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: A0A3S7X2B4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 14 | 18 | PF00656 | 0.677 |
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.397 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.406 |
CLV_PCSK_FUR_1 | 141 | 145 | PF00082 | 0.604 |
CLV_PCSK_FUR_1 | 94 | 98 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 143 | 145 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 53 | 55 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.484 |
CLV_PCSK_PC1ET2_1 | 187 | 189 | PF00082 | 0.660 |
CLV_PCSK_PC1ET2_1 | 96 | 98 | PF00082 | 0.484 |
DEG_APCC_DBOX_1 | 101 | 109 | PF00400 | 0.695 |
DOC_MAPK_gen_1 | 109 | 117 | PF00069 | 0.459 |
DOC_MAPK_MEF2A_6 | 109 | 117 | PF00069 | 0.459 |
DOC_PP2B_LxvP_1 | 44 | 47 | PF13499 | 0.696 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.639 |
DOC_USP7_UBL2_3 | 72 | 76 | PF12436 | 0.680 |
LIG_14-3-3_CanoR_1 | 102 | 108 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 151 | 157 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 23 | 32 | PF00244 | 0.597 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.648 |
LIG_BRCT_BRCA1_1 | 69 | 73 | PF00533 | 0.694 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.401 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.630 |
LIG_LIR_Apic_2 | 129 | 133 | PF02991 | 0.245 |
LIG_SH2_NCK_1 | 149 | 153 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.459 |
LIG_SH3_3 | 165 | 171 | PF00018 | 0.388 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.694 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.715 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.508 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.500 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.437 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.608 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.443 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.698 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.696 |
MOD_N-GLC_1 | 103 | 108 | PF02516 | 0.471 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.728 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.446 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.422 |
MOD_NEK2_2 | 182 | 187 | PF00069 | 0.367 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.677 |
MOD_Plk_1 | 103 | 109 | PF00069 | 0.669 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.671 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.401 |
MOD_SUMO_rev_2 | 68 | 78 | PF00179 | 0.628 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.383 |
TRG_ER_diArg_1 | 141 | 144 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 53 | 56 | PF00400 | 0.607 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8C6 | Leptomonas seymouri | 63% | 98% |
A0A0S4ISL6 | Bodo saltans | 41% | 100% |
A0A1X0NZL1 | Trypanosomatidae | 47% | 100% |
A4HH84 | Leishmania braziliensis | 71% | 100% |
A4I4D0 | Leishmania infantum | 99% | 100% |
C9ZL34 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9ADS9 | Leishmania major | 88% | 100% |
E9AM01 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |