LeishMANIAdb
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Conserved zinc-finger protein

Quick info Localization Expansion Sequence features Structure Function Putative motif mimicry Homologs Download

Quick info

Protein:
Conserved zinc-finger protein
Gene product:
zinc-finger protein, conserved
Species:
Leishmania braziliensis
UniProt:
A4HIG8_LEIBR
TriTrypDb:
LbrM.30.2310 , LBRM2903_300029500 *
Length:
546

Localization

Secreted promastigote
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
Secreted amastigote
Source Evidence on protein Close homologs
Pires et al. no yes: 0
Exosome
Source Evidence on protein Close homologs
Silverman et al. no yes: 0
Glycosome
Source Evidence on protein Close homologs
Jamdhade et al. no yes: 0
Predictions
Source Evidence on protein Close homologs
DeepLoc
SignalP6 no yes: 0, no: 11
NetGPI no yes: 0, no: 11
Cellular components
Term Name Level Count
GO:0005929 cilium 4 1
GO:0042995 cell projection 2 1
GO:0043226 organelle 2 1
GO:0043227 membrane-bounded organelle 3 1
GO:0110165 cellular anatomical entity 1 1
GO:0120025 plasma membrane bounded cell projection 3 1

Expansion

Sequence features

A4HIG8
Sequence
MSA
Disorder
Secondary
Topology
Domains
SignalP
GPI
Phosphorylations
ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A4HIG8

Function

Could not find GO biological_process term for this entry.
Molecular functions
Term Name Level Count
GO:0005488 binding 1 12
GO:0008270 zinc ion binding 6 12
GO:0043167 ion binding 2 12
GO:0043169 cation binding 3 12
GO:0046872 metal ion binding 4 12
GO:0046914 transition metal ion binding 5 12

