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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005681 | spliceosomal complex | 3 | 1 |
GO:0005689 | U12-type spliceosomal complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A4I5V6
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 173 | 175 | PF00675 | 0.762 |
CLV_NRD_NRD_1 | 227 | 229 | PF00675 | 0.717 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.648 |
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.762 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.717 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.501 |
DEG_SPOP_SBC_1 | 142 | 146 | PF00917 | 0.731 |
DEG_SPOP_SBC_1 | 279 | 283 | PF00917 | 0.616 |
DOC_ANK_TNKS_1 | 137 | 144 | PF00023 | 0.650 |
DOC_MAPK_DCC_7 | 256 | 265 | PF00069 | 0.589 |
DOC_PP1_RVXF_1 | 226 | 233 | PF00149 | 0.675 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.811 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.538 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.734 |
LIG_14-3-3_CanoR_1 | 133 | 142 | PF00244 | 0.741 |
LIG_14-3-3_CanoR_1 | 15 | 24 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 191 | 199 | PF00244 | 0.646 |
LIG_14-3-3_CanoR_1 | 227 | 231 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 308 | 312 | PF00244 | 0.499 |
LIG_APCC_ABBA_1 | 210 | 215 | PF00400 | 0.713 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.580 |
LIG_BRCT_BRCA1_1 | 219 | 223 | PF00533 | 0.725 |
LIG_BRCT_BRCA1_1 | 228 | 232 | PF00533 | 0.623 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.714 |
LIG_FHA_1 | 179 | 185 | PF00498 | 0.625 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.737 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.417 |
LIG_FHA_2 | 100 | 106 | PF00498 | 0.723 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.826 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.569 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.625 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.587 |
LIG_KLC1_Yacidic_2 | 211 | 215 | PF13176 | 0.733 |
LIG_LIR_Apic_2 | 93 | 99 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 23 | 27 | PF02991 | 0.596 |
LIG_LIR_Nem_3 | 48 | 53 | PF02991 | 0.470 |
LIG_MYND_1 | 162 | 166 | PF01753 | 0.698 |
LIG_SH2_SRC | 27 | 30 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.743 |
LIG_SH2_STAT5 | 27 | 30 | PF00017 | 0.620 |
LIG_SH3_1 | 186 | 192 | PF00018 | 0.595 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.767 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.684 |
LIG_SH3_3 | 271 | 277 | PF00018 | 0.756 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.671 |
LIG_TRAF2_1 | 110 | 113 | PF00917 | 0.708 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.723 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.573 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.744 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.574 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.682 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.507 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.827 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.587 |
MOD_CK2_1 | 280 | 286 | PF00069 | 0.617 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.371 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.606 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.723 |
MOD_Cter_Amidation | 171 | 174 | PF01082 | 0.728 |
MOD_DYRK1A_RPxSP_1 | 256 | 260 | PF00069 | 0.700 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.583 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.752 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.716 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.651 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.638 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.385 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.722 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.772 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.684 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.621 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.803 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.411 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.559 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.702 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.678 |
MOD_N-GLC_1 | 237 | 242 | PF02516 | 0.716 |
MOD_N-GLC_1 | 254 | 259 | PF02516 | 0.512 |
MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.577 |
MOD_N-GLC_1 | 88 | 93 | PF02516 | 0.530 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.650 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.506 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.411 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.479 |
MOD_PKA_1 | 173 | 179 | PF00069 | 0.717 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.590 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.720 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.648 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.513 |
MOD_Plk_1 | 327 | 333 | PF00069 | 0.647 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.697 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.665 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.732 |
MOD_SUMO_rev_2 | 146 | 155 | PF00179 | 0.734 |
MOD_SUMO_rev_2 | 170 | 179 | PF00179 | 0.721 |
TRG_DiLeu_BaEn_1 | 42 | 47 | PF01217 | 0.519 |
TRG_DiLeu_BaEn_2 | 285 | 291 | PF01217 | 0.718 |
TRG_ER_diArg_1 | 132 | 135 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 251 | 253 | PF00400 | 0.653 |
TRG_Pf-PMV_PEXEL_1 | 186 | 190 | PF00026 | 0.599 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD74 | Leptomonas seymouri | 33% | 99% |
A0A3S7X3N7 | Leishmania donovani | 99% | 100% |
A4HIL1 | Leishmania braziliensis | 67% | 100% |
E9B151 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4Q715 | Leishmania major | 90% | 100% |