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:0005929 | cilium | 4 | 6 |
GO:0042995 | cell projection | 2 | 6 |
GO:0043226 | organelle | 2 | 6 |
GO:0043227 | membrane-bounded organelle | 3 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 6 |
Related structures:
AlphaFold database: E9AU13
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 309 | 313 | PF00656 | 0.484 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.638 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.547 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 261 | 265 | PF00082 | 0.687 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.472 |
DEG_APCC_DBOX_1 | 241 | 249 | PF00400 | 0.419 |
DEG_APCC_DBOX_1 | 90 | 98 | PF00400 | 0.488 |
DEG_SPOP_SBC_1 | 303 | 307 | PF00917 | 0.698 |
DOC_CDC14_PxL_1 | 228 | 236 | PF14671 | 0.599 |
DOC_MAPK_RevD_3 | 227 | 242 | PF00069 | 0.314 |
DOC_PP4_FxxP_1 | 141 | 144 | PF00568 | 0.560 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.587 |
DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.723 |
LIG_14-3-3_CanoR_1 | 122 | 129 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 27 | 31 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 283 | 290 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 298 | 303 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 34 | 41 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 50 | 54 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 74 | 84 | PF00244 | 0.487 |
LIG_BRCT_BRCA1_1 | 67 | 71 | PF00533 | 0.441 |
LIG_Clathr_ClatBox_1 | 262 | 266 | PF01394 | 0.658 |
LIG_DLG_GKlike_1 | 298 | 306 | PF00625 | 0.670 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.587 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.494 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.681 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.507 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.566 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.453 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.620 |
LIG_FHA_2 | 304 | 310 | PF00498 | 0.741 |
LIG_FHA_2 | 336 | 342 | PF00498 | 0.685 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.529 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.497 |
LIG_HP1_1 | 227 | 231 | PF01393 | 0.543 |
LIG_IRF3_LxIS_1 | 164 | 170 | PF10401 | 0.283 |
LIG_IRF3_LxIS_1 | 49 | 56 | PF10401 | 0.447 |
LIG_LIR_Gen_1 | 328 | 336 | PF02991 | 0.679 |
LIG_LIR_Gen_1 | 56 | 66 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 328 | 332 | PF02991 | 0.665 |
LIG_LIR_Nem_3 | 56 | 61 | PF02991 | 0.477 |
LIG_SH2_STAP1 | 58 | 62 | PF00017 | 0.485 |
LIG_SH2_STAT3 | 135 | 138 | PF00017 | 0.583 |
LIG_SH2_STAT3 | 276 | 279 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.648 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.599 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.469 |
LIG_SUMO_SIM_anti_2 | 258 | 266 | PF11976 | 0.645 |
LIG_SUMO_SIM_par_1 | 165 | 170 | PF11976 | 0.570 |
LIG_SUMO_SIM_par_1 | 258 | 266 | PF11976 | 0.682 |
LIG_SUMO_SIM_par_1 | 51 | 56 | PF11976 | 0.498 |
LIG_TRAF2_1 | 339 | 342 | PF00917 | 0.419 |
LIG_TRAF2_1 | 363 | 366 | PF00917 | 0.538 |
LIG_TRAF2_2 | 255 | 260 | PF00917 | 0.716 |
LIG_WRC_WIRS_1 | 326 | 331 | PF05994 | 0.663 |
LIG_WRC_WIRS_1 | 58 | 63 | PF05994 | 0.427 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.371 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.560 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.509 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.602 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.551 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.441 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.458 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.626 |
MOD_CK2_1 | 298 | 304 | PF00069 | 0.704 |
MOD_CK2_1 | 335 | 341 | PF00069 | 0.645 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.488 |
MOD_GlcNHglycan | 168 | 172 | PF01048 | 0.491 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.460 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.407 |
MOD_GlcNHglycan | 199 | 203 | PF01048 | 0.482 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.468 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.545 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.524 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.600 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.469 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.497 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.736 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.547 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.506 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.512 |
MOD_N-GLC_1 | 190 | 195 | PF02516 | 0.293 |
MOD_N-GLC_1 | 21 | 26 | PF02516 | 0.526 |
MOD_N-GLC_1 | 315 | 320 | PF02516 | 0.691 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.625 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.324 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.648 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.438 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.488 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.467 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.572 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.567 |
MOD_PIKK_1 | 129 | 135 | PF00454 | 0.631 |
MOD_PIKK_1 | 21 | 27 | PF00454 | 0.545 |
MOD_PIKK_1 | 315 | 321 | PF00454 | 0.429 |
MOD_PK_1 | 218 | 224 | PF00069 | 0.578 |
MOD_PKA_1 | 34 | 40 | PF00069 | 0.509 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.498 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.512 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.547 |
MOD_PKA_2 | 297 | 303 | PF00069 | 0.532 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.489 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.432 |
MOD_Plk_1 | 193 | 199 | PF00069 | 0.467 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.659 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.479 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.575 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.498 |
MOD_Plk_4 | 57 | 63 | PF00069 | 0.488 |
MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.722 |
TRG_DiLeu_BaEn_4 | 341 | 347 | PF01217 | 0.419 |
TRG_DiLeu_BaLyEn_6 | 258 | 263 | PF01217 | 0.624 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.534 |
TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.478 |
TRG_ER_diArg_1 | 145 | 147 | PF00400 | 0.609 |
TRG_ER_diArg_1 | 241 | 243 | PF00400 | 0.362 |
TRG_ER_diArg_1 | 33 | 35 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 8 | 11 | PF00400 | 0.565 |
TRG_Pf-PMV_PEXEL_1 | 261 | 266 | PF00026 | 0.565 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7XBW4 | Leishmania donovani | 82% | 100% |
A4HQ95 | Leishmania braziliensis | 68% | 100% |
A4IDZ3 | Leishmania infantum | 83% | 100% |
Q4Q0I2 | Leishmania major | 76% | 100% |