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:0005739 | mitochondrion | 5 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0034702 | monoatomic ion channel complex | 4 | 1 |
GO:0034703 | cation channel complex | 5 | 1 |
GO:0034704 | calcium channel complex | 6 | 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 |
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:0110165 | cellular anatomical entity | 1 | 4 |
GO:1902495 | transmembrane transporter complex | 3 | 1 |
GO:1990246 | uniplex complex | 4 | 1 |
GO:1990351 | transporter complex | 2 | 1 |
GO:0016020 | membrane | 2 | 3 |
Related structures:
AlphaFold database: E9AL21
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 12 |
GO:0006811 | monoatomic ion transport | 4 | 12 |
GO:0006812 | monoatomic cation transport | 5 | 12 |
GO:0006816 | calcium ion transport | 7 | 12 |
GO:0006851 | mitochondrial calcium ion transmembrane transport | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0030001 | metal ion transport | 6 | 12 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0055085 | transmembrane transport | 2 | 12 |
GO:0070588 | calcium ion transmembrane transport | 6 | 12 |
GO:0098655 | monoatomic cation transmembrane transport | 4 | 12 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 12 |
GO:0098662 | inorganic cation transmembrane transport | 5 | 12 |
GO:1990542 | mitochondrial transmembrane transport | 3 | 12 |
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 1 |
GO:0006874 | intracellular calcium ion homeostasis | 7 | 1 |
GO:0006875 | obsolete intracellular metal ion homeostasis | 6 | 1 |
GO:0019725 | cellular homeostasis | 2 | 1 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 1 |
GO:0036444 | calcium import into the mitochondrion | 5 | 1 |
GO:0042592 | homeostatic process | 3 | 1 |
GO:0048878 | chemical homeostasis | 4 | 1 |
GO:0050801 | monoatomic ion homeostasis | 5 | 1 |
GO:0051560 | mitochondrial calcium ion homeostasis | 8 | 1 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 1 |
GO:0055074 | calcium ion homeostasis | 8 | 1 |
GO:0055080 | monoatomic cation homeostasis | 6 | 1 |
GO:0055082 | intracellular chemical homeostasis | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0072503 | obsolete cellular divalent inorganic cation homeostasis | 6 | 1 |
GO:0072507 | obsolete divalent inorganic cation homeostasis | 7 | 1 |
GO:0098771 | inorganic ion homeostasis | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0005509 | calcium ion binding | 5 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 177 | 181 | PF00656 | 0.305 |
CLV_C14_Caspase3-7 | 30 | 34 | PF00656 | 0.578 |
CLV_C14_Caspase3-7 | 61 | 65 | PF00656 | 0.502 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.368 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 249 | 251 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.287 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.568 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.476 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.568 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.430 |
CLV_PCSK_PC1ET2_1 | 369 | 371 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 18 | 22 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.582 |
DEG_APCC_DBOX_1 | 1 | 9 | PF00400 | 0.536 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.439 |
DEG_SPOP_SBC_1 | 32 | 36 | PF00917 | 0.481 |
DEG_SPOP_SBC_1 | 72 | 76 | PF00917 | 0.424 |
DOC_CDC14_PxL_1 | 378 | 386 | PF14671 | 0.369 |
DOC_CKS1_1 | 112 | 117 | PF01111 | 0.410 |
DOC_CYCLIN_RxL_1 | 249 | 262 | PF00134 | 0.310 |
DOC_PP1_RVXF_1 | 81 | 87 | PF00149 | 0.546 |
DOC_PP4_FxxP_1 | 243 | 246 | PF00568 | 0.307 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.443 |
DOC_USP7_MATH_2 | 425 | 431 | PF00917 | 0.483 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.466 |
LIG_14-3-3_CanoR_1 | 18 | 23 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 193 | 199 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 265 | 270 | PF00244 | 0.343 |
LIG_14-3-3_CanoR_1 | 298 | 304 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 373 | 379 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 38 | 43 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 428 | 432 | PF00244 | 0.602 |
LIG_BIR_III_2 | 64 | 68 | PF00653 | 0.419 |
LIG_BIR_III_4 | 180 | 184 | PF00653 | 0.261 |
LIG_deltaCOP1_diTrp_1 | 282 | 288 | PF00928 | 0.297 |
LIG_DLG_GKlike_1 | 265 | 272 | PF00625 | 0.483 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.553 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.535 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.405 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.322 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.391 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.295 |
LIG_FHA_2 | 232 | 238 | PF00498 | 0.491 |
LIG_FHA_2 | 298 | 304 | PF00498 | 0.483 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.506 |
LIG_LIR_Apic_2 | 114 | 120 | PF02991 | 0.349 |
LIG_LIR_Apic_2 | 242 | 246 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 184 | 194 | PF02991 | 0.259 |
LIG_LIR_Gen_1 | 224 | 233 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 302 | 312 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 390 | 397 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 407 | 417 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 128 | 133 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 184 | 189 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 191 | 195 | PF02991 | 0.230 |
LIG_LIR_Nem_3 | 207 | 213 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.155 |
LIG_LIR_Nem_3 | 268 | 272 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 287 | 291 | PF02991 | 0.290 |
LIG_LIR_Nem_3 | 302 | 307 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 338 | 343 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 371 | 375 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 390 | 396 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 407 | 412 | PF02991 | 0.257 |
