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 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4I4H4
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 7 |
GO:0005509 | calcium ion binding | 5 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 209 | 213 | PF00656 | 0.729 |
CLV_C14_Caspase3-7 | 24 | 28 | PF00656 | 0.431 |
CLV_MEL_PAP_1 | 140 | 146 | PF00089 | 0.543 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.544 |
CLV_PCSK_FUR_1 | 158 | 162 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.551 |
CLV_PCSK_PC1ET2_1 | 207 | 209 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.402 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.556 |
DOC_AGCK_PIF_1 | 357 | 362 | PF00069 | 0.337 |
DOC_CKS1_1 | 279 | 284 | PF01111 | 0.515 |
DOC_MAPK_gen_1 | 31 | 38 | PF00069 | 0.418 |
DOC_MAPK_gen_1 | 70 | 78 | PF00069 | 0.649 |
DOC_PP2B_LxvP_1 | 333 | 336 | PF13499 | 0.472 |
DOC_PP4_FxxP_1 | 134 | 137 | PF00568 | 0.549 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.575 |
DOC_USP7_MATH_2 | 46 | 52 | PF00917 | 0.405 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.555 |
LIG_14-3-3_CanoR_1 | 158 | 168 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 188 | 192 | PF00244 | 0.739 |
LIG_14-3-3_CanoR_1 | 314 | 320 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 33 | 37 | PF00244 | 0.356 |
LIG_APCC_ABBA_1 | 193 | 198 | PF00400 | 0.529 |
LIG_BRCT_BRCA1_1 | 189 | 193 | PF00533 | 0.595 |
LIG_CaM_IQ_9 | 50 | 66 | PF13499 | 0.446 |
LIG_Clathr_ClatBox_1 | 44 | 48 | PF01394 | 0.377 |
LIG_deltaCOP1_diTrp_1 | 352 | 360 | PF00928 | 0.418 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.542 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.531 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.415 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.486 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.475 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.640 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.530 |
LIG_FHA_2 | 296 | 302 | PF00498 | 0.292 |
LIG_LIR_Gen_1 | 148 | 157 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 304 | 311 | PF02991 | 0.372 |
LIG_LIR_Gen_1 | 337 | 347 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 352 | 362 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 39 | 47 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 148 | 153 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 190 | 196 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 304 | 309 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 320 | 325 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 337 | 342 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 352 | 357 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 358 | 363 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 39 | 44 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 75 | 80 | PF02991 | 0.620 |
LIG_PALB2_WD40_1 | 301 | 309 | PF16756 | 0.421 |
LIG_PTAP_UEV_1 | 245 | 250 | PF05743 | 0.508 |
LIG_PTB_Apo_2 | 249 | 256 | PF02174 | 0.425 |
LIG_PTB_Phospho_1 | 249 | 255 | PF10480 | 0.431 |
LIG_SH2_CRK | 255 | 259 | PF00017 | 0.443 |
LIG_SH2_CRK | 41 | 45 | PF00017 | 0.359 |
LIG_SH2_CRK | 80 | 84 | PF00017 | 0.496 |
LIG_SH2_GRB2like | 80 | 83 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 267 | 270 | PF00017 | 0.649 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.584 |
LIG_SH3_2 | 246 | 251 | PF14604 | 0.539 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.661 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.597 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.408 |
LIG_SUMO_SIM_par_1 | 315 | 321 | PF11976 | 0.409 |
LIG_SUMO_SIM_par_1 | 340 | 345 | PF11976 | 0.416 |
LIG_TRAF2_1 | 114 | 117 | PF00917 | 0.562 |
LIG_TRAF2_1 | 298 | 301 | PF00917 | 0.447 |
LIG_TRAF2_1 | 318 | 321 | PF00917 | 0.228 |
LIG_UBA3_1 | 22 | 31 | PF00899 | 0.362 |
MOD_CDK_SPK_2 | 212 | 217 | PF00069 | 0.577 |
MOD_CDK_SPxxK_3 | 14 | 21 | PF00069 | 0.418 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.697 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.712 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.600 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.555 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.516 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.561 |
MOD_CK2_1 | 295 | 301 | PF00069 | 0.452 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.223 |
MOD_Cter_Amidation | 205 | 208 | PF01082 | 0.544 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.626 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.575 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.542 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.558 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.712 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.616 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.678 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.620 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.684 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.522 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.413 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.461 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.591 |
MOD_N-GLC_1 | 212 | 217 | PF02516 | 0.715 |
MOD_N-GLC_1 | 290 | 295 | PF02516 | 0.447 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.493 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.667 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.426 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.362 |
MOD_NEK2_2 | 145 | 150 | PF00069 | 0.522 |
MOD_PIKK_1 | 268 | 274 | PF00454 | 0.487 |
MOD_PKA_1 | 160 | 166 | PF00069 | 0.565 |
MOD_PKA_2 | 106 | 112 | PF00069 | 0.694 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.554 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.553 |
MOD_PKA_2 | 244 | 250 | PF00069 | 0.489 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.401 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.538 |
MOD_PKB_1 | 158 | 166 | PF00069 | 0.512 |
MOD_Plk_1 | 290 | 296 | PF00069 | 0.463 |
MOD_Plk_2-3 | 112 | 118 | PF00069 | 0.507 |
MOD_Plk_2-3 | 338 | 344 | PF00069 | 0.440 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.510 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.443 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.356 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.423 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.592 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.485 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.555 |
MOD_SUMO_rev_2 | 198 | 204 | PF00179 | 0.616 |
TRG_DiLeu_BaEn_2 | 47 | 53 | PF01217 | 0.400 |
TRG_DiLeu_BaLyEn_6 | 95 | 100 | PF01217 | 0.453 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 339 | 342 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 362 | 365 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.520 |
TRG_ER_diArg_1 | 157 | 160 | PF00400 | 0.462 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7W0 | Leptomonas seymouri | 47% | 100% |
A0A1X0NZT2 | Trypanosomatidae | 29% | 100% |
A0A3Q8IRA6 | Leishmania donovani | 100% | 100% |
A4HHC9 | Leishmania braziliensis | 72% | 100% |
E9ADX5 | Leishmania major | 95% | 100% |
E9ALV6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 98% |