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: A4I808
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 122 | 126 | PF00656 | 0.614 |
CLV_C14_Caspase3-7 | 181 | 185 | PF00656 | 0.626 |
CLV_C14_Caspase3-7 | 264 | 268 | PF00656 | 0.471 |
CLV_C14_Caspase3-7 | 57 | 61 | PF00656 | 0.459 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.624 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.750 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.729 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.563 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 75 | 77 | PF00082 | 0.748 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.613 |
DEG_APCC_DBOX_1 | 136 | 144 | PF00400 | 0.526 |
DEG_APCC_DBOX_1 | 20 | 28 | PF00400 | 0.519 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.609 |
DOC_CKS1_1 | 236 | 241 | PF01111 | 0.503 |
DOC_CKS1_1 | 322 | 327 | PF01111 | 0.447 |
DOC_CYCLIN_RxL_1 | 48 | 57 | PF00134 | 0.483 |
DOC_CYCLIN_yCln2_LP_2 | 164 | 170 | PF00134 | 0.551 |
DOC_MAPK_gen_1 | 146 | 154 | PF00069 | 0.538 |
DOC_MAPK_gen_1 | 230 | 236 | PF00069 | 0.552 |
DOC_MAPK_gen_1 | 286 | 295 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 88 | 97 | PF00069 | 0.565 |
DOC_PP1_RVXF_1 | 255 | 262 | PF00149 | 0.540 |
DOC_PP2B_LxvP_1 | 164 | 167 | PF13499 | 0.612 |
DOC_PP4_FxxP_1 | 322 | 325 | PF00568 | 0.440 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.800 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.659 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.650 |
LIG_14-3-3_CanoR_1 | 127 | 131 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 352 | 357 | PF00244 | 0.460 |
LIG_Actin_WH2_2 | 5 | 23 | PF00022 | 0.595 |
LIG_APCC_ABBA_1 | 130 | 135 | PF00400 | 0.536 |
LIG_BRCT_BRCA1_1 | 116 | 120 | PF00533 | 0.558 |
LIG_BRCT_BRCA1_1 | 267 | 271 | PF00533 | 0.436 |
LIG_BRCT_BRCA1_1 | 318 | 322 | PF00533 | 0.474 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.608 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.629 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.498 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.471 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.446 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.622 |
LIG_FHA_2 | 117 | 123 | PF00498 | 0.650 |
LIG_HCF-1_HBM_1 | 339 | 342 | PF13415 | 0.395 |
LIG_LIR_Apic_2 | 319 | 325 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 244 | 253 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 270 | 279 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 339 | 350 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 339 | 345 | PF02991 | 0.424 |
LIG_NRBOX | 359 | 365 | PF00104 | 0.434 |
LIG_RPA_C_Fungi | 240 | 252 | PF08784 | 0.471 |
LIG_SH2_STAT3 | 351 | 354 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 323 | 326 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.236 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.440 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.607 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.583 |
LIG_SH3_3 | 149 | 155 | PF00018 | 0.647 |
LIG_SH3_3 | 164 | 170 | PF00018 | 0.547 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.531 |
LIG_SUMO_SIM_par_1 | 206 | 213 | PF11976 | 0.595 |
LIG_SUMO_SIM_par_1 | 51 | 57 | PF11976 | 0.482 |
LIG_TRFH_1 | 130 | 134 | PF08558 | 0.489 |
LIG_TRFH_1 | 342 | 346 | PF08558 | 0.421 |
LIG_UBA3_1 | 139 | 146 | PF00899 | 0.523 |
LIG_ULM_U2AF65_1 | 257 | 262 | PF00076 | 0.545 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.623 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.563 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.427 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.582 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.407 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.613 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.656 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.610 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.563 |
MOD_CK2_1 | 206 | 212 | PF00069 | 0.570 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.590 |
MOD_GlcNHglycan | 115 | 119 | PF01048 | 0.591 |
MOD_GlcNHglycan | 2 | 6 | PF01048 | 0.630 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.575 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.538 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.559 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.712 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.514 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.644 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.594 |
MOD_N-GLC_1 | 156 | 161 | PF02516 | 0.553 |
MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.633 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.636 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.615 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.540 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.480 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.673 |
MOD_PK_1 | 352 | 358 | PF00069 | 0.429 |
MOD_PKA_1 | 352 | 358 | PF00069 | 0.464 |
MOD_PKA_1 | 75 | 81 | PF00069 | 0.639 |
MOD_PKA_2 | 126 | 132 | PF00069 | 0.647 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.547 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.655 |
MOD_PKB_1 | 148 | 156 | PF00069 | 0.550 |
MOD_PKB_1 | 258 | 266 | PF00069 | 0.554 |
MOD_PKB_1 | 286 | 294 | PF00069 | 0.479 |
MOD_Plk_1 | 150 | 156 | PF00069 | 0.551 |
MOD_Plk_1 | 182 | 188 | PF00069 | 0.612 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.538 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.711 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.643 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.630 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.628 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.446 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.600 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.651 |
TRG_DiLeu_BaEn_1 | 339 | 344 | PF01217 | 0.425 |
TRG_DiLeu_BaEn_4 | 40 | 46 | PF01217 | 0.562 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 342 | 345 | PF00928 | 0.413 |
TRG_ER_diArg_1 | 148 | 150 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 229 | 231 | PF00400 | 0.608 |
TRG_ER_diArg_1 | 257 | 260 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 295 | 298 | PF00400 | 0.476 |
TRG_ER_diArg_1 | 49 | 52 | PF00400 | 0.523 |
TRG_Pf-PMV_PEXEL_1 | 215 | 220 | PF00026 | 0.600 |
TRG_Pf-PMV_PEXEL_1 | 331 | 335 | PF00026 | 0.439 |
TRG_Pf-PMV_PEXEL_1 | 43 | 48 | PF00026 | 0.622 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X5J3 | Leishmania donovani | 99% | 100% |
A4HKD7 | Leishmania braziliensis | 61% | 100% |
E9B2S5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4Q5D2 | Leishmania major | 84% | 100% |