Membrane associated proteins, LETM1 and EF-hand domain-containing 1 Uncharacterized
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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005743 | mitochondrial inner membrane | 5 | 12 |
GO:0016020 | membrane | 2 | 12 |
GO:0019866 | organelle inner membrane | 4 | 12 |
GO:0031090 | organelle membrane | 3 | 12 |
GO:0031966 | mitochondrial membrane | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005739 | mitochondrion | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
Related structures:
AlphaFold database: A4I4E9
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006811 | monoatomic ion transport | 4 | 2 |
GO:0006812 | monoatomic cation transport | 5 | 2 |
GO:0006816 | calcium ion transport | 7 | 2 |
GO:0006851 | mitochondrial calcium ion transmembrane transport | 4 | 2 |
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 1 |
GO:0006875 | obsolete intracellular metal ion homeostasis | 6 | 1 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019725 | cellular homeostasis | 2 | 1 |
GO:0030001 | metal ion transport | 6 | 2 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 1 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 2 |
GO:0042592 | homeostatic process | 3 | 1 |
GO:0048878 | chemical homeostasis | 4 | 1 |
GO:0050801 | monoatomic ion homeostasis | 5 | 1 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 1 |
GO:0055080 | monoatomic cation homeostasis | 6 | 1 |
GO:0055082 | intracellular chemical homeostasis | 3 | 1 |
GO:0055085 | transmembrane transport | 2 | 2 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0070588 | calcium ion transmembrane transport | 6 | 2 |
GO:0098655 | monoatomic cation transmembrane transport | 4 | 2 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 2 |
GO:0098662 | inorganic cation transmembrane transport | 5 | 2 |
GO:0098771 | inorganic ion homeostasis | 6 | 1 |
GO:1990542 | mitochondrial transmembrane transport | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0043021 | ribonucleoprotein complex binding | 3 | 12 |
GO:0043022 | ribosome binding | 4 | 12 |
GO:0044877 | protein-containing complex binding | 2 | 12 |
GO:0005215 | transporter activity | 1 | 2 |
GO:0005432 | calcium:sodium antiporter activity | 7 | 2 |
GO:0005509 | calcium ion binding | 5 | 2 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 2 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 2 |
GO:0015081 | sodium ion transmembrane transporter activity | 6 | 2 |
GO:0015085 | calcium ion transmembrane transporter activity | 6 | 2 |
GO:0015291 | secondary active transmembrane transporter activity | 4 | 2 |
GO:0015297 | antiporter activity | 5 | 2 |
GO:0015298 | obsolete solute:monoatomic cation antiporter activity | 5 | 2 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 2 |
GO:0015368 | calcium:monoatomic cation antiporter activity | 7 | 2 |
GO:0022804 | active transmembrane transporter activity | 3 | 2 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 2 |
GO:0022857 | transmembrane transporter activity | 2 | 2 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043169 | cation binding | 3 | 2 |
GO:0046872 | metal ion binding | 4 | 2 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 2 |
GO:0140828 | metal cation:monoatomic cation antiporter activity | 6 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 255 | 259 | PF00656 | 0.381 |
CLV_C14_Caspase3-7 | 378 | 382 | PF00656 | 0.561 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 467 | 469 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.287 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.290 |
CLV_PCSK_PC1ET2_1 | 403 | 405 | PF00082 | 0.618 |
CLV_PCSK_PC7_1 | 236 | 242 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 403 | 407 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 458 | 462 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 56 | 60 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 91 | 95 | PF00082 | 0.287 |
DEG_APCC_DBOX_1 | 325 | 333 | PF00400 | 0.419 |
