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: E9AP53
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 170 | 174 | PF00656 | 0.522 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.432 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 66 | 68 | PF00082 | 0.553 |
CLV_PCSK_PC1ET2_1 | 27 | 29 | PF00082 | 0.654 |
CLV_PCSK_PC7_1 | 135 | 141 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.722 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.563 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.611 |
DEG_SPOP_SBC_1 | 151 | 155 | PF00917 | 0.614 |
DOC_CKS1_1 | 54 | 59 | PF01111 | 0.545 |
DOC_CKS1_1 | 82 | 87 | PF01111 | 0.620 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.702 |
DOC_USP7_UBL2_3 | 59 | 63 | PF12436 | 0.619 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.700 |
LIG_14-3-3_CanoR_1 | 121 | 127 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 149 | 157 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 28 | 36 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 41 | 50 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 51 | 57 | PF00244 | 0.682 |
LIG_APCC_ABBA_1 | 230 | 235 | PF00400 | 0.546 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.653 |
LIG_EVH1_1 | 81 | 85 | PF00568 | 0.621 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.689 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.549 |
LIG_LIR_Gen_1 | 159 | 167 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 125 | 129 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 130 | 134 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 154 | 160 | PF02991 | 0.650 |
LIG_LIR_Nem_3 | 64 | 68 | PF02991 | 0.572 |
LIG_PTB_Apo_2 | 125 | 132 | PF02174 | 0.523 |
LIG_SH2_CRK | 201 | 205 | PF00017 | 0.469 |
LIG_SH2_GRB2like | 160 | 163 | PF00017 | 0.622 |
LIG_SH2_NCK_1 | 160 | 164 | PF00017 | 0.619 |
LIG_SH2_NCK_1 | 69 | 73 | PF00017 | 0.655 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.584 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.681 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.537 |
LIG_SH3_3 | 51 | 57 | PF00018 | 0.631 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.615 |
LIG_SUMO_SIM_anti_2 | 3 | 8 | PF11976 | 0.594 |
LIG_TYR_ITIM | 124 | 129 | PF00017 | 0.599 |
MOD_CDK_SPxK_1 | 53 | 59 | PF00069 | 0.633 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.755 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.705 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.620 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.480 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.619 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.591 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.572 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.628 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.704 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.528 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.360 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.625 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.661 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.650 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.562 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.588 |
MOD_N-GLC_1 | 218 | 223 | PF02516 | 0.507 |
MOD_N-GLC_1 | 29 | 34 | PF02516 | 0.686 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.645 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.778 |
MOD_OFUCOSY | 103 | 109 | PF10250 | 0.606 |
MOD_PKA_1 | 135 | 141 | PF00069 | 0.688 |
MOD_PKA_1 | 149 | 155 | PF00069 | 0.557 |
MOD_PKB_1 | 39 | 47 | PF00069 | 0.504 |
MOD_PKB_1 | 74 | 82 | PF00069 | 0.650 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.576 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.781 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.725 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.558 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.695 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.563 |
TRG_ENDOCYTIC_2 | 160 | 163 | PF00928 | 0.635 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.706 |
TRG_ER_diArg_1 | 65 | 67 | PF00400 | 0.431 |
TRG_Pf-PMV_PEXEL_1 | 93 | 98 | PF00026 | 0.580 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ69 | Leptomonas seymouri | 60% | 100% |
A0A3Q8I9J1 | Leishmania donovani | 92% | 100% |
A4H726 | Leishmania braziliensis | 76% | 100% |
A4HVF5 | Leishmania infantum | 91% | 100% |
Q4QGD5 | Leishmania major | 90% | 100% |