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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9AKS7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 300 | 304 | PF00656 | 0.668 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.398 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.284 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 95 | 97 | PF00082 | 0.402 |
CLV_PCSK_PC1ET2_1 | 115 | 117 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.463 |
CLV_Separin_Metazoa | 51 | 55 | PF03568 | 0.418 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.374 |
DOC_CYCLIN_RxL_1 | 13 | 23 | PF00134 | 0.460 |
DOC_MAPK_gen_1 | 102 | 111 | PF00069 | 0.406 |
DOC_MAPK_gen_1 | 135 | 144 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 79 | 87 | PF00069 | 0.546 |
DOC_MAPK_gen_1 | 95 | 101 | PF00069 | 0.385 |
DOC_MAPK_HePTP_8 | 99 | 111 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 102 | 111 | PF00069 | 0.420 |
DOC_MAPK_NFAT4_5 | 104 | 112 | PF00069 | 0.410 |
DOC_SPAK_OSR1_1 | 139 | 143 | PF12202 | 0.259 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.618 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.655 |
LIG_14-3-3_CanoR_1 | 139 | 145 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 175 | 180 | PF00244 | 0.299 |
LIG_CtBP_PxDLS_1 | 49 | 53 | PF00389 | 0.389 |
LIG_deltaCOP1_diTrp_1 | 131 | 140 | PF00928 | 0.312 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.529 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.495 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.651 |
LIG_FHA_2 | 180 | 186 | PF00498 | 0.379 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.472 |
LIG_FHA_2 | 282 | 288 | PF00498 | 0.655 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.411 |
LIG_IBAR_NPY_1 | 245 | 247 | PF08397 | 0.584 |
LIG_LIR_Gen_1 | 173 | 184 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 287 | 296 | PF02991 | 0.648 |
LIG_LIR_Nem_3 | 173 | 179 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 287 | 291 | PF02991 | 0.642 |
LIG_NRBOX | 80 | 86 | PF00104 | 0.257 |
LIG_PCNA_yPIPBox_3 | 183 | 196 | PF02747 | 0.511 |
LIG_SH2_CRK | 176 | 180 | PF00017 | 0.511 |
LIG_SH2_CRK | 223 | 227 | PF00017 | 0.562 |
LIG_SH2_STAP1 | 146 | 150 | PF00017 | 0.483 |
LIG_SH2_STAP1 | 176 | 180 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.393 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.530 |
LIG_TYR_ITIM | 174 | 179 | PF00017 | 0.295 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.681 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.696 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.379 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.458 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.709 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.444 |
MOD_GlcNHglycan | 191 | 195 | PF01048 | 0.561 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.701 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.579 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.549 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.675 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.409 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.553 |
MOD_NEK2_2 | 170 | 175 | PF00069 | 0.347 |
MOD_PIKK_1 | 270 | 276 | PF00454 | 0.655 |
MOD_PK_1 | 102 | 108 | PF00069 | 0.260 |
MOD_PKA_2 | 140 | 146 | PF00069 | 0.408 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.505 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.640 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.517 |
MOD_Plk_2-3 | 44 | 50 | PF00069 | 0.489 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.456 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.446 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.453 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.655 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.564 |
TRG_ENDOCYTIC_2 | 212 | 215 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 223 | 226 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 238 | 241 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.398 |
TRG_ER_diArg_1 | 134 | 137 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.542 |
TRG_ER_diArg_1 | 95 | 97 | PF00400 | 0.406 |
TRG_Pf-PMV_PEXEL_1 | 260 | 264 | PF00026 | 0.568 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HVD6 | Leptomonas seymouri | 56% | 96% |
A0A0S4KF96 | Bodo saltans | 32% | 100% |
A0A1X0NKJ3 | Trypanosomatidae | 44% | 100% |
A0A3S5H5Q7 | Leishmania donovani | 91% | 97% |
A4H4L4 | Leishmania braziliensis | 80% | 100% |
A4HSU0 | Leishmania infantum | 91% | 97% |
C9ZTF2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
Q4QJ30 | Leishmania major | 90% | 100% |
V5B7V1 | Trypanosoma cruzi | 49% | 100% |