These Kinetoplastid proteins share considerable homology with the animal TMEM65 proteins at their membrane domains, with a unique EF-hand at the N-terminus.. While the animal orthologs have a mitochondrial transit signal, it seems to be absent from the Kinetoplastid proteins. The latter have an alanine-rich segment of unclear function.
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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
GO:0005739 | mitochondrion | 5 | 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: A4ICC4
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 11 |
GO:0005509 | calcium ion binding | 5 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 186 | 190 | PF00656 | 0.249 |
CLV_C14_Caspase3-7 | 341 | 345 | PF00656 | 0.354 |
CLV_C14_Caspase3-7 | 90 | 94 | PF00656 | 0.592 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.354 |
CLV_NRD_NRD_1 | 244 | 246 | PF00675 | 0.250 |
CLV_NRD_NRD_1 | 68 | 70 | PF00675 | 0.330 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.392 |
CLV_PCSK_KEX2_1 | 244 | 246 | PF00082 | 0.261 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.328 |
CLV_PCSK_PC1ET2_1 | 114 | 116 | PF00082 | 0.383 |
CLV_PCSK_PC1ET2_1 | 122 | 124 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.625 |
DEG_SPOP_SBC_1 | 30 | 34 | PF00917 | 0.627 |
DOC_CDC14_PxL_1 | 264 | 272 | PF14671 | 0.369 |
DOC_CKS1_1 | 231 | 236 | PF01111 | 0.504 |
DOC_CYCLIN_RxL_1 | 303 | 314 | PF00134 | 0.344 |
DOC_PP1_RVXF_1 | 226 | 232 | PF00149 | 0.442 |
DOC_PP1_RVXF_1 | 327 | 333 | PF00149 | 0.375 |
DOC_PP4_FxxP_1 | 231 | 234 | PF00568 | 0.440 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.727 |
DOC_USP7_UBL2_3 | 224 | 228 | PF12436 | 0.452 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.780 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.559 |
LIG_14-3-3_CanoR_1 | 123 | 130 | PF00244 | 0.615 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.657 |
LIG_BRCT_BRCA1_1 | 190 | 194 | PF00533 | 0.348 |
LIG_Clathr_ClatBox_1 | 269 | 273 | PF01394 | 0.335 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.651 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.263 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.513 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.291 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.732 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.590 |
LIG_LIR_Gen_1 | 280 | 290 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 293 | 301 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 331 | 340 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 280 | 285 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 293 | 298 | PF02991 | 0.376 |
LIG_LIR_Nem_3 | 300 | 304 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 331 | 335 | PF02991 | 0.328 |
LIG_Pex14_2 | 105 | 109 | PF04695 | 0.556 |
LIG_PTB_Apo_2 | 289 | 296 | PF02174 | 0.379 |
LIG_SH2_GRB2like | 195 | 198 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.389 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.326 |
LIG_SUMO_SIM_par_1 | 160 | 165 | PF11976 | 0.363 |
LIG_TRAF2_1 | 85 | 88 | PF00917 | 0.629 |
MOD_CDK_SPK_2 | 98 | 103 | PF00069 | 0.559 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.737 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.702 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.768 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.606 |
MOD_GlcNHglycan | 110 | 113 | PF01048 | 0.387 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.580 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.303 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.245 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.517 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.555 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.402 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.712 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.380 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.692 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.487 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.394 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.622 |
MOD_N-GLC_1 | 177 | 182 | PF02516 | 0.501 |
MOD_N-GLC_1 | 196 | 201 | PF02516 | 0.170 |
MOD_N-GLC_1 | 290 | 295 | PF02516 | 0.590 |
MOD_N-GLC_2 | 208 | 210 | PF02516 | 0.417 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.745 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.339 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.272 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.374 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.637 |
MOD_PIKK_1 | 333 | 339 | PF00454 | 0.361 |
MOD_PKA_1 | 122 | 128 | PF00069 | 0.642 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.711 |
MOD_Plk_1 | 176 | 182 | PF00069 | 0.279 |
MOD_Plk_1 | 196 | 202 | PF00069 | 0.141 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.282 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.170 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.679 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.776 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.470 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.554 |
MOD_SUMO_rev_2 | 341 | 348 | PF00179 | 0.456 |
TRG_DiLeu_BaLyEn_6 | 265 | 270 | PF01217 | 0.262 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.378 |
TRG_ER_diArg_1 | 244 | 246 | PF00400 | 0.461 |
TRG_ER_diArg_1 | 67 | 69 | PF00400 | 0.527 |
TRG_NLS_MonoExtC_3 | 120 | 126 | PF00514 | 0.691 |
TRG_Pf-PMV_PEXEL_1 | 303 | 307 | PF00026 | 0.566 |
TRG_Pf-PMV_PEXEL_1 | 318 | 322 | PF00026 | 0.572 |
TRG_Pf-PMV_PEXEL_1 | 5 | 9 | PF00026 | 0.490 |
TRG_Pf-PMV_PEXEL_1 | 53 | 57 | PF00026 | 0.437 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P806 | Leptomonas seymouri | 80% | 99% |
A0A0S4J8V3 | Bodo saltans | 34% | 100% |
A0A0S4JY67 | Bodo saltans | 55% | 100% |
A0A1X0NL71 | Trypanosomatidae | 56% | 100% |
A0A3R7NFF7 | Trypanosoma rangeli | 30% | 90% |
A0A3S7XCB7 | Leishmania donovani | 96% | 100% |
A4HQK4 | Leishmania braziliensis | 85% | 100% |
E9AUB9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4Q071 | Leishmania major | 96% | 100% |
V5BGX0 | Trypanosoma cruzi | 34% | 84% |
V5BHN9 | Trypanosoma cruzi | 55% | 100% |