Metal Binding, 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:0005737 | cytoplasm | 2 | 1 | 
| GO:0005930 | axoneme | 2 | 1 | 
| GO:0110165 | cellular anatomical entity | 1 | 1 | 
Related structures:
AlphaFold database: A4IA71
| 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 | 163 | 167 | PF00656 | 0.458 | 
| CLV_C14_Caspase3-7 | 309 | 313 | PF00656 | 0.328 | 
| CLV_C14_Caspase3-7 | 345 | 349 | PF00656 | 0.474 | 
| CLV_NRD_NRD_1 | 104 | 106 | PF00675 | 0.408 | 
| CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.581 | 
| CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.597 | 
| CLV_PCSK_KEX2_1 | 104 | 106 | PF00082 | 0.334 | 
| CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.418 | 
| CLV_PCSK_PC1ET2_1 | 19 | 21 | PF00082 | 0.502 | 
| CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.414 | 
| CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.490 | 
| CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.424 | 
| CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.463 | 
| DEG_APCC_DBOX_1 | 104 | 112 | PF00400 | 0.327 | 
| DEG_APCC_DBOX_1 | 241 | 249 | PF00400 | 0.504 | 
| DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.674 | 
| DOC_CYCLIN_RxL_1 | 16 | 26 | PF00134 | 0.434 | 
| DOC_CYCLIN_RxL_1 | 262 | 270 | PF00134 | 0.435 | 
| DOC_PP2B_LxvP_1 | 296 | 299 | PF13499 | 0.503 | 
| DOC_PP2B_LxvP_1 | 323 | 326 | PF13499 | 0.455 | 
| DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.466 | 
| DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.510 | 
| DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.564 | 
| DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.554 | 
| DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.549 | 
| DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.609 | 
| DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.587 | 
| DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.382 | 
| LIG_Actin_WH2_2 | 88 | 106 | PF00022 | 0.483 | 
| LIG_BRCT_BRCA1_1 | 204 | 208 | PF00533 | 0.529 | 
| LIG_BRCT_BRCA1_1 | 340 | 344 | PF00533 | 0.508 | 
| LIG_eIF4E_1 | 319 | 325 | PF01652 | 0.479 | 
| LIG_FHA_1 | 291 | 297 | PF00498 | 0.501 | 
| LIG_FHA_1 | 299 | 305 | PF00498 | 0.520 | 
| LIG_FHA_1 | 88 | 94 | PF00498 | 0.382 | 
| LIG_FHA_2 | 145 | 151 | PF00498 | 0.558 | 
| LIG_FHA_2 | 161 | 167 | PF00498 | 0.455 | 
| LIG_FHA_2 | 307 | 313 | PF00498 | 0.331 | 
| LIG_FHA_2 | 373 | 379 | PF00498 | 0.480 | 
| LIG_FHA_2 | 50 | 56 | PF00498 | 0.351 | 
| LIG_FHA_2 | 75 | 81 | PF00498 | 0.449 | 
| LIG_LIR_Apic_2 | 348 | 354 | PF02991 | 0.513 | 
| LIG_LIR_Gen_1 | 188 | 198 | PF02991 | 0.414 | 
| LIG_LIR_Gen_1 | 406 | 413 | PF02991 | 0.455 | 
| LIG_LIR_Gen_1 | 90 | 100 | PF02991 | 0.470 | 
| LIG_LIR_Nem_3 | 173 | 177 | PF02991 | 0.379 | 
| LIG_LIR_Nem_3 | 188 | 194 | PF02991 | 0.367 | 
| LIG_LIR_Nem_3 | 406 | 412 | PF02991 | 0.476 | 
| LIG_LIR_Nem_3 | 90 | 95 | PF02991 | 0.470 | 
| LIG_Pex14_1 | 340 | 344 | PF04695 | 0.481 | 
| LIG_Pex14_2 | 155 | 159 | PF04695 | 0.431 | 
| LIG_Pex14_2 | 373 | 377 | PF04695 | 0.394 | 
| LIG_RPA_C_Fungi | 233 | 245 | PF08784 | 0.541 | 
| LIG_SH2_CRK | 178 | 182 | PF00017 | 0.382 | 
| LIG_SH2_CRK | 351 | 355 | PF00017 | 0.501 | 
| LIG_SH2_STAP1 | 320 | 324 | PF00017 | 0.477 | 
| LIG_SH2_STAT3 | 396 | 399 | PF00017 | 0.464 | 
| LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.420 | 
| LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.428 | 
| LIG_SUMO_SIM_anti_2 | 188 | 196 | PF11976 | 0.385 | 
| LIG_SUMO_SIM_anti_2 | 90 | 97 | PF11976 | 0.475 | 
| LIG_TRAF2_1 | 170 | 173 | PF00917 | 0.398 | 
| LIG_TRAF2_1 | 52 | 55 | PF00917 | 0.448 | 
| LIG_TRAF2_1 | 59 | 62 | PF00917 | 0.402 | 
