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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4IBW6
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 8 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043169 | cation binding | 3 | 8 |
GO:0046872 | metal ion binding | 4 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 244 | 248 | PF00656 | 0.719 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 136 | 138 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.458 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.444 |
CLV_PCSK_FUR_1 | 140 | 144 | PF00082 | 0.482 |
CLV_PCSK_FUR_1 | 190 | 194 | PF00082 | 0.524 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 136 | 138 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 353 | 355 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 189 | 191 | PF00082 | 0.514 |
CLV_PCSK_PC1ET2_1 | 305 | 307 | PF00082 | 0.394 |
CLV_PCSK_PC1ET2_1 | 353 | 355 | PF00082 | 0.383 |
CLV_PCSK_PC7_1 | 136 | 142 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.453 |
DOC_CKS1_1 | 362 | 367 | PF01111 | 0.360 |
DOC_MAPK_gen_1 | 305 | 314 | PF00069 | 0.433 |
DOC_PP2B_LxvP_1 | 266 | 269 | PF13499 | 0.651 |
DOC_PP4_FxxP_1 | 292 | 295 | PF00568 | 0.452 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.383 |
DOC_USP7_UBL2_3 | 185 | 189 | PF12436 | 0.539 |
DOC_USP7_UBL2_3 | 217 | 221 | PF12436 | 0.536 |
DOC_USP7_UBL2_3 | 305 | 309 | PF12436 | 0.502 |
DOC_USP7_UBL2_3 | 57 | 61 | PF12436 | 0.411 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.360 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.704 |
LIG_14-3-3_CanoR_1 | 34 | 40 | PF00244 | 0.508 |
LIG_14-3-3_CterR_2 | 374 | 377 | PF00244 | 0.509 |
LIG_Actin_WH2_2 | 250 | 265 | PF00022 | 0.669 |
LIG_deltaCOP1_diTrp_1 | 228 | 232 | PF00928 | 0.638 |
LIG_LIR_Apic_2 | 239 | 243 | PF02991 | 0.566 |
LIG_LIR_Apic_2 | 290 | 295 | PF02991 | 0.453 |
LIG_LIR_Apic_2 | 298 | 302 | PF02991 | 0.428 |
LIG_LIR_Apic_2 | 359 | 365 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 22 | 32 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 228 | 237 | PF02991 | 0.653 |
LIG_LIR_Gen_1 | 52 | 60 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 73 | 83 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 228 | 232 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 52 | 56 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 73 | 79 | PF02991 | 0.438 |
LIG_SH2_CRK | 308 | 312 | PF00017 | 0.489 |
LIG_SH2_CRK | 362 | 366 | PF00017 | 0.383 |
LIG_SH2_NCK_1 | 240 | 244 | PF00017 | 0.570 |
LIG_SH2_PTP2 | 53 | 56 | PF00017 | 0.487 |
LIG_SH2_SRC | 240 | 243 | PF00017 | 0.567 |
LIG_SH2_STAP1 | 63 | 67 | PF00017 | 0.519 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.487 |
LIG_SH3_3 | 13 | 19 | PF00018 | 0.590 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.323 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.667 |
LIG_TRAF2_1 | 106 | 109 | PF00917 | 0.504 |
LIG_TRAF2_1 | 128 | 131 | PF00917 | 0.566 |
LIG_TRAF2_1 | 153 | 156 | PF00917 | 0.498 |
LIG_TRAF2_1 | 165 | 168 | PF00917 | 0.508 |
LIG_TRAF2_1 | 169 | 172 | PF00917 | 0.512 |
LIG_TRAF2_1 | 176 | 179 | PF00917 | 0.501 |
LIG_TYR_ITIM | 51 | 56 | PF00017 | 0.487 |
LIG_UBA3_1 | 35 | 40 | PF00899 | 0.446 |
MOD_CDK_SPK_2 | 4 | 9 | PF00069 | 0.652 |
MOD_CDK_SPxK_1 | 361 | 367 | PF00069 | 0.360 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.745 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.560 |
MOD_GlcNHglycan | 171 | 176 | PF01048 | 0.441 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.486 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.557 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.513 |
MOD_N-GLC_1 | 348 | 353 | PF02516 | 0.383 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.671 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.734 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.470 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.446 |
MOD_NEK2_2 | 19 | 24 | PF00069 | 0.653 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.577 |
MOD_PKA_2 | 332 | 338 | PF00069 | 0.383 |
MOD_Plk_2-3 | 52 | 58 | PF00069 | 0.431 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.448 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.360 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.704 |
MOD_SUMO_rev_2 | 258 | 265 | PF00179 | 0.644 |
TRG_DiLeu_BaEn_1 | 46 | 51 | PF01217 | 0.419 |
TRG_DiLeu_BaEn_4 | 202 | 208 | PF01217 | 0.494 |
TRG_DiLeu_BaLyEn_6 | 31 | 36 | PF01217 | 0.404 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 53 | 56 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.419 |
TRG_ER_diArg_1 | 113 | 116 | PF00400 | 0.477 |
TRG_ER_diArg_1 | 140 | 143 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 190 | 193 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 306 | 308 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 373 | 376 | PF00400 | 0.481 |
TRG_NES_CRM1_1 | 46 | 58 | PF08389 | 0.425 |
TRG_NLS_MonoCore_2 | 188 | 193 | PF00514 | 0.492 |
TRG_NLS_MonoExtC_3 | 188 | 193 | PF00514 | 0.492 |
TRG_NLS_MonoExtC_3 | 304 | 309 | PF00514 | 0.478 |
TRG_NLS_MonoExtN_4 | 188 | 193 | PF00514 | 0.496 |
TRG_NLS_MonoExtN_4 | 302 | 309 | PF00514 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 102 | 107 | PF00026 | 0.591 |
TRG_Pf-PMV_PEXEL_1 | 113 | 117 | PF00026 | 0.451 |
TRG_Pf-PMV_PEXEL_1 | 198 | 202 | PF00026 | 0.492 |
TRG_Pf-PMV_PEXEL_1 | 354 | 358 | PF00026 | 0.397 |
TRG_Pf-PMV_PEXEL_1 | 37 | 42 | PF00026 | 0.599 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3I7 | Leptomonas seymouri | 80% | 95% |
A0A0S4JE94 | Bodo saltans | 55% | 100% |
A0A3S5H806 | Leishmania donovani | 100% | 100% |
E9AFQ3 | Leishmania major | 96% | 100% |
E9AIX0 | Leishmania braziliensis | 88% | 100% |
E9B6V6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |