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: 3 |
NetGPI | no | yes: 0, no: 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HTM2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.523 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.791 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.486 |
CLV_PCSK_FUR_1 | 286 | 290 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.791 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.486 |
CLV_PCSK_PC1ET2_1 | 131 | 133 | PF00082 | 0.505 |
CLV_PCSK_PC1ET2_1 | 212 | 214 | PF00082 | 0.577 |
CLV_PCSK_PC7_1 | 208 | 214 | PF00082 | 0.587 |
CLV_PCSK_PC7_1 | 319 | 325 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.521 |
DEG_APCC_DBOX_1 | 122 | 130 | PF00400 | 0.498 |
DOC_CYCLIN_RxL_1 | 52 | 62 | PF00134 | 0.521 |
DOC_CYCLIN_yCln2_LP_2 | 14 | 20 | PF00134 | 0.569 |
DOC_MAPK_gen_1 | 170 | 178 | PF00069 | 0.517 |
DOC_MAPK_gen_1 | 208 | 216 | PF00069 | 0.633 |
DOC_MAPK_gen_1 | 239 | 248 | PF00069 | 0.560 |
DOC_PP1_RVXF_1 | 155 | 161 | PF00149 | 0.436 |
DOC_PP1_RVXF_1 | 210 | 217 | PF00149 | 0.578 |
DOC_PP2B_LxvP_1 | 14 | 17 | PF13499 | 0.583 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.668 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.573 |
LIG_14-3-3_CanoR_1 | 191 | 196 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 201 | 207 | PF00244 | 0.620 |
LIG_14-3-3_CanoR_1 | 213 | 223 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 233 | 242 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 294 | 298 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 338 | 342 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 94 | 103 | PF00244 | 0.580 |
LIG_APCC_ABBA_1 | 24 | 29 | PF00400 | 0.501 |
LIG_BRCT_BRCA1_1 | 60 | 64 | PF00533 | 0.574 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.548 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.512 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.706 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.651 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.636 |
LIG_GBD_Chelix_1 | 158 | 166 | PF00786 | 0.479 |
LIG_LIR_Nem_3 | 53 | 57 | PF02991 | 0.597 |
LIG_SH2_CRK | 54 | 58 | PF00017 | 0.571 |
LIG_SH2_STAP1 | 7 | 11 | PF00017 | 0.646 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.583 |
LIG_SH3_1 | 221 | 227 | PF00018 | 0.594 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.594 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.674 |
LIG_SH3_3 | 63 | 69 | PF00018 | 0.561 |
LIG_SUMO_SIM_par_1 | 16 | 21 | PF11976 | 0.618 |
LIG_SUMO_SIM_par_1 | 55 | 62 | PF11976 | 0.546 |
MOD_CDC14_SPxK_1 | 291 | 294 | PF00782 | 0.663 |
MOD_CDK_SPxK_1 | 288 | 294 | PF00069 | 0.657 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.610 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.631 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.579 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.533 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.574 |
MOD_GlcNHglycan | 60 | 64 | PF01048 | 0.574 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.574 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.592 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.576 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.699 |
MOD_N-GLC_1 | 143 | 148 | PF02516 | 0.502 |
MOD_N-GLC_1 | 50 | 55 | PF02516 | 0.610 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.520 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.553 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.569 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.576 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.611 |
MOD_PK_1 | 139 | 145 | PF00069 | 0.527 |
MOD_PK_1 | 191 | 197 | PF00069 | 0.567 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.619 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.674 |
MOD_PKB_1 | 231 | 239 | PF00069 | 0.652 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.680 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.545 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.653 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.578 |
TRG_DiLeu_BaLyEn_6 | 14 | 19 | PF01217 | 0.575 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.566 |
TRG_ER_diArg_1 | 116 | 119 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 230 | 233 | PF00400 | 0.769 |
TRG_ER_diArg_1 | 239 | 241 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 274 | 276 | PF00400 | 0.634 |
TRG_ER_diArg_1 | 326 | 329 | PF00400 | 0.756 |
TRG_ER_diArg_1 | 337 | 339 | PF00400 | 0.523 |
TRG_NLS_Bipartite_1 | 116 | 134 | PF00514 | 0.503 |
TRG_NLS_MonoExtC_3 | 129 | 135 | PF00514 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 110 | 114 | PF00026 | 0.566 |
TRG_Pf-PMV_PEXEL_1 | 136 | 141 | PF00026 | 0.614 |
TRG_Pf-PMV_PEXEL_1 | 55 | 60 | PF00026 | 0.523 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WQC8 | Leishmania donovani | 99% | 80% |
A4HAZ7 | Leishmania braziliensis | 40% | 73% |