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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4I9Q9
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 6 |
GO:0005509 | calcium ion binding | 5 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043169 | cation binding | 3 | 6 |
GO:0046872 | metal ion binding | 4 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 205 | 211 | PF00089 | 0.524 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.449 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.749 |
DEG_SPOP_SBC_1 | 63 | 67 | PF00917 | 0.698 |
DOC_MAPK_JIP1_4 | 76 | 82 | PF00069 | 0.705 |
DOC_PP1_RVXF_1 | 206 | 212 | PF00149 | 0.524 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 27 | 31 | PF00917 | 0.791 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.554 |
DOC_USP7_UBL2_3 | 246 | 250 | PF12436 | 0.697 |
LIG_14-3-3_CanoR_1 | 233 | 237 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 240 | 246 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 61 | 70 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 7 | 15 | PF00244 | 0.713 |
LIG_BIR_III_4 | 180 | 184 | PF00653 | 0.449 |
LIG_CaM_IQ_9 | 125 | 141 | PF13499 | 0.751 |
LIG_deltaCOP1_diTrp_1 | 119 | 128 | PF00928 | 0.718 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.526 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.729 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.661 |
LIG_FHA_2 | 14 | 20 | PF00498 | 0.707 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.434 |
LIG_LIR_Gen_1 | 119 | 128 | PF02991 | 0.718 |
LIG_LIR_Gen_1 | 176 | 186 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 119 | 125 | PF02991 | 0.720 |
LIG_LIR_Nem_3 | 127 | 131 | PF02991 | 0.591 |
LIG_LIR_Nem_3 | 158 | 162 | PF02991 | 0.647 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 176 | 182 | PF02991 | 0.718 |
LIG_LIR_Nem_3 | 184 | 189 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 237 | 242 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 9 | 15 | PF02991 | 0.659 |
LIG_LYPXL_S_1 | 11 | 15 | PF13949 | 0.641 |
LIG_LYPXL_yS_3 | 12 | 15 | PF13949 | 0.638 |
LIG_Pex14_2 | 155 | 159 | PF04695 | 0.656 |
LIG_SH2_CRK | 20 | 24 | PF00017 | 0.719 |
LIG_SH2_SRC | 189 | 192 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.723 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.524 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.749 |
LIG_SUMO_SIM_anti_2 | 215 | 225 | PF11976 | 0.517 |
LIG_TRAF2_1 | 215 | 218 | PF00917 | 0.524 |
LIG_WRC_WIRS_1 | 125 | 130 | PF05994 | 0.712 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.806 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.709 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.715 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.454 |
MOD_CK2_1 | 78 | 84 | PF00069 | 0.609 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.754 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.744 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.543 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.601 |
MOD_GlcNHglycan | 25 | 30 | PF01048 | 0.781 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.564 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.496 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.680 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.714 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.610 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.741 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.516 |
MOD_N-GLC_1 | 155 | 160 | PF02516 | 0.575 |
MOD_N-GLC_1 | 78 | 83 | PF02516 | 0.708 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.712 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.639 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.612 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.524 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.717 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.705 |
MOD_Plk_1 | 155 | 161 | PF00069 | 0.729 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.709 |
MOD_SUMO_rev_2 | 17 | 23 | PF00179 | 0.644 |
TRG_DiLeu_BaEn_1 | 19 | 24 | PF01217 | 0.717 |
TRG_DiLeu_BaEn_1 | 218 | 223 | PF01217 | 0.524 |
TRG_ENDOCYTIC_2 | 12 | 15 | PF00928 | 0.665 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.555 |
TRG_ER_diArg_1 | 239 | 241 | PF00400 | 0.449 |
TRG_Pf-PMV_PEXEL_1 | 21 | 25 | PF00026 | 0.736 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X7M0 | Leishmania donovani | 100% | 100% |
A4HAL6 | Leishmania braziliensis | 62% | 91% |
E9B4S5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q3A2 | Leishmania major | 91% | 100% |