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: E9AZP0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 147 | 153 | PF00089 | 0.447 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.553 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.534 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.696 |
CLV_PCSK_PC1ET2_1 | 176 | 178 | PF00082 | 0.467 |
CLV_PCSK_PC1ET2_1 | 88 | 90 | PF00082 | 0.696 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.434 |
DEG_APCC_DBOX_1 | 174 | 182 | PF00400 | 0.534 |
DEG_APCC_KENBOX_2 | 106 | 110 | PF00400 | 0.535 |
DOC_CKS1_1 | 90 | 95 | PF01111 | 0.432 |
DOC_MAPK_gen_1 | 128 | 136 | PF00069 | 0.328 |
DOC_MAPK_MEF2A_6 | 56 | 63 | PF00069 | 0.602 |
DOC_PP1_RVXF_1 | 120 | 127 | PF00149 | 0.536 |
DOC_PP4_FxxP_1 | 90 | 93 | PF00568 | 0.464 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.509 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.469 |
LIG_14-3-3_CanoR_1 | 128 | 133 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 150 | 156 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 161 | 168 | PF00244 | 0.520 |
LIG_14-3-3_CanoR_1 | 185 | 189 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 89 | 93 | PF00244 | 0.690 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.638 |
LIG_BRCT_BRCA1_1 | 14 | 18 | PF00533 | 0.484 |
LIG_Clathr_ClatBox_1 | 136 | 140 | PF01394 | 0.489 |
LIG_DLG_GKlike_1 | 128 | 136 | PF00625 | 0.466 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.460 |
LIG_FHA_2 | 136 | 142 | PF00498 | 0.465 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.440 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.551 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.658 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.613 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.635 |
LIG_LIR_Gen_1 | 101 | 110 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 131 | 139 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 101 | 106 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 131 | 136 | PF02991 | 0.584 |
LIG_PDZ_Class_2 | 185 | 190 | PF00595 | 0.447 |
LIG_Pex14_2 | 133 | 137 | PF04695 | 0.466 |
LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.629 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.679 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.582 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.599 |
LIG_TRAF2_1 | 10 | 13 | PF00917 | 0.567 |
LIG_TRAF2_1 | 138 | 141 | PF00917 | 0.512 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.531 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.538 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.585 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.614 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.531 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.584 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.576 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.582 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.602 |
MOD_GlcNHglycan | 80 | 84 | PF01048 | 0.595 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.519 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.640 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.574 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.655 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.432 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.534 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.604 |
MOD_NEK2_2 | 98 | 103 | PF00069 | 0.338 |
MOD_PIKK_1 | 8 | 14 | PF00454 | 0.635 |
MOD_PKA_1 | 128 | 134 | PF00069 | 0.468 |
MOD_PKA_1 | 88 | 94 | PF00069 | 0.637 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.468 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.502 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.437 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.577 |
MOD_Plk_1 | 164 | 170 | PF00069 | 0.605 |
MOD_Plk_1 | 73 | 79 | PF00069 | 0.737 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.472 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.622 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.619 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.459 |
TRG_ER_diArg_1 | 128 | 130 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 174 | 177 | PF00400 | 0.551 |
TRG_NES_CRM1_1 | 104 | 118 | PF08389 | 0.560 |
TRG_NLS_MonoExtN_4 | 173 | 179 | PF00514 | 0.372 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7T0 | Leptomonas seymouri | 45% | 95% |
A0A3S7X1A2 | Leishmania donovani | 84% | 100% |
A4HGB9 | Leishmania braziliensis | 74% | 100% |
E9ADJ8 | Leishmania major | 87% | 100% |
E9AHH7 | Leishmania infantum | 85% | 100% |