LIG_NRBOX | 194 | 200 | PF00104 | 0.246 |
LIG_PCNA_yPIPBox_3 | 245 | 258 | PF02747 | 0.442 |
LIG_Pex14_1 | 284 | 288 | PF04695 | 0.295 |
LIG_SH2_CRK | 133 | 137 | PF00017 | 0.371 |
LIG_SH2_CRK | 421 | 425 | PF00017 | 0.597 |
LIG_SH2_NCK_1 | 112 | 116 | PF00017 | 0.481 |
LIG_SH2_NCK_1 | 421 | 425 | PF00017 | 0.597 |
LIG_SH2_SRC | 117 | 120 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.212 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.338 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.473 |
LIG_SUMO_SIM_anti_2 | 388 | 393 | PF11976 | 0.237 |
LIG_SUMO_SIM_anti_2 | 407 | 414 | PF11976 | 0.149 |
LIG_SUMO_SIM_par_1 | 218 | 225 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 333 | 338 | PF11976 | 0.343 |
LIG_TRAF2_1 | 222 | 225 | PF00917 | 0.311 |
LIG_TRAF2_1 | 300 | 303 | PF00917 | 0.492 |
LIG_TYR_ITIM | 131 | 136 | PF00017 | 0.377 |
LIG_TYR_ITIM | 317 | 322 | PF00017 | 0.498 |
LIG_UBA3_1 | 209 | 217 | PF00899 | 0.278 |
LIG_WRC_WIRS_1 | 240 | 245 | PF05994 | 0.291 |
MOD_CDC14_SPxK_1 | 158 | 161 | PF00782 | 0.500 |
MOD_CDK_SPxK_1 | 155 | 161 | PF00069 | 0.471 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.421 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.483 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.491 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.636 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.453 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.493 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.478 |
MOD_CK2_1 | 185 | 191 | PF00069 | 0.261 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.335 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.409 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.387 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.491 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.439 |
MOD_GlcNHglycan | 216 | 220 | PF01048 | 0.402 |
MOD_GlcNHglycan | 29 | 33 | PF01048 | 0.750 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.453 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.393 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.399 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.619 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.379 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.357 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.642 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.572 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.518 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.673 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.436 |
MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.471 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.328 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.434 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.362 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.628 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.307 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.683 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.539 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.363 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.349 |
MOD_OFUCOSY | 47 | 52 | PF10250 | 0.390 |
MOD_PKA_1 | 25 | 31 | PF00069 | 0.494 |
MOD_PKA_1 | 265 | 271 | PF00069 | 0.435 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.639 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.353 |
MOD_PKA_2 | 297 | 303 | PF00069 | 0.488 |
MOD_PKA_2 | 427 | 433 | PF00069 | 0.598 |
MOD_Plk_1 | 436 | 442 | PF00069 | 0.309 |
MOD_Plk_2-3 | 333 | 339 | PF00069 | 0.335 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.497 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.451 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.333 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.460 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.220 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.313 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.416 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.471 |
TRG_DiLeu_BaEn_1 | 191 | 196 | PF01217 | 0.246 |
TRG_DiLeu_BaEn_1 | 303 | 308 | PF01217 | 0.412 |
TRG_DiLeu_BaEn_2 | 404 | 410 | PF01217 | 0.251 |
TRG_DiLeu_BaLyEn_6 | 80 | 85 | PF01217 | 0.404 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.333 |
TRG_ENDOCYTIC_2 | 186 | 189 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.532 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 126 | 129 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 136 | 139 | PF00400 | 0.389 |
TRG_ER_diArg_1 | 264 | 266 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 325 | 327 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 372 | 374 | PF00400 | 0.382 |
TRG_ER_diArg_1 | 432 | 434 | PF00400 | 0.570 |
TRG_ER_diArg_1 | 81 | 84 | PF00400 | 0.670 |
TRG_NLS_MonoCore_2 | 136 | 141 | PF00514 | 0.503 |
TRG_NLS_MonoExtN_4 | 137 | 142 | PF00514 | 0.501 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P773 | Leptomonas seymouri | 74% | 100% |
A0A0S4IPF8 | Bodo saltans | 44% | 100% |
A0A1X0NK53 | Trypanosomatidae | 49% | 100% |
A0A3S5H5W0 | Leishmania donovani | 95% | 100% |
A0A422NT64 | Trypanosoma rangeli | 44% | 100% |
A4H4V4 | Leishmania braziliensis | 86% | 100% |
A4HT58 | Leishmania infantum | 94% | 100% |
A4IG32 | Danio rerio | 22% | 92% |
B1H2N3 | Xenopus tropicalis | 20% | 95% |
C9ZUW0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 94% |
D2HZB0 | Ailuropoda melanoleuca | 21% | 93% |
Q0IIL1 | Bos taurus | 20% | 94% |
Q4QIT3 | Leishmania major | 93% | 100% |
Q4R518 | Macaca fascicularis | 22% | 94% |
Q6P6Q9 | Rattus norvegicus | 21% | 94% |
Q86XE3 | Homo sapiens | 20% | 85% |
Q8CD10 | Mus musculus | 21% | 100% |
Q8IYU8 | Homo sapiens | 22% | 100% |
Q8VCX5 | Mus musculus | 21% | 94% |
Q99P63 | Rattus norvegicus | 21% | 100% |
Q9BPX6 | Homo sapiens | 22% | 94% |
Q9CTY5 | Mus musculus | 22% | 86% |
V5B8U7 | Trypanosoma cruzi | 47% | 97% |