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: 2 |
NetGPI | no | yes: 0, no: 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: E9APE9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.838 |
CLV_PCSK_FUR_1 | 134 | 138 | PF00082 | 0.766 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.839 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.744 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.657 |
CLV_PCSK_PC1ET2_1 | 105 | 107 | PF00082 | 0.839 |
CLV_PCSK_PC1ET2_1 | 136 | 138 | PF00082 | 0.756 |
CLV_PCSK_PC1ET2_1 | 175 | 177 | PF00082 | 0.604 |
CLV_PCSK_PC1ET2_1 | 256 | 258 | PF00082 | 0.657 |
CLV_PCSK_PC7_1 | 171 | 177 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.798 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.613 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.538 |
DEG_SCF_FBW7_1 | 36 | 43 | PF00400 | 0.515 |
DOC_CKS1_1 | 118 | 123 | PF01111 | 0.587 |
DOC_CKS1_1 | 170 | 175 | PF01111 | 0.775 |
DOC_CKS1_1 | 37 | 42 | PF01111 | 0.514 |
DOC_CKS1_1 | 49 | 54 | PF01111 | 0.551 |
DOC_CYCLIN_RxL_1 | 171 | 180 | PF00134 | 0.797 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.637 |
DOC_USP7_UBL2_3 | 175 | 179 | PF12436 | 0.730 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.765 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.750 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 36 | 41 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.600 |
LIG_14-3-3_CanoR_1 | 197 | 202 | PF00244 | 0.708 |
LIG_14-3-3_CanoR_1 | 55 | 59 | PF00244 | 0.558 |
LIG_BRCT_BRCA1_1 | 190 | 194 | PF00533 | 0.826 |
LIG_Clathr_ClatBox_1 | 147 | 151 | PF01394 | 0.549 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.576 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.517 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.549 |
LIG_LIR_Apic_2 | 43 | 49 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 26 | 36 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 17 | 21 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 26 | 31 | PF02991 | 0.517 |
LIG_SH2_NCK_1 | 212 | 216 | PF00017 | 0.754 |
LIG_SH2_STAP1 | 190 | 194 | PF00017 | 0.826 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.441 |
LIG_SH3_1 | 46 | 52 | PF00018 | 0.550 |
LIG_SH3_3 | 119 | 125 | PF00018 | 0.473 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.692 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.633 |
LIG_SUMO_SIM_par_1 | 146 | 151 | PF11976 | 0.549 |
LIG_TYR_ITIM | 163 | 168 | PF00017 | 0.433 |
MOD_CDK_SPK_2 | 50 | 55 | PF00069 | 0.697 |
MOD_CDK_SPxK_1 | 169 | 175 | PF00069 | 0.720 |
MOD_CDK_SPxK_1 | 82 | 88 | PF00069 | 0.723 |
MOD_CDK_SPxxK_3 | 169 | 176 | PF00069 | 0.726 |
MOD_CDK_SPxxK_3 | 48 | 55 | PF00069 | 0.694 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.662 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.789 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.490 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.506 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.481 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.814 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.554 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.680 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.786 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.656 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.668 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.831 |
MOD_Cter_Amidation | 103 | 106 | PF01082 | 0.822 |
MOD_Cter_Amidation | 173 | 176 | PF01082 | 0.748 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.651 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.502 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.671 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.659 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.748 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.645 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.698 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.714 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.719 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.640 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.589 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.732 |
MOD_LATS_1 | 248 | 254 | PF00433 | 0.719 |
MOD_N-GLC_1 | 222 | 227 | PF02516 | 0.698 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.811 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.666 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.717 |
MOD_NEK2_2 | 54 | 59 | PF00069 | 0.697 |
MOD_PK_1 | 197 | 203 | PF00069 | 0.691 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.668 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.599 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.696 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.671 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.617 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.746 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.611 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.720 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.691 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.606 |
MOD_ProDKin_1 | 36 | 42 | PF00069 | 0.574 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.797 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.765 |
MOD_SUMO_rev_2 | 110 | 117 | PF00179 | 0.774 |
TRG_DiLeu_BaLyEn_6 | 173 | 178 | PF01217 | 0.757 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.549 |
TRG_NLS_MonoExtN_4 | 102 | 109 | PF00514 | 0.703 |
TRG_Pf-PMV_PEXEL_1 | 176 | 180 | PF00026 | 0.773 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
Q4QG29 | Leishmania major | 79% | 100% |