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: A0A3S7WYF3
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_NRD_NRD_1 | 11 | 13 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.571 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.555 |
CLV_PCSK_KEX2_1 | 408 | 410 | PF00082 | 0.663 |
CLV_PCSK_PC1ET2_1 | 408 | 410 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.676 |
DEG_APCC_DBOX_1 | 10 | 18 | PF00400 | 0.513 |
DEG_APCC_DBOX_1 | 241 | 249 | PF00400 | 0.473 |
DEG_SCF_FBW7_1 | 21 | 27 | PF00400 | 0.418 |
DOC_CKS1_1 | 21 | 26 | PF01111 | 0.429 |
DOC_CYCLIN_RxL_1 | 237 | 250 | PF00134 | 0.523 |
DOC_MAPK_gen_1 | 11 | 17 | PF00069 | 0.513 |
DOC_MAPK_gen_1 | 200 | 209 | PF00069 | 0.552 |
DOC_MAPK_MEF2A_6 | 202 | 211 | PF00069 | 0.553 |
DOC_MAPK_MEF2A_6 | 258 | 267 | PF00069 | 0.541 |
DOC_PP2B_LxvP_1 | 229 | 232 | PF13499 | 0.391 |
DOC_PP2B_LxvP_1 | 292 | 295 | PF13499 | 0.545 |
DOC_PP2B_LxvP_1 | 73 | 76 | PF13499 | 0.725 |
DOC_PP4_FxxP_1 | 126 | 129 | PF00568 | 0.493 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.769 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.529 |
LIG_14-3-3_CanoR_1 | 108 | 118 | PF00244 | 0.734 |
LIG_14-3-3_CanoR_1 | 12 | 18 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 135 | 145 | PF00244 | 0.740 |
LIG_14-3-3_CanoR_1 | 365 | 372 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 77 | 86 | PF00244 | 0.626 |
LIG_APCC_ABBA_1 | 304 | 309 | PF00400 | 0.396 |
LIG_BRCT_BRCA1_1 | 18 | 22 | PF00533 | 0.491 |
LIG_BRCT_BRCA1_1 | 337 | 341 | PF00533 | 0.545 |
LIG_EH_1 | 127 | 131 | PF12763 | 0.477 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.734 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.355 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.503 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.380 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.483 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.701 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.543 |
LIG_LIR_Gen_1 | 116 | 126 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 201 | 211 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 220 | 229 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 338 | 349 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 201 | 207 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 220 | 225 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 313 | 318 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 338 | 344 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 87 | 92 | PF02991 | 0.652 |
LIG_NRBOX | 339 | 345 | PF00104 | 0.447 |
LIG_NRBOX | 396 | 402 | PF00104 | 0.465 |
LIG_Pex14_2 | 126 | 130 | PF04695 | 0.486 |
LIG_SH2_CRK | 226 | 230 | PF00017 | 0.396 |
LIG_SH2_CRK | 394 | 398 | PF00017 | 0.451 |
LIG_SH2_STAP1 | 394 | 398 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.391 |
LIG_SH3_1 | 44 | 50 | PF00018 | 0.511 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.535 |
LIG_SUMO_SIM_anti_2 | 205 | 211 | PF11976 | 0.494 |
LIG_SUMO_SIM_anti_2 | 243 | 250 | PF11976 | 0.491 |
LIG_SUMO_SIM_anti_2 | 31 | 38 | PF11976 | 0.410 |
LIG_SUMO_SIM_par_1 | 13 | 19 | PF11976 | 0.524 |
LIG_SUMO_SIM_par_1 | 243 | 250 | PF11976 | 0.397 |
LIG_SUMO_SIM_par_1 | 31 | 38 | PF11976 | 0.332 |
LIG_SUMO_SIM_par_1 | 332 | 338 | PF11976 | 0.510 |
LIG_SUMO_SIM_par_1 | 396 | 402 | PF11976 | 0.544 |
LIG_TRAF2_1 | 299 | 302 | PF00917 | 0.571 |
LIG_TYR_ITIM | 224 | 229 | PF00017 | 0.396 |
LIG_TYR_ITIM | 392 | 397 | PF00017 | 0.407 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.613 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.632 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.533 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.547 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.668 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.562 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.755 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.693 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.703 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.505 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.526 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.373 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.718 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.654 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.718 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.647 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.591 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.548 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.626 |
MOD_N-GLC_1 | 84 | 89 | PF02516 | 0.739 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.759 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.588 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.430 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.486 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.618 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.705 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.746 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.520 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.507 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.639 |
MOD_Plk_1 | 152 | 158 | PF00069 | 0.574 |
MOD_Plk_1 | 271 | 277 | PF00069 | 0.540 |
MOD_Plk_1 | 329 | 335 | PF00069 | 0.415 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.739 |
MOD_Plk_4 | 252 | 258 | PF00069 | 0.455 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.574 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.543 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.665 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.443 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.530 |
MOD_SUMO_rev_2 | 305 | 314 | PF00179 | 0.508 |
MOD_SUMO_rev_2 | 387 | 393 | PF00179 | 0.522 |
TRG_DiLeu_BaEn_1 | 167 | 172 | PF01217 | 0.580 |
TRG_DiLeu_BaEn_1 | 220 | 225 | PF01217 | 0.406 |
TRG_DiLeu_BaLyEn_6 | 376 | 381 | PF01217 | 0.518 |
TRG_DiLeu_BaLyEn_6 | 9 | 14 | PF01217 | 0.542 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 257 | 260 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 394 | 397 | PF00928 | 0.415 |
TRG_ER_diArg_1 | 11 | 13 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 122 | 124 | PF00400 | 0.648 |
TRG_NES_CRM1_1 | 201 | 213 | PF08389 | 0.519 |
TRG_NLS_MonoExtC_3 | 406 | 411 | PF00514 | 0.655 |
TRG_NLS_MonoExtN_4 | 404 | 411 | PF00514 | 0.640 |
TRG_Pf-PMV_PEXEL_1 | 370 | 375 | PF00026 | 0.481 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBQ7 | Leptomonas seymouri | 65% | 100% |
A0A0S4IZX9 | Bodo saltans | 30% | 91% |
A0A1X0NX67 | Trypanosomatidae | 41% | 100% |
A0A422NQ90 | Trypanosoma rangeli | 51% | 100% |
A4HDH1 | Leishmania braziliensis | 70% | 100% |
A4I0V2 | Leishmania infantum | 100% | 100% |
D0A781 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9AWV6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4QAL8 | Leishmania major | 83% | 100% |
V5BR35 | Trypanosoma cruzi | 49% | 100% |