Seems to form a single continuous helix according to predictions. Kinetoplastid-only protein.
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: 5 |
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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: E9AM01
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 14 | 18 | PF00656 | 0.669 |
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.335 |
CLV_PCSK_FUR_1 | 141 | 145 | PF00082 | 0.542 |
CLV_PCSK_FUR_1 | 94 | 98 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.416 |
CLV_PCSK_PC1ET2_1 | 191 | 193 | PF00082 | 0.683 |
CLV_PCSK_PC1ET2_1 | 96 | 98 | PF00082 | 0.416 |
DEG_APCC_DBOX_1 | 101 | 109 | PF00400 | 0.635 |
DOC_MAPK_gen_1 | 109 | 117 | PF00069 | 0.461 |
DOC_MAPK_MEF2A_6 | 109 | 117 | PF00069 | 0.461 |
DOC_PP2B_LxvP_1 | 44 | 47 | PF13499 | 0.682 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.429 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.632 |
DOC_USP7_UBL2_3 | 72 | 76 | PF12436 | 0.690 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.327 |
LIG_14-3-3_CanoR_1 | 102 | 108 | PF00244 | 0.631 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.660 |
LIG_BRCT_BRCA1_1 | 6 | 10 | PF00533 | 0.678 |
LIG_BRCT_BRCA1_1 | 69 | 73 | PF00533 | 0.723 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.348 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.602 |
LIG_LIR_Apic_2 | 127 | 133 | PF02991 | 0.281 |
LIG_SH2_NCK_1 | 149 | 153 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.387 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.426 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.724 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.747 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.697 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.501 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.475 |
MOD_GlcNHglycan | 5 | 9 | PF01048 | 0.498 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.400 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.727 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.696 |
MOD_N-GLC_1 | 103 | 108 | PF02516 | 0.420 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.726 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.419 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.444 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.618 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.618 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.412 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.324 |
MOD_SUMO_rev_2 | 68 | 78 | PF00179 | 0.628 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.351 |
TRG_ER_diArg_1 | 141 | 144 | PF00400 | 0.357 |
TRG_ER_diArg_1 | 53 | 56 | PF00400 | 0.644 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8C6 | Leptomonas seymouri | 63% | 100% |
A0A0S4ISL6 | Bodo saltans | 39% | 100% |
A0A1X0NZL1 | Trypanosomatidae | 48% | 100% |
A0A3S7X2B4 | Leishmania donovani | 87% | 100% |
A4HH84 | Leishmania braziliensis | 76% | 100% |
A4I4D0 | Leishmania infantum | 87% | 100% |
C9ZL34 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9ADS9 | Leishmania major | 89% | 100% |