| LIG_TRAF2_1 | 66 | 69 | PF00917 | 0.377 | 
| LIG_UBA3_1 | 75 | 84 | PF00899 | 0.475 | 
| LIG_WRC_WIRS_1 | 33 | 38 | PF05994 | 0.542 | 
| MOD_CDC14_SPxK_1 | 101 | 104 | PF00782 | 0.475 | 
| MOD_CDK_SPxK_1 | 98 | 104 | PF00069 | 0.376 | 
| MOD_CDK_SPxxK_3 | 363 | 370 | PF00069 | 0.586 | 
| MOD_CDK_SPxxK_3 | 98 | 105 | PF00069 | 0.418 | 
| MOD_CK1_1 | 222 | 228 | PF00069 | 0.603 | 
| MOD_CK2_1 | 144 | 150 | PF00069 | 0.546 | 
| MOD_CK2_1 | 167 | 173 | PF00069 | 0.408 | 
| MOD_CK2_1 | 225 | 231 | PF00069 | 0.541 | 
| MOD_CK2_1 | 299 | 305 | PF00069 | 0.538 | 
| MOD_CK2_1 | 49 | 55 | PF00069 | 0.396 | 
| MOD_CK2_1 | 63 | 69 | PF00069 | 0.308 | 
| MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.520 | 
| MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.503 | 
| MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.417 | 
| MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.557 | 
| MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.382 | 
| MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.462 | 
| MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.503 | 
| MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.522 | 
| MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.494 | 
| MOD_GSK3_1 | 202 | 209 | PF00069 | 0.459 | 
| MOD_GSK3_1 | 240 | 247 | PF00069 | 0.500 | 
| MOD_GSK3_1 | 276 | 283 | PF00069 | 0.474 | 
| MOD_GSK3_1 | 32 | 39 | PF00069 | 0.482 | 
| MOD_GSK3_1 | 45 | 52 | PF00069 | 0.405 | 
| MOD_GSK3_1 | 83 | 90 | PF00069 | 0.444 | 
| MOD_N-GLC_1 | 159 | 164 | PF02516 | 0.488 | 
| MOD_N-GLC_1 | 299 | 304 | PF02516 | 0.484 | 
| MOD_N-GLC_1 | 63 | 68 | PF02516 | 0.437 | 
| MOD_N-GLC_1 | 98 | 103 | PF02516 | 0.465 | 
| MOD_NEK2_1 | 11 | 16 | PF00069 | 0.461 | 
| MOD_NEK2_1 | 159 | 164 | PF00069 | 0.479 | 
| MOD_NEK2_1 | 208 | 213 | PF00069 | 0.447 | 
| MOD_NEK2_1 | 267 | 272 | PF00069 | 0.499 | 
| MOD_NEK2_1 | 36 | 41 | PF00069 | 0.516 | 
| MOD_NEK2_1 | 46 | 51 | PF00069 | 0.460 | 
| MOD_PIKK_1 | 46 | 52 | PF00454 | 0.586 | 
| MOD_PK_1 | 206 | 212 | PF00069 | 0.391 | 
| MOD_Plk_1 | 187 | 193 | PF00069 | 0.390 | 
| MOD_Plk_1 | 206 | 212 | PF00069 | 0.316 | 
| MOD_Plk_1 | 225 | 231 | PF00069 | 0.540 | 
| MOD_Plk_1 | 299 | 305 | PF00069 | 0.528 | 
| MOD_Plk_1 | 63 | 69 | PF00069 | 0.421 | 
| MOD_Plk_4 | 187 | 193 | PF00069 | 0.388 | 
| MOD_Plk_4 | 244 | 250 | PF00069 | 0.449 | 
| MOD_Plk_4 | 299 | 305 | PF00069 | 0.504 | 
| MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.609 | 
| MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.586 | 
| MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.376 | 
| MOD_SUMO_for_1 | 213 | 216 | PF00179 | 0.510 | 
| MOD_SUMO_rev_2 | 161 | 170 | PF00179 | 0.565 | 
| MOD_SUMO_rev_2 | 226 | 235 | PF00179 | 0.533 | 
| TRG_DiLeu_BaEn_1 | 388 | 393 | PF01217 | 0.446 | 
| TRG_DiLeu_BaLyEn_6 | 17 | 22 | PF01217 | 0.403 | 
| TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.383 | 
| TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.358 | 
| TRG_ER_diArg_1 | 103 | 105 | PF00400 | 0.377 | 
| TRG_Pf-PMV_PEXEL_1 | 20 | 24 | PF00026 | 0.496 | 
| TRG_Pf-PMV_PEXEL_1 | 58 | 62 | PF00026 | 0.461 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N1I2R2 | Leptomonas seymouri | 66% | 100% | 
| A0A0S4J207 | Bodo saltans | 35% | 97% | 
| A0A1X0PAP2 | Trypanosomatidae | 42% | 100% | 
| A0A3Q8IHP2 | Leishmania donovani | 99% | 100% | 
| A0A422N4H8 | Trypanosoma rangeli | 42% | 100% | 
| A4HB14 | Leishmania braziliensis | 84% | 100% | 
| C9ZM35 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% | 
| E9B584 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% | 
| Q4Q2P9 | Leishmania major | 95% | 100% | 
| V5B5A3 | Trypanosoma cruzi | 42% | 100% |