A conserved mitochondrial transporter, might be an ADP/ATP translocase
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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: A4HM54
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 288 | 290 | PF00675 | 0.511 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.660 |
CLV_PCSK_PC1ET2_1 | 48 | 50 | PF00082 | 0.668 |
CLV_PCSK_PC7_1 | 284 | 290 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.640 |
DEG_SPOP_SBC_1 | 194 | 198 | PF00917 | 0.300 |
DOC_PP2B_LxvP_1 | 186 | 189 | PF13499 | 0.435 |
DOC_PP2B_LxvP_1 | 63 | 66 | PF13499 | 0.392 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.449 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.286 |
LIG_14-3-3_CanoR_1 | 191 | 195 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 246 | 250 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 38 | 43 | PF00244 | 0.317 |
LIG_APCC_ABBA_1 | 21 | 26 | PF00400 | 0.406 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.591 |
LIG_BRCT_BRCA1_1 | 12 | 16 | PF00533 | 0.485 |
LIG_BRCT_BRCA1_1 | 165 | 169 | PF00533 | 0.440 |
LIG_BRCT_BRCA1_1 | 251 | 255 | PF00533 | 0.322 |
LIG_deltaCOP1_diTrp_1 | 171 | 177 | PF00928 | 0.347 |
LIG_EH1_1 | 176 | 184 | PF00400 | 0.391 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.339 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.348 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.365 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.294 |
LIG_LIR_Gen_1 | 110 | 120 | PF02991 | 0.584 |
LIG_LIR_Gen_1 | 13 | 24 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 171 | 182 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 258 | 265 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 110 | 115 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 13 | 19 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 171 | 177 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 258 | 262 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 276 | 280 | PF02991 | 0.682 |
LIG_Pex14_2 | 72 | 76 | PF04695 | 0.485 |
LIG_SH2_CRK | 120 | 124 | PF00017 | 0.563 |
LIG_SH2_CRK | 134 | 138 | PF00017 | 0.462 |
LIG_SH2_CRK | 277 | 281 | PF00017 | 0.604 |
LIG_SH2_STAP1 | 165 | 169 | PF00017 | 0.460 |
LIG_SH2_STAP1 | 93 | 97 | PF00017 | 0.639 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.638 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.298 |
LIG_TRAF2_1 | 232 | 235 | PF00917 | 0.394 |
LIG_UBA3_1 | 123 | 132 | PF00899 | 0.600 |
LIG_WRC_WIRS_1 | 136 | 141 | PF05994 | 0.401 |
LIG_WRC_WIRS_1 | 182 | 187 | PF05994 | 0.352 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.230 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.401 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.464 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.464 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.348 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.376 |
MOD_GlcNHglycan | 202 | 206 | PF01048 | 0.630 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.414 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.455 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.399 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.344 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.585 |
MOD_N-GLC_1 | 273 | 278 | PF02516 | 0.491 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.412 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.249 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.360 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.324 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.524 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.615 |
MOD_NEK2_2 | 11 | 16 | PF00069 | 0.452 |
MOD_NEK2_2 | 135 | 140 | PF00069 | 0.369 |
MOD_NEK2_2 | 206 | 211 | PF00069 | 0.307 |
MOD_PIKK_1 | 55 | 61 | PF00454 | 0.381 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.374 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.371 |
MOD_PKA_2 | 37 | 43 | PF00069 | 0.397 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.364 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.392 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.383 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.633 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.286 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.582 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.565 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 24 | 27 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 277 | 280 | PF00928 | 0.752 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.367 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4JQQ1 | Bodo saltans | 37% | 98% |
A0A1X0NJA4 | Trypanosomatidae | 47% | 100% |
A0A3S7X8R5 | Leishmania donovani | 86% | 100% |
A4IAR6 | Leishmania infantum | 86% | 100% |
D0A2E6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9AEJ2 | Leishmania major | 85% | 100% |
E9B5Q3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5BNB5 | Trypanosoma cruzi | 47% | 100% |