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: E9AK45
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 126 | 132 | PF00089 | 0.593 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.630 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.538 |
DEG_SCF_TRCP1_1 | 25 | 31 | PF00400 | 0.509 |
DOC_CKS1_1 | 279 | 284 | PF01111 | 0.624 |
DOC_CYCLIN_yCln2_LP_2 | 124 | 130 | PF00134 | 0.593 |
DOC_PP2B_LxvP_1 | 124 | 127 | PF13499 | 0.641 |
DOC_USP7_MATH_1 | 128 | 132 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.572 |
DOC_USP7_UBL2_3 | 310 | 314 | PF12436 | 0.598 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.774 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.721 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.774 |
LIG_14-3-3_CanoR_1 | 129 | 133 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 232 | 238 | PF00244 | 0.593 |
LIG_14-3-3_CanoR_1 | 249 | 259 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 321 | 329 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 331 | 338 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 86 | 95 | PF00244 | 0.344 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.505 |
LIG_BRCT_BRCA1_1 | 185 | 189 | PF00533 | 0.383 |
LIG_deltaCOP1_diTrp_1 | 164 | 169 | PF00928 | 0.519 |
LIG_deltaCOP1_diTrp_1 | 182 | 189 | PF00928 | 0.372 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.423 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.469 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.643 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.580 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.531 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.535 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.483 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.342 |
LIG_LIR_Apic_2 | 291 | 297 | PF02991 | 0.649 |
LIG_LIR_Gen_1 | 156 | 166 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 156 | 162 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 31 | 35 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 97 | 102 | PF02991 | 0.479 |
LIG_SH2_NCK_1 | 294 | 298 | PF00017 | 0.638 |
LIG_SH2_STAT3 | 302 | 305 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.648 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.675 |
LIG_SH3_3 | 260 | 266 | PF00018 | 0.619 |
LIG_SH3_3 | 276 | 282 | PF00018 | 0.592 |
LIG_SUMO_SIM_anti_2 | 209 | 217 | PF11976 | 0.583 |
LIG_SUMO_SIM_anti_2 | 6 | 14 | PF11976 | 0.359 |
LIG_SUMO_SIM_par_1 | 265 | 270 | PF11976 | 0.645 |
LIG_SxIP_EBH_1 | 319 | 333 | PF03271 | 0.538 |
LIG_TRFH_1 | 189 | 193 | PF08558 | 0.444 |
LIG_UBA3_1 | 11 | 16 | PF00899 | 0.354 |
MOD_CDK_SPxK_1 | 189 | 195 | PF00069 | 0.578 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.654 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.574 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.610 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.670 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.338 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.673 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.463 |
MOD_CK2_1 | 255 | 261 | PF00069 | 0.659 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.349 |
MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.581 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.692 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.571 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.563 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.531 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.724 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.537 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.455 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.526 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.627 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.626 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.695 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.688 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.601 |
MOD_LATS_1 | 199 | 205 | PF00433 | 0.510 |
MOD_LATS_1 | 284 | 290 | PF00433 | 0.661 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.664 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.545 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.463 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.418 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.672 |
MOD_PIKK_1 | 131 | 137 | PF00454 | 0.654 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.556 |
MOD_PIKK_1 | 214 | 220 | PF00454 | 0.508 |
MOD_PIKK_1 | 296 | 302 | PF00454 | 0.621 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.671 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.681 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.582 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.594 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.533 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.517 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.620 |
MOD_Plk_1 | 79 | 85 | PF00069 | 0.376 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.620 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.497 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.578 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.774 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.609 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.725 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.775 |
MOD_SUMO_rev_2 | 109 | 114 | PF00179 | 0.569 |
TRG_DiLeu_BaEn_1 | 7 | 12 | PF01217 | 0.354 |
TRG_DiLeu_BaLyEn_6 | 263 | 268 | PF01217 | 0.637 |
TRG_PTS1 | 335 | 338 | PF00515 | 0.676 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H5B7 | Leishmania donovani | 82% | 100% |
A4H441 | Leishmania braziliensis | 55% | 100% |
A4HS58 | Leishmania infantum | 81% | 100% |
E9ACP8 | Leishmania major | 79% | 100% |