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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4Q8E3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 177 | 181 | PF00656 | 0.496 |
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.261 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.204 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.231 |
CLV_PCSK_SKI1_1 | 289 | 293 | PF00082 | 0.246 |
CLV_Separin_Metazoa | 313 | 317 | PF03568 | 0.446 |
DOC_CKS1_1 | 241 | 246 | PF01111 | 0.476 |
DOC_MAPK_RevD_3 | 306 | 321 | PF00069 | 0.404 |
DOC_PP2B_LxvP_1 | 398 | 401 | PF13499 | 0.401 |
DOC_PP2B_LxvP_1 | 65 | 68 | PF13499 | 0.492 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.397 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.452 |
DOC_USP7_UBL2_3 | 387 | 391 | PF12436 | 0.380 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.446 |
LIG_14-3-3_CanoR_1 | 119 | 127 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 143 | 149 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 289 | 294 | PF00244 | 0.446 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.445 |
LIG_BIR_III_4 | 299 | 303 | PF00653 | 0.484 |
LIG_BRCT_BRCA1_1 | 212 | 216 | PF00533 | 0.476 |
LIG_BRCT_BRCA1_1 | 345 | 349 | PF00533 | 0.446 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.454 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.470 |
LIG_FHA_2 | 26 | 32 | PF00498 | 0.492 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.492 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.400 |
LIG_LIR_Gen_1 | 58 | 67 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 58 | 62 | PF02991 | 0.481 |
LIG_RPA_C_Fungi | 358 | 370 | PF08784 | 0.416 |
LIG_SH2_CRK | 253 | 257 | PF00017 | 0.323 |
LIG_SH2_SRC | 139 | 142 | PF00017 | 0.302 |
LIG_SH2_STAP1 | 112 | 116 | PF00017 | 0.345 |
LIG_SH2_STAP1 | 382 | 386 | PF00017 | 0.322 |
LIG_SH2_STAT3 | 251 | 254 | PF00017 | 0.280 |
LIG_SH2_STAT3 | 47 | 50 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 109 | 112 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 277 | 280 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.281 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.351 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.311 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.281 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.345 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.339 |
LIG_SUMO_SIM_anti_2 | 60 | 66 | PF11976 | 0.309 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.345 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.339 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.512 |
MOD_CK2_1 | 25 | 31 | PF00069 | 0.345 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.274 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.359 |
MOD_CK2_1 | 362 | 368 | PF00069 | 0.390 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.236 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.171 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.217 |
MOD_GlcNHglycan | 299 | 303 | PF01048 | 0.281 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.470 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.294 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.304 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.341 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.383 |
MOD_N-GLC_1 | 221 | 226 | PF02516 | 0.294 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.281 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.281 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.281 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.364 |
MOD_NEK2_2 | 369 | 374 | PF00069 | 0.543 |
MOD_PIKK_1 | 100 | 106 | PF00454 | 0.281 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.345 |
MOD_PKA_2 | 362 | 368 | PF00069 | 0.369 |
MOD_PKB_1 | 287 | 295 | PF00069 | 0.345 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.367 |
MOD_Plk_1 | 221 | 227 | PF00069 | 0.354 |
MOD_Plk_1 | 352 | 358 | PF00069 | 0.345 |
MOD_Plk_1 | 401 | 407 | PF00069 | 0.463 |
MOD_Plk_2-3 | 25 | 31 | PF00069 | 0.281 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.345 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.271 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.359 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.281 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.372 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.315 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.281 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.331 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.281 |
MOD_SUMO_rev_2 | 313 | 322 | PF00179 | 0.347 |
TRG_DiLeu_BaEn_4 | 31 | 37 | PF01217 | 0.280 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 279 | 282 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 97 | 100 | PF00928 | 0.359 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.347 |
TRG_ER_diArg_1 | 183 | 185 | PF00400 | 0.302 |
TRG_ER_diArg_1 | 397 | 400 | PF00400 | 0.450 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I9S4 | Leptomonas seymouri | 57% | 100% |
A0A3Q8IAY9 | Leishmania donovani | 92% | 100% |
A4HGH0 | Leishmania braziliensis | 77% | 100% |
A4I3K2 | Leishmania infantum | 92% | 100% |
E9AZU2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
O34940 | Bacillus subtilis (strain 168) | 24% | 100% |
P0DOV6 | Pseudomonas putida | 26% | 100% |
Q9I922 | Xenopus laevis | 23% | 100% |