Glycosylation, Glucosidase II beta subunit-like
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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4HTL3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 131 | 135 | PF00656 | 0.628 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.438 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.777 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.777 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.438 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.593 |
DEG_SCF_FBW7_1 | 240 | 246 | PF00400 | 0.632 |
DEG_SPOP_SBC_1 | 200 | 204 | PF00917 | 0.549 |
DOC_CKS1_1 | 240 | 245 | PF01111 | 0.631 |
DOC_CYCLIN_yCln2_LP_2 | 8 | 14 | PF00134 | 0.470 |
DOC_PP2B_LxvP_1 | 8 | 11 | PF13499 | 0.470 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.630 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 245 | 250 | PF00397 | 0.725 |
LIG_14-3-3_CanoR_1 | 70 | 78 | PF00244 | 0.303 |
LIG_14-3-3_CanoR_1 | 83 | 89 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 97 | 105 | PF00244 | 0.573 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.594 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.731 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.489 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.709 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.649 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.387 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.337 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.577 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.470 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.626 |
LIG_FHA_2 | 186 | 192 | PF00498 | 0.736 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.375 |
LIG_LIR_Apic_2 | 86 | 92 | PF02991 | 0.610 |
LIG_LIR_Gen_1 | 3 | 12 | PF02991 | 0.470 |
LIG_LIR_LC3C_4 | 227 | 232 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 3 | 8 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 59 | 65 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 72 | 77 | PF02991 | 0.402 |
LIG_PDZ_Class_2 | 291 | 296 | PF00595 | 0.599 |
LIG_SH2_CRK | 167 | 171 | PF00017 | 0.729 |
LIG_SH2_CRK | 23 | 27 | PF00017 | 0.470 |
LIG_SH2_CRK | 5 | 9 | PF00017 | 0.470 |
LIG_SH2_CRK | 62 | 66 | PF00017 | 0.470 |
LIG_SH2_CRK | 89 | 93 | PF00017 | 0.629 |
LIG_SH2_GRB2like | 167 | 170 | PF00017 | 0.730 |
LIG_SH2_SRC | 167 | 170 | PF00017 | 0.730 |
LIG_SH2_STAP1 | 212 | 216 | PF00017 | 0.628 |
LIG_SH2_STAP1 | 74 | 78 | PF00017 | 0.566 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.615 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.660 |
LIG_SH3_3 | 246 | 252 | PF00018 | 0.644 |
LIG_SH3_3 | 278 | 284 | PF00018 | 0.679 |
LIG_SUMO_SIM_anti_2 | 206 | 215 | PF11976 | 0.650 |
LIG_SUMO_SIM_par_1 | 229 | 236 | PF11976 | 0.629 |
LIG_TRAF2_1 | 153 | 156 | PF00917 | 0.740 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.470 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.678 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.632 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.696 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.565 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.602 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.516 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.390 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.768 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.733 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.425 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.406 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.727 |
MOD_GlcNHglycan | 235 | 238 | PF01048 | 0.609 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.748 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.592 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.639 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.607 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.764 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.348 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.375 |
MOD_N-GLC_1 | 114 | 119 | PF02516 | 0.643 |
MOD_N-GLC_1 | 38 | 43 | PF02516 | 0.470 |
MOD_N-GLC_1 | 44 | 49 | PF02516 | 0.362 |
MOD_N-GLC_1 | 84 | 89 | PF02516 | 0.607 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.544 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.664 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.470 |
MOD_PIKK_1 | 96 | 102 | PF00454 | 0.615 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.297 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.615 |
MOD_Plk_1 | 114 | 120 | PF00069 | 0.646 |
MOD_Plk_1 | 38 | 44 | PF00069 | 0.505 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.613 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.653 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.503 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.738 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.714 |
TRG_DiLeu_BaLyEn_6 | 22 | 27 | PF01217 | 0.470 |
TRG_ENDOCYTIC_2 | 23 | 26 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.492 |
TRG_ER_diArg_1 | 23 | 25 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 285 | 288 | PF00400 | 0.668 |
TRG_ER_diArg_1 | 96 | 98 | PF00400 | 0.761 |
TRG_Pf-PMV_PEXEL_1 | 288 | 292 | PF00026 | 0.659 |
TRG_Pf-PMV_PEXEL_1 | 48 | 52 | PF00026 | 0.438 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WQB1 | Leishmania donovani | 99% | 100% |
A4H5G3 | Leishmania braziliensis | 56% | 99% |
E9AME4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 97% |
Q4QIA4 | Leishmania major | 82% | 97% |