DEG_APCC_DBOX_1 | 339 | 347 | PF00400 | 0.426 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.644 |
DEG_SPOP_SBC_1 | 484 | 488 | PF00917 | 0.613 |
DOC_AGCK_PIF_2 | 443 | 448 | PF00069 | 0.459 |
DOC_CYCLIN_RxL_1 | 80 | 90 | PF00134 | 0.487 |
DOC_CYCLIN_yCln2_LP_2 | 110 | 116 | PF00134 | 0.344 |
DOC_MAPK_gen_1 | 315 | 323 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 326 | 332 | PF00069 | 0.375 |
DOC_MAPK_gen_1 | 36 | 43 | PF00069 | 0.663 |
DOC_MAPK_gen_1 | 70 | 78 | PF00069 | 0.560 |
DOC_MAPK_gen_1 | 80 | 86 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 202 | 211 | PF00069 | 0.337 |
DOC_PP1_RVXF_1 | 54 | 60 | PF00149 | 0.552 |
DOC_PP1_RVXF_1 | 61 | 67 | PF00149 | 0.521 |
DOC_PP2B_LxvP_1 | 110 | 113 | PF13499 | 0.344 |
DOC_PP2B_LxvP_1 | 187 | 190 | PF13499 | 0.308 |
DOC_PP4_FxxP_1 | 201 | 204 | PF00568 | 0.381 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.419 |
DOC_USP7_UBL2_3 | 16 | 20 | PF12436 | 0.699 |
DOC_USP7_UBL2_3 | 32 | 36 | PF12436 | 0.670 |
DOC_USP7_UBL2_3 | 365 | 369 | PF12436 | 0.484 |
DOC_USP7_UBL2_3 | 408 | 412 | PF12436 | 0.446 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.381 |
LIG_14-3-3_CanoR_1 | 275 | 283 | PF00244 | 0.287 |
LIG_14-3-3_CanoR_1 | 3 | 7 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 315 | 319 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 340 | 344 | PF00244 | 0.498 |
LIG_Actin_WH2_2 | 34 | 51 | PF00022 | 0.672 |
LIG_Actin_WH2_2 | 57 | 75 | PF00022 | 0.556 |
LIG_APCC_ABBA_1 | 104 | 109 | PF00400 | 0.344 |
LIG_APCC_ABBAyCdc20_2 | 134 | 140 | PF00400 | 0.362 |
LIG_BRCT_BRCA1_1 | 439 | 443 | PF00533 | 0.353 |
LIG_Clathr_ClatBox_1 | 251 | 255 | PF01394 | 0.301 |
LIG_eIF4E_1 | 52 | 58 | PF01652 | 0.547 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.730 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.341 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.284 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.483 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.428 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.374 |
LIG_FHA_2 | 485 | 491 | PF00498 | 0.580 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.476 |
LIG_LIR_Apic_2 | 199 | 204 | PF02991 | 0.337 |
LIG_LIR_Apic_2 | 303 | 309 | PF02991 | 0.276 |
LIG_LIR_Gen_1 | 100 | 110 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 195 | 204 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 288 | 294 | PF02991 | 0.287 |
LIG_LIR_Gen_1 | 298 | 309 | PF02991 | 0.287 |
LIG_LIR_Gen_1 | 440 | 450 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 100 | 105 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 195 | 201 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 288 | 293 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 298 | 304 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 383 | 389 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 440 | 446 | PF02991 | 0.365 |
LIG_MYND_1 | 120 | 124 | PF01753 | 0.276 |
LIG_NRP_CendR_1 | 501 | 502 | PF00754 | 0.813 |
LIG_PCNA_PIPBox_1 | 390 | 399 | PF02747 | 0.385 |
LIG_PCNA_yPIPBox_3 | 390 | 404 | PF02747 | 0.386 |
LIG_Pex14_2 | 55 | 59 | PF04695 | 0.563 |
LIG_SH2_CRK | 221 | 225 | PF00017 | 0.338 |
LIG_SH2_CRK | 40 | 44 | PF00017 | 0.626 |
LIG_SH2_STAP1 | 68 | 72 | PF00017 | 0.538 |
LIG_SH2_STAT3 | 68 | 71 | PF00017 | 0.534 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.368 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.362 |
LIG_SH3_3 | 468 | 474 | PF00018 | 0.494 |
LIG_SH3_4 | 32 | 39 | PF00018 | 0.638 |
LIG_Sin3_3 | 108 | 115 | PF02671 | 0.363 |
LIG_TRAF2_1 | 479 | 482 | PF00917 | 0.619 |
LIG_TRAF2_1 | 488 | 491 | PF00917 | 0.592 |
LIG_TYR_ITIM | 299 | 304 | PF00017 | 0.276 |
LIG_TYR_ITIM | 43 | 48 | PF00017 | 0.646 |
LIG_UBA3_1 | 405 | 413 | PF00899 | 0.374 |
LIG_WRC_WIRS_1 | 160 | 165 | PF05994 | 0.283 |
MOD_CDK_SPxxK_3 | 228 | 235 | PF00069 | 0.381 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.691 |
MOD_CK1_1 | 342 | 348 | PF00069 | 0.497 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.444 |
