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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 14 |
GO:0110165 | cellular anatomical entity | 1 | 14 |
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: A0A3S7XCB7
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 | 185 | 189 | PF00656 | 0.287 |
CLV_C14_Caspase3-7 | 340 | 344 | PF00656 | 0.469 |
CLV_C14_Caspase3-7 | 89 | 93 | PF00656 | 0.640 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.386 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.395 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 66 | 68 | PF00082 | 0.384 |
CLV_PCSK_PC1ET2_1 | 113 | 115 | PF00082 | 0.430 |
CLV_PCSK_PC1ET2_1 | 121 | 123 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.657 |
DEG_SPOP_SBC_1 | 29 | 33 | PF00917 | 0.694 |
DOC_CDC14_PxL_1 | 263 | 271 | PF14671 | 0.397 |
DOC_CKS1_1 | 230 | 235 | PF01111 | 0.540 |
DOC_CYCLIN_RxL_1 | 302 | 313 | PF00134 | 0.454 |
DOC_PP1_RVXF_1 | 225 | 231 | PF00149 | 0.489 |
DOC_PP1_RVXF_1 | 326 | 332 | PF00149 | 0.417 |
DOC_PP4_FxxP_1 | 230 | 233 | PF00568 | 0.488 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.747 |
DOC_USP7_UBL2_3 | 223 | 227 | PF12436 | 0.500 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.781 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.610 |
LIG_14-3-3_CanoR_1 | 122 | 129 | PF00244 | 0.694 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.724 |
LIG_BRCT_BRCA1_1 | 189 | 193 | PF00533 | 0.361 |
LIG_Clathr_ClatBox_1 | 268 | 272 | PF01394 | 0.397 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.717 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.670 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.309 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.528 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.346 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.765 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.639 |
LIG_LIR_Gen_1 | 279 | 289 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 292 | 300 | PF02991 | 0.286 |
LIG_LIR_Gen_1 | 330 | 339 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 279 | 284 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 292 | 297 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 299 | 303 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 330 | 334 | PF02991 | 0.364 |
LIG_Pex14_2 | 104 | 108 | PF04695 | 0.607 |
LIG_PTB_Apo_2 | 288 | 295 | PF02174 | 0.415 |
LIG_SH2_GRB2like | 194 | 197 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.434 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.434 |
LIG_SUMO_SIM_par_1 | 159 | 164 | PF11976 | 0.417 |
LIG_TRAF2_1 | 84 | 87 | PF00917 | 0.643 |
MOD_CDK_SPK_2 | 97 | 102 | PF00069 | 0.611 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.731 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.730 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.784 |
MOD_CK2_1 | 33 | 39 | PF00069 | 0.652 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.408 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.569 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.350 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.273 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.489 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.601 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.425 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.714 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.414 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.714 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.524 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.414 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.667 |
MOD_N-GLC_1 | 176 | 181 | PF02516 | 0.538 |
MOD_N-GLC_1 | 195 | 200 | PF02516 | 0.192 |
MOD_N-GLC_1 | 289 | 294 | PF02516 | 0.626 |
MOD_N-GLC_2 | 207 | 209 | PF02516 | 0.451 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.740 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.379 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.138 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.381 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.630 |
MOD_PIKK_1 | 332 | 338 | PF00454 | 0.409 |
MOD_PKA_1 | 121 | 127 | PF00069 | 0.754 |
MOD_PKA_2 | 121 | 127 | PF00069 | 0.723 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.334 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.138 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.285 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.197 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.747 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.779 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.515 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.604 |
MOD_SUMO_rev_2 | 340 | 347 | PF00179 | 0.474 |
TRG_DiLeu_BaLyEn_6 | 264 | 269 | PF01217 | 0.318 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.427 |
TRG_ER_diArg_1 | 243 | 245 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 66 | 68 | PF00400 | 0.584 |
TRG_NLS_MonoExtC_3 | 119 | 125 | PF00514 | 0.727 |
TRG_Pf-PMV_PEXEL_1 | 302 | 306 | PF00026 | 0.612 |
TRG_Pf-PMV_PEXEL_1 | 317 | 321 | PF00026 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 5 | 9 | PF00026 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 52 | 56 | PF00026 | 0.463 |
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% |
A4HQK4 | Leishmania braziliensis | 85% | 100% |
A4ICC4 | Leishmania infantum | 96% | 100% |
C9ZPD7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 81% |
E9AUB9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q071 | Leishmania major | 95% | 100% |
V5BGX0 | Trypanosoma cruzi | 34% | 84% |
V5BHN9 | Trypanosoma cruzi | 55% | 100% |