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: 5 |
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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: E9AME3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 204 | 208 | PF00656 | 0.392 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.537 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.537 |
DEG_SCF_FBW7_2 | 55 | 61 | PF00400 | 0.381 |
DEG_SPOP_SBC_1 | 163 | 167 | PF00917 | 0.396 |
DOC_CKS1_1 | 55 | 60 | PF01111 | 0.379 |
DOC_CYCLIN_yCln2_LP_2 | 174 | 180 | PF00134 | 0.383 |
DOC_MAPK_MEF2A_6 | 189 | 197 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 71 | 80 | PF00069 | 0.403 |
DOC_USP7_MATH_1 | 163 | 167 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.365 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.358 |
DOC_USP7_UBL2_3 | 67 | 71 | PF12436 | 0.475 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.376 |
LIG_Actin_WH2_2 | 167 | 184 | PF00022 | 0.389 |
LIG_BRCT_BRCA1_1 | 245 | 249 | PF00533 | 0.372 |
LIG_BRCT_BRCA1_1 | 99 | 103 | PF00533 | 0.250 |
LIG_deltaCOP1_diTrp_1 | 253 | 259 | PF00928 | 0.476 |
LIG_EH_1 | 234 | 238 | PF12763 | 0.440 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.437 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.453 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.420 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.556 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.372 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.488 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.364 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.392 |
LIG_FHA_2 | 248 | 254 | PF00498 | 0.479 |
LIG_LIR_Gen_1 | 106 | 116 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 242 | 252 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 257 | 266 | PF02991 | 0.356 |
LIG_LIR_LC3C_4 | 271 | 276 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 106 | 111 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 113 | 119 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 213 | 219 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 257 | 262 | PF02991 | 0.356 |
LIG_SH2_CRK | 216 | 220 | PF00017 | 0.384 |
LIG_SH2_GRB2like | 151 | 154 | PF00017 | 0.415 |
LIG_SH2_NCK_1 | 56 | 60 | PF00017 | 0.368 |
LIG_SH2_STAP1 | 151 | 155 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.385 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.413 |
LIG_SUMO_SIM_anti_2 | 175 | 182 | PF11976 | 0.384 |
LIG_SUMO_SIM_anti_2 | 271 | 279 | PF11976 | 0.441 |
LIG_SUMO_SIM_anti_2 | 290 | 297 | PF11976 | 0.715 |
LIG_WRC_WIRS_1 | 111 | 116 | PF05994 | 0.612 |
LIG_WRC_WIRS_1 | 241 | 246 | PF05994 | 0.534 |
LIG_WRC_WIRS_1 | 66 | 71 | PF05994 | 0.401 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.680 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.428 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.368 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.712 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.369 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.432 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.485 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.607 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.431 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.543 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.638 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.429 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.401 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.436 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.363 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.243 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.402 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.363 |
MOD_N-GLC_1 | 157 | 162 | PF02516 | 0.675 |
MOD_N-GLC_1 | 42 | 47 | PF02516 | 0.656 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.587 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.599 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.506 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.403 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.519 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.339 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.285 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.320 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.453 |
MOD_NEK2_2 | 240 | 245 | PF00069 | 0.532 |
MOD_NEK2_2 | 51 | 56 | PF00069 | 0.282 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.359 |
MOD_PKA_1 | 281 | 287 | PF00069 | 0.690 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.519 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.684 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.466 |
MOD_Plk_1 | 206 | 212 | PF00069 | 0.394 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.493 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.502 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.502 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.381 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.347 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.406 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.257 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.370 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.376 |
TRG_DiLeu_BaEn_1 | 176 | 181 | PF01217 | 0.382 |
TRG_DiLeu_BaEn_1 | 299 | 304 | PF01217 | 0.648 |
TRG_DiLeu_LyEn_5 | 299 | 304 | PF01217 | 0.700 |
TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.386 |
TRG_ER_diArg_1 | 119 | 122 | PF00400 | 0.714 |
TRG_ER_diArg_1 | 281 | 283 | PF00400 | 0.612 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I287 | Leptomonas seymouri | 38% | 100% |
A0A3S7WQ88 | Leishmania donovani | 73% | 100% |
A4H5G2 | Leishmania braziliensis | 56% | 96% |
A4HTL2 | Leishmania infantum | 72% | 100% |
Q4QIA5 | Leishmania major | 71% | 98% |