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: 4 |
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 |
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: A4ICR0
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 257 | 261 | PF00656 | 0.516 |
CLV_C14_Caspase3-7 | 359 | 363 | PF00656 | 0.330 |
CLV_C14_Caspase3-7 | 504 | 508 | PF00656 | 0.434 |
CLV_C14_Caspase3-7 | 534 | 538 | PF00656 | 0.477 |
CLV_NRD_NRD_1 | 468 | 470 | PF00675 | 0.410 |
CLV_NRD_NRD_1 | 504 | 506 | PF00675 | 0.400 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.363 |
CLV_PCSK_PC1ET2_1 | 470 | 472 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 310 | 314 | PF00082 | 0.398 |
DEG_ODPH_VHL_1 | 263 | 276 | PF01847 | 0.334 |
DOC_CDC14_PxL_1 | 415 | 423 | PF14671 | 0.354 |
DOC_MAPK_gen_1 | 202 | 209 | PF00069 | 0.360 |
DOC_MAPK_gen_1 | 270 | 280 | PF00069 | 0.307 |
DOC_MAPK_MEF2A_6 | 202 | 209 | PF00069 | 0.360 |
DOC_MAPK_MEF2A_6 | 270 | 278 | PF00069 | 0.311 |
DOC_MAPK_MEF2A_6 | 420 | 429 | PF00069 | 0.334 |
DOC_MAPK_NFAT4_5 | 273 | 281 | PF00069 | 0.333 |
DOC_MAPK_RevD_3 | 493 | 506 | PF00069 | 0.356 |
DOC_PP2B_LxvP_1 | 370 | 373 | PF13499 | 0.365 |
DOC_PP4_FxxP_1 | 280 | 283 | PF00568 | 0.331 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.313 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.626 |
DOC_USP7_UBL2_3 | 266 | 270 | PF12436 | 0.405 |
DOC_USP7_UBL2_3 | 310 | 314 | PF12436 | 0.389 |
DOC_USP7_UBL2_3 | 365 | 369 | PF12436 | 0.401 |
DOC_USP7_UBL2_3 | 453 | 457 | PF12436 | 0.349 |
DOC_USP7_UBL2_3 | 532 | 536 | PF12436 | 0.473 |
DOC_WW_Pin1_4 | 188 | 193 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.655 |
LIG_14-3-3_CanoR_1 | 211 | 217 | PF00244 | 0.458 |
LIG_APCC_ABBA_1 | 354 | 359 | PF00400 | 0.327 |
LIG_BRCT_BRCA1_1 | 320 | 324 | PF00533 | 0.350 |
LIG_BRCT_BRCA1_1 | 488 | 492 | PF00533 | 0.336 |
LIG_eIF4E_1 | 441 | 447 | PF01652 | 0.389 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.422 |
LIG_FHA_1 | 199 | 205 | PF00498 | 0.381 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.369 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.326 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.494 |
LIG_FHA_2 | 435 | 441 | PF00498 | 0.391 |
LIG_FHA_2 | 496 | 502 | PF00498 | 0.356 |
LIG_LIR_Apic_2 | 279 | 283 | PF02991 | 0.332 |
LIG_LIR_Apic_2 | 301 | 305 | PF02991 | 0.435 |
LIG_LIR_Apic_2 | 334 | 340 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 350 | 357 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 489 | 497 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 301 | 307 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 334 | 339 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 436 | 441 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 489 | 495 | PF02991 | 0.319 |
LIG_Pex14_2 | 364 | 368 | PF04695 | 0.323 |
LIG_PTB_Apo_2 | 168 | 175 | PF02174 | 0.518 |
LIG_SH2_CRK | 337 | 341 | PF00017 | 0.303 |
LIG_SH2_GRB2like | 353 | 356 | PF00017 | 0.351 |
LIG_SH2_STAP1 | 213 | 217 | PF00017 | 0.450 |
LIG_SH2_STAP1 | 459 | 463 | PF00017 | 0.490 |
LIG_SH2_STAT3 | 125 | 128 | PF00017 | 0.575 |
LIG_SH2_STAT3 | 161 | 164 | PF00017 | 0.642 |
LIG_SH2_STAT3 | 175 | 178 | PF00017 | 0.420 |
LIG_SH2_STAT3 | 455 | 458 | PF00017 | 0.346 |
LIG_SH2_STAT3 | 52 | 55 | PF00017 | 0.640 |
LIG_SH2_STAT3 | 84 | 87 | PF00017 | 0.516 |
LIG_SH2_STAT3 | 95 | 98 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.596 |
LIG_SH2_STAT5 | 302 | 305 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 353 | 356 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.568 |