Putative motif mimicry

Leishmania From To Domain/Motif Score
CLV_C14_Caspase3-7 254 258 PF00656 0.408
CLV_C14_Caspase3-7 443 447 PF00656 0.391
CLV_NRD_NRD_1 136 138 PF00675 0.227
CLV_NRD_NRD_1 246 248 PF00675 0.424
CLV_PCSK_KEX2_1 119 121 PF00082 0.412
CLV_PCSK_KEX2_1 136 138 PF00082 0.243
CLV_PCSK_KEX2_1 246 248 PF00082 0.551
CLV_PCSK_PC1ET2_1 119 121 PF00082 0.412
CLV_PCSK_PC7_1 115 121 PF00082 0.447
CLV_PCSK_PC7_1 132 138 PF00082 0.130
CLV_PCSK_SKI1_1 247 251 PF00082 0.444
CLV_PCSK_SKI1_1 4 8 PF00082 0.441
CLV_PCSK_SKI1_1 418 422 PF00082 0.577
DEG_APCC_DBOX_1 245 253 PF00400 0.433
DEG_SCF_TRCP1_1 254 259 PF00400 0.421
DOC_ANK_TNKS_1 119 126 PF00023 0.415
DOC_CYCLIN_yClb1_LxF_4 379 384 PF00134 0.408
DOC_CYCLIN_yCln2_LP_2 15 21 PF00134 0.258
DOC_CYCLIN_yCln2_LP_2 376 382 PF00134 0.479
DOC_MAPK_gen_1 353 362 PF00069 0.648
DOC_MAPK_MEF2A_6 170 177 PF00069 0.308
DOC_PP1_RVXF_1 379 385 PF00149 0.407
DOC_PP2B_LxvP_1 376 379 PF13499 0.371
DOC_USP7_MATH_1 538 542 PF00917 0.411
DOC_USP7_UBL2_3 355 359 PF12436 0.445
LIG_14-3-3_CanoR_1 211 215 PF00244 0.441
LIG_14-3-3_CanoR_1 246 250 PF00244 0.494
LIG_14-3-3_CanoR_1 296 304 PF00244 0.535
LIG_14-3-3_CanoR_1 381 385 PF00244 0.371
LIG_14-3-3_CanoR_1 4 12 PF00244 0.302
LIG_14-3-3_CanoR_1 432 438 PF00244 0.446
LIG_14-3-3_CanoR_1 481 490 PF00244 0.437
LIG_Actin_WH2_2 368 383 PF00022 0.373
LIG_Actin_WH2_2 387 404 PF00022 0.398
LIG_Actin_WH2_2 494 512 PF00022 0.421
LIG_APCC_ABBA_1 166 171 PF00400 0.388
LIG_BIR_II_1 1 5 PF00653 0.495
LIG_BRCT_BRCA1_1 130 134 PF00533 0.487
LIG_BRCT_BRCA1_1 444 448 PF00533 0.526
LIG_FHA_1 381 387 PF00498 0.431
LIG_FHA_1 481 487 PF00498 0.496
LIG_FHA_1 5 11 PF00498 0.258
LIG_FHA_1 91 97 PF00498 0.256
LIG_FHA_2 224 230 PF00498 0.477
LIG_FHA_2 287 293 PF00498 0.462
LIG_KLC1_Yacidic_2 70 74 PF13176 0.511
LIG_LIR_Apic_2 463 469 PF02991 0.391
LIG_LIR_Gen_1 217 227 PF02991 0.383
LIG_LIR_Gen_1 228 239 PF02991 0.386
LIG_LIR_Gen_1 70 80 PF02991 0.678
LIG_LIR_Nem_3 217 223 PF02991 0.397
LIG_LIR_Nem_3 228 234 PF02991 0.460
LIG_LIR_Nem_3 314 319 PF02991 0.568
LIG_LIR_Nem_3 419 424 PF02991 0.450
LIG_LIR_Nem_3 445 451 PF02991 0.469
LIG_PDZ_Class_2 541 546 PF00595 0.367
LIG_SH2_NCK_1 220 224 PF00017 0.389
LIG_SH2_SRC 64 67 PF00017 0.495
LIG_SH2_STAP1 216 220 PF00017 0.527
LIG_SH2_STAP1 482 486 PF00017 0.486
LIG_SH2_STAT3 162 165 PF00017 0.258
LIG_SH2_STAT5 105 108 PF00017 0.355
LIG_SH2_STAT5 162 165 PF00017 0.243
LIG_SH2_STAT5 216 219 PF00017 0.317
LIG_SH2_STAT5 267 270 PF00017 0.516
LIG_SH2_STAT5 482 485 PF00017 0.578
LIG_SH2_STAT5 72 75 PF00017 0.589
LIG_SH3_1 78 84 PF00018 0.355
LIG_SH3_3 449 455 PF00018 0.355
LIG_SH3_3 78 84 PF00018 0.355
LIG_SUMO_SIM_anti_2 539 546 PF11976 0.353
LIG_SUMO_SIM_par_1 17 22 PF11976 0.211
LIG_SUMO_SIM_par_1 317 323 PF11976 0.591
LIG_WRC_WIRS_1 231 236 PF05994 0.360
LIG_WRC_WIRS_1 368 373 PF05994 0.416
MOD_CK1_1 128 134 PF00069 0.574
MOD_CK1_1 358 364 PF00069 0.513
MOD_CK1_1 367 373 PF00069 0.482