MOD_CK1_1 | 486 | 492 | PF00069 | 0.560 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.276 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.445 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.475 |
MOD_CK2_1 | 484 | 490 | PF00069 | 0.588 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.487 |
MOD_Cter_Amidation | 499 | 502 | PF01082 | 0.804 |
MOD_DYRK1A_RPxSP_1 | 228 | 232 | PF00069 | 0.381 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.544 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.528 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.708 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.612 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.267 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.713 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.312 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.381 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.367 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.471 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.473 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.389 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.379 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.252 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.560 |
MOD_N-GLC_1 | 268 | 273 | PF02516 | 0.562 |
MOD_N-GLC_1 | 433 | 438 | PF02516 | 0.645 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.296 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.332 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.617 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.283 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.387 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.545 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.486 |
MOD_NEK2_2 | 141 | 146 | PF00069 | 0.301 |
MOD_NEK2_2 | 279 | 284 | PF00069 | 0.362 |
MOD_PIKK_1 | 128 | 134 | PF00454 | 0.287 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.618 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.391 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.287 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.376 |
MOD_PKA_2 | 339 | 345 | PF00069 | 0.474 |
MOD_Plk_1 | 295 | 301 | PF00069 | 0.325 |
MOD_Plk_1 | 415 | 421 | PF00069 | 0.402 |
MOD_Plk_1 | 433 | 439 | PF00069 | 0.332 |
MOD_Plk_1 | 490 | 496 | PF00069 | 0.562 |
MOD_Plk_2-3 | 490 | 496 | PF00069 | 0.615 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.667 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.325 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.268 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.465 |
MOD_Plk_4 | 438 | 444 | PF00069 | 0.373 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.381 |
MOD_SUMO_rev_2 | 486 | 494 | PF00179 | 0.594 |
TRG_DiLeu_BaEn_1 | 247 | 252 | PF01217 | 0.289 |
TRG_DiLeu_BaLyEn_6 | 80 | 85 | PF01217 | 0.500 |
TRG_DiLeu_LyEn_5 | 247 | 252 | PF01217 | 0.301 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.277 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.584 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.560 |
TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.509 |
TRG_ER_diArg_1 | 134 | 137 | PF00400 | 0.315 |
TRG_ER_diArg_1 | 145 | 148 | PF00400 | 0.235 |
TRG_ER_diArg_1 | 171 | 173 | PF00400 | 0.337 |
TRG_ER_diArg_1 | 234 | 236 | PF00400 | 0.287 |
TRG_ER_diArg_1 | 239 | 241 | PF00400 | 0.287 |
TRG_ER_diArg_1 | 7 | 9 | PF00400 | 0.688 |
TRG_NLS_MonoExtC_3 | 410 | 415 | PF00514 | 0.509 |
TRG_NLS_MonoExtN_4 | 408 | 415 | PF00514 | 0.435 |
TRG_Pf-PMV_PEXEL_1 | 412 | 416 | PF00026 | 0.713 |
TRG_Pf-PMV_PEXEL_1 | 83 | 87 | PF00026 | 0.286 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD73 | Leptomonas seymouri | 86% | 99% |
A0A0S4JFV9 | Bodo saltans | 52% | 100% |
A0A1X0NZY3 | Trypanosomatidae | 62% | 100% |
A0A3S5IR30 | Trypanosoma rangeli | 65% | 100% |
A0A3S7X2D5 | Leishmania donovani | 100% | 100% |
A4HHA3 | Leishmania braziliensis | 94% | 100% |
C9ZLK0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 100% |
E9ADU9 | Leishmania major | 99% | 100% |
E9ALY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 100% |
V5DI32 | Trypanosoma cruzi | 64% | 100% |