LIG_SH3_2 | 119 | 124 | PF14604 | 0.566 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.568 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.499 |
LIG_SH3_3 | 416 | 422 | PF00018 | 0.356 |
LIG_TRAF2_1 | 498 | 501 | PF00917 | 0.373 |
LIG_TYR_ITSM | 332 | 339 | PF00017 | 0.313 |
LIG_UBA3_1 | 204 | 208 | PF00899 | 0.314 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.554 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.566 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.417 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.592 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.507 |
MOD_CK2_1 | 391 | 397 | PF00069 | 0.374 |
MOD_CK2_1 | 495 | 501 | PF00069 | 0.345 |
MOD_Cter_Amidation | 315 | 318 | PF01082 | 0.365 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.618 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.653 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.384 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.357 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.388 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.291 |
MOD_GlcNHglycan | 401 | 405 | PF01048 | 0.421 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.548 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.568 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.451 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.334 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.421 |
MOD_N-GLC_1 | 131 | 136 | PF02516 | 0.599 |
MOD_N-GLC_1 | 258 | 263 | PF02516 | 0.459 |
MOD_N-GLC_1 | 404 | 409 | PF02516 | 0.366 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.304 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.442 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.293 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.341 |
MOD_NEK2_2 | 340 | 345 | PF00069 | 0.311 |
MOD_NEK2_2 | 423 | 428 | PF00069 | 0.462 |
MOD_OFUCOSY | 484 | 490 | PF10250 | 0.313 |
MOD_PIKK_1 | 113 | 119 | PF00454 | 0.654 |
MOD_PIKK_1 | 47 | 53 | PF00454 | 0.681 |
MOD_PIKK_1 | 78 | 84 | PF00454 | 0.613 |
MOD_PIKK_1 | 93 | 99 | PF00454 | 0.524 |
MOD_PK_1 | 203 | 209 | PF00069 | 0.353 |
MOD_Plk_1 | 258 | 264 | PF00069 | 0.489 |
MOD_Plk_1 | 300 | 306 | PF00069 | 0.362 |
MOD_Plk_1 | 404 | 410 | PF00069 | 0.360 |
MOD_Plk_1 | 423 | 429 | PF00069 | 0.336 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.616 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.536 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.308 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.311 |
MOD_ProDKin_1 | 188 | 194 | PF00069 | 0.474 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.654 |
MOD_SUMO_for_1 | 312 | 315 | PF00179 | 0.400 |
MOD_SUMO_rev_2 | 239 | 246 | PF00179 | 0.586 |
MOD_SUMO_rev_2 | 262 | 272 | PF00179 | 0.501 |
MOD_SUMO_rev_2 | 311 | 319 | PF00179 | 0.366 |
MOD_SUMO_rev_2 | 499 | 508 | PF00179 | 0.393 |
MOD_SUMO_rev_2 | 528 | 538 | PF00179 | 0.476 |
TRG_DiLeu_BaEn_2 | 487 | 493 | PF01217 | 0.322 |
TRG_ENDOCYTIC_2 | 213 | 216 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 336 | 339 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 353 | 356 | PF00928 | 0.323 |
TRG_ER_diArg_1 | 469 | 472 | PF00400 | 0.381 |
TRG_NLS_MonoExtN_4 | 467 | 473 | PF00514 | 0.375 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7W2 | Leptomonas seymouri | 68% | 100% |
A0A3S7XAD2 | Leishmania donovani | 100% | 100% |
A4HNT4 | Leishmania braziliensis | 84% | 100% |
E9ASJ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 99% |
Q4Q202 | Leishmania major | 96% | 100% |