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 |
Related structures:
AlphaFold database: E9AFQ1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.417 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.492 |
CLV_PCSK_PC1ET2_1 | 286 | 288 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 133 | 137 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.737 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.478 |
CLV_Separin_Metazoa | 238 | 242 | PF03568 | 0.459 |
DEG_APCC_DBOX_1 | 60 | 68 | PF00400 | 0.451 |
DEG_SCF_FBW7_2 | 231 | 238 | PF00400 | 0.429 |
DEG_SPOP_SBC_1 | 155 | 159 | PF00917 | 0.673 |
DOC_CKS1_1 | 232 | 237 | PF01111 | 0.425 |
DOC_CYCLIN_yCln2_LP_2 | 114 | 120 | PF00134 | 0.506 |
DOC_MAPK_MEF2A_6 | 206 | 214 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 3 | 12 | PF00069 | 0.606 |
DOC_PP2B_LxvP_1 | 210 | 213 | PF13499 | 0.394 |
DOC_PP4_FxxP_1 | 5 | 8 | PF00568 | 0.590 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 290 | 294 | PF00917 | 0.489 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.576 |
DOC_WW_Pin1_4 | 231 | 236 | PF00397 | 0.348 |
LIG_14-3-3_CanoR_1 | 226 | 232 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 29 | 35 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 36 | 40 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 7 | 13 | PF00244 | 0.546 |
LIG_CSL_BTD_1 | 42 | 45 | PF09270 | 0.316 |
LIG_deltaCOP1_diTrp_1 | 40 | 46 | PF00928 | 0.440 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.683 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.759 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.424 |
LIG_FHA_1 | 277 | 283 | PF00498 | 0.481 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.342 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.337 |
LIG_FHA_2 | 102 | 108 | PF00498 | 0.459 |
LIG_FHA_2 | 214 | 220 | PF00498 | 0.459 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.315 |
LIG_FXI_DFP_1 | 182 | 186 | PF00024 | 0.468 |
LIG_LIR_Gen_1 | 89 | 99 | PF02991 | 0.301 |
LIG_LIR_LC3C_4 | 208 | 212 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 124 | 129 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 184 | 188 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 40 | 46 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 89 | 95 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 97 | 102 | PF02991 | 0.318 |
LIG_SH2_SRC | 217 | 220 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.313 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.486 |
LIG_SH3_1 | 241 | 247 | PF00018 | 0.415 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.500 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.565 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.594 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.331 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.288 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.514 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.620 |
MOD_CK2_1 | 213 | 219 | PF00069 | 0.407 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.510 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.634 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.654 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.573 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.699 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.420 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.418 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.460 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.498 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.593 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.654 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.650 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.584 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.501 |
MOD_N-GLC_1 | 121 | 126 | PF02516 | 0.464 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.365 |
MOD_NEK2_1 | 145 | 150 | PF00069 | 0.509 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.462 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.454 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.310 |
MOD_OFUCOSY | 69 | 76 | PF10250 | 0.439 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.552 |
MOD_PKA_2 | 145 | 151 | PF00069 | 0.733 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.453 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.321 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.512 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.425 |
MOD_Plk_1 | 222 | 228 | PF00069 | 0.522 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.480 |
MOD_Plk_4 | 213 | 219 | PF00069 | 0.435 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.412 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.439 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.575 |
MOD_ProDKin_1 | 231 | 237 | PF00069 | 0.349 |
MOD_SUMO_for_1 | 271 | 274 | PF00179 | 0.500 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.512 |
TRG_ER_diArg_1 | 240 | 243 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 266 | 268 | PF00400 | 0.424 |
TRG_Pf-PMV_PEXEL_1 | 86 | 90 | PF00026 | 0.386 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HY73 | Leptomonas seymouri | 50% | 100% |
A0A0S4JF57 | Bodo saltans | 35% | 100% |
A0A1X0P581 | Trypanosomatidae | 36% | 100% |
A0A3R7NNI3 | Trypanosoma rangeli | 37% | 100% |
A0A3S7X9V8 | Leishmania donovani | 92% | 100% |
A4HN94 | Leishmania braziliensis | 71% | 98% |
A4IBW4 | Leishmania infantum | 92% | 100% |
C9ZYP7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9B6V4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5BCR5 | Trypanosoma cruzi | 35% | 100% |