MOD_CK1_1 39 45 PF00069 0.365
MOD_CK2_1 191 197 PF00069 0.489
MOD_CK2_1 223 229 PF00069 0.491
MOD_CK2_1 286 292 PF00069 0.371
MOD_CK2_1 49 55 PF00069 0.519
MOD_GlcNHglycan 1 4 PF01048 0.399
MOD_GlcNHglycan 116 119 PF01048 0.447
MOD_GlcNHglycan 254 257 PF01048 0.403
MOD_GlcNHglycan 313 316 PF01048 0.470
MOD_GlcNHglycan 350 353 PF01048 0.575
MOD_GlcNHglycan 363 366 PF01048 0.487
MOD_GlcNHglycan 38 41 PF01048 0.286
MOD_GSK3_1 210 217 PF00069 0.532
MOD_GSK3_1 252 259 PF00069 0.353
MOD_GSK3_1 440 447 PF00069 0.473
MOD_GSK3_1 51 58 PF00069 0.352
MOD_GSK3_1 536 543 PF00069 0.330
MOD_N-GLC_1 23 28 PF02516 0.317
MOD_N-GLC_1 274 279 PF02516 0.507
MOD_N-GLC_1 348 353 PF02516 0.652
MOD_NEK2_1 127 132 PF00069 0.570
MOD_NEK2_1 150 155 PF00069 0.337
MOD_NEK2_1 173 178 PF00069 0.439
MOD_NEK2_1 260 265 PF00069 0.453
MOD_NEK2_1 324 329 PF00069 0.490
MOD_NEK2_1 348 353 PF00069 0.679
MOD_NEK2_1 36 41 PF00069 0.300
MOD_NEK2_1 380 385 PF00069 0.383
MOD_NEK2_1 420 425 PF00069 0.477
MOD_NEK2_1 48 53 PF00069 0.445
MOD_PIKK_1 150 156 PF00454 0.382
MOD_PIKK_1 295 301 PF00454 0.471
MOD_PIKK_1 408 414 PF00454 0.473
MOD_PIKK_1 453 459 PF00454 0.534
MOD_PK_1 440 446 PF00069 0.454
MOD_PKA_2 114 120 PF00069 0.427
MOD_PKA_2 210 216 PF00069 0.438
MOD_PKA_2 245 251 PF00069 0.433
MOD_PKA_2 252 258 PF00069 0.386
MOD_PKA_2 295 301 PF00069 0.592
MOD_PKA_2 380 386 PF00069 0.377
MOD_PKA_2 453 459 PF00069 0.577
MOD_PKA_2 480 486 PF00069 0.426
MOD_Plk_1 107 113 PF00069 0.399
MOD_Plk_1 223 229 PF00069 0.306
MOD_Plk_1 23 29 PF00069 0.272
MOD_Plk_1 256 262 PF00069 0.459
MOD_Plk_1 274 280 PF00069 0.481
MOD_Plk_1 322 328 PF00069 0.546
MOD_Plk_1 390 396 PF00069 0.405
MOD_Plk_2-3 191 197 PF00069 0.525
MOD_Plk_2-3 334 340 PF00069 0.585
MOD_Plk_4 191 197 PF00069 0.465
MOD_Plk_4 210 216 PF00069 0.469
MOD_Plk_4 274 280 PF00069 0.511
MOD_Plk_4 364 370 PF00069 0.606
MOD_Plk_4 390 396 PF00069 0.475
MOD_Plk_4 444 450 PF00069 0.413
MOD_Plk_4 540 546 PF00069 0.358
TRG_ENDOCYTIC_2 220 223 PF00928 0.388
TRG_ENDOCYTIC_2 72 75 PF00928 0.663
TRG_ER_diArg_1 135 137 PF00400 0.272
TRG_ER_diArg_1 245 247 PF00400 0.536
TRG_ER_diArg_1 32 35 PF00400 0.308
TRG_ER_diArg_1 399 402 PF00400 0.406
TRG_Pf-PMV_PEXEL_1 422 427 PF00026 0.372

Homologs

Protein Taxonomy Sequence identity Coverage
A0A0N1I9X5 Leptomonas seymouri 66% 99%
A0A0S4IQV6 Bodo saltans 43% 98%
A0A1X0P2R0 Trypanosomatidae 49% 95%
A0A3Q8IC39 Leishmania donovani 82% 100%
A0A3R7M632 Trypanosoma rangeli 50% 97%
A4I5R4 Leishmania infantum 82% 100%
C9ZR32 Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) 37% 97%
E9B109 Leishmania mexicana (strain MHOM/GT/2001/U1103) 81% 100%
Q4Q757 Leishmania major 80% 100%
Q9D2H5 Mus musculus 23% 76%
V5DCZ6 Trypanosoma cruzi 51% 97%

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LeishMANIAdb - Server version: v0.0.2. - Database version: v0.0.1. - ChangeLog - © 2022-2025 Protein Bioinformatics Research Group, Institute of Enzymology, RCNS