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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0020023 | kinetoplast | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: E9B6Y0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 191 | 195 | PF00656 | 0.349 |
CLV_C14_Caspase3-7 | 227 | 231 | PF00656 | 0.482 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.451 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.439 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.396 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.714 |
DEG_SPOP_SBC_1 | 32 | 36 | PF00917 | 0.750 |
DOC_PP4_FxxP_1 | 139 | 142 | PF00568 | 0.390 |
DOC_PP4_FxxP_1 | 56 | 59 | PF00568 | 0.677 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.747 |
DOC_USP7_UBL2_3 | 151 | 155 | PF12436 | 0.437 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.658 |
LIG_14-3-3_CanoR_1 | 187 | 197 | PF00244 | 0.304 |
LIG_14-3-3_CanoR_1 | 66 | 71 | PF00244 | 0.716 |
LIG_Actin_WH2_2 | 171 | 189 | PF00022 | 0.425 |
LIG_APCC_ABBAyCdc20_2 | 167 | 173 | PF00400 | 0.487 |
LIG_eIF4E_1 | 218 | 224 | PF01652 | 0.477 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.376 |
LIG_FHA_2 | 142 | 148 | PF00498 | 0.426 |
LIG_LIR_Apic_2 | 54 | 59 | PF02991 | 0.676 |
LIG_LIR_Apic_2 | 69 | 73 | PF02991 | 0.541 |
LIG_LIR_Gen_1 | 143 | 153 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 219 | 229 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 143 | 148 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 215 | 221 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 40 | 46 | PF02991 | 0.683 |
LIG_PDZ_Class_2 | 226 | 231 | PF00595 | 0.434 |
LIG_SH2_NCK_1 | 221 | 225 | PF00017 | 0.444 |
LIG_SH2_PTP2 | 70 | 73 | PF00017 | 0.636 |
LIG_SH2_SRC | 70 | 73 | PF00017 | 0.656 |
LIG_SH2_STAP1 | 145 | 149 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.675 |
LIG_SUMO_SIM_anti_2 | 131 | 137 | PF11976 | 0.446 |
LIG_SUMO_SIM_anti_2 | 95 | 100 | PF11976 | 0.439 |
LIG_TYR_ITIM | 98 | 103 | PF00017 | 0.349 |
LIG_TYR_ITSM | 39 | 46 | PF00017 | 0.684 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.725 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.606 |
MOD_CK2_1 | 141 | 147 | PF00069 | 0.381 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.462 |
MOD_CK2_1 | 66 | 72 | PF00069 | 0.659 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.543 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.700 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.403 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.352 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.727 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.493 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.377 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.728 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.624 |
MOD_N-GLC_2 | 183 | 185 | PF02516 | 0.568 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.424 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.421 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.278 |
MOD_NEK2_2 | 166 | 171 | PF00069 | 0.450 |
MOD_NEK2_2 | 75 | 80 | PF00069 | 0.635 |
MOD_PIKK_1 | 158 | 164 | PF00454 | 0.459 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.495 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.402 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.698 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.659 |
MOD_SUMO_rev_2 | 38 | 46 | PF00179 | 0.566 |
MOD_SUMO_rev_2 | 69 | 76 | PF00179 | 0.664 |
TRG_DiLeu_BaEn_2 | 71 | 77 | PF01217 | 0.597 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 149 | 152 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 43 | 46 | PF00928 | 0.681 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.655 |
TRG_ER_diArg_1 | 107 | 110 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 124 | 127 | PF00400 | 0.378 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.645 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMV6 | Leptomonas seymouri | 62% | 97% |
A0A0S4JR13 | Bodo saltans | 33% | 97% |
A0A1X0P4Y8 | Trypanosomatidae | 46% | 100% |
A0A3S7XA10 | Leishmania donovani | 96% | 100% |
A0A422P1A7 | Trypanosoma rangeli | 45% | 100% |
A4HNB8 | Leishmania braziliensis | 85% | 100% |
A4IBZ1 | Leishmania infantum | 96% | 100% |
C9ZYL3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AFS8 | Leishmania major | 95% | 100% |