 140 | 149 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 142 | 151 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 198 | 207 | PF00069 | 0.466 |
DOC_PP2B_LxvP_1 | 169 | 172 | PF13499 | 0.338 |
DOC_PP2B_LxvP_1 | 232 | 235 | PF13499 | 0.529 |
DOC_PP2B_LxvP_1 | 42 | 45 | PF13499 | 0.470 |
DOC_PP4_FxxP_1 | 66 | 69 | PF00568 | 0.432 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.390 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.619 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.310 |
LIG_14-3-3_CanoR_1 | 15 | 19 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 305 | 312 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 375 | 380 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 48 | 58 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 75 | 81 | PF00244 | 0.597 |
LIG_APCC_ABBA_1 | 244 | 249 | PF00400 | 0.343 |
LIG_BRCT_BRCA1_1 | 277 | 281 | PF00533 | 0.392 |
LIG_EH_1 | 67 | 71 | PF12763 | 0.411 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.489 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.422 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.755 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.572 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.322 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.643 |
LIG_LIR_Gen_1 | 141 | 151 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 160 | 169 | PF02991 | 0.301 |
LIG_LIR_Gen_1 | 278 | 289 | PF02991 | 0.393 |
LIG_LIR_LC3C_4 | 183 | 187 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 160 | 165 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 194 | 200 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 278 | 284 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 28 | 33 | PF02991 | 0.550 |
LIG_NRBOX | 279 | 285 | PF00104 | 0.390 |
LIG_NRBOX | 336 | 342 | PF00104 | 0.398 |
LIG_Pex14_2 | 66 | 70 | PF04695 | 0.425 |
LIG_SH2_CRK | 166 | 170 | PF00017 | 0.341 |
LIG_SH2_CRK | 334 | 338 | PF00017 | 0.391 |
LIG_SH2_STAP1 | 334 | 338 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.383 |
LIG_SH3_3 | 256 | 262 | PF00018 | 0.249 |
LIG_SUMO_SIM_anti_2 | 145 | 151 | PF11976 | 0.505 |
LIG_SUMO_SIM_anti_2 | 183 | 190 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 117 | 123 | PF11976 | 0.245 |
LIG_SUMO_SIM_par_1 | 183 | 190 | PF11976 | 0.337 |
LIG_SUMO_SIM_par_1 | 255 | 260 | PF11976 | 0.245 |
LIG_SUMO_SIM_par_1 | 272 | 278 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 336 | 342 | PF11976 | 0.419 |
LIG_TRAF2_1 | 239 | 242 | PF00917 | 0.454 |
LIG_TYR_ITIM | 164 | 169 | PF00017 | 0.341 |
LIG_TYR_ITIM | 332 | 337 | PF00017 | 0.355 |
MOD_CK1_1 | 129 | 135 | PF00069 | 0.523 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.519 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.318 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.544 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.544 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.481 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.505 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.362 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.698 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.678 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.634 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.655 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.565 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.601 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.558 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.436 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.480 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.608 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.664 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.376 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.515 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.670 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.400 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.747 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.401 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.566 |
MOD_PKA_2 | 304 | 310 | PF00069 | 0.437 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.658 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.587 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.497 |
MOD_PKB_1 | 48 | 56 | PF00069 | 0.440 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.351 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.314 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.408 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.307 |
MOD_SUMO_rev_2 | 327 | 333 | PF00179 | 0.477 |
TRG_DiLeu_BaEn_1 | 107 | 112 | PF01217 | 0.433 |
TRG_DiLeu_BaEn_1 | 160 | 165 | PF01217 | 0.349 |
TRG_DiLeu_BaEn_4 | 241 | 247 | PF01217 | 0.348 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 197 | 200 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 334 | 337 | PF00928 | 0.361 |
TRG_ER_diArg_1 | 62 | 64 | PF00400 | 0.606 |
TRG_NES_CRM1_1 | 141 | 153 | PF08389 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 310 | 315 | PF00026 | 0.406 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBQ7 | Leptomonas seymouri | 63% | 100% |
A0A0S4IZX9 | Bodo saltans | 31% | 83% |
A0A1X0NX67 | Trypanosomatidae | 43% | 97% |
A0A3S7WYF3 | Leishmania donovani | 84% | 92% |
A0A422NQ90 | Trypanosoma rangeli | 51% | 100% |
A4HDH1 | Leishmania braziliensis | 69% | 99% |
A4I0V2 | Leishmania infantum | 84% | 92% |
D0A781 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
Q4QAL8 | Leishmania major | 83% | 69% |
V5BR35 | Trypanosoma cruzi | 51% | 100% |