Although obviously looks like a transporter, only very weak homologies exist outside KInetoplastids
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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: A0A3S5H5N8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 93 | 97 | PF00656 | 0.557 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.388 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.304 |
DOC_ANK_TNKS_1 | 201 | 208 | PF00023 | 0.486 |
DOC_MAPK_gen_1 | 29 | 36 | PF00069 | 0.519 |
DOC_MAPK_HePTP_8 | 26 | 38 | PF00069 | 0.477 |
DOC_MAPK_MEF2A_6 | 29 | 38 | PF00069 | 0.516 |
DOC_MAPK_RevD_3 | 15 | 30 | PF00069 | 0.454 |
DOC_PP4_FxxP_1 | 201 | 204 | PF00568 | 0.493 |
LIG_14-3-3_CanoR_1 | 152 | 160 | PF00244 | 0.531 |
LIG_BRCT_BRCA1_1 | 125 | 129 | PF00533 | 0.373 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.489 |
LIG_LIR_Apic_2 | 199 | 204 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 139 | 149 | PF02991 | 0.324 |
LIG_LIR_Gen_1 | 72 | 83 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 112 | 118 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 139 | 144 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 72 | 78 | PF02991 | 0.378 |
LIG_Pex14_1 | 107 | 111 | PF04695 | 0.331 |
LIG_Pex14_1 | 117 | 121 | PF04695 | 0.402 |
LIG_SH2_CRK | 111 | 115 | PF00017 | 0.331 |
LIG_SH2_STAP1 | 111 | 115 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.331 |
LIG_TYR_ITIM | 109 | 114 | PF00017 | 0.331 |
LIG_UBA3_1 | 13 | 22 | PF00899 | 0.333 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.366 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.544 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.469 |
MOD_CMANNOS | 117 | 120 | PF00535 | 0.398 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.343 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.403 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.578 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.342 |
MOD_N-GLC_1 | 24 | 29 | PF02516 | 0.411 |
MOD_N-GLC_1 | 5 | 10 | PF02516 | 0.310 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.417 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.558 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.261 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.350 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.294 |
MOD_NEK2_2 | 196 | 201 | PF00069 | 0.223 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.272 |
MOD_Plk_1 | 24 | 30 | PF00069 | 0.613 |
MOD_Plk_1 | 5 | 11 | PF00069 | 0.310 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.324 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.324 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.307 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.325 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.360 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.318 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.322 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.331 |
TRG_ER_diArg_1 | 28 | 30 | PF00400 | 0.595 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZR4 | Leptomonas seymouri | 62% | 100% |
A0A1X0NL26 | Trypanosomatidae | 35% | 85% |
A0A3R7N0V5 | Trypanosoma rangeli | 32% | 97% |
A4H4I9 | Leishmania braziliensis | 78% | 100% |
A4HSR4 | Leishmania infantum | 100% | 100% |
C9ZTB3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 94% |