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: E9B1B5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.375 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.351 |
CLV_PCSK_PC7_1 | 189 | 195 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.405 |
CLV_Separin_Metazoa | 56 | 60 | PF03568 | 0.383 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.384 |
DEG_SPOP_SBC_1 | 230 | 234 | PF00917 | 0.427 |
DOC_CKS1_1 | 88 | 93 | PF01111 | 0.445 |
DOC_CYCLIN_RxL_1 | 105 | 114 | PF00134 | 0.373 |
DOC_CYCLIN_yCln2_LP_2 | 62 | 68 | PF00134 | 0.445 |
DOC_MAPK_gen_1 | 105 | 113 | PF00069 | 0.373 |
DOC_MAPK_gen_1 | 59 | 68 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 105 | 113 | PF00069 | 0.377 |
DOC_PP1_RVXF_1 | 158 | 164 | PF00149 | 0.415 |
DOC_PP4_FxxP_1 | 68 | 71 | PF00568 | 0.410 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.295 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.335 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.273 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.410 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.332 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.449 |
LIG_14-3-3_CanoR_1 | 25 | 29 | PF00244 | 0.452 |
LIG_Actin_WH2_2 | 175 | 191 | PF00022 | 0.389 |
LIG_APCC_ABBA_1 | 1 | 6 | PF00400 | 0.432 |
LIG_APCC_ABBA_1 | 51 | 56 | PF00400 | 0.328 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.583 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.457 |
LIG_LIR_Apic_2 | 31 | 35 | PF02991 | 0.406 |
LIG_LIR_Gen_1 | 49 | 58 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 6 | 16 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 225 | 230 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 49 | 54 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 6 | 12 | PF02991 | 0.364 |
LIG_MAD2 | 133 | 141 | PF02301 | 0.475 |
LIG_NRBOX | 57 | 63 | PF00104 | 0.345 |
LIG_PTB_Apo_2 | 173 | 180 | PF02174 | 0.408 |
LIG_SH2_CRK | 100 | 104 | PF00017 | 0.451 |
LIG_SH2_NCK_1 | 100 | 104 | PF00017 | 0.451 |
LIG_SH2_NCK_1 | 32 | 36 | PF00017 | 0.398 |
LIG_SH2_SRC | 45 | 48 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.584 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.459 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.480 |
LIG_TRAF2_1 | 8 | 11 | PF00917 | 0.387 |
LIG_UBA3_1 | 106 | 110 | PF00899 | 0.344 |
LIG_WRC_WIRS_1 | 21 | 26 | PF05994 | 0.412 |
LIG_WW_3 | 102 | 106 | PF00397 | 0.425 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.716 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.343 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.486 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.287 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.365 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.574 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.559 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.455 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.397 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.515 |
MOD_N-GLC_1 | 145 | 150 | PF02516 | 0.594 |
MOD_N-GLC_1 | 16 | 21 | PF02516 | 0.410 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.409 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.561 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.405 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.344 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.738 |
MOD_NEK2_2 | 20 | 25 | PF00069 | 0.405 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.489 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.499 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.450 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.401 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.625 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.413 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.330 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.447 |
TRG_DiLeu_BaEn_1 | 225 | 230 | PF01217 | 0.457 |
TRG_DiLeu_BaLyEn_6 | 102 | 107 | PF01217 | 0.409 |
TRG_DiLeu_BaLyEn_6 | 124 | 129 | PF01217 | 0.544 |
TRG_DiLeu_BaLyEn_6 | 57 | 62 | PF01217 | 0.342 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.550 |
TRG_ER_diArg_1 | 58 | 60 | PF00400 | 0.359 |
TRG_Pf-PMV_PEXEL_1 | 59 | 64 | PF00026 | 0.314 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2I1 | Leptomonas seymouri | 57% | 100% |
A0A3Q8IJQ2 | Leishmania donovani | 90% | 100% |
A4HIS8 | Leishmania braziliensis | 73% | 100% |
A4I630 | Leishmania infantum | 91% | 100% |
Q4Q6U9 | Leishmania major | 89% | 100% |