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1ZZ1

Crystal structure of a HDAC-like protein with SAHA bound

Functional Information from GO Data
ChainGOidnamespacecontents
A0016787molecular_functionhydrolase activity
A0046872molecular_functionmetal ion binding
B0016787molecular_functionhydrolase activity
B0046872molecular_functionmetal ion binding
C0016787molecular_functionhydrolase activity
C0046872molecular_functionmetal ion binding
D0016787molecular_functionhydrolase activity
D0046872molecular_functionmetal ion binding
Functional Information from PDB Data
site_idAC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN A 2451
ChainResidue
AASP180
AHIS182
AASP268
ASHH2452

site_idAC2
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN B 2551
ChainResidue
BASP180
BHIS182
BASP268
BSHH2552

site_idAC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN C 2651
ChainResidue
CHIS182
CASP268
CSHH2652
CASP180

site_idAC4
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN D 2751
ChainResidue
DASP180
DHIS182
DASP268
DSHH2752

site_idAC5
Number of Residues5
DetailsBINDING SITE FOR RESIDUE K A 2450
ChainResidue
AASP178
AASP180
AHIS182
ASER201
ALEU202

site_idAC6
Number of Residues5
DetailsBINDING SITE FOR RESIDUE K B 2550
ChainResidue
BASP178
BASP180
BHIS182
BSER201
BLEU202

site_idAC7
Number of Residues5
DetailsBINDING SITE FOR RESIDUE K C 2650
ChainResidue
CASP178
CASP180
CHIS182
CSER201
CLEU202

site_idAC8
Number of Residues5
DetailsBINDING SITE FOR RESIDUE K D 2750
ChainResidue
DASP178
DASP180
DHIS182
DSER201
DLEU202

site_idAC9
Number of Residues5
DetailsBINDING SITE FOR RESIDUE K A 2449
ChainResidue
ATRP191
AASP194
AVAL197
ATYR226
AHOH2501

site_idBC1
Number of Residues5
DetailsBINDING SITE FOR RESIDUE K B 2549
ChainResidue
BTRP191
BASP194
BVAL197
BTYR226
BHOH2604

site_idBC2
Number of Residues6
DetailsBINDING SITE FOR RESIDUE K C 2649
ChainResidue
CTRP191
CASP194
CVAL197
CTYR226
CHOH2767
CHOH2774

site_idBC3
Number of Residues5
DetailsBINDING SITE FOR RESIDUE K D 2749
ChainResidue
DTRP191
DASP194
DVAL197
DTYR226
DHOH2822

site_idBC4
Number of Residues12
DetailsBINDING SITE FOR RESIDUE SHH A 2452
ChainResidue
AASP98
AILE100
AHIS142
AHIS143
APHE152
AASP180
AHIS182
APHE208
AASP268
ATYR312
AZN2451
AHOH2583

site_idBC5
Number of Residues14
DetailsBINDING SITE FOR RESIDUE SHH B 2552
ChainResidue
BLEU21
BASP98
BILE100
BHIS142
BHIS143
BPHE152
BASP180
BHIS182
BPHE208
BASP268
BTYR312
BZN2551
BHOH2739
CPHE341

site_idBC6
Number of Residues11
DetailsBINDING SITE FOR RESIDUE SHH C 2652
ChainResidue
CASP98
CILE100
CHIS142
CHIS143
CPHE152
CASP180
CHIS182
CPHE208
CASP268
CTYR312
CZN2651

site_idBC7
Number of Residues11
DetailsBINDING SITE FOR RESIDUE SHH D 2752
ChainResidue
DHIS182
DPHE208
DASP268
DTYR312
DZN2751
DHOH2897
DILE100
DHIS142
DHIS143
DPHE152
DASP180

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: Proton donor/acceptor => ECO:0000250|UniProtKB:Q48935
ChainResidueDetails
AALA144
BALA144
CALA144
DALA144

site_idSWS_FT_FI2
Number of Residues12
DetailsBINDING: BINDING => ECO:0000269|PubMed:27756124, ECO:0007744|PDB:5G1C
ChainResidueDetails
AVAL181
DVAL181
DHIS183
DALA269
AHIS183
AALA269
BVAL181
BHIS183
BALA269
CVAL181
CHIS183
CALA269

site_idSWS_FT_FI3
Number of Residues4
DetailsSITE: Polarizes the scissile carbonyl of the substrate => ECO:0000250|UniProtKB:Q48935
ChainResidueDetails
ASER313
BSER313
CSER313
DSER313

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PDB entries from 2024-07-24

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