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 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
GO:0005747 | mitochondrial respiratory chain complex I | 4 | 1 |
GO:0030964 | NADH dehydrogenase complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0045271 | respiratory chain complex I | 4 | 1 |
GO:0098796 | membrane protein complex | 2 | 1 |
GO:0098798 | mitochondrial protein-containing complex | 2 | 1 |
GO:0098800 | inner mitochondrial membrane protein complex | 3 | 1 |
GO:0098803 | respiratory chain complex | 3 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1902495 | transmembrane transporter complex | 3 | 1 |
GO:1990204 | oxidoreductase complex | 3 | 1 |
GO:1990351 | transporter complex | 2 | 1 |
Related structures:
AlphaFold database: A4HKL1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.617 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.614 |
CLV_PCSK_PC7_1 | 38 | 44 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 45 | 49 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.534 |
DOC_MAPK_DCC_7 | 19 | 29 | PF00069 | 0.282 |
DOC_MAPK_MEF2A_6 | 23 | 31 | PF00069 | 0.296 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.713 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 182 | 187 | PF00397 | 0.718 |
LIG_14-3-3_CanoR_1 | 162 | 166 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 177 | 183 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 45 | 51 | PF00244 | 0.271 |
LIG_14-3-3_CanoR_1 | 71 | 77 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 92 | 100 | PF00244 | 0.419 |
LIG_14-3-3_CterR_2 | 204 | 206 | PF00244 | 0.774 |
LIG_Actin_WH2_2 | 138 | 156 | PF00022 | 0.663 |
LIG_Actin_WH2_2 | 6 | 21 | PF00022 | 0.282 |
LIG_APCC_ABBA_1 | 120 | 125 | PF00400 | 0.509 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.417 |
LIG_CtBP_PxDLS_1 | 190 | 194 | PF00389 | 0.629 |
LIG_eIF4E_1 | 105 | 111 | PF01652 | 0.447 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.655 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.339 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.392 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.283 |
LIG_LIR_Apic_2 | 181 | 186 | PF02991 | 0.678 |
LIG_LIR_Gen_1 | 115 | 123 | PF02991 | 0.227 |
LIG_LIR_Gen_1 | 139 | 147 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 115 | 121 | PF02991 | 0.227 |
LIG_PCNA_PIPBox_1 | 176 | 185 | PF02747 | 0.661 |
LIG_Pex14_2 | 114 | 118 | PF04695 | 0.358 |
LIG_SH2_CRK | 183 | 187 | PF00017 | 0.749 |
LIG_SH2_GRB2like | 77 | 80 | PF00017 | 0.389 |
LIG_SH2_NCK_1 | 183 | 187 | PF00017 | 0.690 |
LIG_SH2_STAP1 | 123 | 127 | PF00017 | 0.634 |
LIG_SH2_STAT3 | 202 | 205 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.630 |
LIG_SH2_STAT5 | 17 | 20 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.389 |
LIG_SH3_1 | 183 | 189 | PF00018 | 0.690 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.699 |
LIG_SUMO_SIM_anti_2 | 63 | 70 | PF11976 | 0.419 |
LIG_SUMO_SIM_anti_2 | 8 | 14 | PF11976 | 0.294 |
LIG_TRAF2_1 | 149 | 152 | PF00917 | 0.577 |
LIG_WRC_WIRS_1 | 179 | 184 | PF05994 | 0.618 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.292 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.592 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.205 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.625 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.554 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.666 |
MOD_N-GLC_1 | 25 | 30 | PF02516 | 0.482 |
MOD_N-GLC_1 | 43 | 48 | PF02516 | 0.507 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.362 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.383 |
MOD_NEK2_2 | 196 | 201 | PF00069 | 0.750 |
MOD_NEK2_2 | 25 | 30 | PF00069 | 0.282 |
MOD_PIKK_1 | 126 | 132 | PF00454 | 0.531 |
MOD_PIKK_1 | 99 | 105 | PF00454 | 0.398 |
MOD_PK_1 | 43 | 49 | PF00069 | 0.292 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.641 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.401 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.420 |
MOD_PKB_1 | 43 | 51 | PF00069 | 0.311 |
MOD_Plk_1 | 25 | 31 | PF00069 | 0.282 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.307 |
MOD_Plk_1 | 62 | 68 | PF00069 | 0.351 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.316 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.663 |
MOD_Plk_4 | 62 | 68 | PF00069 | 0.292 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.631 |
MOD_ProDKin_1 | 182 | 188 | PF00069 | 0.718 |
MOD_SUMO_rev_2 | 146 | 156 | PF00179 | 0.604 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.597 |
TRG_ER_diArg_1 | 14 | 16 | PF00400 | 0.275 |
TRG_ER_diArg_1 | 41 | 43 | PF00400 | 0.261 |
TRG_ER_diArg_1 | 91 | 93 | PF00400 | 0.411 |
TRG_NES_CRM1_1 | 133 | 146 | PF08389 | 0.610 |
TRG_Pf-PMV_PEXEL_1 | 30 | 35 | PF00026 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 54 | 59 | PF00026 | 0.482 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4J0 | Leptomonas seymouri | 81% | 100% |
A0A0S4JR38 | Bodo saltans | 55% | 100% |
A0A1X0NU58 | Trypanosomatidae | 71% | 100% |
A0A3Q8IL84 | Leishmania donovani | 86% | 100% |
A4I844 | Leishmania infantum | 87% | 100% |
D0AAB1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 73% | 100% |
E9B302 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q554 | Leishmania major | 86% | 100% |
V5BKR8 | Trypanosoma cruzi | 71% | 100% |