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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: E9B3S0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 299 | 303 | PF00656 | 0.745 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.395 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.716 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.534 |
CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.435 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.465 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.370 |
CLV_PCSK_FUR_1 | 77 | 81 | PF00082 | 0.301 |
CLV_PCSK_FUR_1 | 92 | 96 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.716 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 76 | 78 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.326 |
DEG_APCC_DBOX_1 | 213 | 221 | PF00400 | 0.523 |
DEG_SCF_FBW7_1 | 1 | 8 | PF00400 | 0.393 |
DEG_SPOP_SBC_1 | 153 | 157 | PF00917 | 0.630 |
DEG_SPOP_SBC_1 | 285 | 289 | PF00917 | 0.710 |
DOC_CDC14_PxL_1 | 244 | 252 | PF14671 | 0.452 |
DOC_CYCLIN_RxL_1 | 193 | 203 | PF00134 | 0.627 |
DOC_CYCLIN_RxL_1 | 44 | 54 | PF00134 | 0.619 |
DOC_CYCLIN_RxL_1 | 74 | 87 | PF00134 | 0.716 |
DOC_MAPK_gen_1 | 214 | 220 | PF00069 | 0.526 |
DOC_MAPK_gen_1 | 45 | 51 | PF00069 | 0.582 |
DOC_MAPK_gen_1 | 76 | 84 | PF00069 | 0.714 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.763 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.609 |
LIG_14-3-3_CanoR_1 | 215 | 221 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 256 | 261 | PF00244 | 0.688 |
LIG_14-3-3_CanoR_1 | 94 | 99 | PF00244 | 0.647 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.614 |
LIG_eIF4E_1 | 12 | 18 | PF01652 | 0.380 |
LIG_eIF4E_1 | 330 | 336 | PF01652 | 0.530 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.604 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.656 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.539 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.277 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.560 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.742 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.411 |
LIG_GBD_Chelix_1 | 327 | 335 | PF00786 | 0.452 |
LIG_LIR_Gen_1 | 227 | 238 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 333 | 340 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 227 | 233 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 24 | 29 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 333 | 337 | PF02991 | 0.316 |
LIG_PCNA_APIM_2 | 194 | 200 | PF02747 | 0.483 |
LIG_SH2_GRB2like | 12 | 15 | PF00017 | 0.489 |
LIG_SH2_SRC | 12 | 15 | PF00017 | 0.336 |
LIG_SH2_SRC | 246 | 249 | PF00017 | 0.452 |
LIG_SH2_SRC | 334 | 337 | PF00017 | 0.530 |
LIG_SH2_SRC | 72 | 75 | PF00017 | 0.657 |
LIG_SH2_STAP1 | 168 | 172 | PF00017 | 0.678 |
LIG_SH2_STAP1 | 29 | 33 | PF00017 | 0.530 |
LIG_SH2_STAP1 | 98 | 102 | PF00017 | 0.759 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 330 | 333 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 334 | 337 | PF00017 | 0.464 |
LIG_SH3_3 | 102 | 108 | PF00018 | 0.724 |
LIG_SH3_3 | 170 | 176 | PF00018 | 0.576 |
LIG_SH3_3 | 232 | 238 | PF00018 | 0.435 |
LIG_SH3_3 | 248 | 254 | PF00018 | 0.390 |
LIG_SUMO_SIM_anti_2 | 154 | 164 | PF11976 | 0.607 |
LIG_SUMO_SIM_anti_2 | 203 | 209 | PF11976 | 0.393 |
LIG_TYR_ITIM | 228 | 233 | PF00017 | 0.505 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.665 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.773 |
MOD_CK2_1 | 220 | 226 | PF00069 | 0.448 |
MOD_CK2_1 | 276 | 282 | PF00069 | 0.721 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.418 |
MOD_Cter_Amidation | 119 | 122 | PF01082 | 0.394 |
MOD_DYRK1A_RPxSP_1 | 104 | 108 | PF00069 | 0.727 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.462 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.375 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.535 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.600 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.448 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.784 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.602 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.436 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.692 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.717 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.778 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.610 |
MOD_N-GLC_1 | 189 | 194 | PF02516 | 0.456 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.809 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.693 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.463 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.759 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.583 |
MOD_NEK2_2 | 29 | 34 | PF00069 | 0.530 |
MOD_PKA_1 | 256 | 262 | PF00069 | 0.737 |
MOD_PKA_1 | 94 | 100 | PF00069 | 0.536 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.802 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.750 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.648 |
MOD_PKB_1 | 92 | 100 | PF00069 | 0.533 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.572 |
MOD_Plk_1 | 35 | 41 | PF00069 | 0.720 |
MOD_Plk_1 | 98 | 104 | PF00069 | 0.697 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.691 |
MOD_Plk_4 | 158 | 164 | PF00069 | 0.608 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.662 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.530 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.750 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.414 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.530 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.381 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.551 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.731 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.610 |
MOD_SUMO_rev_2 | 57 | 65 | PF00179 | 0.584 |
TRG_DiLeu_BaLyEn_6 | 235 | 240 | PF01217 | 0.530 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 334 | 337 | PF00928 | 0.530 |
TRG_ER_diArg_1 | 121 | 124 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 44 | 47 | PF00400 | 0.600 |
TRG_ER_diArg_1 | 76 | 79 | PF00400 | 0.684 |
TRG_ER_diArg_1 | 82 | 85 | PF00400 | 0.683 |
TRG_ER_diArg_1 | 92 | 95 | PF00400 | 0.573 |
TRG_Pf-PMV_PEXEL_1 | 47 | 52 | PF00026 | 0.371 |
TRG_Pf-PMV_PEXEL_1 | 94 | 99 | PF00026 | 0.331 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X6H6 | Leishmania donovani | 82% | 100% |
A4HLE2 | Leishmania braziliensis | 60% | 99% |
A4I8V1 | Leishmania infantum | 82% | 100% |
Q4Q4A4 | Leishmania major | 80% | 100% |